Antioxidative effects of Alisma orientale extract in palmitate-induced cellular injury

被引:47
作者
Han, Chang Woo [2 ]
Kang, Eun Sil [1 ]
Ham, Sun Ah [1 ]
Woo, Hong Jung [3 ]
Lee, Jang Hoon [3 ]
Seo, Han Geuk [1 ]
机构
[1] Konkuk Univ, Dept Anim Biotechnol, Seoul 143701, South Korea
[2] Pusan Natl Univ, Sch Korean Med, Dept Internal Med, Yangsan, South Korea
[3] Kyung Hee Univ, Coll Oriental Med, Dept Oriental Internal Med, Seoul, South Korea
关键词
Alisma orientale; HepG2; c-Jun NH2-terminal kinase; nonalcoholic fatty liver disease; reactive oxygen species; FATTY LIVER-DISEASE; RHIZOMA DRIED RHIZOME; LIPID-PEROXIDATION; INSULIN-RESISTANCE; REACTIVE OXYGEN; NONALCOHOLIC STEATOHEPATITIS; HEPATOCYTE LIPOAPOPTOSIS; TERPENE COMPONENTS; SIGNALING PATHWAY; METHANOL EXTRACT;
D O I
10.3109/13880209.2012.673629
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Context: Alisma orientale (Sam.) Juzepczuk (Alismataceae) is an indigenous medicinal herb that has been traditionally used for diuretic, hypolipidemic, anti-inflammatory, and antidiabetic proposes in northern and eastern Asia. Objective: This study examined the mechanisms underlying the cytoprotective effect of an aqueous extract of A. orientale (AEAO) against long-chain saturated fatty acid-induced cellular injury. Materials and methods: HepG2 cells were treated with 0.5 mM palmitate to generate a cellular model of nonalcoholic fatty liver disease (NAFLD). Using this cellular model, the cytoprotective effect of AEAO (100 mu g/mL) against long-chain saturated fatty acid-induced cellular injury was evaluated by measuring the steatosis, ROS accumulation, and apoptosis. Results: AEAO significantly attenuated palmitate-induced intracellular steatosis and cellular damage up to 54 and 33%, respectively. Palmitate-induced intracellular levels of reactive oxygen species (ROS) and reactive aldehydes were significantly reduced in the presence of AEAO to 40 and 75%, respectively, suggesting that oxidative stress plays a role in the palmitate-induced damage. AEAO inhibited the palmitate-mediated activation of c-Jun NH2-terminal kinase (JNK), a kinase that is correlated with NAFLD. Inhibition of JNK by SP600125 or addition of AEAO significantly reduced palmitate-induced steatosis, ROS accumulation, and apoptosis, indicating that the protective effects of AEAO against palmitate-induced cellular damage result from blocking ROS-activated JNK signaling. Discussion and conclusion: The combined properties of AEAO in cellular steatosis and ROS production are beneficial for treating NAFLD, which includes complex metabolic changes, such that modulation of a single target is often not sufficient to achieve the desired therapeutic effect.
引用
收藏
页码:1281 / 1288
页数:8
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