Alstermark B, Lundberg A, Sasaki S
Exp Brain Res. 1984;56(2):279-92. doi: 10.1007/BF00236284.
A further analysis has been made of inhibitory pathways to motoneurones via C3-C4 propriospinal neurones (PNs). Intracellular recording was made from triceps brachi motoneurones and effects from higher centres and forelimb afferents on corticospinal IPSPs were investigated after transection of the corticospinal tract at the C5/C6 border. The shortest latencies of the IPSPs evoked by stimulation of the pyramid were as brief as those of the pyramidal EPSPs (Illert et al. 1977). It is postulated that the minimal linkage of the pyramidal IPSPs is disynaptic via inhibitory C3-C4 PNs projecting directly to motoneurones. It was confirmed that pyramidal IPSPs usually are depressed by volleys in forelimb motor axon collaterals (Illert and Tanaka 1978). A quantitative comparison was made of the recurrent depression of pyramidal IPSPs and of IPSPs caused by activation of the Ia inhibitory interneurones. The result support the hypothesis of two parallel inhibitory cortico-motoneuronal pathways via C3-C4 PNs, one disynaptic via the inhibitory PNs and the other trisynaptic via excitatory PNs and Ia inhibitory interneurones. Pyramidal volleys also evoked late IPSPs which in some cases were not depressed from forelimb motor axon collaterals. It is postulated that the late IPSPs are partly due to activation of inhibitory C3-C4 PNs. Disynaptic pyramidal IPSPs were effectively facilitated by volleys in rubro-, tecto- and reticulospinal fibres - but not from vestibulospinal fibres - showing a convergence from the former descending tracts on common inhibitory C3-C4 PNs. Projection from forelimb afferents and corticospinal fibres on common inhibitory C3-C4 PNs was revealed by strong facilitation of disynaptic pyramidal IPSPs from cutaneous forelimb afferents. No corresponding effect was evoked from C2 neck afferents. Stimulation in the lateral reticular nucleus (LRN) evoked monosynaptic IPSPs in some motoneurones. The results of threshold mapping in and around the LRN suggest that the IPSPs are caused by antidromic stimulation of ascending collaterals of inhibitory neurones also projecting to motoneurones, possibly the inhibitory C3-C4 PNs.
对经由C3 - C4脊髓 propriospinal 神经元(PNs)至运动神经元的抑制通路进行了进一步分析。从肱三头肌运动神经元进行细胞内记录,并在C5/C6边界处切断皮质脊髓束后,研究了高级中枢和前肢传入神经对皮质脊髓抑制性突触后电位(IPSPs)的影响。刺激锥体引起的IPSPs的最短潜伏期与锥体兴奋性突触后电位(EPSPs)的潜伏期一样短(Illert等人,1977年)。据推测,锥体IPSPs的最小联系是通过直接投射到运动神经元的抑制性C3 - C4 PNs进行双突触联系。已证实,锥体IPSPs通常会被前肢运动轴突侧支的冲动所抑制(Illert和Tanaka,1978年)。对锥体IPSPs的反复抑制以及由Ia抑制性中间神经元激活引起的IPSPs进行了定量比较。结果支持经由C3 - C4 PNs的两条平行抑制性皮质 - 运动神经元通路的假说,一条通过抑制性PNs进行双突触联系,另一条通过兴奋性PNs和Ia抑制性中间神经元进行三突触联系。锥体冲动还诱发了晚期IPSPs,在某些情况下,这些晚期IPSPs不会被前肢运动轴突侧支抑制。据推测,晚期IPSPs部分是由于抑制性C3 - C4 PNs的激活所致。双突触锥体IPSPs在红核脊髓、顶盖脊髓和网状脊髓纤维的冲动作用下得到有效易化,但前庭脊髓纤维的冲动则无此作用,这表明前三者下行束在共同的抑制性C3 - C4 PNs上存在汇聚。前肢皮肤传入神经对双突触锥体IPSPs的强烈易化作用揭示了前肢传入神经和皮质脊髓纤维在共同的抑制性C3 - C4 PNs上的投射。C2颈部传入神经未引起相应效应。刺激外侧网状核(LRN)在一些运动神经元中诱发了单突触IPSPs。在LRN及其周围进行阈值定位的结果表明,这些IPSPs是由逆向刺激也投射到运动神经元的抑制性神经元的升支引起的,可能是抑制性C3 - C4 PNs。