Soffe S R
Department of Zoology, Bristol University, United Kingdom.
J Neurosci. 1993 Oct;13(10):4456-69. doi: 10.1523/JNEUROSCI.13-10-04456.1993.
Xenopus embryos show two distinct rhythmic motor patterns: swimming and struggling. Both can be generated by spinal cord circuitry and evoked by stimulation of a single skin sensory pathway (Soffe, 1991b). This presents a valuable opportunity to explore mechanisms for vertebrate motor pattern switching. Swimming and struggling have been compared using intracellular recording from spinal neurons in immobilized embryos. Underlying synaptic drive was similar; motoneurons and premotor interneurons were excited in phase with ipsilateral motor root discharge and inhibited in phase with contralateral motor root discharge. Excitation was stronger during struggling and associated with short bursts of impulses, contrasting with single spikes per cycle during swimming. Excitation was reduced in both patterns by local application of 1 mM kynurenic acid, indicating excitatory amino acid mediation. Inhibition was antagonized by 1 microM strychnine, indicating glycine mediation. Many motoneurons (76%) and premotor interneurons (68%) fired during both swimming and struggling, including examples of all three spinal premotor interneuron classes. Most of the remaining motoneurons (20%) and premotor interneurons (24%) fired only during struggling, providing roughly 30% more active neurons than during swimming. To investigate whether new neuronal classes become active during struggling, recordings were made from sensory neurons and sensory interneurons. Rohon-Beard sensory neurons did not fire during either swimming or struggling. Dorsolateral commissural sensory interneurons received rhythmic, strychnine-sensitive inhibition during both swimming and struggling and also did not fire. Neither of these neuronal classes is therefore recruited to the circuitry for struggling. Although behaviorally distinct, Xenopus embryo swimming and struggling motor patterns appear to employ similar synaptic drive. I propose that this reflects the common nature of much of the premotor circuitry that drives them. Extra neurons are recruited to this circuitry during struggling, but only from within classes that also participate in swimming.
游泳和挣扎。这两种模式都可由脊髓回路产生,并可通过刺激单一皮肤感觉通路诱发(索夫,1991b)。这为探索脊椎动物运动模式转换机制提供了一个宝贵的机会。利用固定胚胎中脊髓神经元的细胞内记录对游泳和挣扎进行了比较。潜在的突触驱动相似;运动神经元和运动前中间神经元与同侧运动根放电同步兴奋,与对侧运动根放电同步抑制。挣扎时兴奋更强,且与短脉冲串相关,这与游泳时每个周期单个尖峰形成对比。通过局部应用1 mM犬尿喹啉酸,两种模式下的兴奋均降低,表明是兴奋性氨基酸介导。1 microM士的宁可拮抗抑制作用,表明是甘氨酸介导。许多运动神经元(76%)和运动前中间神经元(68%)在游泳和挣扎时都放电,包括所有三类脊髓运动前中间神经元。其余大多数运动神经元(20%)和运动前中间神经元(24%)仅在挣扎时放电,比游泳时活跃神经元多约30%。为了研究在挣扎时是否有新的神经元类别变得活跃,对感觉神经元和感觉中间神经元进行了记录。罗霍恩-比尔感觉神经元在游泳或挣扎时均不放电。背外侧连合感觉中间神经元在游泳和挣扎时均接受节律性、对士的宁敏感的抑制,也不放电。因此,这两类神经元都未被招募到挣扎的回路中。尽管在行为上有明显差异,但非洲爪蟾胚胎的游泳和挣扎运动模式似乎采用了相似的突触驱动。我认为这反映了驱动它们的许多运动前回路的共同性质。在挣扎时,额外的神经元被招募到这个回路中,但仅来自也参与游泳的类别。