The augmentation of pituitary adenylate cyclase-activating polypeptide (PACAP) in streptozotocin-induced diabetic rats

被引:17
作者
Tamakawa, H
Miyata, A
Satoh, K
Miyake, Y
Matsuo, H
Arimura, A
Kangawa, K
机构
[1] Natl Cardiovasc Ctr, Res Inst, Dept Biochem, Suita, Osaka 565, Japan
[2] Natl Cardiovasc Ctr, Inst Biofunct Res Ltd, Suita, Osaka 565, Japan
[3] Tulane Univ, Hebert Ctr, US Japan Biomed Res Labs, Belle Chasse, LA 70037 USA
基金
日本科学技术振兴机构;
关键词
PACAP; streptozotocin; diabetic rat; RIA; PACAP/VIP receptor; RT-PCR;
D O I
10.1016/S0196-9781(98)00107-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pituitary adenylate cyclase activating polypeptide (PACAP), which was isolated from ovine hypothalamic extract, has been shown to have a physiological role in the regulation of insulin or islet functions. In streptozotocin (STZ)-induced diabetic rats, we examined the content of PACAP immunoreactivity and gene expression of three specific receptors. Four weeks after administration of STZ (50 mg/kg), plasma glucose levels increased 3.3-fold, and plasma insulin levels decreased to one-tenth as compared with the control. The content of PACAP immunoreactivity in the pancreas potently increased by 30%, but the content of vasoactive intestinal polypeptide (VIP) immunoreactivity was not changed. In the other tissues, the content of PACAP immunoreactivity did not significantly change except in the hypothalamus, which showed a 10% increment. In the expression level of PACAP/VIP receptors, semi-quantitative RT-PCR analysis revealed that VIP1/PACAP receptor mRNA significantly increased as compared with the other two types of receptors in the pancreas of STZ-induced diabetic rats. These findings suggest that PACAP and VIP1/PACAP receptor might be involved in the pathophysiology of diabetes mellitus, (C) 1998 Elsevier Science Inc.
引用
收藏
页码:1497 / 1502
页数:6
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