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Novel Heart Failure Therapy Targeting Transcriptional Pathway in Cardiomyocytes by a Natural Compound, Curcumin

机译:天然化合物姜黄素靶向心肌细胞转录途径的新型心力衰竭治疗

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Hypertensive heart disease and post-myocardial-infarction heart failure (HF) are leading causes of cardiovascular mortality in industrialized countries. To date, pharmacological agents that block cell surface receptors for neurohormonal factors have been used, but despite such conventional therapy, HF is increasing in incidence worldwide. During the development and deterioration process of HF, cardiomyocytes undergo maladaptive hypertrophy, which markedly influences their gene expression. Regulation of histone acetylation by histone acetyltransferase (eg, p300) and histone deacetylase plays an important role in this process. Increasing evidence suggests that the excessive acetylation of cardiomyocyte nuclei is a hallmark of maladaptive cardiomyocyte hypertrophy. Curcumin inhibits p300-mediated nuclear acetylation, suggesting its usefulness in HF treatment. Clinical application of this natural compound, which is inexpensive and safe, should be established in the near future.??( Circ J ?2010; 74: 1059?-?1066)
机译:高血压心脏病和心肌梗死后心力衰竭(HF)是工业化国家心血管疾病死亡的主要原因。迄今为止,已经使用了阻断神经激素因子的细胞表面受体的药理剂,但是尽管进行了这种常规治疗,HF在世界范围内的发病率仍在增加。在HF的发生和恶化过程中,心肌细胞经历了适应不良的肥大,从而显着影响其基因表达。组蛋白乙酰转移酶(例如p300)和组蛋白脱乙酰酶对组蛋白乙酰化的调节在该过程中起重要作用。越来越多的证据表明,心肌细胞核过度乙酰化是适应不良的心肌肥大的标志。姜黄素抑制p300介导的核乙酰化,表明其可用于HF治疗。这种廉价,安全的天然化合物的临床应用应在不久的将来确立。(Circ J?2010; 74:1059?-?1066)

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