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在高串联电阻条件下,使用双全细胞电压钳技术准确测量电耦合细胞之间的连接电导。

Accurate measurement of junctional conductance between electrically coupled cells with dual whole-cell voltage-clamp under conditions of high series resistance.

机构信息

Department of Biomedicine, University of Bergen, Jonas Lies vei 91, N-5009 Bergen, Norway.

出版信息

J Neurosci Methods. 2010 Mar 15;187(1):13-25. doi: 10.1016/j.jneumeth.2009.12.003. Epub 2010 Jan 14.

Abstract

Accurate measurement of the junctional conductance (G(j)) between electrically coupled cells can provide important information about the functional properties of coupling. With the development of tight-seal, whole-cell recording, it became possible to use dual, single-electrode voltage-clamp recording from pairs of small cells to measure G(j). Experiments that require reduced perturbation of the intracellular environment can be performed with high-resistance pipettes or the perforated-patch technique, but an accompanying increase in series resistance (R(s)) compromises voltage-clamp control and reduces the accuracy of G(j) measurements. Here, we present a detailed analysis of methodologies available for accurate determination of steady-state G(j) and related parameters under conditions of high R(s), using continuous or discontinuous single-electrode voltage-clamp (CSEVC or DSEVC) amplifiers to quantify the parameters of different equivalent electrical circuit model cells. Both types of amplifiers can provide accurate measurements of G(j), with errors less than 5% for a wide range of R(s) and G(j) values. However, CSEVC amplifiers need to be combined with R(s)-compensation or mathematical correction for the effects of nonzero R(s) and finite membrane resistance (R(m)). R(s)-compensation is difficult for higher values of R(s) and leads to instability that can damage the recorded cells. Mathematical correction for R(s) and R(m) yields highly accurate results, but depends on accurate estimates of R(s) throughout an experiment. DSEVC amplifiers display very accurate measurements over a larger range of R(s) values than CSEVC amplifiers and have the advantage that knowledge of R(s) is unnecessary, suggesting that they are preferable for long-duration experiments and/or recordings with high R(s).

摘要

准确测量电耦合细胞的连接电导 (G(j)) 可以提供关于耦合功能特性的重要信息。随着紧密密封、全细胞记录的发展,使用双、单电极电压钳记录从小型细胞对来测量 G(j) 成为可能。需要减少对细胞内环境干扰的实验可以使用高阻管或穿孔贴片技术进行,但伴随而来的串联电阻 (R(s)) 的增加会影响电压钳控制并降低 G(j) 测量的准确性。在这里,我们提出了一种详细的分析方法,用于在高 R(s) 条件下准确确定稳态 G(j) 和相关参数,使用连续或不连续单电极电压钳 (CSEVC 或 DSEVC) 放大器来量化不同等效电路模型细胞的参数。这两种类型的放大器都可以提供 G(j) 的准确测量,对于广泛的 R(s) 和 G(j) 值,误差小于 5%。然而,CSEVC 放大器需要与 R(s) 补偿或数学校正相结合,以消除非零 R(s) 和有限膜电阻 (R(m)) 的影响。对于更高的 R(s) 值,R(s) 补偿会变得困难,并导致可能损坏记录细胞的不稳定性。对 R(s) 和 R(m) 的数学校正可以产生非常准确的结果,但取决于整个实验中对 R(s) 的准确估计。DSEVC 放大器在比 CSEVC 放大器更大的 R(s) 值范围内显示出非常准确的测量结果,并且具有不需要了解 R(s) 的优势,这表明它们更适合长时间实验和/或具有高 R(s) 的记录。

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