Center for Translational Medicine of the First Affiliated Hospital, Sun Yatsen University, Guangzhou, China.
Braz J Med Biol Res. 2020 Mar 2;53(3):e9201. doi: 10.1590/1414-431X20199201. eCollection 2020.
Methylophiopogonanone A (MO-A), a homoisoflavonoid extracted from Ophiopogon japonicus, has been shown to attenuate myocardial apoptosis and improve cerebral ischemia/reperfusion injury. However, the hypolipidemic effects remain unknown. This study was performed to investigate a potential hypolipidemic effect of MO-A in hyperlipidemia rats, as well as its underlying mechanism of action. A rat model of hyperlipidemia was induced by a high-fat diet (HFD). Animals were randomly divided into three groups (n=8/group): normal control group (NC), HFD group, and HFD+MO-A (10 mg·kg-1·d-1) treatment group. The effects of MO-A on serum lipids, body weight, activity of lipoprotein metabolism enzyme, and gene expression of lipid metabolism were evaluated in HFD-induced rats. In HFD-induced rats, pretreatment with MO-A decreased the body weight gain and reduced serum and hepatic lipid levels. In addition, pretreatment with MO-A improved the activities of lipoprotein lipase and hepatic lipase in serum and liver, down-regulated mRNA expression of acetyl CoA carboxylase and sterol regulatory element-binding protein 1c, and up-regulated mRNA expression of low-density lipoprotein receptor and peroxisome proliferator-activated receptor α in the liver. Our results indicated that MO-A showed strong ability to ameliorate the hyperlipidemia in HFD-induced rats. MO-A might be a potential candidate for prevention of overweight and dyslipidemia induced by HFD.
甲基ophiopogonanone A(MO-A),从麦冬提取的homoisoflavonoid,已被证明可以减轻心肌细胞凋亡,改善脑缺血/再灌注损伤。然而,其降血脂作用尚不清楚。本研究旨在探讨 MO-A 在高脂血症大鼠中的潜在降血脂作用及其作用机制。采用高脂饮食(HFD)诱导大鼠高脂血症模型。动物随机分为三组(每组 8 只):正常对照组(NC)、HFD 组和 HFD+MO-A(10mg·kg-1·d-1)治疗组。评价 MO-A 对 HFD 诱导大鼠血脂、体重、脂蛋白代谢酶活性及脂质代谢基因表达的影响。在 HFD 诱导的大鼠中,MO-A 预处理可降低体重增加,降低血清和肝脂质水平。此外,MO-A 预处理可改善血清和肝脏中脂蛋白脂肪酶和肝脂肪酶的活性,下调乙酰辅酶 A 羧化酶和固醇调节元件结合蛋白 1c 的 mRNA 表达,上调肝脏中低密度脂蛋白受体和过氧化物酶体增殖物激活受体α的 mRNA 表达。我们的结果表明,MO-A 对 HFD 诱导的大鼠高脂血症有很强的改善作用。MO-A 可能是预防 HFD 引起的超重和血脂异常的潜在候选药物。