Title :
Effects of Osthole on Protein Expression of CYP7A1, DGAT2 and PPARalpha/gamma in Fat Milk-Induced Fatty Liver Rats
Author :
Yan, Zhang ; Xie Mei-lin ; Xue Jie ; Gu Zhen-lun
Author_Institution :
Med. Sch., Dept. of Pharmacology, Soochow Univ., Suzhou
Abstract :
To determine the effect of osthole on protein expression of PPARalpha/gamma and related target molecules such as CYP7A and DGAT in the liver of hyperlipidemic fatty liver (HFL) rats, and to investigate the possible mechanism of treating HFL. HFL rat model was established by feeding the Sprague-Dawley rats with fat milk for 6 weeks. The experimental rats were then treated with 5-20 mg/kg osthole for 6 weeks. The proteins expression of PPARalpha/gamma, CYP7A1, and DGAT2 in rat liver was measured by western blot analyses. After administration of osthole, expression of PPARalpha and PPARgamma proteins in HFL rat liver was increased by 49% ~ 133% and 19% ~ 113% in the osthole groups as compared with model group, respectively (P<0.05 or P<0.01). The related target proteins were increased by 85% ~ 147% for CYP7A1 and decreased by 35% ~ 62% for DGAT2 by the osthole-treatment, respectively (P<0.01). Osthole possessed therapeutic effects on fat milk-induced fatty liver in rats, and the mechanism might be attributed to regulating the protein expression of CYP7A1 and DGAT2 via increasing PPARalpha/gamma.
Keywords :
biochemistry; drugs; genetics; liver; molecular biophysics; patient treatment; proteins; 7alpha-hydroxylase; CYP7A target molecules; DGAT target molecules; PPARalpha/gamma target molecules; Sprague-Dawley rats; diacylgycerol acyltransferase; fat milk; gene expression; hyperlipidemic fatty liver rats; osthole effect; peroxisome-proliferator-activated receptors; protein expression; time 6 week; western blot analyses; Animal structures; Biochemistry; Blood; Dairy products; Drugs; Hospitals; Lipidomics; Liver; Proteins; Rats;
Conference_Titel :
Bioinformatics and Biomedical Engineering, 2008. ICBBE 2008. The 2nd International Conference on
Conference_Location :
Shanghai
Print_ISBN :
978-1-4244-1747-6
Electronic_ISBN :
978-1-4244-1748-3
DOI :
10.1109/ICBBE.2008.63