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Pharmacology of Neurotransmitter Release

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  • © 2008

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Part of the book series: Handbook of Experimental Pharmacology (HEP, volume 184)

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Table of contents (17 chapters)

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About this book

It has been known for half a century that neurotransmitters are released in preformed quanta, that the quanta represent transmitter-storing vesicles, and that release occurs by exocytosis. The focus of this book is twofold. In the first part, the molecular events of exocytosis are analysed. This includes a discussion of presynaptic calcium channels, the core proteins of the secretory machinery, and the actions of clostridial toxins and a -latrotoxin, famous for their potency as well as their crucial role in the elucidation of the steps of exocytosis. In the book’s second part, the presynaptic receptors for endogenous chemical signals are presented that make neurotransmitter release a highly regulated process. These include ligand-gated ion channels and presynaptic G-protein-coupled receptors. The targets of presynaptic receptors within the exocytosis cascade, and their therapeutic potential, are subjects addressed in the majority of chapters.

Editors and Affiliations

  • Howard Hughes Medical Institute and Center for Basic Neuroscience, UT Southwestern Medical Center, Dallas, USA

    Thomas C. Südhof

  • Institut für Experimentelle und Klinische Pharmakologie und Toxikologie, Albert-Ludwigs-Universität Freiburg, Germany

    Klaus Starke

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