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Effects of capsaicin on adipogenic differentiation in bovine bone marrow mesenchymal stem cell.


ABSTRACT: Capsaicin is a major constituent of hot chili peppers that influences lipid metabolism in animals. In this study, we explored the effects of capsaicin on adipogenic differentiation of bovine bone marrow mesenchymal stem cells (BMSCs) in a dose- and time-dependent manner. The BMSCs were treated with various concentrations of capsaicin (0, 0.1, 1, 5, and 10 ?M) for 2, 4, and 6 days. Capsaicin suppressed fat deposition significantly during adipogenic differentiation. Peroxisome proliferator-activated receptor gamma, cytosine-cytosine-adenosine-adenosine-thymidine/enhancer binding protein alpha, fatty acid binding protein 4, and stearoyl-CoA desaturase expression decreased after capsaicin treatment. We showed that the number of apoptotic cells increased in dose- and time-dependent manners. Furthermore, we found that capsaicin increased the expression levels of apoptotic genes, such as B-cell lymphoma 2-associated X protein and caspase 3. Overall, capsaicin inhibits fat deposition by triggering apoptosis.

SUBMITTER: Jeong JY 

PROVIDER: S-EPMC4213691 | biostudies-literature | 2014 Dec

REPOSITORIES: biostudies-literature

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Effects of capsaicin on adipogenic differentiation in bovine bone marrow mesenchymal stem cell.

Jeong Jin Young JY   Suresh Sekar S   Park Mi Na MN   Jang Mi M   Park Sungkwon S   Gobianand Kuppannan K   You Seungkwon S   Yeon Sung-Heom SH   Lee Hyun-Jeong HJ  

Asian-Australasian journal of animal sciences 20141201 12


Capsaicin is a major constituent of hot chili peppers that influences lipid metabolism in animals. In this study, we explored the effects of capsaicin on adipogenic differentiation of bovine bone marrow mesenchymal stem cells (BMSCs) in a dose- and time-dependent manner. The BMSCs were treated with various concentrations of capsaicin (0, 0.1, 1, 5, and 10 μM) for 2, 4, and 6 days. Capsaicin suppressed fat deposition significantly during adipogenic differentiation. Peroxisome proliferator-activat  ...[more]

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