Hormone-dependence of sarin lethality in rats: Sex differences and stage of the estrous cycle

Carl D Smith1, Linnzi K M Wright1, Gregory E Garcia1

  • 1US Army Medical Research Institute of Chemical Defense (USAMRICD), Aberdeen Proving Ground, MD 21010, United States.

Insights

Female rats' sensitivity to lethal chemical warfare nerve agents (CWNAs) like sarin varies with their hormonal cycle. Proestrus females showed higher sarin LD50, suggesting cycle stage impacts toxicity studies.

Area of Science:

  • Toxicology
  • Neuroscience
  • Endocrinology

Background:

  • Chemical warfare nerve agents (CWNAs) pose significant health risks, with rodent models crucial for research.
  • Most CWNA toxicity studies exclude females or fail to account for hormonal cycle variations.
  • Gonadal hormones in females may influence sensitivity to CWNA lethality.

Purpose of the Study:

  • To determine the median lethal dose (LD50) of sarin in male, ovariectomized (OVEX) female, and cycling female rats.
  • To assess baseline plasma esterase activity across different groups.
  • To investigate the impact of the estrous cycle on sarin toxicity.

Main Methods:

  • Determined 24-hour LD50 of sarin in male, OVEX female, and female rats at diestrus, proestrus, and estrus.
  • Measured plasma acetylcholinesterase, butyrylcholinesterase, and carboxylesterase activity.
  • Compared LD50 values and esterase activity across experimental groups.

Main Results:

  • Females in proestrus exhibited a significantly higher sarin LD50 compared to OVEX and estrous females.
  • Observed sex differences in plasma esterase activity were inconsistent and unlikely to significantly impact LD50.
  • Hormonal cyclicity in female rodents influences sarin toxicity outcomes.

Conclusions:

  • Female rodent sensitivity to sarin is modulated by the estrous cycle stage.
  • Controlling for the hormonal cycle is essential for minimizing variability in CWNA toxicity studies.
  • Further research is needed to elucidate the mechanisms underlying these hormonal influences on CWNA toxicity, beyond plasma esterase activity.