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组胺诱导人脐静脉培养内皮细胞产生的内向电流。

Histamine-induced inward currents in cultured endothelial cells from human umbilical vein.

作者信息

Bregestovski P, Bakhramov A, Danilov S, Moldobaeva A, Takeda K

机构信息

Institute of Experimental Cardiology, U.S.S.R. Cardiology Research Center, Moscow.

出版信息

Br J Pharmacol. 1988 Oct;95(2):429-36. doi: 10.1111/j.1476-5381.1988.tb11663.x.

Abstract
  1. The membrane response to applied histamine of cultured endothelial cells from human umbilical vein was studied by use of whole cell and single channel patch clamp techniques. A value of -27 +/- 1.4 mV was found for the resting potential under whole cell current clamp. No voltage-gated currents were seen at either the macroscopic or single channel levels. 2. At holding potentials of -20 to -40 mV, histamine evoked slow rising, long lasting whole cell inward currents. The inward current was associated with depolarization and decreased input resistance. The calcium ionophore A23187 provoked similar whole cell inward currents. 3. Single channel currents were observed in cell-attached and inside-out patches for both histamine and A23187. The single channel conductance was about 20 pS with a mean open time of 5 ms and a reversal potential of 0 mV in symmetrical potassium solutions. Internal sodium blocked outward going currents. 4. For cell-attached patches, histamine-dependent channel activity required external calcium and was also seen when histamine was present in the bath but not the pipette. Recording from inside-out patches revealed that decreases in 'internal' calcium resulted in the disappearance of channel activity. 5. The histamine-dependent inward current appears to involve calcium-dependent activation of cationic channels.
摘要
  1. 运用全细胞和单通道膜片钳技术,研究了人脐静脉培养内皮细胞对所施加组胺的膜反应。在全细胞电流钳制下,静息电位值为-27±1.4 mV。在宏观或单通道水平均未观察到电压门控电流。2. 在-20至-40 mV的钳制电位下,组胺诱发缓慢上升、持续时间长的全细胞内向电流。该内向电流与去极化和输入电阻降低有关。钙离子载体A23187引发类似的全细胞内向电流。3. 在细胞贴附式和内面向外式膜片中均观察到组胺和A23187的单通道电流。在对称钾溶液中,单通道电导约为20 pS,平均开放时间为5 ms,反转电位为0 mV。胞内钠离子阻断外向电流。4. 对于细胞贴附式膜片,组胺依赖性通道活性需要细胞外钙,当组胺存在于浴液而非微管中时也可观察到该活性。从内面向外式膜片记录显示,“胞内”钙的减少导致通道活性消失。5. 组胺依赖性内向电流似乎涉及阳离子通道的钙依赖性激活。

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