Mard Seyyed Ali, Veisi Ali, Ahangarpour Akram, Gharib-Naseri Mohammad Kazem
Physiology Research Center, Research Center for Infectious Diseases of Digestive System, Department of Physiology, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Physiology Research Center, Department of Physiology, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Iran J Basic Med Sci. 2016 Feb;19(2):172-7.
This study was performed to investigate the effects of mucosal acidification on mRNA expression and protein synthesis of cystathionine gamma lyase (CSE), cystathionine beta synthase (CBS), and mucosal release of H2S in gastric mucosa in rats.
Thirty-two rats were randomly assigned into 4 groups (8 in each), including: the control group, HCl (10 mM) treated group, HCl (100 mM) treated group, and one group to study the effect of Nω-Nitro-L-arginine methyl ester hydrochloride (L-NAME). Anesthetized rats underwent tracheostomy and midline laparotomy. Ninety min after the instillation of neutral or acidic solutions, animals were sacrificed and the gastric mucosa was collected to measure the H2S concentration by ELISA method and to quantify mRNA expression of CSE and CBS by quantitative real-time PCR (qRT-PCR). Protein synthesis was also detected by Western blot method.
Mucosal acidification with 10 and 100 HCl, significantly increased mucosal levels of H2S (P<0.01 and P<0.001) and mRNA (P<0.01 and P<0.001) and protein expressions of CSE (P<0.01 and P<0.001). L-NAME treatment reversed H2S release to control level.
Our findings indicated that mucosal acidification with HCl increased mucosal release of H2S through upregulation of CSE gene and its protein expression. This effect is mainly mediated through the involvement of nitric oxide.
本研究旨在探讨黏膜酸化对大鼠胃黏膜中胱硫醚γ裂解酶(CSE)、胱硫醚β合酶(CBS)的mRNA表达、蛋白质合成以及H2S黏膜释放的影响。
32只大鼠随机分为4组(每组8只),包括:对照组、10 mM HCl处理组、100 mM HCl处理组以及一组用于研究盐酸Nω-硝基-L-精氨酸甲酯(L-NAME)作用的组。对麻醉的大鼠进行气管切开术和正中剖腹术。在滴注中性或酸性溶液90分钟后,处死动物并收集胃黏膜,通过ELISA法测量H2S浓度,并通过定量实时PCR(qRT-PCR)定量CSE和CBS的mRNA表达。蛋白质合成也通过蛋白质印迹法检测。
用10 mM和100 mM HCl进行黏膜酸化,显著增加了黏膜H2S水平(P<0.01和P<0.001)、CSE的mRNA(P<0.01和P<0.001)和蛋白质表达(P<0.01和P<0.001)。L-NAME处理使H2S释放恢复到对照水平。
我们的研究结果表明,用HCl进行黏膜酸化通过上调CSE基因及其蛋白质表达增加了黏膜H2S释放。这种作用主要通过一氧化氮介导。