Eisenberg R S
J Gen Physiol. 1967 Jul;50(6):1785-806. doi: 10.1085/jgp.50.6.1785.
The input impedance of muscle fibers of the crab was determined with microelectrodes over the frequency range 1 cps to 10 kc/sec. Care was taken to analyze, reduce, and correct for capacitive artifact. One dimensional cable theory was used to determine the properties of the equivalent circuit of the membrane admittance, and the errors introduced by the neglect of the three dimensional spread of current are discussed. In seven fibers the equivalent circuit of an element of the membrane admittance must contain a DC path and two capacitances, each in series with a resistance. In two fibers, the element of membrane admittance could be described by one capacitance in parallel with a resistance. In several fibers there was evidence for a third very large capacitance. The values of the elements of the equivalent circuit depend on which of several equivalent circuits is chosen. The circuit (with a minimum number of elements) that was considered most reasonably consistent with the anatomy of the fiber has two branches in parallel: one branch having a resistance R(e) in series with a capacitance C(e); the other branch having a resistance R(b) in series with a parallel combination of a resistance R(m) and a capacitance C(m). The average circuit values (seven fibers) for this model, treating the fiber as a cylinder of sarcolemma without infoldings or tubular invaginations, are R(e) = 21 ohm cm(2); C(e) = 47 microf/cm(2); R(b) = 10.2 ohm cm(2); R(m) = 173 ohm cm(2); C(m) = 9.0 microf/cm(2). The relation of this equivalent circuit and another with a nonminimum number of circuit elements to the fine structure of crab muscle is discussed. In the above equivalent circuit R(m) and C(m) are attributed to the sarcolemma; R(e) and C(e), to the sarcotubular system; and R(b), to the amorphous material found around crab fibers. Estimates of actual surface area of the sarcolemma and sarcotubular system permit the average circuit values to be expressed in terms of unit membrane area. The values so expressed are consistent with the dielectric properties of predominantly lipid membranes.
利用微电极在1 cps至10 kc/秒的频率范围内测定了蟹肌肉纤维的输入阻抗。已注意分析、减少并校正电容性伪迹。使用一维电缆理论来确定膜导纳等效电路的特性,并讨论了因忽略电流的三维扩散而引入的误差。在七根纤维中,膜导纳元件的等效电路必须包含一条直流路径和两个电容,每个电容与一个电阻串联。在两根纤维中,膜导纳元件可用一个电容与一个电阻并联来描述。在几根纤维中,有证据表明存在第三个非常大的电容。等效电路元件的值取决于选择几个等效电路中的哪一个。被认为与纤维解剖结构最合理一致的(元件数量最少的)电路有两个并联分支:一个分支有一个电阻R(e)与一个电容C(e)串联;另一个分支有一个电阻R(b)与一个电阻R(m)和一个电容C(m)的并联组合串联。将纤维视为没有褶皱或管状内陷的肌膜圆柱体时,该模型(七根纤维)的平均电路值为:R(e) = 21欧姆·厘米²;C(e) = 47微法/厘米²;R(b) = 10.2欧姆·厘米²;R(m) = 173欧姆·厘米²;C(m) = 9.0微法/厘米²。讨论了这个等效电路以及另一个具有非最小数量电路元件的等效电路与蟹肌肉精细结构的关系。在上述等效电路中R(m)和C(m)归因于肌膜;R(e)和C(e)归因于肌管系统;R(b)归因于在蟹纤维周围发现的无定形物质。对肌膜和肌管系统实际表面积的估计使得平均电路值可以用单位膜面积来表示。如此表示的值与主要为脂质膜的介电特性一致。