![]() |
|
|
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
3 Department of Nutrition, Mahidol University, Bangkok 10400, Thailand 4 Department of Biochemistry, Mahidol University, Bangkok 10700, Thailand 5 Department of Human Nutrition, The Ohio State University, Columbus, OH 43210 6 Department of Nutrition, University of North Carolina, Greensboro, NC 27402
The xanthones,
- and
-mangostin (MG), are major bioactive compounds found in mangosteen and are reported to have antiinflammatory properties in several murine models. Given the association between obesity, chronic low-grade inflammation, and insulin resistance, we examined the effects of
- and
-MG on markers of inflammation and insulin resistance in primary cultures of newly differentiated human adipocytes treated with lipopolysaccharide (LPS).
- and
-MG decreased the induction by LPS of inflammatory genes, including tumor necrosis factor-
, interleukin (IL)-1β, IL-6, IL-8, monocyte chemoattractant protein-1, and Toll-like receptor-2. Moreover,
- and
-MG attenuated LPS activation of the mitogen-activated protein kinases (MAPK) c-jun NH2-terminal kinase, extracellular signal-related kinase, and p38.
- and
-MG also attenuated LPS activation of c-Jun and activator protein (AP)-1 activity.
-MG was more effective than
-MG on an equimolar basis. Furthermore,
-MG but not
-MG attenuated LPS-mediated I
B-
degradation and nuclear factor-
B (NF-
B) activity. In addition,
-MG prevented the suppression by LPS of insulin-stimulated glucose uptake and PPAR-
and adiponectin gene expression. Taken together, these data demonstrate that MG attenuates LPS-mediated inflammation and insulin resistance in human adipocytes, possibly by inhibiting the activation of MAPK, NF-
B, and AP-1.
* To whom correspondence should be addressed. E-mail: mkmcinto{at}uncg.edu.
Manuscript received 2 March 2009. Initial review completed 23 March 2009. Revision accepted 29 March 2009.