Parnas I, Dudel J, Cohen I, Franke C
J Neurosci. 1984 Jul;4(7):1912-23. doi: 10.1523/JNEUROSCI.04-07-01912.1984.
In the deep abdominal extensor muscles of spiny lobsters (Panulirus-pennicillatus), the common excitor axon of segment II was eliminated by intracellular injection of pronase. At 1 to 23 days after the operation, the quantal content of excitatory postsynaptic currents (EPSCs), elicited by stimulation of the specific excitor of the L1 muscle, was determined in a specific area of the L1 muscle, both in the operated and in the contralateral control side. The EPSCs in the operated muscles had about a 5 times higher quantal content compared to those in the controls, the change developing within 1 to 2 days after operation. In camera lucida drawings of preparations stained with methylene blue, increased branching of the remaining excitatory axon was obvious at more than 4 days after the operation. To investigate the possibility of contribution of central mechanisms (Rotshenker, S. (1979) J. Physiol. (Lond.) 292: 535-547). to this effect, the bundle of five axons to the deep abdominal extensors of segment II was cut immediately after injection of pronase into the common excitor axon. This caused a reduction of the quantal content of EPSCs and shrinking of the field of innervation in the operated L1 muscle as compared to the control. Therefore, axonal continuity or central connections seem to be necessary for the development of an increased innervation by the specific excitor to L1 after eliminating the common excitor axon. Possible postsynaptic effects of the elimination of the common excitor axon were controlled by recording synaptic single channel currents elicited by the excitatory transmitter glutamate, using the patch clamp method. These single current events did not show appreciable changes in operated L1 muscles. Therefore, the presynaptic strengthening effect on the nerve terminals of the specific L1 excitor is predominant after elimination of the common excitor axon.
在多刺龙虾(Panulirus - pennicillatus)的腹部深层伸肌中,通过细胞内注射链霉蛋白酶消除了第二节段的共同兴奋性轴突。在手术后1至23天,在L1肌肉的特定区域测定了由L1肌肉的特定兴奋性刺激所引发的兴奋性突触后电流(EPSC)的量子含量,同时测定了手术侧和对侧对照侧的情况。与对照侧相比,手术侧肌肉中的EPSC量子含量高出约5倍,这种变化在手术后1至2天内就已出现。在亚甲蓝染色制剂的明场绘图中,术后4天以上可明显看到剩余兴奋性轴突的分支增加。为了研究中枢机制(Rotshenker, S. (1979) J. Physiol. (Lond.) 292: 535 - 547)对此效应的贡献可能性,在将链霉蛋白酶注入共同兴奋性轴突后,立即切断了通往第二节段腹部深层伸肌的五条轴突束。与对照相比,这导致手术侧L1肌肉中EPSC的量子含量降低以及神经支配区域缩小。因此,轴突连续性或中枢连接似乎对于在消除共同兴奋性轴突后特定兴奋性刺激对L1的神经支配增加的发展是必要的。通过使用膜片钳技术记录由兴奋性递质谷氨酸引发的突触单通道电流,来控制消除共同兴奋性轴突可能产生的突触后效应。这些单电流事件在手术侧L1肌肉中未显示出明显变化。因此,在消除共同兴奋性轴突后,对特定L1兴奋性刺激的神经末梢的突触前增强效应占主导。