Under both natural and laboratory conditions, female rats in estrus exhibit spontaneous and predictable patterns of sexual contacts with males which appear to regulate or pace the temporal characteristics of copulatory stimuli received. Two consequences of the females' pacing of copulatory stimulation are an abbreviation of the length of the period of estrus and acute increases in serum concentrations of the 5a-reduced androgen, 3a-androstanediol. These data suggest that this androgen, released from the ovary in response to temporally-appropriate coital stimuli, contributes to decreasing sexual responsiveness at the end of estrus. The experiments proposed in this application will define the characteristics of the behavioral stimuli which contribute to estrus abbreviation and 3a-androstanediol release, determine whether increases in circulating 3a-androstanediol play a physiological role in estrus abbreviation, and determine whether increased levels of 3a-androstanediol are a result of pituitary hormone release. These studies will examine the reciprocal relationships between the endocrine system and sexual responsiveness in the female rat -- which relationships may serve to regulate reproductive processes insuring species survival. In addition, these studies will elucidate whether 5a-reduced androgens, known to have strong inhibitory effects on sexual receptivity in ovariectomized hormone-primed rats, play a role under physiological conditions in modulating the display of sexual behavior in the intact female rat.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD021802-03
Application #
3320947
Study Section
Biopsychology Study Section (BPO)
Project Start
1986-08-01
Project End
1989-07-31
Budget Start
1988-08-01
Budget End
1989-07-31
Support Year
3
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Boston University
Department
Type
Schools of Arts and Sciences
DUNS #
604483045
City
Boston
State
MA
Country
United States
Zip Code
02118
Polston, E K; Heitz, M; Barnes, W et al. (2001) NMDA-mediated activation of the medial amygdala initiates a downstream neuroendocrine memory responsible for pseudopregnancy in the female rat. J Neurosci 21:4104-10
Polston, E K; Erskine, M S (2001) Excitotoxic lesions of the medial amygdala differentially disrupt prolactin secretory responses in cycling and mated female rats. J Neuroendocrinol 13:13-21
Lee, J W; Erskine, M S (2000) Changes in pain threshold and lumbar spinal cord immediate-early gene expression induced by paced and nonpaced mating in female rats. Brain Res 861:26-36
Lee, J W; Erskine, M S (2000) Pseudorabies virus tracing of neural pathways between the uterine cervix and CNS: effects of survival time, estrogen treatment, rhizotomy, and pelvic nerve transection. J Comp Neurol 418:484-503
Polston, E K; Centorino, K M; Erskine, M S (1998) Diurnal fluctuations in mating-induced oxytocinergic activity within the paraventricular and supraoptic nuclei do not influence prolactin secretion. Endocrinology 139:4849-59
Erskine, M S; Hanrahan, S B (1997) Effects of paced mating on c-fos gene expression in the female rat brain. J Neuroendocrinol 9:903-12
Frye, C A; McCormick, C M; Coopersmith, C et al. (1996) Effects of paced and non-paced mating stimulation on plasma progesterone, 3 alpha-diol and corticosterone. Psychoneuroendocrinology 21:431-9
Frye, C A; Van Keuren, K R; Erskine, M S (1996) Behavioral effects of 3 alpha-androstanediol. I: Modulation of sexual receptivity and promotion of GABA-stimulated chloride flux. Behav Brain Res 79:109-18
Lee, J W; Erskine, M S (1996) Vaginocervical stimulation suppresses the expression of c-fos induced by mating in thoracic, lumbar and sacral segments of the female rat. Neuroscience 74:237-49
Coopersmith, C; Gans, S E; Rowe, D W et al. (1996) Infusions of lidocaine into the amygdala, but not the preoptic area, block pseudopregnancy in the rat. J Neuroendocrinol 8:259-66

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