Roselli C E, Stadelman H, Horton L E, Resko J A
Endocrinology. 1987 Jan;120(1):97-106. doi: 10.1210/endo-120-1-97.
The conversion of androgens to active metabolites by neural tissue is believed to be an essential component in the cellular mechanism of androgen-induced neuroendocrine responses. In this study, we measured the in vitro aromatization and 5 alpha-reduction of androgens in incubations of microdissected brain regions from four intact and five castrated (6 weeks) adult male rhesus monkeys. Individual nuclei were microdissected from 600-microns frozen brain sections and homogenized in a potassium phosphate buffer. Aromatase activity was measured by a radiometric assay that uses the incorporation of tritium from [1 beta-3H]androstenedione into 3H2O as an index of estrogen formation. We estimated 5 alpha-reductase activity by isolating 5 alpha-dihydrotestosterone on two different chromatography systems and measuring the amount of this product formed from [1 alpha,2 alpha-3H]testosterone. We acidified a portion of each homogenate and determined LHRH content by RIA. Between brain nuclei, aromatase activity varied 1500-fold, whereas 5 alpha-reductase activity varied only 3-fold. Both enzyme activities were highest in amygdaloid, medial preoptic, and medial diencephalic nuclei and lowest in the caudate nucleus. Aromatase activities in the supraoptic nucleus, periventricular area, medial preoptic area-anterior hypothalamus, and lateral hypothalamus were significantly (P less than 0.05) lower in castrated males. Castration did not significantly affect 5 alpha-reductase activity, except for an increase in the basolateral amygdala. The highest concentrations of LHRH were in the infundibular nucleus-median eminence and were 30 times greater than amounts measured in preoptic and medial hypothalamic nuclei. The LHRH contents of the infundibular nucleus-median eminence, ventral medial nucleus, and lateral hypothalamus were significantly lower in castrated males (P less than 0.05). In addition, we observed a significant correlation between aromatase activity and LHRH content in the basal hypothalamus of intact males (r = 0.947; P less than 0.05; n = 8), but not in the preoptic-anterior hypothalamus (r = 0.068; P greater than 0.05; n = 10). No correlation was observed between 5 alpha-reductase activity and LHRH content in either area. These data indicate that castration selectively affects androgen metabolism and LHRH content in discrete regions of the brain of male monkeys and suggest that aromatase and 5 alpha-reductase are regulated differentially in the primate brain.
神经组织将雄激素转化为活性代谢物被认为是雄激素诱导神经内分泌反应细胞机制的重要组成部分。在本研究中,我们测量了来自4只完整和5只阉割(6周)成年雄性恒河猴的显微切割脑区孵育物中雄激素的体外芳香化和5α-还原。从600微米厚的冷冻脑切片中显微切割出单个核,并在磷酸钾缓冲液中匀浆。芳香化酶活性通过放射性测定法测量,该方法利用[1β-3H]雄烯二酮中的氚掺入3H2O作为雌激素形成的指标。我们通过在两种不同的色谱系统上分离5α-二氢睾酮并测量由[1α,2α-3H]睾酮形成的该产物的量来估计5α-还原酶活性。我们将每份匀浆的一部分酸化,并通过放射免疫分析测定促性腺激素释放激素(LHRH)含量。在脑核之间,芳香化酶活性变化1500倍,而5α-还原酶活性仅变化3倍。两种酶活性在杏仁核、内侧视前核和内侧间脑核中最高,在尾状核中最低。阉割雄性动物的视上核、室周区、内侧视前区-下丘脑前部和外侧下丘脑的芳香化酶活性显著降低(P<0.05)。阉割除了使基底外侧杏仁核的5α-还原酶活性增加外,对5α-还原酶活性没有显著影响。促性腺激素释放激素浓度最高的部位是漏斗核-正中隆起,比视前核和下丘脑内侧核中的测量值高30倍。阉割雄性动物的漏斗核-正中隆起、腹内侧核和外侧下丘脑的促性腺激素释放激素含量显著降低(P<0.05)。此外,我们观察到完整雄性动物下丘脑基部的芳香化酶活性与促性腺激素释放激素含量之间存在显著相关性(r=0.947;P<0.05;n=8),但在视前-下丘脑前部未观察到相关性(r=0.068;P>0.05;n=10)。在这两个区域中,均未观察到5α-还原酶活性与促性腺激素释放激素含量之间的相关性。这些数据表明,阉割选择性地影响雄性猴子大脑离散区域中的雄激素代谢和促性腺激素释放激素含量,并表明芳香化酶和5α-还原酶在灵长类动物大脑中受到不同的调节。