首页> 美国卫生研究院文献>American Journal of Physiology - Regulatory Integrative and Comparative Physiology >Orexin-A enhances feeding in male rats by activating hindbrain catecholamine neurons
【2h】

Orexin-A enhances feeding in male rats by activating hindbrain catecholamine neurons

机译:Orexin-A通过激活后脑儿茶酚胺神经元来增强雄性大鼠的进食

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

Both lateral hypothalamic orexinergic neurons and hindbrain catecholaminergic neurons contribute to control of feeding behavior. Orexin fibers and terminals are present in close proximity to hindbrain catecholaminergic neurons, and fourth ventricular (4V) orexin injections that increase food intake also increase c-Fos expression in hindbrain catecholamine neurons, suggesting that orexin neurons may stimulate feeding by activating catecholamine neurons. Here we examine that hypothesis in more detail. We found that 4V injection of orexin-A (0.5 nmol/rat) produced widespread activation of c-Fos in hindbrain catecholamine cell groups. In the A1 and C1 cell groups in the ventrolateral medulla, where most c-Fos-positive neurons were also dopamine β hydroxylase (DBH) positive, direct injections of a lower dose (67 pmol/200 nl) of orexin-A also increased food intake in intact rats. Then, with the use of the retrogradely transported immunotoxin, anti-DBH conjugated to saporin (DSAP), which targets and destroys DBH-expressing catecholamine neurons, we examined the hypothesis that catecholamine neurons are required for orexin-induced feeding. Rats given paraventricular hypothalamic injections of DSAP, or unconjugated saporin (SAP) as control, were implanted with 4V or lateral ventricular (LV) cannulas and tested for feeding in response to ventricular injection of orexin-A (0.5 nmol/rat). Both LV and 4V orexin-A stimulated feeding in SAP controls, but DSAP abolished these responses. These results reveal for the first time that catecholamine neurons are required for feeding induced by injection of orexin-A into either LV or 4V.
机译:下丘脑外侧食欲神经元神经元和后脑儿茶酚胺能神经元都有助于控制进食行为。食欲素纤维和末端紧邻后脑儿茶酚胺能神经元,第四次进食(4V)食欲素注射剂增加食物摄入量也会增加后脑儿茶酚胺神经元的c-Fos表达,这表明食欲素神经元可以通过激活儿茶酚胺神经元来刺激进食。在这里,我们更详细地检查该假设。我们发现4V注射的orexin-A(0.5 nmol /大鼠)在后脑儿茶酚胺细胞群中产生了广泛的c-Fos活化。在腹侧延髓的A1和C1细胞组中,大多数c-Fos阳性神经元也是多巴胺β羟化酶(DBH)阳性,直接注射较低剂量(67 pmol / 200 nl)的orexin-A也增加了食物完整大鼠的摄入量。然后,通过使用逆向转运的免疫毒素(抗-DBH缀合到saporin(DSAP)上)来靶向并破坏表达DBH的儿茶酚胺神经元,我们检验了儿茶酚胺神经元是食欲素诱导的喂养所必需的假设。给予DSAP的脑室下丘脑旁注射或未结合的saporin(SAP)作为对照的大鼠植入4V或外侧心室(LV)套管,并测试对心室注射orexin-A的反应(0.5 nmol /大鼠)。 LV和4V orexin-A均可刺激SAP对照的进食,但DSAP消除了这些反应。这些结果首次揭示了儿茶酚胺神经元是通过将orexin-A注入LV或4V诱导诱导进食所必需的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号