Devaux Jerome, Gola Maurice, Jacquet Guy, Crest Marcel
Laboratoire Intégration des Informations Sensorielles, Centre National de la Recherche Scientifique, 31 Chemin Joseph-Aiguier, 13402 Marseille Cedex 20, France.
J Neurophysiol. 2002 Mar;87(3):1376-85. doi: 10.1152/jn.00646.2001.
Four blockers of voltage-gated potassium channels (Kv channels) were tested on the compound action potentials (CAPs) of rat optic nerves in an attempt to determine the regulation of Kv channel expression during the process of myelination. Before myelination occurred, 4-aminopyridine (4-AP) increased the amplitude, duration, and refractory period of the CAPs. On the basis of their pharmacological sensitivity, 4-AP-sensitive channels were divided in two groups, the one sensitive to kaliotoxin (KTX), dendrotoxin-I (DTX-I), and 4-AP, and the other sensitive only to 4-AP. In addition, tetraethylammonium chloride (TEA) applied alone broadened the CAPs. At the onset of myelination, DTX-I induced a more pronounced effect than KTX; this indicates that a fourth group of channels sensitive to 4-AP and DTX-I but insensitive to KTX had developed. The effects of KTX and DTX-I gradually disappeared during the period of myelination. Electron microscope findings showed that the disappearance of these effects was correlated with the ongoing process of myelination. This was confirmed by the fact that DTX-I and KTX enlarged the CAPs of demyelinated adult optic nerves. These results show that KTX- and DTX-sensitive channels are sequestrated in paranodal regions. During the process of myelination, KTX had less pronounced effects than DTX-I on demyelinated nerves, which suggests that the density of the KTX-sensitive channels decreased during this process. By contrast, 4-AP increased the amplitude, duration, and refractory period of the CAPs at all the ages tested and to a greater extent than KTX and DTX-I. The effects of TEA alone also gradually disappeared during this period. However, effects of TEA on CAPs were observed when this substance was applied after 4-AP to the adult optic nerve; this shows that TEA-sensitive channels are not masked by the myelin sheath. In conclusion, the process of myelination seems to play an important part in the regulation and setting of Kv channels in optic nerve axons.
对四种电压门控钾通道(Kv通道)阻滞剂进行了测试,以研究其对大鼠视神经复合动作电位(CAP)的影响,从而确定髓鞘形成过程中Kv通道表达的调控机制。在髓鞘形成之前,4-氨基吡啶(4-AP)增加了CAP的幅度、持续时间和不应期。根据其药理敏感性,对4-AP敏感的通道分为两组,一组对蝎毒素(KTX)、树突毒素-I(DTX-I)和4-AP敏感,另一组仅对4-AP敏感。此外,单独应用四乙铵氯化物(TEA)可使CAP增宽。在髓鞘形成开始时,DTX-I比KTX诱导出更明显的效应;这表明已形成了第四组对4-AP和DTX-I敏感但对KTX不敏感的通道。在髓鞘形成期间,KTX和DTX-I的效应逐渐消失。电子显微镜检查结果表明,这些效应的消失与正在进行的髓鞘形成过程相关。DTX-I和KTX可增大脱髓鞘成年视神经的CAP,这一事实证实了上述结论。这些结果表明,对KTX和DTX敏感的通道被隔离在结旁区域。在髓鞘形成过程中,KTX对脱髓鞘神经的影响不如DTX-I明显,这表明在此过程中对KTX敏感的通道密度降低。相比之下,在所有测试年龄,4-AP均增加了CAP的幅度、持续时间和不应期,且比KTX和DTX-I的作用更大。在此期间,单独应用TEA的效应也逐渐消失。然而,当在4-AP之后将TEA应用于成年视神经时,可观察到TEA对CAP的效应;这表明对TEA敏感的通道未被髓鞘所掩盖。总之,髓鞘形成过程似乎在视神经轴突中Kv通道的调控和设定中起重要作用。