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章鱼胺——一种在小龙虾神经肌肉接头处具有突触前活性依赖性作用的神经激素。

Octopamine--a neurohormone with presynaptic activity-dependent effects at crayfish neuromuscular junctions.

作者信息

Breen C A, Atwood H L

出版信息

Nature. 1983;303(5919):716-8. doi: 10.1038/303716a0.

Abstract

Octopamine, the phenol analogue of noradrenaline, is a neurosecretory product found in many vertebrate and invertebrate species. In the American lobster, octopamine produces an increase in muscular tension during activation of the motor nerve and may induce spontaneous contractions at concentrations of 10(-7) M (refs 1,2). In the lobster, postsynaptic mechanisms, including a change in Ca2+ conductance of the muscle membrane, are thought to be responsible for potentiation of contraction. In contrast, studies on insects have implicated both pre- and postsynaptic effects: for example, O'Shea and Evans reported that neuromuscular transmission in the locust leg extensor muscle is modulated by octopamine released from a specific neurosecretory neurone which acts on high-affinity octopamine receptors located both on the muscle and on excitatory nerve terminals. The presynaptic receptors mediate an increase in frequency of spontaneous miniature postsynaptic potentials recorded in the muscle. In view of the apparent discrepancy between insect and crustacean results, we have re-examined the effects of octopamine on neuromuscular transmission in a crustacean muscle and report here that enhanced postsynaptic potentials produced by very low levels of octopamine (10(-10) -10(-7) M) are largely attributable to a presynaptic effect which increases quantal release of transmitter. Also, this effect is more pronounced and longer lasting when octopamine is applied to active neuromuscular preparations. This system provides a model for selective consolidation of active synapses by neurohormonal mechanisms. Such an effect could be of general significance in the nervous system, as it would provide a mechanism for selective neurohormonal regulation and strengthening of pathways used during specific activities.

摘要

章鱼胺是去甲肾上腺素的酚类类似物,是在许多脊椎动物和无脊椎动物物种中发现的一种神经分泌产物。在美国龙虾中,章鱼胺在运动神经激活期间会使肌肉张力增加,并且在浓度为10^(-7) M时可能会诱发自发收缩(参考文献1,2)。在龙虾中,包括肌肉膜Ca2+电导变化在内的突触后机制被认为是收缩增强的原因。相比之下,对昆虫的研究表明其具有突触前和突触后效应:例如,奥谢和埃文斯报道,蝗虫腿部伸肌中的神经肌肉传递受到从特定神经分泌神经元释放的章鱼胺的调节,该神经元作用于位于肌肉和兴奋性神经末梢上的高亲和力章鱼胺受体。突触前受体介导肌肉中记录到的自发微小突触后电位频率增加。鉴于昆虫和甲壳类动物的研究结果存在明显差异,我们重新研究了章鱼胺对甲壳类动物肌肉神经肌肉传递的影响,并在此报告,极低水平的章鱼胺(10^(-10) - 10^(-7) M)产生的增强突触后电位在很大程度上归因于突触前效应,该效应增加了递质的量子释放。此外,当将章鱼胺应用于活跃的神经肌肉制剂时,这种效应更明显且持续时间更长。该系统为通过神经激素机制选择性巩固活跃突触提供了一个模型。这种效应在神经系统中可能具有普遍意义,因为它将为特定活动期间使用的通路提供一种选择性神经激素调节和强化的机制。

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