A. Loseke et K. Spanelborowski, SIMPLE OR REPEATED INDUCTION OF SUPEROVULATION - A STUDY ON OVULATIONRATES AND MICROVESSEL CORROSION CASTS IN OVARIES OF GOLDEN-HAMSTERS, Annals of anatomy, 178(1), 1996, pp. 5-14
Repeatedly stimulated ovaries are reported to decrease the ovulation r
ate. One cause among others might be that the microvascular bed has be
en insufficiently developed. Therefore, 30-day-old golden hamsters wer
e superovulated either once or repeatedly. At the light microscopic le
vel, the ovulation rate in serially sectioned ovaries was indirectly d
etermined by the occurrence of corpora lutea and of abnormal follicle
rupture with oocyte release into the cortical stroma (IOR). For the st
udy with scanning electron microscopy (SEM), the microvascular bed of
the ovaries was cast with a polyester resin, and the corrosion casts o
f mature follicles observed. The histological sections of once-stimula
ted ovaries showed a large number of corpora lutea and IOR follicles.
This indicated hyperovulation. In corrosion casts of once-stimulated o
varies, large-sited antral follicles with two layers of a dense capill
ary meshwork were observed. Capillary sprouts were aligned around the
antrum 0 to 12 h after administration of human chorionic gonadotrophin
(hCG), and these radiated towards the center of the antrum after 12 t
o 36 h had elapsed. The ovulation site was recognized at the follicle
apex by three similarly sized structures which were either a sinusoid,
an oocyte replica, or an opening. Repeatedly stimulated ovaries produ
ced a low number of corpora lutea and almost no IOR follicles. This wa
s judged as hypoovulation. The microvessels of mature follicles were r
educed in number and incompletely cast. Widespread resin leakages were
conspicuous in the follicle wall 36 h after hCG injection, but the ca
pillary sprouts radiated towards the center of the antrum. No ovulatio
n site was detectable. It is concluded, that capillary sprouts are ind
uced before luteinization. The ovulation site is indicated by particul
ar changes in its microvascular bed. An insufficiently developed micro
vascular bed may be responsible for hypoovulation in repeatedly stimul
ated ovaries.