Antihyperlipidemic effect of Cyclocarya paliurus (Batal.) Iljinskaja extract and inhibition of apolipoprotein B48 overproduction in hyperlipidemic mice

J Ethnopharmacol. 2015 May 26:166:286-96. doi: 10.1016/j.jep.2015.03.030. Epub 2015 Mar 17.

Abstract

Ethnopharmacological relevance: Cyclocarya paliurus (CP) Batal., the sole species in its genus, is a native plant to China. As a traditional Chinese folk medicine, the tree leaves have been widely used for the treatment of metabolic disorders, including hyperlipidemia, obesity, diabetes and hypertension.

Aim of the study: The study aimed to evaluate the antihyperlipidemic effect of CP ethanol extract, as well as its inhibitory activity on apolipoproteinB48 (apoB48), in normal and hyperlipidemic mice.

Materials and methods: The antihyperlipidemic effect of CP was evaluated in hyperlipidemic mice induced by high-fat diet for 4 weeks. CP ethanol extract (0.37, 0.75 and 1.5g/kg/day) was orally administrated once daily. Lipids and antioxidant profiles, including total cholesterol (TC), triglyceride (TG), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), malondialdehyde (MDA), superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px), together with the indices of hepatic and renal functions were examined. RT-qPCR and western blotting were used to analysis the expression levels of tumor necrosis factor (TNF-α), total- and triglyceride-rich apoB48 (TRL-apoB48), as well as the phosphorylation of the mitogen-activatein kinase (MAPK).

Results: CP as well as simvastatin remarkably lowered the levels of TC, TG, LDL-C and MDA, and at the same time, elevated the HDL-C, SOD and GSH-Px in high-fat diet mice. It also decreased the serum concentration of total- and TRL-apoB48 in the fasting state. CP inhibited TNF-α expression and phosphorylation level of MAPK. Furthermore, the HE staining of liver and kidney, together with hepatic and renal function analysis showed hepato- and renoprotective activities of CP.

Conclusions: These results suggested that CP possesses beneficial potentials for use in treating hyperlipidemia and the underlying lipid-lowering mechanism might associate with a down-regulation of the intestinal-associated lipoprotein apoB48, which may provide evidence about its practical application for treating hyperlipidemia and its complications.

Keywords: Antihyperlipidemic; Antioxidant; ApoB48; Arjunolic acid (PubChem CID: 73641); Cyclocaric acid B (CAS No. 182315-46-4); Cyclocarya paliurus; Isoquercitrin (PubChem CID: 5280804); Kaempferol-3-O-α-l-rhamnopyranoside (PubChem CID: 5316673); Kaempferol-3-O-β-d-glucuronide (PubChem CID: 5282102); MAPK; Pterocaryoside A (CAS No. 168146-85-8).; Pterocaryoside B (CAS No. 168146-27-8); TNF-α.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Apolipoprotein B-48 / antagonists & inhibitors*
  • Cholesterol, HDL / blood
  • Cholesterol, LDL / blood
  • Diet, High-Fat / adverse effects
  • Drugs, Chinese Herbal / chemistry
  • Drugs, Chinese Herbal / pharmacology
  • Ethnopharmacology / methods
  • Glutathione Peroxidase / blood
  • Hyperlipidemias / blood
  • Hyperlipidemias / drug therapy*
  • Hyperlipidemias / metabolism
  • Hypolipidemic Agents / chemistry
  • Hypolipidemic Agents / pharmacology*
  • Juglandaceae / chemistry*
  • Kidney / drug effects
  • Kidney / metabolism
  • Lipids / blood
  • Liver / drug effects
  • Liver / metabolism
  • Male
  • Malondialdehyde / blood
  • Mice
  • Mitogen-Activated Protein Kinase Kinases / metabolism
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology*
  • Plant Leaves / chemistry
  • Superoxide Dismutase / blood
  • Triglycerides / blood
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Antioxidants
  • Apolipoprotein B-48
  • Cholesterol, HDL
  • Cholesterol, LDL
  • Drugs, Chinese Herbal
  • Hypolipidemic Agents
  • Lipids
  • Plant Extracts
  • Triglycerides
  • Tumor Necrosis Factor-alpha
  • Malondialdehyde
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Mitogen-Activated Protein Kinase Kinases