Disparate consequences of heat stress exposure during meiotic maturation: embryo development after chemical activation vs fertilization of bovine oocytes

Reproduction. 2011 Dec;142(6):831-43. doi: 10.1530/REP-11-0032. Epub 2011 Oct 12.

Abstract

Consequences of heat stress exposure during the first 12 h of meiotic maturation differed depending on how and when bovine oocytes were activated. If heat-stressed oocytes underwent IVF at ~24 h, blastocyst development was less than for respective controls and similar to that obtained for nonheat-stressed oocytes undergoing IVF at 30 h (i.e. slightly aged). In contrast, if heat-stressed oocytes underwent chemical activation with ionomycin/6-dimethylaminopurine at 24 h, blastocyst development was not only higher than respective controls, but also equivalent to development obtained after activation of nonheat-stressed oocytes at 30 h. Developmental differences in chemically activated vs IVF-derived embryos were not related to fertilization failure or gross alterations in cytoskeletal components. Rather, ionomycin-induced calcium release and MAP kinase activity were less in heat-stressed oocytes. While underlying mechanisms are multifactorial, ability to obtain equivalent or higher development after parthenogenetic activation demonstrates that oocytes experiencing heat stress during the first 12 h of meiotic maturation have the necessary components to develop to the blastocyst stage, but fail to do so after fertilization.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Actin Cytoskeleton / metabolism
  • Adenine / analogs & derivatives
  • Adenine / pharmacology
  • Aging / physiology
  • Animals
  • Calcium / metabolism
  • Calcium Ionophores / pharmacology
  • Cattle
  • Embryonic Development* / drug effects
  • Female
  • Fertilization
  • Fertilization in Vitro*
  • Hot Temperature*
  • Ionomycin / pharmacology
  • Maturation-Promoting Factor / metabolism
  • Meiosis
  • Mitogen-Activated Protein Kinases / antagonists & inhibitors
  • Mitogen-Activated Protein Kinases / metabolism
  • Oocytes / drug effects
  • Oocytes / growth & development*
  • Oocytes / metabolism

Substances

  • Calcium Ionophores
  • Ionomycin
  • N(6),N(6)-dimethyladenine
  • Maturation-Promoting Factor
  • Mitogen-Activated Protein Kinases
  • Adenine
  • Calcium