HIV protease inhibitors block human preadipocyte differentiation, but not via the PPARγ/RXR heterodimer

被引:68
作者
Wentworth, JM
Burris, TP
Chatterjee, VKK
机构
[1] Addenbrookes Hosp, Dept Med, Cambridge CB2 2QQ, England
[2] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Pharmacol, Piscataway, NJ 08854 USA
关键词
D O I
10.1677/joe.0.164R007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A recent prospective clinical study has shown that antiviral therapy with HIV protease inhibitors (PIs) is associated with a syndrome of peripheral fat wasting (lipodystrophy) and disordered glucose and lipid metabolism (Carr et al. 1999). We have studied the effects of indinavir and saquinavir, two HIV protease inhibitors, on cultured primary human preadipocytes and report that these compounds inhibit their differentiation. However, we find that these agents do not inhibit either transcriptional activation or adipocyte P2 gene induction by the PPAR gamma/RXR nuclear receptor heterodimer. Together, our findings suggest that impaired adipogenesis is the basis of PI-associated lipodystrophy, but that this occurs via a PPAR gamma/RXR-independent mechanism.
引用
收藏
页码:R7 / R10
页数:4
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