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垂体腺苷酸环化酶激活多肽刺激离体灌流大鼠胰腺释放胰岛素。

Pituitary adenylate cyclase activating polypeptide stimulates insulin release from the isolated perfused rat pancreas.

作者信息

Kawai K, Ohse C, Watanabe Y, Suzuki S, Yamashita K, Ohashi S

机构信息

Department of Internal Medicine, University of Tsukuba, Ibaraki-ken, Japan.

出版信息

Life Sci. 1992;50(4):257-61. doi: 10.1016/0024-3205(92)90332-j.

Abstract

Pituitary adenylate cyclase activating polypeptide (PACAP) is a novel hypothalamic peptide structurally related to vasoactive intestinal peptide (VIP) and glucagon like peptide-1(7-36) amide (tGLP-1) in its N-terminal portion. Therefore, their levels of insulinotropic potency were compared using an isolated rat pancreas perfusion. It was found that 0.1 nM PACAP (1-27) amide (PACAP27) significantly stimulated insulin release under a perfusate glucose concentration of 5.5 mM, whereas 1 nM PACAP27 did not under a perfusate glucose concentration of 2.8 mM. The potency was evaluated as tGLP-1 greater than PACAP27 greater than VIP. These results indicate that PACAP is a glucagon superfamily peptide which stimulates insulin release in a glucose dependent manner.

摘要

垂体腺苷酸环化酶激活多肽(PACAP)是一种新型的下丘脑肽,其N端部分在结构上与血管活性肠肽(VIP)和胰高血糖素样肽-1(7-36)酰胺(tGLP-1)相关。因此,使用离体大鼠胰腺灌注比较了它们的促胰岛素分泌能力。结果发现,在灌注液葡萄糖浓度为5.5 mM时,0.1 nM PACAP(1-27)酰胺(PACAP27)能显著刺激胰岛素释放,而在灌注液葡萄糖浓度为2.8 mM时,1 nM PACAP27则不能。其效力评估为tGLP-1大于PACAP27大于VIP。这些结果表明,PACAP是一种以葡萄糖依赖方式刺激胰岛素释放的胰高血糖素超家族肽。

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