Department of Pharmacology and Toxicology, Faculty of Pharmacy, Helwan University, Ein Helwan, Cairo, Egypt,
Arch Pharm Res. 2013 Sep;36(9):1140-8. doi: 10.1007/s12272-013-0110-x. Epub 2013 Apr 17.
This study evaluated the effect of methylsulfonylmethane (MSM) on carbon tetrachloride (CCl₄)-induced acute liver injury in rats. A single injection of CCl₄ (2 ml/kg, i.p.) increased serum aminotransferases (ALT and AST) activities. In addition, CCl₄ treatment led to elevation of hepatic malondialdehyde (MDA) content as well as decrease in superoxide dismutase (SOD) and catalase (CAT) activities. Furthermore, cytochrome P450 2E1 (CYP2E1) content was suppressed while proinflammatory cytokines tumour necrosis factor-α (TNF-α) and interleukin-6 (IL-6) levels increased in liver tissue after CCl4 administration. We showed that acute CCl₄-induced damage was accompanied by a rise in Bax/Bcl₂ ratio indicating apoptosis. Pre-treatment with MSM (400 mg/kg) inhibited the increases of serum ALT and AST activities, decreased hepatic MDA, TNF-α, IL-6 and Bax/Bcl₂ ratio compared to CCl₄ treated group. On the other hand, MSM raised SOD and CAT activities as well as CYP2E1 level in liver tissues. The present study shows that MSM possesses a hepatoprotective effect against CCl₄-induced liver injury in rats. This protective effect might be through its antioxidant, anti-inflammatory and antiapoptotic properties.
本研究评估了甲基磺酰甲烷 (MSM) 对四氯化碳 (CCl₄) 诱导的大鼠急性肝损伤的影响。单次注射 CCl₄ (2 ml/kg,ip) 可增加血清转氨酶 (ALT 和 AST) 活性。此外,CCl₄ 处理会导致肝丙二醛 (MDA) 含量升高,超氧化物歧化酶 (SOD) 和过氧化氢酶 (CAT) 活性降低。此外,CYP2E1 含量在 CCl4 给药后降低,而 TNF-α和 IL-6 等促炎细胞因子在肝组织中的水平升高。我们表明,急性 CCl₄ 诱导的损伤伴随着 Bax/Bcl₂ 比值的升高,表明细胞凋亡。与 CCl₄ 处理组相比,MSM (400 mg/kg) 预处理可抑制血清 ALT 和 AST 活性的升高,降低肝 MDA、TNF-α、IL-6 和 Bax/Bcl₂ 比值。另一方面,MSM 可提高肝组织中的 SOD 和 CAT 活性以及 CYP2E1 水平。本研究表明,MSM 对大鼠 CCl₄ 诱导的肝损伤具有保护作用。这种保护作用可能是通过其抗氧化、抗炎和抗凋亡特性实现的。