{"title":"Nitric oxide stimulates prostaglandin synthesis in cultured rabbit gastric cells","authors":"Hironori Uno, Tetsuo Arakawa, Takashi Fukuda, Hidenori Yu, Yasuhiro Fujiwara, Kazuhide Higuchi, Masayasu Inoue , Kenzo Kobayashi","doi":"10.1016/S0090-6980(97)00013-0","DOIUrl":null,"url":null,"abstract":"<div><p>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 × 10<sup>−4</sup>, 5 × 10<sup>−4</sup>, 10<sup>−3</sup> M) increased PGE<sub>2</sub> synthesis, and SNP (10<sup>−3</sup> M) increased PGI<sub>2</sub> synthesis in these cells. Hemoglobin, a scavenger of NO, (10<sup>−5</sup> M) eliminated the increase in PGE<sub>2</sub> synthesis by SNP, but methylene blue, an inhibitor of soluble guanylate cyclase, (5 × 10<sup>−5</sup> M) did not affect the increase in PGE<sub>2</sub> synthesis by SNP. 8-bromo guanosine 3′ : 5′-cyclic monophosphate (8-bromo cGMP), a cGMP analogue, (10<sup>−6</sup>, 10<sup>−5</sup>, 10<sup>−4</sup>, 10<sup>−3</sup> M) did not affect PGE<sub>2</sub> synthesis. These findings suggest that NO increased PGE<sub>2</sub> and PGI<sub>2</sub> synthesis via a cGMP-independent pathway in cultured rabbit gastric cells.</p></div>","PeriodicalId":20653,"journal":{"name":"Prostaglandins","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1997-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0090-6980(97)00013-0","citationCount":"30","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Prostaglandins","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0090698097000130","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 30
Abstract
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 × 10−4, 5 × 10−4, 10−3 M) increased PGE2 synthesis, and SNP (10−3 M) increased PGI2 synthesis in these cells. Hemoglobin, a scavenger of NO, (10−5 M) eliminated the increase in PGE2 synthesis by SNP, but methylene blue, an inhibitor of soluble guanylate cyclase, (5 × 10−5 M) did not affect the increase in PGE2 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 PGE2 synthesis. These findings suggest that NO increased PGE2 and PGI2 synthesis via a cGMP-independent pathway in cultured rabbit gastric cells.