首页> 外文期刊>Peptides: An International Journal >The hypothalamic paraventricular nucleus is not essential for orexigenic NPY or anorexigenic melanocortin action.
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The hypothalamic paraventricular nucleus is not essential for orexigenic NPY or anorexigenic melanocortin action.

机译:下丘脑室旁核对食源性NPY或厌食性黑皮质素作用不是必需的。

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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 inlesioned 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.
机译:下丘脑室旁核(PVN)的双侧电解损伤会导致食欲亢进,体重增加过多。致食性神经肽Y(NPY)系统和致厌性黑皮质素系统在PVN中起调节食物摄入的作用,并参与介导瘦素的厌食作用。我们假设这些系统的反应性的改变可能会导致PVN损伤大鼠的食欲亢进。成年雌性Sprague-Dawley大鼠在PVN中立即接受了假性或电解性损伤,随后将引导套管植入了第三脑室。假手术组和假性高吞噬性PVN损伤的大鼠在手术后第25天向脑室内(i.c.v.)注射118 pmole或470 pmole NPY,并测量食物摄取3 h。与假手术大鼠相比,PVN损伤的老鼠对NPY的食物摄入量几乎高出三倍。但是,对5微克瘦素静脉注射的反应病变大鼠和假大鼠没有什么不同。在手术后7-14天或30-40天开始的另外的大鼠中测试了黑皮质素激动剂MTII对食物摄入的影响。在起燃前立即注射0.1 nmole或1.0 nmole的MTII剂量,并在注射后2 h,24 h和48 h测量食物摄入量。 PVN病变大鼠的食物摄入量的抑制与假手术病变大鼠的食物摄入的抑制率没有差异。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吞咽过多。此外,基于PVN损伤和假对照大鼠对厌食药MTII和瘦素的反应的相似性以及病变大鼠对NPY的超敏性,我们得出结论,PVN对NPY刺激食物摄入或抑制黑皮质素不是必需的食物摄入量的增加以及PVN以外的NPY和黑皮质素受体足以产生这些作用。

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