首页> 外文期刊>Pharmacology, Biochemistry and Behavior >Cortical (3H)ketanserin binding and 5-HT2A receptor-mediated behavioral responses in obese Zucker rats.
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Cortical (3H)ketanserin binding and 5-HT2A receptor-mediated behavioral responses in obese Zucker rats.

机译:肥胖的Zucker大鼠中皮质(3H)酮色林结合和5-HT2A受体介导的行为反应。

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摘要

Past studies have indicated that genetically obese Zucker (fa/fa) rats are hypercorticoid, and that this neuroendocrine alteration plays a key role in the syndrome. In keeping with the proposal that glucocorticoids may upregulate central 5-HT2A receptors, we have studied the effects of acute and repeated 5-HT2A receptor stimulation by 1-(4-iodo-2,5-dimethoxyphenyl)-2-aminopropane (DOI) in lean and obese Zucker rats. Acute injection of DOI (2 mg/kg, SC) elicited a lower number of head shakes in obese rats compared to that measured in lean rats. Conversely, neither DOI-elicited decreases in food intakes and body weights nor cortical [3H]ketanserin binding were affected by obesity. In rats repeatedly pretreated with DOI, biochemical and functional indices of 5-HT2A receptor downregulation failed to reveal an effect of obesity. It is suggested that 5-HT2A receptor-mediated functions, but not their downregulation, may be differentially affected in the hypercorticoid obese Zucker rat.
机译:过去的研究表明,遗传性肥胖的祖克(fa / fa)大鼠是皮质激素,这种神经内分泌改变在该综合征中起关键作用。为了与糖皮质激素可能上调中央5-HT2A受体的提议保持一致,我们研究了1-(4-碘-2,5-二甲氧基苯基)-2-氨基丙烷(DOI)对急性和反复性5-HT2A受体刺激的影响在肥胖的Zucker肥胖大鼠中。与肥胖大鼠相比,肥胖大鼠的DOI急性注射(2 mg / kg,SC)引起的头摇次数更少。相反,肥胖不会影响DOI引起的食物摄入和体重下降,也不影响皮质[3H]酮色林的结合。在多次用DOI预处理的大鼠中,5-HT2A受体下调的生化和功能指标未能显示出肥胖的作用。提示5-HT2A受体介导的功能而不是其下调在高皮质类固醇肥胖Zucker大鼠中可能受到不同的影响。

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