Exposure to organophosphates reduces the expression of neurotrophic factors in neonatal rat brain regions: similarities and differences in the effects of chlorpyrifos and diazinon on the fibroblast growth factor superfamily.BACKGROUND: The fibroblast growth factor Fibroblast growth factors, or FGFs, are a family of growth factors involved in wound healing and embryonic development. The FGFs are heparin-binding proteins and interactions with cell-surface associated heparan sulfate proteoglycans have been shown to be essential for FGF (FGF FGF Fibroblast Growth Factor
FGF Future Generation Foundation (Egypt)
FGF Feel-Good Factor
FGF Federación Gallega de Fútbol (Spain)
FGF Fédération Guinéenne de Football (Guinea) ) superfamily superfamily /su·per·fam·i·ly/ (soo´per-fam?i-le)
1. a taxonomic category between an order and a family.
2. of neurotrophic factors plays critical roles in neural cell development, brain assembly, and recovery from neuronal injury.
OBJECTIVES: We administered two organophosphate pesticides, chlorpyrifos and diazinon diazinon
an organophosphorus insecticide, used in ear tags for cattle and in flea collars and rinses for dogs. Called also dimpylate. See also organophosphorus compound. , to neonatal rats on postnatal postnatal /post·na·tal/ (-na´t'l) occurring after birth, with reference to the newborn.
Of or occurring after birth, especially in the period immediately after birth. days 1-4, using doses below the threshold for systemic toxicity or growth impairment, and spanning the threshold for barely detectable cholinesterase cholinesterase /cho·lin·es·ter·ase/ (-es´ter-as) serum cholinesterase, pseudocholinesterase; an enzyme that catalyzes the hydrolytic cleavage of the acyl group from various esters of choline and some related compounds; determination of inhibition: 1 mg/kg/day chlorpyrifos and 1 or 2 mg/kg/day diazinon.
METHODS: Using microarrays, we then examined the regional expression of mRNAs encoding the FGFs and their receptors (FGFRs) in the forebrain forebrain: see brain. and brain stem.
RESULTS: Chlorpyrifos and diazinon both markedly suppressed fgf20 expression in the forebrain and fgf2 in the brain stem, while elevating brain stem fgfr4 and evoking a small deficit in brain stem fgf22. However, they differed in that the effects on fgf2 and fgfr4 were significantly larger for diazinon, and the two agents also showed dissimilar, smaller effects on fgf11, fgf14, and fgfr1.
CONCLUSIONS: The fact that there are similarities but also notable disparities in the responses to chlorpyrifos and diazinon, and that robust effects were seen even at doses that do not inhibit cholinesterase, supports the idea that organophosphates differ in their propensity to elicit developmental neurotoxicity neurotoxicity /neu·ro·tox·ic·i·ty/ (noor?o-tok-sis´it-e) the quality of exerting a destructive or poisonous effect upon nerve tissue. , unrelated to their anticholinesterase anticholinesterase /an·ti·cho·lin·es·ter·ase/ (-ko?lin-es´ter-as) cholinesterase inhibitor.
n. activity. Effects on neurotrophic factors provide a mechanistic link between organophosphate organophosphate /or·ga·no·phos·phate/ (or?gah-no-fos´fat) an organic ester of phosphoric or thiophosphoric acid; such compounds are powerful acetylcholinesterase inhibitors and are used as insecticides and nerve gases. injury to developing neurons and the eventual, adverse neurodevelopmental outcomes.
KEY WORDS: brain development, chlorpyrifos, diazinon, fibroblast growth factor, fibroblast growth factor receptors, microarrays, neurotoxicity, organophosphate insecticides. Environ Health Perspect 115:909-916 (2007). doi:10.1289/ehp.9901 available via http://dx.doi.org/ [Online 27 February 2007]
The developmental neurotoxicity of organophosphate pesticides represents a biological conundrum that has important ramifications ramifications npl → Auswirkungen pl for human exposures (for review see Colborn 2006; Costa 2006; Landrigan 2001; Mileson et al. 1998; Slotkin 2005; Weiss et al. 2004). All of the organophosphates produce systemic toxicity by inhibiting acetylcholinesterase acetylcholinesterase /ac·e·tyl·cho·lin·es·ter·ase/ (AChE) (-ko?li-nes´ter-as) an enzyme present in the central nervous system, particularly in nervous tissue, muscle, and red cells, that catalyzes the hydrolysis of acetylcholine to , resulting in overt symptoms of cholinergic cholinergic /cho·lin·er·gic/ (ko?lin-er´jik)
1. parasympathomimetic; stimulated, activated, or transmitted by choline (acetylcholine); said of the sympathetic and parasympathetic nerve fibers that liberate acetylcholine at a hyperstimulation; these effects have therefore been assumed to be the common mechanism underlying adverse developmental consequences (Mileson et al. 1998). However, the fetus and neonate neonate /neo·nate/ (ne´o-nat) newborn infant.
A neonatal infant.
a newborn animal. recover from cholinesterase inhibition much more quickly than adults (Chakraborti et al. 1993; Lassiter et al. 1998), yet display greater overall toxicity and damage to the central nervous system (for review see Pope 1999; Slotkin 2004, 2005). Indeed, evidence accumulating over the past decade implicates a host of other mechanisms in the developmental neurotoxicity of the organophosphates that depend instead upon the direct targeting of events specific to the developing brain (for review see Barone et al. 2000; Pope 1999; Rice and Barone 2000; Slotkin 2004). Importantly, many of these processes are vulnerable to organophosphates at doses below those necessary to elicit signs of systemic toxicity and even below the threshold for significant inhibition of cholinesterase (Pope 1999; Slotkin 2004, 2005).
Although a wide variety of intermediate events in brain development connect the initial effects of organophosphates on neural cell differentiation to the eventual synaptic synaptic /syn·ap·tic/ (si-nap´tik)
1. pertaining to or affecting a synapse.
2. pertaining to synapsis.
Of or relating to synapsis or a synapse. and behavioral defects (Pope 1999; Slotkin 2004, 2005), little information is currently available about specific cellular mechanisms that render the developing brain so vulnerable to these agents. Indeed, many events in differentiation and assembly of neural circuits are affected, including the processes of neuronal and glial cell gli·al cell
Any of the cells making up the neuroglia, especially the astrocytes, oligodendroglia, and microglia. replication and differentiation, specification of neurotransmitter neurotransmitter, chemical that transmits information across the junction (synapse) that separates one nerve cell (neuron) from another nerve cell or a muscle. Neurotransmitters are stored in the nerve cell's bulbous end (axon). phenotypes, axonogenesis and synaptogenesis, and synaptic function (Barone et al. 2000; Casida and Quistad 2004; Gupta 2004; Jameson et al. 2006; Pope 1999; Slotkin 1999, 2004). In turn, the diversity of these targets suggests that the organophosphates disrupt some very basic processes in neural cell differentiation. For that reason, a number of investigations have turned to the neurotrophic factors known to play critical roles in neural development and damage/repair processes.
In adults, fully symptomatic organophosphate poisoning produces peripheral neuropathies and then a reactive increase in formation of neurotrophic factors mediating repair and neuritic outgrowth (Pope et al. 1995). Although we are dealing with events in the central nervous system rather than with peripheral neuropathies, it is not unreasonable to hypothesize hy·poth·e·size
v. hy·poth·e·sized, hy·poth·e·siz·ing, hy·poth·e·siz·es
To assert as a hypothesis.
To form a hypothesis. that these factors are equally or even more important at the subtoxic exposures that damage the developing brain. Two sets of neurotrophic factors have been explored to date. First, acetylcholinesterase itself is thought to play a nonenzymatic role in neural development (Brimijoin and Koenigsberger 1999), and we recently demonstrated induction of the neurotoxic neurotoxic
pertaining to or emanating from a neurotoxin.
a case of poisoning by a neurotoxin.
neurotoxic adjective splice variant of acetylcholinesterase at organophosphate exposures below the threshold for detectable inhibition of enzymatic activity in neonatal rat brain after apparently subtoxic exposures to chlorpyrifos or diazinon (Jameson et al. 2007). In addition, two recent studies (Betancourt and Carr 2004; Betancourt et al. 2006) focused on nerve growth factor nerve growth factor
n. Abbr. NGF
A protein that stimulates the growth of sympathetic and sensory nerve cells.
Nerve growth factor and brain-derived neurotrophic factor Brain-derived neurotrophic factor (BDNF) is a neurotrophic factor found in the brain and the periphery. It is a protein that acts on certain neurons of the central nervous system and the peripheral nervous system that helps to support the survival of existing neurons and encourage after exposure of newborn rats to chlorpyrifos or chlorpyrifos oxon, the active metabolite active metabolite Therapeutics A drug metabolite with therapeutic activity similar to the parent compound, which must be considered in therapeutic pharmacokinetics that inhibits cholinesterase. Although these researchers used exposures that were above the threshold for cholinesterase inhibition and somatic somatic /so·mat·ic/ (so-mat´ik)
1. pertaining to or characteristic of the soma or body.
2. pertaining to the body wall in contrast to the viscera.
adj. growth impairment, they found no significant decrease in either protein (Betancourt and Carr 2004) and only a small decrease (10-20%) in the mRNA encoding nerve growth factor (Betancourt et al. 2006).
Thus, if organophosphate effects on neurotrophic factors play an important role in the developmental neurotoxicity of these agents, then other factors are likely to be more highly affected. In the present study, we turned our attention to the large number of fibroblast growth factors (FGFs) and their receptors (FGFRs). The FGF superfamily plays a widespread and vital role in brain development and in the repair from neural injury (Dono 2003). Across the various stages of development, the FGFs promote and maintain neuronal cell replication and are required for differentiation into the terminal transmitter phenotype (Gage et al. 1995; Johe et al. 1996). The different FGFs play specific roles in neuronal cell differentiation, neurite outgrowth, and the recovery from damage in regions such as the striatum striatum /stri·a·tum/ (stri-a´tum) corpus striatum.stria´tal
n. pl. stri·a·ta and hippocampus hippocampus
fabulous marine creature; half fish, half horse. [Rom. Myth. and Art: Hall, 154]
See : Monsters (Hart et al. 2000; Limke et al. 2003; Murase and McKay 2006; Ohmachi et al. 2000; Ray et al. 1993; Takagi et al. 2005). The same regions are known targets for the adverse neurodevelopmental effects of organophosphates (Barone et al. 2000; Slotkin 1999, 2004, 2005), which disrupt the very same cellular events for which the FGFs provide trophic trophic /tro·phic/ (tro´fik) (trof´ik) pertaining to nutrition.
Of, relating to, or characterized by nutrition. signals (Axelrad et al. 2003; Das and Barone 1999; Howard et al. 2005; Song et al. 1998). Accordingly, we used a microarray approach to examine the family of FGFs and their receptors, comparing the effects of two different organophosphates, chlorpyrifos and diazinon, to emphasize points of similarity and difference: if the developmental neurotoxicity of the organophosphates involves neurotrophic mechanisms unrelated to the inhibition of cholinesterase, then there may be significant disparities in their impact on neurotrophic factors. We concentrated on doses that evoke barely detectable inhibition, too low to elicit any signs of cholinergic hyperstimulation (Slotkin et al. 2006b; Song et al. 1997); our assessments were conducted in two brain regions, the brain stem and forebrain, that differ both in anatomical attributes as well as in maturational timetables (Rodier 1988).
Materials and Methods
Animal treatments. All experiments were carried out in accordance with federal and state guidelines and with prior approval of the Duke University Institutional Animal Care and Use Committee Institutional Animal Care and Use Committees are of central importance to the application of laws to animal research in the United States. Most research involving laboratory animals is funded by the United States National Institutes of Health or other federal agencies. ; all animals were treated humanely and with due care for alleviation of distress. Timed-pregnant Sprague-Dawley rats (Charles River, Raleigh, NC, USA) were housed in breeding cages, with a 12-hr light/dark cycle and free access to food and water. On the day of birth, all pups were randomized ran·dom·ize
tr.v. ran·dom·ized, ran·dom·iz·ing, ran·dom·iz·es
To make random in arrangement, especially in order to control the variables in an experiment. and redistributed to the dams with a litter size of 9-10 to maintain a standard nutritional status nutritional status,
n the assessment of the state of nourishment of a patient or subject. .
Chlorpyrifos and diazinon (both from Chem Service, West Chester, PA, USA) were dissolved in dimethylsulfoxide di·meth·yl·sulf·ox·ide
DMSO. to provide consistent absorption (Whitney et al. 1995), and were injected subcutaneously in a volume of 1 mL/kg body weight once daily on postnatal days (PNDs) 1-4; control animals received equivalent injections of dimethylsulfoxide vehicle. For both agents, we used doses below the threshold for growth retardation and systemic toxicity (Campbell et al. 1997; Slotkin et al. 2006a; Whitney et al. 1995): 1 mg/kg for chlorpyrifos and either 1 or 2 mg/kg for diazinon. This chlorpyrifos treatment and the higher dose of diazinon produce neurotoxicity in developing rat brain while eliciting < 20% cholinesterase inhibition, whereas the lower dose of diazinon does not produce any detectable inhibition (Slotkin 1999, 2004; Slotkin et al. 2006b; Song et al. 1997; Whitney et al. 1995), or any of the symptoms of cholinergic hyperstimulation known to be characteristic of anticholinesterase activity (Clegg and van Gemert 1999). These treatments thus resemble the nonsymptomatic exposures reported in pregnant women (De Peyster et al. 1993) and are within the range of expected fetal and childhood exposures after routine home application or in agricultural communities (Gurunathan et al. 1998; Ostrea et al. 2002).
On PND (Personal Navigation Device) A portable GPS-based navigation system that can be used when walking, hiking or in any vehicle. See GPS. 5 (24 hr after the last dose), one male pup was selected from each of five litters in each treatment group. Animals were decapitated de·cap·i·tate
tr.v. de·cap·i·tat·ed, de·cap·i·tat·ing, de·cap·i·tates
To cut off the head of; behead.
[Late Latin d , the cerebellum cerebellum (sĕr'əbĕl`əm), portion of the brain that coordinates movements of voluntary (skeletal) muscles. It contains about half of the brain's neurons, but these particular nerve cells are so small that the cerebellum accounts for was removed, and the brain stem and forebrain were separated by a cut made rostral rostral /ros·tral/ (ros´tral)
1. pertaining to or resembling a rostrum; having a rostrum or beak.
2. situated toward a rostrum or toward the beak (oral and nasal region), which may mean superior (in relationships to the thalamus thalamus (thăl`əməs), mass of nerve cells centrally located in the brain just below the cerebrum and resembling a large egg in size and shape. . Tissues were weighed and flash-frozen in liquid nitrogen and maintained at -45[degrees]C until analyzed. Our study design involved the analysis of 40 separate tissues: one animal from each of five litters for each of the four treatment groups, with two tissues (brain stem, forebrain) from each animal.
Microarray determinations. Tissues were thawed and total RNA RNA: see nucleic acid.
in full ribonucleic acid
One of the two main types of nucleic acid (the other being DNA), which functions in cellular protein synthesis in all living cells and replaces DNA as the carrier of genetic was isolated using the Aurum total RNA Fatty and Fibrous Tissue fibrous tissue
Tissue composed of bundles of collagenous white fibers between which are rows of connective tissue cells. Kit (Bio-Rad Laboratories, Hercules, CA, USA). RNA quality was verified using the RNA 6000 LabChip Kit and the Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA). An aliquot aliquot (al-ee-kwoh) adj. a definite fractional share, usually applied when dividing and distributing a dead person's estate or trust assets. (See: share) of each sample used in the study was withdrawn and combined to make a reference RNA preparation to be included on each array. RNA amplification was carried out using a commercial kit (Low RNA Input Fluorescent Linear Amplification Kit; Agilent).
Each RNA sample was annealed with a primer containing a polydT and a T7 polymerase promoter. Reverse transcriptase Reverse transcriptase
Any of the deoxyribonucleic acid (DNA) polymerases present in particles of retroviruses which are able to carry out DNA synthesis using an RNA template. produced a first and second strand cDNA. T7 RNA polymerase T7 RNA Polymerase is an RNA polymerase that catalyzes the formation of RNA in the 5'→ 3' direction. T7 RNA polymerase is extremely promoter-specific and only transcribes bacteriophage T7 DNA or DNA cloned downstream of a T7 promoter. then created cRNA from the double stranded cDNA by incorporating cyanine-3- (for the reference RNA) or cyanine-5- (for the sample RNA) labeled cytidine 5-triphosphate cytidine 5-triphosphate
A nucleotide necessary to the synthesis of RNA and to the production of choline and ethanolamine. ; the quality of the labeled cRNA was again verified and the absolute concentration was measured spectrophotometrically. For each pair of reference cRNA and experimental cRNA hybridized to an array, equal amounts of cRNA (0.75 [micro]g) were hybridized using a commercial kit (In situ Hybridization in situ hybridization A method for localizing a sequence of DNA, mRNA, or protein in a cell or tissue; the use of a DNA or RNA probe to detect a cDNA sequence in chromosome spreads or in interphase nuclei or an RNA sequence of cloned bacterial or cultured Kit-Plus; Agilent). Hybridization hybridization /hy·brid·iza·tion/ (hi?brid-i-za´shun)
1. crossbreeding; the act or process of producing hybrids.
2. molecular hybridization
3. was performed at 60[degrees]C for 17 hr with Agilent Whole Rat Genome Arrays (G4131A). The arrays were washed with Agilent's SSPE SSPE
subacute sclerosing panencephalitis
subacute sclerosing panencephalitis.
SSPE Subacute sclerosing panencephalitis, see there Wash Protocol using a solution of 6x SSPE, 0.005% N-lauroylsarcosine, a solution of 0.06x SSPE, 0.005% N-lauroylsarcosine, and Agilent's Stabilization and Drying Solution. The arrays were scanned on an Agilent G2565BA Microarray Scanner, and data from the scans were compiled with Agilent Feature Extraction Software 8.1. The steps from RNA amplification through extraction of the scanner output data were performed by a private contractor (Cogenics, Research Triangle Park Research Triangle Park, research, business, medical, and educational complex situated in central North Carolina. It has an area of 6,900 acres (2,795 hectares) and is 8 × 2 mi (13 × 3 km) in size. Named for the triangle formed by Duke Univ. , NC, USA).
Array normalizations and error detection were carried out using Silicon Genetics' GeneSpring GX Version 7.2 (Agilent), via the Enhanced Agilent Feature Extraction Import Preprocessor Software that performs some preliminary processing on the input before it is processed by the main program. See preprocessing.
(programming) preprocessor - A program that transforms input data in some way before it is read by the main program. . First, values of poor quality intensity and low dependability were removed using a "filter on flags" feature, where standardized software algorithms determined which spots were "present," "marginal," or "absent"; spots were considered "present" only where the output was uniform, not saturated and significant above background, whereas spots that satisfied the main requirements but were outliers relative to the typical values for the other genes were considered "marginal." Filters were set to retain only the values that were found to be present or marginal for further analysis; however, of the genes that passed the filter, none was marginal.
Data were normalized in three steps using the algorithms supplied with the Feature Extraction software. The first step divides the signal in the Cy5 channel (sample RNA) by that in the Cy3 channel (reference RNA), to give the measured ratio for each gene in the array. The second normalization In relational database management, a process that breaks down data into record groups for efficient processing. There are six stages. By the third stage (third normal form), data are identified only by the key field in their record. adjusts the total signal of each chip to a standard value ("normalize normalize
to convert a set of data by, for example, converting them to logarithms or reciprocals so that their previous non-normal distribution is converted to a normal one. to 50th percentile") determined by the median of all the reliable values on the chip; this renders the output of each chip comparable with that of every other chip in the study. The third normalization step is applied to each gene across all the arrays in the study ("normalize to median"): The median of all the values obtained for a given gene is calculated and used as the normalization standard for that gene, so that, regardless of absolute differences in the expression of the various genes, they are placed on the same scale for comparison.
After normalization, one final quality-control filter was applied in which genes showing excessive biologic variability were discarded; the criterion for retention was that more than half of the eight treatment x region groupings had to have coefficients of variation < 30%.
For some of the genes, the arrays contained multiple probes and/or replicates of the same probe in different locations on the chip, and these were used to verify the reliability of values and the validity of the measures on the chip. In these cases, to avoid artificially inflating the number of positive findings, we limited each gene to a single set of values, selecting those obtained for the probe showing the smallest intragroup (treatment, region) variance; the other values for that gene were used only to corroborate To support or enhance the believability of a fact or assertion by the presentation of additional information that confirms the truthfulness of the item.
The testimony of a witness is corroborated if subsequent evidence, such as a coroner's report or the testimony of other direction and magnitude of change. Through these procedures we identified five defective arrays with sequential production numbers, for which one corner of the array showed a nonuniform overall difference in brightness that affected the readings in that region of the chip. The affected samples were reevaluated on replacement arrays that did not repeat the problem. Our experimental design ensured that the replacement readings were distributed among all the treatment groups because our sample sequence was control, chlorpyrifos, diazinon 1 mg/kg, diazinon 2 mg/kg; thus we did not run the risk of generating a spurious apparent treatment effect from differences among arrays. The defective arrays did allow us to perform an additional quality-control evaluation because most of the spots on the defective arrays were in the portion that did not show the defect. Comparing the values on the replacement arrays to the valid portions of the defective arrays produced a close correspondence of values (correlation coefficient Correlation Coefficient
A measure that determines the degree to which two variable's movements are associated.
The correlation coefficient is calculated as: = 0.98).
Statistical procedures. Because of the requirement to normalize the data across arrays and within each gene, the absolute values for a given gene are meaningless; only the relative differences between regions and treatments can be compared. Accordingly, results for the regional differences in gene expression in control rats are presented as means [+ or -] SEs of the normalized ratios for each gene, but the effects of the treatments are given as the percentage change from control to allow for visual comparison of the relative changes evoked for each gene, regardless of its control ratio. However, statistical comparisons were based on the actual ratios (log-transformed because the data are in the form of ratios) rather than the percent change.
Our design involved planned comparisons of the organophosphate-exposed groups to the controls and between the two different organophosphates, so it was important to consider the false positive rate and to protect against type 1 errors from repeated testing of the same database. Accordingly, before looking at effects on individual genes, we performed a global analysis of variance (ANOVA anova
see analysis of variance.
ANOVA Analysis of variance, see there ) incorporating all treatments, both regions, and all genes in a single comparison. Lower-order ANOVAs were then carried out as permitted by the interactions of treatment with region and gene that justified subdivisions of the data set. Finally, differences for individual treatments for a specified gene in a single brain region were evaluated with Fisher's protected least significant difference test. However, where there was no treatment x region interaction for a given gene; only the main treatment effect was reported without subtesting of effects in individual regions. For ANOVA results, effects were considered significant at p < 0.05 (two-tailed, because we were interested in both increases and decreases in gene expression). In addition to these parametric tests of the direction and magnitude of changes in gene expression, we evaluated the incidence of significant differences as compared with the false positive rate using Fisher's exact test Fisher's exact test
a statistical test for association in a two-by-two table based on the exact hypergeometric distribution of the frequencies within the table. , applying a one-tailed criterion of p < 0.05 because only an increase above the false positive rate would be predicted. Finding a significant decrease in the incidence of detected differences relative to the false positive rate would be biologically implausible and statistically meaningless.
Of the FGF and FGFR genes present on the microarray, 19 genes passed the quality control filters, encoding 15 of the FGFs and all 4 FGFRs (Table 1). In control rats, we did not observe any overall pattern of regional preference for expression of these genes: Of the 19 genes evaluated, only 6 showed significant regional differences, with fgf9, fgf22, and fgfr2 more highly expressed in the brain stem, whereas fgf14, fgf20, and fgfr1 were higher in the forebrain. Organophosphate exposures elicited significant, regionally selective changes in gene expression for the FGFs and FGFRs. Multivariate ANOVA (all treatments, all genes, both regions) showed a significant treatment x region x gene interaction (p < 0.0001), enabling separate evaluations for each gene. Out of the 19 genes, 7 displayed significant main treatment effects or an interaction of treatment x region, as compared with an expected false positive rate of only 1 gene (p < 0.02).
For the genes encoding FGFs, chlorpyrifos exposure produced a significant overall decrement To subtract a number from another number. Decrementing a counter means to subtract 1 or some other number from its current value. (main treatment effect, p < 0.05) and specific reductions in the expression of fgf2, fgf11, fgf20, and fgf22 (Figure 1). By far, the largest effect was on fgf20, which showed a 50% deficit in the forebrain; this region also displayed a significant deficit in fgf2 and fgf11. In contrast, the brain stem showed smaller decreases restricted to fgf2 and fgf22.
The effects of diazinon on the FGF genes displayed similarities to those of chlorpyrifos, but also some differences. The lower dose of diazinon caused a large reduction in forebrain fgf20 expression as did chlorpyrifos, but diazinon failed to decrease forebrain fgf2 or fgf11 significantly, and instead evoked a reduction in fgf14 (Figure 2A). In the brain stem, we again saw a small decrease in fgf2 and fgf22. Increasing the dose of diazinon to 2 mg/kg produced a further divergence from the effects seen with chlorpyrifos (Figure 2B). Although we still saw a significant reduction in fgf20 in the forebrain, no other gene was significantly affected for this region. In the brain stem, the higher dose of diazinon produced an even larger decrease in fgf2 expression than with either chlorpyrifos or the lower diazinon treatment. These regional differences between diazinon and chlorpyrifos were statistically significant (p < 0.02 for the interaction of treatment x region x gene).
Two of the four genes encoding the FGFRs, fgfr1 and fgfr4, showed statistically significant treatment-related changes in expression, but the magnitude of the effect on fgfr1 was quite small, < 10% (Figure 3). In contrast, fgfr4 showed significant increases in expression for all three organophosphate treatment groups, an effect that was restricted to the brain stem. Diazinon produced a larger increase than did chlorpyrifos. Again, the regional differences in the effects of the two organophosphates were statistically distinguishable (p < 0.05 for the interaction of treatment x region x gene).
Earlier work with higher doses of chlorpyrifos administered for longer periods of time--treatments that evoke significant and persistent cholinesterase inhibition and/or growth impairment--identified small (10-20%) decreases in the mRNA encoding nerve growth factor (Betancourt et al. 2006). We also examined expression of the two corresponding genes on our arrays, ngfb (GenBank accession no. XM_227525; GenBank 2007) and ngfg (Genbank NM_031523) but found only a small (6%) decrease in ngfb in the forebrain that did not achieve statistical significance (data not shown). Similarly, we found no significant effects on expression of the gene encoding brain-derived neurotrophic factor (bdnf; Genbank accession no. NM_012513; data not shown).
Our results show that neonatal exposure to doses of organophosphates that are below the threshold for any signs of systemic intoxication intoxication, condition of body tissue affected by a poisonous substance. Poisonous materials, or toxins, are to be found in heavy metals such as lead and mercury, in drugs, in chemicals such as alcohol and carbon tetrachloride, in gases such as carbon monoxide, and or growth deficits, and just at the threshold At the Threshold, whose son Lil E. Tee won the 1992 Kentucky Derby for W. Cal Partee, died March 23 of a stroke at Purdue University School of Veterinary Medicine in West Lafayette, Ind. The 21-year-old stallion stood at Wayne Houston's Stoney Creek Horse Farm near Mooreland, Ind. for any detectable inhibition of cholinesterase, nevertheless causes profound suppression of several members of the FGF superfamily of neurotrophic factors. Indeed, the effects for chlorpyrifos or diazinon in the present study are far larger than those reported previously for other neurotrophic factors, even when the earlier work involved chlorpyrifos treatments at higher doses for longer periods, producing much greater cholinesterase inhibition or frank growth impairment (Betancourt and Carr 2004; Jameson et al. 2007). Furthermore, we found a distinct regional hierarchy corresponding to the maturational and anatomical differences between the brain stem and the forebrain (Rodier 1988). The brain stem matures earlier than the forbrain and contains a high proportion of cell bodies for cholinergic, catecholaminergic, and serotonergic se·ro·to·ner·gic or se·ro·to·ni·ner·gic
Activated by or capable of liberating serotonin, especially in transmitting nerve impulses.
containing or activated by serotonin. neurons; the forebrain develops later and contains the terminal projections of these neurotransmitter systems, all of which are prominent targets for the developmental neurotoxicity of organophosphates (Slotkin 1999, 2004, 2005). In keeping with this regional specificity, fgf20 was suppressed by chlorpyrifos or diazinon in the forebrain, whereas the two organophosphates differentially targeted fgf2 in the brain stem (diazinon > chlorpyrifos). There were also smaller effects on fgf11, fgf14, fgf22, fgfr1, and fgfr4, each of which also displayed either a regionally selective effect or a difference between the two organophosphates. In contrast, no such regional differences were reported for other neurotrophic factors such as nerve growth factor or acetylcholinesterase splice variants associated with neural damage/repair (Betancourt and Carr 2004; Jameson et al. 2007). Indeed, to obtain any effect on nerve growth factor gene expression, the dose and duration of chlorpyrifos exposure have to be increased to the point where cholinesterase is persistently inhibited and/or growth is impaired; even then, there is only a small (10-20%) decrement (Betancourt et al. 2006). In the present study, we used lower doses and shorter durations of exposure that caused barely detectable cholinesterase inhibition and no growth impairment, and found no significant deficits for either nerve growth factor or brain-derived neurotrophic factor, indicating that selective members of the FGF superfamily are indeed far more sensitive to disruption by the organophosphates.
The regional selectivity suggests that the effects of neonatal exposure to organophosphates on expression of FGFs reflects the targeting of specific processes in brain development rather than a global interference with neurotrophic responses. Below, we will consider each of the FGFs in turn, emphasizing their various roles in neural development and plasticity. However, first it is necessary to consider the important differences between chlorpyrifos and diazinon.
In the developing rat brain, treatment with 1 mg/kg chlorpyrifos produces approximately a 10-20% inhibition of cholinesterase (Song et al. 1997), roughly equivalent to that seen at 2 mg/kg diazinon (Slotkin et al. 2006b); the lower dose of diazinon (1 mg/kg) produces no significant inhibition whatsoever (Slotkin et al. 2006b). If the effects of these agents were the result of cholinesterase inhibition, then the chlorpyrifos treatment should produce the same pattern of effects as the higher dose of diazinon, whereas the lower diazinon dose should have no effect at all. In fact, though, all three treatments shared the same major suppression of fgf20 in the forebrain. Furthermore, the low dose of diazinon inhibited brain stem fgf2 and fgf22 expression, and increased fgfr4, just as did chlorpyrifos. It is therefore apparent that these effects are totally unrelated to cholinesterase inhibition, the mechanism that underlies the systemic toxicity of the organophosphates, thus reinforcing the concept that the developmental neurotoxicity of these agents represents a separable sep·a·ra·ble
Possible to separate: separable sheets of paper.
sep set of mechanisms that operate at lower exposures (Colborn 2006; Slotkin 1999, 2004, 2005; U.S. Environmental Protection Agency Environmental Protection Agency (EPA), independent agency of the U.S. government, with headquarters in Washington, D.C. It was established in 1970 to reduce and control air and water pollution, noise pollution, and radiation and to ensure the safe handling and 2006).
It is also noteworthy that we saw several important differences in the effects of chlorpyrifos as compared with diazinon: chlorpyrifos decreased fgf2 and fgf11 in the forebrain, whereas diazinon did not; in the brain stem, diazinon reduced fgf2 and induced fgfr4 much more than did chlorpyrifos, and also had effects on forebrain fgf14 and fgfr1 that were not seen with chlorpyrifos. The similarities and disparities suggest that the two organophosphates are likely to produce many parallels in subsequent neurodevelopmental deficits but may also differ in important ways. Although much more information is available for chlorpyrifos than for diazinon, several findings already suggest differential targeting of neural cell replication, neuritic outgrowth, cytotoxic cy·to·tox·ic
Of, relating to, or producing a toxic effect on cells.
cyto·tox·ic events, and cholinergic and monoaminergic neurotransmitter systems by these two agents (Jameson et al. 2007; Qiao et al. 2001; Slotkin et al. 2006a, 2007).
The two specific members of the FGF superfamily that were most highly affected by neonatal organophosphate exposure were fgf2 and fgf20, both of which have clearly established roles in neurodevelopment, plasticity, damage/repair, and neurodegenerative disorders. The expression of fgf2 shows spatial and temporal relationships to the maturational profile of each brain region (Gomez-Pinilla et al. 1994; Monfils et al. 2006) and up-regulation of this gene is required for the recovery from developmental brain injury (Monfils et al. 2005; Yoshimura et al. 2001). In addition, we recently found that fgf2 is intimately involved in the programming of neural plasticity associated with less injurious in·ju·ri·ous
1. Causing or tending to cause injury; harmful: eating habits that are injurious to one's health.
2. perturbations, such as prenatal stress (Fumagalli et al. 2005). Accordingly, the robust down-regulation of this gene caused by neonatal organophosphate treatment is likely to play an important role in the neurodevelopmental outcomes of such exposures; in particular, our finding of regional selectivity (brain stem > forebrain) is in keeping with the targeting of a specific maturational stage and/or anatomical location and similarly, the preferential sensitivity to diazinon predicts a potentially worsened outcome with this agent. For fgf2, our finding of gross suppression by organophosphates during the brain growth spurt growth spurt Pediatrics A period of rapid growth in middle adolescence; ♀ ↑ ±8 cm/yr ±age 12; ♂ ↑ ±10 cm/yr ± age 14; GS is orderly, affecting acral parts–ie, hands and feet grow before proximal regions, (Dobbing and Sands 1979) is highly likely to have long-term, adverse consequences for neural development and behavioral function. Even a brief period of fgf2 down-regulation interferes directly with neurogenesis neurogenesis /neu·ro·gen·e·sis/ (-jen´e-sis) the development of nervous tissue.
Formation of nervous tissue.
the development of nervous tissue. (Tao et al. 1997), and the period of exposure studied here (first few days after birth) corresponds to the peak proliferation period in a number of neuronal populations, including those of the hippocampal hip·po·cam·pus
n. pl. hip·po·cam·pi
A ridge in the floor of each lateral ventricle of the brain that consists mainly of gray matter and has a central role in memory processes. dentate gyrus dentate gyrus
One of the two interlocking gyri composing the hippocampus. (Kempermann et al. 1997; Rodier 1988). If similar effects occur with organophosphate exposures in earlier or later developmental periods, this could explain why shifting the exposure window often targets the neural cells and regions that are undergoing the most rapid development (Slotkin 1999, 2004, 2005).
In contrast to the organophosphate-evoked reduction in fgf2, which was more prominent in the brain stem, the suppression of fgf20 was selective for the forebrain. What is particularly notable about the regional difference is that fgf20 is preferentially expressed in a subregion sub·re·gion
A subdivision of a region, especially an ecological region.
subre of the forebrain, the striatum (Ohmachi et al. 2000), which contains the majority of dopamine dopamine (dōp`əmēn), one of the intermediate substances in the biosynthesis of epinephrine and norepinephrine. See catecholamine.
One of the catecholamines, widely distributed in the central nervous system. projections, the loss of which results in Parkinson disease Parkinson Disease Definition
Parkinson disease (PD) is a progressive movement disorder marked by tremors, rigidity, slow movements (bradykinesia), and posture instability. . There is growing suspicion that repeated developmental exposures to pesticides that target striatal dopamine projections play a significant role in the later emergence of this neurodegenerative disorder (for review, see Cory-Slechta et al. 2005; Landrigan et al. 2005). Indeed, the relationship of suppressed fgf20 expression to dopaminergic dopaminergic /do·pa·min·er·gic/ (do?pah-men-er´jik) activated or transmitted by dopamine; pertaining to tissues or organs affected by dopamine.
adj. deficits and thence thence
1. From that place; from there: flew to Helsinki and thence to Moscow.
2. From that circumstance or source; therefrom.
3. Archaic From that time; thenceforth. to Parkinson disease is directly supported by human genetic data (Murase and McKay 2006; Takagi et al. 2005; van der Walt et al. 2004) and by the specific role of this neurotrophic factor neurotrophic factor A generic term for any of a family of substances with roles in maintenance and survival of neurons–eg, secretory proteins, nerve growth factors–see there, brain-derived growth factor, neurotrophin-3 in promoting survival of the very neurons that are lost in Parkinson disease (Damier et al. 1999; Yamada et al. 1990).
The requirement for fgf20 is similarly found for development of these neurons and for preventing their death from apoptosis secondary to oxidative stress oxidative stress,
n an imbalance of the prooxidant antioxidant ratio in which too few antioxidants are produced or ingested or too many oxidizing agents are produced. (Murase and McKay 2006); the striatum is especially sensitive to oxidative damage, in part because dopamine itself produces oxidative metabolites Metabolites
Substances produced by metabolism or by a metabolic process.
Mentioned in: Interactions (Hirsch 1994; Olanow and Arendash 1994). Organophosphates target striatal dopamine systems by causing release of dopamine while simultaneously evoking oxidative stress through other cellular mechanisms (Bloomquist et al. 2002; Gupta 2004; Jett and Navoa 2000; Karen et al. 2001; Lazarini et al. 2004; Slotkin et al. 2002, 2005; Slotkin and Seidler 2007). Consequently, these neural pathways are among the most vulnerable to long-term damage after developmental exposure to chlorpyrifos (Aldridge et al. 2005b; Dam et al. 1999; Slotkin et al. 2002, 2007; Slotkin and Seidler 2007). Finally, it should be noted that fgf2 is also deficient in dopaminergic neurons in Parkinson disease (Tooyama et al. 1993) and fgf2 and fgf20 actually act in concert to protect dopaminergic neurons from oxidative injury and to promote their repair (Krieglstein et al. 1998; Ohmachi et al. 2000; Otto and Unsicker 1990; Shults et al. 2000), so that the combined deficit in both these neurotrophic factors, superimposed su·per·im·pose
tr.v. su·per·im·posed, su·per·im·pos·ing, su·per·im·pos·es
1. To lay or place (something) on or over something else.
2. on organophosphateinduced oxidative stress, may render striatal dopamine pathways especially vulnerable. In particular, in Parkinson disease, degeneration begins in the brain stem (Braak et al. 2006), the region in which we found reduced fgf2 expression after neonatal organophosphate exposure. We therefore anticipate that later in life, exposed individuals may show a greater likelihood of neurodegenerative disorders such as Parkinson disease, which is already known to be associated with pesticide exposures in adulthood (Kamel and Hoppin 2004).
In addition to the major changes seen for fgf2 and fgf20 expression, we found significant but smaller effects on other members of the FGF superfamily, including fgf11, fgf14, and fgf22, and also on two of the receptor genes, fgfr1 and fgfr4. Although the roles for these are less well understood, there is substantial evidence for involvement of all of them in neurodevelopment and hence in the developmental neurotoxicity of the organophosphates. Developing neurons show particularly high expression of fgf11 and fgf14 (Luo et al. 2002; Wang et al. 2000), and the latter participates directly in neuronal signaling, axonal axonal
pertaining to or arising from an axon.
an axon dies and cannot be replaced if its cell body is destroyed. trafficking, and development of sodium channels required for neuronal excitability excitability
readiness to respond to a stimulus; irritability. (Lou et al. 2005; Wang et al. 2002). Deficits in fgf14 are associated with the development of movement disorders Movement Disorders Definition
Movement disorders are a group of diseases and syndromes affecting the ability to produce and control movement.
Description (Wang et al. 2002) and it is well established that early exposure to organophosphates compromises the subsequent development of motor activity (Carr et al. 2001; Dam et al. 2000). Similarly, fgf22, a recently discovered member of the FGF family, is involved in neural differentiation of granule cells and acts as an organizer of presynaptic presynaptic /pre·syn·ap·tic/ (-si-nap´tik) situated or occurring proximal to a synapse.
Relating to the area on the proximal side of a synaptic gap. activity (Umemori et al. 2004). Again, hippocampal and cerebellar cerebellar /cer·e·bel·lar/ (ser?e-bel´ar) pertaining to the cerebellum.
Involving the part of the brain (cerebellum), which controls walking, balance, and coordination. granule cells are known to be targeted by developmental exposure to organophosphates (Abdel-Rahman et al. 2003; Roy et al. 2005) in association with profound alterations in the patterns of presynaptic neuronal activity and associated behaviors (Aldridge et al. 2005b; Dam et al. 1999; Icenogle et al. 2004; Levin et al. 2001, 2002; Qiao et al. 2003, 2004; Richardson and Chambers 2004, 2005; Slotkin et al. 2001, 2002; Slotkin and Seidler 2007).
Of the two FGF receptor genes for which we found significant changes, fgfr1 is only weakly expressed in the developing brain but probably serves as an organization factor (Blak et al. 2005); we found only a small effect on this receptor, restricted to diazinon, so that this may ultimately contribute to some differences in outcome between the two organophosphates. We saw a far more robust effect on fgf4, again with a greater action of diazinon as compared to chlorpyrifos. In contrast to fgfr1, fgfr4 is highly expressed in developing brain, especially in the hippocampus (Cool et al. 2002; Limke et al. 2003; Wright et al. 2004) and in cholinergic neurons of the medial habenular nucleus (Miyake and Itoh 1996), and is involved specifically in neurite outgrowth (Hart et al. 2000). Furthermore, this receptor binds fgf2, one of the FGF members highly affected by organophosphate exposure, reinforcing the greater potential contribution of this particular signaling pathway; indeed, the fact that fgf4 was up-regulated suggests that this is a partial, adaptive response to the suppression of fgf2 expression, a conclusion reinforced by the fact that diazinon was more effective than chlorpyrifos for both the down-regulation of brain stem fgf2 and the up-regulation of fgfr4. In keeping with these relationships, developmental exposure to organophosphates especially targets each of the processes associated with fgfr4: neurons of the cholinergic phenotype (Slotkin 1999, 2004, 2005), the hippocampus (Abdel-Rahman et al. 2003; Pung pung
n. New England
A low, one-horse box sleigh.
[Short for dialectal tom-pung, from an Algonquian language of southern New England.]
Noun 1. et al. 2006; Roy et al. 2005; Terry et al. 2003), and neuritic outgrowth (Axelrad et al. 2003; Das and Barone 1999; Howard et al. 2005; Slotkin et al. 2006a; Song et al. 1998).
It is important to note a number of limitations of our approach, which relies on measurement of gene expression at the mRNA level assessed in two, broadly defined brain regions. First, the magnitude of changes was small when compared to the fold-change that can be obtained with in vitro in vitro /in vi·tro/ (in ve´tro) [L.] within a glass; observable in a test tube; in an artificial environment.
In an artificial environment outside a living organism. studies of pesticide neurotoxicity, where typically one assesses the effects on a single cell type at a fixed stage of differentiation (Mense n. 1. Manliness; dignity; comeliness; civility.
v. t. 1. To grace. et al. 2006). That is hardly surprising, given the heterogeneity of the brain stem and the forebrain, so that even a large change in gene expression in a specific cell population would be "washed out" by mRNA from unaffected areas. In fact, treatment of animals with higher doses of organophosphates that produce outright toxicity or even lethality rarely produces changes in gene expression exceeding 10-30% in vivo in vivo /in vi·vo/ (ve´vo) [L.] within the living body.
Within a living organism.
in vivo adv. (Betancourt et al. 2006; Damodaran et al. 2006a, 2006b).
The second limitation is inherent in any study of mRNA: this measure by itself does not provide a definitive answer about the actual rate of synthesis and degradation of the encoded protein, the factors that actually control the concentrations of the corresponding trophic factors or factors within the cell. Nevertheless, there are two important aspects designed into the current study that render the findings relevant and interpretable. First, we included chlorpyrifos as a test compound whose impact has already been confirmed for the relevant end points of neural cell differentiation, axonogenesis, and other developmental processes known to be regulated by FGFs. Second, our interpretations rely on patterns of changes across multiple regions and FGF/FGFR subtypes rather than on a single change in one region. Nevertheless, it is obvious that a direct mechanistic link needs to be established between the changes seen here at the mRNA level and the known outcomes for chlorpyrifos, or the suspected outcomes for diazinon.
Our results are also limited by the fact that we examined only males, whereas there are numerous studies showing significant sex differences in the outcomes of developmental exposure to organophosphates (Aldridge et al. 2004, 2005a, 2005b; Dam et al. 2000; Levin et al. 2001; Ricceri et al. 2006; Slotkin 2005; Slotkin et al. 2001, 2002; Slotkin and Seidler 2007). Here, we were limited primarily by practical considerations of technical capabilities and cost. We expect, however, that males and females will show important differences in transcriptional profiles in accordance with the sex-selective nature of organophosphateinduced neurodevelopmental anomalies. Despite these limitations, though, our results are likely to be relevant to environmental exposures of fetuses and children to organophosphates. Although our studies were modeled primarily on the upper limits of estimated or measured exposures after home or agricultural application (Gurunathan et al. 1998; Ostrea et al. 2002), recent studies indicate that much lower, long-term exposures of pregnant women result in adverse neurodevelopmental outcomes for their children (Eskenazi et al. 2007; Rauh et al. 2006; Young et al. 2005). Accordingly, modeling the potential mechanisms underlying the adverse effects of these agents at exposures below the threshold for cholinesterase inhibition may provide important insights into the etiology of these orders and thus to potential strategies for amelioration a·me·lio·ra·tion
1. The act or an instance of ameliorating.
2. The state of being ameliorated; improvement.
Noun 1. .
In conclusion, our results show that neonatal exposure to low doses of organophosphates, below the threshold for any signs of systemic toxicity and spanning the threshold for any detectable cholinesterase inhibition, evoke profound and regionally selective effects on expression of specific members of the FGF superfamily of neurotrophic factors, with the largest effects seen for fgf2 and fgf20. The fact that there are similarities but also notable disparities in the responses to chlorpyrifos and diazinon, and that robust effects were seen at a dose of diazinon that does not inhibit cholinesterase, supports the idea that organophosphates differ in their propensity to elicit developmental neurotoxicity, unrelated to their anticholinesterase activity. Further, the specific involvement of fgf2 and fgf20 in development of the hippocampus and striatum matches some of the most sensitive regional targets for neurodevelopmental disruption by the organophosphates, reinforcing the potential mechanistic role of suppression of these neurotrophic factors in organophosphate-induced developmental neurotoxicity.
The close relationship between deficiencies in these factors and loss of dopamine neurons in Parkinson disease further indicates the need for long-term studies of the effects of early organophosphate exposure, preferably occupying the entire life span so as to determine whether developmental exposures lead to later emergence of neurodegenerative disorders. Finally, the identification of specific neurotrophic factors targeted by organophosphates may enable the design of targeted, interventional strategies that might prevent or offset neurodevelopmental damage in cases of known exposure. For example, increasing the concentration of FGF2 protein appears to offset the functional outcome of neonatal damage to the motor cortex motor cortex
The region of the cerebral cortex influencing movements of the face, neck and trunk, and arm and leg. Also called excitable area, motor area, Rolando's area. (Monfils et al. 2005), and the neuroprotective effect of nicotine in animal models of Parkinson disease (Quik and Di Monte 2001) is associated with its ability to up-regulate fgf2 expression (Belluardo et al. 2004). The characterization of neurotrophic factors involved in the developmental neurotoxicity of organophosphates thus establishes a mechanistic link between the initial events in neural cell damage and the eventual outcome, while at the same time providing valuable information to enable discrimination between the effects of different organophosphates as well as potential therapeutic interventions to prevent or offset neural damage.
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Theodore A. Slotkin, (1) Frederic J. Seidler, (1) and Fabio Fumagalli (2)
(1) Department of Pharmacology & Cancer Biology, Duke University Medical Center, Durham, North Carolina Durham is a city in the U.S. state of North Carolina. It is the county seat of Durham CountyGR6 and is the fourth-largest city in the state by population. , USA; (2) Center of Neuropharmacology neuropharmacology /neu·ro·phar·ma·col·o·gy/ (-fahr?mah-kol´ah-je) the scientific study of the effects of drugs on the nervous system.
n. , Department of Pharmacological Sciences, University of Milan The university is a member of the League of European Research Universities.
Throughout Milan, the University is normally known as Statale to avoid confusion with other academic institutions in the city. , Milan, Italy
Address correspondence to T.A. Slotkin, Box 3813 DUMC DUMC Duke University Medical Center
DUMC Damascus United Methodist Church (Damascus, MD)
DUMC Demaree United Methodist Church (Illinois) , Duke University Medical Center, Durham, NC 27710 USA. Telephone: (919) 681-8015. Fax: (919) 684-8197. E-mail: email@example.com
This research was supported by grant ES10356 from the National Institutes of Health.
T.A.S. and F.J.S. have provided expert witness testimony on behalf of government agencies, corporations, and/or individuals. F.F. declares he has no competing financial interests.
Received 14 November 2006; accepted 27 February 2007.
Table 1. Control values. Name Gene Genbank accession no. Fibroblast growth factor 1 fgf1 NM_012846 Fibroblast growth factor 2 fgf2 NM_019305 Fibroblast growth factor 3 fgf3 NM_130817 Fibroblast growth factor 9 fgf9 NM_012952 Fibroblast growth factor 11 fgf11 NM_130816 Fibroblast growth factor 12 fgf12 NM_130814 Fibroblast growth factor 13 fgf13 NM_053428 Fibroblast growth factor 14 fgf14 NM_022223 Fibroblast growth factor 15 fgf15 NM_130753 Fibroblast growth factor 17 fgf17 NM_019198 Fibroblast growth factor 18 fgf18 NM_019199 Fibroblast growth factor 20 fgf20 NM_023961 Fibroblast growth factor 21 fgf21 NM_130752 Fibroblast growth factor 22 fgf22 NM_130751 Fibroblast growth factor 23 fgf23 NM_130754 Fibroblast growth factor fgfr1 NM_024146 receptor 1 Fibroblast growth factor fgfr2 BF 557.572 receptor 2 Fibroblast growth factor fgfr3 NM_053429 receptor 3 Fibroblast growth factor fgfr4 XM_344570 receptor 4 Name Brainstem Forebrain Fibroblast growth factor 1 0.98 [+ or -] 0.05 1.00 [+ or -] 0.04 Fibroblast growth factor 2 1.17 [+ or -] 0.09 1.02 [+ or -] 0.03 Fibroblast growth factor 3 1.13 [+ or -] 0.11 0.87 [+ or -] 0.04 Fibroblast growth factor 9 1.37 [+ or -] 0.08 0.81 [+ or -] 0.02* Fibroblast growth factor 11 1.03 [+ or -] 0.13 1.18 [+ or -] 0.10 Fibroblast growth factor 12 1.02 [+ or -] 0.07 1.01 [+ or -] 0.03 Fibroblast growth factor 13 0.97 [+ or -] 0.02 1.00 [+ or -] 0.02 Fibroblast growth factor 14 0.87 [+ or -] 0.06 1.20 [+ or -] 0.04* Fibroblast growth factor 15 1.04 [+ or -] 0.15 1.15 [+ or -] 0.20 Fibroblast growth factor 17 0.96 [+ or -] 0.06 1.00 [+ or -] 0.08 Fibroblast growth factor 18 0.96 [+ or -] 0.04 0.99 [+ or -] 0.04 Fibroblast growth factor 20 0.92 [+ or -] 0.23 1.63 [+ or -] 0.22* Fibroblast growth factor 21 0.99 [+ or -] 0.08 0.97 [+ or -] 0.07 Fibroblast growth factor 22 1.11 [+ or -] 0.02 0.93 [+ or -] 0.04* Fibroblast growth factor 23 1.10 [+ or -] 0.10 0.84 [+ or -] 0.10 Fibroblast growth factor 1.00 [+ or -] 0.02 1.08 [+ or -] 0.02* receptor 1 Fibroblast growth factor 1.10 [+ or -] 0.04 0.96 [+ or -] 0.02* receptor 2 Fibroblast growth factor 0.98 [+ or -] 0.02 1.00 [+ or -] 0.03 receptor 3 Fibroblast growth factor 0.89 [+ or -] 0.03 0.98 [+ or -] 0.03 receptor 4 GenBank accession numbers from GenBank (2007). *Significant difference between brain stem and forebrain.