Printer Friendly

Locus Coeruleus and Dopamine-Dependent Memory Consolidation.

1. Introduction

Many people have vivid memories of the first dinner date with their partner, including details like the name of the restaurant and the food they had. In contrast, it is very difficult to remember what you had for dinner a few weeks ago. Most everyday memories, including episodic-like memories that we may form automatically in the hippocampus (HPC) [1-3], are forgotten, whereas some of them are retained for a long time by a memory stabilization process (initial memory consolidation). Initial selective retention occurs when something novel or salient happens shortly before or after the time of memory encoding, as in "flashbulb memory" [4, 5]. Unexpected novel events create a "halo" of enhanced memory, triggering an initial memory consolidation which extends not only forwards but also backwards in time, boosting retention of trivial memories that would normally be forgotten. Thus, initial consolidation serves as the "gate" to long-term memory, so that only a subset of information is retained for long enough to be subject to stabilization in the neocortex via a complementary process of "systems memory consolidation" [6, 7].

Animal studies of novelty-associated enhancement of memory persistence have enabled analysis of possible mechanisms [8-13] and established that novelty-triggered initial memory consolidation is sensitive to blockade of dopamine (DA) [D.sub.1]/[D.sub.5] receptors and protein synthesis inhibitors in HPC. Pharmacological studies of hippocampal synaptic plasticity have supported the notion that [D.sub.1]/[D.sub.5] receptors act as a gating mechanism for long-term persistence of plastic changes [14,15]. However, the literature remains unclear and often contradictory regarding the neuronal source of DA in HPC. An influential hypothesis called the "HPC-VTA (ventral tegmental area) loop" model, proposed over a decade ago [16], postulates that tyrosine hydroxylase- (T[H.sup.+]-) expressing neurons of VTA project to the hippocampal formation [17, 18] and release DA under circumstances of novelty or surprise [16, 19]. Nevertheless, VTA-T[H.sup.+] axons are sparse in HPC [17,18], raising a possibility that other sources of DA, including dense T[H.sup.+] axons from the locus coeruleus (LC), might play a significant role [20, 21].

To seek the neuronal source of hippocampal DA that mediates the beneficial effect of novelty on memory persistence, we combined an optogenetic approach with an everyday memory task in mice. Surprisingly, we found that LC-T[H.sup.+] neurons, originally defined by their canonical noradrenaline (NA) signaling, mediate postencoding novelty-associated enhancement of memory retention in a manner consistent with possible corelease of DA along with NA in HPC [22] (Figure 1(a)). Our results are complemented by the subsequent direct detection of DA corelease from LC axons in HPC [23]. In this review paper, we discuss the following issues with focus on the LC-DA system: (i) a role of hippocampal [D.sub.1]/[D.sub.5] receptors in the novelty-induced memory enhancement, (ii) two distinct novelty systems (VTA-HPC and LC-HPC systems) of dopamine-releasing (DAergic) memory modulation, (iii) brain areas that might convey environmental novelty signal to HPC, (iv) molecular and anatomical basis for [D.sub.1]/[D.sub.5] receptor-mediated signaling in HPC, and (v) proteins that might mediated the environmental novelty-associated memory enhancement in HPC.

2. Novelty-Induced Memory Enhancement Depends on [D.sub.1]/[D.sub.5] Receptors in HPC

Activity-dependent hippocampal synaptic plasticity (long-term potentiation (LTP) and long-term depression (LTD)) may underpin the neural mechanisms of hippocampus-dependent learning and memory [3, 13, 24, 25]. Frey and colleagues [26] established the separate existence of early- and late-forms of LTP (E-LTP and L-LTP, resp.) in the hippocampal CA1 region, the latter being defined as protein synthesis dependent. Their work also provided the first experimental evidence suggesting that neuromodulators, especially DA, play a significant role in the transition from E-LTP to L-LTP at CA3-CA1 synapses [27]. DA effects are essentially heterosynaptic rather than homosynaptic (i.e., activity of DAergic inputs affect the strength of other synapses). Hippocampal [D.sub.1]/[D.sub.5] receptors play a specific role in control of temporal persistence of LTP at CA3-CA1 synapses ex vivo [12, 14, 15, 28-30]. In awake animals, [D.sub.1]/[D.sub.5] receptor activation is crucial for persistence of LTP in CA1, confirming the results ex vivo [10, 28]. Pharmacological manipulations of hippocampal [D.sub.1]/[D.sub.5] receptors also indicate that DA is required for the persistence of memories including aversive contextual [31-34], spatial [35, 36], object recognition [33] and paired associate [37] learning. Interestingly, Karunakaran and colleagues showed that learning-induced plasticity of hippocampal parvalbumin neurons was specifically required for long-term memory consolidation through [D.sub.1]/[D.sub.5] receptors [38]. Although hippocampal [D.sub.1]/[D.sub.5] receptors may play a disproportionate role in the persistence of hippocampal memory, it has also been implicated in facilitating the induction of ELTP (reviewed in [21]) and, thereby, the entry of information into earlier memory [39].

Since available pharmacological agonists and antagonists of dopamine [D.sub.1]-like receptors do not discriminate [D.sub.1] and [D.sub.5] receptors [40], numerous gene knockout studies were conducted in order to elucidate the precise function of [D.sub.1] and [D.sub.5] receptors in roles of hippocampal synaptic plasticity and memory [41-47] (reviewed in [21]). Yet, differentiating the function of hippocampal [D.sub.1] and [D.sub.5] receptors may seem like a daunting task, because there is a caveat in global knockout studies in that they lack regional selectivity. To overcome this issue, Sarinana and colleagues developed knockout mice lacking either [D.sub.1] or [D.sub.5] receptors selectively in granule cells of the dentate gyrus (DG) [48]. They demonstrated that DG-[D.sub.1] receptor deletion, but not DG-[D.sub.5] receptor deletion, impairs persistence of memory in contextual fear conditioning, highlighting the role of DG-[D.sub.1] receptors in gating persistence of hippocampus-dependent memory (but also see [28]). It should be noted, however, that [D.sub.5] receptor mRNA is also expressed strongly in the CA3 and CA1 [48] and LTP at CA3-CA1 synapses ex vivo and spatial memory are impaired in [D.sub.5] receptor global knockout mice [47]. Thus, it is also possible that hippocampal [D.sub.5] receptor outside DG could have an important role in the persistence of hippocampus-dependent memory.

There are many lines of evidence suggesting that the persistence of memory is determined largely by neural activity that occurs at the time of memory encoding. However, the synaptic tagging and capture (STC) hypothesis of protein synthesis-dependent LTP, developed by Frey and Morris [49-51], offers the intriguing but distinct perspective that the persistence of memory is also dependent on independent neural activity afferent to the same pool of neurons mediating synaptic plasticity that occurs before or after memory traces are encoded. According to this hypothesis, the local setting of "synaptic tags" at activated glutamatergic synapses during memory encoding can be dissociated from synthesis and distribution of plasticity-related proteins (PRPs) that is induced by surrounding events (e.g., unexpected novel events). PRPs are then captured by synaptic tags in order to stabilize synaptic changes--a process that is critical for initial memory consolidation.

Indeed, in vivo electrophysiological experiments showed that exploration of a novel environment results in facilitation of persistence of synaptic plasticity in the CA1 area [52]. This novelty-associated facilitation of persistence of synaptic plasticity in CA1 was prevented by a [D.sub.1]/[D.sub.5] receptor antagonist [10]. Also, considering that exploration of a novel environment leads to upregulation of immediate early genes (IEGs) such as Arc/Arg3.1 and Homer1a/Vesl-1S [8, 53], the STC hypothesis predicts that unrelated novelty exploration before or after memory encoding should enhance the persistence of a recently encoded memory [3]. This prediction was first confirmed using a hippocampus-dependent inhibitory avoidance task in rats [11]. Our group has developed an "everyday" memory task for rats and mice whose use has revealed that (i) unrelated novel experiences can facilitate the persistence of spatial memory and (ii) this novelty-induced enhancement of memory persistence was prevented by the intrahippocampal injection of a [D.sub.1]/[D.sub.5] receptor antagonist (but not by a [beta]-adrenoceptor receptor antagonist), or by blockade of hippocampal protein synthesis [12, 13, 22]. Complementary results have been obtained using different learning tasks including inhibitory avoidance, taste memory, object recognition, and contextual fear conditioning [54-58]. Interestingly, Moncada and colleagues showed that novelty-induced memory persistence is also sensitive for hippocampal [beta]-adrenoceptor blockade in inhibitory avoidance test [56], in line with in vivo electrophysiological results that there are a [D.sub.1]/[D.sub.5] receptor-independent mechanism of STC hypothesis [59]. Recently, Nomoto and colleagues elegantly showed that a [D.sub.1]/[D.sub.5] receptor-dependent mechanism shared hippocampal neural ensemble for a weak object recognition memory and unrelated novelty is necessary for novelty-induced enhancement of memory persistence [60].

3. Two Distinct Novelty Systems of Dopaminergic Memory Modulation in HPC

The prevailing "HPC-VTA loop" model of DAergic consolidation [16] postulates that novelty-associated enhancement of hippocampus-dependent memory is mediated by a subiculum-accumbens-pallidum- VTA-HPC pathway, an idea supported by animal and human studies [32, 61-63]. If this hypothesis holds, then it follows that HPC would receive an innervation from VTA-T[H.sup.+] neurons, environmental novelty would activate VTA-T[H.sup.+] neurons, and activation of VTAT[H.sup.+] neurons should be necessary and sufficient for novelty-induced enhancement of memory persistence. However, T[H.sup.+] axons from VTA mainly target to the ventral HPC [17, 18, 23, 64, 65] and T[H.sup.+] neurons represent only 10% of hippocampus-projecting neurons in VTA [17], resulting in a sparse projection in the dorsal HPC [22, 23]. Optetrode recordings revealed that VTA-T[H.sup.+] neurons were slightly activated by environmental novelty [22, 66]. Postencoding optogenetic activation of VTA-T[H.sup.+] neurons was without a significant effect on memory persistence. Moreover, pharmacological blockade of VTA-T[H.sup.+] neurons during environmental novelty had no effect on novelty-associated memory enhancement [22]. Importantly, the impact of "environmental novelty" may differ qualitatively from that of "reward-associated novelty." Reward expectancy is a critical component of the execution of learned actions until they become habitual [67]. Longstanding data point that the substantia nigra (SN)/VTA system thought to play important role for processing unexpected reward [68-70]. Such reward signals are primarily coded by DA, which modulates the synaptic connections in the striatum within a narrow time window [71]. Considering that memory retention is also enhanced by reward magnitude [12, 22, 72], we now hypothesize that VTA-HPC system might mediate reward-associated novelty which modulates the retention of memory with a narrow time window (Figure 1(b)). Keeping with this hypothesis, there was a narrow time window for impact of pharmacological VTA inactivation on both synaptic plasticity in vivo and memory in the passive avoidance task [73]. Optogenetic activation of hippocampus-projecting VTA-T[H.sup.+] axons can bidirectionally modulate CA3-CA1 synaptic responses ex vivo [74], and optogenetic activation of VTA-T[H.sup.+] axons in HPC at the time of learning enhances spatial memory after 1 hr [66]. Interestingly, VTA activation associated with visual novelty did not correlate with memory enhancement in humans [75]. In contrast, recent study in humans have demonstrated that postlearning SN/VTA-hippocampal interactions contribute to preferential retention of episodic memory that are learned in high-reward contexts [76].

Considering that DA acts not only as a neurotransmitter in its own right but also as the precursor for NA, T[H.sup.+] axons originating from the LC (A6, in rat nomenclature) [77] are another potential source of DA in HPC. The LC has long been implicated in novelty, attention, arousal, and cognition [78-83], and its firing is tied to distinct changes in neocortical activation during sleep [84]. The LC receives prominent direct inputs from many cortical and subcortical areas and sends extensive projections throughout the brain and spinal cord with the exception of the basal ganglia and SN, all of which are dense with axonal projections or cell bodies of DAergic SN/VTA neurons [85, 86]. Dense innervation of all hippocampal areas by LC axons has been demonstrated by prior anatomical studies (Figure 2(a)) [87-93]. Recently, cell type-specific tract tracing experiments have confirmed these observations and further established that T[H.sup.+] axons from LC far outnumber those from VTA (Figure 2(b)) [22, 23]. The LC has two different types of firing patterns: constant "tonic" activity (1-3 Hz) and intermittent "phasic" impulse activity (8-10 Hz) [78], that have been correlated to different behavioural states [94]. The LC neurons are activated in response to environmental novelty that habituates over time (Figures 2(c) and 2(d)) [22, 95, 96].

Pharmacological inhibition of LC prevents the beneficial effect of environmental novelty on memory persistence [22]. Critically, postencoding optogenetic activation of LC-T[H.sup.+] neurons mimics this environmental novelty effect (Figure 3(d)). Surprisingly, this LC-T[H.sup.+] neuron photoactivation-driven memory enhancement is sensitive to hippocampal [D.sub.1]/[D.sub.5] receptor blockade and resistant to [beta]-adrenoceptor blockade (Figure 3(d)). In line with these results, electrical activation of LC results in persistent synaptic plasticity at CA3-CA1 synapses in vivo, which is prevented by [D.sub.1]/[D.sub.5] receptor antagonist (Figure 3(b)) [52]. Furthermore, selective optogenetic activation of hippocampus-projecting LC-T[H.sup.+] axons mediates a [D.sub.1]/[D.sub.5] receptor-sensitive and [beta]-adrenoceptor-resistant enhancement of synaptic transmission and LTP at CA3-CA1 synapses ex vivo [22], consistent with the idea that LC-T[H.sup.+] might release DA in HPC [20, 97]. Our results are complemented by the subsequent direct detection of DA core-lease along with NA from LC-T[H.sup.+] axons in HPC (Figure 3 e)) ([23]. Taken together, these observations collectively indicate that LC-HPC system is activated by environmental novelty and mediates postencoding memory enhancement via the non canonical release of DA in HPC (Figure 1(a)).

In contrast, a recent study showed that electrical activation of LC can mimic the beneficial effect of environmental novelty on memory persistence of the inhibitory avoidance and spatial object recognition tasks in rats in a hippocampal [beta]-adrenoceptor-sensitive manner [61]. Further studies will be required to access how the DAergic and noradrenergic systems interact mechanistically in processing environmental novelty in HPC.

It is not yet clear, however, how the environmental novelty signal reaches the LC-T[H.sup.+] neurons. Computational models [98] have proposed that novelty is computed in the hippocampal CA1 through a process that compares the "predictions" that arrive from CA3 via the Schaffer collaterals with the "reality" that arrives directly from the neocortex via the perforant path. According to this view, CA1 acts as a "comparator" that detects mismatches between predictions from CA3 and actual sensory input from the neocortex [16]. Based on this model, one possibility is that novelty detection occurs in HPC, which then activates LC-T[H.sup.+] neurons that project back to HPC. There has been, however, little direct empirical evidence to support the CA1 comparator model so far. In addition, a recent study [86] found no direct projections from HPC to LC-T[H.sup.+] neurons. Therefore, it is likely that the environmental novelty signal reaches LC-T[H.sup.+] neurons from HPC via a relay (e.g., the medial prefrontal cortex [99]). Second possibility is that LC-HPC projection is part of a parallel circuit independent of the HPC-VTA loop. There are many areas of the brain that will respond stronger to novel stimuli. Among them, the superior colliculus shows strong response to novel visual stimuli [100] as well as novel multisensory information [101]. Neurons in the superior colliculus habituate their novelty response over time in a similar way to the environmental novelty-associated response in LC neurons. It is also noted that the superior colliculus constitutes a large fraction of direct synaptic input to LC-T[H.sup.+] neurons [86].

4. Molecular and Anatomical Basis for [D.sub.1]/[D.sub.5] Receptor-Mediated Signaling in HPC

In catecholamine synthesis pathway, TH is the rate-limiting enzyme under basal conditions. However, when D[beta]H (dopamine-[beta]- hydroxylase), the enzyme that converts DA to NA in synaptic vesicles of LC-T[H.sup.+] terminals, becomes saturated and rate limiting [102, 103], not all of the DA in the vesicle is converted to NA, and the probability of corelease of DA and NA would increase. In support of this hypothesis, it has been demonstrated that chemical and electrical stimulation of LC neurons elicits release of both DA and NA in the medial prefrontal cortex (Figure 3(a)) [97, 104-106] and HPC [107, 108]. Smith and Greene were the first to provide direct electrophysiological evidence for this idea (Figure 3(c)) [20]. More recent optogenetic studies have further provided physiological and biochemical evidence for noncanonical release of DA from LC-T[H.sup.+] axons in HPC (Figures 3(d) and 3(e)) [22, 23]. Taken together, it is thus plausible that LC-T[H.sup.+] axons are the source of DA in the dorsal HPC.

In DA signaling, dopamine transporter- (DAT-) mediated reuptake plays a key role in limiting DA diffusion and defining DA transients [109]. Similar to the sparse expression in the medial prefrontal cortex [110, 111], however, DAT expression is extremely low in HPC [112-114]. Instead, norepinephrine transporter (NET), which also has an affinity for DA [97, 115, 116], is abundantly expressed on the plasma membrane of LC-T[H.sup.+] axons in HPC. As is the case for the medial prefrontal cortex [117], heterologous reuptake by NET contributes to the clearance of DA in HPC [118, 119]. Although the difference between the kinetics and efficacy of DA reuptake by DAT and NET remains elusive, the major DA clearance system in HPC is similar to the medial prefrontal cortex, where slow and sustained pattern of DA release is observed during a large variety of cognitive and motivational functions [120].

Now that it has been established that LC-T[H.sup.+] axons are likely to be an essential constituent of DA signaling in the dorsal HPC, it is imperative to further explore their distribution patterns and as well as their connectivity with hippocampal principal neurons and various types of interneurons. As consistently demonstrated in prior studies by D[beta]H immunohistochemistry as well as autoradiography [88, 89, 91, 93], there are some regional and laminar differences in innervation density of LC axons. To summarize simply, LC innervation covers the entire HPC, and it is especially high in DG. Laminar distribution pattern is also different depending on subregions. In the subiculum and CA1, the density of LC axons is clearly higher in the stratum lacunosum moleculare. In CA3, the highest density is found in the stratum lucidum, where mossy fibers of DG granule cells make synapses on pyramidal neurons. In DG, it is the highest in the polymorph layer in the hilus and the lowest in the granule cell layer (but see [23]). It should be also noted that the density of LC axon is moderately high in the molecular layer. Thus, the differential distribution pattern within each region suggests that the cellular targets of LC-T[H.sup.+] axons might differ depending on the subregions. Furthermore, considering that different subregions exercise distinct functions in information processing within HPC [121], it would be noteworthy that the densest regional LC-T[H.sup.+] innervations in HPC are those of the DG and subiculum, which correspond to its main cortical input and output stations, respectively [122, 123].

Of further consideration is whether specialized DA release sites exist on LC-T[H.sup.+] axons, and if so, how these DA release sites are distributed in HPC, especially in relation to localisation of [D.sub.1] and [D.sub.5] receptors. In this regard, we are still at the very beginning of the path to get the whole picture. For example, the synaptic profile of T[H.sup.+] axons in HPC is still a controversial issue. Previous immunoelectron microscopic analyses have shown that T[H.sup.+] axons often make direct contact with pyramidal neurons and [gamma]-aminobutyric acid-releasing (GABAergic) interneurons [90, 124, 125]. Even at such contact sites, however, the great majority of them do not form synapse-like specializations, including uniform cleft width between the apposed membranes and thickening of the apposed membranes [90, 125, 126]. By contrast, a small fraction of them seem to make symmetrical synapses with soma and dendritic shaft of GABAergic interneurons [90]. In recent years, however, it has become clear that morphologically defined "DA synapse," which is formed between T[H.sup.+] terminals and dendritic elements that exhibit ultrastructural features of symmetrical synapses, is not likely to be the site of DA transmission. Specifically, [D.sub.1] receptors are almost exclusively located at the extrasynaptic membrane [127, 128] and not localized to DA synapses [129]. Thus, future studies are required to determine the release site of DA in LC-T[H.sup.+] axons and their spatial relationship with [D.sub.1] and [D.sub.5] receptors in HPC.

Our current knowledge regarding the expression pattern of [D.sub.1] and [D.sub.5] receptors in HPC is still limited and inconclusive [48, 130-138]. Distribution of [D.sub.1]/[D.sub.5] receptors in HPC was first demonstrated by binding studies using radio-labelled ligands. Although the signal intensity in HPC is much lower than in "DA-rich regions" such as the striatum, low to moderate levels of binding to [D.sub.1]/[D.sub.5] receptors are observed in the molecular layer of DG [130, 139-142]. In situ hybridization studies have further uncovered differential expression patterns of [D.sub.1] receptor mRNA in the ventral and dorsal HPC. [D.sub.1] receptor mRNA is expressed in dispersed cells in CA3/ CA1 and DG in the ventral HPC, while it is mainly expressed in DG granule cells in the dorsal HPC [48, 130, 142]. These observations are further supported by a recent study on transgenic mice expressing eGFP (enhanced green fluorescent protein) under control of the [D.sub.1] receptor promotor, which shows that it is mainly expressed in DG granule cells and a subset of GABAergic interneurons in the hilus and CA1/CA3 [137,138]. In spite of this clear expression pattern, subcellular distribution of [D.sub.1] receptor remains elusive, mainly because [D.sub.1] receptor protein expression in HPC is quite low compared with the striatum. In situ hybridization studies have consistently shown that [D.sub.5] receptor mRNA is dominantly expressed in HPC [48, 131-133]. At the cellular level, there is a consensus that [D.sub.5] receptor is expressed in pyramidal neurons in CA1/CA3 and granule cells in DG [48,131-134]. However, further analyses are needed in order to determine its subcellular localization and expression in GABAergic interneurons.

It is now widely accepted that DA receptors can form both homomers and heteromers with several other classes of receptors, including other G protein-coupled receptors (GPCRs) and ionotropic receptors [143, 144]. [D.sub.1] receptor directly couples with the GluN1 and GluN2A subunits of the N-methyl-D-aspartate (NMDA) receptor and modulates the NMDA receptor currents [145, 146]. Recently, Kern and colleagues showed that [D.sub.1] receptor and ghrelin receptor form heteromers in a complex with Gaq and initiate a noncanonical cAMP-independent signaling pathway that regulate DA-dependent hippocampal synaptic plasticity and memory [147]. Similarly, [D.sub.5] receptor directly couples to the y2 subunit of the GABA subtype-A receptor, modulating the inhibitory current [148].

5. Plasticity-Related Proteins and Novelty-Associated Memory Enhancement in HPC

Optogenetic activation of hippocampus-projecting LC-T[H.sup.+] axons at the time of learning enhances a [D.sub.1]/[D.sub.5] receptor-sensitive 24 hr memory in a spatial object recognition task [23]. However, from the perspective of the STC hypothesis [49, 51], our behavioural protocol [22], in which there is a 30 min delay between encoding and exposure to environmental novelty, can dissociate the encoding phase from the consolidation processes. It could allow us to exclude the possibility of DAergic modulation of memory encoding via, for example, changes in attention [23, 149] and alterations in CREB- (cyclic adenosine monophosphate response element-binding protein-) mediated changes in neuronal excitability [150]. Our proposed mechanism for postencoding environmental novelty-associated memory enhancement is as follows: hippocampal [D.sub.1]/[D.sub.5] receptor activation induced by environmental novelty triggers nuclear gene transcription and nuclear/dendritic synthesis and distribution of PRPs that are captured by "synaptic tags" in order to stabilize synaptic changes within hippocampal excitatory neurons [51].

Pharmacological activation of [D.sub.1]/[D.sub.5] receptors enhances Zif268/Egr-1/Krox-24 and Arc expression in DG in vivo [151]. [D.sub.1]/Dg receptor activation also stimulates local protein synthesis in the dendrites of hippocampal neuron in vitro [152, 153]. On the other hand, LTP-induced expression of Zif268 and Arc in CA1 is significantly reduced in global [D.sub.1] receptor knockout mice [44, 46]. It has been established that exploration of a novel environment causes upregulation of several IEGs in HPC [8, 154-156]. However, important questions remain open regarding the specific role of particular PRPs in novelty-induced enhancement of memory persistence. Although several proteins, including Homer1a, Arc, BDNF (brain-derived neurotrophic factor), AMPA ([alpha]-amino-3-hydroxy-5-methyl-4-isoxazole propionate) receptor, actin and PKM[zeta] (protein kinase M[zeta]), have been suggested as possible key mediators of persistence of long-lasting synaptic plasticity and memory [157], they only provide partial explanations of the phenomenon. For example, synaptic activity-induced Homer1a and Arc gene products are targeted to active or inactive synapses, respectively, in vitro [158, 159], but their roles in environmental novelty-induced memory persistence remain largely unexplored.

The local setting of synaptic tags and the capture of PRPs by tagged synapses might have occurred in activated dendritic spines at glutamatergic synapses in HPC. The capture of PRPs by tagged synapses, critical for initial memory consolidation, results in an increase of both the strength of the synaptic transmission ("functional plasticity") and volume of dendritic spines ("structural plasticity") [51]. Functional and structural plasticity is thought to involve the insertion of AMPA receptors at the postsynaptic membrane [160] and the remodelling of actin cytoskeleton [161, 162], respectively. Thus, we predict the features of PRPs to be as follows: PRPs are (i) enriched in dendritic spines and (ii) involved in the regulation of AMPA receptor trafficking and/or remodelling of actin cytoskeleton. It has been reported that 1755 gene products are enriched in postsynaptic dendritic spines (SynaptomeDB, SynaptomeDB/index.php [163]).

One possible experiment for identifying key PRPs critical for environmental novelty-induced memory boost would be translational profiling acquired under different behavioural and physiological conditions (Figure 4). The intellectual background to this approach is STC hypothesis [49, 51] whereby the mechanisms mediating memory encoding (tag-setting) and consolidation (sequestration of PRPs) are independent events. Previous results [164] support this dissociation between tag-setting (calcium/calmodulin-dependent protein kinase (CaMK) II signaling pathway) and the availability of PRPs (CaMKIV signaling pathway). The critical test session after which tissue is taken would include novelty exploration and optogenetic activation of LC-T[H.sup.+] neurons that can enhance memory retention (Figure 4(a)) [22]. In addition, it would include photoactivation of LCT[H.sup.+] neurons with systemic injection of [D.sub.1]/[D.sub.5] receptor antagonist that might block the relevant synthesis of PRPs mediated by DAergic signaling in hippocampal neurons. These conditions would be compared to a baseline home cage condition. Recently developed techniques "TRAP" (translating ribosome affinity purification) (Figure 4(b)) [165] and "BONCAT" (bioorthogonal noncanonical amino acid tagging) (Figure 4(c)) [153] allow us to selectively isolate translated mRNAs and newly synthesized proteins during the critical test session, respectively. Translational profiles acquired under different behavioural and physiological conditions would be then compared (Figure 4(d)). Specifically, comparisons among a subset of genes translated in these different conditions can be used to zero-in on candidate PRPs.

If candidate PRPs would be identified, the next logical step is to assess whether the candidate PRPs are preferentially targeted to activated spines using two-photon glutamate uncaging with time-lapse imaging [166]. Subsequently, it is imperative to characterise the function of the candidate PRPs that are induced by environmental novelty in novelty-associated enhancement of memory persistence. Methods to optically control the activity of specific proteins [167], when available, would allow us to disable the function of the candidate PRPs by illumination with light during initial memory consolidation in a spatially and temporally precise manner (Figure 4(e)). These sets of experiments would identify key PRPs that mediate novelty-associated enhancement of memory persistence within excitatory neurons in HPC. Among the brain disorders, the breakdown of memory (associated with stress, aging, and age-associated disorders) causes great concern. Identification of proteins that enhance retention of everyday memory will have the potential to reveal new drug targets for treatment or restoration of lost memory function. These proteins will also constitute good candidates for "biomarkers" for impairments such as forgetfulness and age-associated memory decline.

6. Conclusions

Most everyday memories may form automatically in HPC. The key role of this memory system is to filter our unnecessary information but keep the important memories by a mechanism that involves novelty-associated DA release in HPC. Recent optogenetic studies have revealed that projections from noradrenergic LC-T[H.sup.+] neurons to HPC can drive the postencoding environmental novelty-associated enhancement of memory retention through noncanonical release of DA in HPC. These studies also raise an intriguing possibility that the impact of environmental novelty may differ qualitatively from that of reward-associated novelty and projections from VTA-T[H.sup.+] neurons to HPC might mediate reward-associated novelty which modulates the memory retention with a narrow time window. Initial consolidation triggered by two distinct dopaminergic novelty systems could help make encoded memory traces last long enough for the effective function of the more extended process of system consolidation by which hippocampus-dependent memories guide the eventual stabilization of neocortical memory networks.

Conflicts of Interest

No competing interests exist.


This study is supported by grants from The Naito Foundation (Miwako Yamasaki) and The RS MacDonald Seedcorn Fund, Edinburgh Neuroscience (Tomonori Takeuchi). The authors thank Noboru Komiyama, Hiroshi Ichinose, Adrian Duszkiewicz, Lisa Genzel, Isabella Wagner, Duda Kvitsiani, Sadegh Nabavi, Tobias Bast, Masahiko Watanabe, and Robert Greene for the scientific discussion.


[1] D. Marr, "Simple memory: a theory for archicortex," Philosophical Transactions of the Royal Society of London Series B: Biological Sciences, vol. 262, no. 841, pp. 23-81, 1971.

[2] M. Moscovitch, "Recovered consciousness: a hypothesis concerning modularity and episodic memory," Journal of Clinical and Experimental Neuropsychology, vol. 17, no. 2, pp. 276-290, 1995.

[3] R. G. Morris, "Elements of a neurobiological theory of hippocampal function: the role of synaptic plasticity, synaptic tagging and schemas," The European Journal of Neuroscience, vol. 23, no. 11, pp. 2829-2846, 2006.

[4] R. Brown and J. Kulik, "Flashbulb memories," Cognition, vol. 5, no. 1, pp. 73-99, 1977.

[5] J. E. Dunsmoor, V. P. Murty, L. Davachi, and E. A. Phelps, "Emotional learning selectively and retroactively strengthens memories for related events," Nature, vol. 520, no. 7547, pp. 345-348, 2015.

[6] L. R. Squire, "Memory and the hippocampus: a synthesis from findings with rats, monkeys, and humans," Psychological Review, vol. 99, no. 2, pp. 195-231, 1992.

[7] Y. Dudai and M. RGM, "To consolidate or not to consolidate: what are the questions?," in Brain, Perception and Memory: Advances in Cognitive Sciences, J. Bolhuis, Ed., pp. 147-162, OUP, Oxford, 2001.

[8] J. F. Guzowski, B. L. McNaughton, C. A. Barnes, and P. F. Worley, "Environment-specific expression of the immediate-early gene arc in hippocampal neuronal ensembles," Nature Neuroscience, vol. 2, no. 12, pp. 1120-1124, 1999.

[9] S. Li, W. K. Cullen, R. Anwyl, and M. J. Rowan, "Dopamine-dependent facilitation of LTP induction in hippocampal CA1 by exposure to spatial novelty," Nature Neuroscience, vol. 6, no. 5, pp. 526-531, 2003.

[10] N. Lemon and D. Manahan-Vaughan, "Dopamine [D.sub.1]/[D.sub.5] receptors gate the acquisition of novel information through hippocampal long-term potentiation and long-term depression," The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, vol. 26, no. 29, pp. 7723-7729, 2006.

[11] D. Moncada and H. Viola, "Induction of long-term memory by exposure to novelty requires protein synthesis: evidence for a behavioral tagging," The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, vol. 27, no. 28, pp. 7476-7481, 2007.

[12] S. H. Wang, R. L. Redondo, and R. G. Morris, "Relevance of synaptic tagging and capture to the persistence of long-term potentiation and everyday spatial memory," Proceedings of the National Academy of Sciences of the United States of America, vol. 107, no. 45, pp. 19537-19542, 2010.

[13] T. Takeuchi, A. J. Duszkiewicz, and R. G. Morris, "The synaptic plasticity and memory hypothesis: encoding, storage and persistence," Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences, vol. 369, no. 1633, article 20130288, 2014.

[14] U. Frey, H. Matthies, and K. G. Reymann, "The effect of dopaminergic [D.sub.1] receptor blockade during tetanization on the expression of long-term potentiation in the rat CA1 region in vitro," Neuroscience Letters, vol. 129, no. 1, pp. 111-114, 1991.

[15] Y. Y. Huang and E. R. Kandel, "[D.sub.1]/[D.sub.5] receptor agonists induce a protein synthesis-dependent late potentiation in the CA1 region of the hippocampus," Proceedings of the National Academy of Sciences of the United States of America, vol. 92, no. 7, pp. 2446-2450, 1995.

[16] J. E. Lisman and A. A. Grace, "The hippocampal-VTA loop: controlling the entry of information into long-term memory," Neuron, vol. 46, no. 5, pp. 703-713, 2005.

[17] A. Gasbarri, C. Verney, R. Innocenzi, E. Campana, and C. Pacitti, "Mesolimbic dopaminergic neurons innervating the hippocampal formation in the rat: a combined retrograde tracing and immunohistochemical study," Brain Research, vol. 668, no. 1-2, pp. 71-79, 1994.

[18] A. Gasbarri, A. Sulli, and M. G. Packard, "The dopaminergic mesencephalic projections to the hippocampal formation in the rat," Progress in Neuro-Psychopharmacology & Biological Psychiatry, vol. 21, no. 1, pp. 1 -22, 1997.

[19] J. Lisman, A. A. Grace, and E. Duzel, "A neoHebbian framework for episodic memory; role of dopamine-dependent late LTP," Trends in Neurosciences, vol. 34, no. 10, pp. 536-547, 2011.

[20] C. C. Smith and R. W. Greene, "CNS dopamine transmission mediated by noradrenergic innervation," The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, vol. 32, no. 18, pp. 6072-6080, 2012.

[21] N. Hansen and D. Manahan-Vaughan, "Dopamine [D.sub.1]/[D.sub.5] receptors mediate informational saliency that promotes persistent hippocampal long-term plasticity," Cerebral Cortex, vol. 24, no. 4, pp. 845-858, 2014.

[22] T. Takeuchi, A. J. Duszkiewicz, A. Sonneborn et al., "Locus coeruleus and dopaminergic consolidation of everyday memory," Nature, vol. 537, no. 7620, pp. 357-362, 2016.

[23] K. A. Kempadoo, E. V. Mosharov, S. J. Choi, D. Sulzer, and E. R. Kandel, "Dopamine release from the locus coeruleus to the dorsal hippocampus promotes spatial learning and memory," Proceedings of the National Academy of Sciences of the United States of America, vol. 113, no. 51, pp. 14835-14840, 2016.

[24] T. V. Bliss and G. L. Collingridge, "A synaptic model of memory: long-term potentiation in the hippocampus," Nature, vol. 361, no. 6407, pp. 31-39, 1993.

[25] R. C. Malenka and M. F. Bear, "LTP and LTD: an embarrassment of riches," Neuron, vol. 44, no. 1, pp. 5-21, 2004.

[26] U. Frey, M. Krug, K. G. Reymann, and H. Matthies, "Anisomycin, an inhibitor of protein synthesis, blocks late phases of LTP phenomena in the hippocampal CA1 region in vitro," Brain Research, vol. 452, no. 1-2, pp. 57-65, 1988.

[27] U. Frey, H. Schroeder, and H. Matthies, "Dopaminergic antagonists prevent long-term maintenance of posttetanic LTP in the CA1 region of rat hippocampal slices," Brain Research, vol. 522, no. 1, pp. 69-75, 1990.

[28] J. L. Swanson-Park, C. M. Coussens, S. E. Mason-Parker et al., "A double dissociation within the hippocampus of dopamine [D.sub.1]/[D.sub.5] receptor and [beta]-adrenergic receptor contributions to the persistence of long-term potentiation," Neuroscience, vol. 92, no. 2, pp. 485-497, 1999.

[29] C. M. O'Carroll and R. G. Morris, "Heterosynaptic coactivation of glutamatergic and dopaminergic afferents is required to induce persistent long-term potentiation," Neuropharmacology, vol. 47, no. 3, pp. 324-332, 2004.

[30] S. Navakkode, S. Sajikumar, and J. U. Frey, "Synergistic requirements for the induction of dopaminergic [D.sub.1]/[D.sub.5]-receptor- mediated LTP in hippocampal slices of rat CA1 in vitro," Neuropharmacology, vol. 52, no. 7, pp. 1547-1554, 2007.

[31] R. Bernabeu, L. Bevilaqua, P. Ardenghi et al., "Involvement of hippocampal cAMP/cAMP-dependent protein kinase signaling pathways in a late memory consolidation phase of aversively motivated learning in rats," Proceedings of the National Academy of Sciences of the United States of America, vol. 94, no. 13, pp. 7041-7046, 1997.

[32] J. I. Rossato, L. R. Bevilaqua, I. Izquierdo, J. H. Medina, and M. Cammarota, "Dopamine controls persistence of long-term memory storage," Science, vol. 325, no. 5943, pp. 1017-1020, 2009.

[33] C. R. Furini, J. C. Myskiw, B. E. Schmidt, L. A. Marcondes, and I. Izquierdo, "[D.sub.1] and [D.sub.5] dopamine receptors participate on the consolidation of two different memories," Behavioural Brain Research, vol. 271, pp. 212-217, 2014.

[34] J. I. Broussard, K. Yang, A. T. Levine et al., "Dopamine regulates aversive contextual learning and associated in vivo synaptic plasticity in the hippocampus," Cell Reports, vol. 14, no. 8, pp. 1930-1939, 2016.

[35] C. M. O'Carroll, S. J. Martin, J. Sandin, B. Frenguelli, and R. G. Morris, "Dopaminergic modulation of the persistence of one-trial hippocampus-dependent memory," Learning & Memory, vol. 13, no. 6, pp. 760-769, 2006.

[36] W. C. da Silva, C. C. Kohler, A. Radiske, and M. Cammarota, "[D.sub.1]/[D.sub.5] Dopamine receptors modulate spatial memory formation," Neurobiology of Learning and Memory, vol. 97, no. 2, pp. 271-275, 2012.

[37] I. Bethus, D. Tse, and R. G. Morris, "Dopamine and memory: modulation of the persistence of memory for novel hippocampal NMDA receptor-dependent paired associates," The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, vol. 30, no. 5, pp. 1610-1618, 2010.

[38] S. Karunakaran, A. Chowdhury, F. Donato, C. Quairiaux, C. M. Michel, and P. Caroni, "PV plasticity sustained through D1/5 dopamine signaling required for long-term memory consolidation," Nature Neuroscience, vol. 19, no. 3, pp. 454-464, 2016.

[39] M. Pezze and T. Bast, "Dopaminergic modulation of hippocampus-dependent learning: blockade of hippocampal D1-class receptors during learning impairs 1-trial place memory at a 30-min retention delay," Neuropharmacology, vol. 63, no. 4, pp. 710-718, 2012.

[40] C. Missale, S. R. Nash, S. W. Robinson, M. Jaber, and M. G. Caron, "Dopamine receptors: from structure to function," Physiological Reviews, vol. 78, no. 1, pp. 189-225, 1998.

[41] H. Matthies, A. Becker, H. Schroeder, J. Kraus, V. Hollt, and M. Krug, "Dopamine D1-deficient mutant mice do not express the late phase of hippocampal long-term potentiation," Neuroreport, vol. 8, no. 16, pp. 3533-3535, 1997.

[42] D. R. Smith, C. D. Striplin, A. M. Geller et al., "Behavioural assessment of mice lacking [D.sub.1A] dopamine receptors," Neuroscience, vol. 86, no. 1, pp. 135-146, 1998.

[43] M. El-Ghundi, P. J. Fletcher, J. Drago, D. R. Sibley, B. F. O'Dowd, and S. R. George, "Spatial learning deficit in dopamine [D.sub.1] receptor knockout mice," European Journal of Pharmacology, vol. 383, no. 2, pp. 95-106, 1999.

[44] N. Granado, O. Ortiz, L. M. Suarez et al., "[D.sub.1] but not [D.sub.5] dopamine receptors are critical for LTP, spatial learning, and LTP-induced arc and zif268 expression in the hippocampus," Cerebral Cortex, vol. 18, no. 1, pp. 1-12, 2008.

[45] B. Xing, H. Kong, X. Meng, S. G. Wei, M. Xu, and S. B. Li, "Dopamine [D.sub.1] but not [D.sub.3] receptor is critical for spatial learning and related signaling in the hippocampus," Neuroscience, vol. 169, no. 4, pp. 1511-1519, 2010.

[46] O. Ortiz, J. M. Delgado-Garcia, I. Espadas et al., "Associative learning and CA3-CA1 synaptic plasticity are impaired in [D.sub.1]R null, [Drd1a.sup.-/-] mice and in hippocampal siRNA silenced Drd1a mice," The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, vol. 30, no. 37, pp. 12288-12300, 2010.

[47] R. Moraga-Amaro, H. Gonzalez, V. Ugalde et al., "Dopamine receptor D5 deficiency results in a selective reduction of hippocampal NMDA receptor subunit NR2B expression and impaired memory," Neuropharmacology, vol. 103, pp. 222-235, 2016.

[48] J. Sarinana, T. Kitamura, P. Kunzler, L. Sultzman, and S. Tonegawa, "Differential roles of the dopamine 1-class receptors, [D.sub.1]R and D5R, in hippocampal dependent memory," Proceedings of the National Academy of Sciences of the United States of America, vol. 111, no. 22, pp. 8245-8250, 2014.

[49] U. Frey and R. G. Morris, "Synaptic tagging and long-term potentiation," Nature, vol. 385, no. 6616, pp. 533-536, 1997.

[50] U. Frey and R. G. Morris, "Synaptic tagging: implications for late maintenance of hippocampal long-term potentiation," Trends in Neurosciences, vol. 21, no. 5, pp. 181-188, 1998.

[51] R. L. Redondo and R. G. Morris, "Making memories last: the synaptic tagging and capture hypothesis," Nature Reviews Neuroscience, vol. 12, no. 1, pp. 17-30, 2011.

[52] N. Lemon and D. Manahan-Vaughan, "Dopamine D1/D5 receptors contribute to de novo hippocampal LTD mediated by novel spatial exploration or locus coeruleus activity," Cerebral Cortex, vol. 22, no. 9, pp. 2131-2138, 2012.

[53] A. Vazdarjanova and J. F. Guzowski, "Differences in hippocampal neuronal population responses to modifications of an environmental context: evidence for distinct, yet complementary, functions of CA3 and CA1 ensembles," The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, vol. 24, no. 29, pp. 6489-6496, 2004.

[54] M. Merhav and K. Rosenblum, "Facilitation of taste memory acquisition by experiencing previous novel taste is protein-synthesis dependent," Learning & Memory, vol. 15, no. 7, pp. 501-507, 2008.

[55] F. Ballarini, D. Moncada, M. C. Martinez, N. Alen, and H. Viola, "Behavioral tagging is a general mechanism of long-term memory formation," Proceedings of the National Academy of Sciences of the United States of America, vol. 106, no. 34, pp. 14599-14604, 2009.

[56] D. Moncada, F. Ballarini, M. C. Martinez, J. U. Frey, and H. Viola, "Identification of transmitter systems and learning tag molecules involved in behavioral tagging during memory formation," Proceedings of the National Academy of Sciences of the United States of America, vol. 108, no. 31, pp. 12931-12936, 2011.

[57] Y. Lu, Y. Ji, S. Ganesan et al., "TrkB as a potential synaptic and behavioral tag," The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, vol. 31, no. 33, pp. 11762-11771, 2011.

[58] M. Tomaiuolo, C. Katche, H. Viola, and J. H. Medina, "Evidence of maintenance tagging in the hippocampus for the persistence of long-lasting memory storage," Neural Plasticity, vol. 2015, Article ID 603672, 9 pages, 2015.

[59] K. L. Shires, B. M. Da Silva, J. P. Hawthorne, R. G. Morris, and S. J. Martin, "Synaptic tagging and capture in the living rat," Nature Communications, vol. 3, p. 1246, 2012.

[60] M. Nomoto, N. Ohkawa, H. Nishizono et al., "Cellular tagging as a neural network mechanism for behavioural tagging," Nature Communications, vol. 7, article 12319, 2016.

[61] D. Moncada, "Evidence of VTA and LC control of protein synthesis required for the behavioral tagging process," Neurobiology of Learning and Memory, vol. 138, pp. 226-237, 2016.

[62] K. Duncan, A. Tompary, and L. Davachi, "Associative encoding and retrieval are predicted by functional connectivity in distinct hippocampal area CA1 pathways," The Journal of neuroscience: the official journal of the Society for Neuroscience, vol. 34, no. 34, pp. 11188-11198, 2014.

[63] A. Tompary, K. Duncan, and L. Davachi, "Consolidation of associative and item memory is related to post-encoding functional connectivity between the ventral tegmental area and different medial temporal lobe subregions during an unrelated task," The Journal of neuroscience : the official journal of the Society for Neuroscience, vol. 35, no. 19, pp. 7326-7331, 2015.

[64] B. Scatton, H. Simon, M. Le Moal, and S. Bischoff, "Origin of dopaminergic innervation of the rat hippocampal formation," Neuroscience Letters, vol. 18, no. 2, pp. 125-131, 1980.

[65] L. W. Swanson, "The projections of the ventral tegmental area and adjacent regions: a combined fluorescent retrograde tracer and immunofluorescence study in the rat," Brain Research Bulletin, vol. 9, no. 1-6, pp. 321-353, 1982.

[66] C. G. McNamara, A. Tejero-Cantero, S. Trouche, N. Campo-Urriza, and D. Dupret, "Dopaminergic neurons promote hippocampal reactivation and spatial memory persistence," Nature Neuroscience, vol. 17, no. 12, pp. 1658-1660, 2014.

[67] B. J. Everitt, A. Dickinson, and T. W. Robbins, "The neuropsychological basis of addictive behaviour," Brain Research Brain Research Reviews, vol. 36, no. 2-3, pp. 129-138, 2001.

[68] W. Schultz, P. Apicella, T. Ljungberg, R. Romo, and E. Scarnati, "Reward-related activity in the monkey striatum and substantia nigra," Progress in Brain Research, vol. 99, pp. 227-235, 1993.

[69] H. C. Tsai, F. Zhang, A. Adamantidis et al., "Phasic firing in dopaminergic neurons is sufficient for behavioral conditioning," Science, vol. 324, no. 5930, pp. 1080-1084, 2009.

[70] E. E. Steinberg, R. Keiflin, J. R. Boivin, I. B. Witten, K. Deisseroth, and P. H. Janak, "A causal link between prediction errors, dopamine neurons and learning," Nature Neuroscience, vol. 16, no. 7, pp. 966-973, 2013.

[71] S. Yagishita, A. Hayashi-Takagi, G. C. Ellis-Davies, H. Urakubo, S. Ishii, and H. Kasai, "A critical time window for dopamine actions on the structural plasticity of dendritic spines," Science, vol. 345, no. 6204, pp. 1616-1620, 2014.

[72] B. Salvetti, R. G. Morris, and S. H. Wang, "The role of rewarding and novel events in facilitating memory persistence in a separate spatial memory task," Learning & Memory, vol. 21, no. 2, pp. 61-72, 2014.

[73] E. Ghanbarian and F. Motamedi, "Ventral tegmental area inactivation suppresses the expression of CA1 long term potentiation in anesthetized rat," PLoS One, vol. 8, no. 3, article e58844, 2013.

[74] Z. B. Rosen, S. Cheung, and S. A. Siegelbaum, "Midbrain dopamine neurons bidirectionally regulate CA3-CA1 synaptic drive," Nature Neuroscience, vol. 18, no. 12, pp. 1763-1771, 2015.

[75] D. B. Fenker, J. U. Frey, H. Schuetze, D. Heipertz, H. J. Heinze, and E. Duzel, "Novel scenes improve recollection and recall of words," Journal of Cognitive Neuroscience, vol. 20, no. 7, pp. 1250-1265, 2008.

[76] M. J. Gruber, M. Ritchey, S. F. Wang, M. K. Doss, and C. Ranganath, "Post-learning hippocampal dynamics promote preferential retention of rewarding events," Neuron, vol. 89, no. 5, pp. 1110-1120, 2016.

[77] A. Dahlstrom and K. Fuxe, "Localization of monoamines in the lower brain stem," Experientia, vol. 20, no. 7, pp. 398-399, 1964.

[78] G. Aston-Jones and F. E. Bloom, "Activity of norepinephrine-containing locus coeruleus neurons in behaving rats anticipates fluctuations in the sleep-waking cycle," The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, vol. 1, no. 8, pp. 876-886, 1981.

[79] C. Harley, "Noradrenergic and locus coeruleus modulation of the perforant path-evoked potential in rat dentate gyrus supports a role for the locus coeruleus in attentional and memorial processes," Progress in Brain Research, vol. 88, pp. 307-321, 1991.

[80] S. J. Sara, "The locus coeruleus and noradrenergic modulation of cognition," Nature Reviews Neuroscience, vol. 10, no. 3, pp. 211-223, 2009.

[81] M. E. Carter, O. Yizhar, S. Chikahisa et al., "Tuning arousal with optogenetic modulation of locus coeruleus neurons," Nature Neuroscience, vol. 13, no. 12, pp. 1526-1533, 2010.

[82] M. E. Carter, L. de Lecea, and A. Adamantidis, "Functional wiring of hypocretin and LC-NE neurons: implications for arousal," Frontiers in Behavioral Neuroscience, vol. 7, p. 43, 2013.

[83] K. Janitzky, M. T. Lippert, A. Engelhorn et al., "Optogenetic silencing of locus coeruleus activity in mice impairs cognitive flexibility in an attentional set-shifting task," Frontiers in Behavioral Neuroscience, vol. 9, p. 286, 2015.

[84] O. Eschenko, C. Magri, S. Panzeri, and S. J. Sara, "Noradrenergic neurons of the locus coeruleus are phase locked to cortical up-down states during sleep," Cerebral Cortex, vol. 22, no. 2, pp. 426-435, 2012.

[85] E. Szabadi, "Functional neuroanatomy of the central noradrenergic system," Journal of Psychopharmacology, vol. 27, no. 8, pp. 659-693, 2013.

[86] L. A. Schwarz, K. Miyamichi, X. J. Gao et al., "Viral-genetic tracing of the input-output organization of a central noradrenaline circuit," Nature, vol. 524, no. 7563, pp. 88-92, 2015.

[87] T. W. Blackstad, K. Fuxe, and T. Hokfelt, "Noradrenaline nerve terminals in the hippocampal region of the rat and the guinea pig," Zeitschrift fur Zellforschung und Mikroskopische Anatomie, vol. 78, no. 4, pp. 463-473, 1967.

[88] L. W. Swanson and B. K. Hartman, "The central adrenergic system. An immunofluorescence study of the location of cell bodies and their efferent connections in the rat utilizing dopamine-[beta]-hydroxylase as a marker," The Journal of Comparative Neurology, vol. 163, no. 4, pp. 467-505, 1975.

[89] R. Loy, D. A. Koziell, J. D. Lindsey, and R. Y. Moore, "Noradrenergic innervation of the adult rat hippocampal formation," The Journal of Comparative Neurology, vol. 189, no. 4, pp. 699-710, 1980.

[90] T. A. Milner and C. E. Bacon, "GABAergic neurons in the rat hippocampal formation: ultrastructure and synaptic relationships with catecholaminergic terminals," The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, vol. 9, no. 10, pp. 3410-3427, 1989.

[91] S. Oleskevich, L. Descarries, and J. C. Lacaille, "Quantified distribution of the noradrenaline innervation in the hippocampus of adult rat," The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, vol. 9, no. 11, pp. 3803-3815, 1989.

[92] A. M. Moudy, D. D. Kunkel, and P. A. Schwartzkroin, "Development of dopamine-beta-hydroxylase--positive fiber innervation of the rat hippocampus," Synapse (New York, NY), vol. 15, no. 4, pp. 307-318, 1993.

[93] Z. Q. Xu, T. J. Shi, and T. Hokfelt, "Galanin/GMAP- and NPY-like immunoreactivities in locus coeruleus and noradrenergic nerve terminals in the hippocampal formation and cortex with notes on the galanin-R1 and -R2 receptors," The Journal of Comparative Neurology, vol. 392, no. 2, pp. 227-251, 1998.

[94] G. Aston-Jones and J. D. Cohen, "An integrative theory of locus coeruleus-norepinephrine function: adaptive gain and optimal performance," Annual Review of Neuroscience, vol. 28, pp. 403-450, 2005.

[95] S. J. Sara, A. Vankov, and A. Herve, "Locus coeruleus-evoked responses in behaving rats: a clue to the role of noradrenaline in memory," Brain Research Bulletin, vol. 35, no. 5-6, pp. 457-465, 1994.

[96] A. Vankov, A. Herve-Minvielle, and S. J. Sara, "Response to novelty and its rapid habituation in locus coeruleus neurons of the freely exploring rat," The European Journal of Neuroscience, vol. 7, no. 6, pp. 1180-1187, 1995.

[97] P. Devoto and G. Flore, "On the origin of cortical dopamine: is it a co-transmitter in noradrenergic neurons?," Current Neuropharmacology, vol. 4, no. 2, pp. 115-125, 2006.

[98] M. E. Hasselmo and B. P. Wyble, "Free recall and recognition in a network model of the hippocampus: simulating effects of scopolamine on human memory function," Behavioural Brain Research, vol. 89, no. 1-2, pp. 1-34, 1997.

[99] E. Jodo, C. Chiang, and G. Aston-Jones, "Potent excitatory influence of prefrontal cortex activity on noradrenergic locus coeruleus neurons," Neuroscience, vol. 83, no. 1, pp. 63-79, 1998.

[100] S. E. Boehnke, D. J. Berg, R. A. Marino, P. F. Baldi, L. Itti, and D. P. Munoz, "Visual adaptation and novelty responses in the superior colliculus," The European Journal of Neuroscience, vol. 34, no. 5, pp. 766-779, 2011.

[101] T. J. Perrault Jr., B. E. Stein, and B. A. Rowland, "Non-stationarity in multisensory neurons in the superior colliculus," Frontiers in Psychology, vol. 2, p. 144, 2011.

[102] N. G. Ahn and J. P. Klinman, "Nature of rate-limiting steps in a compartmentalized enzyme system. Quantitation of dopamine transport and hydroxylation rates in resealed chromaffin granule ghosts," The Journal of Biological Chemistry, vol. 264, no. 21, pp. 12259-12265, 1989.

[103] A. Deutch and R. Roth, Neurobiology of Mental Illness, Oxford University Press, 4th edition, 2013.

[104] O. Curet, T. Dennis, and B. Scatton, "The formation of deaminated metabolites of dopamine in the locus coeruleus depends upon noradrenergic neuronal activity," Brain Research, vol. 335, no. 2, pp. 297-301, 1985.

[105] P. Devoto, G. Flore, P. Saba, M. Fa, and G. L. Gessa, "Corelease of noradrenaline and dopamine in the cerebral cortex elicited by single train and repeated train stimulation of the locus coeruleus," BMC Neuroscience, vol. 6, p. 31, 2005.

[106] P. Devoto, G. Flore, P. Saba, M. Fa, and G. L. Gessa, "Stimulation of the locus coeruleus elicits noradrenaline and dopamine release in the medial prefrontal and parietal cortex," Journal of Neurochemistry, vol. 92, no. 2, pp. 368-374, 2005.

[107] B. Scatton, T. Dennis, and O. Curet, "Increase in dopamine and DOPAC levels in noradrenergic terminals after electrical stimulation of the ascending noradrenergic pathways," Brain Research, vol. 298, no. 1, pp. 193-196, 1984.

[108] L. Quintin, G. Hilaire, and J. F. Pujol, "Variations in 3,4-dihy-droxyphenylacetic acid concentration are correlated to single cell firing changes in the rat locus coeruleus," Neuroscience, vol. 18, no. 4, pp. 889-899, 1986.

[109] S. J. Cragg and M. E. Rice, "DAncing past the DAT at a DA synapse," Trends in Neurosciences, vol. 27, no. 5, pp. 270-277, 2004.

[110] B. J. Ciliax, C. Heilman, L. L. Demchyshyn et al., "The dopamine transporter: immunochemical characterization and localization in brain," The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, vol. 15, no. 3, Part 1, pp. 1714-1723, 1995.

[111] S. R. Sesack, V. A. Hawrylak, C. Matus, M. A. Guido, and A. I. Levey, "Dopamine axon varicosities in the prelimbic division of the rat prefrontal cortex exhibit sparse immunoreactivity for the dopamine transporter," The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, vol. 18, no. 7, pp. 2697-2708, 1998.

[112] C. L. Coulter, H. K. Happe, D. A. Bergman, and L. C. Murrin, "Localization and quantification of the dopamine transporter: comparison of [[sup.3]H]WIN 35,428 and [[sup.125I]]RTI-55," Brain Research, vol. 690, no. 2, pp. 217-224, 1995.

[113] B. H. Schott, C. I. Seidenbecher, D. B. Fenker et al., "The dopaminergic midbrain participates in human episodic memory formation: evidence from genetic imaging," The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, vol. 26, no. 5, pp. 1407-1417, 2006.

[114] O. B. Kwon, D. Paredes, C. M. Gonzalez et al., "Neuregulin-1 regulates LTP at CA1 hippocampal synapses through activation of dopamine D4 receptors," Proceedings of the National Academy of Sciences of the United States of America, vol. 105, no. 40, pp. 15587-15592, 2008.

[115] A. S. Horn, "Structure-activity relations for the inhibition of catecholamine uptake into synaptosomes from noradrenaline and dopaminergic neurones in rat brain homogenates," British Journal of Pharmacology, vol. 47, no. 2, pp. 332-338, 1973.

[116] T. Pacholczyk, R. D. Blakely, and S. G. Amara, "Expression cloning of a cocaine- and antidepressant-sensitive human noradrenaline transporter," Nature, vol. 350, no. 6316, pp. 350-354, 1991.

[117] J. A. Moron, A. Brockington, R. A. Wise, B. A. Rocha, and B. T. Hope, "Dopamine uptake through the norepinephrine transporter in brain regions with low levels of the dopamine transporter: evidence from knock-out mouse lines," The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, vol. 22, no. 2, pp. 389-395, 2002.

[118] S. Schroeter, S. Apparsundaram, R. G. Wiley, L. H. Miner, S. R. Sesack, and R. D. Blakely, "Immunolocalization of the cocaine- and antidepressant-sensitive 1-norepinephrine transporter," The Journal of Comparative Neurology, vol. 420, no. 2, pp. 211-232, 2000.

[119] A. Borgkvist, T. Malmlof, K. Feltmann, M. Lindskog, and B. Schilstrom, "Dopamine in the hippocampus is cleared by the norepinephrine transporter," The International Journal of Neuropsychopharmacology, vol. 15, no. 4, pp. 531-540, 2012.

[120] W. Schultz, "Behavioral dopamine signals," Trends in Neurosciences, vol. 30, no. 5, pp. 203-210, 2007.

[121] R. P. Kesner and E. T. Rolls, "A computational theory of hippocampal function, and tests of the theory: new developments," Neuroscience and Biobehavioral Reviews, vol. 48, pp. 92-147, 2015.

[122] L. W. Swanson and W. M. Cowan, "An autoradiographic study of the organization of the efferent connections of the hippocampal formation in the rat," The Journal of Comparative Neurology, vol. 172, no. 1, pp. 49-84, 1977.

[123] A. Hjorth-Simonsen and B. Jeune, "Origin and termination of the hippocampal perforant path in the rat studied by silver impregnation," The Journal of Comparative Neurology, vol. 144, no. 2, pp. 215-232, 1972.

[124] M. Frotscher and C. Leranth, "Catecholaminergic innervation of pyramidal and GABAergic nonpyramidal neurons in the rat hippocampus. Double label immunostaining with antibodies against tyrosine hydroxylase and glutamate decarboxylase," Histochemistry, vol. 88, no. 3-6, pp. 313-319, 1988.

[125] D. Umbriaco, S. Garcia, C. Beaulieu, and L. Descarries, "Relational features of acetylcholine, noradrenaline, serotonin and GABA axon terminals in the stratum radiatum of adult rat hippocampus (CA1)," Hippocampus, vol. 5, no. 6, pp. 605-620, 1995.

[126] Y. Murata, T. Chiba, P. Brundin, A. Bjorklund, and O. Lindvall, "Formation of synaptic graft-host connections by noradrenergic locus coeruleus neurons transplanted into the adult rat hippocampus," Experimental Neurology, vol. 110, no. 3, pp. 258-267, 1990.

[127] K. K. Yung, J. P. Bolam, A. D. Smith, S. M. Hersch, B. J. Ciliax, and A. I. Levey, "Immunocytochemical localization of [D.sub.1] and D2 dopamine receptors in the basal ganglia of the rat: light and electron microscopy," Neuroscience, vol. 65, no. 3, pp. 709-730, 1995.

[128] I. Caille, B. Dumartin, and B. Bloch, "Ultrastructural localization of [D.sub.1] dopamine receptor immunoreactivity in rat striatonigral neurons and its relation with dopaminergic innervation," Brain Research, vol. 730, no. 1-2, pp. 17-31, 1996.

[129] M. Uchigashima, T. Ohtsuka, K. Kobayashi, and M. Watanabe, "Dopamine synapse is a neuroligin-2-mediated contact between dopaminergic presynaptic and GABAergic postsynaptic structures," Proceedings of the National Academy of Sciences of the United States of America, vol. 113, no. 15, pp. 4206-4211, 2016.

[130] R. T. Fremeau Jr., G. E. Duncan, M. G. Fornaretto et al., "Localization of [D.sub.1] dopamine receptor mRNA in brain supports a role in cognitive, affective, and neuroendocrine aspects of dopaminergic neurotransmission," Proceedings of the National Academy of Sciences of the United States of America, vol. 88, no. 9, pp. 3772-3776, 1991.

[131] M. Tiberi, K. R. Jarvie, C. Silvia et al., "Cloning, molecular characterization, and chromosomal assignment of a gene encoding a second D1 dopamine receptor subtype: differential expression pattern in rat brain compared with the D1A receptor," Proceedings of the National Academy of Sciences of the United States of America, vol. 88, no. 17, pp. 7491-7495, 1991.

[132] R. K. Sunahara, H. C. Guan, B. F. O'Dowd et al., "Cloning of the gene for a human dopamine D5 receptor with higher affinity for dopamine than D1," Nature, vol. 350, no. 6319, pp. 614-619, 1991.

[133] J. H. Meador-Woodruff, A. Mansour, D. K. Grandy, S. P. Damask, O. Civelli, and S. J. Watson Jr., "Distribution of [D.sub.5] dopamine receptor mRNA in rat brain," Neuroscience Letters, vol. 145, no. 2, pp. 209-212, 1992.

[134] Z. U. Khan, A. Gutierrez, R. Martin, A. Penafiel, A. Rivera, and A. de la Calle, "Dopamine [D.sub.5] receptors of rat and human brain," Neuroscience, vol. 100, no. 4, pp. 689-699, 2000.

[135] F. Laplante, D. R. Sibley, and R. Quirion, "Reduction in acetylcholine release in the hippocampus of dopamine D5 receptor-deficient mice," Neuropsychopharmacology, vol. 29, no. 9, pp. 1620-1627, 2004.

[136] Y. Mu, C. Zhao, and F. H. Gage, "Dopaminergic modulation of cortical inputs during maturation of adult-born dentate granule cells," The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, vol. 31, no. 11, pp. 4113-4123, 2011.

[137] G. Gangarossa, S. Longueville, D. De Bundel et al., "Characterization of dopamine D1 and D2 receptor-expressing neurons in the mouse hippocampus," Hippocampus, vol. 22, no. 12, pp. 2199-2207, 2012.

[138] E. Puighermanal, L. Cutando, J. Boubaker-Vitre et al., "Anatomical and molecular characterization of dopamine [D.sub.1] receptor-expressing neurons of the mouse C[A.sub.1] dorsal hippocampus," Brain Structure & Function, vol. 222, no. 4, pp. 1897-1911, 2016.

[139] T. M. Dawson, P. Barone, A. Sidhu, J. K. Wamsley, and T. N. Chase, "Quantitative autoradiographic localization of D-1 dopamine receptors in the rat brain: use of the iodinated ligand [[sup.125]I]SCH 23982," Neuroscience Letters, vol. 68, no. 3, pp. 261-266, 1986.

[140] T. M. Dawson, D. R. Gehlert, R. T. McCabe, A. Barnett, and J. K. Wamsley, "D-1 dopamine receptors in the rat brain: a quantitative autoradiographic analysis," The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, vol. 6, no. 8, pp. 2352-2365, 1986.

[141] M. Camps, P. H. Kelly, and J. M. Palacios, "Autoradiographic localization of dopamine [D.sub.1] and [D.sub.2] receptors in the brain of several mammalian species," Journal of Neural Transmission. General Section, vol. 80, no. 2, pp. 105-127, 1990.

[142] A. Mansour, J. H. Meador-Woodruff, Q. Zhou, O. Civelli, H. Akil, and S. J. Watson, "A comparison of [D.sub.1] receptor binding and mRNA in rat brain using receptor autoradiographic and in situ hybridization techniques," Neuroscience, vol. 46, no. 4, pp. 959-971, 1992.

[143] M. L. Perreault, A. Hasbi, B. F. O'Dowd, and S. R. George, "Heteromeric dopamine receptor signaling complexes: emerging neurobiology and disease relevance," Neuropsychopharmacology, vol. 39, no. 1, pp. 156-168, 2014.

[144] J. M. Beaulieu, S. Espinoza, and R. R. Gainetdinov, "Dopamine receptors--IUPHAR review 13," British Journal of Pharmacology, vol. 172, no. 1, pp. 1-23, 2015.

[145] F. J. Lee, S. Xue, L. Pei et al., "Dual regulation of NMDA receptor functions by direct protein-protein interactions with the dopamine D1 receptor," Cell, vol. 111, no. 2, pp. 219-230, 2002.

[146] L. Pei, F. J. Lee, A. Moszczynska, B. Vukusic, and F. Liu, "Regulation of dopamine D1 receptor function by physical interaction with the NMDA receptors," The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, vol. 24, no. 5, pp. 1149-1158, 2004.

[147] A. Kern, M. Mavrikaki, C. Ullrich, R. Albarran-Zeckler, A. F. Brantley, and R. G. Smith, "Hippocampal dopamine/DRD1 signaling dependent on the ghrelin receptor," Cell, vol. 163, no. 5, pp. 1176-1190, 2015.

[148] F. Liu, Q. Wan, Z. B. Pristupa, X. M. Yu, Y. T. Wang, and H. B. Niznik, "Direct protein-protein coupling enables crosstalk between dopamine D5 and [gamma]-aminobutyric acid a receptors," Nature, vol. 403, no. 6767, pp. 274-280, 2000.

[149] C. G. Kentros, N. T. Agnihotri, S. Streater, R. D. Hawkins, and E. R. Kandel, "Increased attention to spatial context increases both place field stability and spatial memory," Neuron, vol. 42, no. 2, pp. 283-295, 2004.

[150] T. Rogerson, D. J. Cai, A. Frank et al., "Synaptic tagging during memory allocation," Nature Reviews Neuroscience, vol. 15, no. 3, pp. 157-169, 2014.

[151] G. Gangarossa, M. Di Benedetto, G. J. O'Sullivan et al., "Convulsant doses of a dopamine D1 receptor agonist result in Erk-dependent increases in Zif268 and arc/Arg3.1 expression in mouse dentate gyrus," PLoS One, vol. 6, no. 5, article e19415, 2011.

[152] W. B. Smith, S. R. Starck, R. W. Roberts, and E. M. Schuman, "Dopaminergic stimulation of local protein synthesis enhances surface expression of GluR1 and synaptic transmission in hippocampal neurons," Neuron, vol. 45, no. 5, pp. 765-779, 2005.

[153] J. J. Hodas, A. Nehring, N. Hoche et al., "Dopaminergic modulation of the hippocampal neuropil proteome identified by bioorthogonal noncanonical amino acid tagging (BONCAT)," Proteomics, vol. 12, no. 15-16, pp. 2464-2476, 2012.

[154] A. Vazdarjanova, B. L. McNaughton, C. A. Barnes, P. F. Worley, and J. F. Guzowski, "Experience-dependent coincident expression of the effector immediate-early genes Arc and Homer 1a in hippocampal and neocortical neuronal networks," The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, vol. 22, no. 23, pp. 10067-10071, 2002.

[155] A. Rinaldi, S. Romeo, C. Agustin-Pavon, A. Oliverio, and A. Mele, "Distinct patterns of Fos immunoreactivity in striatum and hippocampus induced by different kinds of novelty in mice," Neurobiology of Learning and Memory, vol. 94, no. 3, pp. 373-381, 2010.

[156] W. Yoshioka, N. Endo, A. Kurashige et al., "Fluorescence laser microdissection reveals a distinct pattern of gene activation in the mouse hippocampal region," Scientific Reports, vol. 2, p. 783, 2012.

[157] S. Sajikumar, Synaptic Tagging and Capture: From Synapses to Behavior, Springer, New York, NY, USA, 2015.

[158] D. Okada, F. Ozawa, and K. Inokuchi, "Input-specific spine entry of soma-derived Vesl-1S protein conforms to synaptic tagging," Science, vol. 324, no. 5929, pp. 904-909, 2009.

[159] H. Okuno, K. Akashi, Y. Ishii et al., "Inverse synaptic tagging of inactive synapses via dynamic interaction of arc/Arg3.1 with CaMKII[beta]," Cell, vol. 149, no. 4, pp. 886-898, 2012.

[160] Y. Hayashi, S. H. Shi, J. A. Esteban, A. Piccini, J. C. Poncer, and R. Malinow, "Driving AMPA receptors into synapses by LTP and CaMKII: requirement for GluR1 and PDZ domain interaction," Science, vol. 287, no. 5461, pp. 2262-2267, 2000.

[161] M. Matsuzaki, N. Honkura, G. C. Ellis-Davies, and H. Kasai, "Structural basis of long-term potentiation in single dendritic spines," Nature, vol. 429, no. 6993, pp. 761-766, 2004.

[162] K. Okamoto, T. Nagai, A. Miyawaki, and Y. Hayashi, "Rapid and persistent modulation of actin dynamics regulates postsynaptic reorganization underlying bidirectional plasticity," Nature Neuroscience, vol. 7, no. 10, pp. 1104-1112, 2004.

[163] M. Pirooznia, T. Wang, D. Avramopoulos et al., "SynaptomeDB: an ontology-based knowledgebase for synaptic genes," Bioinformatics, vol. 28, no. 6, pp. 897-899, 2012.

[164] R. L. Redondo, H. Okuno, P. A. Spooner, B. G. Frenguelli, H. Bito, and R. G. Morris, "Synaptic tagging and capture: differential role of distinct calcium/calmodulin kinases in protein synthesis-dependent long-term potentiation," The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, vol. 30, no. 14, pp. 4981-4989, 2010.

[165] M. Heiman, A. Schaefer, S. Gong et al., "A translational profiling approach for the molecular characterization of CNS cell types," Cell, vol. 135, no. 4, pp. 738-748, 2008.

[166] M. Bosch, J. Castro, T. Saneyoshi, H. Matsuno, M. Sur, and Y. Hayashi, "Structural and molecular remodeling of dendritic spine substructures during long-term potentiation," Neuron, vol. 82, no. 2, pp. 444-459, 2014.

[167] X. X. Zhou, M. Pan, and M. Z. Lin, "Investigating neuronal function with optically controllable proteins," Frontiers in Molecular Neuroscience, vol. 8, p. 37, 2015.

[168] J. Y. Lin, S. B. Sann, K. Zhou et al., "Optogenetic inhibition of synaptic release with chromophore-assisted light inactivation (CALI)," Neuron, vol. 79, no. 2, pp. 241-253, 2013.

Miwako Yamasaki (1) and Tomonori Takeuchi (1, 2)

(1) Department of Anatomy, Hokkaido University Graduate School of Medicine, Sapporo, Hokkaido 060-8638, Japan

(2) Centre for Discovery Brain Science, Edinburgh Neuroscience, The University of Edinburgh, 1 George Square, Edinburgh EH8 9JZ, UK

Correspondence should be addressed to Miwako Yamasaki; k- and Tomonori Takeuchi;

Received 5 February 2017; Revised 6 June 2017; Accepted 18 June 2017; Published 16 October 2017

Academic Editor: Pamela B. Mello-Carpes

Caption: Figure 1: Two distinct novelty systems. There are two types of novelty: "environmental novelty" (e.g., new environment with objects never seen before) and "reward-associated novelty" (e.g., new reward in an unexpected location). They are associated with release of dopamine (DA) in the hippocampus (HPC) but might be processed by different systems with different time windows. (a) The locus coeruleus- (LC-) HPC system mediates environmental novelty which modulates the retention of memory with a broad time window (~1hr). (b) The ventral tegmental area- (VTA-) HPC system might mediate reward-associated novelty which modulates the memory with a narrow time window.

Caption: Figure 2: Hippocampal projections from LC neurons and increased LC neuron activity by environmental novelty. (a) Immunofluorescence of D[beta]H in HPC. (a) is reproduced from [88]. (b) T[H.sup.+] axons in the dorsal HPC originate from LC-T[H.sup.+] neurons. Quantification shows stronger T[H.sup.+] projections from LC than from VTA in CA1, CA3, and DG. *** p < 0.001, paired t-test. (b) is reproduced from [22]. (c) Response to novelty and its habituation in LC neurons. (c) is reproduced from [96]. (d) LC-T[H.sup.+] neurons show strong response to environmental novelty that habituates over 5 min. (d) is reproduced from [22].

Caption: Figure 3: Noncanonical release of DA from LC-T[H.sup.+] axons in HPC. (a) LC electorical stimulation-induced increase of NA (top) and DA (bottom) in the medial prefrontal cortex. (a) is reproduced from [106]. (b) LC electorical stimulation-mediated [D.sub.1]/[D.sub.5] receptor-sensitive facilitation of CA3-CA1 LTD in vivo. (b) is reproduced from [52]. (c) TH knockdown in LC prevents [D.sub.1]/[D.sub.5] receptor-mediated enhancement of excitatory transmission in HPC. (c) is reproduced from [20]. (d) Optogenetic activation of LC-T[H.sup.+] neurons enhances persistence of memory in a manner consistent with release of DA in HPC * p < 0.05 versus chance, t-test. (d) is reproduced from [22]. (e) Optogenetic activation of LC-T[H.sup.+] axons in HPC produces an increase in DA release in the dorsal HPC. * p < 0.05, t-test. (e) is reproduced from [23].

Caption: Figure 4: Identification of key PRPs (plasticity-related proteins) by using optogenetics and translational profiling. (a) The critical test session would include (i) a behavioural condition that enhances memory (novelty), (ii) optogenetic activation of LC neurons (LC on), and (iii) LC activation with [D.sub.1]/[D.sub.5] receptor blocker (LC on with [D.sub.1]/[D.sub.5]-R blocker) that might block the relevant synthesis of PRPs mediated by DAergic signaling in key target neurons. These conditions are compared to a home cage condition. (b) The TRAP technology, involving cell type-specific expression of green fluorescent protein- (GFP-) tagged ribosomal protein and GFP immunoprecipitation, enables the selective isolation of "translated mRNAs" in genetically defined neurons. (c) BONCAT (bioorthogonal noncanonical amino acid tagging) technology, involving labelling of newly synthesized proteins by AHA (azidohomoalanine), which can be later tagged for isolation and identification by mass spectrometry. (d) Candidate PRPs would be identified through the Venn diagram overlap of experimental conditions. (e) Optogenetic inhibition of a candidate PRP using "miniSOG," a genetically encoded singlet oxygen generator [168]. After light illumination, singlet oxygen ([sup.1][O.sub.2]) is generated by miniSOG leading to the inactivation of fusion protein of interest.
COPYRIGHT 2017 Hindawi Limited
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2017 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Author:Yamasaki, Miwako; Takeuchi, Tomonori
Publication:Neural Plasticity
Article Type:Report
Date:Jan 1, 2017
Previous Article:Visual Plasticity in Adults.
Next Article:The Effect of Glucocorticoid and Glucocorticoid Receptor Interactions on Brain, Spinal Cord, and Glial Cell Plasticity.

Terms of use | Privacy policy | Copyright © 2022 Farlex, Inc. | Feedback | For webmasters |