Smith Steven R
Pennington Biomedical Research Center, 6400 Perkins Road, Baton Rouge, LA 70808, USA.
Curr Drug Targets CNS Neurol Disord. 2004 Oct;3(5):431-9. doi: 10.2174/1568007043337030.
The metabolic syndrome is a cluster of easy-to-measure clinical phenotypes that serve as markers for increased risk for CVD and diabetes. There is no universal agreement as to the underlying pathophysiology of the metabolic syndrome. At its core, the metabolic syndrome is the result of energy excess; therefore treating obesity is a good strategy to reverse the clinical features of the metabolic syndrome. Hypertension is a special case, may not be part of the core pathophysiology of the metabolic syndrome, and will not be discussed. After a brief review of recent developments in the pathophysiology of the metabolic syndrome, this review will concentrate on peripheral targets in the following categories: ectopic fat and fat oxidation, intrinsic defects in substrate switching and mitochondrial biogenesis, lipolysis and lipid turnover, adipose tissue as an endocrine organ, nutrient / energy sensing systems, and inflammation. The advantages and pitfalls of these targets will be discussed with an eye towards the relevant literature.
代谢综合征是一组易于测量的临床表型,可作为心血管疾病(CVD)和糖尿病风险增加的标志物。关于代谢综合征的潜在病理生理学,尚无普遍共识。代谢综合征的核心是能量过剩;因此,治疗肥胖是逆转代谢综合征临床特征的一个好策略。高血压是一个特殊情况,可能不是代谢综合征核心病理生理学的一部分,本文将不做讨论。在简要回顾代谢综合征病理生理学的最新进展后,本综述将集中讨论以下几类外周靶点:异位脂肪与脂肪氧化、底物转换和线粒体生物发生的内在缺陷、脂肪分解与脂质周转、作为内分泌器官的脂肪组织、营养/能量传感系统以及炎症。将结合相关文献讨论这些靶点的优势与缺陷。