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Experimental Physiology 90.4 pp 577-586
DOI: 10.1113/expphysiol.2004.029611
© The Physiological Society 2005
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Inhibition of carbachol-evoked oscillatory currents by the NO donor sodium nitroprusside in guinea-pig ileal myocytes

Seung-Soo Chung1, Duck-Sun Ahn1, Hong-Ghi Lee2, Young-Ho Lee12 and Taick-Sang Nam12

1 Department of Physiology, College of Medicine, Yonsei University, Seoul 120-752, Republic of Korea 2 BK 21 Project for Medical Sciences, Yonsei University, Seoul 120-752, Republic of Korea

The effect of sodium nitroprusside (SNP) on carbachol (CCh)-evoked inward cationic current (Icat) oscillations in guinea-pig ileal longitudinal myocytes was investigated using the whole-cell patch-clamp technique and permeabilized longitudinal muscle strips. SNP (10 µM) completely inhibited Icat oscillations evoked by 1 µM CCh. 1H-(1,2,4) Oxadiazole [4,3-a] quinoxaline-1-one (ODQ; 1 µM) almost completely prevented the inhibitory effect of SNP on Icat oscillations. 8-Bromo-guanosine 3',5'-cyclic monophosphate (8-Br-cGMP; 30 µM) in the pipette solution completely abolished Icat oscillations. However, a pipette solution containing Rp-8-Br-cGMP (30 µM) almost completely abolished the inhibitory effect of SNP on Icat oscillations. When the intracellular calcium concentration ([Ca2+]i) was held at a resting level using BAPTA (10 mM) and Ca2+ (4.6 µM) in the pipette solution, CCh (1 µM) evoked only the sustained component of Icat without any oscillations and SNP did not affect the current. A high concentration of inositol 1,4,5-trisphosphate (IP3; 30 µM) in the patch pipette solutions significantly reduced the inhibitory effect of SNP (10 µM) on Icat oscillations. SNP significantly inhibited the Ca2+ release evoked by either CCh or IP3 but not by caffeine in permeabilized preparations of longitudinal muscle strips. These results suggest that the inhibitory effects of SNP on Icat oscillations are mediated, in part, by functional modulation of the IP3 receptor, and not by the inhibition of cationic channels themselves or by muscarinic receptors in the plasma membrane. This inhibition seems to be mediated by an increased cGMP concentration in a protein kinase G-dependent manner.

(Received 9 December 2004; accepted after revision 18 March 2005; first published online 15 April 2005)
Corresponding author T.-S. Nam: Department of Physiology, College of Medicine, Yonsei University 134, Shinchon-Dong, Seodaemun-Gu, Seoul 120-752, Republic of Korea. Email: tsnam{at}yumc.yonsei.ac.kr


Seung-Soo Chung and Duck-Sun Ahn contributed equally to this work.




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