Lipid-lowering and antiatherogenic effects of Vitex megapotamica (Spreng.) Moldenke in a mice experimental model

J Ethnopharmacol. 2018 Apr 6:215:14-20. doi: 10.1016/j.jep.2017.12.030. Epub 2017 Dec 20.

Abstract

Ethnopharmacological relevance: Vitex megapotamica (Spreng.) Moldenke is a deciduous tree, native of South America. Its leaves are traditionally used to treat cardiovascular diseases. This activity is related to the presence of flavonoids, the major compounds of the crude extract.

Aim of the study: This study investigated the effects of the oral administration of crude extract and standardized fractions from V. megapotamica leaves on lipid profile and on the formation of atherosclerotic plaque in C57BL/6 LDLr-KO mice treated with high-fat diet (HFD).

Materials and methods: Male C57BL/6 LDLr-KO mice were fed with HFD (cholesterol, 1.25%) for 30 days. They were treated with hydroethanolic extract (500 or 1000mg/kg/day) or fractions (125 or 250mg/kg/day). After 30 days of treatment, it was evaluated the serum lipid profile, atherogenic index, and atherosclerotic plaque.

Results: All doses of the hydroethanolic extract reduced significantly the levels of total cholesterol, triglycerides, LDL-c and the atherogenic index. The n-butanolic fraction also reduced significantly the levels of total cholesterol, triglycerides, LDL-c and the atherogenic index, at all doses, with exception for the triglycerides, which only the lower dose was effective. The residual fraction reduced significantly the levels of total cholesterol, LDL-c and the atherogenic index, at all doses, with exception for the atherogenic index, which only the higher dose was effective. The atherosclerotic plaque formation was impaired only by the lower dose of the hydroethanolic extract.

Conclusions: Overall, our data suggest that V. megapotamica has potential for the treatment of dyslipidemias.

Keywords: Atherogenic index; C57BL/6 LDLr-KO mice; Flavonoids; Hypolipidemia; Tarumã; Vitex megapotamica.

MeSH terms

  • Animals
  • Diet, High-Fat / adverse effects
  • Hyperlipidemias / blood
  • Hyperlipidemias / chemically induced*
  • Hyperlipidemias / drug therapy*
  • Hypolipidemic Agents / administration & dosage
  • Hypolipidemic Agents / pharmacology*
  • Lipids / blood
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Phytotherapy
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology*
  • Plant Lectins / chemistry
  • Receptors, LDL / genetics
  • Receptors, LDL / metabolism
  • Vitex / chemistry*

Substances

  • Hypolipidemic Agents
  • Lipids
  • Plant Extracts
  • Plant Lectins
  • Receptors, LDL