ANGIOTENSIN-CONVERTING ENZYME-INHIBITION REVERSES LUTEAL-PHASE STEROID-PRODUCTION IN OOCYTE DONORS

被引:17
作者
MORRIS, RS
PAULSON, RJ
LINDHEIM, SR
LEGRO, RS
LOBO, RA
SAUER, MV
机构
[1] UNIV SO CALIF,LOS ANGELES CTR WOMENS & CHILDRENS HOSP,SCH MED,DIV REPROD ENDOCRINOL,LOS ANGELES,CA 90033
[2] UNIV SO CALIF,CALIF MED CTR,IN VITRO FERTILIZAT PROGRAM,LOS ANGELES,CA 90033
关键词
OVARIAN-DERIVED PRORENIN TO ANGIOTENSIN CASCADE (ODPAC) ANGIOTENSIN-CONVERTING ENZYME (ACE) INHIBITION; CAPTOPRIL; OOCYTE DONATION; OVARIAN STEROID SYNTHESIS; OVARIAN HYPERSTIMULATION SYNDROME (OHSS);
D O I
10.1016/S0015-0282(16)57493-7
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To determine whether angiotensin-converting enzyme (ACE) inhibition would affect ovarian steroid synthesis in the oocyte donors undergoing controlled ovarian hyperstimulation (COH). Setting: The IVF program of the University of Southern California. Design: Prospective matched clinical trial. Patients: Twelve oocyte donors were studied in 28 hyperstimulation cycles. Interventions: Donors underwent a standard COH protocol; Follicle aspiration was performed 34 hours after administration of hCG. After the procedure, seven donors were administered the ACE inhibitor, captopril, 6.25 mg orally twice daily for 4 days, The remaining patients served as controls. Main Outcome Measures: Serum E(2), P, plasma prorenin, active renin, and angiotensin II (Ang II). Results: Angiotensin II increased after aspiration in both groups but was significantly lower in those receiving captopril, Peak P in the captopril group was significantly lower than controls (81.8 +/- 27.8 versus 208.5 +/- 23.9 ng/mL [conversion factor to SI unit, 3.180]). Peak E(2) was significantly higher (2,222.4 +/- 875.3 versus 425.6 +/- 490.4 pg/mL [conversion factor to SI unit, 3.671]). Active renin and Ang II correlated with P. Conclusions: In stimulated cycles, inhibition of Ang II production appears to raise serum E(2) and lower P levels. Angiotensin II, therefore, may have a role in the regulation of ovarian steroid synthesis.
引用
收藏
页码:854 / 858
页数:5
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