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      Central role of ceramide biosynthesis in body weight regulation, energy metabolism, and the metabolic syndrome.

      American Journal of Physiology - Endocrinology and Metabolism

      Adipose Tissue, pathology, Animals, Body Weight, physiology, Ceramides, biosynthesis, blood, Energy Metabolism, Fatty Acids, Monounsaturated, pharmacology, Ion Channels, metabolism, Lysophospholipids, Male, Metabolic Syndrome X, Mice, Mice, Inbred C57BL, Mitochondrial Proteins, Obesity, Organ Size, Sphingolipids, Sphingosine, analogs & derivatives, Suppressor of Cytokine Signaling Proteins

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          Abstract

          Although obesity is associated with multiple features of the metabolic syndrome (insulin resistance, leptin resistance, hepatic steatosis, chronic inflammation, etc.), the molecular changes that promote these conditions are not completely understood. Here, we tested the hypothesis that elevated ceramide biosynthesis contributes to the pathogenesis of obesity and the metabolic syndrome. Chronic treatment for 8 wk of genetically obese (ob/ob), and, high-fat diet-induced obese (DIO) mice with myriocin, an inhibitor of de novo ceramide synthesis, decreased circulating ceramides. Decreased ceramide was associated with reduced weight, enhanced metabolism and energy expenditure, decreased hepatic steatosis, and improved glucose hemostasis via enhancement of insulin signaling in the liver and muscle. Inhibition of de novo ceramide biosynthesis decreased adipose expression of suppressor of cytokine signaling-3 (SOCS-3) and induced adipose uncoupling protein-3 (UCP3). Moreover, ceramide directly induced SOCS-3 and inhibited UCP3 mRNA in cultured adipocytes suggesting a direct role for ceramide in regulation of metabolism and energy expenditure. Inhibition of de novo ceramide synthesis had no effect on adipose tumor necrosis factor-alpha (TNF-alpha) expression but dramatically reduced adipose plasminogen activator inhibitor-1 (PAI-1) and monocyte chemoattactant protein-1 (MCP-1). This study highlights a novel role for ceramide biosynthesis in body weight regulation, energy expenditure, and the metabolic syndrome.

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          Author and article information

          Journal
          10.1152/ajpendo.91014.2008
          2711669
          19435851

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