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肥胖(fa/fa) Zucker大鼠下丘脑室旁核中神经肽Y分泌增加。

Increased neuropeptide Y secretion in the hypothalamic paraventricular nucleus of obese (fa/fa) Zucker rats.

作者信息

Dryden S, Pickavance L, Frankish H M, Williams G

机构信息

Department of Medicine, University of Liverpool, UK.

出版信息

Brain Res. 1995 Sep 4;690(2):185-8. doi: 10.1016/0006-8993(95)00628-4.

Abstract

NPY is synthesized in the hypothalamic arcuate nucleus (ARC), and NPY injected into the paraventricular nucleus (PVN), the main site of NPY release, induces hyperphagia and reduces energy expenditure. Hypothalamic NPY mRNA and NPY levels are increased in fatty Zucker rats, consistent with increased NPY release. This could explain the hyperphagia and reduced energy expenditure, which lead to obesity in the fatty Zucker rat. We have therefore compared NPY secretion in the PVN of conscious fatty and lean Zucker rats using push-pull sampling. The NPY secretory profile was consistently higher in fatty Zucker rats than in lean rats throughout the 3-h study period (P < 0.01), and mean NPY secretion over the whole 3 h was increased 2-fold in the fatty rats (P < 0.001). We conclude that fatty Zucker rats have increased NPY release in the PVN. This observation further supports the hypothesis that increased activity of the NPYergic ARC-PVN pathway may contribute to obesity in the fatty Zucker syndrome.

摘要

神经肽Y(NPY)在下丘脑弓状核(ARC)合成,将NPY注入神经肽Y释放的主要部位室旁核(PVN)会诱发摄食亢进并减少能量消耗。肥胖型 Zucker 大鼠下丘脑的神经肽Y信使核糖核酸(mRNA)和神经肽Y水平升高,这与神经肽Y释放增加一致。这可以解释肥胖型 Zucker 大鼠的摄食亢进和能量消耗减少,而这会导致肥胖。因此,我们使用推挽式采样法比较了清醒的肥胖型和瘦型 Zucker 大鼠室旁核中的神经肽Y分泌情况。在整个3小时的研究期间,肥胖型 Zucker 大鼠的神经肽Y分泌情况始终高于瘦型大鼠(P < 0.01),肥胖型大鼠在整个3小时内的神经肽Y平均分泌量增加了2倍(P < 0.001)。我们得出结论,肥胖型 Zucker 大鼠室旁核中的神经肽Y释放增加。这一观察结果进一步支持了以下假说:神经肽Y能的弓状核-室旁核通路活性增加可能导致肥胖型 Zucker 综合征中的肥胖。

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