The role of nitric oxide (NO) in the regulation of acid secretion w'/> Role of nitric oxide in regulation of gastric acid secretion in rats: effects of NO donors and NO synthase inhibitor
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Role of nitric oxide in regulation of gastric acid secretion in rats: effects of NO donors and NO synthase inhibitor

机译:一氧化氮在大鼠胃酸分泌调节中的作用:NO供体和NO合酶抑制剂的作用

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class="enumerated" style="list-style-type:decimal">The role of nitric oxide (NO) in the regulation of acid secretion was examined in the anaesthetized rat.A rat stomach was mounted in an ex vivo chamber, instilled with 2 ml of saline every 15 min, and the recovered sample was titrated at pH 7.0 against 0.1 N NaOH by use of an automatic titrator for acid secretion. Gastric mucosal blood flow (GMBF) was measured simultaneously by laser Doppler flowmeter.Intragastric application of NO donors such as FK409 (3 and 6 mg ml−1) and sodium nitroprusside (SNP; 6 and 12 mg  ml−1) as well as i.p. administration of cimetidine (60 mg kg−1), a histamine H2-receptor antagonist, significantly inhibited the increase in acid secretion in response to pentagastrin (60 μg kg−1 h−1, i.v.), in doses that increased gastric mucosal blood flow (GMBF).Intragastric application of FK409 (6 mg ml−1) increased both basal and stimulated acid secretion induced by YM-14673 (0.3 mg kg−1, i.v.), an analogue of thyrotropin-releasing hormone (TRH), but had no effect on the acid secretory response induced by histamine (4 mg kg−1 h−1, i.v.).Pretreatment with NG-nitro-L-arginine methyl ester (L-NAME; 10 mg kg−1, i.v.) did not affect basal acid secretion, but significantly potentiated the increase in acid secretion induced by YM-14673 and slightly augmented the acid secretory response to pentagastrin.Both pentagastrin and YM-14673 increased the release of nitrite plus nitrate (NOx), stable NO metabolites, into the gastric lumen, and these changes were completely inhibited by prior administration of L-NAME (10 mg kg−1, i.v.).Pentagastrin caused an increase in luminal release of histamine and this response was significantly suppressed by intragastric application of FK409 (6 mg ml−1).These results suggest that either exogenous or endogenous NO has an inhibitory action on gastric acid secretion through suppression of histamine release from enterochromaffin-like (ECL) cells.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 在麻醉的大鼠中检查了一氧化氮(NO)在酸分泌调节中的作用。 将大鼠的胃置于离体腔中,每15分钟注入2 µml生理盐水,然后回收的样品用自动滴定仪在pH = 7.0的条件下用0.1 N NaOH滴定以进行酸分泌。通过激光多普勒流量计同时测量胃粘膜血流量。 在胃内应用NO供体,如FK409(3和6μmgml -1 )和硝普钠( SNP; 6和12 mg ml −1 )以及ip组胺H2受体拮抗剂西咪替丁(60μmgkg -1 )的给药显着抑制了对五肽胃泌素(60μμgkg -1 h的酸分泌的增加) −1 ,iv),以增加胃粘膜血流量(GMBF)的剂量。 在胃内施用FK409(6 mg ml -1 )增加了促甲状腺激素释放激素(TRH)的类似物YM-14673(0.3 mg kg -1 ,iv)诱导的基础和刺激性酸分泌,但对诱导的酸分泌反应没有影响通过组胺(4 mg kg −1 h -1 ,iv)。 用N G -nitro-预处理L-精氨酸甲酯(L-NAME; 10 mg kg -1 ,静脉注射)不影响基础酸分泌,但可显着增强YM-14673诱导的酸分泌增加,并略微增加该酸五肽胃泌素的分泌反应。 五肽胃泌素和YM-14673均可增加亚硝酸盐和硝酸盐(NOx)的释放表NO代谢物进入胃腔,并且这些变化被事先给予L-NAME(10(mg kg −1 ,iv)完全抑制。 pentagastrin引起增加在组胺的腔内释放中,并且在胃内施用FK409(6 mg ml −1 )显着抑制了这种反应。 这些结果表明,外源性或内源性NO均具有抑制作用抑制肠嗜铬细胞样(ECL)细胞释放组胺对胃酸分泌的影响。

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