The neuropeptide PACAP contributes to the glucagon response to insulin-induced hypoglycaemia in mice

被引:18
|
作者
Persson, K [1 ]
Ahrén, B [1 ]
机构
[1] Lund Univ, Dept Med, S-22184 Lund, Sweden
来源
ACTA PHYSIOLOGICA SCANDINAVICA | 2002年 / 175卷 / 01期
关键词
glucagon secretion; hypoglycaemia; mice; PACAP;
D O I
10.1046/j.1365-201X.2002.00977.x
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The neuropeptide pituitary adenylate cyclase-activating polypeptide (PACAP) is a neuropeptide in the autonomic nerves innervating the pancreatic islets and previous studies have shown that it stimulates insulin and glucagon secretion. It is known that autonomic nerve activation contributes to the glucagon response to hypoglycaemia, In the present study, we evaluated whether PACAP is involved in this glucagon response by examining the glucagon response to insulin-induced hypoglycaemia in mice genetically deleted of the specific PACAP receptor, the PAC1 receptor, We found that insulin (1 U kg(-1) ip) reduced circulating glucose to a hypoglycaemic level of approximate to2.5 mmol L-1 in PAC1R-/- mice and their wild-type counterparts with no difference between the groups. However, the glucagon response to this hypoglycaemia was markedly impaired in the PAC1R-/- mice, Thus, after 120 min, plasma glucagon was 437+/-79 ng L-1 in wild-type mice vs. only 140+/-36 ng L-1 in PAC1R-/- mice (P=0.004), In contrast, the glucagon response to intravenously administered arginine (0.25 g kg(-1)) was the same in the two groups of mice. We conclude that PACAP through activation of PAC1 receptors contribute to the glucagon response to insulin-induced hypoglycaemia. Therefore, the glucagon response to hypoglycaemia is dependent not only or the classical neurotransmitters but also on the neuropeptide PACAP.
引用
收藏
页码:25 / 28
页数:4
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