Dale N, Roberts A
J Physiol. 1985 Jun;363:35-59. doi: 10.1113/jphysiol.1985.sp015694.
The neuronal basis of the excitation received by motoneurones during swimming in curarized Xenopus embryos has been investigated further. Extracellular stimulation of axons in the fibre tracts of the spinal cord has been used to evoke unitary excitatory post-synaptic potentials (p.s.p.s) in motoneurones. The p.s.p.s. had a rise time of 3-5 ms and a long falling phase lasting up to 200 ms. These potentials consist of two components: a 'fast' p.s.p. which is insensitive to 50 microM-(+/-)-2-amino-5-phosphonovaleric acid (APV) but is blocked by 2 mM-cis-2,3-piperidine dicarboxylic acid (PDA) and is therefore probably mediated by kainate/quisqualate receptors, and a 'slow' p.s.p. which is blocked by both APV and PDA and is therefore probably mediated by N-methyl-D-aspartate (NMDA) receptors. Paired intracellular recordings from motoneurones and interneurones have revealed a class of spinal cord interneurone which makes descending excitatory amino-acid-dependent synapses onto motoneurones and commissural interneurones. The p.s.p.s evoked by intracellular stimulation of these excitatory interneurones consist of 'fast' and 'slow' components identical in shape and pharmacological properties to those of the extracellularly evoked potentials. One neurone may, therefore, be able to release a transmitter which activates both NMDA and non-NMDA receptors on the same post-synaptic neurone generating fast and slow post-synaptic potentials. The excitatory interneurones play an important role in the generation of the swimming pattern in the curarized Xenopus embryo. Like motoneurones, they fire once per swimming cycle in phase with the ipsilateral motoneurones and receive a background excitation during swimming that is excitatory amino acid mediated. They are therefore part of the swimming rhythm generator. The temporal summation of the extracellularly evoked p.s.p.s shows that these excitatory interneurones are sufficient to generate the excitatory drive received by motoneurones during swimming.
对箭毒化非洲爪蟾胚胎游泳时运动神经元所接收兴奋的神经基础进行了进一步研究。通过对脊髓纤维束中的轴突进行细胞外刺激,以诱发运动神经元的单一兴奋性突触后电位(p.s.p.s)。这些p.s.p.s的上升时间为3 - 5毫秒,下降相较长,持续长达200毫秒。这些电位由两个成分组成:一个“快速”p.s.p.,它对50微摩尔(±)-2-氨基-5-膦酸戊酸(APV)不敏感,但被2毫摩尔顺式-2,3-哌啶二羧酸(PDA)阻断,因此可能由海人藻酸/使君子氨酸受体介导;以及一个“慢速”p.s.p.,它被APV和PDA都阻断,因此可能由N-甲基-D-天冬氨酸(NMDA)受体介导。对运动神经元和中间神经元进行的成对细胞内记录揭示了一类脊髓中间神经元,它们在运动神经元和联合中间神经元上形成下行兴奋性氨基酸依赖性突触。这些兴奋性中间神经元的细胞内刺激所诱发的p.s.p.s由“快速”和“慢速”成分组成,其形状和药理学特性与细胞外诱发电位的相同。因此,一个神经元可能能够释放一种递质,该递质激活同一突触后神经元上的NMDA和非NMDA受体,产生快速和慢速突触后电位。兴奋性中间神经元在箭毒化非洲爪蟾胚胎游泳模式的产生中起重要作用。与运动神经元一样,它们在每个游泳周期与同侧运动神经元同步放电一次,并在游泳期间接受兴奋性氨基酸介导的背景兴奋。因此,它们是游泳节律发生器的一部分。细胞外诱发p.s.p.s的时间总和表明,这些兴奋性中间神经元足以产生游泳时运动神经元所接收的兴奋驱动。