Institute of Clinical Neurosciences, Royal Prince Alfred Hospital and The University of Sydney, Sydney, Australia.
J Physiol. 2010 Jul 1;588(Pt 13):2503-15. doi: 10.1113/jphysiol.2010.190884. Epub 2010 May 17.
This study investigated the excitability and accommodative properties of low-threshold human motor axons to test whether these motor axons have greater expression of the persistent Na(+) conductance, I(NaP). Computer-controlled threshold tracking was used to study 22 single motor units and the data were compared with compound motor potentials of various amplitudes recorded in the same experimental session. Detailed comparisons were made between the single units and compound potentials that were 40% or 5% of maximal amplitude, the former because this is the compound potential size used in most threshold tracking studies of axonal excitability, the latter because this is the compound potential most likely to be composed entirely of motor axons with low thresholds to electrical recruitment. Measurements were made of the strength-duration relationship, threshold electrotonus, current-voltage relationship, recovery cycle and latent addition. The findings did not support a difference in I(NaP). Instead they pointed to greater activity of the hyperpolarization-activated inwardly rectifying current (I(h)) as the basis for low threshold to electrical recruitment in human motor axons. Computer modelling confirmed this finding, with a doubling of the hyperpolarization-activated conductance proving the best single parameter adjustment to fit the experimental data. We suggest that the hyperpolarization-activated cyclic nucleotide-gated (HCN) channel(s) expressed on human motor axons may be active at rest and contribute to resting membrane potential.
本研究旨在探究低阈值人类运动轴突的兴奋性和适应特性,以检验这些运动轴突是否具有更高表达的持续钠(Na+)电导(INaP)。采用计算机控制的阈跟踪技术研究了 22 个单运动单位,并将数据与同一实验中记录的不同幅度的复合运动电位进行了比较。对单单位和复合电位进行了详细比较,复合电位分别为最大幅度的 40%或 5%,前者是因为这是大多数轴突兴奋性阈跟踪研究中使用的复合电位大小,后者是因为这是最有可能完全由低阈值电招募的运动轴突组成的复合电位。对强度-时间关系、阈电紧张、电流-电压关系、恢复周期和潜伏性相加进行了测量。研究结果不支持 INaP 存在差异。相反,它们指向更大的超极化激活内向整流电流(I(h))活性,作为人类运动轴突电招募低阈值的基础。计算机建模证实了这一发现,超极化激活电导增加一倍被证明是拟合实验数据的最佳单一参数调整。我们认为,人类运动轴突上表达的超极化激活环核苷酸门控(HCN)通道可能在静息时活跃,并有助于静息膜电位。