Publications by authors named "Y Minokoshi"

Activation of brown and beige fat biogenesis promotes metabolic health in rodents and humans, but typically requires cold exposure or pharmacological activation of β-adrenergic receptors, which may pose cardiovascular risks. Dietary intervention represents a clinically viable alternative strategy to induce beige cells and thus enhance metabolic health, though the underlying mechanisms remain poorly understood. In this study, we identified specific microbiota members in both mice and humans that promote browning of white adipose tissue (WAT) and ameliorate metabolic disorders in the context of a low-protein diet (LPD).

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Inflammation and thermogenesis in white adipose tissue (WAT) at different sites influence the overall effects of obesity on metabolic health. In mice fed a high-fat diet (HFD), inflammatory responses are less pronounced in inguinal WAT (ingWAT) than in epididymal WAT (epiWAT). Here we show that ablation and activation of steroidogenic factor 1 (SF1)-expressing neurons in the ventromedial hypothalamus (VMH) oppositely affect the expression of inflammation-related genes and the formation of crown-like structures by infiltrating macrophages in ingWAT, but not in epiWAT, of HFD-fed mice, with these effects being mediated by sympathetic nerves innervating ingWAT.

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Article Synopsis
  • Low body temperature is linked to poor outcomes in heart failure patients, with brown adipose tissue (BAT) playing a significant role in metabolic health and potentially influencing heart failure.
  • BAT dysfunction, demonstrated through reduced thermogenic capacity and hypoxia after heart stressors like thoracic aortic constriction (TAC) or myocardial infarction (MI), leads to adverse effects on heart function and body temperature regulation.
  • Elevated levels of plasma TMAO were associated with decreased heart energy production and function, suggesting that therapies focused on improving BAT function and reducing TMAO levels could benefit heart failure patients.
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Article Synopsis
  • Monocarboxylates like lactate and pyruvate play key roles as building blocks for important metabolic processes, including glucose and lipid synthesis, through pathways like the TCA cycle.
  • The transportation of these monocarboxylates is primarily managed by monocarboxylate transporters (MCTs), which rely on the protein basigin (BSG) for proper function and location in the cell membrane.
  • Research shows that when BSG is depleted, MCT1 transport decreases, leading to disrupted gluconeogenesis and altered metabolic pathways, but this can improve conditions like hyperglycemia and insulin resistance when observed in BSG-deficient mice on a high-fat diet.
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