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Metformin improves lipid metabolism disorders through reducing the expression of microsomal triglyceride transfer protein in OLETF rats.

Authors :
Wang, Nianhong
Zhang, Junqing
Wu, Yiming
Liu, Jia
Liu, Lin
Guo, Xiaohui
Source :
Diabetes Research & Clinical Practice. Dec2016, Vol. 122, p170-178. 9p.
Publication Year :
2016

Abstract

<bold>Objective: </bold>This study aimed to investigate the role of MTP on lipid metabolism disorders in insulin-resistant rats and the potential mechanism through which metformin can improve lipid metabolism disorders.<bold>Methods: </bold>30 OLETF rats served as research subjects and 18 LETO rats of the same strain served as the control group (LETO group). After the first oral glucose tolerance test (at 8-week-old), 6 rats were randomly killed from each group. The remaining 24 OLETF rats were randomly divided into untreated group (OLETF group) and treated group (OLETF/M group, cured with metformin). By the end of the 10th and 20th week of treatment, MTP in the liver was measured for all rats in the study.<bold>Results: </bold>All OLETF rats exhibited diabetic phenotypes at 18-week-old, with their triglyceride level higher than in LETO rats at the same age. In OLETF rats, MTP level in the liver was higher than in LETO rats at 18-week-old, and the difference was significant at 28-week-old [(13.79±1.47) vs. (8.20±1.14), p<0.05]. Treatment with metformin for 20weeks decreased triglyceride [(1.06±0.23) vs. (2.20±0.62) mmol/L, p<0.05] and total cholesterol [(1.90±0.19) vs. (2.36±0.14) mmol/L, p<0.05] in OLETF rats. Metformin also decreased MTP level in the liver [(7.65±1.31) vs. (13.79±1.47), p<0.01].<bold>Conclusions: </bold>MTP may be associated with the lipid metabolism disorder in OLETF rats and metformin could improve lipid metabolism through reducing the expression of MTP. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01688227
Volume :
122
Database :
Academic Search Index
Journal :
Diabetes Research & Clinical Practice
Publication Type :
Academic Journal
Accession number :
120141803
Full Text :
https://doi.org/10.1016/j.diabres.2016.10.006