Drosophila Ryanodine Receptors Mediate General Anesthesia by Halothane
Autor: | Jon W. Marsh, Brigit High, Harold E. Smith, David J. Sandstrom, Howard A. Nash, Shuying Gao |
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Rok vydání: | 2013 |
Předmět: |
Male
Molecular Sequence Data Anesthesia General Biology Inhibitory postsynaptic potential Article Cell Line Immobilization In vivo medicine Animals Point Mutation Amino Acid Sequence Ryanodine receptor Ryanodine Receptor Calcium Release Channel Hyperpolarization (biology) In vitro Electrophysiology Drosophila melanogaster Anesthesiology and Pain Medicine Anesthesia Anesthetics Inhalation Anesthetic Halothane medicine.drug |
Zdroj: | Anesthesiology. 118:587-601 |
ISSN: | 0003-3022 |
DOI: | 10.1097/aln.0b013e31827e52c6 |
Popis: | Background—Although in vitro studies have identified numerous possible targets, the molecules that mediate the in vivo effects of volatile anesthetics remain largely unknown. The mammalian ryanodine receptor (Ryr) is a known halothane target, and we hypothesized that it has a central role in anesthesia. Methods—Gene function of the Drosophila Ryr (dRyr) was manipulated in the whole body or in specific tissues using a collection of mutants and transgenes, and responses to halothane were measured with a reactive climbing assay. Cellular responses to halothane were studied using Ca 2+ imaging and patch clamp electrophysiology. Results—Halothane potency strongly correlates with dRyr gene copy number, and missense mutations in regions known to be functionally important in mammalian Ryrs gene cause dominant hypersensitivity. Tissue-specific manipulation of dRyr shows that expression in neurons and glia, but not muscle, mediates halothane sensitivity. In cultured cells, halothane-induced Ca 2+ efflux is strictly dRyr-dependent, suggesting a close interaction between halothane and dRyr. Ca 2+ imaging and electrophysiology of Drosophila central neurons reveal halothane-induced Ca 2+ flux that is altered in dRyr mutants and correlates with strong hyperpolarization. Conclusions—In Drosophila, neurally-expressed dRyr mediates a substantial proportion of halothane's anesthetic effects in vivo, is potently activated by halothane in vitro, and activates an inhibitory conductance. Our results provide support for Ryr as an important mediator of immobilization by volatile anesthetics. |
Databáze: | OpenAIRE |
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