Graduate Program in Neuroscience and Departments of Entomology and Neuroscience, University of Minnesota, Saint Paul, Minnesota 55108, USA.
J Neurosci. 2010 Feb 10;30(6):2373-83. doi: 10.1523/JNEUROSCI.5765-09.2010.
The coordination of multiple neural oscillators is key for the generation of productive locomotor movements. In the medicinal leech, we determined that activation and coordination of the segmental crawl oscillators, or unit burst generators, are dependent on signals descending from the cephalic ganglion. In nearly intact animals, removing descending input (reversibly with a sucrose block) prevented overt crawling, but not swimming. Cephalic depolarization was sufficient for coordination. To determine whether descending signals were necessary for the generation and maintenance of posterior-directed intersegmental phase delays, we induced fictive crawling in isolated whole nerve cords using dopamine (DA) and blocked descending inputs. After blockade, we observed a significant loss of intersegmental coordination. Appropriate phase delays were also absent in DA-treated chains of ganglia. In chains, when one ganglion was removed from its neighbors, crawling in that ganglion emerged robust and stable, underscoring that these oscillators operate best with either all or none of their intersegmental inputs. To study local oscillator coupling, we induced fictive crawling (with DA) in a single oscillator within a chain. Although appropriate intersegmental phase delays were always absent, when one ganglion was treated with DA, neighboring ganglia began to show crawl-like bursting, with motoneuron spikes/burst greatest in untreated posterior ganglia. We further determined that this local excitatory drive excluded the swim-gating cell, 204. In conclusion, both long-distance descending and local interoscillator coupling contribute to crawling. This dual contribution helps to explain the inherent flexibility of crawling, and provides a foundation for understanding other dynamic locomotor behaviors across animal groups.
多个神经振荡器的协调是产生高效运动的关键。在医用水蛭中,我们确定了节段性爬行振荡器(或单位爆发发生器)的激活和协调依赖于来自头神经节的信号。在几乎完整的动物中,去除下行输入(用蔗糖块可逆地去除)会阻止明显的爬行,但不会阻止游泳。头神经节的去极化足以协调。为了确定下行信号是否对产生和维持向后的节间相位延迟是必要的,我们使用多巴胺(DA)在分离的全神经索中诱导虚拟爬行,并阻断下行输入。阻断后,我们观察到节间协调明显丧失。在 DA 处理的神经节链中也没有适当的相位延迟。在链中,当一个神经节与其相邻神经节分离时,该神经节中的爬行会出现强大而稳定的状态,这强调了这些振荡器在具有全部或无节间输入时表现最佳。为了研究局部振荡器耦合,我们在链中的单个振荡器中诱导虚拟爬行(用 DA)。尽管总是没有适当的节间相位延迟,但当一个神经节用 DA 处理时,相邻的神经节开始显示出类似爬行的爆发,未处理的后神经节中的运动神经元尖峰/爆发最大。我们进一步确定这种局部兴奋性驱动排除了游泳门控细胞 204。总之,远距离下行和局部振荡器之间的耦合都有助于爬行。这种双重贡献有助于解释爬行的固有灵活性,并为理解跨动物群的其他动态运动行为提供了基础。