Cardiovascular Research Group, Mazankowski Alberta Heart Institute, University of Alberta, Alberta T6G 2S2, Canada.
Physiol Rev. 2010 Jan;90(1):207-58. doi: 10.1152/physrev.00015.2009.
There is a constant high demand for energy to sustain the continuous contractile activity of the heart, which is met primarily by the beta-oxidation of long-chain fatty acids. The control of fatty acid beta-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 beta-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 beta-oxidation of fatty acids in obesity and diabetes can compromise cardiac function. Furthermore, alterations in fatty acid beta-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 beta-oxidation and how alterations in fatty acid beta-oxidation can contribute to heart disease. The implications of inhibiting fatty acid beta-oxidation as a potential novel therapeutic approach for the treatment of various forms of heart disease are also discussed.
心脏的持续收缩活动需要持续的能量供应,这主要通过长链脂肪酸的β氧化来满足。脂肪酸β氧化的控制非常复杂,旨在确保脂肪酸的供应和氧化足以满足心脏的能量需求。脂肪酸通过β氧化的代谢不是孤立调节的;而是响应于收缩工作的改变、竞争底物的存在(即葡萄糖、乳酸、酮体、氨基酸)、激素环境的变化以及氧供应的限制而发生的。脂肪酸代谢的改变可导致心脏病理学。例如,肥胖和糖尿病中脂肪酸的过度摄取和β氧化可损害心脏功能。此外,在缺血期间和之后以及在衰竭的心脏中脂肪酸β氧化的改变也可导致心脏病理学。本文综述了心肌脂肪酸β氧化的调节以及脂肪酸β氧化的改变如何导致心脏病。还讨论了抑制脂肪酸β氧化作为治疗各种形式心脏病的潜在新治疗方法的意义。