Nitric oxide stimulates prostaglandin synthesis in cultured rabbit gastric cells

被引:33
作者
Uno, H [1 ]
Arakawa, T [1 ]
Fukuda, T [1 ]
Yu, H [1 ]
Fujiwara, Y [1 ]
Higuchi, K [1 ]
Inoue, M [1 ]
Kobayashi, K [1 ]
机构
[1] OSAKA CITY UNIV,SCH MED,DEPT BIOCHEM 1,ABENO KU,OSAKA 545,JAPAN
来源
PROSTAGLANDINS | 1997年 / 53卷 / 03期
关键词
nitric oxide; prostaglandin; cultured rabbit gastric cell;
D O I
10.1016/S0090-6980(97)00013-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Both prostaglandins (PGs) and nitric oxide (NO) have cytoprotective and hyperemic effects in the stomach. However, the effect of NO on PG synthesis in gastric mucosal cells is unclear. We examined whether sodium nitroprusside (SNP), a releaser of NO, stimulates PG synthesis in cultured rabbit gastric mucus-producing cells. These cells did not release NO themselves. Co-incubation with SNP (2 x 10(-4), 5 x 10(-4), 10(-3) M) increased PGE(2) synthesis, and SNP (10(-3) M) increased PGI(2) synthesis in these cells. Hemoglobin, a scavenger of NO, (10(-5) M) eliminated the increase in PGE(2) synthesis by SNP, but methylene blue, an inhibitor of soluble guanylate cyclase, (5 x 10(-5) M) did not affect the increase in PGE(2) synthesis by SNP. 8-bromo guanosine 3':5'-cyclic monophosphate (8-bromo cGMP), a cGMP analogue, (10(-6), 10(-5), 10(-4), 10(-3) M) did not affect PGE(2) synthesis. These findings suggest that MO increased PGE(2) and PGI(2) synthesis via a cGMP-independent pathway in cultured rabbit gastric cells. (C) 1997 by Elsevier Science Inc.
引用
收藏
页码:153 / 162
页数:10
相关论文
共 29 条
[1]   NONSTEROIDAL ANTIINFLAMMATORY DRUGS INHIBIT EXPRESSION OF THE INDUCIBLE NITRIC-OXIDE SYNTHASE GENE [J].
AEBERHARD, EE ;
HENDERSON, SA ;
ARABOLOS, NS ;
GRISCAVAGE, JM ;
CASTRO, FE ;
BARRETT, CT ;
IGNARRO, LJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 208 (03) :1053-1059
[2]   INVITRO ADAPTIVE CYTOPROTECTION IN GASTRIC CELLS ISOLATED FROM RAT STOMACH [J].
ARAKAWA, T ;
NAKAMURA, A ;
FUKUDA, T ;
HIGUCHI, K ;
NAKAMURA, H ;
KOBAYASHI, K .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 1990, 12 :S32-S38
[3]   ABSENCE OF EFFECT OF 16,16-DIMETHYL PROSTAGLANDIN-E2 ON REDUCTION OF GASTRIC-MUCOSAL BLOOD-FLOW CAUSED BY INDOMETHACIN IN RATS [J].
ARAKAWA, T ;
NAKAMURA, H ;
CHONO, S ;
SATOH, H ;
FUKUDA, T ;
SAEKI, Y ;
KOBAYASHI, K .
DIGESTIVE DISEASES AND SCIENCES, 1989, 34 (09) :1369-1373
[4]   NITRIC-OXIDE GENERATORS AND CGMP STIMULATE MUCUS SECRETION BY RAT GASTRIC-MUCOSAL CELLS [J].
BROWN, JF ;
KEATES, AC ;
HANSON, PJ ;
WHITTLE, BJR .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (03) :G418-G422
[5]   DIFFERENTIAL DISTRIBUTION OF NITRIC-OXIDE SYNTHASE BETWEEN CELL-FRACTIONS ISOLATED FROM THE RAT GASTRIC-MUCOSA [J].
BROWN, JF ;
TEPPERMAN, BL ;
HANSON, PJ ;
WHITTLE, BJR ;
MONCADA, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 184 (02) :680-685
[6]   INVOLVEMENT OF NITRIC-OXIDE IN THE REFLEX RELAXATION OF THE STOMACH TO ACCOMMODATE FOOD OR FLUID [J].
DESAI, KM ;
SESSA, WC ;
VANE, JR .
NATURE, 1991, 351 (6326) :477-479
[7]   ROLE OF NITRIC-OXIDE IN EICOSANOID SYNTHESIS AND UTERINE MOTILITY IN ESTROGEN-TREATED RAT UTERI [J].
FRANCHI, AM ;
CHAUD, M ;
RETTORI, V ;
SUBURO, A ;
MCCANN, SM ;
GIMENO, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (02) :539-543
[8]   ANALYSIS OF NITRATE, NITRITE, AND [N-15]-LABELED NITRATE IN BIOLOGICAL-FLUIDS [J].
GREEN, LC ;
WAGNER, DA ;
GLOGOWSKI, J ;
SKIPPER, PL ;
WISHNOK, JS ;
TANNENBAUM, SR .
ANALYTICAL BIOCHEMISTRY, 1982, 126 (01) :131-138
[9]   NITRIC-OXIDE ENHANCES PROSTAGLANDIN-H SYNTHASE-1 ACTIVITY BY A HEME-INDEPENDENT MECHANISM - EVIDENCE IMPLICATING NITROSOTHIOLS [J].
HAJJAR, DP ;
LANDER, HM ;
PEARCE, SFA ;
UPMACIS, RK ;
POMERANTZ, KB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (12) :3340-3346
[10]   SIGNAL TRANSDUCTION MECHANISMS INVOLVING NITRIC-OXIDE [J].
IGNARRO, LJ .
BIOCHEMICAL PHARMACOLOGY, 1991, 41 (04) :485-490