[应激条件下大鼠胃黏膜NO合酶系统参数及环加氧酶抑制]。

I. Fomenko, T. Bondarchuk, L. P. Bilets'ka, N. B. Panasiuk, O. Skliarov
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引用次数: 2

摘要

在水约束应激模型大鼠实验中,研究了不同来源的非甾体类抗炎药对胃粘膜形态学状态和no合酶系统参数变化的影响。在水约束应激模型大鼠中,给予非选择性环氧抑制剂萘普生可增强胃粘膜损伤的严重程度。同时,no -合成酶诱导型和组成型同工型的活性均降低。脂质过氧化参数保持在限水胁迫时的水平。研究表明,使用释放h2s的非甾体类抗炎药ATB-346具有优势,其细胞保护作用表现为减少胃损伤总面积。然而,脂质过氧化和no -合成酶系统参数与萘普生组无明显差异,表明母体分子(萘普生)对no -系统功能的调节作用普遍存在,给予双COX/LOX抑制剂化合物2A5DHT比萘普生对胃损伤的影响更小。iNOS活性明显高于萘普生作用下的iNOS活性。
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[Parameters of NO synthase system of gastric mucosa in rats under stress conditions and inhibition of cyclooxygenase].
In experiments on rats with modeled water-restrained stress, the influence of nonsteroidal anti-inflammatory drugs of different genesis on morphological status of gastric mucosa and changes of NO-synthase system parameters have been studied Administration of nonselective cyclooxygenese inhibitor naproxen in the water-restrained stress model in rats potentiated the increase of severity of damage of gastric mucosa. At the same time, the activity of both inducible and constitutive isoforms ofNO-sythase decreased. The parameters of lipoperoxidation remained at the level observed during water-restrained stress. It was shown the advantages of the use of H2S-releasinfg nonsteroidal anti-inflammatory drug ATB-346, which are associated with its cytoprotective effect of the drug manifested by a decreased total area of gastric damage. However, parameters of lipoperoxidation and NO-syntase system did not differ substantially from those in the group treated with napoxen, indicating the prevalence of parent molecule (naproxen) in regulation of function of NO-system Administration of dual COX/LOX inhibitor, the compound 2A5DHT, caused a decrease of gastric damage as compared to the effect ofnaproxen. The activity of iNOS remained much higher than under condition of the naproxen action.
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