Abstract

The effect of Fufang Jiangzhi No. 3 on cholesterol-bile acid metabolism in New Zealand white rabbit fed with cholesterol-rich diet was studied. 24 male New Zealand white rabbits were randomly assigned into control group (Group A), hypercholesterolemia model group (Group B), and Fufang Jiangzhi No. 3 treatment group (Group C). Groups B and C were fed with cholesterol-rich diet (containing 1% cholesterol) 120 g/day during 4 weeks’ administration in order to establish hypercholesterolemia model while Group A was fed with common rabbit fodder 120 g/day. Group C received Fufang Jiangzhi No. 3 by intragastric administration (0.5 bag/20 ml distilled water, every morning) at the same time as the start of the cholesterol-rich diet exposure. Serum CHO, LDL-C and BA assessment of 24 rabbits was performed at the end of the experiment. The activity of CYP7A1 in the liver was measured by enzymelinked immunosorbent assay (ELISAs). The expressions of CYP7A1 mRNA, bile salt export pump (BSEP) mRNA and small heterodimer partner (SHP) mRNA in the liver were measured by real time polymerase chain reaction (RT-PCR). Serum CHO in Group B was much higher than that in Group A (P<0.05), moreover, the serum CHO in Group C was lower than that in Group B ( P<0.05). The level of BSEP mRNA and SHP mRNA in Group C were much lower than those of Group B ( P<0.01). These results suggested that Fufang Jiangzhi No. 3 can up-regulate the expression of CYP7A1 mRNA and enhance the activity of CYP7A1. It may be one of the mechanisms involved in its preventive effect in cholesterolrich diet-induced hyperchlesterolemia in New Zealand white rabbit.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.