Sodium nitroprusside regulates the relaxation of the longitudinal muscle in the gut

被引:4
作者
Tepavcevic, S. N. [1 ,2 ]
Isenovic, E. R. [1 ,2 ]
Varagic, V. M. [3 ]
Milovanovic, S. R. [4 ]
机构
[1] Inst Vinca, Lab Mol Biol & Endocrinol, Belgrade 11001, Serbia
[2] Inst Vinca, Lab Radiobiol & Mol Genet, Belgrade 11001, Serbia
[3] Inst Biol Res Dr Sinisa Stankovic, Fac Med, Belgrade, Serbia
[4] Fac Med, Foca, Bosnia & Herceg
来源
PHARMAZIE | 2008年 / 63卷 / 02期
关键词
D O I
10.1691/ph.2008.7649
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Nitric oxide (NO) has been shown to mediate nonadrenergic-noncholinergic relaxation in gastrointestinal (GI) smooth muscle cells. As GI smooth muscles relaxations are partly dependent on NO, we decided to investigate the effect of sodium nitroprusside (SNP) on the longitudinal muscle contraction of the isolated guinea pig ileum. Increasing concentrations of SNP (10(-10)M, 10(-9)M, 10(-8)M, 10(-7)M, 10(-6)M and 10(-5)M) reduced ileum contractions stimulated by electrical stimulation (ES) (8-76%; p < 0.05) and by acetylcholine (Ach) (23-62%; p < 0.05) significantly and in a concentration-dependent manner. Furthermore, treatment with an inhibitor of the soluble guanylate cyclase, methylene blue (10 mM), antagonized significantly the relaxing effect of SNP (0-39%; p < 0.05, p < 0.01, p < 0.001 for ES- and 4-27%; p < 0.05 for Ach-induced contractions). The results show that treatment with 1 mu M manganese-containing superoxide dismutase (MnSOD) and 10 mu M L-arginine (L-arg) caused a significant decrease in SNP induced relaxations (6-55%; p < 0.05, p < 0.001 and 2-46%; p < 0.05, p < 0.01 for ES- and 15-28%; p < 0.05, p < 0.01, p < 0.001 and 12-32%; p < 0.05, p < 0.01 for Ach-induced contractions, respectively). In conclusion, our data suggest that SNP, which releases NO, is able to depress longitudinal muscle contraction of the isolated guinea pig ileum, suggesting that exogenous application of NO inhibits intestinal contractions of smooth muscle cells and that cGMP mediates the response to NO. In addition, MnSOD and L-arg decreased the relaxing effect of SNP on the isolated ileum of the guinea pig.
引用
收藏
页码:151 / 155
页数:5
相关论文
共 50 条
[21]   The role of intracellular Ca2+ pool in sodium nitroprusside-induced relaxation of rat aorta smooth muscle cells [J].
I. V. Kovalev ;
M. B. Baskakov ;
L. V. Kapilevich ;
M. A. Medvedev ;
A. A. Panov ;
A. G. Popov .
Bulletin of Experimental Biology and Medicine, 1999, 127 :160-162
[22]   Signaling for contraction and relaxation in smooth muscle of the gut [J].
Murthy, KS .
ANNUAL REVIEW OF PHYSIOLOGY, 2006, 68 :345-374
[23]   SODIUM IN SMOOTH-MUSCLE RELAXATION [J].
MA, TS ;
BOSE, D .
AMERICAN JOURNAL OF PHYSIOLOGY, 1977, 232 (01) :C59-C66
[24]   Nitric oxide and sodium nitroprusside-induced relaxation of the human umbilical artery [J].
Lovren, F ;
Triggle, C .
BRITISH JOURNAL OF PHARMACOLOGY, 2000, 131 (03) :521-529
[25]   A novel mechanism of vascular relaxation induced by sodium nitroprusside in the isolated rat aorta [J].
Bonaventura, Daniella ;
Lunardi, Claure N. ;
Rodrigues, Gerson J. ;
Neto, Mario A. ;
Bendhack, Lusiane M. .
NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2008, 18 (04) :287-295
[26]   EFFECT OF OUABAIN AND ALTERATIONS IN POTASSIUM CONCENTRATION ON RELAXATION INDUCED BY SODIUM-NITROPRUSSIDE [J].
RAPOPORT, RM ;
MURAD, F .
BLOOD VESSELS, 1983, 20 (05) :255-264
[27]   Methylgloxal enhances sodium nitroprusside-induced relaxation in isolated blood vessel [J].
Mukohda, Masashi ;
Yamawaki, Hideyuki ;
Okada, Muneyoshi ;
Hara, Yukio .
JOURNAL OF PHARMACOLOGICAL SCIENCES, 2009, 109 :165P-165P
[28]   INFLUENCE OF HYPOXIA ON SODIUM NITROPRUSSIDE-INDUCED RELAXATION OF ISOLATED RABBIT VESSELS [J].
IWASAKI, S ;
OHASHI, M ;
TAKAYANAGI, I .
JAPANESE JOURNAL OF PHARMACOLOGY, 1987, 43 :P287-P287
[29]   On the outside looking in: longitudinal muscle development in the gut [J].
Young, H. M. .
NEUROGASTROENTEROLOGY AND MOTILITY, 2008, 20 (05) :431-433
[30]   The NO donor sodium nitroprusside: Evaluation of skeletal muscle vascular and metabolic dysfunction [J].
Hirai, Daniel M. ;
Copp, Steven W. ;
Ferguson, Scott K. ;
Holdsworth, Clark T. ;
Musch, Timothy I. ;
Poole, David C. .
MICROVASCULAR RESEARCH, 2013, 85 :104-111