Dopamine maintains network synchrony via direct modulation of gap junctions in the crustacean cardiac ganglion

Author:

Lane Brian J1ORCID,Kick Daniel R1ORCID,Wilson David K1,Nair Satish S2ORCID,Schulz David J1ORCID

Affiliation:

1. Division of Biological Sciences, University of Missouri, Columbia, United States

2. Department of Electrical Engineering and Computer Science, University of Missouri, Columbia, United States

Abstract

The Large Cell (LC) motor neurons of the crab cardiac ganglion have variable membrane conductance magnitudes even within the same individual, yet produce identical synchronized activity in the intact network. In a previous study we blocked a subset of K+ conductances across LCs, resulting in loss of synchronous activity (Lane et al., 2016). In this study, we hypothesized that this same variability of conductances makes LCs vulnerable to desynchronization during neuromodulation. We exposed the LCs to serotonin (5HT) and dopamine (DA) while recording simultaneously from multiple LCs. Both amines had distinct excitatory effects on LC output, but only 5HT caused desynchronized output. We further determined that DA rapidly increased gap junctional conductance. Co-application of both amines induced 5HT-like output, but waveforms remained synchronized. Furthermore, DA prevented desynchronization induced by the K+ channel blocker tetraethylammonium (TEA), suggesting that dopaminergic modulation of electrical coupling plays a protective role in maintaining network synchrony.

Funder

National Institutes of Health

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference62 articles.

1. Coregulation of ion channel conductances preserves output in a computational model of a crustacean cardiac motor neuron;Ball;Journal of Neuroscience,2010

2. Beyond the connectome: how neuromodulators shape neural circuits;Bargmann;BioEssays,2012

3. Feedback from motor neurones to pacemaker neurones in lobster cardiac ganglion contributes to regulation of burst frequency;Berlind;The Journal of Experimental Biology,1989

4. Dopamine and 5-hydroxytryptamine actions on the cardiac ganglion of the lobster Homarus americanus;Berlind;Journal of Comparative Physiology A: Sensory, Neural, and Behavioral Physiology,1998

5. Monoamine pharmacology of the lobster cardiac ganglion;Berlind;Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology,2001

Cited by 18 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3