Lipid accumulation in non-adipose tissue and lipotoxicity

被引:381
作者
van Herpen, N. A. [1 ,2 ]
Schrauwen-Hinderling, V. B. [1 ]
机构
[1] Univ Maastricht, Dept Human Biol, Nutr & Toxicol Res Inst Maastricht, NL-6200 MD Maastricht, Netherlands
[2] Top Inst Food & Nutr, NL-6700 AN Wageningen, Netherlands
关键词
lipid accumulation; non-adipose tissue; lipotoxicity; ectopic fat;
D O I
10.1016/j.physbeh.2007.11.049
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
Obesity is a well-known risk factor for the development of type 2 diabetes mellitus and cardiovascular disease. importantly, obesity is not only associated with lipid accumulation in adipose tissue, but also in non-adipose tissues. The latter is also known as ectopic lipid accumulation and may be a possible link between obesity and its comorbidities such as insulin resistance, type 2 diabetes mellitus and cardiovascular disease. In skeletal muscle and liver, lipid accumulation has been associated with the development of insulin resistance, an early hallmark of developing type 2 diabetes mellitus. More specifically, accumulation of intermediates of lipid metabolism, such as diacylglycerol (DAG) and Acyl-CoA have been shown to interfere with insulin signaling in these tissues. initially, muscular and hepatic insulin resistance can be overcome by an increased insulin production by the pancreas, resulting in hyperinsulinemia. However, during the progression towards overt type 2 diabetes, pancreatic failure occurs resulting in reduced insulin production. Interestingly, also in the pancreas lipid accumulation has been shown to precede dysfunction. Finally, accumulation of fat in the heart has been associated with cardiac dysfunction and heart failure, which may be an explanation for diabetic cardiomyopathy. Taken together, we conclude that evidence for deleterious effects of lipid accumulation in non-adipose tissue (lipotoxicity) is strong. However, while ample human data is available for skeletal muscle and the liver, future research should focus on lipid accumulation in the pancreas and the heart. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:231 / 241
页数:11
相关论文
共 122 条
[1]   Recent concepts in non-alcoholic fatty liver disease [J].
Adams, LA ;
Angulo, P .
DIABETIC MEDICINE, 2005, 22 (09) :1129-1133
[2]  
Aggarwal BB, 1996, EUR CYTOKINE NETW, V7, P93
[3]  
[Anonymous], UPD TREND TABL INCL
[4]   Effects of intravenous and dietary lipid challenge on intramyocellular lipid content and the relation with insulin sensitivity in humans [J].
Bachmann, OP ;
Dahl, DB ;
Brechtel, K ;
Machann, J ;
Haap, M ;
Maier, T ;
Loviscach, M ;
Stumvoll, M ;
Claussen, CA ;
Schick, F ;
Häring, HU ;
Jacob, S .
DIABETES, 2001, 50 (11) :2579-2584
[5]   Pioglitazone reduces hepatic fat content and augments splanchnic glucose uptake in patients with type 2 diabetes [J].
Bajaj, M ;
Suraamornkul, S ;
Pratipanawatr, T ;
Hardies, LJ ;
Pratipanawatr, W ;
Glass, L ;
Cersosimo, E ;
Miyazaki, Y ;
DeFronzo, RA .
DIABETES, 2003, 52 (06) :1364-1370
[6]   Lipoprotein secretion and triglyceride stores in the heart [J].
Björkegren, J ;
Véniant, M ;
Kim, SK ;
Withycombe, SK ;
Wood, PA ;
Hellerstein, MK ;
Neese, RA ;
Young, SG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (42) :38511-38517
[7]   Effects of acute changes of plasma free fatty acids on intramyocellular fat content and insulin resistance in healthy subjects [J].
Boden, G ;
Lebed, B ;
Schatz, M ;
Homko, C ;
Lemieux, S .
DIABETES, 2001, 50 (07) :1612-1617
[8]   In vivo determination of intra-myocellular lipids in human muscle by means of localized H-1-MR-spectroscopy [J].
Boesch, C ;
Slotboom, J ;
Hoppeler, H ;
Kreis, R .
MAGNETIC RESONANCE IN MEDICINE, 1997, 37 (04) :484-493
[9]   Chronic exposure to free fatty acid reduces pancreatic β cell insulin content by increasing basal insulin secretion that is not compensated for by a corresponding increase in proinsulin biosynthesis translation [J].
Bollheimer, LC ;
Skelly, RH ;
Chester, MW ;
McGarry, JD ;
Rhodes, CJ .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (05) :1094-1101
[10]   Long chain coenzyme A esters activate the pore-forming subunit (Kir6.2) of the ATP-regulated potassium channel [J].
Bränström, R ;
Leibiger, IB ;
Leibiger, B ;
Corkey, BE ;
Berggren, PO ;
Larsson, O .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (47) :31395-31400