The role of perinatal testosterone on exploratory behavior, sexual motivation, and spatial working memory in adult rats

C. Gopalan, Paige Niepoetter, Avery Ogle, Sai Medavaka, Samantha A. Olendorff, Kevin R. Tucker
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Abstract

Aim: Sex differentiation occurs during the perinatal period (four days before and after birth) in the rat brain. The brain remains a female brain unless exposed to testosterone, which gets metabolized to 17β-estradiol and dihydrotestosterone. While aromatase converts testosterone to 17β-estradiol, 5α-reductase converts testosterone to dihydrotestosterone. 17β-estradiol exerts its effects by binding to an estrogen receptor, whereas dihydrotestosterone via an androgen receptor. The role of dihydrotestosterone and 17β-estradiol during the organizational phase of brain differentiation was tested using adult rat behaviors. The study sought to examine the effects of perinatal manipulations on adult rat behaviors. Materials and methods: Timed-pregnant rats received either the vehicle (5% ethanol and 95% sesame oil), exemestane (4 mg/kg/ml; aromatase inhibitor), or flutamide (20 mg/kg/ml; androgen receptor blocker) subcutaneously during the last four days of pregnancy. Pups from each group continued to receive their treatments during the first four days after birth. From postnatal day 65, these animals were subjected to open field, sexual motivation, and spatial working memory tests. Results: Male rats receiving flutamide exhibited exploratory behavior significantly more compared to exemestane and control groups. Male rats receiving exemestane had substantially higher plasma testosterone and displayed an increased interest in the estrus rat than the control and flutamide group. Conclusion: Androgen receptor blockade resulted in increased exploratory behavior in male rats where 17β-estradiol was testosterone's primary metabolite. The blocking of aromatase using exemestane resulted in higher levels of plasma testosterone and enhanced sexual motivation in male rats. Thus, 17β-estradiol and dihydrotestosterone's presence during the organizational phase is essential for normal socio-sexual and exploratory behaviors.
围产期睾酮对成年大鼠探索性行为、性动机和空间工作记忆的影响
目的:大鼠脑性别分化发生在围生期(出生前后4天)。大脑仍然是女性的大脑,除非暴露在睾酮中,睾酮被代谢成17β-雌二醇和二氢睾酮。芳香化酶将睾酮转化为17β-雌二醇,而5α-还原酶将睾酮转化为二氢睾酮。17β-雌二醇通过结合雌激素受体发挥作用,而二氢睾酮通过雄激素受体发挥作用。利用成年大鼠的行为学研究双氢睾酮和17β-雌二醇在脑分化组织阶段的作用。这项研究试图检验围产期操作对成年大鼠行为的影响。材料和方法:定时妊娠大鼠分别给予5%乙醇和95%香油的对照物,依西美坦(4 mg/kg/ml;芳香酶抑制剂),或氟他胺(20mg /kg/ml;在怀孕的最后四天皮下注射雄激素受体阻滞剂。每组幼鼠在出生后的前四天继续接受治疗。从出生后第65天开始,对这些动物进行开阔场地、性动机和空间工作记忆测试。结果:与依西美坦和对照组相比,服用氟他胺的雄性大鼠表现出更多的探索行为。与对照组和氟他胺组相比,接受依西美坦治疗的雄性大鼠血浆睾酮水平明显升高,对发情的兴趣也增加。结论:雄激素受体阻断导致雄性大鼠探索行为增加,其中17β-雌二醇是睾酮的主要代谢物。使用依西美坦阻断芳香化酶导致雄性大鼠血浆睾酮水平升高和性动机增强。因此,17β-雌二醇和双氢睾酮在组织阶段的存在对于正常的社会性行为和探索性行为是必不可少的。
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