Preliminary study on efficacy and mechanism of Atractylodes Macrocephelae Rhizoma extracts in metabolic hyperlipidemia rats.
- Author:
Qi-jing TANG
;
Su-hong CHEN
;
Dan-dan PAN
;
Bo LI
;
Gui-yan LV
- Publication Type:Journal Article
- MeSH:
Acyl Coenzyme A;
antagonists & inhibitors;
genetics;
metabolism;
Animals;
Atractylodes;
chemistry;
Drugs, Chinese Herbal;
administration & dosage;
Humans;
Hydroxymethylglutaryl-CoA Reductase Inhibitors;
administration & dosage;
Hyperlipidemias;
drug therapy;
enzymology;
metabolism;
Lipoproteins, HDL;
metabolism;
Male;
Rats;
Rats, Sprague-Dawley;
Rhizome;
chemistry;
Triglycerides;
metabolism
- From:
China Journal of Chinese Materia Medica
2015;40(9):1803-1807
- CountryChina
- Language:Chinese
-
Abstract:
Hyperlipidemia is a major factor causing coronary heart disease and atherosclerosis. The high-density lipoprotein cholesterol (HDL-C) is a major indicator for measuring lipid levels. However, there is no an effective medicine that can obviously increase HDL-C at present. According to previous laboratory studies, atractylodes macrocephalae extracts could significantly increase HDL-C level. In this study, the metabolic hyperlipidemia rat model was established by feeding high-sugar and fat diets and alcohol-drinking to explore the effect and mechanism of atractylodes macrocephalae extracts on hyperlipidemia rats. According to the findingins, different doses of atractylodes macrocephalae extracts could reduce the levels of TC, TG, LDL-C, ACAT and increase the contents of LCAT, HDL-C. Particularly, the atractylodes macrocephalae extracts (100 mg · kg(-1) group showed increase in HDL-C by about 50% and significant declines in HMG-CoA reductase, TC, TG. In conclusion, Atractylodes Macrocephelae Rhizoma extracts could effectively regulate the dyslipidemia of hyperlipidemia rats, especially on HDL-C. Its mechanism may be related to reduction in cholesterol synthesis by inhibiting HMG-CoA reductase in livers and increase in lipid metabolism and transport by regulating LCAT and ACAT levels.