Myocardial Fatty Acid Metabolism in Health and Disease

2010 ◽  
Vol 90 (1) ◽  
pp. 207-258 ◽  
Author(s):  
Gary D. Lopaschuk ◽  
John R. Ussher ◽  
Clifford D. L. Folmes ◽  
Jagdip S. Jaswal ◽  
William C. Stanley

There is a constant high demand for energy to sustain the continuous contractile activity of the heart, which is met primarily by the β-oxidation of long-chain fatty acids. The control of fatty acid β-oxidation is complex and is aimed at ensuring that the supply and oxidation of the fatty acids is sufficient to meet the energy demands of the heart. The metabolism of fatty acids via β-oxidation is not regulated in isolation; rather, it occurs in response to alterations in contractile work, the presence of competing substrates (i.e., glucose, lactate, ketones, amino acids), changes in hormonal milieu, and limitations in oxygen supply. Alterations in fatty acid metabolism can contribute to cardiac pathology. For instance, the excessive uptake and β-oxidation of fatty acids in obesity and diabetes can compromise cardiac function. Furthermore, alterations in fatty acid β-oxidation both during and after ischemia and in the failing heart can also contribute to cardiac pathology. This paper reviews the regulation of myocardial fatty acid β-oxidation and how alterations in fatty acid β-oxidation can contribute to heart disease. The implications of inhibiting fatty acid β-oxidation as a potential novel therapeutic approach for the treatment of various forms of heart disease are also discussed.

1997 ◽  
Vol 24 (5) ◽  
pp. 461-464
Author(s):  
Tjibbe de Groot ◽  
Bart Maris ◽  
Carine Boonen ◽  
Guy Bormans ◽  
Luc Mortelmans ◽  
...  

2009 ◽  
Vol 34 (3) ◽  
pp. 315-322 ◽  
Author(s):  
Gregory R. Steinberg

During moderate-intensity exercise, fatty acids are the predominant substrate for working skeletal muscle. The release of fatty acids from adipose tissue stores, combined with the ability of skeletal muscle to actively fine tune the gradient between fatty acid and carbohydrate metabolism, depending on substrate availability and energetic demands, requires a coordinated system of metabolic control. Over the past decade, since the discovery that AMP-activated protein kinase (AMPK) was increased in accordance with exercise intensity, there has been significant interest in the proposed role of this ancient stress-sensing kinase as a critical integrative switch controlling metabolic responses during exercise. In this review, studies examining the role of AMPK as a regulator of fatty acid metabolism in both adipose tissue and skeletal muscle during exercise will be discussed. Exercise induces activation of AMPK in adipocytes and regulates triglyceride hydrolysis and esterfication through phosphorylation of hormone sensitive lipase (HSL) and glycerol-3-phosphate acyl-transferase, respectively. In skeletal muscle, exercise-induced activation of AMPK is associated with increases in fatty acid uptake, phosphorylation of HSL, and increased fatty acid oxidation, which is thought to occur via the acetyl-CoA carboxylase-malony-CoA-CPT-1 signalling axis. Despite the importance of AMPK in regulating fatty acid metabolism under resting conditions, recent evidence from transgenic models of AMPK deficiency suggest that alternative signalling pathways may also be important for the control of fatty acid metabolism during exercise.


2004 ◽  
Vol 68 (6) ◽  
pp. 595-598 ◽  
Author(s):  
Nobuaki Shikama ◽  
Tomoo Nakagawa ◽  
Yasuo Takiguchi ◽  
Nobuyuki Aotsuka ◽  
Yoichi Kuwabara ◽  
...  

1995 ◽  
Vol 2 (3) ◽  
pp. 256-266 ◽  
Author(s):  
N TAMAKI ◽  
Y FUJIBAYASHI ◽  
Y MAGATA ◽  
Y YONEKURA ◽  
J KONISHI

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