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首页> 外文期刊>Journal of Neurophysiology >GABAA-receptor-mediated conductance and action potential waveform in cutaneous and muscle afferent neurons of the adult rat: differential expression and response to nerve injury.
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GABAA-receptor-mediated conductance and action potential waveform in cutaneous and muscle afferent neurons of the adult rat: differential expression and response to nerve injury.

机译:成年大鼠皮肤和肌肉传入神经元中GABAA受体介导的电导和动作电位波形:差异表达和对神经损伤的反应。

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1. Whole cell patch-clamp recordings were obtained from identified cutaneous and muscle afferent neurons (33-60 microns diam) in dissociated L4 and L5 dorsal root ganglia (DRGs) from normal rats and from rats 2-3 wk after sciatic nerve ligation or crush injury. gamma-Aminobutyric acid (GABA)-induced conductance was compared in normal and injured neurons from both functional classes of sensory neurons. 2. Control cutaneous afferent neurons had a peak GABA-mediated conductance of 287 +/- 27 (SE) nS compared with 457 +/- 42 nS for control muscle afferent neurons. 3. An inflection on the downslope of the action potential was observed in 47% of cutaneous afferent neurons compared with 20% of muscle afferent neurons. 4. After ligation and transection of the sciatic nerve there was no change in the GABA-mediated conductance of muscle afferent neurons or in the action potential waveform (23% inflected). However, the cutaneous afferent neurons displayed a greater than two-fold increase in their GABA-mediated conductance and displayed a prominent reduction in the number of neurons with inflected action potentials (13% inflected). Input resistance was similar in cutaneous and muscle afferent neurons and decreased after ligation in cutaneous but not muscle afferents. Resting potential averaged from -50 to -56 mV in normal and ligated groups for both cutaneous and muscle afferent neurons. 5. After crush injury in cutaneous afferent neurons where the transected axons were allowed to regenerate into the distal nerve stump, GABAA-receptor-mediated conductance was elevated compared with controls. However, action potential waveform was not altered by crush injury, suggesting a differential regulation of these two properties in cutaneous afferent neurons. 6. These data indicate that injury-induced plasticity of GABAA-receptor-mediated conductance and action potential waveform occurs in cutaneous but not muscle afferent DRG neurons. It appears that peripherally derived influences are critical in maintaining the electrophysiological phenotype of cutaneous afferent neurons but not muscle afferent neurons.
机译:1.全细胞膜片钳记录是从正常大鼠和坐骨神经结扎后2-3 wk分离的L4和L5背根神经节(DRGs)中分离出的皮肤和肌肉传入神经元(直径为33-60微米)获得的。挤压伤。在正常和受伤的神经元中,从两种功能类别的感觉神经元中比较了γ-氨基丁酸(GABA)诱导的电导。 2.对照皮肤传入神经元的峰值GABA介导的电导为287 +/- 27(SE)nS,而对照肌肉传入神经元为457 +/- 42nS。 3.在47%的皮肤传入神经元中观察到动作电位下坡的变化,而在20%的肌肉传入神经元中观察到。 4.坐骨神经结扎和横切后,GABA介导的肌肉传入神经元电导或动作电位波形没有变化(23%的变化)。但是,皮肤传入神经元的GABA介导的电导增加了两倍以上,并且动作电位发生变化的神经元数量显着减少(发生变化的占13%)。皮肤和肌肉传入神经元的输入阻力相似,结扎后在皮肤而非肌肉传入神经中降低。在正常和结扎组中,皮肤和肌肉传入神经元的静息电位平均为-50至-56 mV。 5.皮肤传入神经元被挤压损伤后,横断的轴突被允许再生为远端神经残端,与对照组相比,GABAA受体介导的电导率升高。然而,动作电位波形并未因挤压损伤而改变,表明在皮肤传入神经元中这两种特性的差异调节。 6.这些数据表明,损伤诱导的GABAA受体介导的可塑性和动作电位波形发生在皮肤而非肌肉传入的DRG神经元中。看来,外周来源的影响对于维持皮肤传入神经元而非肌肉传入神经元的电生理表型至关重要。

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