Functional interactions between the SK2 channel and the nicotinic acetylcholine receptor in enteric neurons of the guinea pig ileum

被引:10
作者
Nakajima, Hidemitsu
Goto, Hiroto
Azuma, Yasu-Taka
Fujita, Akikazu
Takeuchi, Tadayoshi
机构
[1] Osaka Prefecture Univ, Lab Vet Pharmacol, Grad Sch Life & Environm Sci, Naka Ku, Sakai, Osaka 5998531, Japan
[2] Nagoya Univ, Grad Sch Med, Dept Anat & Mol Cell Biol, Showa Ku, Nagoya, Aichi, Japan
关键词
acetylcholine release; guinea pig ileum; nicotinic acetylcholine receptor; SK2; subunit; small conductance Ca2+-activated K+ channels;
D O I
10.1111/j.1471-4159.2007.04960.x
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 neurotransmitter acetylcholine (ACh) plays a critical role in gastrointestinal function. The role of the small conductance Ca2+-activated K+ (SK) channel in ACh release was examined using myenteric plexus preparations of guinea pig ileum. Apamin, an inhibitor of the SK channel, significantly enhanced nicotine-induced ACh release, but neither electrical field stimulation- nor 5-hydroxytryptamine-induced ACh release, suggesting that SK channels might be selectively involved in the regulation of nicotine-induced ACh release. Therefore, we investigated the distribution of SK2 and SK3 subunits and the interaction between SK2 channels and nicotinic ACh receptors (nAChRs) in the guinea pig ileum. The immunoreactivity of SK2 subunits was located in enteric neuronal cells. Furthermore, SK2-immunoreactive cells stained with an antibody for choline acetyltransferase, a marker for cholinergic neurons, and with an antibody for the alpha 3/5 subunits of nAChR. In contrast, immunoreactivity of SK3 subunits was not found in enteric neurons. A co-immunoprecipitation assay with Triton X-100-soluble membrane fractions prepared from the ileum revealed an association of the SK2 subunit with the alpha 3/5 subunits of nAChR. These results suggest that SK2 channels negatively regulate the excitation of enteric neurons via functional interactions with nAChRs.
引用
收藏
页码:2428 / 2438
页数:11
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