Ishimura K, Yoshinaga-Hirabayashi T, Tsuri H, Kominami S, Takemori S, Fujita H
Department of Anatomy, Osaka University Medical School, Japan.
Histochemistry. 1990;94(3):225-9. doi: 10.1007/BF00266622.
The localization of cytochrome P-450 of 17 alpha-hydroxylase/C17-C20 lyase (P-450(17 alpha, lyase] and the changes of the enzyme activity were studied immunocytochemically and biochemically in the ovaries of immature rats treated with PMSG (pregnant mare serum gonadotropin) and hCG (human chorionic gonadotropin). Immunocytochemically, P-450(17 alpha, lyase) was localized in both the theca interna cells and interstitial gland cells of the ovaries of immature rats treated with PMSG for 48 h. After hCG administration, the immunoreactive cells rapidly decreased in number in the PMSG-pretreated rat ovary. Namely, 6 h after the hCG injection, positive staining for P-450(17 alpha, lyase) was recognized only in a few theca interna cells, while 12 h after the injection to immunostained cells were detected in the ovary. Forty-eight hours after the hGC treatment (96 h after the PMSG injection), most of the theca interna cells and the interstitial gland cells became immunopositive for P-450(17 alpha, lyase) again. The 17 alpha-hydroxylating activity of P-450(17 alpha, lyase) was 0.5, 0.22 and 0.03 nmol/min/mg protein in the ovarian microsomes of PMSG-treated, PMSG + hCG(3 h)-treated and PMSG + hCG(6 h)-treated rats, respectively. Changes of the hydroxylase activities in all the experimental groups are almost parallel to those of P-450 contents in the microsomes.(ABSTRACT TRUNCATED AT 250 WORDS)
采用免疫细胞化学和生物化学方法,研究了用孕马血清促性腺激素(PMSG)和人绒毛膜促性腺激素(hCG)处理的未成熟大鼠卵巢中17α-羟化酶/C17-C20裂解酶细胞色素P-450(P-450(17α,裂解酶))的定位及酶活性变化。免疫细胞化学研究发现,用PMSG处理48小时的未成熟大鼠卵巢中,P-450(17α,裂解酶)定位于卵泡内膜细胞和间质腺细胞。给予hCG后,PMSG预处理的大鼠卵巢中免疫反应阳性细胞数量迅速减少。即hCG注射后6小时,仅在少数卵泡内膜细胞中检测到P-450(17α,裂解酶)阳性染色,而注射后12小时卵巢中未检测到免疫染色细胞。hCG处理48小时后(PMSG注射后96小时),大多数卵泡内膜细胞和间质腺细胞再次对P-450(17α,裂解酶)呈免疫阳性。PMSG处理、PMSG + hCG(3小时)处理和PMSG + hCG(6小时)处理的大鼠卵巢微粒体中,P-450(17α,裂解酶)的17α-羟化活性分别为0.5、0.22和0.03 nmol/分钟/毫克蛋白。所有实验组羟化酶活性的变化与微粒体中P-450含量的变化几乎平行。(摘要截短至250字)