Black Joel A, Cummins Theodore R, Yoshimura Naoki, de Groat William C, Waxman Stephen G
Department of Neurology and PVA/EPVA Neuroscience Research Center, Yale University School of Medicine, New Haven, CT 06510, USA.
Brain Res. 2003 Feb 14;963(1-2):132-8. doi: 10.1016/s0006-8993(02)03957-4.
Tetrodotoxin-resistant (TTX-R) sodium channels Na(v)1.8/SNS and Na(v)1.9/NaN are preferentially expressed in small diameter dorsal root ganglia (DRG) neurons. The urinary bladder is innervated by small afferent neurons from L6/S1 DRG, of which approximately 75% exhibit high-threshold action potentials that are mediated by TTX-R sodium channels. Following transection of the spinal cord at T8, the bladder becomes areflexic and then gradually hyper-reflexic, and there is an attenuation of the TTX-R sodium currents in bladder afferent neurons. In the present study, we demonstrate that Na(v)1.8 is expressed in both bladder and non-bladder afferent neurons, while Na(v)1.9 is expressed in non-bladder afferent neurons but is rarely observed in bladder afferent neurons. In spinal cord transected rats 28-32 days following transection, there is a decreased expression of Na(v)1.8 sodium channels in bladder afferents, but no change in the expression of Na(v)1.8 in non-bladder afferent neurons. Both bladder and non-bladder afferent neurons exhibit limited increases in Na(v)1.9 expression following spinal cord transection. These results demonstrate that the expression of TTX-R channels in bladder afferent neurons changes after spinal cord transection, and these changes may contribute to the increased excitability of these neurons following spinal cord injury.
河豚毒素抗性(TTX-R)钠通道Na(v)1.8/SNS和Na(v)1.9/NaN优先在小直径背根神经节(DRG)神经元中表达。膀胱由来自L6/S1 DRG的小传入神经元支配,其中约75%表现出由TTX-R钠通道介导的高阈值动作电位。在T8水平横断脊髓后,膀胱变得无反射,然后逐渐出现反射亢进,并且膀胱传入神经元中的TTX-R钠电流减弱。在本研究中,我们证明Na(v)1.8在膀胱和非膀胱传入神经元中均有表达,而Na(v)1.9在非膀胱传入神经元中表达,但在膀胱传入神经元中很少观察到。在横断脊髓28 - 32天后的大鼠中,膀胱传入神经中Na(v)1.8钠通道的表达降低,但非膀胱传入神经元中Na(v)1.8的表达没有变化。脊髓横断后,膀胱和非膀胱传入神经元中Na(v)1.9的表达均有有限增加。这些结果表明,脊髓横断后膀胱传入神经元中TTX-R通道的表达发生变化,这些变化可能导致脊髓损伤后这些神经元兴奋性增加。