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在ob/ob小鼠中,KiSS-1神经元是瘦素的直接作用靶点。

KiSS-1 neurones are direct targets for leptin in the ob/ob mouse.

作者信息

Smith J T, Acohido B V, Clifton D K, Steiner R A

机构信息

Department of Physiology and Biophysics, School of Medicine, University of Washington, Seattle, 98195-7290, USA.

出版信息

J Neuroendocrinol. 2006 Apr;18(4):298-303. doi: 10.1111/j.1365-2826.2006.01417.x.

Abstract

Leptin is an adipocyte-derived hormone that acts on the hypothalamus to influence feeding, metabolism and reproduction, but the cellular and molecular targets for the action of leptin in the brain have yet to be fully elucidated. Kisspeptins are encoded by the Kiss1 gene, which is expressed in the hypothalamus and has been implicated in the neuroendocrine regulation of gonadotrophin-releasing hormone secretion. We tested the hypothesis that kisspeptin-expressing neurones are targets for leptin. First, we examined whether leptin regulates the expression of Kiss1 by comparing levels of KiSS-1 mRNA in the arcuate nucleus among groups of mice having different circulating levels of leptin: (i) wild-type (WT); (ii) leptin-deficient ob/ob; and (iii) ob/ob mice treated with leptin. All mice were castrated to control for endogenous concentrations of gonadal steroids. KiSS-1 mRNA was significantly reduced in ob/ob compared to WT mice and levels of KiSS-1 mRNA in ob/ob mice treated with leptin were increased, but not fully restored to that found in WT animals. Second, we performed double-label in situ hybridisation for KiSS-1 mRNA and the leptin receptor (Ob-Rb) mRNA and found that almost one-half (approximately 40%) of KiSS-1 mRNA-expressing cells in the arcuate nucleus expressed Ob-Rb mRNA. These results demonstrate that KiSS-1 neurones are direct targets for regulation by leptin and suggest that the reproductive deficits associated with leptin-deficient states may be attributable, in part, to diminished expression of Kiss1.

摘要

瘦素是一种由脂肪细胞分泌的激素,作用于下丘脑以影响进食、新陈代谢和生殖,但瘦素在大脑中的细胞和分子作用靶点尚未完全阐明。亲吻素由Kiss1基因编码,该基因在下丘脑中表达,并参与促性腺激素释放激素分泌的神经内分泌调节。我们检验了表达亲吻素的神经元是瘦素作用靶点这一假说。首先,我们通过比较不同循环瘦素水平小鼠组(i)野生型(WT);(ii)瘦素缺乏的ob/ob小鼠;(iii)用瘦素治疗的ob/ob小鼠弓状核中KiSS-1 mRNA水平,来研究瘦素是否调节Kiss1的表达。所有小鼠均被阉割以控制内源性性腺类固醇浓度。与WT小鼠相比,ob/ob小鼠中KiSS-1 mRNA显著降低,用瘦素治疗的ob/ob小鼠中KiSS-1 mRNA水平升高,但未完全恢复到WT动物中的水平。其次,我们对KiSS-1 mRNA和瘦素受体(Ob-Rb)mRNA进行了双标记原位杂交,发现弓状核中几乎一半(约40%)表达KiSS-1 mRNA的细胞也表达Ob-Rb mRNA。这些结果表明,KiSS-1神经元是瘦素调节的直接靶点,并提示与瘦素缺乏状态相关的生殖缺陷可能部分归因于Kiss1表达的减少。

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