Abstract
Plasma prorenin and active renin were measured before and after human chorionic gonadotropin (hCG) administration in two groups of patients undergoing ovarian stimulation for 4-6 days with follicle-stimulating hormone alone or in combination with luteinizing hormone, for in vitro fertilization. Baseline total plasma renin (prorenin plus active renin; n = 12) averaged 25 +/- 8 ng/ml per hr (mean +/- SD). Total renin did not change during ovarian stimulation but it increased to 46 +/- 16 ng/ml per hr (P less than 0.05) 1 or 2 days later, just before hCG administration. Thirty-six hours after hCG administration, just before laparoscopy and egg retrieval, total renin was 123 +/- 97 ng/ml per hr; a peak of 182 +/- 143 ng/ml per hr occurred 2-6 days later--i.e., during the luteal phase of the menstrual cycle. In eight of the patients who did not conceive, total renin returned to baseline 14 days after hCG administration. In four who conceived, a nadir was reached (57 +/- 13 ng/ml per hr) 8-12 days after hCG administration and then total renin increased again as the plasma beta hCG measurement began to rise. By day 16 it averaged 225 +/- 157 ng/ml per hr. In a second group of five patients active renin and prorenin were measured separately. Active renin comprised less than 20% of the total renin at all times. It was unchanged until day 4 after hCG administration and then increased significantly only when plasma progesterone was high. Thus, the initial response to hCG was entirely due to an increase in prorenin. A highly significant correlation was observed between the number of follicles and the total renin increases on the day of aspiration (r = 0.93, P less than 0.001) and at the peak (r = 0.89, P less than 0.001). After hCG administration, a temporal relationship was observed between the rise in total renin and plasma estradiol and progesterone levels. These results demonstrate that plasma prorenin increases markedly after administration of hCG and that the rise is directly related to the number of ovarian follicles and to plasma estrogen and progesterone levels. The findings suggest that prorenin is produced by the mature ovarian follicle and by the corpus luteum in response to gonadotropin stimulation.
Full text
PDF




Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Acker G. M., Galen F. X., Devaux C., Foote S., Papernik E., Pesty A., Menard J., Corvol P. Human chorionic cells in primary culture: a model for renin biosynthesis. J Clin Endocrinol Metab. 1982 Nov;55(5):902–909. doi: 10.1210/jcem-55-5-902. [DOI] [PubMed] [Google Scholar]
- BROWN J. J., DAVIES D. L., LEVER A. F., ROBERTSON J. I. VARIATIONS IN PLASMA RENIN DURING THE MENSTRUAL CYCLE. Br Med J. 1964 Oct 31;2(5417):1114–1115. doi: 10.1136/bmj.2.5417.1114. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Culler M. D., Tarlatzis B. C., Lightman A., Fernandez L. A., Decherney A. H., Negro-Vilar A., Naftolin F. Angiotensin II-like immunoreactivity in human ovarian follicular fluid. J Clin Endocrinol Metab. 1986 Mar;62(3):613–615. doi: 10.1210/jcem-62-3-613. [DOI] [PubMed] [Google Scholar]
- Derkx F. H., Alberda A. T., Zeilmaker G. H., Schalekamp M. A. High concentrations of immunoreactive renin, prorenin and enzymatically-active renin in human ovarian follicular fluid. Br J Obstet Gynaecol. 1987 Jan;94(1):4–9. doi: 10.1111/j.1471-0528.1987.tb02243.x. [DOI] [PubMed] [Google Scholar]
- Derkx F. H., Steunkel C., Schalekamp M. P., Visser W., Huisveld I. H., Schalekamp M. A. Immunoreactive renin, prorenin, and enzymatically active renin in plasma during pregnancy and in women taking oral contraceptives. J Clin Endocrinol Metab. 1986 Oct;63(4):1008–1015. doi: 10.1210/jcem-63-4-1008. [DOI] [PubMed] [Google Scholar]
- Derkx F. H., Wenting G. J., Man in 't Veld A. J., Verhoeven R. P., Schalekamp M. A. Control of enzymatically inactive renin in man under various pathological conditions: implications for the interpretation of renin measurements in peripheral and renal venous plasma. Clin Sci Mol Med. 1978 May;54(5):529–538. doi: 10.1042/cs0540529. [DOI] [PubMed] [Google Scholar]
- Elliott M. E., Siegel F. L., Hadjokas N. E., Goodfriend T. L. Angiotensin effects on calcium and steroidogenesis in adrenal glomerulosa cells. Endocrinology. 1985 Mar;116(3):1051–1059. doi: 10.1210/endo-116-3-1051. [DOI] [PubMed] [Google Scholar]
- Fernandez L. A., Tarlatzis B. C., Rzasa P. J., Caride V. J., Laufer N., Negro-Vilar A. F., DeCherney A. H., Naftolin F. Renin-like activity in ovarian follicular fluid. Fertil Steril. 1985 Aug;44(2):219–223. doi: 10.1016/s0015-0282(16)48740-6. [DOI] [PubMed] [Google Scholar]
- Fernandez L. A., Twickler J., Mead A. Neovascularization produced by angiotensin II. J Lab Clin Med. 1985 Feb;105(2):141–145. [PubMed] [Google Scholar]
- Fishman M. C., Zimmerman E. A., Slater E. E. Renin and angiotensin: the complete system within the neuroblastoma x glioma cell. Science. 1981 Nov 20;214(4523):921–923. doi: 10.1126/science.6272392. [DOI] [PubMed] [Google Scholar]
- Glorioso N., Atlas S. A., Laragh J. H., Jewelewicz R., Sealey J. E. Prorenin in high concentrations in human ovarian follicular fluid. Science. 1986 Sep 26;233(4771):1422–1424. doi: 10.1126/science.3529392. [DOI] [PubMed] [Google Scholar]
- Hsueh W. A., Luetscher J. A., Carlson E. J., Grislis G., Fraze E., McHargue A. Changes in active and inactive renin throughout pregnancy. J Clin Endocrinol Metab. 1982 May;54(5):1010–1016. doi: 10.1210/jcem-54-5-1010. [DOI] [PubMed] [Google Scholar]
- Jones G. S., Acosta A. A., Garcia J. E., Bernardus R. E., Rosenwaks Z. The effect of follicle-stimulating hormone without additional luteinizing hormone on follicular stimulation and oocyte development in normal ovulatory women. Fertil Steril. 1985 May;43(5):696–702. doi: 10.1016/s0015-0282(16)48550-x. [DOI] [PubMed] [Google Scholar]
- Jones G. S. Update on in vitro fertilization. Endocr Rev. 1984 Winter;5(1):62–75. doi: 10.1210/edrv-5-1-62. [DOI] [PubMed] [Google Scholar]
- Jones H. W., Jr, Jones G. S., Andrews M. C., Acosta A., Bundren C., Garcia J., Sandow B., Veeck L., Wilkes C., Witmyer J. The program for in vitro fertilization at Norfolk. Fertil Steril. 1982 Jul;38(1):14–21. [PubMed] [Google Scholar]
- Lumbers E. R. Activation of renin in human amniotic fluid by low pH. Enzymologia. 1971 Jun 30;40(6):329–336. [PubMed] [Google Scholar]
- McNatty K. P., Makris A., DeGrazia C., Osathanondh R., Ryan K. J. The production of progesterone, androgens, and estrogens by granulosa cells, thecal tissue, and stromal tissue from human ovaries in vitro. J Clin Endocrinol Metab. 1979 Nov;49(5):687–699. doi: 10.1210/jcem-49-5-687. [DOI] [PubMed] [Google Scholar]
- Moon Y. S., Tsang B. K., Simpson C., Armstrong D. T. 17 beta-Estradiol biosynthesis in cultured granulosa and thecal cells of human ovarian follicles: stimulation by follicle-stimulating hormone. J Clin Endocrinol Metab. 1978 Aug;47(2):263–267. doi: 10.1210/jcem-47-2-263. [DOI] [PubMed] [Google Scholar]
- Muasher S. J., Garcia J. E., Rosenwaks Z. The combination of follicle-stimulating hormone and human menopausal gonadotropin for the induction of multiple follicular maturation for in vitro fertilization. Fertil Steril. 1985 Jul;44(1):62–69. doi: 10.1016/s0015-0282(16)48678-4. [DOI] [PubMed] [Google Scholar]
- Okamura T., Clemens D. L., Inagami T. Renin, angiotensins, and angiotensin-converting enzyme in neuroblastoma cells: evidence for intracellular formation of angiotensins. Proc Natl Acad Sci U S A. 1981 Nov;78(11):6940–6943. doi: 10.1073/pnas.78.11.6940. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Poisner A. M., Wood G. W., Poisner R. Release of inactive renin from human fetal membranes and isolated trophoblasts. Clin Exp Hypertens A. 1982;4(11-12):2007–2017. doi: 10.3109/10641968209062366. [DOI] [PubMed] [Google Scholar]
- Ryan K. J., Petro Z. Steroid biosynthesis by human ovarian granulosa and thecal cells. J Clin Endocrinol Metab. 1966 Jan;26(1):46–52. doi: 10.1210/jcem-26-1-46. [DOI] [PubMed] [Google Scholar]
- Sealey J. E., Atlas S. A., Glorioso N., Manapat H., Laragh J. H. Cyclical secretion of prorenin during the menstrual cycle: synchronization with luteinizing hormone and progesterone. Proc Natl Acad Sci U S A. 1985 Dec;82(24):8705–8709. doi: 10.1073/pnas.82.24.8705. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sealey J. E., Atlas S. A., Laragh J. H. Prorenin and other large molecular weight forms of renin. Endocr Rev. 1980 Fall;1(4):365–391. doi: 10.1210/edrv-1-4-365. [DOI] [PubMed] [Google Scholar]
- Sealey J. E., Cholst I., Glorioso N., Troffa C., Weintraub I. D., James G., Laragh J. H. Sequential changes in plasma luteinizing hormone and plasma prorenin during the menstrual cycle. J Clin Endocrinol Metab. 1987 Jul;65(1):1–5. doi: 10.1210/jcem-65-1-1. [DOI] [PubMed] [Google Scholar]
- Sealey J. E., Glorioso N., Itskovitz J., Laragh J. H. Prorenin as a reproductive hormone. New form of the renin system. Am J Med. 1986 Dec;81(6):1041–1046. doi: 10.1016/0002-9343(86)90402-x. [DOI] [PubMed] [Google Scholar]
- Sealey J. E., Glorioso N., Itskovitz J., Troffa C., Cholst I., Rosenwaks Z. Plasma prorenin during early pregnancy: ovarian secretion under gonadotropin control? J Hypertens Suppl. 1986 Dec;4(5):S92–S95. [PubMed] [Google Scholar]
- Sealey J. E., Glorioso N., Toth A., Atlas S. A., Laragh J. H. Stimulation of plasma prorenin by gonadotropic hormones. Am J Obstet Gynecol. 1985 Nov 1;153(5):596–597. doi: 10.1016/0002-9378(85)90495-8. [DOI] [PubMed] [Google Scholar]
- Sealey J. E., McCord D., Taufield P. A., Ales K. A., Druzin M. L., Atlas S. A., Laragh J. H. Plasma prorenin in first-trimester pregnancy: relationship to changes in human chorionic gonadotropin. Am J Obstet Gynecol. 1985 Nov 1;153(5):514–519. doi: 10.1016/0002-9378(85)90464-8. [DOI] [PubMed] [Google Scholar]
- Sealey J. E., White R. P., Laragh J. H., Rubin A. L. Plasma prorenin and renin in anephric patients. Circ Res. 1977 Oct;41(4 Suppl 2):17–21. doi: 10.1161/01.res.41.4.17. [DOI] [PubMed] [Google Scholar]
- Skinner S. L., Cran E. J., Gibson R., Taylor R., Walters W. A., Catt K. J. Angiotensins I and II, active and inactive renin, renin substrate, renin activity, and angiotensinase in human liquor amnii and plasma. Am J Obstet Gynecol. 1975 Mar 1;121(5):626–630. doi: 10.1016/0002-9378(75)90463-9. [DOI] [PubMed] [Google Scholar]
- Smith J. B., Smith L., Brown E. R., Barnes D., Sabir M. A., Davis J. S., Farese R. V. Angiotensin II rapidly increases phosphatidate-phosphoinositide synthesis and phosphoinositide hydrolysis and mobilizes intracellular calcium in cultured arterial muscle cells. Proc Natl Acad Sci U S A. 1984 Dec;81(24):7812–7816. doi: 10.1073/pnas.81.24.7812. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Veeck L. L., Wortham J. W., Jr, Witmyer J., Sandow B. A., Acosta A. A., Garcia J. E., Jones G. S., Jones H. W., Jr Maturation and fertilization of morphologically immature human oocytes in a program of in vitro fertilization. Fertil Steril. 1983 May;39(5):594–602. doi: 10.1016/s0015-0282(16)47052-4. [DOI] [PubMed] [Google Scholar]
- Wallenstein S., Zucker C. L., Fleiss J. L. Some statistical methods useful in circulation research. Circ Res. 1980 Jul;47(1):1–9. doi: 10.1161/01.res.47.1.1. [DOI] [PubMed] [Google Scholar]
- Yen S. S., Llerena O., Little B., Pearson O. H. Disappearance rates of endogenous luteinizing hormone and chorionic gonadotropin in man. J Clin Endocrinol Metab. 1968 Dec;28(12):1763–1767. doi: 10.1210/jcem-28-12-1763. [DOI] [PubMed] [Google Scholar]

