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刘 晶, 孙 莉, 丁亚军, 林 娜, 舒 斌, 朱崇泉. 肌醇硫酸酯铝抗胃溃疡的作用机制[J]. 中国药科大学学报, 2011, 42(1): 73-77.
引用本文: 刘 晶, 孙 莉, 丁亚军, 林 娜, 舒 斌, 朱崇泉. 肌醇硫酸酯铝抗胃溃疡的作用机制[J]. 中国药科大学学报, 2011, 42(1): 73-77.
LIU Jing, SUN Li, DING Ya-jun, LIN Na, SHU Bin, ZHU Chong-quan. Potential mechanisms of sulfuric acid ester inositol aluminum against peptic ulcer[J]. Journal of China Pharmaceutical University, 2011, 42(1): 73-77.
Citation: LIU Jing, SUN Li, DING Ya-jun, LIN Na, SHU Bin, ZHU Chong-quan. Potential mechanisms of sulfuric acid ester inositol aluminum against peptic ulcer[J]. Journal of China Pharmaceutical University, 2011, 42(1): 73-77.

肌醇硫酸酯铝抗胃溃疡的作用机制

Potential mechanisms of sulfuric acid ester inositol aluminum against peptic ulcer

  • 摘要: 为了研究肌醇硫酸酯铝对大鼠乙酸烧灼胃溃疡的保护作用机制,采用乙酸建立大鼠慢性胃溃疡模型。将192只SD大鼠随机分为6组:正常组、肌醇硫酸酯铝高、中、低剂量组、达喜组和奥美拉唑组。各组于给药后的第3、8天分别处死16只大鼠,其中8只采用免疫组织化学染色法测定表皮生长因子(EGF)、表皮生长因子受体(EGFR)、碱性成纤维细胞生长因子(bFGF)、转化生长因子β(TGFβ)、血管内皮生长因子(VEGF),8只测定胃溃疡指数、一氧化氮(NO)含量、超氧化物歧化酶(SOD)活性和丙二醛(MDA)的含量。结果表明,与模型对照组相比,肌醇硫酸酯铝会增加EGF、EGFR、bFGF、TGFβ、VEGF的表达,并有统计学差异(P<0.05、P<0.01)。肌醇硫酸酯铝可以预防穿孔的发生,降低胃溃疡指数,提高溃疡抑制率,同时可降低MDA含量、提高组织中的SOD活性及NO含量(P<0.05)。研究结果表明:肌醇硫酸酯铝治疗胃溃疡的机制可能与促进EGF、EGFR、bFGF、TGFβ、VEGF的表达,降低MDA含量,提高组织中的SOD活性及NO含量有关。

     

    Abstract: In this study,a chronic model of gastric ulcer by acetic acid was prepared to verify the protection of sulfuric acid ester inositol aluminum in rats.192 SD rats were randomly divided into 6 groups,and each orally given with CMC-Na,sulfuric acid ester inositol aluminum (200,400 and 800 mg/kg),talcid (400 mg/kg) and omeprazole (12 mg/kg),respectively.16 rats in each group were sacrificed separately at day 3 and day 8 after the administration;half of the 16 rats were used for the measurement of EGF,EGFR,bFGF,TGFβ,VEGF contents with the immunohistochemical staining method and another half were used for the examination of gastric ulcer index,carbon monoxide content,superoxide dismutase activity and malonaldehyde content.Compared with the model group (CMC-Na treated),the EGF, EGFR,bFGF,TGFβ,VEGF contents in the sulfuric acid ester inositol aluminum treated groups were increased obviously (P<0.05,P<0.01).Furthermore,sulfuric acid ester inositol aluminum administration was found to prevent stomach perforation,reduce the gastric ulcer index,increase the gastric ulcer inhibition rate, reduce the MDA content,and increase the SOD activity and the NO content of the organization (P<0.05). Therefore,the protection of the sulfuric acid ester inositol aluminum on gastric ulcer might be related to the increment of EGF,EGFR,bFGF,TGFβ,VEGF,NO contents,and the SOD activity as well as the reduction of MDA content.

     

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