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对猫脊髓中运动神经元非交互抑制的最后一级中间核中间神经元所产生抑制作用的药理学分析。

Pharmacologic analysis of inhibition produced by last-order intermediate nucleus interneurons mediating nonreciprocal inhibition of motoneurons in cat spinal cord.

作者信息

Rudomin P, Jiménez I, Quevedo J, Solodkin M

机构信息

Department of Physiology, Biophysics and Neurosciences, Centro de Investigacion y de Estudios Avanzados del IPN, México, D.F.

出版信息

J Neurophysiol. 1990 Jan;63(1):147-60. doi: 10.1152/jn.1990.63.1.147.

Abstract
  1. The aim of this study was to investigate the effects of drugs blocking glycinergic and GABAergic transmission on the postsynaptic inhibition of hindlimb motoneurons produced by activation of last-order laminae V-VI interneurons, which are coexcited by muscle and cutaneous afferents and have axonal branches projecting to the Clarke's column. 2. In anesthetized cats with right spinal cord hemisected and both dorsal columns cut between L4 and L5 segments, stimulation of the Clarke's column (CC) at L3-L4 level produced a short-latency, presumably monosynaptic, inhibitory potential that could be recorded either from L7 or S1 ventral rootlets by means of the sucrose-gap technique (iVRP) or intracellularly from hindlimb motoneurons (IPSP). These potentials have been attributed to antidromic activation of a population of last-order interneurons mediating nonreciprocal inhibition of motoneurons. 3. The early iVRP and IPSP produced by CC stimulation was practically abolished 10-20 s after the intravenous injection of strychnine (0.1 mg/kg) and replaced by an excitatory synaptic potential followed by delayed, slow, strychnine-resistant inhibitory potential. 4. Monosynaptic reflexes (MSR) elicited by stimulation of group I gastrocnemius (GS) afferents were inhibited during the occurrence of the CC-iVRP. This inhibition was significantly reduced after intravenous strychnine. On the other hand, the inhibition of the GS-MSR, produced by conditioning stimulation of the posterior biceps and semitendinosus (PBSt) nerve with trains of pulses applied 25-35 ms before the test stimulus, was practically unchanged after the intravenous injection of strychnine. 5. The CC-iVRP and the associated inhibition of GS-MSRs were not significantly affected after the intravenous injection of 0.1 mg/kg of picrotoxin, which clearly reduced the dorsal root potentials (DRP), the late component of the iVRP, and the inhibition of MSRs produced by PBSt volleys. 6. The effect of strychnine and picrotoxin was tested on the monosynaptic iVRP elicited by single intermediate nucleus interneurons that were antidromically activated from the CC and responded both to low-threshold cutaneous fibers and to group I or group II afferents. In three experiments where the interneuronal activity could be kept after the drug injection, it was possible to show that strychnine abolished the interneuronally elicited iVRP, which was replaced by an excitatory synaptic potential with onset preceding the interneuronal activity. In another experiment, it was possible to show that the interneuronally elicited iVRP was not affected by an intra-aortic injection of picrotoxin (0.5 mg/kg) that reduced to one-half the DRP and the iVRP produced by group I PBSt volleys.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 本研究的目的是探讨阻断甘氨酸能和γ-氨基丁酸能传递的药物对由最后一级V - VI层中间神经元激活所产生的后肢运动神经元突触后抑制的影响,这些中间神经元由肌肉和皮肤传入神经共同兴奋,且其轴突分支投射到克拉克柱。2. 在右侧脊髓半横切且L4和L5节段之间的双侧背柱切断的麻醉猫中,在L3 - L4水平刺激克拉克柱(CC)产生一个短潜伏期、推测为单突触的抑制电位,该电位可通过蔗糖间隙技术(iVRP)从L7或S1腹侧小根记录,或从后肢运动神经元细胞内记录(IPSP)。这些电位归因于介导运动神经元非相互抑制的一群最后一级中间神经元的逆向激活。3. 静脉注射士的宁(0.1 mg/kg)后10 - 20秒,CC刺激产生的早期iVRP和IPSP实际上被消除,并被一个兴奋性突触电位取代,随后是延迟的、缓慢的、对士的宁有抗性的抑制电位。4. 在CC - iVRP出现期间,刺激I组腓肠肌(GS)传入神经所引发的单突触反射(MSR)受到抑制。静脉注射士的宁后,这种抑制作用显著降低。另一方面,在用测试刺激前25 - 35毫秒施加的一串脉冲对肱二头肌和半腱肌(PBSt)神经进行条件刺激所产生的GS - MSR抑制,在静脉注射士的宁后实际上没有变化。5. 静脉注射0.1 mg/kg荷包牡丹碱后,CC - iVRP及相关的GS - MSR抑制没有受到显著影响,而荷包牡丹碱明显降低了背根电位(DRP)、iVRP的晚期成分以及PBSt串刺激所产生的MSR抑制。6. 测试了士的宁和荷包牡丹碱对由单个中间核中间神经元引发的单突触iVRP的影响,这些中间神经元从CC逆向激活,对低阈值皮肤纤维以及I组或II组传入神经都有反应。在三个药物注射后中间神经元活动仍可维持的实验中,能够表明士的宁消除了中间神经元引发 的iVRP,该电位被一个在中间神经元活动之前开始的兴奋性突触电位取代。在另一个实验中,能够表明中间神经元引发的iVRP不受主动脉内注射荷包牡丹碱(0.5 mg/kg)的影响,该注射使I组PBSt串刺激产生的DRP和iVRP降低了一半。(摘要截断于400字)

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