The islet circadian clock: entrainment mechanisms, function and role in glucose homeostasis

被引:24
|
作者
Rakshit, K. [1 ]
Qian, J. [2 ]
Colwell, C. S. [2 ]
Matveyenko, A. V. [1 ]
机构
[1] Mayo Clin, Sch Med, Dept Physiol & Biomed Engn, Rochester, MN 55905 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Psychiat & Biobehav Sci, Lab Circadian & Sleep Med, Los Angeles, CA 90095 USA
来源
基金
美国国家卫生研究院;
关键词
-cell; circadian clock; circadian disruption; insulin secretion; islet; T2DM; BETA-CELL FAILURE; INSULIN-SECRETION; ACCELERATES DEVELOPMENT; DIURNAL-VARIATION; OXIDATIVE STRESS; SLEEP DURATION; METABOLISM; DISRUPTION; TOLERANCE; RHYTHMS;
D O I
10.1111/dom.12523
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Circadian regulation of glucose homeostasis and insulin secretion has long been appreciated as an important feature of metabolic control in humans. Circadian disruption is becoming increasingly prevalent in today's society and is likely responsible in part for the considerable rise in type 2 diabetes (T2DM) and metabolic syndrome worldwide. Thus, understanding molecular mechanisms driving the inter-relationship between circadian disruption and T2DM is important in context of disease prevention and therapeutics. In this regard, the goal of this article is to highlight the role of the circadian system, and islet circadian clocks in particular, as potential regulators of -cell function and survival. To date, studies have shown that islet clocks respond to changes in feeding patterns, and regulate a multitude of critical cellular processes in insulin secreting -cells (e.g. insulin exocytosis, mitochondrial function and response to oxidative stress). Subsequently, either genetic or environmental disruption of normal islet clock performance compromises -cell function and leads to loss of glycaemic control. Future work is warranted to further unravel the role of circadian clocks in human islet function in health and contributions to pathogenesis of T2DM.
引用
收藏
页码:115 / 122
页数:8
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