翼足类软体动物足部5 -羟色胺能神经元簇包含两种形态亚型,具有不同的神经支配目标。

Q4 Neuroscience
Jennifer B Plyler, Richard A Satterlie
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引用次数: 1

摘要

翼足类软体动物Clione limacina的每个足神经节包含一组血清素免疫反应神经元,这些神经元已被证明可以调节翼状旁足的慢抽搐肌肉组织的收缩,并有助于游泳加速。每个神经元簇有不同数量的神经元,在5到9之间,但左右神经节之间没有显著差异。在电生理记录的实验中,染料注射(羧基荧光素),发现集群包含两个子集的神经元。大多数通过n4神经支配同侧翼。每个神经元簇中的两个神经元向脚神经节的n3和n8神经发送信号。n3神经的突起支配颈部体壁,n8神经的突起支配尾部体壁。两组神经元的基线电生理活动不同,因为“翅膀”神经元具有持续的小突触活动,而“体壁”神经元只有很少的突触输入。讨论了Pd-SW簇在游泳加速(翅膀神经元)和控制体内流体压力和翅膀血腔室(体壁神经元)中的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pedal serotonergic neuron clusters of the pteropod mollusc, Clione limacina, contain two morphological subtypes with different innervation targets.

Each pedal ganglion of the pteropod mollusc Clione limacina contains a cluster of serotonin-immunoreactive neurons that have been shown to modulate contractions of the slow-twitch musculature of the wing-like parapodia, and contribute to swim accelerations. Each cluster has a variable number of neurons, between 5 and 9, but there is no significant difference between right and left ganglia. In experiments with electrophysiological recordings followed by dye-injection (carboxyfluorescein), the clusters were found to contain two subsets of neurons. The majority innervate the ipsilateral wing via nerve n4. Two of the neurons in each cluster send processes out of the pedal ganglion in nerves n3 and n8. The processes in nerve n3 innervate the body wall of the neck region, while those in nerve n8 innervate the body wall of the tail. The baseline electrophysiological activity of the two subsets of neurons was different as "wing" neurons had constant barrages of small synaptic activity, while the "body wall" neurons had few synaptic inputs. The potential roles of the Pd-SW cluster in swim acceleration (wing neurons) and control of fluid pressure in the body and wing hemocoelic compartments (body wall neurons) are discussed.

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来源期刊
Invertebrate Neuroscience
Invertebrate Neuroscience NEUROSCIENCES-
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Invertebrate Neurosciences publishes peer-reviewed original articles, reviews and technical reports describing recent advances in the field of invertebrate neuroscience. The journal reports on research that exploits the simplicity and experimental tractability of the invertebrate preparations to underpin fundamental advances in neuroscience. Articles published in Invertebrate Neurosciences serve to highlight properties of signalling in the invertebrate nervous system that may be exploited in the field of antiparisitics, molluscicides and insecticides. Aspects of particular interest include: Functional analysis of the invertebrate nervous system; Molecular neuropharmacology and toxicology; Neurogenetics and genomics; Functional anatomy; Neurodevelopment; Neuronal networks; Molecular and cellular mechanisms of behavior and behavioural plasticity.
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