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Merck
CN
  • Dissociation of Adaptive Thermogenesis from Glucose Homeostasis in Microbiome-Deficient Mice.

Dissociation of Adaptive Thermogenesis from Glucose Homeostasis in Microbiome-Deficient Mice.

Cell metabolism (2020-02-23)
Tibor I Krisko, Hayley T Nicholls, Curtis J Bare, Corey D Holman, Gregory G Putzel, Robert S Jansen, Natalie Sun, Kyu Y Rhee, Alexander S Banks, David E Cohen
摘要

Recent studies suggest that a key mechanism whereby the gut microbiome influences energy balance and glucose homeostasis is through the recruitment of brown and beige adipocytes, primary mediators of the adaptive thermogenic response. To test this, we assessed energy expenditure and glucose metabolism in two complementary mouse models of gut microbial deficiency, which were exposed to a broad range of thermal and dietary stresses. Neither ablation of the gut microbiome, nor the substantial microbial perturbations induced by cold ambient temperatures, influenced energy expenditure during cold exposure or high-fat feeding. Nevertheless, we demonstrated a critical role for gut microbial metabolism in maintaining euglycemia through the production of amino acid metabolites that optimized hepatic TCA (tricarboxylic acid) cycle fluxes in support of gluconeogenesis. These results distinguish the dispensability of the gut microbiome for the regulation of energy expenditure from its critical contribution to the maintenance of glucose homeostasis.

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单克隆抗 β-肌动蛋白抗体 小鼠抗, clone AC-15, ascites fluid
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乙酸钠, anhydrous, Molecular Biology, ≥99%
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丙酸钠, ≥99.0%
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丁酸钠, ≥98.5% (GC)
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橙黄 G, for NA electrophoresis