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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Gastroprotective effect of taurine zinc solid dispersions against absolute ethanol-induced gastric lesions is mediated by enhancement of antioxidant activity and endogenous PGE(2) production and attenuation of NO production
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Gastroprotective effect of taurine zinc solid dispersions against absolute ethanol-induced gastric lesions is mediated by enhancement of antioxidant activity and endogenous PGE(2) production and attenuation of NO production

机译:通过增强抗氧化活性和内源性PGE(2)生产和衰减,牛磺酸锌固体分散体对绝对乙醇诱导的胃病变的胃保护作用介导的

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Zinc plays a key role in maintaining gastric mucosal integrity, while alcohol dependency can lead to low zinc status. Complexes containing zinc have been reported to have better ability to protect gastric mucosa than the compounds alone. In this study, taurine zinc [Zn(NH3CH2CH2SO3)(2)] solid dispersions (SDs) were synthesized and investigated in an ethanol-induced ulcer model in rats. Gastric ulcer index; gastric mucosa malondialdehyde (MDA) level, glutathione (GSH) content, superoxide dismutase (SOD) activity and prostaglandin E-2 (PGE(2)) production; and serum nitric oxide (NO) were assessed and histological analysis of the gastric mucosa tissue was performed. Taurine zinc (100, 200 mg/kg) SDs protected rat gastric mucosa from ethanol-induced injury. Moreover, the gastroprotective effect of taurine zinc SDs was accompanied by a decrease in serum NO and significant increase in gastric prostaglandin E-2 (PGE(2)). When indomethacin, a non-selective COX inhibitor was administered before the last dose of taurine zinc, the gastroprotective effect of taurine zinc was weakened. Furthermore, taurine zinc (200 mg/kg) SDs protected against ulceration more significantly than the same dose of taurine alone, suggesting a synergistic effect between taurine and zinc. These results indicate taurine zinc protects the gastric mucosa against ethanol-induced damage by elevating antioxidants, decreasing lipid peroxidation and inhibiting the production of nitric oxide. The gastroprotective effect of taurine zinc was also partially mediated by endogenous PGE(2) production. (C) 2014 Elsevier By. All rights reserved,
机译:锌在维持胃粘膜完整性方面发挥着关键作用,而酒精依赖可以导致低锌状态。据报道,含有锌的配合物具有更好的能力来保护胃粘膜的能力而不是单独的化合物。在该研究中,在大鼠乙醇诱导的溃疡模型中合成并研究了牛磺酸锌[Zn(NH 3 CH 2 CH 2 SO 3)(2)]固体分散体(SDS)。胃溃疡指数;胃粘膜丙二醛(MDA)水平,谷胱甘肽(GSH)含量,超氧化物歧化酶(SOD)活性和前列腺素E-2(PGE(2))生产;评估血清一氧化氮(NO),进行胃粘膜组织的组织学分析。牛磺酸锌(100,200mg / kg)SDS保护来自乙醇诱导损伤的大鼠胃粘膜。此外,牛磺酸锌SDS的胃保护作用伴随着血清NO和胃前列腺素E-2(PGE(2))的显着增加。当Indomethacin时,在最后剂量的牛磺酸锌之前施用非选择性Cox抑制剂,牛磺酸锌的胃保护作用削弱。此外,牛磺酸锌(200mg / kg)SDS保护比单独的同一剂牛磺酸更显着的溃疡,这表明牛磺酸和锌之间的协同效应。这些结果表明,牛磺酸锌通过升高抗氧化剂,降低脂质过氧化并抑制一氧化氮的产生来保护胃粘膜抗乙醇诱导的损伤。牛磺酸锌的胃保护作用也由内源性PGE(2)产生部分介导。 (c)2014年elestvier。版权所有,

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