Virtue Sam, Vidal-Puig Antonio
Institute of Metabolic Science, Metabolic Research Laboratories, University of Cambridge, Box 289, Level 4, Addenbrooke's Hospital, Cambridge CB2 0QQ, UK.
Biochim Biophys Acta. 2010 Mar;1801(3):338-49. doi: 10.1016/j.bbalip.2009.12.006. Epub 2010 Jan 6.
While the link between obesity and type 2 diabetes is clear on an epidemiological level, the underlying mechanism linking these two common disorders is not as clearly understood. One hypothesis linking obesity to type 2 diabetes is the adipose tissue expandability hypothesis. The adipose tissue expandability hypothesis states that a failure in the capacity for adipose tissue expansion, rather than obesity per se is the key factor linking positive energy balance and type 2 diabetes. All individuals possess a maximum capacity for adipose expansion which is determined by both genetic and environmental factors. Once the adipose tissue expansion limit is reached, adipose tissue ceases to store energy efficiently and lipids begin to accumulate in other tissues. Ectopic lipid accumulation in non-adipocyte cells causes lipotoxic insults including insulin resistance, apoptosis and inflammation. This article discusses the links between adipokines, inflammation, adipose tissue expandability and lipotoxicity. Finally, we will discuss how considering the concept of allostasis may enable a better understanding of how diabetes develops and allow the rational design of new anti diabetic treatments.
虽然在流行病学层面上,肥胖与2型糖尿病之间的联系很明显,但将这两种常见疾病联系起来的潜在机制却没有那么容易理解。一种将肥胖与2型糖尿病联系起来的假说是脂肪组织扩张性假说。脂肪组织扩张性假说认为,脂肪组织扩张能力的失败,而非肥胖本身,是将正能量平衡与2型糖尿病联系起来的关键因素。所有个体都拥有由遗传和环境因素共同决定的最大脂肪扩张能力。一旦达到脂肪组织扩张极限,脂肪组织就会停止有效储存能量,脂质开始在其他组织中积累。非脂肪细胞中的异位脂质积累会导致脂毒性损伤,包括胰岛素抵抗、细胞凋亡和炎症。本文讨论了脂肪因子、炎症、脂肪组织扩张性和脂毒性之间的联系。最后,我们将讨论考虑内稳态概念如何能更好地理解糖尿病的发展,并有助于合理设计新的抗糖尿病治疗方法。