Phillips Maureen L, Schultz Bruce D
Department of Anatomy and Physiology, Kansas State University, 1600 Denison Avenue, Manhattan, KS 66506, USA.
Biol Reprod. 2002 Apr;66(4):1016-23. doi: 10.1095/biolreprod66.4.1016.
Epithelial cells were isolated from adult porcine vas deferens and grown in the absence or presence of steroid hormones. Transepithelial resistance (R(te)), basal short circuit current (I(sc)), and the effects of selected ion transport modulators on these parameters were evaluated in modified Ussing chambers at three time points (5-8, 11-14, and 18-22 days postseeding). At the earliest time point, no significant differences were observed. At the middle time point, when compared with R(te) in untreated control monolayers, R(te) in monolayers exposed to 17beta-estradiol, aldosterone, cortisol, cortisone, prednisolone, prednisone, and dexamethasone was significantly lower; in contrast, R(te) in monolayers exposed to testosterone, dihydrotestosterone, or progesterone did not differ from that in control monolayers. Treatments with cortisol, prednisolone, and dexamethasone were associated with an elevated basal I(sc) that was amiloride sensitive, indicating ongoing Na(+) absorption by these monolayers. R(te) was increased by amiloride treatment in glucocorticoid-treated monolayers but remained significantly less than that of control monolayers. At the third time point, the postamiloride R(te) of glucocorticoid-treated monolayers was not different from that of control monolayers. Responses to ATP, forskolin, bumetanide, and DASU-02 were not affected by steroid treatment at any time point. Taken together, these results suggest that estrogens and corticosteroids can modulate epithelial function in the distal excurrent duct of the adult male reproductive system. At physiological or pharmacological concentrations, these hormones would be expected to modify the luminal environment (both the ionic composition and pH) to which sperm are exposed and thus affect male fertility.
从成年猪输精管中分离出上皮细胞,并在无类固醇激素或有类固醇激素存在的情况下进行培养。在改良的尤斯灌流小室中,于接种后的三个时间点(接种后5 - 8天、11 - 14天和18 - 22天)评估跨上皮电阻(R(te))、基础短路电流(I(sc))以及所选离子转运调节剂对这些参数的影响。在最早的时间点,未观察到显著差异。在中间时间点,与未处理的对照单层细胞的R(te)相比,暴露于17β - 雌二醇、醛固酮、皮质醇、可的松、泼尼松龙、泼尼松和地塞米松的单层细胞的R(te)显著降低;相反,暴露于睾酮、双氢睾酮或孕酮的单层细胞的R(te)与对照单层细胞的R(te)没有差异。皮质醇、泼尼松龙和地塞米松处理导致基础I(sc)升高,且该升高对阿米洛利敏感,表明这些单层细胞存在持续的Na(+)吸收。在糖皮质激素处理的单层细胞中,阿米洛利处理可增加R(te),但仍显著低于对照单层细胞。在第三个时间点,糖皮质激素处理的单层细胞在阿米洛利处理后的R(te)与对照单层细胞的R(te)没有差异。在任何时间点,对ATP、福斯高林、布美他尼和DASU - 02的反应均不受类固醇处理的影响。综上所述,这些结果表明雌激素和皮质类固醇可调节成年雄性生殖系统远端输出管中的上皮功能。在生理或药理浓度下,这些激素有望改变精子所接触的管腔环境(离子组成和pH值),从而影响男性生育能力。