Zhao Wei, Zhu Feng, Shen Weiwei, Fu Aifen, Zheng Lin, Yan Zhaowen, Zhao Lingzi, Fu Guohui
Key Laboratory of Cell Differentiation and Apoptosis of Chinese Ministry of Education, Institutes of Medical Sciences, Department of Pathology, Shanghai Jiaotong University School of Medicine, Shanghai 200025, China.
Acta Biochim Biophys Sin (Shanghai). 2009 Apr;41(4):301-8. doi: 10.1093/abbs/gmp014.
The compound 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid (DIDS) is an efficient anion exchanger inhibitor that can block the activities of anion exchanger 2 (AE2), which plays an indispensable role in gastric acid secretion. DIDS also has potent anti-oxidative and antiapoptosis activities. This study aimed to investigate the effect of DIDS on ethanol-induced mucosal damage in rats and to evaluate the underlying mechanisms that mediate the action of the compound. The rats received 1 ml of absolute ethanol or saline orally. DIDS [50 mg/kg intravenous (i.v.)] was given 5 min before ethanol administration. Gastric lesions were evaluated macroscopically, microscopically, and electron microscopically at 60 min after ethanol challenge. Gastric myeloperoxidase (MPO) activity, malonyldialdehyde (MDA) level, prostaglandin E2 (PGE2) synthesis, and cyclooxygenase-2 (COX-2) expression were assessed. For the evaluation of the effect of DIDS on gastric acid secretion, histamine-stimulatory gastric acid secretion was examined with or without pretreatment of DIDS (50 mg/kg; i.v.). Ethanol-induced gastric lesions were characterized by increasing gastric MDA level, MPO activity, and COX-2 expression, and decreasing PGE2 synthesis. It was found that DIDS significantly reduced the extent of gastric mucosal damage and reversed tissue MDA level and MPO activity. DIDS further enhanced the expression of COX-2 and reversed the decrease of PGE2. Our results suggested that DIDS is beneficial in rat model of gastric injury through mechanisms that involve inhibiting inflammatory cell infiltration and lipid peroxidation and up-regulating the COX-2/PGE2 pathway.
化合物4,4'-二异硫氰基芪-2,2'-二磺酸(DIDS)是一种有效的阴离子交换抑制剂,可阻断阴离子交换蛋白2(AE2)的活性,而AE2在胃酸分泌中起不可或缺的作用。DIDS还具有强大的抗氧化和抗凋亡活性。本研究旨在探讨DIDS对乙醇诱导的大鼠胃黏膜损伤的影响,并评估介导该化合物作用的潜在机制。大鼠口服1 ml无水乙醇或生理盐水。在给予乙醇前5分钟静脉注射DIDS[50 mg/kg]。乙醇攻击60分钟后,通过宏观、微观和电子显微镜评估胃损伤情况。评估胃髓过氧化物酶(MPO)活性、丙二醛(MDA)水平、前列腺素E2(PGE2)合成及环氧合酶-2(COX-2)表达。为评估DIDS对胃酸分泌的影响,在有或无DIDS(50 mg/kg;静脉注射)预处理的情况下检测组胺刺激的胃酸分泌。乙醇诱导的胃损伤表现为胃MDA水平、MPO活性和COX-2表达增加,PGE2合成减少。结果发现,DIDS显著减轻胃黏膜损伤程度,逆转组织MDA水平和MPO活性。DIDS进一步增强COX-2表达,逆转PGE2的降低。我们的结果表明,DIDS通过抑制炎症细胞浸润和脂质过氧化以及上调COX-2/PGE2途径,对大鼠胃损伤模型有益。