EXTRACELLULAR SEROTONIN IN THE LATERAL HYPOTHALAMIC AREA IS INCREASEDDURING THE POSTEJACULATORY INTERVAL AND IMPAIRS COPULATION IN MALE RATS

Citation
Ds. Lorrain et al., EXTRACELLULAR SEROTONIN IN THE LATERAL HYPOTHALAMIC AREA IS INCREASEDDURING THE POSTEJACULATORY INTERVAL AND IMPAIRS COPULATION IN MALE RATS, The Journal of neuroscience, 17(23), 1997, pp. 9361-9366
Citations number
26
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
02706474
Volume
17
Issue
23
Year of publication
1997
Pages
9361 - 9366
Database
ISI
SICI code
0270-6474(1997)17:23<9361:ESITLH>2.0.ZU;2-7
Abstract
Serotonin (5-HT) is generally inhibitory to masculine sexual behavior, It has been suggested that 5-HT released after ejaculation may promot e the sexual quiescence of the postejaculatory interval (PEI). The fol lowing experiments were conducted to test (1) whether extracellular 5- HT increases in either the anterior lateral hypothalamic area (LHA(A)) or the medial preoptic area (MPOA) of male rats after ejaculation; (2 ) whether increasing 5-HT in these sites, by microinjecting the select ive serotonin reuptake inhibitor alaproclate, could inhibit copulatory abilities; and (3) whether copulation deficits produced by alaproclat e were attributable to locomotor impairments, The effects of local app lication of alaproclate on extracellular 5-HT levels in the LHA(A) and the MPOA were also tested. Extracellular serotonin was measured in al l experiments using in vivo microdialysis. Ejaculation was correlated with enhanced 5-HT release from the LHA(A); no 5-HT increases were obs erved before ejaculation, and levels were decreased toward basal value s during a subsequent copulatory series. Elevating 5-HT in the LHA(A) by microinjecting alaproclate inhibited copulation by increasing the l atency to mount, intromit, and ejaculate, This inhibition did not resu lt from nonspecific locomotor impairments. In the MPOA, 5-HT release r emained stable throughout copulation, and microinjecting alaproclate i nto this site did not significantly alter sexual behavior. These data support the large body of evidence suggesting that 5-HT is inhibitory to masculine sexual behavior. Furthermore, the LHA(A), but not the MPO A, may be one site responsible for serotonergic inhibition of copulati on during the PEI.