Landmesser L T, Szente M
J Physiol. 1986 Nov;380:157-74. doi: 10.1113/jphysiol.1986.sp016278.
Motoneurone cell death and spontaneous embryonic motility were blocked in chick embryos by daily in ovo injections of d-tubocurarine from stage 28-36 (E5-10). Isolated spinal cord-hind-limb preparations were prepared from these embryos and movement sequences in response to electrical stimulation of the thoracic cord were assessed, after drug wash-out, by electromyogram (e.m.g.) or muscle-nerve recordings. In embryos in which complete blockade of lumbar motoneurone cell death was later confirmed histologically, flexor and extensor motoneurone pools were found to be activated in alternating bursts as occurs in control embryos. Thus the development of the basic cord circuits responsible for these patterns of motoneurone activation does not require motoneurone cell death. Partial blockade of motoneurone cell death by guanosine 3',5'-phosphate (cyclic GMP) was also without effect on muscle activation patterns. In ovo injection of d-tubocurarine or alpha-bungarotoxin in doses sufficient to block embryonic motility was found to have a direct effect on the spinal cord, preventing the patterned activation of motoneurone pools in alternating bursts. Cords removed from treated embryos behaved similarly to cords in which these drugs were applied acutely in the bath. Minor changes in muscle activation patterns that occurred with chronic drug treatment were also observed in acutely treated cords and appear to be a direct and persistent effect of the drugs on cord circuits. It is possible to conclude that cholinergic circuits within the chick lumbar cord play a role in the normal patterned activation of flexor and extensor motoneurone pools. Systemically applied drugs can have access to these circuits, indicating a need for caution when interpreting the results of drugs applied in this manner to developing embryos. We also conclude that neither the activation of motoneurones in patterned bursts, nor the afferent feed-back from the movements that result, are required to form the basic spinal cord circuits responsible for the activation of extensor and flexor motoneurone pools in alternating bursts.
从第28至36期(E5 - 10)开始,每天对鸡胚进行卵内注射d - 筒箭毒碱,可导致运动神经元细胞死亡和胚胎自发运动受阻。从这些胚胎中制备出分离的脊髓 - 后肢标本,在药物洗脱后,通过肌电图(e.m.g.)或肌肉 - 神经记录来评估对胸段脊髓进行电刺激时的运动序列。在后来经组织学证实腰段运动神经元细胞死亡完全被阻断的胚胎中,发现屈肌和伸肌运动神经元池像在对照胚胎中一样以交替爆发的形式被激活。因此,负责这些运动神经元激活模式的基本脊髓回路的发育并不需要运动神经元细胞死亡。鸟苷3',5'-磷酸(环磷酸鸟苷)对运动神经元细胞死亡的部分阻断对肌肉激活模式也没有影响。发现以足以阻断胚胎运动的剂量进行卵内注射d - 筒箭毒碱或α - 银环蛇毒素对脊髓有直接作用,可阻止运动神经元池以交替爆发的形式进行模式化激活。从经处理的胚胎中取出的脊髓表现与在浴中急性应用这些药物的脊髓相似。在急性处理的脊髓中也观察到了慢性药物处理时发生的肌肉激活模式的微小变化,这似乎是药物对脊髓回路的直接和持续作用。可以得出结论,鸡腰段脊髓内的胆碱能回路在屈肌和伸肌运动神经元池的正常模式化激活中起作用。全身应用的药物可以作用于这些回路,这表明在解释以这种方式应用于发育中胚胎的药物结果时需要谨慎。我们还得出结论,形成负责伸肌和屈肌运动神经元池交替爆发激活的基本脊髓回路,既不需要运动神经元以模式化爆发的形式激活,也不需要由此产生的运动的传入反馈。