首页 | 本学科首页   官方微博 | 高级检索  
     


Electrochemical Measurements of Optogenetically Stimulated Quantal Amine Release from Single Nerve Cell Varicosities in Drosophila Larvae
Authors:Dr. Soodabeh Majdi  Dr. E. Carina Berglund  Johan Dunevall  Dr. Alexander I. Oleinick  Prof. Christian Amatore  Prof. David E. Krantz  Prof. Andrew G. Ewing
Affiliation:1. Department of Chemistry and Chemical Engineering, Chalmers University of Technology Department, Kemiv?gen 10, 41296 Gothenburg (Sweden);2. Department of Chemistry and Molecular Biology, University of Gothenburg, Kemiv?gen 10, 41296 Gothenburg (Sweden);3. Ecole Normale Supérieure‐PSL Research University, Département de Chimie, Sorbonne Universités‐UPMC Univ Paris 06, CNRS UMR 8640 PASTEUR, 24, rue Lhomond, 75005 Paris (France);4. Department of Psychiatry and Biobehavioral Sciences, Gonda Center for Neuroscience and Genetics Research, David Geffen School of Medicine at, University of California, Los Angeles, CA (USA)
Abstract:The nerve terminals found in the body wall of Drosophila melanogaster larvae are readily accessible to experimental manipulation. We used the light‐activated ion channel, channelrhodopsin‐2, which is expressed by genetic manipulation in Type II varicosities to study octopamine release in Drosophila. We report the development of a method to measure neurotransmitter release from exocytosis events at individual varicosities in the Drosophila larval system by amperometry. A microelectrode was placed in a region of the muscle containing a varicosity and held at a potential sufficient to oxidize octopamine and the terminal stimulated by blue light. Optical stimulation of Type II boutons evokes exocytosis of octopamine, which is detected through oxidization at the electrode surface. We observe 22700±4200 molecules of octopamine released per vesicle. This system provides a genetically accessible platform to study the regulation of amine release at an intact synapse.
Keywords:amperometry  channelrhodopsin  Drosophila larvae  octopamine  varicosity
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号