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Hepatoprotective Effects of Met-enkephalin on Acetaminophen-Induced Liver Lesions in Male CBA Mice

机译:Met-脑啡肽对乙酰氨基酚诱发的男性CBA小鼠肝损伤的肝保护作用

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摘要

Recent histopathological investigations in patients with hepatitis suggested possible involvement of Met-enkephalin and its receptors in the pathophysiology of hepatitis. Consequently, we evaluated the potential hepatoprotective effects of this endogenous opioid pentapeptide in the experimental model of acetaminophen induced hepatotoxicity in male CBA mice. Met-enkephalin exhibited strong hepatoprotective effects in a dose of 7.5 mg/kg, which corresponds to the protective dose reported for several different animal disease models. In this group plasma alanine aminotransferase and aspartate aminotransferase enzyme activities, as well as liver necrosis score were significantly reduced in comparison to control animals treated with physiological saline (p > 0.01). The specificity of the peptide hepatoprotection was investigated from the standpoint of the receptor and peptide blockade. It was concluded that Met-enkephalin effects on the liver were mediated via delta and zeta opioid receptors. Genotoxic testing of Met-enkephalin confirmed the safety of the peptide.
机译:最近对肝炎患者的组织病理学研究表明,Met-脑啡肽及其受体可能与肝炎的病理生理有关。因此,我们在对乙酰氨基酚诱导的雄性CBA小鼠肝毒性实验模型中评估了这种内源性阿片类五肽的潜在肝保护作用。 Met-脑啡肽在7.5 mg / kg的剂量下表现出强大的肝保护作用,相当于几种不同动物疾病模型报道的保护剂量。与用生理盐水治疗的对照组动物相比,该组的血浆丙氨酸氨基转移酶和天冬氨酸氨基转移酶活性以及肝坏死评分显着降低(p> 0.01)。从受体和肽阻滞的角度研究了肽肝保护的特异性。结论是,Met-脑啡肽对肝脏的作用是通过δ和ζ-阿片样物质受体介导的。 Met-脑啡肽的基因毒性测试证实了该肽的安全性。

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