首页> 美国卫生研究院文献>The Journal of Neuroscience >Peptide Cotransmitter Release from Motorneuron B16 inAplysia californica: Costorage Corelease and Functional Implications
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Peptide Cotransmitter Release from Motorneuron B16 inAplysia californica: Costorage Corelease and Functional Implications

机译:加州电动车中Motorneuron B16的肽共递质释放:Costorage共释放和功能含义

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摘要

Many neurons contain multiple peptide cotransmitters in addition to their classical transmitters. We are using the accessory radula closer neuromuscular system of Aplysia, which participates in feeding in these animals, to define the possible consequences of multiple modulators converging on single targets. How these modulators are released onto their targets is of critical importance in understanding the outcomes of their modulatory actions and their physiological role. Here we provide direct evidence that the partially antagonistic families of modulatory peptides, the myomodulins and buccalins, synthesized by motorneuron B16 are costored and coreleased in fixed ratios. We show that this release is calcium-dependent and independent of muscle contraction. Furthermore, we show that peptide release is initiated at the low end of the physiological range of motorneuron firing frequency and that it increases with increasing motorneuron firing frequency. The coordination of peptide release with the normal operating range of a neuron may be a general phenomenon and suggests that the release of peptide cotransmitters may exhibit similar types of regulation and plasticity as have been observed for classical transmitters. Stimulation paradigms that increase muscle contraction amplitude or frequency also increase peptide release from motor neuron B16. The net effect of the modulatory peptide cotransmitters released from motorneuron B16 would be to increase relaxation rate and therefore allow more frequent and/or larger contractions to occur without increased resistance to antagonist muscles. The end result of this modulation could be to maximize the efficiency of feeding.
机译:许多神经元除其经典的递质外还包含多种肽共递质。我们正在使用海ly附属的小弓closer近端神经肌肉系统,该系统参与喂养这些动物,以定义多个调节剂汇聚在单个靶标上的可能后果。这些调节剂如何释放到其靶标上对于理解其调节作用的结果及其生理作用至关重要。在这里,我们提供直接证据,证明由运动神经元B16合成的调节性肽,肌调节蛋白和颊钙蛋白的部分拮抗性家族被固定并共释放。我们表明,这种释放是钙依赖性的,并且与肌肉收缩无关。此外,我们表明,肽释放在运动神经元激发频率的生理范围的低端开始,并且随着运动神经元激发频率的增加而增加。肽释放与神经元正常工作范围的协调可能是普遍现象,并表明肽共递质的释放可能表现出与经典递质相同的调节和可塑性。增加肌肉收缩幅度或频率的刺激范例也增加了从运动神经元B16释放的肽。从运动神经元B16释放的调节肽共递质的净作用将是增加松弛率,并因此允许更频繁和/或更大的收缩发生而不增加对拮抗肌的抵抗力。这种调制的最终结果可能是使进料效率最大化。

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