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Lipid lowering effects of Momordica charantia (Bitter Melon) in HIV-1-protease inhibitor-treated human hepatoma cells, HepG2
Article first published online: 29 JAN 2009
DOI: 10.1038/sj.bjp.0706821
2006 British Pharmacological Society
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Nerurkar, P. V., Lee, Y. K., Linden, E. H., Lim, S., Pearson, L., Frank, J. and Nerurkar, V. R. (2006), Lipid lowering effects of Momordica charantia (Bitter Melon) in HIV-1-protease inhibitor-treated human hepatoma cells, HepG2. British Journal of Pharmacology, 148: 1156–1164. doi: 10.1038/sj.bjp.0706821
Publication History
- Issue published online: 29 JAN 2009
- Article first published online: 29 JAN 2009
- (Received December 29, 2005, Revised March 13, 2006, Accepted May 25, 2006)
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Keywords:
- Ritonavir;
- lopinavir;
- HAART;
- bitter melon;
- triglycerides;
- apoB;
- apoC-III;
- apoA-I;
- apolipoproteins;
- hyperlipidemia
- 1Hyperlipidemic effects of HIV-1-protease inhibitors (PI) are associated with increased hepatic production of triglyceride (TG)-rich lipoproteins, rather than lipoprotein clearance. PI are known to increase apolipoprotein B (apoB) secretion, apoC-III mRNA expression and decrease apoA-1 secretion. Nutritional therapy remains an important strategy to manage PI-associated hyperlipidemia.
- 2This study investigated the in vitro efficacy of Asian vegetable, Momordica charantia or bitter melon (BM) to ameliorate PI-associated apoB and lipid abnormalities in HepG2 cells.
- 3Our study demonstrates that bitter melon juice (BMJ) significantly reduced apoB secretion and apoC-III mRNA expression and normalized apoA-I expression in PI-treated HepG2 cells. BMJ also significantly reduced cellular TG and microsomal TG transfer protein, suggesting that lipid bioavailability and lipidation of apoB assembly may play a role in decreased apoB secretion.
- 4Identifying molecular targets of BM may offer alternative dietary strategies to decrease PI-associated hyperlipidemia and improve quality of life among HIV-1-infected patients.
British Journal of Pharmacology (2006) 148, 1156–1164. doi:10.1038/sj.bjp.0706821

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