5-Hydroxytryptamine Generates Tonic Inward Currents on Pacemaker Activity of Interstitial Cells of Cajal from Mouse Small Intestine
Author(s) -
Pawan K. Shahi,
Seok Choi,
Dong Chuan Zuo,
Cheol Ho Yeum,
Pyung Jin Yoon,
Jun Lee,
Young Dae Kim,
Chan Guk Park,
Man Yoo Kim,
Hye Rang Shin,
Hyun Jung Oh,
Jae Yeoul Jun
Publication year - 2011
Publication title -
korean journal of physiology and pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.514
H-Index - 29
eISSN - 2093-3827
pISSN - 1226-4512
DOI - 10.4196/kjpp.2011.15.3.129
Subject(s) - interstitial cell of cajal , antagonist , tonic (physiology) , receptor , pacemaker potential , 5 ht receptor , receptor antagonist , chemistry , serotonin , medicine , endocrinology , small intestine , pharmacology , biology , electrophysiology , smooth muscle
In this study we determined whether or not 5-hydroxytryptamine (5-HT) has an effect on the pacemaker activities of interstitial cells of Cajal (ICC) from the mouse small intestine. The actions of 5-HT on pacemaker activities were investigated using a whole-cell patch-clamp technique, intracellular Ca(2+) ([Ca(2+)](i)) analysis, and RT-PCR in ICC. Exogenously-treated 5-HT showed tonic inward currents on pacemaker currents in ICC under the voltage-clamp mode in a dose-dependent manner. Based on RT-PCR results, we found the existence of 5-HT(2B, 3, 4, and 7) receptors in ICC. However, SDZ 205557 (a 5-HT(4) receptor antagonist), SB 269970 (a 5-HT7 receptor antagonist), 3-tropanylindole - 3 - carboxylate methiodide (3-TCM; a 5-HT(3) antagonist) blocked the 5-HT-induced action on pacemaker activity, but not SB 204741 (a 5-HT(2B) receptor antagonist). Based on [Ca(2+)](i) analysis, we found that 5-HT increased the intensity of [Ca(2+)](i). The treatment of PD 98059 or JNK II inhibitor blocked the 5-HT-induced action on pacemaker activity of ICC, but not SB 203580. In summary, these results suggest that 5-HT can modulate pacemaker activity through 5-HT(3, 4, and 7) receptors via [Ca(2+)](i) mobilization and regulation of mitogen-activated protein kinases.
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