Morrison Christopher D, Huypens Peter, Stewart Laura K, Gettys Thomas W
Laboratory of Neurosignaling, Pennington Biomedical Research Center, Baton Rouge, LA, USA.
Biochim Biophys Acta. 2009 May;1792(5):409-16. doi: 10.1016/j.bbadis.2008.09.005. Epub 2008 Sep 25.
Insulin and leptin play complementary roles in regulating the consumption, uptake, oxidation and storage of nutrients. Chronic consumption of diets that contain a high proportion of calories from saturated fat induces a progressive deterioration in function of both hormones. Certain rat lines and strains of mice are particularly sensitive to the obesogenic and diabetogenic effects of high fat diets, and have been used extensively to study the developmental progression of insulin and leptin resistance in relation to the increasing adiposity that is characteristic of their response to these diets. Some aspects of the diminished efficacy of each hormone are secondary to increased adiposity but a consensus is emerging to support the view that direct effects of dietary components or their metabolites, independent of the resulting obesity, play important roles in development of insulin and leptin resistance. In this minireview, we will examine the implications of crosstalk between leptin and insulin signaling during the development of diet-induced obesity, emphasizing potential interactions between pathways that occur among target sites, and exploring how these interactions may influence the progression of obesity and diabetes.
胰岛素和瘦素在调节营养物质的消耗、摄取、氧化和储存方面发挥着互补作用。长期食用富含饱和脂肪热量的饮食会导致这两种激素的功能逐渐恶化。某些大鼠品系和小鼠品系对高脂肪饮食的致肥胖和致糖尿病作用特别敏感,并已被广泛用于研究胰岛素和瘦素抵抗的发展进程,这与它们对这些饮食反应所特有的肥胖增加有关。每种激素效力降低的某些方面是肥胖增加的继发结果,但越来越多的共识支持这样一种观点,即饮食成分或其代谢产物的直接作用,独立于由此产生的肥胖,在胰岛素和瘦素抵抗的发展中起重要作用。在这篇小型综述中,我们将研究饮食诱导肥胖发展过程中瘦素和胰岛素信号之间相互作用的影响,强调靶位点之间发生的信号通路之间的潜在相互作用,并探讨这些相互作用如何影响肥胖和糖尿病的进展。