Role of KCa Channels in SNAP-Induced Relaxation of Aorta from Renal Hypertensive Rats.
- Author:
Seok CHOI
1
;
Hyoung KIM
;
Jae Yeoul JUN
;
Pyung Jin YOON
;
Hyun Lee KIM
;
Jong Hoon CHUNG
;
Cheol Ho YEUM
Author Information
1. Department of Physiology, College of Medicine, Chosun University, Gwangju, Korea. chyum@chosun.ac.kr
- Publication Type:Original Article
- Keywords:
SNAP;
Ca2+-activated K+ channels;
Vasorelaxation;
Renal hypertension
- MeSH:
Animals;
Aorta*;
Aorta, Thoracic;
Cyclic GMP;
Guanylate Cyclase;
Humans;
Hypertension;
Hypertension, Renal;
Methylene Blue;
Muscle, Smooth, Vascular;
Nitric Oxide;
Phenylephrine;
Placebos;
Potassium Channels, Calcium-Activated;
Rats*;
Relaxation*;
Renal Artery;
S-Nitroso-N-Acetylpenicillamine;
Tissue Donors;
Vasodilation
- From:Korean Journal of Nephrology
2007;26(4):398-403
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: S-nitroso-N-acetylpenicillamine (SNAP), a nitric oxide (NO) donor, is thought to relax vascular smooth muscle by stimulation of soluble guanylate cyclase, accumulation of its product cyclic GMP (cGMP) level. Evidence has emerged that NO-induced vasodilatation is also mediated by stimulating Ca2+-activated K+ (KCa) channels directly or indirectly through cGMP. The aim of the present study was to investigate possible involvement or alteration of KCa channels in the mechanism of vasodilation induced by SNAP in two-kidney, one-clip (2K1C) hypertensive rats. METHODS: 2K1C hypertension was made by clipping the left renal artery and age-matched control rats received a sham treatment. Using rings prepared from thoracic aortae, we studied changes in isometric tension of the rings in response to SNAP to evaluate effects of a soluble guanylate cyclase inhibitor methylene blue (MB), and a specific blocker of KCa channel iberiotoxin (ITX). RESULTS: Aortic rings from 2K1C hypertensive and sham-clipped control rats precontracted with phenylephrine showed similar relaxation to SNAP. MB markedly suppressed the SNAP-induced relaxation in both groups, leaving about 30% of MB-resistant relaxation. ITX nearly completely eliminated the MB-resistant relaxation in control rats, but it did not affect 2K1C rats. CONCLUSION: These results suggest that SNAP-induced vasorelaxation is mediated through cGMP- dependent and cGMP-independent KCa channel involving mechanisms, the latter may be altered in 2K1C renal hypertension.
