Methylophiopogonanone A, an Ophiopogon homoisoflavonoid, alleviates high-fat diet-induced hyperlipidemia: assessment of its potential mechanism.
Zhao LiYing-Ying WuBei-Xin YuPublished in: Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas (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.
Keyphrases
- high fat diet
- insulin resistance
- adipose tissue
- weight gain
- high fat diet induced
- gene expression
- low density lipoprotein
- high glucose
- binding protein
- diabetic rats
- body weight
- ischemia reperfusion injury
- oxidative stress
- transcription factor
- fatty acid
- metabolic syndrome
- skeletal muscle
- body mass index
- drug induced
- type diabetes
- subarachnoid hemorrhage
- heart failure
- dna methylation
- physical activity
- weight loss
- birth weight
- human health