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Action of octopamine and tyramine on muscles of Drosophila melanogaster larvae

机译:章鱼胺和酪胺对果蝇幼虫肌肉的作用

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Octopamine (OA) and tyramine (TA) play important roles in homeostatic mechanisms, behavior, and modulation of neuromuscular junctions in arthropods. However, direct actions of these amines on muscle force production that are distinct from effects at the neuromuscular synapse have not been well studied. We utilize the technical benefits of the Drosophila larval preparation to distinguish the effects of OA and TA on the neuromuscular synapse from their effects on contractility of muscle cells. In contrast to the slight and often insignificant effects of TA, the action of OA was profound across all metrics assessed. We demonstrate that exogenous OA application decreases the input resistance of larval muscle fibers, increases the amplitude of excitatory junction potentials (EJPs), augments contraction force and duration, and at higher concentrations (10~-5 and 10~-4 M) affects muscle cells 12 and 13 more than muscle cells 6 and 7. Similarly, OA increases the force of synaptically driven contractions in a cell-specific manner. Moreover, such augmentation of contractile force persisted during direct muscle depolarization concurrent with synaptic block. OA elicited an even more profound effect on basal tonus. Application of 10~-5 M OA increased synaptically driven contractions by -1.1 mN but gave rise to a 28-mN increase in basal tonus in the absence of synaptic activation. Augmentation of basal tonus exceeded any physiological stimulation paradigm and can potentially be explained by changes in intramuscular protein mechanics. Thus we provide evidence for independent but complementary effects of OA on chemical synapses and muscle contractility.
机译:章鱼胺(OA)和酪胺(TA)在节肢动物的稳态机制,行为和神经肌肉接头的调节中起重要作用。但是,这些胺对肌肉力量产生的直接作用与对神经肌肉突触的作用不同,因此尚未得到很好的研究。我们利用果蝇幼虫制剂的技术优势来区分OA和TA对神经肌肉突触的影响与对肌肉细胞收缩性的影响。与TA的轻微且通常无关紧要的影响相反,OA在评估的所有指标中的作用都是深远的。我们证明外源OA的使用会降低幼虫肌纤维的输入阻力,增加兴奋性连接电位(EJPs)的幅度,增加收缩力和持续时间,并且在较高浓度(10〜-5和10〜-4 M)下会影响肌肉细胞12和13比肌肉细胞6和7多。类似地,OA以细胞特异性方式增加突触驱动的收缩力。而且,这种收缩力的增加在直接肌肉去极化与突触阻滞的同时持续存在。 OA对基底突突产生了更深远的影响。在没有突触激活的情况下,使用10〜-5 M OA可使突触驱动的收缩增加-1.1 mN,但使基底突突增加28 mN。基底环的增强超出了任何生理刺激范式,并且可能由肌内蛋白质力学的变化来解释。因此,我们为OA对化学突触和肌肉收缩的独立但互补的作用提供了证据。

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