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肠抑素注入大鼠第三脑室后可抑制食物摄入。

Enterostatin suppresses food intake following injection into the third ventricle of rats.

作者信息

Shargill N S, Tsujii S, Bray G A, Erlanson-Albertsson C

机构信息

Department of Medicine, University of Southern California, Los Angeles.

出版信息

Brain Res. 1991 Mar 22;544(1):137-40. doi: 10.1016/0006-8993(91)90895-3.

Abstract

The effect on food intake of an activation peptide from pancreatic pro-colipase, called enterostatin, has been studied after parenteral or third ventricular administration. The activation peptide (enterostatin = Val-Pro-Asp-Pro-Arg = VPDPR) reduced food intake when given intraperitoneally. Low doses of this peptide also reduced food intake when given into the third ventricle, but high doses were ineffective. Enterostatin did not modify the stimulatory effects on food intake of clonidine, an alpha 2-adrenergic agonist, suggesting that its anorectic effects are not mediated via the alpha 2-adrenergic system. These data suggest that enterostatin, an activation peptide from pro-colipase, may play a role in producing satiety.

摘要

一种源自胰蛋白酶原前体的激活肽——肠抑胃素,经肠胃外给药或第三脑室给药后,其对食物摄取的影响已得到研究。该激活肽(肠抑胃素=缬氨酸-脯氨酸-天冬氨酸-脯氨酸-精氨酸=VPDPR)经腹腔注射时可减少食物摄取量。低剂量的该肽经第三脑室给药时也可减少食物摄取量,但高剂量则无效。肠抑胃素不会改变α2-肾上腺素能激动剂可乐定对食物摄取的刺激作用,这表明其厌食作用并非通过α2-肾上腺素能系统介导。这些数据表明,源自胰蛋白酶原前体的激活肽肠抑胃素可能在产生饱腹感方面发挥作用。

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