2004
DOI: 10.1016/j.neures.2004.02.011
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Expression of estrogen receptors (α, β) and androgen receptor in serotonin neurons of the rat and mouse dorsal raphe nuclei; sex and species differences

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Cited by 102 publications
(71 citation statements)
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“…An electrophysiological study revealed that firing activity of the 5-HT neurons in the DRN, but not MRN, was higher in the females than males (48). Additionally, several studies revealed that gonadal steroid hormones such as androgen and estrogen can regulate neural activity in the DRN in a genderspecific manner (66,67). Thus, the region-specific 5-HTergic mechanisms in the neural circuit including the BLA and hippocampus may underlie gender differences in emotional regulation (68,69).…”
Section: Discussionmentioning
confidence: 99%
“…An electrophysiological study revealed that firing activity of the 5-HT neurons in the DRN, but not MRN, was higher in the females than males (48). Additionally, several studies revealed that gonadal steroid hormones such as androgen and estrogen can regulate neural activity in the DRN in a genderspecific manner (66,67). Thus, the region-specific 5-HTergic mechanisms in the neural circuit including the BLA and hippocampus may underlie gender differences in emotional regulation (68,69).…”
Section: Discussionmentioning
confidence: 99%
“…This pattern suggests not only estradiolmediated regulation of hippocampal input and output signaling in the dentate gyrus and subiculum, but also that this regulation is primarily via the ERβ (Östlund et al 2003). ERβ immunoreactivity has been observed in the dorsal raphe nucleus (Mitra et al 2003;Sheng et al 2004). Using in vivo extracellular unitary recordings of rat dorsal raphe nucleus 5-HT neurons, Robichaud and Debonnel (2005) showed that 17β-estradiol, and testosterone, increased the firing activity of 5-HT neurons in both males and females.…”
Section: Discussionmentioning
confidence: 99%
“…Double immunofluorescent staining was performed for co-localization studies. Sections were pre-incubated, bleached (18), and stained with a mixture of antiWfs1n (diluted 1:200) and mouse monoclonal antiinsulin (diluted 1:100; Santa Cruz Biotechnology, Santa Cruz, CA, USA), anti-glucagon (diluted 1:200; Sigma-Aldrich, St Louis, MO, USA), or anti-somatostatin (diluted 1:25; Biomeda Corporation, Foster City, CA, USA) in 0.1 M sodium phosphate buffer containing 0.3% Triton X-100, 0.1% sodium azide, and 3% normal goat serum (PBT-NGS) for 24 h at 20 8C. Next, the sections were incubated with a mixture of two secondary antibodies in PBT-NGS for 24 h at 20 8C.…”
Section: Methodsmentioning
confidence: 99%