Vascular Disease and Therapeutics Group, Basil Hetzel Institute, Queen Elizabeth Hospital, University of Adelaide, Adelaide, South Australia, Australia.
Curr Opin Cardiol. 2010 Jul;25(4):329-34. doi: 10.1097/HCO.0b013e328339f191.
We focus on the molecular and cellular basis of the improvement in myocardial energetics, which might represent an attractive therapeutic option in some forms of acute and chronic heart disease.
Myocardial dysfunction, whether related to left ventricular hypertrophy, heart failure or myocardial ischaemia, is frequently associated with impairment of myocardial energy balance. It is now apparent that this energetic impairment plays a pivotal role, not only in the evolution and outcomes of these disorders but also frequently in their pathogenesis. Despite the fact that energetic impairment may arise for many complex reasons, and the difficulty both in assessing the impairment in vivo and in determining its precise mechanism(s), a number of drugs have become available for treatment of ischaemia and heart failure, as well as potentially for limitation of pathological left ventricular hypertrophy, which act primarily by altering myocardial metabolism so as to improve energetic status. Recent studies with perhexiline and trimetazidine, agents which induce a 'metabolic shift' from long-chain fatty acid to glucose utilization, have demonstrated the utility of this therapeutic principle.
There is ongoing need for more complete mechanistic understanding of the 'metabolic agents', as well as for the large-scale clinical trials of their impact on health outcomes.
我们专注于改善心肌能量代谢的分子和细胞基础,这可能代表了某些形式的急性和慢性心脏病的一种有吸引力的治疗选择。
心肌功能障碍,无论是与左心室肥厚、心力衰竭还是心肌缺血有关,通常都伴有心肌能量平衡的损害。现在很明显,这种能量损伤不仅在这些疾病的演变和结果中起着关键作用,而且在其发病机制中也经常起着关键作用。尽管能量损伤可能由于许多复杂的原因而产生,并且在体内评估损伤和确定其确切机制方面存在困难,但已有许多药物可用于治疗缺血和心力衰竭,以及潜在地限制病理性左心室肥厚,这些药物主要通过改变心肌代谢来改善能量状态。最近对丙戊茶碱和曲美他嗪的研究表明,这些药物诱导了从长链脂肪酸到葡萄糖利用的“代谢转变”,证明了这一治疗原则的实用性。
人们仍然需要更全面地了解“代谢药物”的机制,以及需要进行大规模的临床试验来评估它们对健康结果的影响。