Division of Molecular Medicine, Bose Institute, P-1/12, CIT Scheme VII M, Kolkata-700054, India.
Free Radic Res. 2010 Mar;44(3):340-55. doi: 10.3109/10715760903513017.
The present study was carried out to investigate whether taurine plays any beneficial role in acetaminophen (APAP)-induced acute hepatotoxicity. APAP exposure increased the plasma levels of ALT, ALP, LDH, TNF-alpha and NO production. Moreover, APAP treatment reduced the glutathione level and antioxidant enzyme activities, increased lipid peroxidation and caused hepatic DNA fragmentation which ultimately leads to cellular necrosis. Also, incubation of hepatocytes with APAP reduced cell viability, enhanced ROS generation and increased CYP2E1 activity. APAP overdose caused injury in the hepatic tissue and hepatocytes via the upregulation of CYP2E1 and JNK. Taurine treatment was effective in counteracting APAP-induced hepatic damages, oxidative stress and cellular necrosis. Results indicate that APAP overdose caused hepatic injury due to its metabolism to hepatotoxic NAPQI (N-acetyl-p-benzoquinone imine), usually catalysed by CYP2E1, and via the direct activation of JNK-dependent cell death pathway. Taurine possesses prophylactic as well as therapeutic potentials against APAP-induced hepatic injury.
本研究旨在探讨牛磺酸是否对乙酰氨基酚(APAP)诱导的急性肝毒性有任何有益作用。APAP 暴露会增加 ALT、ALP、LDH、TNF-α 和 NO 产生的血浆水平。此外,APAP 处理会降低谷胱甘肽水平和抗氧化酶活性,增加脂质过氧化作用,并导致肝 DNA 片段化,最终导致细胞坏死。而且,用 APAP 孵育肝细胞会降低细胞活力,增强 ROS 的产生,并增加 CYP2E1 活性。APAP 过量通过上调 CYP2E1 和 JNK 导致肝组织和肝细胞损伤。牛磺酸治疗可有效对抗 APAP 诱导的肝损伤、氧化应激和细胞坏死。结果表明,APAP 过量导致肝损伤是由于其代谢为肝毒性 NAPQI(N-乙酰-p-苯醌亚胺),通常由 CYP2E1 催化,并通过 JNK 依赖性细胞死亡途径的直接激活。牛磺酸具有预防和治疗 APAP 诱导的肝损伤的潜力。