Bovine oocyte and embryo development following meiotic inhibition with butyrolactone I

Mol Reprod Dev. 2000 Oct;57(2):204-9. doi: 10.1002/1098-2795(200010)57:2<204::AID-MRD12>3.0.CO;2-N.

Abstract

In this study we have shown that butyrolactone I (BL-I), a potent inhibitor of cyclin-dependent kinases, inhibits meiotic resumption in bovine oocytes by blocking germinal vesicle breakdown in a dose-dependent manner. A concentration 100 microM blocked over 60% of oocytes, while 150 microM inhibited almost all oocytes compared to the control in which over 80% resumed meiosis. Following a second 24 hr culture under conditions permissive to normal maturation, almost all (95%) of blocked oocytes resumed meiosis and progressed to metaphase II. In terms of developmental competence, oocytes maintained in meiotic arrest for 24 hr with 100 microM exhibited a similar capacity to develop to the blastocyst stage as nonblocked control oocytes following maturation, fertilization, and culture in vitro. Cryopreservation was employed as a tool to detect differences in the oocyte viability between blocked and control oocytes. Cleavage of oocytes was significantly reduced following vitrification and activation both in BL-I treated (40.2% vs. 71.9%, P < 0.05) and the control groups (45.6% vs. 81.7%, P < 0.05). However, BL-I treated oocytes were less likely to develop into blastocysts following vitrification (20.0% from vitrified vs 42.5% from nonvitrified cleaved oocytes, P < 0.05, based on cleaved oocytes) compared to nontreated oocytes (34.0% from vitrified vs. 42. 9% from nonvitrified oocytes, P < 0.05). These results demonstrate the feasibility of maintaining bovine oocytes in artificial meiotic arrest without compromising their subsequent developmental competence and may represent a tool for improving the development of less competent oocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4-Butyrolactone / analogs & derivatives*
  • 4-Butyrolactone / pharmacology
  • Animals
  • Cattle
  • Cyclin-Dependent Kinases / antagonists & inhibitors
  • Embryonic and Fetal Development / drug effects*
  • Enzyme Inhibitors / pharmacology
  • Female
  • In Vitro Techniques
  • Male
  • Meiosis / drug effects*
  • Oocytes / drug effects*
  • Oocytes / growth & development*

Substances

  • Enzyme Inhibitors
  • butyrolactone I
  • Cyclin-Dependent Kinases
  • 4-Butyrolactone