Jankowska E, Lundberg A, Rudomin P, Sykova E
Brain Res. 1982 May 20;240(1):117-29. doi: 10.1016/0006-8993(82)90649-7.
An analysis was made of effects of 0.1-1.0 mg/kg 4-aminopyridine (4-AP) i.v. on excitatory and inhibitory spinal reflex pathways in lightly anaesthetized or decerebrated cats. The effects appeared within the first minutes of the injection, reached maximum after about 10-15 min and remained stable during at least several hours. 4-AP enhanced the following synaptic actions on motoneurones: monosynaptic excitation from Ia afferents and descending tracts, disynaptic and polysynaptic excitation from group Ib, group II, cutaneous and high threshold muscle afferents, disynaptic inhibition from Ia and Ib afferents and recurrent and polysynaptic inhibition from different afferents. 4-AP also increased primary afferent depolarization and excitation of ascending tract cells by peripheral stimuli. In the case of the disynaptic inhibitory pathways it has been shown that 4-AP may enhance the excitation of the interposed interneurones but it also increases the action of these interneurones on the motoneurones; monosynaptic inhibition evoked in motoneurones by electrical stimulation of the axons of the inhibitory interneurones was used as a test response in these experiments. No indications were found of direct effects of 4-AP on excitability of afferent fibres or motoneurones to electrical stimuli. No systematic changes were either found in the membrane potential of motoneurones or in the duration of action potentials of these neurones or primary afferents. It is therefore concluded that small doses of 4-AP enhance synaptic transmission in the spinal cord by an action at a presynaptic level.
分析了静脉注射0.1 - 1.0毫克/千克4 - 氨基吡啶(4 - AP)对轻度麻醉或去大脑猫的脊髓兴奋性和抑制性反射通路的影响。这些影响在注射后的最初几分钟内出现,约10 - 15分钟后达到最大值,并在至少几个小时内保持稳定。4 - AP增强了以下对运动神经元的突触作用:来自Ia传入纤维和下行束的单突触兴奋、来自Ib类、II类、皮肤和高阈值肌肉传入纤维的双突触和多突触兴奋、来自Ia和Ib传入纤维的双突触抑制以及来自不同传入纤维的回返性和多突触抑制。4 - AP还增加了初级传入去极化以及外周刺激对上行束细胞的兴奋。对于双突触抑制通路,已表明4 - AP可能增强中间神经元的兴奋,但它也增加了这些中间神经元对运动神经元的作用;在这些实验中,通过电刺激抑制性中间神经元的轴突在运动神经元中诱发的单突触抑制被用作测试反应。未发现4 - AP对传入纤维或运动神经元对电刺激的兴奋性有直接影响。也未在运动神经元的膜电位或这些神经元或初级传入纤维的动作电位持续时间中发现系统性变化。因此得出结论,小剂量的4 - AP通过在突触前水平起作用来增强脊髓中的突触传递。