Alstermark B, Ohlson S
Department of Integrative Medical Biology, Section of Physiology, Umeå University, S-901 87 Umeå, Sweden.
Neurosci Res. 2000 Nov;38(3):249-56. doi: 10.1016/s0168-0102(00)00160-7.
Intracellular recording was made from propriospinal neurones (PNs) in the C3-C4 spinal cord segments in the cat (alpha-chloralose anaesthesia). The effect of electrical stimulation of corticospinal neurones (CSNs) in the cortex was investigated. Short C3-C4 PNs were identified by antidromic activation of their axons in the ventral horn in C6/C7 and in the lateral reticular nucleus. Long PNs were antidromically identified from Th12-13. In short PNs, monosynaptic excitory postsynoptic potentials (EPSPs) were elicited from the rostral part of the lateral sigmoid gyrus, the lateral part of the anterior sigmoid gyrus in area 4 gamma and in the adjacent area 6. Two subtypes of short PNs were identified. PNs of type I received monosynaptic EPSPs from the rostral part of the lateral sigmoid gyrus, the lateral part of the anterior sigmoid gyrus in area 4 gamma, which is from the same region as disynaptic cortical EPSPs were evoked in forelimb motoneurones. PNs of type II received monosynaptic EPSPs from regions slightly more rostrally in the anterior sigmoid gyrus in area 4 gamma and in the adjacent area 6, which is outside the region from which disynaptic EPSPs could be evoked in forelimb motoneurones. Long PNs received monosynaptic EPSPs, like the short PNs, by stimulation in the rostral part of the lateral sigmoid gyrus, the lateral part of the anterior sigmoid gyrus in area 4 gamma and in the adjacent area 6. In contrast, the long PNs also received monosynaptic EPSPs from area 3b near the border of area 1. The present results show segregation of the cortical control to functionally different premotoneuronal systems and suggest that this control could in part be separated for subtypes of short C3-C4 PNs.
在猫(α-氯醛糖麻醉)的C3 - C4脊髓节段,对脊髓固有神经元(PNs)进行细胞内记录。研究了皮层中皮质脊髓神经元(CSNs)电刺激的效应。短的C3 - C4 PNs通过其轴突在C6/C7腹角和外侧网状核中的逆行激活来识别。长PNs从Th12 - 13进行逆行识别。在短PNs中,单突触兴奋性突触后电位(EPSPs)由外侧乙状结肠回的前部、4γ区的前乙状结肠回外侧部分以及相邻的6区诱发。识别出了两种短PNs亚型。I型PNs从外侧乙状结肠回的前部、4γ区的前乙状结肠回外侧部分接受单突触EPSPs,该区域与在前肢运动神经元中诱发双突触皮质EPSPs的区域相同。II型PNs从4γ区的前乙状结肠回和相邻6区中稍靠前的区域接受单突触EPSPs,该区域在前肢运动神经元中不能诱发双突触EPSPs。长PNs像短PNs一样,通过刺激外侧乙状结肠回的前部、4γ区的前乙状结肠回外侧部分以及相邻的6区接受单突触EPSPs。相比之下,长PNs还从靠近1区边界的3b区接受单突触EPSPs。目前的结果显示了皮质对功能不同的运动前神经元系统的控制分离,并表明这种控制在一定程度上可能因短C3 - C4 PNs的亚型而有所不同。