Fetcho J R
Department of Physiology, State University of New York, School of Biomedical Sciences, Buffalo.
Brain Behav Evol. 1991;37(5):298-316. doi: 10.1159/000114367.
Most swimming vertebrates, particularly fishes and amphibians, avoid predators by producing an escape behavior initiated by a single action potential in one of a pair of cells, the Mauthner cells, located in the hindbrain. The most prominent feature of this behavior is a rapid, forceful bend of body and tail which leads to a characteristic C bend (stage 1) early in the escape. The spinal output of the Mauthner cell is largely responsible for this bend. Each Mauthner cell sends an axon down the length of the spinal cord on the side opposite the soma. When one Mauthner axon fires, it massively excites the ipsilateral musculature by (1) monosynaptic excitation of the large primary motoneurons that innervate the fast white muscle fibers and (2) polysynaptic excitation of motoneurons which is most likely mediated through an identified class of descending interneurons. While motoneurons on the side of the C bend are excited, excitation of those on the opposite side is blocked by inhibition of primary motoneurons and descending interneurons. This inhibition is mediated by commissural interneurons that are electrotonically coupled to the Mauthner axon and cross the spinal cord to monosynaptically inhibit cells on the opposite side. They inhibit not only primary motoneurons and descending interneurons, but also the commissural inhibitory interneurons on the opposite side. The inhibition of contralateral primary motoneurons and descending interneurons prevents motor activity on the side opposite the C bend from opposing that bend, while the inhibition of commissural interneurons prevents them from interfering, via their inhibitory connections, with excitation of motoneurons on the side of the bend. The spinal network responsible for the bend has several similarities with the spinal network for swimming in other anamniotic vertebrates, including lampreys and embryonic frogs. These similarities reveal important, primitive features of axial motor networks among vertebrates.
大多数会游泳的脊椎动物,尤其是鱼类和两栖动物,会通过产生一种逃避行为来躲避捕食者,这种行为由位于后脑的一对细胞(即毛特纳细胞)中的一个产生的单动作电位引发。这种行为最显著的特征是身体和尾巴快速、有力地弯曲,在逃避初期会导致特征性的C形弯曲(阶段1)。毛特纳细胞的脊髓输出在很大程度上导致了这种弯曲。每个毛特纳细胞沿着与胞体相对一侧的脊髓长度发送一条轴突。当一条毛特纳轴突放电时,它会通过以下方式大量兴奋同侧肌肉组织:(1)对支配快速白肌纤维的大型初级运动神经元进行单突触兴奋;(2)对运动神经元进行多突触兴奋,这很可能是通过一类已确定的下行中间神经元介导的。当C形弯曲一侧的运动神经元被兴奋时,另一侧运动神经元的兴奋会被初级运动神经元和下行中间神经元的抑制所阻断。这种抑制是由连合中间神经元介导的,它们通过电紧张耦合与毛特纳轴突相连,并穿过脊髓对另一侧的细胞进行单突触抑制。它们不仅抑制初级运动神经元和下行中间神经元,还抑制另一侧的连合抑制性中间神经元。对同侧初级运动神经元和下行中间神经元的抑制可防止C形弯曲另一侧的运动活动与该弯曲对抗,而对连合中间神经元的抑制可防止它们通过抑制性连接干扰弯曲一侧运动神经元的兴奋。负责这种弯曲的脊髓网络与其他无羊膜脊椎动物(包括七鳃鳗和胚胎青蛙)游泳时的脊髓网络有几个相似之处。这些相似之处揭示了脊椎动物轴向运动网络的重要原始特征。