Bipolar Disorder Clinical Trial
Official title:
Chronobiologic Effects of Gonadal Steroid Manipulations in Volunteer Subjects
For many years researchers have been trying to better understand the regulation of sleep and
activity by studying circadian (daily) rhythms of human beings. It appears that the hormones
estrogen, progesterone, and testosterone play a role in the regulation of circadian rhythm
in animals. Researchers believe these hormones may also play a similar role in the
regulation of human circadian rhythms. Little research has been conducted on how these
hormones affect human circadian rhythms.
This study is designed to learn more about how specific hormones influence men and women's
daily rhythms. This study will use women from another research study being conducted at the
NIMH called, "The central nervous system effects of pharmacologically induced
hypogonadotropic hypogonadism with and without estrogen and progesterone". Male subjects
will be recruited from another NIMH study called, "The central nervous system effects of
pharmacologically induced hypogonadotropic hypogonadism with and without testosterone
replacement".
In order to test the possibility that gonadal steroids (estrogen, progesterone, and
testosterone) change circadian rhythms and the sleep-wake cycle in humans, participants will
undergo chronobiologic evaluations. The chronobiologic evaluations will look at sleep and
rest periods, activity as measured by a wrist monitor, and 24 hour inpatient
electroencephalograph (EEG), rectal temperature, and melatonin monitoring.
It is hypothesized that gonadal steroids modulate circadian rhythms and the sleep-wake cycle in humans, as they do in animals. This hypothesis will be tested by performing chronobiologic evaluations on women enrolled in protocol 92-M-0174 ("The central nervous system effects of pharmacologically induced hypogonadotropic hypogonadism with and without estrogen and progesterone") and on men enrolled in protocol 94-M-0037 (The central nervous system effects of pharmacologically induced hypogonadotropic hypogonadism with and without testosterone replacement"). Based on the animal literature, we hypothesize that melatonin and sleep onset will be phase-advanced in women on estrogen, compared with those on progesterone or in a hypogonadal state. We also hypothesize that the amplitude of the activity cycle will be decreased in the progesterone, as compared with the estrogen, condition. Based on findings in amenorrheic women and in those on oral contraceptives, we hypothesize that the amplitude of melatonin secretion will be increased in the hypogonadal state, compared with the other two conditions. Finally, based on literature cited below, we hypothesize that mean prolactin levels will be higher in the testosterone plus Lupron condition and in the estrogen plus Lupron condition than in the other hormonal conditions. ;
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