The objective of the study was to investigate the effects of estrogen on se
verity and duration of myoclonus in the rat cardiac arrest model of posthyp
oxic myoclonus. Female sex hormones affect a variety of movement disorders
and alter dopaminergic and serotonergic pharmacology. Although women repres
ented three-fourths of patients from the original report of Lance and Adams
and 80% of the largest published series, the impact of estrogens on myoclo
nus has never been studied. Twelve previously ovariectomized female rats un
derwent 8 minutes of mechanically induced cardiac arrest and were resuscita
ted according to a standardized protocol. On the same day, they were random
ly assigned to subcutaneous treatment with a 21-day, 0.5-mg, 17 beta -estra
diol or matching placebo pellet. Animals were tested daily with 7 sets of 4
5 auditory stimuli for 10 days, and myoclonus scores were obtained using a
5-point interval scale. Comparisons were based on two-sample Wilcoxon rank-
sum tests. Estrogen treatment significantly enhanced myoclonus intensity an
d duration: mean peak myoclonus score, 210.2 +/- 18.0 versus 180 +/- 28.5 (
p = 0.031); mean number of days above baseline, 9.2 +/- 0.4 versus 5.7 +/-
2.3 (p = 0.004); mean score on day 10, 90.7 +/- 38.7 versus 27.0 +/- 20.6 (
p = 0.016). All estrogen-treated animals were above baseline on day 10 comp
ared with none in the placebo group. Estrogen enhances and prolongs posthyp
oxic myoclonus, suggesting that female gender and estrogen status may play
a pivotal role as a risk factor for human posthypoxic myoclonus.