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下丘脑室旁核对于促食欲的神经肽Y或抑制食欲的黑皮质素作用并非必不可少。

The hypothalamic paraventricular nucleus is not essential for orexigenic NPY or anorexigenic melanocortin action.

作者信息

Dube Michael G, Kalra Satya P, Kalra Pushpa S

机构信息

Department of Physiology and Functional Genomics, McKnight Brain Institute, University of Florida, College of Medicine, P.O. Box 100274, Gainesville, FL 32610-0274, USA.

出版信息

Peptides. 2006 Sep;27(9):2239-48. doi: 10.1016/j.peptides.2006.04.005. Epub 2006 Jun 8.

Abstract

Bilateral electrolytic lesions of the paraventricular nucleus of the hypothalamus (PVN) produce hyperphagia with excess weight gain. The orexigenic neuropeptide Y (NPY) system and the anorexigenic melanocortin system act in the PVN to regulate food intake, and participate in mediating the anorexic effects of leptin. We hypothesized that changes in the responsiveness of these systems may contribute to the hyperphagia observed in PVN-lesioned rats. Adult female Sprague-Dawley rats received either sham or electrolytic lesions in the PVN immediately followed by implantation of a guide cannula into the third cerebroventricle. Twenty-five days following surgery groups of sham and hyperphagic PVN-lesioned rats were injected intracerebroventricularly (i.c.v.) with either 118 pmole or 470 pmole of NPY and food intake was measured for 3 h. Food intake in response to NPY was nearly three-fold higher in PVN-lesioned rats as compared to sham rats. However, the response to 5 microg leptin i.c.v. was not different in lesioned versus sham rats. The effect of the melanocortin agonist MTII on food intake was tested in additional rats beginning either 7-14 days or 30-40 days following surgery. Doses of 0.1 nmole or 1.0 nmole of MTII were injected immediately before lights-off and food intake was measured at 2 h, 24 h and 48 h post-injection. Suppression of food intake in PVN-lesioned rats was not different from that in sham-lesioned rats. These data suggest that hyper-responsiveness to NPY may account in part for the hyperphagia observed in PVN-lesioned rats. Furthermore, based on the similarities of responses of PVN-lesioned and sham control rats to the anorexigenic agents MTII and leptin and the hypersensitivity of lesioned rats to NPY, we conclude that the PVN is not essential for NPY stimulation of food intake or for melanocortin suppression of food intake and that NPY and melanocortin receptors outside of the PVN are sufficient to produce these effects.

摘要

下丘脑室旁核(PVN)的双侧电解损伤会导致食欲亢进并伴有体重过度增加。促食欲神经肽Y(NPY)系统和抑食欲黑皮质素系统在PVN中发挥作用以调节食物摄入,并参与介导瘦素的厌食作用。我们推测这些系统反应性的变化可能导致PVN损伤大鼠出现食欲亢进。成年雌性Sprague-Dawley大鼠接受PVN的假手术或电解损伤,随后立即将引导套管植入第三脑室。术后25天,对假手术组和食欲亢进的PVN损伤大鼠组进行脑室内(i.c.v.)注射118皮摩尔或470皮摩尔的NPY,并测量3小时内的食物摄入量。与假手术大鼠相比,PVN损伤大鼠对NPY的食物摄入量反应高出近三倍。然而,脑室内注射5微克瘦素时,损伤大鼠与假手术大鼠的反应并无差异。在术后7 - 14天或30 - 40天开始,在另外的大鼠中测试黑皮质素激动剂MTII对食物摄入的影响。在熄灯前立即注射0.1纳摩尔或1.0纳摩尔的MTII,并在注射后2小时、24小时和48小时测量食物摄入量。PVN损伤大鼠的食物摄入抑制与假手术损伤大鼠没有差异。这些数据表明,对NPY的高反应性可能部分解释了PVN损伤大鼠中观察到的食欲亢进。此外,基于PVN损伤大鼠和假手术对照大鼠对抑食欲剂MTII和瘦素的反应相似性以及损伤大鼠对NPY的超敏反应,我们得出结论,PVN对于NPY刺激食物摄入或黑皮质素抑制食物摄入并非必不可少,并且PVN之外的NPY和黑皮质素受体足以产生这些作用。

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