Faculty of Medicine, Institute of Pharmacology and Clinical Pharmacology, Comenius University, Sasinkova 4, 811 08 Bratislava, Slovakia.
Centre of Experimental Medicine, v.v.i., Institute of Normal and Pathological Physiology, Slovak Academy of Sciences, Sienkiewiczova 1, 813 71 Bratislava, Slovakia.
Int J Mol Sci. 2024 May 7;25(10):5093. doi: 10.3390/ijms25105093.
Identifying alterations caused by aging could be an important tool for improving the diagnosis of cardiovascular diseases. Changes in vascular tone regulation involve various mechanisms, like NO synthase activity, activity of the sympathetic nervous system, production of prostaglandin, endothelium-dependent relaxing, and contracting factors, etc. Surprisingly, Ca-dependent Cl channels (CaCCs) are involved in all alterations of the vascular tone regulation mentioned above. Furthermore, we discuss these mechanisms in the context of ontogenetic development and aging. The molecular and electrophysiological mechanisms of CaCCs activation on the cell membrane of the vascular smooth muscle cells (VSMC) and endothelium are explained, as well as the age-dependent changes that imply the activation or inhibition of CaCCs. In conclusion, due to the diverse intracellular concentration of chloride in VSMC and endothelial cells, the activation of CaCCs depends, in part, on intracellular Ca concentration, and, in part, on voltage, leading to fine adjustments of vascular tone. The activation of CaCCs declines during ontogenetic development and aging. This decline in the activation of CaCCs involves a decrease in protein level, the impairment of Ca influx, and probably other alterations in vascular tone regulation.
鉴定由衰老引起的改变可能是改善心血管疾病诊断的重要工具。血管张力调节的变化涉及多种机制,如一氧化氮合酶活性、交感神经系统活性、前列腺素的产生、内皮依赖性舒张和收缩因子等。令人惊讶的是,Ca 依赖性 Cl 通道(CaCCs)参与了上述所有血管张力调节的改变。此外,我们还讨论了这些机制在个体发育和衰老过程中的作用。解释了 CaCCs 在血管平滑肌细胞(VSMC)和内皮细胞膜上的激活的分子和电生理机制,以及年龄依赖性变化,这些变化暗示了 CaCCs 的激活或抑制。总之,由于 VSMC 和内皮细胞中氯离子的细胞内浓度不同,CaCCs 的激活部分取决于细胞内 Ca 浓度,部分取决于电压,从而导致血管张力的精细调节。CaCCs 的激活在个体发育和衰老过程中下降。CaCCs 激活的这种下降涉及蛋白水平的降低、Ca 内流的损害,以及血管张力调节的其他可能改变。