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Role of adipose tissue in body-weight regulation: mechanisms regulating leptin production and energy balance

机译:脂肪组织在体重调节中的作用:调节瘦素产生和能量平衡的机制

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Adipose tissue performs complex metabolic and endocrine functions. Among the endocrine products produced by adipose tissue are tumour necrosis factor ?±, interleukin 6, acylation-stimulating protein and leptin. The present review will focus primarily on mechanisms regulating leptin production and leptin action, and the implications of this regulation in the control of energy balance. Leptin acts in the central nervous system where it interacts with a number of hypothalamic neuropeptide systems to regulate feeding behaviour and energy expenditure. The presence of extreme obesity in animals and human subjects with mutations of the leptin gene or the leptin receptor demonstrates that normal leptin production and action are critical for maintaining energy balance. Insulin is the major regulator of leptin production by adipose tissue. Insulin infusions increase circulating leptin concentrations in human subjects. Plasma leptin levels are markedly decreased in insulin-deficient diabetic rodents, and the low leptin levels contribute to diabetic hyperphagia. Based on in vitro studies, the effect of insulin to stimulate leptin production appears to involve increased glucose metabolism. Blockade of glucose transport or glycolysis inhibits leptin expression and secretion in isolated adipocytes. Evidence suggests that anaerobic metabolism of glucose to lactate does not stimulate leptin production. Alterations in insulin-mediated glucose metabolism in adipose tissue are likely to mediate the effects of energy restriction to decrease, and refeeding to increase, circulating leptin levels. Changes in glucose metabolism may also explain the observation that high-fat meals lower 24 h circulating leptin levels relative to high-carbohydrate meals in human subjects, suggesting a mechanism that may contribute to the effects that high-fat diets have in promoting increased energy intake, weight gain and obesity. The decreased circulating leptin observed during energy restriction is related to increased sensations of hunger in human subjects. Thus, decreases in leptin during energy-restricted weight-loss regimens may contribute to the strong propensity for weight regain. A better understanding of the precise mechanisms regulating leptin production and leptin action may lead to new approaches for managing obesity.
机译:脂肪组织执行复杂的代谢和内分泌功能。脂肪组织产生的内分泌产物中有肿瘤坏死因子α±,白介素6,酰化刺激蛋白和瘦素。本审查将主要侧重于调节瘦素产生和瘦素作用的机制,以及该调节对能量平衡控制的影响。瘦素在中枢神经系统中起作用,并与许多下丘脑神经肽系统相互作用,从而调节进食行为和能量消耗。在动物和人类中,存在瘦素基因或瘦素受体突变的极端肥胖症表明,正常的瘦素产生和作用对于维持能量平衡至关重要。胰岛素是脂肪组织生产瘦素的主要调节剂。胰岛素输注会增加人体受试者的循环瘦素浓度。在胰岛素缺乏的糖尿病啮齿动物中血浆瘦素水平显着降低,而瘦素水平低则导致糖尿病性食欲过高。根据体外研究,胰岛素刺激瘦素产生的作用似乎与葡萄糖代谢增加有关。葡萄糖转运或糖酵解的阻滞抑制了分离的脂肪细胞中瘦素的表达和分泌。有证据表明葡萄糖厌氧代谢为乳酸不会刺激瘦素的产生。脂肪组织中胰岛素介导的葡萄糖代谢的改变可能介导能量限制的作用降低,再进食以增加循环瘦素水平。葡萄糖代谢的变化也可能解释了以下观察结果:高脂肪饮食相对于人类受试者的高碳水化合物饮食可降低24小时循环瘦素水平,这表明可能有助于高脂肪饮食促进能量摄入增加的机制,体重增加和肥胖。在能量限制期间观察到的循环瘦素减少与人类受试者饥饿感的增加有关。因此,在能量受限的减肥方案中,瘦素的减少可能有助于体重增加。对调节瘦素产生和瘦素作用的精确机制的更好的理解可能会导致新的肥胖管理方法。

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