期刊
JOURNAL OF NEUROCHEMISTRY
卷 84, 期 6, 页码 1256-1265出版社
BLACKWELL PUBLISHING LTD
DOI: 10.1046/j.1471-4159.2003.01607.x
关键词
DOI binding; in situ hybridization; 5-HT2A mRNA; 5-HT2C mRNA; G(q/11) proteins; hormones
The aim of the present studies was to determine the effects of reduced or absent serotonin (5-HT) transporters (5-HTTs) on 5-HT2A and 5-HT2C receptors. The density of 5-HT2C receptors was significantly increased in the amygdala and choroid plexus of 5-HTT knockout mice. On the other hand, the density of 5-HT2A receptors was significantly increased in the hypothalamus and septum, but reduced in the striatum, of 5-HTT knockout mice. However, 5-HT2A mRNA was not changed in any brain region measured. 5-HT2C mRNA was significantly reduced in the choroid plexus and lateral habenula nucleus of these mice. The function of 5-HT2A receptors was evaluated by hormonal responses to (+/-)-1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane (DOI). Oxytocin, but not adrenocorticotrophic hormone or corticosterone, responses to DOI were significantly greater in 5-HTT knockout mice. In addition, G(q) and G(11) proteins were not significantly changed in any brain region measured. The present results suggest that the constitutive alteration in the function of 5-HTTs changes the density of 5-HT2A and 5-HT2C receptors in a brain region-specific manner. These changes may not be mediated by alterations in their gene expression or in the level of G(q/11) proteins. The alterations in these receptors may be related to the altered behaviors of 5-HTT knockout mice.
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