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皮质酮和氢化可的松对人 Kv1.5 通道电流的抑制作用。

Inhibitory effects of cortisone and hydrocortisone on human Kv1.5 channel currents.

机构信息

Department of Physiology, Institute of Bioscience and Biotechnology, BK21 plus Graduate Program, Kangwon National University School of Medicine, Chuncheon 200-701, Republic of Korea.

Department of Physiology, Institute of Bioscience and Biotechnology, BK21 plus Graduate Program, Kangwon National University School of Medicine, Chuncheon 200-701, Republic of Korea.

出版信息

Eur J Pharmacol. 2015 Jan 5;746:158-66. doi: 10.1016/j.ejphar.2014.11.007. Epub 2014 Nov 18.

Abstract

Glucocorticoids are the primary hormones that respond to stress and protect organisms from dangerous situations. The glucocorticoids hydrocortisone and its dormant form, cortisone, affect the cardiovascular system with changes such as increased blood pressure and cardioprotection. Kv1.5 channels play a critical role in the maintenance of cellular membrane potential and are widely expressed in pancreatic β-cells, neurons, myocytes, and smooth muscle cells of the pulmonary vasculature. We examined the electrophysiological effects of both cortisone and hydrocortisone on human Kv1.5 channels expressed in Xenopus oocytes using a two-microelectrode voltage clamp technique. Both cortisone and hydrocortisone rapidly and irreversibly suppressed the amplitude of Kv1.5 channel current with IC50 values of 50.2±4.2μM and 33.4±3.2μM, respectively, while sustained the current trace shape of Kv1.5 current. The inhibitory effect of cortisone on Kv1.5 decreased progressively from -10mV to +30mV, while hydrocortisone׳s inhibition of the channel did not change across the same voltage range. Both cortisone and hydrocortisone blocked Kv1.5 channel currents in a non-use-dependent manner and neither altered the channel׳s steady-state activation or inactivation curves. These results show that cortisone and hydrocortisone inhibited Kv1.5 channel currents differently, and that Kv1.5 channels were more sensitive to hydrocortisone than to cortisone.

摘要

糖皮质激素是应对压力和保护生物体免受危险情况的主要激素。糖皮质激素氢化可的松及其休眠形式可的松,通过增加血压和心脏保护等变化影响心血管系统。Kv1.5 通道在维持细胞膜电位方面起着至关重要的作用,并且在胰腺β细胞、神经元、心肌细胞和肺血管平滑肌细胞中广泛表达。我们使用双电极电压钳技术检查了可的松和氢化可的松对在非洲爪蟾卵母细胞中表达的人 Kv1.5 通道的电生理影响。可的松和氢化可的松均快速且不可逆地抑制 Kv1.5 通道电流的幅度,IC50 值分别为 50.2±4.2μM 和 33.4±3.2μM,同时维持 Kv1.5 电流的电流迹线形状。可的松对 Kv1.5 的抑制作用从-10mV 逐渐降低到+30mV,而氢化可的松对通道的抑制作用在相同的电压范围内没有变化。可的松和氢化可的松均以非使用依赖性方式阻断 Kv1.5 通道电流,并且都不改变通道的稳态激活或失活曲线。这些结果表明,可的松和氢化可的松对 Kv1.5 通道电流的抑制作用不同,并且 Kv1.5 通道对氢化可的松比可的松更敏感。

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