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Oxidative stress in portal hypertension-induced rats with particular emphasis on nitric oxide and trace metals

机译:门静脉高压症大鼠的氧化应激特别是一氧化氮和微量金属

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摘要

AIM: To investigate the oxidative-stress-related changes in rats with portal hypertension with particular emphasis on nitric oxide (NO) and trace metals.METHODS: Cirrhosis was induced by partial portal vein ligation (PVL) in Wistar rats. The lipid peroxidation marker (malondialdehyde, MDA), antioxidant defense enzymes including superoxide dismutase (SOD), catalase (CAT), glutathione (GSH), and agents known to have antioxidant features including nitric oxide (NO), zinc (Zn), copper (Cu) were determined both in serum and in liver tissue at 4 wk after surgery in PVL and sham-operated rats. Portal pressure of all experimental animals was measured. MDA was detected by thiobarbituric acid reactivity assay. SOD activity was determined by inhibition of nitroblue tetrazolium reduction with xanthine/xanthine oxidase used as a superoxide generator. CAT activity was determined by the breakdown of hydrogen peroxide. GSH concentrations were measured by using metaphosphoric acid for protein precipitation and 5’-5’-dithio-bis-2-nitrobenzoic acid for color development. NO was detected by the Griess method after reduction of nitrate to nitrite with nitrate reductase, and the concentrations of Zn and Cu were measured by a Shimadzu 680 AA atomic absorption spectrometer. Histopathological confirmation was done under light microscope. Statistical analyses were done by Student’s t-test, and significance of the difference was tested by the unpaired Mann-Whitney test. P<0.05 was considered statistically significant.RESULTS: Histopathological studies confirmed PVL-induced cirrhotic changes. There was a statistically significant difference in portal pressure between PVL and control groups (P<0.001). The results showed significant increases in the levels of MDA and NO in both tissue and serum (P<0.05 and P<0.001, respectively in tissue; P<0.001 for each in serum), and Zn only in tissue (P<0.001) in rats with PVL compared with sham-operated rats. Besides, PVL rats exhibited reduced plasma and tissue GSH, CAT, SOD (P<0.001 for each). Serum and tissue Cu concentration did not change.CONCLUSION: Our findings suggest that PVL in rats induces important biochemical and molecular changes related to oxidative stress in the liver.
机译:目的:探讨门静脉高压症大鼠的氧化应激相关变化,特别是一氧化氮(NO)和微量金属。方法:Wistar大鼠门静脉部分结扎(PVL)诱发肝硬化。脂质过氧化标记(丙二醛,MDA),抗氧化剂防御酶,包括超氧化物歧化酶(SOD),过氧化氢酶(CAT),谷胱甘肽(GSH),以及已知具有抗氧化特性的试剂,包括一氧化氮(NO),锌(Zn),铜在PVL和假手术大鼠中,在术后4 wk测定血清和肝组织中的(Cu)。测量所有实验动物的门静脉压力。通过硫代巴比妥酸反应性测定法检测MDA。 SOD活性是通过用黄嘌呤/黄嘌呤氧化酶(用作超氧化物发生器)抑制硝基蓝四唑还原而确定的。 CAT的活性是通过过氧化氢的分解来确定的。通过使用偏磷酸沉淀蛋白质和使用5'-5'-二硫代-双-2-硝基苯甲酸显色来测量GSH浓度。用硝酸还原酶将硝酸盐还原为亚硝酸盐后,用Griess法检测到NO,用Shimadzu 680 AA原子吸收光谱仪测量Zn和Cu的浓度。在光学显微镜下进行组织病理学证实。统计分析是通过Student t检验进行的,差异的显着性是通过未配对的Mann-Whitney检验进行检验的。 P <0.05被认为具有统计学意义。结果:组织病理学研究证实PVL引起的肝硬化改变。 PVL与对照组之间的门脉压力有统计学上的显着差异(P <0.001)。结果显示,在组织和血清中,MDA和NO含量显着增加(分别在组织中P <0.05和P <0.001;在血清中每种P <0.001),仅组织中Zn(P <0.001)。 PVL大鼠与假手术大鼠相比。此外,PVL大鼠的血浆和组织GSH,CAT,SOD均降低(每组P <0.001)。血清和组织中铜的浓度没有变化。结论:我们的发现表明,PVL在大鼠体内可诱导与肝脏氧化应激相关的重要生化和分子变化。

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