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Nociceptin signaling involves a calcium-based depolarization in Tetrahymena thermophila.

1. Introduction

Nociceptin/orphanin FQ (hereafter referred to as nociceptin) is a peptide involved in vertebrate pain signaling. The endogenous receptor for this ligand is ORL-1/NCR [1, 2]. A number of signaling pathways have been implicated in vertebrate nociceptin signaling. A partial listing of molecules involved in this signaling cascade would include [G.sub.i/o] proteins [1], neuronal nitric oxide synthase (nNOS) [3], and Erk-dependent signaling [4]. In addition, signaling through the nociceptin receptor induces a reduction in calcium influx via P/Q-type calcium channels in rat brain [5].

Tetrahymena thermophila are free-living, unicellular eukaryotes. While T. thermophila do not feel pain, they are capable of sensing chemoattractants and chemorepellents in their environment. This allows them to find food and possibly to escape predation [6]. A recent review by Csaba [7] details the response of T. thermophila to a number of chemoattractants and chemorepellents, including their response to many vertebrate hormones. Indeed, T. thermophila appear to synthesize and respond to a number of vertebrate hormones, including serotonin, melatonin, adrenocorticotropic hormone, and insulin [7].

A number of chemorepellents which have been characterized in T. thermophila are polycationic peptides, including lysozyme [8], thelysozymefragmentCB2 [9], PACAP [10], and nociceptive peptides including bradykinin and substance P 11]. Lysozyme signaling involves a calcium-based depolarization [12]. Lysozyme and PACAP appear to share a signaling pathway [9], which involves cAMP and phospholipase C [13], as well as NOS and cGMP [14]. A related peptide, VIP, also uses these signaling pathways and cross-adapts with lysozyme and PACAP, suggesting that Tetrahymena are signaling through a generalized polycation receptor [15].

Nociceptin is a polycationic peptide that is commercially available in three different isoforms. Nociceptin carries a charge of +4 at pH 7.0, while nociceptin-NH2 carries a charge of +5 at pH 7.0. Nociceptin-[Arg.sub.14][Lys.sub.15] carries a charge of +6 at pH 7.0. Our hypothesis was that all three of the nociceptin analogues would be chemorepellents in T. thermophila and that more highly charged nociceptin isoforms will have a lower E[C.sub.100] in behavioral assays than isoforms which carry a lesser charge.

2. Materials and Methods

2.1. Cell Cultures. Tetrahymena thermophila, strain B2086,a generous gift from Hennessey [6] (SUNY Buffalo), was used for all of the experiments. Cells were grown at 25[degrees]C in the axenic medium of Dentler [16], without shaking or addition of antibiotics. Two-day old cell cultures were used for all behavioral assays described below.

2.2. Chemicals and Solutions. Behavioral assays were carried out in a buffer of pH 7.0 containing 10 mM Trizma base,0.5mM MOPS, and 50 [micro]M Ca[Cl.sub.2]. All repellents and inhibitors used were dissolved in this buffer.

All nociceptin isoforms, thapsigargin, J-113397, and EGTA, were purchased from Tocris Biosciences, Bristol, UK.

2.3. Behavioral Assays. Behavioral assays were carried out as previously described [8, 10, 17]. Ten milliliters of T. thermophila culture was washed by centrifugation in a clinical centrifuge at high speed, and the pellet was reconstituted in 10 mL buffer. This wash step was repeated twice, and cells were reconstituted in 5 mL of buffer for use in behavioral assays. To perform the behavioral assays, 300 [micro]L of cell suspension was transferred to the first well of a microtiter plate. Cells were then transferred individually using a micropipette into the second well of the microtiter plate, which contained 300 [micro]L of buffer as a control. Cells were then transferred to a third well containing 300 [micro]L of nociceptin. Behavior of the cells was observed for the first 5 seconds after transfer to the third well, and the percentage of cells exhibiting avoidance behavior was noted. Varying concentrations of each peptide were used until we determined the minimum concentration at which 90% of the cells exhibited avoidance behavior (E[C.sub.100]). Each trial represents 10 cells. A minimum of 6 trials was performed for each data point.

Pharmacological inhibition assays were performed similar to the behavioral assays described previously. After being washed in buffer, cells were exposed to pharmacological agents known to block specific signaling pathways and incubated for 15 minutes to 2 hours. Cells were then transferred to a solution containing nociceptin at E[C.sub.100] and then monitored for avoidance behavior. Each trial represents 10 cells. A minimum of 6 trials was performed for each data point.

Cross-adaptation assays were performed as previously described [10, 17]. Briefly, 300 [micro]L of cells were placed into the first well of a 3-well microtiter plate. Cells were then individually transferred to the second well of the 3-well microtiter plate, which contained a repellent. The cells were allowed to adapt to this repellent for 10-15 minutes or until cells showed baseline avoidance (an avoidance of no more than 20%). Cells were then individually transferred to the third well of the 3-well microtiter plate, which contained the repellent to be tested for cross-adaptation and monitored for avoidance behavior. Data which showed 20% or fewer cells exhibiting avoidance was considered "baseline avoidance." Baseline avoidance is the number of cells in our assay which show avoidance behavior when being transferred from one well containing buffer to another well containing the same buffer and usually ranges from 5 to 20%. Cells exhibiting baseline avoidance in response to this assay were considered to be cross-adapted. Each trial represents 10 cells. A minimum of 6 trials was performed for each data point.

2.4. Electrophysiology. Standard one-electrode whole-cell membrane potential recordings were recorded as the previously reported procedures in Tetrahymena thermophila [9, 12]. The recording buffer contained were carried out in a buffer of pH 7.0 containing 10 mM Trizma base, 0.5 mM MOPS, and 1 mM Ca[Cl.sub.2]. Membrane potentials were displayed on a digital oscilloscope and retained on a chart recorder during continuous bath perfusion at a rate of approximately 20.0 mL/min. The recording bath had a volume of approximately 1 mL. Solutions were changed by switching valves connected either to buffer or to the experimental solution without changing the flow rate of the perfusion system.

3. Results

All isoforms of nociceptin were chemorepellents in T. thermophila (Figure 1). Nociceptin, which has a charge of +4 at our assay pH of 7.0, had an E[C.sub.100] of 100 [micro]M in our behavioral assay. Nociceptin-NH2, which has a charge of +5 under assay conditions, had an E[C.sub.100] of 50 [micro]M, while nociceptin-[Arg.sub.14][Lys.sub.15] which has a charge of +6 under assay conditions had an E[C.sub.100] of 25 [micro]M. Avoidance was observed for 1-5 seconds but was seen for as long as 10-15 minutes (not shown). After cells acclimated to the nociceptin, they returned to forward swimming.

Cross-adaptation assays (Table 1) show that all three isoforms of nociceptin cross-adapt with one another. However, nociceptin-adapted cells did not cross-adapt to PACAP-38, and PACAP-adapted cells did not cross-adapt to nociceptin. Since all three nociceptin isoforms cross-adapted to one another, implying a common signaling pathway, we used 50 [micro]M nociceptin-NH2 in all subsequent pharmacological and behavioral assays.

Studies with pharmacological agents known to block G-protein signaling, tyrosine kinase signaling, and broad spectrum kinase activity had no effect on avoidance behavior in T. thermophila (Table 2). However, studies with the calcium chelator, EGTA, and the SERCA ATPase inhibitor, thapsigargin, both affected nociceptin avoidance (Figure 2). A concentration of 50 [micro]M EGTA was sufficient to reduce avoidance to a baseline avoidance of 20%. Thapsigargin, however, never reduced avoidance to baseline under the conditions of our assay. The highest concentration of thapsigargin we were able to achieve in our assay was 300 [micro]M. Thapsigargin reduced avoidance by 50% at a concentration of 100 [micro]M; however, increasing the concentration to 300 [micro]M did not decrease avoidance beyond that seen with 100 [micro]M thapsigargin.

Whole-cell electrophysiology studies indicate that nociceptin-NH2 is a depolarizing signal in T. thermophila (Figure 3). A nociceptin-NH2 concentration of just 5 was sufficient to elicit a depolarization of approximately 20 mV, though this concentration does not cause behavioral avoidance above baseline levels in Tetrahymena (Figures 3(a) and 1). Fifty [micro]M nociceptin-NH2, which is the E[C.sub.100] for behavioral avoidance in Tetrahymena, elicited a depolarization of approximately 40 mV (Figure 3(b)). The depolarization produced by 50 nociceptin-NH2 was eliminated by the addition of 1mM EGTA to the external medium (Figure 3(c)).

J-113397, a competitive inhibitor of the human nociceptin receptor, inhibited the behavioral response to 50 [micro]M nociceptin-NH2 in Tetrahymena thermophila when applied extracellularly (Figure 4). Baseline avoidance to nociceptin was achieved by the addition of 50 [micro]M of J-113397.

4. Discussion

Our results confirmed our hypothesis that all three nociceptin isoforms tested would serve as chemorepellents in T thermophila (Figure 1). In addition, the E[C.sub.100] of each compound was correlated with the charge, with the most highly charged isoform having the lowest E[C.sub.100], although all of the E[C.sub.100] values were in a similar range. The correlation of lower E[C.sub.100] values with a higher charge is consistent with what we have seen using other charged peptides in T. thermophila. For example, when we have used various peptides derived from ACTH, the more highly charged peptides caused avoidance at lower concentrations than did the less highly charged peptides [11]. In addition, our previous studies with PACAP and VIP [15] show that PACAP is effective at causing avoidance at a 1000-fold lower concentration than VIP, though presumably acting through the same receptor and/or signaling pathway. The isoform of PACAP that we used in the 2003 study, PACAP-38-NH2, has a net charge of +11 at pH 7.0, while VIP has a net charge of just +4 at the same pH. While factors other than charge are certainly involved in the interaction between these peptides and their putative receptor, it is highly probable that charge is playing a role in these interactions, possibly by increasing the affinity of ligand for its receptor. In the case of nociceptin, the charge differences were relatively small as were the differences in E[C.sub.100].

Cells acclimated to nociception within 10-15 minutes of first being exposed to it (not shown). All isoforms of nociceptin were cross-adapted to one another, indicating that all forms of nociceptin were using the same receptor and/or signaling pathway. This is similar to what has previously been shown for lysozyme [8] and PACAP/VIP [15]. Since PACAP, lysozyme, and VIP appear to share a common receptor [10, 15], we cross-adapted cells to nociceptin and PACAP to determine whether nociceptin was using the same receptor/signaling pathway as the three previously studied polycationic ligands. As Table 1 shows, PACAP-adapted cells did not cross-adapt to nociceptin and nociceptin-adapted cells did not cross-adapt to PACAP. This indicates that nociceptin signals through a pathway that does not involve the previously described polycation receptor.

The previously studied PACAP response appears to be mediated through a G-protein-coupled receptor which uses adenylyl cyclase, phospholipase C, and nitric oxide synthase [10,13-15]. In order to further ascertain whether nociceptin was using a separate signaling pathway, we used pharmacological inhibitors to block G-protein-linked receptors and associated pathways. None of these inhibitors blocked avoidance to nociceptin (Table 2), giving further evidence that the previously described polycation receptor is not being used in nociceptin signaling. This also differs from the vertebrate nociceptin receptor, which signals through [G.sub.i/o] proteins [1].

Since a tyrosine kinase has been implicated in GTP signaling in T. thermophila [18] as well as insulin signaling [19], we also tested a battery of protein kinase and tyrosine kinase inhibitors to determine whether nociceptin signaling would be inhibited. None of these inhibitors affected nociceptin signaling (Table 2). Interestingly, genomic studies of Tetrahymena [20] show no evidence of the presence of a tyrosine kinase in this organism.

Since a calcium-based depolarization is elicited by the addition of lysozyme [12] as well as the lysozyme fragment, CB2 [8], to T. thermophila, we wished to determine whether calcium was involved in nociceptin signaling in this organism. Studies with the external calcium chelator, EGTA (Figure 2) indicated that extracellular calcium was necessary for behavioral avoidance to nociceptin, since concentrations of EGTA above 50 reduced avoidance down to baseline. Baseline avoidance in this organism is determined by counting the number of cells that show avoidance behavior when transferred from one well of buffer to another well of the same buffer [10]. The SERCA ATPase inhibitor, thapsigargin, was used to determine whether internal calcium stores were required in order for avoidance to occur. As seen in Figure 2, exposure of cells to 100 thapsigargin reduced avoidance by approximately 50%. However, the avoidance response was not completely inhibited, indicating that while intracellular calcium may play a role in avoidance, lack of intracellular calcium stores depleted by thapsigargin may be partially compensated for by allowing extracellular calcium into the cytosol. Notably, the thapsigargin concentration used in this study was much higher than what we used in a previous study [18], in which only 1 nM thapsigargin was necessary in order to block the behavioral response to GTP. This is further evidence that extracellular calcium is primarily responsible for nociceptin avoidance. Calcium is not necessary for avoidance to all peptides, however, since avoidance of netrin-1, semaphorin 3C, and fragments of ACTH is unaffected by addition of either EGTA or thapsigargin [11].

Whole-cell electrophysiology studies indicate that nociceptin causes a depolarization in T. thermophila (Figure 3), even at concentrations that normally do not cause a behavioral response in this organism (Figures 3(a) and 1). When the E[C.sub.100] of nociceptin-NH2 was used, the amplitude of the depolarization increased (Figure 3(b)). Finally, we were able to remove the depolarization by the addition of EGTA to the external medium (Figure 3(c)), implying that calcium is involved in the depolarization. This is similar to the previously described responses to lysozyme [12]and the lysozyme fragment, CB2 [9].

The involvement of calcium in nociceptin avoidance in T. thermophila is rather different from the human response to nociceptin, which involves closing calcium channels [5]. However, we did use J-113397, which is a competitive inhibitor of the human nociceptin receptor [21], in order to determine if it could also block T. thermophila avoidance to nociceptin. As shown in Figure 4,50 J-113397 was effective in reducing avoidance to baseline. This drug had no effect on avoidance to ACTH fragments (data not shown), suggesting that the response was specific to nociceptin. While we have not identified the receptor or signaling pathway that nociceptin is using in T. thermophila, these data suggest that there may be commonalities between the human nociceptin receptor and a possible nociceptin-binding protein in T. thermophila.

In summary, we have shown that nociceptin is a chemo-repellent in Tetrahymena which elicits a depolarization. It does not act through the previously described polycation receptor nor does it signal through a G-protein-mediated receptor like the vertebrate nociceptin receptor. However, the J113397 studies imply that Tetrahymena may possess some type of receptor that shares binding characteristics with the human nociceptin receptor. Further studies may help elucidate the signaling mechanisms used in nociceptin avoidance in T. thermophila. If the receptor is identified, comparisons between the human nociceptin receptor and the unknown nociceptin-sensing mechanism in T. thermophila would be instructive.

5. Conclusions

The vertebrate signaling peptide, nociceptin, is a chemorepellent in Tetrahymena thermophila. The effectiveness of signaling is impacted by the charge of the nociceptin isoform, with more highly charged forms of nociceptin requiring lower concentrations to signal effectively. Nociceptin does not signal through the previously described polycation receptor of Tetrahymena thermophila nor does it signal through a G-protein-linked receptor, as it does in humans. However, nociceptin avoidance in Tetrahymena thermophila is blocked by addition of J-113397, a competitive inhibitor of the vertebrate nociceptin receptor. This suggests that the vertebrate nociceptin receptor and its analog in Tetrahymena may share common binding characteristics. Finally, nociceptin signaling provokes a depolarization, which pharmacological studies suggest may be caused by an influx of calcium.

Abbreviations

ACTH:          Adrenocorticotropic hormone
E[C.sub.100]:  Concentration of chemorepellent that causes
               avoidance in 100% of individuals
EGTA:          Ethylene glycol tetraacetic acid
I[C.sub.50]:   Concentration of inhibitor that blocks 50%
               of avoidance
PACAP:         Pituitary adenylyl cyclase activating
               polypeptide
VIP:           Vasoactive intestinal peptide.


http://dx.doi.org/10.1155/2013/573716

Conflict of Interests

None of the authors of this paper has any financial relationship with the vendors mentioned in this paper. There is no conflict of interests to declare.

References

[1] B. E. Hawes, M. P. Graziano, and D. G. Lambert, "Cellular actions of nociceptin: transduction mechanisms," Peptides, vol. 21,no 7,pp 961-967,2000

[2] E. Hashiba, C. Harrison, G. Calo' et al., "Characterisation and comparison of novel ligands for the nociceptin/orphanin FQ receptor," Naunyn-Schmiedeberg's Archives of Pharmacology, vol. 363, no. 1, pp. 28-33, 2001.

[3] L. Xu, E. Okuda-Ashitaka, S. Matsumura et al., "Signal pathways coupled to activation of neuronal nitric oxide synthase in the spinal cord by nociceptin/orphanin FQ," Neuropharmacology, vol.52, no.5, pp. 1318-1325,2007.

[4] C. Goeldner, D. Reiss, J. Wichmann, H. Meziane, B. L. Kieffer, and A. M. Ouagazzal, "Nociceptin receptor impairs recognition memory via interaction with NMDA receptor-dependent mitogen-activated protein kinase/extracellular signal-regulated kinase signaling in the hippocampus," Journal of Neuroscience, vol. 28, no. 9, pp. 2190-2198, 2008.

[5] H.S. Gompf, M.G. Moldavan, R.P. Irwin, and C.N. Allen, "Nociceptin/orphanin FQ (N/OFQ) inhibits excitatory and inhibitory synaptic signaling in the suprachiasmatic nucleus (SCN)," Neuroscience, vol.132, no.4, pp.955-965,2005.

[6] T. M. Hennessey, "Responses of the ciliates Tetrahymena and Paramecium to external ATP and GTP," Purinergic Signalling,

vol. 1, no. 2, pp. 101-110, 2005.

[7] G. Csaba, "The hormonal system of the unicellular Tetrahymena: a review with evolutionary aspects," Acta Microbiologica et Immunologica Hungarica, vol. 59, no. 2, pp. 131-156.

[8] H. G. Kuruvilla, M. Y. Kim, and T. M. Hennessey, "Chemosensory adaptation to lysozyme and GTP involves independently regulated receptors in Tetrahymena thermophila," Journal of Eukaryotic Microbiology, vol.44, no.3, pp.263-268,1997.

[9] H. G. Kuruvilla and T. M. Hennessey, "Chemosensory responses of Tetrahymena thermophila to CB2, a 24-amino-acid fragment of lysozyme," Journal of Comparative Physiology A, vol. 184, no. 5, pp. 529-534, 1999.

[10] S.R. Mace, J.G. Dean, J.R. Murphy, J.L. Rhodes, and H.G. Kuruvilla, "PACAP-38 is a chemorepellent and an agonist for the lysozyme receptor in Tetrahymena thermophila," Journal of Comparative Physiology A, vol. 186, no. 1, pp. 39-43, 2000.

[11] S. Ort, T. Warren, J. Morrow, E. Infante, A. Yager, and H. Kuruvilla, "Polycationic peptides are chemorepellents in Tetrahymena thermophila," manuscript in preparation.

[12] H. G. Kuruvilla and T. M. Hennessey, "Purification and characterization of a novel chemorepellent receptor from Tetrahymena thermophila," Journal of Membrane Biology, vol.162, no.1, pp. 51-57, 1998.

[13] D. L. Hassenzahl, N. K. Yorgey, M. D. Keedyetal., "Chemorepellent signaling through the PACAP/lysozyme receptor is mediated through cAMP and PKC in Tetrahymena thermophila," Journal of Comparative Physiology A, vol. 187, no. 3, pp. 171-176, 2001.

[14] J. Lucas, M. Riddle, J. Bartholomew et al., "PACAP-38 signaling in Tetrahymena thermophila involves NO and cGMP," Acta Protozoologica, vol. 43, no. 1, pp. 15-20, 2004.

[15] M. Keedy, N. Yorgey, J. Hilty, A. Price, D. Hassenzahl, and H. Kuruvilla, "Pharmacological evidence suggests that the lysozyme/PACAP receptor of Tetrahymena thermophila is a polycation receptor," Acta Protozoologica, vol. 42, no. 1, pp. 11-17, 2003.

[16] W. L. Dentler, "Fractionation of Tetrahymena ciliary membranes with Triton X-114 and the identification of a ciliary membrane ATPase," Journal of Cell Biology, vol.107, no. 6, pp. 2679-2688, 1988.

[17] E. D. Robinette, K. T. Gulley, K. J. Cassity et al., "A comparison of the polycation receptors of Paramecium tetraurelia and Tetrahymena thermophila," Journal of Eukaryotic Microbiology, vol.55, no.2, pp.86-90,2008.

[18] J. Bartholomew, J. Reichart, R. Mundy et al., "GTP avoidance in Tetrahymena thermophila requires tyrosine kinase activity, intracellular calcium, NOS, and guanylyl cyclase," Purinergic Signalling, vol.4, no.2, pp.171-181,2008.

[19] P. Kovacs and G. Csaba, "Effect of inhibitors and activators of tyrosine kinase on insulin imprinting in Tetrahymena" Cell Biochemistry and Function, vol. 10, no. 4, pp. 267-271,1992.

[20] J. A. Eisen, R. S. Coyne, M. Wu et al., "Macronuclear genome sequence of the ciliate Tetrahymena thermophila, a model eukaryote," PLoS Biology, vol. 4, no. 9, articlee286, 2006.

[21] C. Trapella, R. Guerrini, L. Piccagli et al., "Identification of an achiral analogue of J-113397 as potent nociceptin/orphanin FQ receptor antagonist," Bioorganic and Medicinal Chemistry, vol. 14, no. 3, pp. 692-704, 2006.

Thomas Lampert, (1) Cheryl Nugent, (2) John Weston, (2) Nathanael Braun, (2) and Heather Kuruvilla (2)

(1) Department of Biological Sciences, State University of New York at Buffalo, 109 Cooke Hall, Buffalo, NY14260, USA

(2) Department of Science and Mathematics, Cedarville University, 251 North Main Street, Cedarville, OH 45314, USA

Correspondence should be addressed to Heather Kuruvilla; heatherkuruvilla@cedarville.edu

Received 7 March 2013; Accepted 9 April 2013

Academic Editor: Hubert Vaudry

TABLE 1: Nociceptin cross-adaptation studies. Cells were adapted to
a given ligand by incubating them in that ligand for 10-15 minutes
or until avoidance behavior ceased. Cells were then moved into
another ligand and were scored positively or negatively for
avoidance. Cross-adaptation with various analogues of nociceptin
all show avoidance values that are at or below baseline ([less than or
equal to] 20%; [10]). However, cross- adaptation with the
polycationic peptide, PACAP, does not cross-adapt with nociception,
implying that nociception is using a pathway that is distinct from the
previously described lysozyme/PACAP receptor [10,15]. N represents
the number of trials conducted. Each trial consisted of 10 cells,
which were individually scored as positive or negative for avoidance.

                          Nociceptin          Nociceptin-
                                              N[H.sub.2]

Nociceptin                9.2 [+ or -] 8.2    5 [+ or -] 8.3
                          N=13                N=6

Nociceptin-N[H.sub.2]     5 [+ or -] 7.5      16.9 [+ or -] 12.2
                          N = 9               N=8

Nociceptin [Arg.sub.14]   3.3 [+ or -] 5.8    13.3 [+ or -] 12.1
[Lys.sub.15]              N = 6               N=6

PACAP 1-38                97.5 [+ or -] 4.6   100 [+ or -] 0
                          N = 8               N=10

                          Nociceptin            PACAP 1-38
                          [Arg.sub.14]
                          [Lys.sub.15]

Nociceptin                0[+ or -]0            96.6 [+ or -] 5.8
                          N = 6                 N = 6

Nociceptin-N[H.sub.2]     14.5 [+ or -] 12.4    100 [+ or -] 0
                          N =12                 N = 6

Nociceptin [Arg.sub.14]   16.6 [+ or -] 16.3    91.25 [+ or -] 9.9
[Lys.sub.15]              N = 6                 N = 8

PACAP 1-38                100[+ or -] 0         13.3[+ or -] 5.8
                          N =10                 N = 6

TABLE 2: Pharmacological inhibitors which act on G-protein mediated
receptor pathways and tyrosine kinase pathways do not significantly
impact nociception avoidance. N represents the number of trials
conducted. Each trial consisted of 10 cells, which were
individually scored as positive or negative for avoidance.

Pharmacological inhibitor          Pathway inhibited

Control                                  None
50 [micro]M RpcAMPs                Adenylyl cyclase
1mM GDP-[beta]-S                      G-proteins
1 [micro]M U-73122                  Phospholipase C
1 [micro]M U-73345           Inactive analogue of U-73122
10 [micro]M calphostin C           Protein kinase C
1 mM 1400 W                               NOS
100 [micro]M tyrphostin 47     Receptor tyrosine kinases
100 [micro]M AG126                Map kinase pathway
150 [micro]M SU 6668           Receptor tyrosine kinases
300 [micro]M apigenin               Protein kinases
3 mM H-9                            Protein kinases

Pharmacological inhibitor    Percentage of cells    N
                             avoiding nociceptin

Control                      94.28 [+ or -] 5.34      8
50 [micro]M RpcAMPs          96.67 [+ or -] 5.16      6
1mM GDP-[beta]-S             100.0 [+ or -] 0.0       6
1 [micro]M U-73122           97.78 [+ or -] 4.40      9
1 [micro]M U-73345           96.67 [+ or -] 5.16      6
10 [micro]M calphostin C     96.0 [+ or -] 5.0       10
1 mM 1400 W                  96.0 [+ or -] 5.0       10
100 [micro]M tyrphostin 47   92.5 [+ or -] 9.57       6
100 [micro]M AG126           96.0 [+ or -] 6.99      10
150 [micro]M SU 6668         91.66 [+ or -] 4.08      6
300 [micro]M apigenin        91.2 [+ or -] 6.4        8
3 mM H-9                     96.6 [+ or -] 5.1        6
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Title Annotation:Research Article
Author:Lampert, Thomas; Nugent, Cheryl; Weston, John; Braun, Nathanael; Kuruvilla, Heather
Publication:International Journal of Peptides
Article Type:Report
Geographic Code:1USA
Date:Jan 1, 2013
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