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Biology of Reproduction, Vol 11, 145-152, Copyright © 1974 by Society for the Study of Reproduction
1 Department of Endocrinology, Growth and Reproduction, Erasmus University,
P.O. Box 1738, Rotterdam Denuded ovarian oocytes, obtained from prepuberal rats, were incubated under oil
and their development was studied by time-lapse cinemicrography. Polar bodies were
formed about 8 h after autopsy and showed active movements immediately following
abstriction. The oocyte membrane did not show contraction wrinkles during polar body
formation as had been observed in mouse oocytes. Unfertilized tubal oocytes formed
a second polar body in vitro about 45 min after isolation. Rat ovarian oocytes were able to utilize pyruvate, lactate, and possibly even an endogenous energy source for maturation. The absence of oxygen prevented maturation. It
is suggested that oxygen (oxidation-reduction potential changes) may trigger oocyte maturation in Vivo. The formation of the second polar body in vitro is not inhibited by KCN, carbonyl
cyanide p-trifluoromethoxyphenyl hydrazone, or the absence of oxygen, which indicates
that the initiation of the second maturation division, unlike that of the first meiotic
division, does not require generation of ATP by oxidative metabolism. Tubal oocytes
lose the capacity to form a second polar body in the evening on the day of estrus.
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