Moschovakis A K, Sholomenko G N, Burke R E
Laboratory of Neural Control, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892.
Exp Brain Res. 1991;83(3):489-501. doi: 10.1007/BF00229826.
Low threshold (less than or equal to 2 x T) cutaneous afferents in the superficial peroneal (SP) and medial plantar (PLNT) nerves both produce short-latency excitatory postsynaptic potentials (EPSPs) in flexor digitorum longus (FDL) alpha-motoneurons, with minimum central latencies (less than or equal to 1.8 ms) that indicate a disynaptic connection. However, SP and PLNT EPSPs in FDL motoneurons are differentially modulated during fictive stepping in decerebrate cats. The early components in SP EPSPs are systematically enhanced during the early flexion phase of fictive stepping (Schmidt et al. 1988) while those in PLNT EPSPs are markedly depressed during flexion. In addition, transmission in the PLNT----FDL pathway is enhanced during occasional step cycles in which the FDL displays firing during the extension phase. This enhancement affects only the trisynaptic components of PLNT EPSPs, is simultaneous with the extension FDL burst, and is not found in SP EPSPs. These results indicate that the SP----FDL and PLNT----FDL pathways are composed of entirely different sets of segmental last-order interneurons, each of which receives sensory information from contiguous, relatively limited regions of skin on the most distal parts of the hindpaw. Possible functional consequences of these interneuronal organizations are discussed.
腓浅神经(SP)和足底内侧神经(PLNT)中的低阈值(小于或等于2×T)皮肤传入纤维,均可在趾长屈肌(FDL)α运动神经元中产生短潜伏期兴奋性突触后电位(EPSP),其最小中枢潜伏期(小于或等于1.8毫秒)表明为双突触连接。然而,在去大脑猫的模拟步行过程中,FDL运动神经元中的SP和PLNT EPSP受到不同的调制。SP EPSP的早期成分在模拟步行的早期屈曲阶段会系统性增强(施密特等人,1988年),而PLNT EPSP的早期成分在屈曲期间则会显著抑制。此外,在偶尔的步周期中,当FDL在伸展阶段放电时,PLNT - FDL通路的传递会增强。这种增强仅影响PLNT EPSP的三突触成分,与FDL伸展爆发同时出现,而在SP EPSP中未发现。这些结果表明,SP - FDL和PLNT - FDL通路由完全不同的节段性终末中间神经元组成,每个中间神经元从后爪最远端相邻的、相对有限的皮肤区域接收感觉信息。文中讨论了这些中间神经元组织可能产生的功能后果。