Wang Ling-Peng, Luo Jian, Hu Hai-Feng, Zhang Li, Li Ya-Li, Ai Li-Man, Wang Yu-Ling, Ma Yi-Tong, Mu Hu-Yati, Hou Yue-Mei
Department of Cardiology of The First Affiliated Hospital, Xinjiang Medical University Urumqi 830000, Xinjiang, China.
Department of Internal Medicine (VIP) of The First Affiliated Hospital, Xinjiang Medical University Urumqi 830000, Xinjiang, China.
Int J Clin Exp Med. 2015 Feb 15;8(2):2506-15. eCollection 2015.
Our previous studies showed that expression and functional profile of voltage-dependent potassium channels Kv1.3 were increased in lymphocytes of spontaneously hypertensive rats (SHR) compared to normotensive rats, suggesting a crucial role for lymphocyte Kv1.3 in the development of hypertension. Here, we further investigated whether the expression and functional profile of Kv1.3 was related to increased blood pressure in SHR with age of 4, 8, 16 and 24 wk.
Systolic blood pressure was measured through pressure device around the tail. mRNA and protein expression were assessed by real-time PCR and western blot in lymphocytes of SHR. Current density of Kv channels in lymphocytes was measured by patch-clamp.
Systolic blood pressure was elevated in an age-dependent manner (ANOVA P < 0.05). mRNA and protein level of Kv1.3 were significantly increased in an age-dependent manner in lymphocyte of SHR (ANOVA P < 0.05). Moreover, the current density of Kv was dramatically enhanced in an age-dependent manner (ANOVA P < 0.05).
The systolic blood pressure positively correlated with expression as well as current density of potassium channels in lymphocytes of SHR at age of 8, 16 and 24 wk. In conclusion, Kv1.3 channels were upregulated in an age-dependent manner in SHR and correlates with systolic blood pressure during aging. The present study implies that Kv1.3 blockers may be applied as a therapeutic treatment for the development of hypertension during aging.
我们之前的研究表明,与正常血压大鼠相比,自发性高血压大鼠(SHR)淋巴细胞中电压依赖性钾通道Kv1.3的表达和功能特征增加,提示淋巴细胞Kv1.3在高血压发展中起关键作用。在此,我们进一步研究了4、8、16和24周龄SHR中Kv1.3的表达和功能特征是否与血压升高有关。
通过尾部周围的压力装置测量收缩压。采用实时PCR和蛋白质印迹法评估SHR淋巴细胞中的mRNA和蛋白质表达。通过膜片钳测量淋巴细胞中Kv通道的电流密度。
收缩压以年龄依赖性方式升高(方差分析P<0.05)。SHR淋巴细胞中Kv1.3的mRNA和蛋白质水平以年龄依赖性方式显著增加(方差分析P<0.05)。此外,Kv的电流密度以年龄依赖性方式显著增强(方差分析P<0.05)。
8、16和24周龄SHR淋巴细胞中收缩压与钾通道的表达及电流密度呈正相关。总之,Kv1.3通道在SHR中以年龄依赖性方式上调,并与衰老过程中的收缩压相关。本研究提示Kv1.3阻滞剂可能作为衰老过程中高血压发展的一种治疗方法。