Chair of Molecular Nutritional Medicine, TUM School of Life Sciences, Technical University of Munich, Freising, Germany.
EKFZ - Else Kröner-Fresenius Center for Nutritional Medicine, Technical University of Munich, Freising, Germany.
Sci Rep. 2019 Jan 15;9(1):131. doi: 10.1038/s41598-018-37464-z.
Supplementation of cholate to a high fat diet can protect mice from diet-induced, increased body mass gain. It has been hypothesized that uncoupling protein 1 dependent, non-shivering thermogenesis in brown adipocytes provides the mechanism of increased energy expenditure to counteract excessive energy intake. We scrutinized this conjecture in wildtype mice and mice genetically devoid of a functional uncoupling protein 1 gene (C57BL/6J) as well as mice of the 129S6/SvEvTac strain that, in comparison, display an extraordinary capacity to recruit ectopic brown adipocytes. Protection from diet-induced, increased body mass gain by cholate supplementation was absent in 129S6/SvEvTac mice, a consequence of much lower bile acid absorption and spillover in this strain. Conversely, Ucp1-KO mice did not differ from C57BL/6J wildtype controls in any parameter assessed. Daily energy expenditure and resting metabolic rate of C57BL/6J mice remained unaffected by cholate supplementation. We conclude that protection of mice from diet-induced, increased body mass gain by cholate supplementation depends on the specific genetic background of C57BL/6J mice, does not involve increased energy expenditure and is independent of uncoupling protein 1 dependent non-shivering thermogenesis.
向高脂肪饮食中补充胆酸盐可以保护小鼠免受饮食引起的体重增加。据推测,解偶联蛋白 1 依赖性非颤抖性产热棕色脂肪细胞提供了增加能量消耗的机制,以抵消过量的能量摄入。我们在野生型小鼠和缺乏功能性解偶联蛋白 1 基因的小鼠(C57BL/6J)以及 129S6/SvEvTac 品系的小鼠中仔细研究了这一假设,与野生型相比,129S6/SvEvTac 品系的小鼠具有非凡的募集异位棕色脂肪细胞的能力。129S6/SvEvTac 小鼠由于胆汁酸吸收和溢出较低,因此缺乏胆酸盐补充对饮食引起的体重增加的保护作用。相反,Ucp1-KO 小鼠在任何评估参数上均与 C57BL/6J 野生型对照无差异。C57BL/6J 小鼠的每日能量消耗和静息代谢率不受胆酸盐补充的影响。我们得出结论,胆酸盐补充保护小鼠免受饮食引起的体重增加取决于 C57BL/6J 小鼠的特定遗传背景,不涉及增加能量消耗,并且独立于解偶联蛋白 1 依赖性非颤抖性产热。