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Differential sympathetic outflow to adipose depots is required for visceral fat loss in response to calorie restriction

机译:响应卡路里限制,内脏脂肪损失需要有不同的交感性流出到脂肪库

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The sympathetic nervous system (SNS) regulates energy homeostasis in part by governing fatty acid liberation from adipose tissue. We first examined whether SNS activity toward discrete adipose depots changes in response to a weight loss diet in mice. We found that SNS activity toward each adipose depot is unique in timing, pattern of activation, and habituation with the most dramatic contrast between visceral and subcutaneous adipose depots. Sympathetic drive toward visceral epididymal adipose is more than doubled early in weight loss and then suppressed later in the diet when weight loss plateaued. Coincident with the decline in SNS activity toward visceral adipose is an increase in activity toward subcutaneous depots indicating a switch in lipolytic sources. In response to calorie restriction, SNS activity toward retroperitoneal and brown adipose depots is unaffected. Finally, pharmacological blockage of sympathetic activity on adipose tissue using the β3-adrenergic receptor antagonist, SR59230a, suppressed loss of visceral adipose mass in response to diet. These findings indicate that SNS activity toward discrete adipose depots is dynamic and potentially hierarchical. This pattern of sympathetic activation is required for energy liberation and loss of adipose tissue in response to calorie-restricted diet.
机译:交感神经系统(SNS)部分地通过控制从脂肪组织释放的脂肪酸来调节能量稳态。我们首先检查了SNS对离散脂肪库的活性是否响应小鼠的减肥饮食而改变。我们发现,对每个脂肪库的SNS活性在时机,激活模式和习惯化方面都是独特的,内脏和皮下脂肪库之间的差异最为明显。在减肥初期,对内脏附睾脂肪的同情驱动力增加了一倍以上,而在减肥达到平稳状态后,在饮食中则受到抑制。与SNS对内脏脂肪的活性下降相吻合的是对皮下贮库的活性增加,表明脂解源的转换。响应热量限制,SNS对腹膜后和棕色脂肪贮库的活性不受影响。最后,使用β3-肾上腺素能受体拮抗剂SR59230a对脂肪组织上的交感活性进行药理学阻滞,可以抑制饮食对内脏脂肪量的损失。这些发现表明,SNS对离散脂肪库的活动是动态的,并且可能是分层的。响应热量限制饮食,能量释放和脂肪组织损失需要这种交感激活模式。

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