| Literature DB >> 28754711 |
Minji Kim1, Tomoya Furuzono1, Kanae Yamakuni1, Yongjia Li1, Young-Il Kim1, Haruya Takahashi1, Ryuji Ohue-Kitano1,2, Huei-Fen Jheng1, Nobuyuki Takahashi1,2, Yuriko Kano3, Rina Yu4, Shigenobu Kishino5, Jun Ogawa2,5, Kunitoshi Uchida6,7,8, Jun Yamazaki8, Makoto Tominaga6,7, Teruo Kawada1,2, Tsuyoshi Goto9,2.
Abstract
Gut microbiota can regulate the host energy metabolism; however, the underlying mechanisms that could involve gut microbiota-derived compounds remain to be understood. Therefore, in this study, we investigated the effects of KetoA [10-oxo-12(Z)-octadecenoic acid]-a linoleic acid metabolite produced by gut lactic acid bacteria-on whole-body energy metabolism and found that dietary intake of KetoA could enhance energy expenditure in mice, thereby protecting mice from diet-induced obesity. By using Ca2+ imaging and whole-cell patch-clamp methods, KetoA was noted to potently activate transient receptor potential vanilloid 1 (TRPV1) and enhance noradrenalin turnover in adipose tissues. In addition, KetoA up-regulated genes that are related to brown adipocyte functions, including uncoupling protein 1 (UCP1) in white adipose tissue (WAT), which was later diminished in the presence of a β-adrenoreceptor blocker. By using obese and diabetic model KK-Ay mice, we further show that KetoA intake ameliorated obesity-associated metabolic disorders. In the absence of any observed KetoA-induced antiobesity effect or UCP1 up-regulation in TRPV1-deficient mice, we prove that the antiobesity effect of KetoA was caused by TRPV1 activation-mediated browning in WAT. KetoA produced in the gut could therefore be involved in the regulation of host energy metabolism.-Kim, M., Furuzono, T., Yamakuni, K., Li, Y., Kim, Y.-I., Takahashi, H., Ohue-Kitano, R., Jheng, H.-F., Takahashi, N., Kano, Y., Yu, R., Kishino, S., Ogawa, J., Uchida, K., Yamazaki, J., Tominaga, M., Kawada, T., Goto, T. 10-oxo-12(Z)-octadecenoic acid, a linoleic acid metabolite produced by gut lactic acid bacteria, enhances energy metabolism by activation of TRPV1. © FASEB.Entities:
Keywords: UCP1; beige cells; fatty acids; gut microbiota; obesity
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Year: 2017 PMID: 28754711 DOI: 10.1096/fj.201700151R
Source DB: PubMed Journal: FASEB J ISSN: 0892-6638 Impact factor: 5.191