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Human Reproduction, Vol. 8, No. 7, pp. 1011-1014, 1993
© 1993 European Society of Human Reproduction and Embryology

other

Relaxin induces ovulations in the in-vitro perfused rat ovary

M. Brännström1 and A.H. MacLennan

Department of Obstetrics and Gynaecology, Reproductive Medicine Unit, University of Adelaide, The Queen Elizabeth Hospital Woodville Road, Woodville, SA 5011, Australia

Correspondence: 1To whom correspondence should be addressed

The effects of human recombinant relaxin on ovulation and ovarian steroidogenesis were investigated in vitro using a perfused rat ovary model. Ovaries of equine chorionic gonadotrophin (ECG; 20 IU)-primed Sprague—Dawley rats were perfused for 21 h. Ovarian release of oestradiol and progesterone was measured during the perfusion period and the number of ovulations was estimated by counting the released oocytes at termination of the experiment. Non-treated control ovaries did not ovulate whereas addition of ovine luteinizing hormone (LH; 100 ng/ml) resulted in a mean (± SEM) number of ovulations of 3.0 ± 0.8 from all treated ovaries. Relaxin (10 µg/ml) induced mean (± SEM) number of ovulations at 2.4 ± 0.2 in all treated ovaries but did not further increase the ovulation rate when combined with LH (mean ± SEM 3.2 ± 0.4). All ovulated oocytes in the groups stimulated by LH showed signs of nuclear maturation (germinal vesicle breakdown) when harvested, in contrast to ovulated oocytes in the relaxin group, which were immature (presence of germinal vesicle). Progesterone and oestradiol release was significantly increased in the LH-stimulated groups but not in the group treated only with relaxin, in comparison to the untreated control group. These results demonstrate that relaxin may have a paracrine role within the ovary and may facilitate ovulation, possibly by promoting connective tissue remodelling of the follicle wall.

Key words: Ovary/ovulation/rat/relaxin


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