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前列腺素和促黄体生成素释放激素对大鼠颗粒细胞中磷脂酸-磷脂酰肌醇标记的影响。

Effects of prostaglandins and luteinizing hormone-releasing hormone on phosphatidic acid-phosphatidylinositol labeling in rat granulosa cells.

作者信息

Minegishi T, Leung P C

出版信息

Can J Physiol Pharmacol. 1985 Apr;63(4):320-4. doi: 10.1139/y85-058.

DOI:10.1139/y85-058
PMID:3924380
Abstract

In cultures of rat granulosa cells, luteinizing hormone-releasing hormone (LHRH) increases 32P incorporation into both phosphatidylinositol (PI) and phosphatidic acid (PA). After 20 min, the level of radioactivity was three- to four-fold (p less than 0.01) above control in the PI and PA fractions, respectively. The stimulatory effect of LHRH on 32P incorporation was limited to PI and PA. Similar to the effects of LHRH, a rapid and marked increase of 32P incorporation into both PI and PA is observed upon addition of prostaglandin F2 alpha (PGF2 alpha) (10(-5)M) to rat granulosa cells. Incorporation of radioactivity into PA was already increased (p less than 0.05) by 2 min following PGF2 alpha addition, while the increase in 32P-labeled PI became significant (p less than 0.01) by 5 min. In contrast to PGF2 alpha, the labeling of PI and PA following the addition of PGE2 (10(-5)M) was not significantly different from control levels during the entire 10 min of incubation. The sensitivity of the increased PA-PI labeling induced by LHRH and PGF2 alpha is compared in another experiment. After 20 min incubation 10(-6)M LHRH increased PI and PA labeling by six- and four-fold, respectively. Although the effect of PGF2 alpha is less than that of LHRH, 10(-5)M PGF2 alpha significantly (p less than 0.01) increased PI and PA labeling by three- and two-fold, respectively. By contrast, 10(-6)M PGE2 failed to affect 32P incorporation into the various phospholipid fractions, but a small enhancement (p less than 0.05) of PI and PA labeling was observed only at 10(-5)M PGE2.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在大鼠颗粒细胞培养物中,促黄体生成激素释放激素(LHRH)可增加32P掺入磷脂酰肌醇(PI)和磷脂酸(PA)的量。20分钟后,PI和PA组分中的放射性水平分别比对照高3至4倍(p<0.01)。LHRH对32P掺入的刺激作用仅限于PI和PA。与LHRH的作用类似,向大鼠颗粒细胞中添加前列腺素F2α(PGF2α,10(-5)M)后,PI和PA中的32P掺入迅速且显著增加。添加PGF2α后2分钟,PA中的放射性掺入就已增加(p<0.05),而32P标记的PI在5分钟时增加显著(p<0.01)。与PGF2α相反,添加前列腺素E2(PGE2,10(-5)M)后,在整个10分钟的孵育过程中,PI和PA的标记与对照水平无显著差异。在另一项实验中比较了LHRH和PGF2α诱导的PA-PI标记增加的敏感性。孵育20分钟后,10(-6)M LHRH分别使PI和PA标记增加6倍和4倍。尽管PGF2α的作用小于LHRH,但10(-5)M PGF2α分别使PI和PA标记显著(p<0.01)增加3倍和2倍。相比之下,10(-6)M PGE2未能影响32P掺入各种磷脂组分,但仅在10(-5)M PGE2时观察到PI和PA标记有小幅增强(p<0.05)。(摘要截于250字)

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