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Curcumin prevents high fat diet induced insulin resistance and obesity via attenuating lipogenesis in liver and inflammatory pathway in adipocytes.
- Source :
-
PloS one [PLoS One] 2012; Vol. 7 (1), pp. e28784. Date of Electronic Publication: 2012 Jan 09. - Publication Year :
- 2012
-
Abstract
- Background: Mechanisms underlying the attenuation of body weight gain and insulin resistance in response to high fat diet (HFD) by the curry compound curcumin need to be further explored. Although the attenuation of the inflammatory pathway is an accepted mechanism, a recent study suggested that curcumin stimulates Wnt signaling pathway and hence suppresses adipogenic differentiation. This is in contrast with the known repressive effect of curcumin on Wnt signaling in other cell lineages.<br />Methodology and Principal Findings: We conducted the examination on low fat diet, or HFD fed C57BL/6J mice with or without curcumin intervention for 28 weeks. Curcumin significantly attenuated the effect of HFD on glucose disposal, body weight/fat gain, as well as the development of insulin resistance. No stimulatory effect on Wnt activation was observed in the mature fat tissue. In addition, curcumin did not stimulate Wnt signaling in vitro in primary rat adipocytes. Furthermore, curcumin inhibited lipogenic gene expression in the liver and blocked the effects of HFD on macrophage infiltration and the inflammatory pathway in the adipose tissue.<br />Conclusions and Significance: We conclude that the beneficial effect of curcumin during HFD consumption is mediated by attenuating lipogenic gene expression in the liver and the inflammatory response in the adipose tissue, in the absence of stimulation of Wnt signaling in mature adipocytes.
- Subjects :
- Adipocytes drug effects
Adipocytes metabolism
Adipose Tissue drug effects
Adipose Tissue metabolism
Adipose Tissue pathology
Adiposity drug effects
Animals
Curcumin administration & dosage
Dietary Fats pharmacology
Dietary Supplements
Gene Expression Regulation drug effects
Glucose metabolism
Hep G2 Cells
Humans
Inflammation genetics
Insulin pharmacology
Lipogenesis genetics
Liver drug effects
Liver pathology
Male
Mice
Mice, Inbred C57BL
Obesity metabolism
Phosphorylation drug effects
Proto-Oncogene Proteins c-akt metabolism
Rats
Signal Transduction drug effects
Time Factors
Weight Gain drug effects
Adipocytes pathology
Curcumin pharmacology
Inflammation pathology
Insulin Resistance
Lipogenesis drug effects
Liver metabolism
Obesity prevention & control
Subjects
Details
- Language :
- English
- ISSN :
- 1932-6203
- Volume :
- 7
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- PloS one
- Publication Type :
- Academic Journal
- Accession number :
- 22253696
- Full Text :
- https://doi.org/10.1371/journal.pone.0028784