Sharpe R M, Swanston I A, Cooper I, Tsonis C G, McNeilly A S
MRC Reproductive Biology Unit, Centre for Reproductive Biology, Edinburgh.
J Endocrinol. 1988 Nov;119(2):315-26. doi: 10.1677/joe.0.1190315.
Immunoreactive inhibin was measured in testicular interstitial fluid (IF) from rats during sexual maturation or after impairment of spermatogenesis induced by ethane dimethanesulphonate (EDS), unilateral cryptorchidism or local heating (43 degrees C, 30 min) of the testes, to ascertain its usefulness as a marker of changing Sertoli cell function. Cultures of isolated seminiferous tubules were also studied. Inhibin was measured by a radioimmunoassay directed towards the first 26 amino acids of the N-terminus of the alpha-subunit, and the results confirmed for selected pools of IF by in-vitro bioassay using dispersed ovine pituitary cells. During puberty, IF levels of immunoactive inhibin fell by more than 90% (P less than 0.001) between 30 and 60 days of age, a decrease paralleled by the levels of androgen-binding protein (ABP), another Sertoli cell product secreted into IF. These changes also paralleled, but preceded, the fall (60%; P less than 0.001) in serum levels of FSH between 40 and 70 days, while the serum and IF levels of testosterone increased more than two-fold over this period. When adult rats were injected with EDS to destroy the Leydig cells, testosterone levels in IF and serum were undetectable at 3 and 7 days after treatment, were just detectable at 14 days and thereafter returned slowly towards normal by 42 days. The initial androgen withdrawal following EDS treatment caused a progressive reduction in testicular weight up to 21 days and this was accompanied by a significant increase in the serum levels of FSH and a two- to threefold increase in the IF levels of immunoactive inhibin (and also of ABP). Serum FSH and IF levels of immunoactive inhibin returned to within the normal range by 42 days when testosterone levels had normalized. In contrast, in two other experimental situations in which a marked decrease in testicular weight coupled with an increase in IF levels of ABP occurs, different results for the IF levels of immunoactive inhibin were obtained. Thus, in rats exposed to local heating of the testes, IF levels of immunoactive inhibin remained unchanged from control values at 21-40 days after treatment, a finding confirmed by bioassay results. In rats made unilaterally cryptorchid for 10 months, levels of immunoactive inhibin in IF were reduced by 60% (P less than 0.01) in the abdominal compared with the contralateral scrotal testis.(ABSTRACT TRUNCATED AT 400 WORDS)
为确定免疫反应性抑制素作为支持细胞功能变化标志物的效用,对性成熟期间或经乙烷二甲磺酸盐(EDS)、单侧隐睾或睾丸局部加热(43摄氏度,30分钟)诱导精子发生受损后的大鼠睾丸间质液(IF)中的免疫反应性抑制素进行了测量。还对分离的生精小管培养物进行了研究。通过针对α亚基N端前26个氨基酸的放射免疫测定法测量抑制素,并使用分散的绵羊垂体细胞通过体外生物测定法对选定的IF样本的结果进行了确认。在青春期,30至60日龄之间免疫反应性抑制素的IF水平下降超过90%(P<0.001),这种下降与雄激素结合蛋白(ABP)的水平平行,ABP是另一种分泌到IF中的支持细胞产物。这些变化也与40至70日龄之间血清促卵泡激素(FSH)水平的下降(60%;P<0.001)平行,但先于此下降,而在此期间血清和IF中的睾酮水平增加了两倍多。当成年大鼠注射EDS以破坏睾丸间质细胞时,治疗后3天和7天IF和血清中的睾酮水平无法检测到,14天时刚刚可检测到,此后到42天时缓慢恢复正常。EDS治疗后最初的雄激素撤退导致睾丸重量在21天内逐渐减轻,同时血清FSH水平显著升高,免疫反应性抑制素(以及ABP)的IF水平增加两到三倍。当睾酮水平恢复正常时,血清FSH和免疫反应性抑制素的IF水平在42天时恢复到正常范围内。相比之下,在另外两种实验情况下,出现了睾丸重量显著减轻以及ABP的IF水平增加的情况,免疫反应性抑制素的IF水平得到了不同的结果。因此,在睾丸局部加热的大鼠中,治疗后21至40天免疫反应性抑制素的IF水平与对照值相比保持不变,生物测定结果证实了这一发现。在单侧隐睾10个月的大鼠中,与对侧阴囊睾丸相比,腹部睾丸IF中的免疫反应性抑制素水平降低了60%(P<0.01)。(摘要截取自400字)