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Membrane potential, chloride exchange, and chloride conductance in Ehrlich mouse ascites tumour cells.

机译:Ehrlich小鼠腹水肿瘤细胞的膜电位,氯离子交换和氯离子传导。

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摘要

1. The steady-state tracer exchange flux of chloride was measured at 10-150 mM external chloride concentration, substituting either lactate or sucrose for chloride. The chloride flux saturates in both cases with a K 1/2 about 50 and 15 mM, respectively. 2. The inhibitory effect of other monovalent anions on the chloride transport was investigated by measuring the 36Cl- efflux into media where either bromide, nitrate, or thiocyanate had been substituted for part of the chloride. The sequence of increasing affinity for the chloride transport system was found to be: Br- less than Cl- less than SCN- = NO3-. 3. The chloride steady-state exchange flux in the presence of nitrate can be described by Michaelis-Menten kinetics with nitrate as a competitive inhibitor of the chloride flux. 4. The apparent activation energy (EA) was determined to be 67 +/- 6.2 kJ/mole, and was constant between 7 and 38 degrees C. 5. The membrane potential (Vm) was measured as a function of the concentration of external K+, substituting K+ for Na+. The transference number of K+ (tK) was estimated from the slope of Vm vs. log10 (K+)e, and tCl and tNa were calculated, neglecting current carried by ions other than Cl-, K+, and Na+. The diffusional net flux of K+ was calculated from the steady-state exchange flux of 42K+, assuming the flux ratio equation to be valid. From this value the K+ conductance and the Na+ and Cl- conductances were calculated. The experiments showed that GCl, GNa, and GK are all about 14 muS/cm2. 6. The net (conductive) chloride permeability derived from the chloride conductance was 4 x 10(-8) cm/sec compared with the apparent permeability of 6 x 10(-7) cm/sec as calculated from the chloride tracer exchange flux. These data suggest that about 95% of the chloride transport is mediated by an electrically silent exchange diffusion. 7. Comparable effects of phloretin (0.25 mM) on the net (conductive) permeability and the apparent permeability to chloride (about 80% inhibition) may indicate that the chloride exchange and conductance pathways are not completely separate and distinct modes of transport, but may involve common elements. The reduced chloride permeability in the presence of phloretin is estimated to be two orders of magnitude larger than the ground permeability of the cell membrane.
机译:1.在外部氯化物浓度为10-150 mM时,用乳酸盐或蔗糖代替氯化物,测量了氯化物的稳态示踪剂交换通量。在这两种情况下,氯化物通量分别以大约为50和15 mM的K 1/2饱和。 2.通过测量36Cl-排入溴化物,硝酸盐或硫氰酸盐已替代部分氯离子的介质中,研究了其他一价阴离子对氯离子迁移的抑制作用。发现对氯离子转运系统的亲和力增加的顺序为:Br-小于Cl-小于SCN- = NO3-。 3.硝酸盐存在下的氯化物稳态交换通量可通过Michaelis-Menten动力学描述,其中硝酸盐是氯化物通量的竞争性抑制剂。 4.表观活化能(EA)被确定为67 +/- 6.2 kJ / mole,并且在7到38摄氏度之间恒定。5.膜电位(Vm)被测量为外部浓度的函数K +,用K +代替Na +。由Vm对log 10(K +)e的斜率估算K +(tK)的迁移数,并计算tCl和tNa,忽略除Cl-,K +和Na +以外的离子携带的电流。假设通量比方程有效,则由42K +的稳态交换通量计算出K +的扩散净通量。根据该值,计算出K +电导以及Na +和Cl-电导。实验表明,GCl,GNa和GK均约为14μS/ cm2。 6.源自氯化物电导的净(导电)氯化物渗透率为4 x 10(-8)cm / sec,而根据氯化物示踪剂交换通量计算的表观渗透率为6 x 10(-7)cm / sec。这些数据表明,约95%的氯化物传输是通过电沉默交换扩散介导的。 7.伞菌素(0.25 mM)对净(导电)通透性和对氯的表观通透性(约80%抑制)的可比作用可能表明,氯离子交换和电导途径不是完全分开和不同的运输方式,但可能涉及共同要素。估计在存在促视黄素的情况下降低的氯离子渗透率比细胞膜的地面渗透率大两个数量级。

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