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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Hypothalamic neuronal histamine mediates the thyrotropin-releasing hormone-induced suppression of food intake.
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Hypothalamic neuronal histamine mediates the thyrotropin-releasing hormone-induced suppression of food intake.

机译:下丘脑神经元组胺介导促甲状腺激素释放激素诱导的食物摄取抑制。

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We examined the involvement of thyrotropin-releasing hormone (TRH) and TRH type 1 and 2 receptors (TRH-R1 and TRH-R2, respectively) in the regulation of hypothalamic neuronal histamine. Infusion of 100 nmol TRH into the rat third cerebroventricle (3vt) significantly decreased food intake (p < 0.05) compared to controls infused with phosphate- buffered saline. This TRH-induced suppression of food intake was attenuated partially in histamine-depleted rats pre-treated with alpha-fluoromethylhistidine (a specific suicide inhibitor of histidine decarboxylase) and in mice with targeted disruption of histamine H1 receptors. Infusion of TRH into the 3vt increased histamine turnover as assessed by pargyline-induced accumulation of tele-methylhistamine (t-MH, a major metabolite of neuronal histamine in the brain) in the tuberomammillary nucleus (TMN), the paraventricular nucleus, and the ventromedial hypothalamic nucleus in rats. In addition, TRH-induced decrease of food intake and increase of histamine turnoverwere in a dose-dependent manner. Microinfusion of TRH into the TMN increased t-MH content, histidine decarboxylase (HDC) activity and expression of HDC mRNA in the TMN. Immunohistochemical analysis revealed that TRH-R2, but not TRH-R1, was expressed within the cell bodies of histaminergic neurons in the TMN of rats. These results indicate that hypothalamic neuronal histamine mediates the TRH-induced suppression of feeding behavior.
机译:我们研究了促甲状腺激素释放激素(TRH)和TRH 1型和2型受体(分别为TRH-R1和TRH-R2)在下丘脑神经元组胺的调节中的参与。与注入磷酸盐缓冲盐水的对照组相比,将100 nmol TRH注入大鼠第三脑室(3vt)显着降低了食物摄入(p <0.05)。 TRH诱导的食物摄取抑制在用α-氟甲基组氨酸(组氨酸脱羧酶的特异性自杀抑制剂)预处理的组胺消耗大鼠中和在靶向破坏组胺H1受体的小鼠中得到部分减弱。将TRH注入3vt可提高组胺转化率,这是通过Pargyline诱导的在瘤体乳头核(TMN),脑室旁核和腹膜内的远端甲基组胺(t-MH,是大脑中神经元组胺的主要代谢产物)积累而评估的大鼠下丘脑核。此外,TRH诱导的食物摄入减少和组胺周转的增加呈剂量依赖性。将TRH微注入TMN可提高t-MH含量,组氨酸脱羧酶(HDC)活性和HDN mRNA在TMN中的表达。免疫组织化学分析显示,TRH-R2而非TRH-R1在大鼠TMN的组胺能神经元细胞体内表达。这些结果表明下丘脑神经元组胺介导TRH诱导的摄食行为抑制。

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