Kozuka Yuji, Kawamata Mikito, Furue Hidemasa, Ishida Takashi, Tanaka Satoshi, Namiki Akiyoshi, Yamakage Michiaki
Department of Anesthesiology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Department of Anesthesiology, Sapporo Medical University School of Medicine, Sapporo, Japan Department of Anesthesiology and Resuscitology, Shinshu University School of Medicine, Matsumoto, Japan
Mol Pain. 2016 Aug 28;12. doi: 10.1177/1744806916665827. Print 2016.
After spinal cord injury, central neuropathic pain develops in the majority of spinal cord injury patients. Spinal hemisection in rats, which has been developed as an animal model of spinal cord injury in humans, results in hyperexcitation of spinal dorsal horn neurons soon after the hemisection and thereafter. The hyperexcitation is likely caused by permanent elimination of the descending pain systems. We examined the change in synaptic transmission of substantia gelatinosa neurons following acute spinal hemisection by using an in vivo whole-cell patch-clamp technique.
An increased spontaneous action potential firings of substantia gelatinosa neurons was detected in hemisected rats compared with that in control animals. The frequencies and amplitudes of spontaneous excitatory postsynaptic currents and of evoked excitatory postsynaptic currentss in response to non-noxious and noxious stimuli were not different between hemisected and control animals. On the contrary, the amplitude and frequency of spontaneous inhibitory postsynaptic currents of substantia gelatinosa neurons in hemisected animals were significantly smaller and lower, respectively, than those in control animals (P < 0.01). Large amplitude and high-frequency spontaneous inhibitory postsynaptic currents, which could not be elicited by mechanical stimuli, were seen in 44% of substantia gelatinosa neurons in control animals but only in 17% of substantia gelatinosa neurons in hemisected animals. In control animals, such large amplitude spontaneous inhibitory postsynaptic currents were suppressed by spinal application of tetrodotoxin (1 µM). Cervical application of lidocaine (2%, 10 µl) also inhibited such large amplitude of inhibitory postsynaptic currents. The proportion of multi-receptive substantia gelatinosa neurons, which exhibit action potential firing in response to non-noxious and noxious stimuli, was much larger in hemisected animals than in control animals.
These suggest that substantia gelatinosa neurons receive tonic inhibition by spinal inhibitory interneurons which generate persistent action potentials. Spinal hemisection results in hyperexcitation of substantia gelatinosa neurons at least in part by eliminating the tonic descending control of spinal inhibitory interneurons from supraspinal levels.
脊髓损伤后,大多数脊髓损伤患者会出现中枢神经性疼痛。大鼠脊髓半切术已被开发为人类脊髓损伤的动物模型,在半切术后不久及之后会导致脊髓背角神经元的过度兴奋。这种过度兴奋可能是由于下行疼痛系统的永久性消除所致。我们使用体内全细胞膜片钳技术研究了急性脊髓半切术后胶状质神经元突触传递的变化。
与对照动物相比,在半切大鼠中检测到胶状质神经元的自发放电动作电位增加。在半切动物和对照动物之间,对非伤害性和伤害性刺激的自发放电兴奋性突触后电流以及诱发的兴奋性突触后电流的频率和幅度没有差异。相反,半切动物中胶状质神经元的自发放电抑制性突触后电流的幅度和频率分别明显小于和低于对照动物(P < 0.01)。在对照动物中,44%的胶状质神经元可见不能由机械刺激诱发的大幅度高频自发放电抑制性突触后电流,但在半切动物中仅在17%的胶状质神经元中可见。在对照动物中,脊髓应用河豚毒素(1 μM)可抑制这种大幅度自发放电抑制性突触后电流。颈部应用利多卡因(2%,10 μl)也可抑制这种大幅度抑制性突触后电流。对半切动物和对照动物中对非伤害性和伤害性刺激均表现出动作电位发放的多感受性胶状质神经元的比例进行比较,发现半切动物中的比例远高于对照动物。
这些结果表明,胶状质神经元接受脊髓抑制性中间神经元的紧张性抑制,这些中间神经元产生持续性动作电位。脊髓半切至少部分通过消除脊髓上水平对脊髓抑制性中间神经元的紧张性下行控制而导致胶状质神经元过度兴奋。