Department of Pharmacology and Toxicology, Faculty of Pharmacy, Comenius University in Bratislava, Odbojarov 10, 83232 Bratislava, Slovakia.
Institute of Pharmacology and Clinical Pharmacology, Faculty of Medicine, Comenius University in Bratislava, Spitalska 24, 81372 Bratislava, Slovakia.
Medicina (Kaunas). 2019 Jul 16;55(7):380. doi: 10.3390/medicina55070380.
: Many studies indicate the involvement of transient receptor potential (TRP) channels in the development of heart hypertrophy. However, the data is often conflicted and has originated in animal models. Here, we provide systematic analysis of TRP channels expression in human failing myocardium. : Left-ventricular tissue samples were isolated from explanted hearts of NYHA III-IV patients undergoing heart transplants (n = 43). Quantitative real-time PCR was performed to assess the mRNA levels of TRPC, TRPM and TRPV channels. Analysis of functional, clinical and biochemical data was used to confirm an end-stage heart failure diagnosis. Compared to myocardium samples from healthy donor hearts (n = 5), we detected a distinct increase in the expression of TRPC1, TRPC5, TRPM4 and TRPM7, and decreased expression of TRPC4 and TRPV2. These changes were not dependent on gender, clinical or biochemical parameters, nor functional parameters of the heart. We detected, however, a significant correlation of TRPC1 and MEF2c expression. : The end-stage heart failure displays distinct expressional changes of TRP channels. Our findings provide a systematic description of TRP channel expression in human heart failure. The results highlight the complex interplay between TRP channels and the need for deeper analysis of early stages of hypertrophy and heart failure development.
许多研究表明瞬时受体电位(TRP)通道参与了心肌肥厚的发生。然而,这些数据往往存在冲突,并且来源于动物模型。在这里,我们对人类衰竭心肌中 TRP 通道的表达进行了系统分析。
从接受心脏移植(n = 43)的 NYHA III-IV 级患者的心脏中分离出左心室组织样本。进行实时定量 PCR 以评估 TRPC、TRPM 和 TRPV 通道的 mRNA 水平。对功能、临床和生化数据的分析用于确认终末期心力衰竭的诊断。与来自健康供体心脏的心肌样本(n = 5)相比,我们检测到 TRPC1、TRPC5、TRPM4 和 TRPM7 的表达明显增加,而 TRPC4 和 TRPV2 的表达降低。这些变化不依赖于性别、临床或生化参数,也不依赖于心脏的功能参数。然而,我们检测到 TRPC1 和 MEF2c 表达之间存在显著相关性。
终末期心力衰竭显示出 TRP 通道的明显表达变化。我们的研究结果提供了人类心力衰竭中 TRP 通道表达的系统描述。这些结果强调了 TRP 通道之间的复杂相互作用,需要对心肌肥厚和心力衰竭发展的早期阶段进行更深入的分析。