期刊
METABOLISM-CLINICAL AND EXPERIMENTAL
卷 77, 期 -, 页码 58-64出版社
W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.metabol.2017.08.006
关键词
Cinnamaldehyde; Obesity; Thermogenesis; Subcutaneous adipocytes
资金
- Human Frontier Science Program Young Investigator Grant [RGY0082/2014]
- Mallinckrodt grant from the Edward Mallinckrodt Jr. Foundation
- National Institutes of Health [R01DK107583, F31DK112625]
- American Heart Association [17POST33060001]
Objective. Cinnamaldehyde (CA) is a food compound that has previously been observed to be protective against obesity and hyperglycemia in mouse models. In this study, we aimed to elucidate the mechanisms behind this protective effect by assessing the cell autonomous response of primary adipocytes to CA treatment. Methods. Primary murine adipocytes were treated with CA and thermogenic and metabolic responses were assessed after both acute and chronic treatments. Human adipose stem cells were differentiated and treated with CA to assess whether the CA mediated signaling is conserved in humans. Results. CA significantly activated PICA signaling, increased expression levels of thermogenic genes and induced phosphorylation of HSL and PLIN1 in murine primary adipocytes. Inhibition of PKA or p38 MAPK enzymatic activity markedly inhibited the CA-induced thermogenic response. In addition, chronic CA treatment regulates metabolic reprogramming, which was partially diminished in FGF21KO adipocytes. Importantly, both acute and chronic effects of CA were observed in human adipose stem cells isolated from multiple donors of different ethnicities and ages and with a variety of body mass indexes (BMI). Conclusions. CA activates thermogenic and metabolic responses in mouse and human primary subcutaneous adipocytes in a cell-autonomous manner, giving a mechanistic explanation for the anti-obesity effects of CA observed previously and further supporting its potential metabolic benefits on humans. Given the wide usage of cinnamon in the food industry, the notion that this popular food additive, instead of a drug, may activate thermogenesis, could ultimately lead to therapeutic strategies against obesity that are much better adhered to by participants. (C) 2017 Elsevier Inc. All rights reserved.
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