2005
DOI: 10.1016/j.bbr.2005.04.015
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Anxiolytic effect of estradiol in the median raphe nucleus mediated by 5-HT1A receptors

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Cited by 42 publications
(28 citation statements)
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“…For example, the anorectic effects of fenfluramine are enhanced during the estrous phase of the female rat reproductive cycle [23]. Further, there is a precedent in the literature for interactions between the 5-HT 1A receptor and estrogen in measures relevant to moos such as the production of receptive sexual behavior [24] and also antidepressant [25] and anxiolytic [26] effects. In the present experiments sucrose intakes were averaged across the 4-6 day reproductive cycle of mice [17] and thus estrus cycle was not monitored.…”
Section: Discussionmentioning
confidence: 99%
“…For example, the anorectic effects of fenfluramine are enhanced during the estrous phase of the female rat reproductive cycle [23]. Further, there is a precedent in the literature for interactions between the 5-HT 1A receptor and estrogen in measures relevant to moos such as the production of receptive sexual behavior [24] and also antidepressant [25] and anxiolytic [26] effects. In the present experiments sucrose intakes were averaged across the 4-6 day reproductive cycle of mice [17] and thus estrus cycle was not monitored.…”
Section: Discussionmentioning
confidence: 99%
“…Second, although the hippocampus and VMH are logical areas to begin investigating the brain region-and ER subtype-specific effects of E 2 for anxiety, and socio-sexual behavior, it is likely that these are not the only brain regions involved in the behavioral effects observed. For instance, direct E 2 administration to the medial amygdala or median raphe nucleus decreases anxiety and depressive behavior of ovx rats demonstrating that these brain regions are sensitive to E 2 's effects and involved in affective responses (Walf and Frye, 2003;Andrade et al, 2005;Walf and Frye, 2006). Indeed, in the case of the amygdala, ERa and ERb expression varies with reproductive status and mating stimuli (Greco et al, 2003a, b).…”
Section: Discussionmentioning
confidence: 99%
“…The cyclic fluctuations of oestrogens enhance the response to stress, which confers susceptibility to depression and anxiety (Seeman 1997). Shiroma et al (2005) and Andrade et al (2005) supposed that a reduction in E2 could be related to the development or exacerbations of anxiety or depression or other psychic disorders such as schizophrenia (Rao and Kolsch 2003;Huber et al 2004).…”
Section: Discussionmentioning
confidence: 99%