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大鼠皮质集合管中的全细胞电流:低钠饮食增加氨氯地平敏感性电导。

Whole-cell currents in rat cortical collecting tubule: low-Na diet increases amiloride-sensitive conductance.

作者信息

Frindt G, Sackin H, Palmer L G

机构信息

Department of Physiology and Biophysics, Cornell University Medical College, New York, New York 10021.

出版信息

Am J Physiol. 1990 Mar;258(3 Pt 2):F562-7. doi: 10.1152/ajprenal.1990.258.3.F562.

Abstract

Individual principal cells within the rat cortical collecting tubule were studied under voltage-clamp conditions using the whole-cell variation of the patch-clamp technique. Isolated tubules were split to expose the apical membrane surface and bathed in NaCl medium at 23 degrees C. When carboxyfluorescein was included in the patch pipette, the dye diffused rapidly into the cell being clamped but did not spread to neighboring cells, indicating a lack of cell-to-cell coupling. Average cell capacitance under whole-cell clamp conditions with KCl in the pipette was 18 +/- 2 pF (n = 10 cells) in rats maintained on a normal diet, consistent with that expected from morphometric measurements of cell surface area. The capacitance increased to 36 +/- 7 pF (n = 8 cells) for rats kept on a low-Na diet, indicating that cell membrane area was increased under these conditions. The amiloride-sensitive whole-cell conductance (GNa), assumed to equal the conductance through apical Na channels, was determined as the slope of the current-voltage relation near zero holding potential. GNa was 6.0 +/- 1.7 nS/cell (n = 12) for rats maintained on a low-Na diet compared with 0.06 +/- 0.08 nS/cell (n = 13) for rats kept on a normal diet. The amiloride-insensitive whole-cell conductance averaged 9.1 +/- 2.0 nS/cell, with no significant difference between low-Na and normal groups. Sodium channel density (N) was estimated from GNa, the mean open probability of the channel, and the single-channel conductance. N equals 3,000 channels/cells in rats on a low-Na diet compared with N less than 100 channels/cell for rats on a normal diet.

摘要

采用膜片钳技术的全细胞记录模式,在电压钳条件下对大鼠皮质集合管中的单个主细胞进行了研究。将分离的肾小管切开以暴露顶端膜表面,并置于23℃的NaCl培养基中。当膜片电极内液中含有羧基荧光素时,染料迅速扩散到被钳制的细胞内,但未扩散到相邻细胞,这表明不存在细胞间耦联。在正常饮食的大鼠中,膜片电极内液为KCl时,全细胞钳制条件下的平均细胞电容为18±2 pF(n = 10个细胞),这与根据细胞表面积形态测量所预期的值一致。对于低钠饮食的大鼠,电容增加到36±7 pF(n = 8个细胞),表明在这些条件下细胞膜面积增加。假定等于通过顶端钠通道的电导的氨氯地平敏感全细胞电导(GNa),被确定为接近零钳制电位时电流-电压关系的斜率。低钠饮食的大鼠GNa为6.0±1.7 nS/细胞(n = 12),而正常饮食的大鼠为0.06±0.08 nS/细胞(n = 13)。氨氯地平不敏感全细胞电导平均为9.1±2.0 nS/细胞,低钠组和正常组之间无显著差异。钠通道密度(N)由GNa、通道的平均开放概率和单通道电导估算得出。低钠饮食的大鼠N等于3000个通道/细胞,而正常饮食的大鼠N小于100个通道/细胞。

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