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Development of the rat oocyte in vitro: inhibition and induction of maturation in the presence or absence of the cumulus oophorus
Authors:N Dekel  W H Beers
Institution:The Rockefeller University, 1230 York Avenue, New York, New York 10021 USA
Abstract:The effect in vitro of oocyte maturation inhibitors and the ability of preparations of luteinizing hormone to relieve the arrest induced by these substances was studied in preparations of cumulus-free (naked) rat oocytes, and compared to previously obtained results from oocytes enclosed by their cumulus cells. The development of both the cumulus-oocyte complex and naked oocyte is arrested in vitro by cyclic AMP derivatives or cyclic nucleotide phosphodiesterase inhibitors. While gonadotropins can overcome the effect of these substances in the cumulus oocyte complex, they have no effect on naked oocytes. Cholera enterotoxin, an irreversible activator of adenylate cyclase, maintains developmental arrest in cultured cumulus oocyte complexes but not in naked oocytes. Preparations of luteinizing hormone can partially overcome the effect of cholera enterotoxin in the complexes. Furthermore, the acceleration of oocyte maturation in vitro observed in the presence of gonadotropins, which is seen in cumulus oocyte complexes, can be mimicked by stripping the oocyte of its associated cumulus cells. The results of these and other studies suggest that: (1) the cytoplasmic levels of cyclic AMP in the isolated oocyte are high enough to maintain meiotic arrest if a phosphodiesterase inhibitor is present; (2) the oocyte contains an active phosphodiesterase; (3) the oolemma may lack the adenylate cyclase system and; (4) gonadotropins seem to affect the oocyte indirectly, via the cumulus cells, possibly by interrupting communication between the two cell types.
Keywords:(o)LH  (ovine)luteinizing hormone  GV  germinal vesicle  cAMP  cyclic AMP  dibutyryl cyclic AMP  iBuMeXan  3-isobutyl-1-methylxanthine  IU  international units  PMSG  pregnant mare serum gonadotropin  L-15  Leibovitz's L-15 tissue culture medium  half maximally effective dose
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