TY - JOUR
T1 - Angiotensin-converting enzyme inhibition reverses luteal phase steroid production in oocyte donors
AU - Morris, R. S.
AU - Paulson, R. J.
AU - Lindhelm, S. R.
AU - Legro, R. S.
AU - Lobo, R. A.
AU - Sauer, M. V.
PY - 1995
Y1 - 1995
N2 - Objective: To determine whether angiotensin-converting enzyme (ACE) inhibition would affect ovarian steroid synthesis in the oocyte donors undergoing controlled ovarian hyperstimulalion (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 Main Outcome Measures: Serum E2, P, plasma prorenin, active renin, and angiotensin II (Ang II). Results: Angiotensin II increased after aspiration in both groups hut 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 E2 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 E2 and lower P levels. Angiotensin II, therefore, may have a role in the regulation of ovarian steroid synthesis.
AB - Objective: To determine whether angiotensin-converting enzyme (ACE) inhibition would affect ovarian steroid synthesis in the oocyte donors undergoing controlled ovarian hyperstimulalion (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 Main Outcome Measures: Serum E2, P, plasma prorenin, active renin, and angiotensin II (Ang II). Results: Angiotensin II increased after aspiration in both groups hut 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 E2 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 E2 and lower P levels. Angiotensin II, therefore, may have a role in the regulation of ovarian steroid synthesis.
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U2 - 10.1016/s0015-0282(16)57493-7
DO - 10.1016/s0015-0282(16)57493-7
M3 - Article
C2 - 7890074
AN - SCOPUS:0028934020
SN - 0015-0282
VL - 63
SP - 854
EP - 858
JO - Fertility and Sterility
JF - Fertility and Sterility
IS - 4
ER -