Varga Z, Bene L, Pieri C, Damjanovich S, Gáspár R
Department of Biophysics, University Medical School, Debrecen, Hungary.
Biochem Biophys Res Commun. 1996 Jan 26;218(3):828-32. doi: 10.1006/bbrc.1996.0147.
Using flow cytometric membrane potential measurements with the oxonol dye, we determined that 5.7-57 microM juglone depolarizes human lymphocytes in a dose dependent manner. The depolarizing effect of juglone was verified by patch-clamp. Juglone decreased whole-cell n-type K+ currents in human peripheral blood lymphocytes and accelerated inactivation; however, it did not influence the kinetics of activation of the K+ conductance. The percentage increase in K+ channel inactivation rate and the degree of drug induced block was independent of membrane potential, K+ channel block by juglone fully developed within 4 minutes and was not removable by washing with drug free extracellular solution. Blocking of n-type K+ channels by juglone is in concert with its depolarizing effect on human lymphocytes.
使用恶嗪醇染料进行流式细胞术膜电位测量,我们确定5.7 - 57微摩尔胡桃醌以剂量依赖方式使人类淋巴细胞去极化。通过膜片钳验证了胡桃醌的去极化作用。胡桃醌降低了人类外周血淋巴细胞中的全细胞n型钾电流并加速了失活;然而,它并不影响钾离子电导的激活动力学。钾离子通道失活率的增加百分比和药物诱导的阻断程度与膜电位无关,胡桃醌对钾离子通道的阻断在4分钟内完全形成,并且不能通过用无药物的细胞外溶液冲洗而消除。胡桃醌对n型钾离子通道的阻断与其对人类淋巴细胞的去极化作用一致。