Zhang Yili, Khorkova Olga, Rodriguez Rosa, Golowasch Jorge
Federated Department of Biological Sciences, Rutgers University-Newark, Newark, NJ, USA.
J Neurophysiol. 2009 Jan;101(1):372-86. doi: 10.1152/jn.01290.2007. Epub 2008 Jul 2.
Central pattern generators (CPGs) are neuronal networks that control vitally important rhythmic behaviors including breathing, heartbeat, and digestion. Understanding how CPGs recover activity after their rhythmic activity is disrupted has important theoretical and practical implications. Previous experimental and modeling studies indicated that rhythm recovery after central neuromodulatory input loss (decentralization) could be based entirely on activity-dependent mechanisms, but recent evidence of long-term conductance regulation by neuromodulators suggest that neuromodulator-dependent mechanisms may also be involved. Here we examined the effects of altering activity and the neuromodulatory environment before decentralization of the pyloric CPG in Cancer borealis on the initial phase of rhythmic activity recovery after decentralization. We found that pretreatments altering the network activity through shifting the ionic balance or the membrane potential of pyloric pacemaker neurons reduced the delay of recovery initiation after decentralization, consistent with the recovery process being triggered already during the pretreatment period through an activity-dependent mechanism. However, we observed that pretreatment with neuromodulators GABA and proctolin, acting via metabotropic receptors, also affected the initial phase of the recovery of pyloric activity after decentralization. Their distinct effects appear to result from interactions of their metabotropic effects with their effects on neuronal activity. Thus we show that the initial phase of the recovery process can be accounted for by the existence of distinct activity-and neuromodulator-dependent pathways. We propose a computational model that includes activity- and neuromodulator-dependent mechanisms of the activity recovery process, which successfully explains the experimental observations and predicts the results of key biological experiments.
中枢模式发生器(CPGs)是控制包括呼吸、心跳和消化等至关重要的节律性活动的神经网络。了解CPGs在其节律性活动被破坏后如何恢复活动具有重要的理论和实际意义。先前的实验和建模研究表明,中枢神经调节输入丧失(去神经支配)后的节律恢复可能完全基于活动依赖机制,但最近有关神经调节剂长期电导调节的证据表明,神经调节剂依赖机制可能也参与其中。在这里,我们研究了在北方瘤蟹幽门CPG去神经支配之前改变活动和神经调节环境对去神经支配后节律性活动恢复初始阶段的影响。我们发现,通过改变幽门起搏器神经元的离子平衡或膜电位来改变网络活动的预处理减少了去神经支配后恢复起始的延迟,这与恢复过程在预处理期间就已通过活动依赖机制触发一致。然而,我们观察到,用通过代谢型受体起作用的神经调节剂GABA和促肠肌肽进行预处理,也会影响去神经支配后幽门活动恢复的初始阶段。它们的不同作用似乎源于其代谢型作用与其对神经元活动的作用之间的相互作用。因此,我们表明恢复过程的初始阶段可以由不同的活动和神经调节剂依赖途径的存在来解释。我们提出了一个计算模型,该模型包括活动恢复过程中活动和神经调节剂依赖机制,成功解释了实验观察结果并预测了关键生物学实验的结果。