MacVicar B A, Llinás R R
J Neurosci Res. 1985;13(1-2):323-35. doi: 10.1002/jnr.490130121.
Intracellular recordings were obtained from growing tips of regenerating giant axons in the lamprey spinal cord, the recording sites verified by Lucifer yellow injection. In the presence of extracellular Ba++ (3-6 mM), tetraethylammonium (10-15 mM), and 4-aminopyridine (4-6 mM), action potentials showed prolonged plateaus. The fast initial phase of the action potential, but not the plateau (Ba++-spike), was blocked by tetrodotoxin (10(-6) gm/ml). The Ba++ spike was associated with increased membrane conductance and could be terminated with hyperpolarizing current pulses. Normal axons did not generate similar Ba++ spikes. However, TTX-resistant, voltage-dependant conductance changes could be elicited in normal axons if much higher concentrations of Ba++ (18-30 mM) were used. Their rate of rise was slower than in regenerating axons (0.6 V/sec vs 3.2 V/sec; n = 5), and the response did not outlast the current pulse. The Ba++ responses in normal and regenerating axons were blocked by ions known to block voltage-gated Ca++ conductances (Co++, Ni++, or Cd++). Therefore, these spikes probably represent Ba++ entry through voltage-dependent Ca++ channels, suggesting the presence of a higher-than-average voltage-dependent Ca++ conductance in the growing axon. However, Ca++-dependent spikes could not be obtained under any conditions in either normal or regenerating axons. Simultaneous intracellular recordings from growth cones and axons indicated that the Ba++ spike was initiated, in most cases, at the growth cone. The Ba++ spikes were recorded in regenerating axons for as long as 50 days following cord transection and were not correlatable with the "dying-back" phenomenon in cut axons, which usually is over before day 6. The concept of a higher-than-average voltage-dependent Ca++ conductance in growing tips of regenerating axons is in agreement with the hypothesis that Ca++ is important in regeneration and that regeneration may be related to the process of chemical synaptic transmission.
在七鳃鳗脊髓再生巨轴突的生长尖端进行细胞内记录,记录部位通过荧光黄注射进行验证。在细胞外存在Ba++(3 - 6 mM)、四乙铵(10 - 15 mM)和4 - 氨基吡啶(4 - 6 mM)时,动作电位显示出延长的平台期。动作电位的快速初始阶段,而非平台期(Ba++峰),被河豚毒素(10(-6)克/毫升)阻断。Ba++峰与膜电导增加相关,并且可以通过超极化电流脉冲终止。正常轴突不会产生类似的Ba++峰。然而,如果使用更高浓度的Ba++(18 - 30 mM),在正常轴突中可以引发对河豚毒素有抗性的、电压依赖性的电导变化。它们的上升速率比再生轴突中的慢(0.6伏/秒对3.2伏/秒;n = 5),并且反应不会持续到电流脉冲结束。正常和再生轴突中的Ba++反应被已知可阻断电压门控Ca++电导的离子(Co++、Ni++或Cd++)阻断。因此,这些峰可能代表Ba++通过电压依赖性Ca++通道进入,表明在生长的轴突中存在高于平均水平的电压依赖性Ca++电导。然而,在正常或再生轴突的任何条件下都无法获得Ca++依赖性峰。从生长锥和轴突同时进行的细胞内记录表明,在大多数情况下,Ba++峰起始于生长锥。在脊髓横断后长达50天的时间里,在再生轴突中记录到了Ba++峰,并且与切断轴突中的“回退”现象无关,“回退”现象通常在第6天之前就结束了。再生轴突生长尖端存在高于平均水平的电压依赖性Ca++电导这一概念与Ca++在再生中很重要且再生可能与化学突触传递过程相关的假设一致。