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Testosterone Induces Molecular Changes in Dopamine Signaling Pathway Molecules in the Adolescent Male Rat Nigrostriatal Pathway

  • Tertia D. Purves-Tyson,

    Affiliations Schizophrenia Research Institute, Sydney, New South Wales, Australia, Schizophrenia Research Laboratory, Neuroscience Research Australia, Sydney, New South Wales, Australia, School of Medical Sciences, University of New South Wales, Sydney, New South Wales, Australia

  • Samantha J. Owens,

    Affiliations Schizophrenia Research Institute, Sydney, New South Wales, Australia, Schizophrenia Research Laboratory, Neuroscience Research Australia, Sydney, New South Wales, Australia, School of Medical Sciences, University of New South Wales, Sydney, New South Wales, Australia

  • Kay L. Double,

    Affiliation Discipline of Biomedical Science, School of Medical Sciences, Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia

  • Reena Desai,

    Affiliation ANZAC Research Institute, University of Sydney, Concord Hospital, Concord, New South Wales, Australia

  • David J. Handelsman,

    Affiliation ANZAC Research Institute, University of Sydney, Concord Hospital, Concord, New South Wales, Australia

  • Cynthia Shannon Weickert

    c.weickert@neura.edu.au

    Affiliations Schizophrenia Research Institute, Sydney, New South Wales, Australia, Schizophrenia Research Laboratory, Neuroscience Research Australia, Sydney, New South Wales, Australia, School of Psychiatry, University of New South Wales, Sydney, New South Wales, Australia

Testosterone Induces Molecular Changes in Dopamine Signaling Pathway Molecules in the Adolescent Male Rat Nigrostriatal Pathway

  • Tertia D. Purves-Tyson, 
  • Samantha J. Owens, 
  • Kay L. Double, 
  • Reena Desai, 
  • David J. Handelsman, 
  • Cynthia Shannon Weickert
PLOS
x

Abstract

Adolescent males have an increased risk of developing schizophrenia, implicating testosterone in the precipitation of dopamine-related psychopathology. Evidence from adult rodent brain indicates that testosterone can modulate nigrostriatal dopamine. However, studies are required to understand the role testosterone plays in maturation of dopamine pathways during adolescence and to elucidate the molecular mechanism(s) by which testosterone exerts its effects. We hypothesized that molecular indices of dopamine neurotransmission [synthesis (tyrosine hydroxylase), breakdown (catechol-O-methyl transferase; monoamine oxygenase), transport [vesicular monoamine transporter (VMAT), dopamine transporter (DAT)] and receptors (DRD1-D5)] would be changed by testosterone or its metabolites, dihydrotestosterone and 17β-estradiol, in the nigrostriatal pathway of adolescent male rats. We found that testosterone and dihydrotestosterone increased DAT and VMAT mRNAs in the substantia nigra and that testosterone increased DAT protein at the region of the cell bodies, but not in target regions in the striatum. Dopamine receptor D2 mRNA was increased and D3 mRNA was decreased in substantia nigra and/or striatum by androgens. These data suggest that increased testosterone at adolescence may change dopamine responsivity of the nigrostriatal pathway by modulating, at a molecular level, the capacity of neurons to transport and respond to dopamine. Further, dopamine turnover was increased in the dorsal striatum following gonadectomy and this was prevented by testosterone replacement. Gene expression changes in the dopaminergic cell body region may serve to modulate both dendritic dopamine feedback inhibition and reuptake in the dopaminergic somatodendritic field as well as dopamine release and re-uptake dynamics at the presynaptic terminals in the striatum. These testosterone-induced changes of molecular indices of dopamine neurotransmission in males are primarily androgen receptor-driven events as estradiol had minimal effect. We conclude that nigrostriatal responsivity to dopamine may be modulated by testosterone acting via androgen receptors to alter gene expression of molecules involved in dopamine signaling during adolescence.

Introduction

Schizophrenia is slightly more common in males than females [1]. The peak age of onset of schizophrenia in males is concomitant with higher testosterone levels at adolescence and young adulthood, suggesting testosterone may be linked to the onset of psychosis in vulnerable individuals [2]. Increased dopamine within the nigrostriatal pathway of patients with schizophrenia is proposed as a driver of psychosis [3][5] supported by the effectiveness of antipsychotics (which block dopamine D2 receptors) in diminishing symptoms of hallucinations and delusions [6]. Imaging studies provide direct evidence of dysregulation of striatal dopamine transmission in schizophrenia underlying the development of psychosis [7], [8] but the underlying molecular cause(s) of this dopamine dysregulation are unknown. Understanding the molecular mechanisms by which testosterone modulates the maturation and regulation of nigrostriatal dopamine responsivity during adolescence is crucial to understanding the possible role of testosterone in schizophrenia risk.

Dopaminergic transmission involves signaling by five G-protein coupled receptors divided into inhibitory receptors (DRD2, DRD3, DRD4) and excitatory receptors (DRD1, DRD5), as well as the regulation of dopamine movement across membranes via dopamine transporter (DAT) and vesicular monoamine transporter (VMAT2). Dopamine is broken down by catechol-O-methyl transferase (COMT) and monoamine oxidase (MAOA and MAOB) enzymes to the main metabolites, 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) (reviewed in [9]). Dopamine homeostasis is maintained by dopamine biosynthesis, transport and breakdown, all potentially modulated by testosterone-induced changes in gene expression and/or protein levels of the molecules involved.

In order for testosterone to change gene expression, it can bind directly to the transcription factors, androgen receptor (AR) or, following conversion to estradiol by aromatase, to estrogen receptors (ERα, ERβ). Testosterone is also converted to dihydrotestosterone (DHT), a more potent, pure androgen which initiates transcription mainly via ARs [10] (although it can also act through ERβ [11]). All three receptors are expressed in dopaminergic neurons in the adult rodent midbrain [12][15] and ERα and AR expression has been confirmed in the adolescent male rat midbrain [16].

Previously, we found that testosterone increased TH in the adolescent substantia nigra [16]; and here, we predicted that activation of sex steroid receptors in male adolescence would lead to increased striatal TH protein and dopamine. Evidence regarding the mechanism(s) by which testosterone modulates nigrostriatal dopamine neurotransmission in the adult mammalian brain is, however, conflicting [17][21]. Circulating testosterone levels are positively correlated with protein levels of tyrosine hydroxylase (TH), the rate-limiting enzyme in dopamine synthesis, in the striatum of adolescent male rhesus macaques [22]. In addition, gonadectomy reduced TH activity in the striatum of adult male rats and this reduction was prevented by testosterone [23].We recently reported that testosterone increased COMT and MAO mRNAs in the adolescent male rat substantia nigra (SN), implying increased dopamine turnover capacity in the nigrostriatal pathway in male adolescence [16]. Further studies in adult rats suggest other components of dopamine signaling can also be modified by androgens [6], [24][26]. In the current work, we tested the hypothesis that testosterone can induce androgen receptor-driven changes in gene expression of multiple molecules involved in the regulation of dopamine neurotransmission in the nigrostriatal pathway in adolescent male rat brain.

In the current work, we investigated which molecular indices of dopamine neurotransmission are modulated by testosterone and whether testosterone actions in the adolescent male rat nigrostriatal pathway are driven primarily by androgenic or estrogenic mechanisms. We achieved this by gonadectomizing 45-day old male rats (adolescence) and replacing endogenous testosterone with either testosterone (T), DHT or 17β-estradiol (estradiol, E) until 60 days of age (young adults). Unexpectedly, dopamine was unchanged in the dorsal striatum by gonadectomy or with testosterone replacement, but dopamine turnover was increased by gonadectomy. Gene expression for dopamine transporters (DAT and VMAT2) and protein levels of DAT were increased in the substantia nigra by androgens but not estradiol. DAT protein levels were unchanged in the striatum. We show that, in contrast to our previously reported data in the substantia nigra [16], striatal COMT and MAO gene expression is unchanged by sex steroids. We report distinct dopamine receptor (D1, D2, D3, D5) mRNAs are modulated in areas of dopaminergic cell bodies and post-synaptic targets (D2 and D5) of the nigrostriatal pathway, mostly via AR activation. Our results indicate that in adolescent male rats, testosterone may alter the dopamine neurotransmission within the nigrostriatal pathway by attenuating dopamine turnover in the striatum and by modulating mRNA levels of dopamine receptors and changing dopamine transporter levels in the midbrain.

Materials and Methods

Experimental animals

All animal experiments were approved by the Animal Care and Ethics Committee of the University of New South Wales (Ethics number ACEC10/40) in accordance with the National Health and Medical Research Council of Australia's Code of Practice for the Care and Use of Animals for Experimental Purposes, which also conforms to standard international guidelines. Male Sprague-Dawley rats were used for all experiments (Animal Resource Centre, Perth, WA, Australia). Rats were group housed (3–4/cage) in 12/12 hr light/dark phases with constant humidity and temperature and free access to water and standard rat chow. All surgery was performed under ketamine hydrochloride and xylazine hydrochloride anaesthesia, and all efforts were made to minimize suffering. A total of 78 experimental animals were used.

Gonadectomy and sex steroid replacement.

Male rats were gonadectomised at 45 days of age and given continuous replacement testosterone (T), DHT or 17β-estradiol (E) by subdermal silastic implant [27][29] for two weeks. Male Sprague-Dawley rats experience an increase in circulating testosterone between 45 and 60 days of age [30][34] and at 60 days of age are considered young adults. There were five groups (∼15 rats/group): intact (Intact); gonadectomy alone (Gdx); gonadectomy plus testosterone (Gdx+T); gonadectomy plus DHT (Gdx+DHT); gonadectomy plus estradiol (Gdx+E). Rats were anaesthetized with an intraperitoneal injection of ketamine hydrochloride (60 mg/kg) and xylazine hydrochloride (10 mg/kg) (Provet, Castle Hill, Australia). Intact animals underwent abdominal surgery but gonads were left in place. Silastic implants were placed subcutaneously between the shoulder blades at time of gonadectomy. Gdx and Intact groups were given empty implants. Implants were 1 cm long, internal diameter 1.47 mm, outer diameter 1.95 mm and filled with crystalline steroid (ends sealed with silastic adhesive). The implants have been characterized in previous studies and achieve supraphysiological, steady-state serum hormone levels and androgen implants maintain seminal vesicle weights comparable to that in untreated animals [16], [28], [35]. T, DHT and E were quantified in serum using stable isotope dilution liquid chromatography-tandem mass spectroscopy as described [36] and adapted for rodents [37]. The limit of quantitation is 0.025 ng/ml T, 0.1 ng/ml DHT and 5 pg/ml E as previously reported [16]. Concentrations of circulating sex steroids and seminal vesicle weights confirm that successful sex steroid replacement was achieved in these rats as reported previously [16]. Briefly, in Intact rats circulating concentrations of T and DHT were 2.8 ± 0.6 and 0.2 ± 0.03 ng/ml respectively and E was 7.3 pg/ml. In Gdx rats, T was 0.03 ± 0.001 ng/ml and DHT and E were not detectable. In Gdx+T rats, T was 23.1 ± 12.0 ng/ml and DHT and E were not detectable. In the Gdx+DHT group, DHT was 21.42 ± 10.6 ng/ml and T was not detectable. In the Gdx+E group, E was 17.0 ± 6.7 pg/ml.

Brain dissection.

At 60 days of age, rats were anaesthetized with 60 mg/kg sodium pentobarbital (Euthal, Delvet, Seven Hills, Australia) and decapitated. Brains were removed and tissue blocks containing midbrain and striatum were dissected following a Rat Brain Atlas [38]. The midbrain block was trimmed transversely at the cerebral aqueduct and two lateral segments of midbrain on either side of the ventral tegmental area containing the substantia nigra (SN) were collected. The block containing striatum (between bregma 2.28 mm and 0.36 mm) was trimmed on either side of the midline along the lateral ventricles and ventrally to remove non-striatal tissue. In the striatal blocks, the striatum above the line of the anterior commissures was collected as dorsal striatum and referred to in the study as striatum. The striatum was separated from the overlying corpus callosum and stored. Trunk blood was collected on the day of euthanasia in 0.8 ml serum gel tubes (Z serum MiniCollect tube, GreinerBioOne, Wemmel, Belgium) and serum collected by centrifugation. Left and right hemisphere segments were randomly assigned for either protein or RNA extraction. 6–15 mg of tissue was separated from dorsal striatum segments allocated for RNA to utilize for reverse-phase, high pressure liquid chromatography.

Dopamine and metabolite measurement

Dorsal striatum samples were analysed for dopamine, DOPAC and HVA, using high pressure liquid chromatography with electrochemical detection as previously described [39], [40]. Frozen tissue samples were sonicated (S-250A Sonicator; Branson Ultrasonics, Danbury, CT, USA) for 30 s in 19× the tissue weight of 150 mM H3PO4 and 500 µM diethylenetriaminepenta-acetic acid (Sigma, St Louis, MO, USA) followed by centrifugation (44,5000 g, 25 min, 4°C; Optima L-90K ultracentrifuge; Beckman Coulter, Palo Alto, CA, USA) and supernatant collected and stored (−80°C).

High pressure liquid chromatography was performed with a Prominence system (Shimadzu, Kyoto, Japan) composed of degasser (DGU-20A3), liquid chromatographer (LC-20AD), autosampler (SIL-20A) and communications module (CBM-20A). Samples were injected onto a Gemini C18 column (150×4.60 mm, 110 Å, 5 µm particle size; Phenomenex, Torrance, CA, USA) connected to an electrochemical detector (Antec Leyden Intro, Zoeterwoude, NV, Netherlands) with an Ag/AgCl reference electrode at a potential of +0.72 V and 40°C. Isocratic mobile phase contained 16% methanol, 84% 0.01 M monobasic sodium phosphate, 0.1 mM ethylenediaminetetraacetic acid, 0.65 mM 1-octane sulfonic acid, 0.5 mM triethylamine at pH 3.4, adjusted with hydrochloric acid (Sigma). Injection volumes were 20–35 µL with a 0.75 mL/min flow rate and a 23.5 min run time.

External standards (1 µM dopamine, 1 µM DOPAC and 2 µM HVA; Sigma) were run daily (9 days in total) to produce a six-point standard curve for dopamine (0.95–17.07 ng), DOPAC (0.84–15.13 ng) and HVA (1.82–32.79 ng) to quantify samples run on the same day. Peak area analysis was with Class VP7.3 SP1 software (Shimadzu). Aliquots of 20–35 µL of samples, pooled from a subset of thirty-five rats (seven samples from each group) were injected daily and used to normalise between measurements acquired on different days. Dopamine turnover was calculated as DOPAC+HVA/dopamine.

Immunoblotting

Dorsal striatum or substantia nigra tissue blocks were homogenized (0.1 M Tris, pH 7.5, 50% glycerol, proteinase inhibitor cocktail (Sigma Cat# P8340) and aprotinin 0.015 mM, Sigma) using a handheld electric homogenizer (Polytron, Kinematica, Lucerne, Switzerland). Protein concentration was determined using the Bradford protein assay (Sigma). An aliquot of each sample was combined and used as a standard and run in duplicate on each gel to allow standardization between blots (internal control). Standard curves with between 0.5 and 20 µg substantia nigra or dorsal striatum protein were run and TH and DAT expression was determined to be within a linear range and 3 µg protein/sample was used. SDS-PAGE (10% acrylamide for TH and 8% acrylamide for DAT) was performed and proteins were transferred to nitrocellulose (45 µm, Biorad, CA, USA). Primary antibodies were anti-TH (host species rabbit, 1∶5000; Chemicon), anti-DAT (host species rabbit, 1∶300, H-20 sc14002, Santa Cruz) and anti-β-actin (host species mouse, 1∶5000; MAB1501, Millipore). Secondary antibodies were goat anti-mouse or anti-rabbit horseradish peroxidase conjugated (1∶4000, Millipore). Immunoreactive bands were detected using the LumiGlo detection kit (LumiGlo Reagent; Cell Signaling, Danvers, MA, USA) on hyperfilm (Amersham, GE Healthcare, Uppsala, Sweden). The immunoblots were scanned and band densities converted to numerical values using ImageJ software (ImageJ 1.43u, National Institutes of Health, USA). Relative intensities of TH and DAT bands (on separate blots) were normalized to relative intensity of β-actin bands on the same immunoblot.

RNA extraction and cDNA synthesis

Total RNA was extracted from SN and dorsal striatum samples in 800–1000 µl TRIzol (Life Technologies, Grand Island, NY, USA) as recommended by the manufacturer. RNA was quantified using a ND-1000 spectrophotometer (Nanodrop Technologies, Wilmington, DE, USA) and RNA integrity was assessed with high resolution capillary electrophoresis (Agilent Bioanalyzer 2100, Agilent Technologies, Palo Alto, CA, USA). Two aliquots of 3 µg RNA from each sample were reverse transcribed with SuperScript III First-Strand Synthesis Supermix and random hexamers, according to the manufacturer's protocol (Life Technologies). The 2 aliquots of cDNA from each sample were pooled and diluted for qPCR. A parallel reaction was performed without reverse transcriptase.

Quantitative real-time PCR (qPCR)

Transcripts of interest were measured by TaqMan Gene Expression Assays (Table 1) (Applied Biosystems, Foster City, CA, USA) using an ABI Prism 7900HT Fast Real-Time PCR System and a 384-well format. Three housekeeping genes were used to calculate the normalizing control for gene expression (termed geometric mean) and were selected on the basis that they were unchanged by the treatment. GusB, 18S rRNA and GAPDH, were used in the SN and GusB, GAPDH and YWHAZ were used in the striatum (Table 1, Gene names and Taqman probes). The geometric means of the three housekeeping genes used for each region were calculated as described previously [41]. Samples were run alongside a seven-point standard curve using serial dilutions of cDNA derived from SN or striatum RNA pooled from a subset of 25 rats (taken from all treatment groups). No template controls were included. Measurements were performed in triplicate. PCR cycling conditions were: 50°C for 2 min, 95°C for 10 min, 50 cycles of 95°C for 15 s and 60°C for 1 min. PCR data were captured with Sequence Detector Software (SDS version 2.4, Applied Biosystems) and real-time fluorescence intensity plotted with the threshold within the linear phase of the amplification profiles.

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Table 1. Genes of interest and housekeeper genes with ABI Taqman Gene Expression Assay part numbers.

https://doi.org/10.1371/journal.pone.0091151.t001

Statistics

Unless otherwise stated statistical analyses were conducted using SPSS software (IBM SPSS Statistics, version 19) and p<0.05 was considered statistically significant. Population outliers were removed by Grubb's test (GraphPad Prism online calculators) on the normalized qPCR, immunoblotting and HPLC data. Immunoblotting data are presented as change of relative intensity compared to the Gdx group ± SEM. Immunoblotting data were normalized to β-actin expression. qPCR data are presented as percent change of mRNA levels relative to the Gdx group ± SEM. Outlier detection of the triplicates obtained from the qPCR raw data excluded measurement errors [42]. qPCR raw data was normalized by the geomean of the housekeepers. HPLC data is expressed as ng/mg tissue ± SEM. HPLC raw data was normalized to an internal control run each day. Dopamine turnover was calculated before outliers were removed. All data was analyzed by one-way ANOVA followed by Fisher's LSD. Comparisons of DAT protein levels were made using one-directional t tests (GraphPad Prism) due to an a priori hypothesis [43], based on mRNA findings, that DAT protein would be increased by androgens relative to the Intact and Gdx groups.

Results

Circulating sex steroids over a two week adolescent period change mRNAs encoding for pre-synaptic dopamine reuptake, vesicular packaging and dopamine receptor proteins in the substantia nigra

In the substantia nigra, there was a significant effect of treatment group on DAT mRNA (F = 6.1, df =  (4,64), p<0.0001) (Fig. 1A) and VMAT mRNA (F = 4.18, df  =  (4,65), p = 0.005) (Fig. 1B). Both DAT and VMAT mRNAs were increased significantly relative to Intact or Gdx by replacement with T or DHT but not E. DAT mRNA was increased 40% and 50% by T and DHT, respectively, when compared to the Gdx group and 45% and 54% by T and DHT, respectively, when compared to the Intact group. VMAT mRNA was increased 26% and 35% by T and DHT, respectively, when compared to the Gdx group and 27% and 36% by T and DHT, respectively, when compared to the Intact group.

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Figure 1. Effect of gonadectomy and sex steroid replacement on presynaptic dopamine transporter and dopamine receptor mRNA expression in the substantia nigra of adolescent male rats.

DAT (A) and VMAT (B) mRNA expression were increased by androgens but not by 17β-estradiol replacement. (C) DRD2 pan, (D) DRD2 short and (E) DRD2 long mRNAs were increased by testosterone and DHT replacement relative to Intact and Gdx groups. 17β-estradiol replacement had no effect on DRD2pan, D2S or D2L mRNA levels. (F) DRD3 mRNA was decreased by testosterone and DHT replacement relative to Gdx. 17β-estradiol replacement had no effect on DRD3 mRNA. (G) DRD1 mRNA was increased by DHT replacement relative to Gdx. Testosterone and 17β- estradiol replacement had no effect on DRD1 mRNA expression. (H) DRD5 mRNA was increased by testosterone replacement relative to Intact and Gdx groups and increased by DHT and 17β-estradiol replacement relative to the Gdx group. * denotes comparison with Intact, unless comparison is indicated by a line, # denotes comparison with the Gdx group, * and # p<0.05, ** and ## p<0.01, *** and ### p<0.001, n = 12–15/group.

https://doi.org/10.1371/journal.pone.0091151.g001

In the substantia nigra, we also found a significant effect of treatment group on DRD2 pan mRNA (F = 8.5, df  =  (4,65), p<0.0001) (Fig. 1C). DRD2 pan includes two isoforms, DRD2 short (D2S), which has a truncated cytoplasmic loop, and DRD2 long (D2L). There was a significant effect of treatment group on D2S (F = 8.3, df  =  (4,63) p<0.0001) and D2L (F = 6.8, df  =  (4,65) p = 0.0001) as well as DRD3 (F = 3.38, df  =  (4,61), p = 0.015) mRNA expression in the male rats (Fig. 1D, E, F). DRD2 pan, D2S and D2L mRNAs were significantly increased by T and DHT replacement relative to Intact (p<0.005) and Gdx (p<0.011). E replacement had no effect on any DRD2 mRNA isoform. In contrast, DRD3 mRNA was decreased relative to Gdx by T (p = 0.012) and by DHT replacement (p = 0.004) but was unchanged by E replacement.

We found a significant effect of treatment group on DRD1 and DRD5 mRNA expression in the substantia nigra (F = 3.3, df  =  (4,62), p = 0.017 and F = 5.9, df  =  (4,61), p = 0.0005, respectively) (Fig. 1G, H). DHT replacement significantly increased DRD1 mRNA relative to Gdx (p = 0.006). There was only a trend for T to increase DRD1 mRNA expression relative to Gdx (p = 0.064) and E replacement had no effect on DRD1 mRNA. Both T and DHT groups had significantly increased DRD1 mRNA relative to the E group (p = 0.04 and 0.004, respectively). In terms of DRD5 mRNA, T replacement significantly increased transcript levels relative to Intact (p = 0.003) and Gdx (p<0.001). Both DHT replacement and E replacement significantly increased DRD5 mRNA relative to Gdx (Gdx vs. Gdx+DHT, p = 0.007; Gdx vs. Gdx+E, p = 0.003).

Circulating sex steroids over a two week adolescent period do not change levels of mRNAs encoding for proteins involved in dopamine breakdown, but sex steroids do change dopamine receptor mRNA levels in the dorsal striatum

In the striatum, COMT, MAOA and MAOB mRNAs were unchanged by gonadectomy and sex steroid replacement [COMT, F = 1.218, df  =  (4,66), p = 0.311 (Fig. 2A); MAOA, F = 1.36, df  =  (4,69), p = 0.257 (Fig. 2B); MAOB, F = 0.787, df  =  (4,68), p = 0.538 (data not shown)].

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Figure 2. Effect of gonadectomy and sex steroid replacement on dopamine metabolic enzyme and dopamine receptor mRNA expression in the dorsal striatum of adolescent male rats.

There was no effect of treatment group on mRNA expression of COMT (A) or MAOA (B). (C) DRD2 pan mRNA was increased by testosterone, DHT and 17β-estradiol replacement relative to the Intact group. (D) DRD2 short mRNA was increased relative to the Intact group by testosterone and DHT replacement but not by17β-estradiol replacement. (E) There was a trend for treatment group to change DRD2 long mRNA expression (F =  2.36, df  =  (4,65), p = 0.063). There were no statistically significant sex steroid-related changes in (F) DRD3 mRNA (F = 1.62, df  =  (4,65), p = 0.18) or (G) DRD1 mRNA (F = 2.10, df  =  (4,65), p = 0.015) (H) DRD5 mRNA expression was increased relative to the Intact group by Gdx, testosterone and DHT replacement but not by 17β-estradiol replacement. * denotes comparison with intact, * p<0.05, ** p<0.01, n = 12–16/group.

https://doi.org/10.1371/journal.pone.0091151.g002

In the striatum, we also found a significant effect of treatment group on DRD2 pan mRNA (F = 2.72, df  =  (4,66) p = 0.036). DRD2 pan mRNA was increased by T, DHT and E relative to the Intact group (Fig. 2C). The significant increase in DRD2 pan as a result of androgen replacement may be driven by significant increases in DRD2S mRNA (F = 2.85, df  =  (4,67), p = 0.03) by T and DHT (Fig. 2D). There were no significant changes in DRD2L mRNA expression due to sex steroid treatment (F = 2.36, df  =  (4,65), p = 0.063)(Fig. 2E). There were no statistically significant sex steroid-related changes in striatal DRD3 mRNA (F = 1.62, df  =  (4,65) p = 0.18) (Fig. 2F) or DRD1 mRNA (F = 2.10, df  =  (4,65), p = 0.091) (Fig. 2G). There was a significant effect of treatment group on DRD5 mRNA expression in the striatum (F = 3.34, df  =  (4,65), p = 0.015) (Fig. 2H). DRD5 mRNA expression was increased by gonadectomy alone relative to Intact (Gdx vs Intact, p = 0.035) and this increase was not attenuated by the replacement of T or DHT (Intact vs Gdx+T, p = 0.001, Intact vs. Gdx+DHT, p = 0.048) but was prevented by E replacement (Intact vs Gdx+E, ns)(Fig. 2H).

Dopamine transporter protein is increased by testosterone in the substantia nigra

In the substantia nigra, we found that sex steroid effects on DAT protein reached trend levels of statistical significance overall (F = 2.52, df  =  (4,41), p = 0.056) (Fig 3). A priori, planned comparisons revealed significant increases in DAT protein in response to testosterone (Gdx vs. Gdx+T, p = 0.024, t = 2.15, df  = 16) but not in response to DHT (Gdx vs. Gdx+DHT, p = 0.09, t = 1.36, df  = 16) (Fig. 3). We did not detect a significant increase in DAT protein levels in the testosterone or DHT groups compared to the Intact group (Intact vs. Gdx+T, p = 0.075, t = 1.51, df  = 17; Intact vs. Gdx+DHT, p = 0.16, t = 0.96, df  = 17). We have previously reported testosterone-induced increases in TH protein levels in the substantia nigra [16]

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Figure 3. Effect of gonadectomy and sex steroid replacement on dopamine transporter protein in the substantia nigra of adolescent male rats.

In the substantia nigra there was a trend for treatment group to change DAT protein (F = 2.52, df  =  (4,41), p = 0.056). Representative immunoblots of a subset of substantia nigra samples show DAT (50 kDa) and β-actin (43 kDa). A priori, planned comparisons, based on mRNA data, revealed that testosterone replacement increased DAT protein compared to the gonadectomised group. * p<0.05, n = 9–10/group. (MWM, molecular weight marker; std, internal standard).

https://doi.org/10.1371/journal.pone.0091151.g003

Proteins involved in dopamine transport and dopamine synthesis appear unchanged by testosterone in the dorsal striatum

There was a trend towards a change in DAT protein levels (normalized to β-actin levels) in the dorsal striatum according to treatment group (F = 2.39, df  =  (4,45) p = 0.07). However, a priori, planned comparisons revealed no effect of testosterone or DHT relative to Intact or Gdx groups on DAT protein levels in the dorsal striatum (all p>0.05, Fig. 4A).

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Figure 4. Effect of gonadectomy and sex steroid replacement on dopamine transporter protein and tyrosine hydroxylase protein in adolescent male rat dorsal striatum.

(A) DAT protein was unchanged in the dorsal striatum by gonadectomy and sex steroid replacement (F = 2.39, df  =  (4,45), p = 0.07). Representative immunoblots of a subset of dorsal striatum samples from all five groups show DAT (50 kDa) and β-actin (43 kDa). (B) TH protein was unchanged by gonadectomy or sex steroid replacement in the dorsal striatum (F = 0.41, df  =  (4,45), p = 0.78). Representative immunoblots of a subset of dorsal striatum samples from all five groups show TH protein (60 kDa) and β-actin protein (43 kDa). * p<0.05, n = 9–10/group. (MWM, molecular weight marker; std, internal standard).

https://doi.org/10.1371/journal.pone.0091151.g004

Striatal TH protein levels (normalized to β-actin levels) were also unchanged by gonadectomy or by sex steroid replacement in the dorsal striatum (F = 0.41, df  =  (4,45), p = 0.78) (Fig. 4B).

Dopamine turnover in the dorsal striatum is increased by testosterone removal

Dopamine and HVA levels were unchanged in the striatum in any treatment group (F = 0.74, df  =  (4,67), p = 0.57 and F = 0.8, df  =  (4,61), p = 0.53, respectively) (Fig. 5A, C). There was a significant effect of treatment group on levels of the DOPAC in the striatum (F = 5.3, df  =  (4,68), p = 0.001). Striatal DOPAC was increased in the Gdx group compared to the Intact group (p = 0.004) and this was prevented by testosterone replacement (Gdx vs. Gdx+T, p = 0.003), but not by DHT or E (Fig. 5B). The increase in DOPAC in the Gdx group resulted in a significant group effect on dopamine turnover (DOPAC+HVA/DA) (F = 3.2, df  =  (4,64), p = 0.019; n = 11–16) (Fig. 5D). Dopamine turnover was increased in the Gdx group (Intact vs. Gdx, p = 0.005) and the increase was prevented by androgens (Gdx vs T, p = 0.04; Gdx vs. DHT, p = 0.012), but not by E (Gdx vs. Gdx+E, ns) (Fig. 5D).

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Figure 5. The effect of gonadectomy and sex steroid replacement on dopamine, dopamine metabolites and dopamine turnover in the dorsal striatum of adolescent male rats.

There was no significant effect of treatment group on dopamine (A) or HVA (C). Gonadectomy increased DOPAC (B) and this increase was attenuated by testosterone replacement only. Dopamine turnover (D) was significantly increased by gonadectomy and this was attenuated by testosterone and DHT replacement but not 17β-estradiol replacement. * denotes comparison with Intact unless comparison indicated by a line, # denotes comparison with the Gdx group, * and # p<0.05; ** and ## p<0.01, n = 11–16/group for all.

https://doi.org/10.1371/journal.pone.0091151.g005

Discussion

Summary of findings

We provide data to support our hypothesis that testosterone may modulate, via mainly androgen receptor-driven changes, gene expression of multiple molecules involved in the regulation of dopamine within the nigrostriatal pathway in adolescent male rat brain. In the substantia nigra, testosterone increased several dopamine receptor mRNAs [D1, D2 (short and long), D5] as well as dopamine transporter (VMAT2, DAT) gene expression and DAT protein but decreased DRD3 mRNA. This novel data, combined with our previous findings of increased TH protein and COMT and MOA mRNAs in the substantia nigra [16] with testosterone during an adolescent period (PND45-60), suggests that the dopaminergic system may be coordinately modified to accommodate more midbrain dopamine signaling when males mature. Adolescent sex steroids also regulated both D2 and D5 dopamine receptor mRNAs in the dorsal striatum (summarized in Table 2). Our data highlight in adolescent male rats that 1) there are several different points at which testosterone can modulate molecular indices of dopamine signaling, 2) there is a greater degree of testosterone regulation of dopamine-related molecular parameters in the substantia nigra compared to the striatum and 3) testosterone induces a coordinated increase in DRD2S mRNA levels in the substantia nigra and striatum.

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Table 2. Summary of gene expression and protein changes in response to sex steroid replacement relative to the Gdx group.

https://doi.org/10.1371/journal.pone.0091151.t002

Testosterone has differential effects on dopamine in the substantia nigra versus striatum

Dopamine production is rate limited by TH levels and TH activity. Previous studies in rodent brain have reported both increases and decreases in striatal dopamine in response to sex steroids [19][21], [44]. We have reported that testosterone replacement increased TH protein levels in the substantia nigra in adolescent male rats [16], however, we now show that contrary to our prediction that testosterone would increase TH in the striatum as well, no increase in striatal TH protein or increase in striatal dopamine levels was detected. In fact, dopamine turnover (a measure of dopamine activity) in the striatum was increased upon testosterone removal and this stimulatory effect was attenuated by testosterone replacement. The somewhat surprising increase in dopamine turnover in the striatum following gonadectomy could reflect an increase in dopamine packaging and release that is maintained in balance by dopamine reuptake and breakdown. However, when comparing gonadectomised and intact rats, changes in dopamine breakdown enzyme or transporter mRNAs or proteins (where measured) were not found in the striatum, thus the changes in dopamine turnover after gonadectomy may reflect post-transcriptional or post-translational changes in the activity of these proteins.

Testosterone may regulate dopamine neurotransmission at dopaminergic cell soma and terminals

Gene expression changes in dopaminergic cell bodies can alter protein levels in both presynaptic axon terminals at a distance from the cell bodies and/or locally in somatodendritic fields. Our previously reported increase in TH protein in the region of the dopaminergic cell bodies [16] combined with the lack of increase in TH protein or dopamine in the terminals in the striatum suggests that increases in dopamine synthesis via androgens may occur at the level of cell bodies and dendrites rather than at the terminals. In support of the preference for testosterone to induce local changes in molecular indices of dopamine signaling, we find that increases in DAT protein are found proximal to the soma, in the substantia nigra and not distal, in the striatum. Increased dendritic synthesis, release and uptake of dopamine could serve to modify feedback inhibition of dopamine neurons within the substantia nigra, thereby regulating dopamine neuron excitability and indirectly modifying dopamine release at axon terminals [45], [46]. The fact that localized changes in molecules impacting local self-regulation of dopamine neurons may be more directly influenced by testosterone could have relevance for schizophrenia as a recent meta-analysis of imaging studies concluded that the largest dopaminergic abnormality in schizophrenia is presynaptic [4], which implicates an intrinsic dysfunction in dopamine neurons themselves. DAT [47][49] and VMAT [50] have been localized to both the somatodendritic field and terminals of nigrostriatal dopaminergic neurons in the rat and human. Our reported increase in VMAT and DAT mRNAs in the substantia nigra in response to testosterone could lead to increased DAT and VMAT protein in either the dendrites and/or in the terminals and our data (increased DAT protein only in the region of cell bodies not at the terminals) supports that dopamine neuron dendrites are more likely targets of testosterone-induced changes. Testosterone-induced increased somatodendritic dopamine transport and dopamine breakdown [16] in the substantia nigra would serve to not only maintain dopaminergic homeostasis but also provide more precise temporal control over the activity of the dopaminergic neuron cell bodies. Further, the increase in DAT and VMAT mRNAs by testosterone was not accompanied by changes in TH protein or dopamine levels in the striatum perhaps suggesting that synthesis and steady state levels are stable at the terminals, whereas in the substantia nigra both TH and DAT protein are increased by testosterone. Thus, our data suggest that dopamine neurotransmission may be enhanced at the cell bodies and dendrites of dopamine neurons in response to testosterone at male adolescence. Ultimately, the functional outcome of these molecular changes would be determined by the balance between theses changes e.g. increased DRD2 in the somatodendritic field (see below) would increase feedback inhibition of the DA neurons, but increased DAT would serve to clear DA from the extracellular space more rapidly, thereby potentially reducing feedback inhibition.

Testosterone regulates the level of dopamine receptor mRNAs in the nigrostriatal pathway

In support of a local change proximal to dopamine neurons in the substantia nigra, we find that 3 out of 5 dopamine receptor mRNAs are increased in response to adolescent testosterone in the substantia nigra perhaps reflecting changes in available dopamine. We also report increased DRD2 gene expression in response to testosterone in both the region of the dopaminergic cell bodies and in the region of the medium spiny neurons of the dorsal striatum. As such, there are multiple sites at which increases in DRD2 expression could modulate dopamine sensitivity of the nigrostriatal pathway: at the cell bodies and dendrites of dopamine neurons within the midbrain, at the pre-synaptic dopamine terminals in the striatum and at the post-synaptic neurons in the striatum. DRD2 activation at the dopaminergic cell bodies results in the attenuation of dopaminergic neuron excitability via feedback inhibition. DRD2 and DRD3 are considered autoreceptors in dopaminergic neurons where DRD2 at the presynaptic terminal provides inhibitory control over dopamine release and DRD2 and DRD3 control electrical activity of the dopamine neurons at the cell body. The testosterone-induced changes we report in DRD2 gene expression in the nigrostriatal pathway at adolescence are of particular interest as DRD2 receptors are the target of all antipsychotic treatments for schizophrenia, with DRD2 receptors in the dorsal striatum suggested to be the most responsive to changes in tissue dopamine levels [7]. Our evidence indicates that testosterone also increases DRD1 and DRD5 (excitatory receptors) in the substantia nigra and DRD5 in the striatum, suggesting more generalized sensitivity to secreted dopamine via testosterone exposure. Interestingly, gonadectomy also increased DRD5 mRNA in the striatum and increased DRD5 mRNA was attenuated by estradiol and not androgens and this effect of estrogen suggests that the balance of sex steroids may play a role in the regulation of striatal DRD5 gene expression. It is important to acknowledge that DHT can also have effects via conversion to 3β-diol, which has a high affinity for ERβ and DHT effects may therefore include an estrogenic component [11]. In conclusion, the action of dopamine would, in combination with DA synthesis, transport and metabolism, depend on the balance of excitatory and inhibitory dopamine receptors and their location within the nigrostriatal pathway and the gene expression profile of these DA-related molecules can be modulated by sex steroids in male adolescence.

The mechanism of testosterone regulation of molecular indices of dopamine neurotransmission is mostly androgenic

Crucial to developing new drug targets for therapy in dopamine-related neural disorders is knowledge of the underlying mechanism(s) driving the changes in dopamine regulating proteins. The majority of the gene expression changes reported here are only induced by DHT and testosterone, and not by estradiol, indicating that in adolescent males androgen receptor, not ERα, activation is critical for these responses. It is less clear whether ERβ is involved or not as DHT, via conversion to 3β-diol has a high affinity for ERβ [11]. The minimal estrogenic effects driven by testosterone may provide some insight in to the greater sensitivity of males to schizophrenia [51][53] and to dopamine-potentiating drugs of abuse such as amphetamine, which, in males, could potentially be due to a combination of a lower level of protective estrogen-driven effects [2] as well as potentiating dominant androgen-driven effects. Compounding these AR-driven effects is our evidence that in addition to modulating dopamine regulating proteins and mRNAs, testosterone also creates a self-reinforcing, positive feedback loop in the adolescent male rat midbrain to create a more androgen responsive state by increasing AR gene expression whilst decreasing ERα gene expression [16].

Limitations of our study

It is important to note the lack of detectable differences in gene expression between intact and gonadectomised rats. Differences in dopamine pathway-related gene expression between intact and gonadectomised rats in our study may be subtle and difficult to detect due to differences between the natural gradual increase in testosterone over adolescence and the immediate, supraphysiological, steady state levels achieved with implants. Intact animals may require a longer exposure to high testosterone to allow the changes we see in gene expression, that we report in sex steroid replaced animals, to occur. The lack of detectable differences between intact and gonadectomised rats could occur if gonadectomy had occurred after the adolescent increase in testosterone. Although androgen-dependent physiological changes (preputial separation) at adolescence are reported in male Sprague-Dawley rats as early as day postnatal day 38 [54] they are more commonly reported between postnatal days 45 and 48 [55]. The majority of studies agree, however, that testosterone levels continue to rise between 45 to 60 days of age [30][34], and measurements of circulating testosterone in our Sprague-Dawley rat colony is in agreement with this (unpublished data). In addition, the male brain is not testosterone naïve prior to when testosterone levels start to increase [31]. We also demonstrate here differences in striatal dopamine turnover between Intact and Gdx animals as well as significant differences in seminal vesicle weights [16] and in BDNF-related pathways in the CNS (unpublished data), all of which support the efficacy of our paradigm. We acknowledge that the serum sex steroid levels achieved via implants are supraphysiological, however our data indicate that molecular indices of dopamine neurotransmission in the adolescent male nigrostriatal pathway can be modulated by sex steroids and the replacement studies allow us to dissociate androgen versus estrogen driven mechanisms of testosterone, both important for sex steroid based drug development. The duration of treatment may also account for at least some of the conflicting data in the literature. Changes reported in the adult rat prefrontal cortex indicate decreased dopamine concentrations four days post gonadectomy but dopamine was increased at 28-days post gonadectomy [56]. We detected no change in dopamine concentration in the dorsal striatum at 14 days after gonadectomy but an increase in dopamine turnover in response to gonadectomy – thus, our data may reflect a transitionary phase between 4 and 28 days of replacement. We did not determine how these dopamine-related changes may vary over time.

A limitation of this study is that we do not know exactly how the dopamine receptor mRNAs are translated into protein as there are different synthetic pools of dopamine receptor mRNA (striatal medium spiny neurons, dopamine neurons) and protein measurements of the receptors in the striatum would reflect a mixture of receptors from different mRNA pools and would not distinguish the source or the cellular location (post-synaptic versus pre-synaptic) of any protein changes in the striatum, making conclusions about protein expression in the dorsal striatum difficult to interpret. However, gene expression data provides valuable information about differential control of these molecules at the mRNA level at different points in the nigrostriatal pathway. In contrast, protein measurements of DAT and TH are more informative as the primary source of these proteins is the dopamine neurons in the nigra, allowing conclusions to be drawn regarding changes in protein expression in the somatodendritic and terminal fields of the nigral neurons. An important follow up to this study will be to determine whether these observed gene expression and protein changes in dopamine-related molecules lead to changes in behavior in response to dopamine-potentiating drugs such as amphetamine.

Conclusions

In general, our data support the hypothesis that the ability of the nigrostriatal pathway to respond to dopamine is modulated by circulating testosterone levels during adolescence. Although the current data does not allow us to draw conclusions regarding the functional outcomes of observed changes it is feasible that in individuals with an underlying susceptibility to schizophrenia the pubertal increase in circulating testosterone at adolescence may serve as a trigger for the presentation of dopamine-related psychosis. Studies in humans suggest that increased testosterone increases striatal dopamine. Studies in women using functional magnetic resonance imaging support the hypothesis that exogenous testosterone affects dopaminergic activity [57] and our study, albeit in males, indicates the potential molecular correlates that may underlie this. Susceptibility to schizophrenia may relate to variations in dopamine-regulating genes or variation in sex steroid-related genes. Indeed, genetic variation in a number of genes involved in dopamine regulation have been linked to schizophrenia risk, including DRD2 [58], [59], VMAT2 (psychotic disorder) [60] and COMT [61], [62]. A variant of the ESR1 gene has also been shown as a genetic risk factor for schizophrenia [63]. In the current work, we have not investigated the functional effects of these changes on brain dopamine but we note that human studies report that increased testosterone increases striatal dopamine [57] and anabolic androgenic steroids, synthetic variants of testosterone, are known to be associated with adverse effects on mental health, including psychosis and aggression [64]. Our study demonstrates changes that may represent the molecular correlates of such effects.

We conclude that the testosterone-induced, AR-driven modulation of molecular indices of dopamine responsivity of the nigrostriatal pathway may involve regulation of dopamine feedback inhibition in the somatodendritic field and post-synaptic dopamine action in the terminal field. Testosterone has widespread effects including regulating mRNA and some protein levels of molecules involved in pre-synaptic dopamine synthesis, dopamine reuptake and dopamine packaging, dopamine breakdown and dopamine reception. Although the functional outcome of these molecular changes have not been measured this knowledge provides clues to the coordinated multi-faceted level of sex steroid control over dopamine neurotransmission to target for drug development, whereby dopamine responsivity of the nigrostriatal pathway can be modulated, perhaps by changing androgen and/or estrogen receptor activation.

Acknowledgments

The authors thank Deborah Rothmond for assistance with qPCRs, and Veronica Cottam for technical assistance with HPLC.

Author Contributions

Conceived and designed the experiments: TPT KD CSW. Performed the experiments: TPT SO RD. Analyzed the data: TPT SO. Contributed reagents/materials/analysis tools: TPT RD CSW KD DH. Wrote the paper: TPT SO KD DH CSW. Supplied steroid implants: DH. Measured circulating sex steroids: DH. Provided critical experimental advice pertaining to sex steroids and critical comment on the manuscript: DH. Provided critical advice pertaining to measurement of sex steroids and carried out these experiments: RD.

References

  1. 1. McGrath J, Saha S, Chant D, Welham J (2008) Schizophrenia: a concise overview of incidence, prevalence, and mortality. Epidemiologic reviews 30: 67–76.
  2. 2. Markham JA (2012) Sex steroids and schizophrenia. Reviews in endocrine & metabolic disorders 13: 187–207.
  3. 3. Howes OD, Kapur S (2009) The dopamine hypothesis of schizophrenia: version III—the final common pathway. Schizophr Bull 35: 549–562.
  4. 4. Howes OD, Kambeitz J, Kim E, Stahl D, Slifstein M, et al. (2012) The Nature of Dopamine Dysfunction in Schizophrenia and What This Means for Treatment: Meta-analysis of Imaging Studies. Arch Gen Psychiatry 69: 776–786.
  5. 5. Abi-Dargham A, Rodenhiser J, Printz D, Zea-Ponce Y, Gil R, et al. (2000) Increased baseline occupancy of D2 receptors by dopamine in schizophrenia. Proceedings of the National Academy of Sciences of the United States of America 97: 8104–8109.
  6. 6. Seeman P (2006) Targeting the dopamine D2 receptor in schizophrenia. Expert opinion on therapeutic targets 10: 515–531.
  7. 7. Kegeles LS, Abi-Dargham A, Frankle WG, Gil R, Cooper TB, et al. (2010) Increased synaptic dopamine function in associative regions of the striatum in schizophrenia. Arch Gen Psychiatry 67: 231–239.
  8. 8. Laruelle M, Abi-Dargham A, Gil R, Kegeles L, Innis R (1999) Increased dopamine transmission in schizophrenia: relationship to illness phases. Biol Psychiatry 46: 56–72.
  9. 9. Beaulieu JM, Gainetdinov RR (2011) The physiology, signaling, and pharmacology of dopamine receptors. Pharmacological reviews 63: 182–217.
  10. 10. Celotti F, Melcangi RC, Martini L (1992) The 5 alpha-reductase in the brain: molecular aspects and relation to brain function. Front Neuroendocrinol 13: 163–215.
  11. 11. Handa RJ, Pak TR, Kudwa AE, Lund TD, Hinds L (2008) An alternate pathway for androgen regulation of brain function: activation of estrogen receptor beta by the metabolite of dihydrotestosterone, 5alpha-androstane-3beta,17beta-diol. Horm Behav 53: 741–752.
  12. 12. Kritzer MF, Creutz LM (2008) Region and sex differences in constituent dopamine neurons and immunoreactivity for intracellular estrogen and androgen receptors in mesocortical projections in rats. J Neurosci 28: 9525–9535.
  13. 13. Perez SE, Chen EY, Mufson EJ (2003) Distribution of estrogen receptor alpha and beta immunoreactive profiles in the postnatal rat brain. Brain Res Dev Brain Res 145: 117–139.
  14. 14. Shughrue PJ, Lane MV, Merchenthaler I (1997) Comparative distribution of estrogen receptor-alpha and -beta mRNA in the rat central nervous system. J Comp Neurol 388: 507–525.
  15. 15. Ravizza T, Veliskova J, Moshe SL (2003) Testosterone regulates androgen and estrogen receptor immunoreactivity in rat substantia nigra pars reticulata. Neurosci Lett 338: 57–61.
  16. 16. Purves-Tyson TD, Handelsman DJ, Double KL, Owens SJ, Bustamante S, et al. (2012) Testosterone regulation of sex steroid-related mRNAs and dopamine-related mRNAs in adolescent male rat substantia nigra. BMC Neuroscience 13: 95.
  17. 17. Beatty WW, Dodge AM, Traylor KL (1982) Stereotyped behavior elicited by amphetamine in the rat: influences of the testes. Pharmacol Biochem Behav 16: 565–568.
  18. 18. Walker QD, Cabassa J, Kaplan KA, Li ST, Haroon J, et al. (2001) Sex differences in cocaine-stimulated motor behavior: disparate effects of gonadectomy. Neuropsychopharmacology 25: 118–130.
  19. 19. Dluzen DE, Ramirez VD (1989) Effects of orchidectomy on nigro-striatal dopaminergic function: behavioral and physiological evidence. J Neuroendocrinol 1: 285–290.
  20. 20. de Souza Silva MA, Mattern C, Topic B, Buddenberg TE, Huston JP (2009) Dopaminergic and serotonergic activity in neostriatum and nucleus accumbens enhanced by intranasal administration of testosterone. Eur Neuropsychopharmacol 19: 53–63.
  21. 21. Thiblin I, Finn A, Ross SB, Stenfors C (1999) Increased dopaminergic and 5-hydroxytryptaminergic activities in male rat brain following long-term treatment with anabolic androgenic steroids. Br J Pharmacol 126: 1301–1306.
  22. 22. Morris RW, Fung SJ, Rothmond DA, Richards B, Ward S, et al. (2010) The effect of gonadectomy on prepulse inhibition and fear-potentiated startle in adolescent rhesus macaques. Psychoneuroendocrinol 35: 896–905.
  23. 23. Abreu P, Hernandez G, Calzadilla CH, Alonso R (1988) Reproductive hormones control striatal tyrosine hydroxylase activity in the male rat. Neurosci Lett 95: 213–217.
  24. 24. Kindlundh AM, Rahman S, Lindblom J, Nyberg F (2004) Increased dopamine transporter density in the male rat brain following chronic nandrolone decanoate administration. Neurosci Lett 356: 131–134.
  25. 25. Meyers B, D'Agostino A, Walker J, Kritzer MF (2010) Gonadectomy and hormone replacement exert region- and enzyme isoform-specific effects on monoamine oxidase and catechol-O-methyltransferase activity in prefrontal cortex and neostriatum of adult male rats. Neuroscience 165: 850–862.
  26. 26. Birgner C, Kindlundh-Hogberg AM, Oreland L, Alsio J, Lindblom J, et al. (2008) Reduced activity of monoamine oxidase in the rat brain following repeated nandrolone decanoate administration. Brain Res 1219: 103–110.
  27. 27. Allan CM, Couse JF, Simanainen U, Spaliviero J, Jimenez M, et al. (2010) Estradiol induction of spermatogenesis is mediated via an estrogen receptor-{alpha} mechanism involving neuroendocrine activation of follicle-stimulating hormone secretion. Endocrinology 151: 2800–2810.
  28. 28. Singh J, O'Neill C, Handelsman DJ (1995) Induction of spermatogenesis by androgens in gonadotropin-deficient (hpg) mice. Endocrinology 136: 5311–5321.
  29. 29. Zirkin BR, Santulli R, Awoniyi CA, Ewing LL (1989) Maintenance of advanced spermatogenic cells in the adult rat testis: quantitative relationship to testosterone concentration within the testis. Endocrinology 124: 3043–3049.
  30. 30. Walker DM, Kirson D, Perez LF, Gore AC (2012) Molecular profiling of postnatal development of the hypothalamus in female and male rats. Biology of reproduction 87: 129.
  31. 31. Saksena SK, Lau IF (1979) Variations in serum androgens, estrogens, progestins, gonadotropins and prolactin levels in male rats from prepubertal to advanced age. Experimental aging research 5: 179–194.
  32. 32. Bai Y, Chang F, Zhou R, Jin PP, Matsumoto H, et al. (2011) Increase of anteroventral periventricular kisspeptin neurons and generation of E2-induced LH-surge system in male rats exposed perinatally to environmental dose of bisphenol-A. Endocrinology 152: 1562–1571.
  33. 33. Blystone CR, Furr J, Lambright CS, Howdeshell KL, Ryan BC, et al. (2007) Prochloraz inhibits testosterone production at dosages below those that affect androgen-dependent organ weights or the onset of puberty in the male Sprague Dawley rat. Toxicological sciences : an official journal of the Society of Toxicology 97: 65–74.
  34. 34. Noriega NC, Howdeshell KL, Furr J, Lambright CR, Wilson VS, et al. (2009) Pubertal administration of DEHP delays puberty, suppresses testosterone production, and inhibits reproductive tract development in male Sprague-Dawley and Long-Evans rats. Toxicological sciences : an official journal of the Society of Toxicology 111: 163–178.
  35. 35. Purves-Tyson TD, Arshi MS, Handelsman DJ, Cheng Y, Keast JR (2007) Androgen and estrogen receptor-mediated mechanisms of testosterone action in male rat pelvic autonomic ganglia. Neuroscience 148: 92–104.
  36. 36. Harwood DT, Handelsman DJ (2009) Development and validation of a sensitive liquid chromatography-tandem mass spectrometry assay to simultaneously measure androgens and estrogens in serum without derivatization. Clinica chimica acta; international journal of clinical chemistry 409: 78–84.
  37. 37. McNamara KM, Harwood DT, Simanainen U, Walters KA, Jimenez M, et al. (2010) Measurement of sex steroids in murine blood and reproductive tissues by liquid chromatography-tandem mass spectrometry. J Steroid Biochem Mol Biol 121: 611–618.
  38. 38. Paxinos G, Watson C (2007) The Rat Brain in Stereotaxic Coordinates: Elsevier.
  39. 39. Kontur P, Dawson R, Monjan A (1984) Manipulation of mobile phase parameters for the HPLC separation of endogenous monoamines in rat brain tissue. J Neurosci Methods 11: 5–18.
  40. 40. Alburges ME, Narang N, Wamsley JK (1993) A sensitive and rapid HPLC-ECD method for the simultaneous analysis of norepinephrine, dopamine, serotonin and their primary metabolites in brain tissue. Biomedical chromatography : BMC 7: 306–310.
  41. 41. Vandesompele J, De Preter K, Pattyn F, Poppe B, Van Roy N, et al. (2002) Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol 3: 1–12.
  42. 42. Weickert CS, Sheedy D, Rothmond DA, Dedova I, Fung S, et al. (2010) Selection of reference gene expression in a schizophrenia brain cohort. Aust N Z J Psychiatry 44: 59–70.
  43. 43. Huck SW (2009) Statistical Misconceptions. Knoxville: Psychology Press, Taylor and Francis Group.
  44. 44. Johnson ML, Day A, Ho CC, David Walker Q, Francis R, et al. (2010) Androgen decreases dopamine neurone survival in rat midbrain. J Neuroendocrinol 22: 238–247.
  45. 45. Lacey MG, Mercuri NB, North RA (1987) Dopamine acts on D2 receptors to increase potassium conductance in neurones of the rat substantia nigra zona compacta. The Journal of physiology 392: 397–416.
  46. 46. Beckstead MJ, Grandy DK, Wickman K, Williams JT (2004) Vesicular dopamine release elicits an inhibitory postsynaptic current in midbrain dopamine neurons. Neuron 42: 939–946.
  47. 47. Ciliax BJ, Drash GW, Staley JK, Haber S, Mobley CJ, et al. (1999) Immunocytochemical localization of the dopamine transporter in human brain. J Comp Neurol 409: 38–56.
  48. 48. Hersch SM, Yi H, Heilman CJ, Edwards RH, Levey AI (1997) Subcellular localization and molecular topology of the dopamine transporter in the striatum and substantia nigra. J Comp Neurol 388: 211–227.
  49. 49. Nirenberg MJ, Vaughan RA, Uhl GR, Kuhar MJ, Pickel VM (1996) The dopamine transporter is localized to dendritic and axonal plasma membranes of nigrostriatal dopaminergic neurons. J Neuroscience 16: 436–447.
  50. 50. Nirenberg MJ, Chan J, Liu Y, Edwards RH, Pickel VM (1996) Ultrastructural localization of the vesicular monoamine transporter-2 in midbrain dopaminergic neurons: potential sites for somatodendritic storage and release of dopamine. J Neuroscience 16: 4135–4145.
  51. 51. Leung A, Chue P (2000) Sex differences in schizophrenia, a review of the literature. Acta psychiatrica Scandinavica Supplementum 401: 3–38.
  52. 52. Aleman A, Kahn RS, Selten JP (2003) Sex differences in the risk of schizophrenia: evidence from meta-analysis. Arch Gen Psychiatry 60: 565–571.
  53. 53. McGrath J, Saha S, Welham J, El Saadi O, MacCauley C, et al. (2004) A systematic review of the incidence of schizophrenia: the distribution of rates and the influence of sex, urbanicity, migrant status and methodology. BMC medicine 2: 13.
  54. 54. Korenbrot CC, Huhtaniemi IT, Weiner RI (1977) Preputial separation as an external sign of pubertal development in the male rat. Biology of reproduction 17: 298–303.
  55. 55. Lewis EM, Barnett JF Jr, Freshwater L, Hoberman AM, Christian MS (2002) Sexual maturation data for Crl Sprague-Dawley rats: criteria and confounding factors. Drug and chemical toxicology 25: 437–458.
  56. 56. Aubele T, Kritzer MF (2011) Gonadectomy and hormone replacement affects in vivo basal extracellular dopamine levels in the prefrontal cortex but not motor cortex of adult male rats. Cereb Cortex 21: 222–232.
  57. 57. Hermans EJ, Bos PA, Ossewaarde L, Ramsey NF, Fernandez G, et al. (2010) Effects of exogenous testosterone on the ventral striatal BOLD response during reward anticipation in healthy women. NeuroImage 52: 277–283.
  58. 58. Glatt SJ, Faraone SV, Tsuang MT (2003) Meta-analysis identifies an association between the dopamine D2 receptor gene and schizophrenia. Mol Psychiatry 8: 911–915.
  59. 59. Glatt SJ, Jonsson EG (2006) The Cys allele of the DRD2 Ser311Cys polymorphism has a dominant effect on risk for schizophrenia: evidence from fixed- and random-effects meta-analyses. American journal of medical genetics Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 141B: 149–154.
  60. 60. Simons CJ, van Winkel R (2012) Intermediate Phenotype Analysis of Patients, Unaffected Siblings, and Healthy Controls Identifies VMAT2 as a Candidate Gene for Psychotic Disorder and Neurocognition. Schizophr Bull.
  61. 61. Egan MF, Goldberg TE, Kolachana BS, Callicott JH, Mazzanti CM, et al. (2001) Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia. Proc Natl Acad Sci U S A 98: 6917–6922.
  62. 62. Akil M, Kolachana BS, Rothmond DA, Hyde TM, Weinberger DR, et al. (2003) Catechol-O-methyltransferase genotype and dopamine regulation in the human brain. J Neurosci 23: 2008–2013.
  63. 63. Weickert CS, Miranda-Angulo AL, Wong J, Perlman WR, Ward SE, et al. (2008) Variants in the estrogen receptor alpha gene and its mRNA contribute to risk for schizophrenia. Hum Mol Genet 17: 2293–2309.
  64. 64. Wood RI (2008) Anabolic-androgenic steroid dependence? Insights from animals and humans. Frontiers in neuroendocrinology 29: 490–506.