Jackson William F
Department of Pharmacology & Toxicology, Michigan State University, East Lansing, MI, USA.
Microcirculation. 2018 Jan;25(1). doi: 10.1111/micc.12421.
VSMCs in resistance arteries and arterioles express a diverse array of K channels with members of the K 1, K 2 and K 7 families being particularly important. Members of the K channel family: (i) are highly expressed in VSMCs; (ii) are active at the resting membrane potential of VSMCs in vivo (-45 to -30 mV); (iii) contribute to the negative feedback regulation of VSMC membrane potential and myogenic tone; (iv) are activated by cAMP-related vasodilators, hydrogen sulfide and hydrogen peroxide; (v) are inhibited by increases in intracellular Ca and vasoconstrictors that signal through G -coupled receptors; (vi) are involved in the proliferative phenotype of VSMCs; and (vii) are modulated by diseases such as hypertension, obesity, the metabolic syndrome and diabetes. Thus, K channels participate in every aspect of the regulation of VSMC function in both health and disease.
阻力动脉和小动脉中的血管平滑肌细胞表达多种钾通道,其中K1、K2和K7家族成员尤为重要。钾通道家族成员:(i) 在血管平滑肌细胞中高度表达;(ii) 在体内血管平滑肌细胞的静息膜电位(-45至-30 mV)时具有活性;(iii) 有助于血管平滑肌细胞膜电位和肌源性张力的负反馈调节;(iv) 被cAMP相关的血管舒张剂、硫化氢和过氧化氢激活;(v) 被细胞内钙增加和通过G偶联受体发出信号的血管收缩剂抑制;(vi) 参与血管平滑肌细胞的增殖表型;(vii) 受到高血压、肥胖、代谢综合征和糖尿病等疾病的调节。因此,钾通道参与了健康和疾病状态下血管平滑肌细胞功能调节的各个方面。