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Activity and Neuromodulatory Input Contribute to the Recovery of Rhythmic Output After Decentralization in a Central Pattern Generator

机译:活动和神经调节输入有助于在中央模式发生器中去中心化后恢复有节奏的输出

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摘要

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.
机译:中央模式发生器(CPG)是神经元网络,可控制至关重要的节律行为,包括呼吸,心跳和消化。了解CPG的节律活动受到破坏后如何​​恢复活动具有重要的理论和实践意义。先前的实验和模型研究表明,中枢神经调节输入丧失(分散)后的节律恢复可能完全基于活动依赖性机制,但最近有关神经调节剂长期电导调节的证据表明,也可能涉及神经调节剂依赖性机制。在这里,我们检查了癌变中幽门CPG分散之前活动的改变和神经调节环境对分散后节律活动恢复的初始阶段的影响。我们发现预处理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,从而降低了分散后恢复启动的延迟,这与预处理过程中通过活动依赖机制已经触发的恢复过程一致。然而,我们观察到神经代谢的GABA和Proctolin通过代谢亲和性受体进行的预处理也影响了分散后幽门活动恢复的初始阶段。它们的独特作用似乎是由于它们的促代谢作用与它们对神经元活动的相互作用所引起的。因此,我们表明,恢复过程的初始阶段可以通过存在与众不同的依赖于活性和依赖神经调节剂的途径来解释。我们提出了一种计算模型,其中包括活动恢复过程中依赖于活动和神经调节剂的机制,该模型成功地解释了实验观察结果并预测了关键生物学实验的结果。

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