一氧化氮合酶抑制剂对内毒素致肝脏脂质过氧化形成的影响。

S Sakaguchi, S Furusawa, K Yokota, K Sasaki, M Takayanagi, Y Takayanagi
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引用次数: 11

摘要

本研究探讨了一氧化氮对内毒素血症时脂质过氧化形成的影响。一氧化氮合酶抑制剂N(G)-单甲基- l-精氨酸乙酸酯(L-NMMA, 20 mg/kg,静脉注射)、N(G)-硝基- l-精氨酸甲酯(L-NAME, 10 mg/kg,静脉注射)和N(G)-硝基- l-精氨酸(L-NA, 10 mg/kg,静脉注射)以及一种相对选择性的诱导型一氧化氮合酶抑制剂氨基胍(10 mg/kg,静脉注射)对内毒素诱导的小鼠死亡没有保护作用。l -精氨酸类似物(L-NMMA、L-NAME、L-NA)腹腔注射内毒素18小时后,小鼠肝脏超氧化物歧化酶活性低于单独内毒素处理小鼠,而l -精氨酸类似物注射内毒素小鼠肝脏黄嘌呤氧化酶活性高于单独内毒素处理小鼠。在l -精氨酸类似物和氨基胍处理的小鼠中,内毒素注射后18小时肝脏中非蛋白巯基和过氧化脂质水平与单独内毒素处理的小鼠没有显着差异。l -精氨酸类似物和氨基胍对内毒素引起的肝脏脂质过氧化形成影响不大。300 μ m氨基胍显著抑制内毒素诱导的J774A细胞内过氧化。然而,氨基胍不影响内毒素诱导的J774A细胞毒性。1细胞。我们的研究结果清楚地表明,过氧化氢酶(10微克/毫升)、d -甘露醇(10毫米)或超氧化物歧化酶(100 U/毫升)处理对内毒素(1微克/毫升)激活的J774A产生一氧化氮的影响很小或没有影响。1细胞。这些发现表明,在内毒素血症期间,一氧化氮对脂质过氧化形成并不重要。因此,一氧化氮不太可能在内毒素血症中自由基生成引起的肝损伤中起重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of nitric oxide synthase inhibitors on lipid peroxide formation in liver caused by endotoxin challenge.

This study investigated the effect of nitric oxide on lipid peroxide formation during endotoxaemia. Nitric oxide synthase inhibitors N(G)-monomethyl-L-arginine acetate (L-NMMA, 20 mg/kg, intravenously), N(G)-nitro-L-arginine-methyl ester (L-NAME, 10 mg/kg, intravenously), and N(G)-nitro-L-arginine (L-NA, 10 mg/kg, intravenously), and a relatively selective inducible nitric oxide synthase inhibitor aminoguanidine (10 mg/kg, intravenously), did not protect against endotoxin-induced death of mice. Superoxide dismutase activity in liver 18 hr after administration of endotoxin (6 mg/kg, intraperitoneally) to L-arginine analogues (L-NMMA, L-NAME, L-NA)-treated mice was lower than in mice treated with endotoxin alone, whereas the administration of L-arginine analogues increased xanthine oxidase activity in the livers of endotoxin-injected mice compared with mice treated with endotoxin alone. In mice treated with L-arginine analogues and aminoguanidine, the levels of non-protein sulfhydryl and lipid peroxide in liver 18 hr after endotoxin injection did not show significant differences from mice treated with endotoxin alone. L-Arginine analogues and aminoguanidine had little effect on lipid peroxide formation in liver caused by endotoxin. Treatment with aminoguanidine (300 microM) significantly inhibited endotoxin-induced intracellular peroxide in J774A.1 cells, however, aminoguanidine did not affect endotoxin-induced cytotoxicity in J774A.1 cells. Our results clearly demonstrate that treatment with catalase (10 microg/ml), D-mannitol (10 mM), or superoxide dismutase (100 U/ml), has little or no effect on nitric oxide production by endotoxin (1 microg/ml)-activated J774A.1 cells. These findings suggest that nitric oxide is not crucial for lipid peroxide formation during endotoxaemia. Therefore, it is unlikely that nitric oxide plays a significant role in liver injury caused by free radical generation in endotoxaemia.

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