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      Identification of a fluorescent general anesthetic, 1-aminoanthracene.

      Proceedings of the National Academy of Sciences of the United States of America
      Anesthetics, General, metabolism, Animals, Anthracenes, pharmacology, Apoferritins, chemistry, Binding Sites, Chloride Channels, Fluorescence, Fluorescent Dyes, Horses, Ion Channel Gating, drug effects, Isoflurane, Larva, cytology, Microscopy, Confocal, Neurons, Propofol, Protein Structure, Secondary, Reflex, Startle, Spectrometry, Fluorescence, Temperature, Xenopus laevis, gamma-Aminobutyric Acid

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          Abstract

          We identified a fluorophore, 1-aminoanthracene (1-AMA), that is anesthetic, potentiates GABAergic transmission, and gives an appropriate dissociation constant, K(d) approximately 0.1 mM, for binding to the general anesthetic site in horse spleen apoferritin (HSAF). 1-AMA fluorescence is enhanced when bound to HSAF. Thus, displacement of 1-AMA from HSAF by other anesthetics attenuates the fluorescence signal and allows determination of K(d), as validated by isothermal titration calorimetry. This provides a unique fluorescence assay for compound screening and anesthetic discovery. Additional electrophysiology experiments in isolated cells indicate that 1-AMA potentiates chloride currents elicited by GABA, similar to many general anesthetics. Furthermore, 1-AMA reversibly immobilizes stage 45-50 Xenopus laevis tadpoles (EC(50) = 16 microM) and fluorescence micrographs show 1-AMA localized to brain and olfactory regions. Thus, 1-AMA provides an unprecedented opportunity for studying general anesthetic distribution in vivo at the cellular and subcellular levels.

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