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对具有遗传易感性的神经回路的代谢印记会使肥胖持续存在。

Metabolic imprinting on genetically predisposed neural circuits perpetuates obesity.

作者信息

Levin B E

机构信息

Department of Neurosciences, New Jersey Medical School, Newark, New Jersey, USA.

出版信息

Nutrition. 2000 Oct;16(10):909-15. doi: 10.1016/s0899-9007(00)00408-1.

Abstract

There is an obesity epidemic in the industrialized world that is not simply explained by excess energy intake and decreased energy expenditure. Persistent obesity develops when genetically predisposed individuals are in a chronic state of positive energy balance. Once established, the obese body weight is avidly defended against both over- and underfeeding. Animal studies have shown that lean individuals who are genetically predisposed toward obesity have abnormalities of neural function that prime them to become obese when caloric density of the diet is raised. These neural abnormalities are gradually "corrected" as obesity becomes fully developed, suggesting that obesity is the normal state for such individuals. Thus, defense of the obese body weight may be perpetuated by the formation of new neural circuits involved in energy-homeostasis pathways that are not then easily abolished. Such neural plasticity can occur in both adult life and during nervous-system development. Early pre- and postnatal metabolic conditions (maternal diabetes, obesity, undernutrition) can lead genetically predisposed offspring to become even more obese as adults. This enhanced obesity is associated with altered brain neural circuitry, and these changes can then be passed on to subsequent generations in a feed-forward cycle of ever-increasing body weight. Thus, the metabolic perturbations associated with obesity during both brain development and adult life can produce "metabolic imprinting" on genetically predisposed neural circuits involved in energy homeostasis. Drugs that reduce body weight decrease the defended body weight and alter neural pathways involved in energy homeostasis but have no permanent effect on body weight or neural function in most individuals. Thus, early intervention in mothers, infants, children, and adults may be the only way to prevent the formation of permanent neural connections that promote and perpetuate obesity in genetically predisposed individuals.

摘要

在工业化世界中,肥胖症流行,这不能简单地用能量摄入过多和能量消耗减少来解释。当具有遗传易感性的个体处于长期正能量平衡状态时,持续性肥胖就会发展。一旦形成,肥胖体重会积极抵御过度喂养和喂养不足。动物研究表明,具有肥胖遗传易感性的瘦人存在神经功能异常,当饮食的热量密度增加时,他们就容易肥胖。随着肥胖完全发展,这些神经异常会逐渐“得到纠正”,这表明肥胖对这些个体来说是正常状态。因此,肥胖体重的维持可能是由于参与能量稳态途径的新神经回路的形成,而这些回路随后不容易被消除。这种神经可塑性在成年期和神经系统发育过程中都可能发生。出生前和出生后的早期代谢状况(母亲糖尿病、肥胖、营养不良)会使具有遗传易感性的后代成年后变得更加肥胖。这种肥胖加剧与大脑神经回路改变有关,然后这些变化可以在前馈循环中传递给后代,导致体重不断增加。因此,在大脑发育和成年期与肥胖相关的代谢紊乱会在参与能量稳态的遗传易感性神经回路上产生“代谢印记”。减轻体重的药物会降低维持的体重,并改变参与能量稳态的神经通路,但对大多数人的体重或神经功能没有永久性影响。因此,对母亲、婴儿、儿童和成年人进行早期干预可能是防止在具有遗传易感性的个体中形成促进和维持肥胖的永久性神经连接的唯一方法。

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