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外周给予PYY(3 - 36)会使小鼠产生条件性味觉厌恶。

Peripheral administration of PYY(3-36) produces conditioned taste aversion in mice.

作者信息

Halatchev Ilia G, Cone Roger D

机构信息

Vollum Institute and Center for the Study of Weight Regulation and Associated Disorders, Oregon Health and Science University, 3181 SW Sam Jackson Park Road, Portland, Oregon 97239, USA.

出版信息

Cell Metab. 2005 Mar;1(3):159-68. doi: 10.1016/j.cmet.2005.02.003.

Abstract

Peptide YY (PYY) is a postprandially released gut hormone. Peripheral administration of one form of the peptide PYY3-36 produces a short-term reduction in food intake in rodents. Initial reports suggested that effects of PYY3-36 on food intake are mediated by increasing the anorexigenic drive from melanocortin neurons in the hypothalamic arcuate nucleus. However, more recent data have demonstrated that the anorexigenic activity of PYY3-36 is not dependent on melanocortin ligands or their receptors in the CNS. We demonstrate here that the anorexigenic actions of PYY3-36 are also not dependent on the vagus nerve, a common pathway of satiety signaling. Peripherally administered PYY3-36 activates neurons in the area postrema and nucleus tractus solitarius, brainstem areas known to mediate effects of certain aversive stimuli. Furthermore, peripheral administration of PYY3-36 causes conditioned taste aversion in mice. Thus, inhibition of food intake by PYY3-36 may result in part from induction of an aversive response.

摘要

肽YY(PYY)是一种餐后释放的肠道激素。外周给予一种形式的肽PYY3-36可使啮齿动物的食物摄入量短期内减少。最初的报告表明,PYY3-36对食物摄入的影响是通过增强下丘脑弓状核中黑皮质素神经元的厌食驱动来介导的。然而,最近的数据表明,PYY3-36的厌食活性并不依赖于中枢神经系统中的黑皮质素配体或其受体。我们在此证明,PYY3-36的厌食作用也不依赖于迷走神经,迷走神经是饱腹感信号传导的常见途径。外周给予PYY3-36可激活最后区和孤束核中的神经元,这两个脑干区域已知可介导某些厌恶刺激的作用。此外,外周给予PYY3-36会导致小鼠出现条件性味觉厌恶。因此,PYY3-36对食物摄入的抑制作用可能部分源于厌恶反应的诱导。

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