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血管紧张素转换酶抑制对促性腺激素刺激的家兔的影响:对雌二醇产生的作用

Angiotensin converting enzyme inhibition of the gonadotropin-stimulated rabbit: effect on estradiol production.

作者信息

Morris R S, Wong I L, Paulson R J

机构信息

Division of Reproductive Endocrinology, University of Southern California School of Medicine, Los Angeles County Women's and Children's Hospital, USA.

出版信息

J Assist Reprod Genet. 1995 May;12(5):326-9. doi: 10.1007/BF02213713.

Abstract

PURPOSE

Our purpose was to determine whether angiotensin converting enzyme (ACE) inhibitors affect gonadotropin-stimulated estradiol (E2) production.

DESIGN

This was a prospective, masked, randomized, placebo-controlled animal trial. Twenty female New Zealand White rabbits were hyperstimulated with gonadotropins. One-half of the rabbits received concomitant treatment with the ACE inhibitor, enalapril; one-half received concomitant treatment with a placebo.

RESULTS

Baseline peripheral E2 (13 +/- 4 vs 11 +/- 2 pg/ml) and angiotensin II (Ang II) (22 +/- 5 vs 27 +/- 7 pg/ml) levels were similar in both groups. Significant inhibition of peripheral Ang II levels was achieved in the enalapril group (32 +/- 6 vs 93 +/- 15 pg/ml; P = 0.005). E2 was significantly higher in the rabbits receiving enalapril versus placebo (369 +/- 58 vs 183 +/- 35 pg/ml, P < 0.03), respectively. By day 10, peripheral E2 had returned to normal levels in both groups (13 +/- 1 vs 13 +/- 1 pg/ml). However, E2 levels in the ovarian effluent were 2.8 times higher in the enalapril rabbits.

CONCLUSION

Peripheral Ang II levels increase after gonadotropin stimulation and ACE inhibitors are able to blunt this increase significantly. ACE inhibition has a significant stimulatory effect on ovarian E2 production. This implies that Ang II may normally inhibit ovarian E2 production in stimulated cycles.

摘要

目的

我们的目的是确定血管紧张素转换酶(ACE)抑制剂是否会影响促性腺激素刺激的雌二醇(E2)生成。

设计

这是一项前瞻性、双盲、随机、安慰剂对照的动物试验。20只雌性新西兰白兔用促性腺激素进行超刺激。其中一半兔子同时接受ACE抑制剂依那普利治疗;另一半接受安慰剂治疗。

结果

两组的基线外周血E2(13±4 vs 11±2 pg/ml)和血管紧张素II(Ang II)(22±5 vs 27±7 pg/ml)水平相似。依那普利组外周血Ang II水平得到显著抑制(32±6 vs 93±15 pg/ml;P = 0.005)。接受依那普利治疗的兔子的E2显著高于接受安慰剂治疗的兔子(分别为369±58 vs 183±35 pg/ml,P < 0.03)。到第10天,两组外周血E2均恢复到正常水平(13±1 vs 13±1 pg/ml)。然而,依那普利组兔子卵巢流出液中的E2水平高出2.8倍。

结论

促性腺激素刺激后外周血Ang II水平升高,ACE抑制剂能够显著抑制这种升高。ACE抑制对卵巢E2生成有显著的刺激作用。这意味着在受刺激的周期中,Ang II可能正常情况下会抑制卵巢E2生成。

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