Effects of muscarinic receptor type 3 knockout on mouse islet secretory responses

被引:32
作者
Zawalich, WS
Zawalich, KC
Tesz, GJ
Taketo, MM
Sterpka, J
Philbrick, W
Matsui, M
机构
[1] Yale Univ, Sch Nursing, New Haven, CT 06536 USA
[2] Kyoto Univ, Grad Sch Med, Sakyo Ku, Kyoto 6068501, Japan
[3] Yale Univ, Sch Med, New Haven, CT 06536 USA
[4] Univ Tokyo, Inst Med Sci, Minato Ku, Tokyo 1088639, Japan
关键词
islets; insulin; secretion; cholinergic;
D O I
10.1016/j.bbrc.2004.01.139
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
The impact of muscarinic type 3 receptor knockout (M3KO) on the cholinergic regulation of insulin secretion and phospholipase C (PLC) activation was determined. Islets isolated from control, wild-type mice or heterozygotes responded with comparable insulin secretory responses to 15 mM glucose. This response was markedly amplified by the inclusion of 10 muM carbachol. While 15 mM glucose-induced release remained similar to wild-type and heterozygote responses in M3KO mice, the stimulatory impact of carbachol was abolished. Stimulation with 15 mM glucose plus 50 muM carbachol increased fractional efflux rates of myo-[2-H-3]inositol from control wild-type and heterozygote islets but not from M3KO islets. Fed plasma insulin levels of M3KO mice were reduced 68% when compared to values obtained from combined wild-type and heterozygote animals. These studies support the conclusion that the M-3 receptor in islets is coupled to PLC activation and insulin secretion and that cholinergic stimulation of the islets may play an important role in the regulation of plasma insulin levels. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:872 / 876
页数:5
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