Gerendai I, Shaha C, Thau R, Bardin C W
Endocrinology. 1984 Oct;115(4):1645-7. doi: 10.1210/endo-115-4-1645.
beta-Endorphin is believed to be synthesized in testicular Leydig cells. To gain more information about the role of this and other endogenous opioid peptides in the testis, opiate antagonists (naloxone and nalmefene, 100 micrograms/testis) were administered intratesticularly to hemicastrated adult rats. Leydig cell function was evaluated by measurement of serum testosterone and testosterone production in vitro. Estimation of androgen binding protein (rABP) was used as an index of Sertoli cell function. Serum testosterone was reduced significantly by intratesticular administration of naloxone and nalmefene in treated animals. Systemic administration of these antagonists had no effect at the doses used. Testes from treated animals incubated in vitro with or without hCG produced significantly less testosterone than vehicle-treated control testes. Hemicastration reduced rABP synthesis and secretion; however, treatment with opiate antagonists did not alter the amount of this protein in the serum or epididymides of these rats. These observations suggest that endogenous testicular opiates modulate testosterone secretion by Leydig cells.
β-内啡肽被认为是在睾丸间质细胞中合成的。为了获取更多关于这种及其他内源性阿片肽在睾丸中作用的信息,将阿片拮抗剂(纳洛酮和纳美芬,100微克/睾丸)经睾丸内注射给半去势成年大鼠。通过测量血清睾酮及体外睾酮生成来评估间质细胞功能。雄激素结合蛋白(rABP)的测定用作支持细胞功能的指标。在处理的动物中,经睾丸内注射纳洛酮和纳美芬后血清睾酮显著降低。以所用剂量全身给药这些拮抗剂则无作用。来自处理动物的睾丸在体外无论有无hCG孵育时产生的睾酮均显著少于用赋形剂处理的对照睾丸。半去势减少了rABP的合成与分泌;然而,用阿片拮抗剂处理并未改变这些大鼠血清或附睾中该蛋白的量。这些观察结果提示内源性睾丸阿片类物质调节间质细胞的睾酮分泌。