EFFECT OF NITRIC-OXIDE ON THE COLONIC SMOOTH-MUSCLE OF PATIENTS WITH HIRSCHSPRUNGS-DISEASE

被引:13
作者
BEALER, JF
NATUZZI, ES
FLAKE, AW
ADZICK, NS
HARRISON, MR
机构
[1] The Fetal Treatment Center, Department of Surgery, University of California, San Francisco, CA
关键词
HIRSCHSPRUNGS DISEASE; NONADRENERGIC NONCHOLINERGIC NERVES; NITRIC OXIDE; S-NITROSO-N-ACETYLPENICILLAMINE;
D O I
10.1016/0022-3468(94)90272-0
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Hirschsprung's disease results in bowel obstruction because of a failure of smooth muscle relaxation in both the aganglionic segment of bowel and the internal anal sphincter (IAS). Nonadrenergic noncholinergic (NANC) nerves, which use nitric oxide (NO) as their chemical messenger, are responsible for relaxing smooth muscle in normal bowel and the IAS. Previous work indicates that the cause of the aganglionic colon's inability to relax may be a lack of NANC nerves. To test this hypothesis, the authors compared the effect of an exogenous source of NO, S-nitroso-N-acetylpenicillamine (SNAP), on the isometric tension of smooth muscle strips taken from the ganglionic colon, aganglionic colon, and IAS of patients with Hirschsprung's disease. Exposure of ganglionic and aganglionic colon specimens to SNAP (10-3 to 10-5 mol/L) resulted in up to 70% reduction of resting tension. This relaxation occurred in a dose-dependent fashion and could be promptly reversed by the addition of the NO antagonist methylene blue. However, SNAP had no demonstrable effect on the smooth muscle strips taken from the IAS of patients with Hirschsprung's disease. This finding suggests that, in the aganglionic colon, a deficiency of NANC nerves contributes to the development of bowel obstruction. However, the failure of the IAS to relax in Hirschsprung's disease appears to be unrelated to NO and the NANC nervous system. © 1994.
引用
收藏
页码:1025 / 1029
页数:5
相关论文
共 29 条
[1]  
BEALER JF, 1994, PEDIATRICS, V93, P647
[2]   NG-NITRO-L-ARGININE REDUCES NONADRENERGIC, NONCHOLINERGIC RELAXATIONS OF HUMAN GUT [J].
BURLEIGH, DE .
GASTROENTEROLOGY, 1992, 102 (02) :679-683
[3]   NITRIC-OXIDE SYNTHASE FROM CEREBELLUM CATALYZES THE FORMATION OF EQUIMOLAR QUANTITIES OF NITRIC-OXIDE AND CITRULLINE FROM L-ARGININE [J].
BUSH, PA ;
GONZALEZ, NE ;
GRISCAVAGE, JM ;
IGNARRO, LJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 185 (03) :960-966
[4]   RELEASE OF NITRIC-OXIDE BY ACTIVATION OF NONADRENERGIC NONCHOLINERGIC NEURONS OF INTERNAL ANAL-SPHINCTER [J].
CHAKDER, S ;
RATTAN, S .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (01) :G7-G12
[5]   RELEASE AND PROPERTIES OF ENDOTHELIUM-DERIVED RELAXING FACTOR (EDRF) FROM ENDOTHELIAL-CELLS IN CULTURE [J].
COCKS, TM ;
ANGUS, JA ;
CAMPBELL, JH ;
CAMPBELL, GR .
JOURNAL OF CELLULAR PHYSIOLOGY, 1985, 123 (03) :310-320
[6]  
CRAVEN PA, 1978, J BIOL CHEM, V253, P8433
[7]   ISOFORMS OF NITRIC-OXIDE SYNTHASE - CHARACTERIZATION AND PURIFICATION FROM DIFFERENT CELL-TYPES [J].
FORSTERMANN, U ;
SCHMIDT, HHHW ;
POLLOCK, JS ;
SHENG, H ;
MITCHELL, JA ;
WARNER, TD ;
NAKANE, M ;
MURAD, F .
BIOCHEMICAL PHARMACOLOGY, 1991, 42 (10) :1849-1857
[8]   REDUCED TISSUE CONTENT OF VASOACTIVE INTESTINAL PEPTIDE IN AGANGLIONIC COLON OF HIRSCHSPRUNGS-DISEASE [J].
FREUND, HR ;
HUMPHREY, CS ;
FISCHER, JE .
AMERICAN JOURNAL OF SURGERY, 1981, 141 (02) :243-244
[9]   SOME OBSERVATIONS ON INTRINSIC NERVOUS MECHANISM IN HIRSCHSPRUNGS DISEASE [J].
FRIGO, GM ;
DELTACCA, M ;
LECCHINI, S ;
CREMA, A .
GUT, 1973, 14 (01) :35-40
[10]   THE NATURE OF ENDOTHELIUM-DERIVED VASCULAR RELAXANT FACTOR [J].
GRIFFITH, TM ;
EDWARDS, DH ;
LEWIS, MJ ;
NEWBY, AC ;
HENDERSON, AH .
NATURE, 1984, 308 (5960) :645-647