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迷走神经刺激可降低大鼠的体重和脂肪量。

Vagus nerve stimulation reduces body weight and fat mass in rats.

机构信息

Department of Biomedical Sciences, University of Cagliari, Cagliari, Italy.

出版信息

PLoS One. 2012;7(9):e44813. doi: 10.1371/journal.pone.0044813. Epub 2012 Sep 28.

Abstract

Among the manifold effects of vagus nerve stimulation (VNS) delivered as an add-on treatment to patients with drug-resistant epilepsy, a moderate loss of body weight has been observed in some individuals. We have now investigated this effect in rats. Exposure of rats to VNS for 4 weeks reduced feed conversion efficiency as well as body weight gain (by ∼25%) and the amount of mesenteric adipose tissue (by ∼45%) in comparison with those in sham-operated control animals. A pair-fed experiment showed that both lower dietary intake and increase energy expenditure independently contributed to the reduction of body weight and mesenteric adipose tissue. Moreover, VNS increased the level of non-esterified fatty acids in plasma and mesenteric adipose tissue by ∼50 and 80%, respectively, without affecting that in the liver. In addition, VNS reduced the amounts of endocannabinoids and increased N-palmitoylethanolamide, an endogenous ligand of the transcription factor PPARα (peroxisome proliferator-activated receptor α) in mesenteric adipose tissue but not in the hypothalamus. These effects were accompanied by increased expression of the gene for brain-derived neurotrophic factor (BDNF) in the hypothalamus and up-regulation of the abundance of PPARα in the liver. Our results suggest that the reduction in body fat induced by VNS in rats may result from the action of both central and peripheral mediators. The reduced feed conversion efficiency associated with VNS may be mediated by hypothalamic BDNF, down-regulation of endocannabinoid tone in mesenteric adipose tissue and a PPARα-dependent increase in fatty acid oxidation in the liver, which in concerted action may account for the anorexic effect and increased energy expenditure.

摘要

在迷走神经刺激(VNS)作为附加治疗用于耐药性癫痫患者的众多影响中,一些人观察到体重适度减轻。我们现在已经在大鼠中研究了这种影响。与假手术对照动物相比,大鼠暴露于 VNS 4 周会降低饲料转化率效率以及体重增加(约 25%)和肠系膜脂肪组织量(约 45%)。配对喂养实验表明,较低的饮食摄入量和增加能量消耗都独立导致体重和肠系膜脂肪组织减少。此外,VNS 使血浆和肠系膜脂肪组织中非酯化脂肪酸水平分别增加了约 50%和 80%,而对肝脏没有影响。此外,VNS 降低了内源性大麻素的含量,并增加了 N-棕榈酰乙醇酰胺(转录因子 PPARα(过氧化物酶体增殖物激活受体 α)的内源性配体)在肠系膜脂肪组织中的含量,但在下丘脑没有影响。这些作用伴随着脑源性神经营养因子(BDNF)基因在下丘脑的表达增加和肝脏中 PPARα丰度的上调。我们的结果表明,VNS 在大鼠中引起的体脂肪减少可能是由中枢和外周介质共同作用的结果。与 VNS 相关的饲料转化率效率降低可能是由下丘脑 BDNF、肠系膜脂肪组织中内源性大麻素张力的下调以及 PPARα依赖性脂肪酸氧化增加介导的,这些协同作用可能解释了厌食作用和能量消耗增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4510/3460935/1136e082f4ab/pone.0044813.g001.jpg

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