脂质代谢和营养分配策略。

A M Morris, D J Calsbeek, R H Eckel
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引用次数: 4

摘要

世界范围内超重和肥胖的日益普遍令人生畏,需要受影响者、卫生保健专业人员、政府和制药行业迅速予以关注。由于超重/肥胖被定义为脂肪组织质量过剩,所有预防和治疗方法都必须考虑将脂肪组织中的脂质储存转向氧化代谢。脂质分配是一个复杂的过程,涉及脂肪和其他常量营养素,特别是碳水化合物之间的相互作用。在等热量环境中,当脂肪被储存时,碳水化合物被氧化,反之亦然。以维持体重的方式影响脂肪分配的过程必须通过器官特异性脂肪转运和代谢的变化来改变。然而,当考虑治疗时,仅改变脂质分配将是无效的,除非也达到负能量平衡,即能量消耗超过能量摄入。本综述的目的是集中在分子包括激素,酶,细胞因子,膜转运蛋白和转录因子直接参与脂肪运输和分配可能是潜在的药物靶点。通过对这些分子进行系统和/或组织特异性修饰来有利地改变身体组成的一些例子已经在小鼠中提供了基因敲除和/或转基因方法。将这一科学转化为人类仍然是一项具有挑战性的任务。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lipid metabolism and nutrient partitioning strategies.

The increasing prevalence of overweight and obesity worldwide is daunting and requires prompt attention by the affected, health care profession, government and the pharmaceutical industry. Because overweight/obesity are defined as an excess of adipose tissue mass, all approaches in prevention and treatment must consider redirecting lipid storage in adipose tissue to oxidative metabolism. Lipid partitioning is a complex process that involves interaction between fat and other macronutrients, particularly carbohydrate. In an isocaloric environment, when fat is stored carbohydrate is oxidized and vice versa. Processes that influence fat partitioning in a manner in which weight is maintained must be modified by changes in organ-specific fat transport and metabolism. When therapy is considered, however, changes in lipid partitioning alone will be ineffective unless a negative energy balance is also achieved, i.e. energy expenditure exceeds energy intake. The intent of this review is to focus on molecules including hormones, enzymes, cytokines, membrane transport proteins, and transcription factors directly involved in fat trafficking and partitioning that could be potential drug targets. Some examples of favorably altering body composition by systemic and/or tissue specific modification of these molecules have already been provided with gene knockout and/or transgenic approaches in mice. The translation of this science to humans remains a challenging task.

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