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Education  |   June 2012
A Novel Fluorescent General Anesthetic Enables Imaging of Sites of Action In Vivo 
Author Affiliations & Notes
  • Roderic G. Eckenhoff, M.D.
    *
  • *Department of Anesthesiology & Critical Care, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania.
Article Information
Education / Pharmacology / Radiological and Other Imaging
Education   |   June 2012
A Novel Fluorescent General Anesthetic Enables Imaging of Sites of Action In Vivo 
Anesthesiology 6 2012, Vol.116, 1363. doi:10.1097/ALN.0b013e31824cb4b1
Anesthesiology 6 2012, Vol.116, 1363. doi:10.1097/ALN.0b013e31824cb4b1
A DIFFICULTY in understanding anesthetic pharmacology lies in the fleeting drug interactions with tissues and cells, which makes difficult the determination of distribution at any level. A better understanding of general anesthetic distribution is important for quantifying “off-target” and “on-target” effects and may be useful in assessing drug efficacy and safety. We have discovered a molecule with anesthetic properties1 that becomes strongly fluorescent when constrained in a hydrophobic pocket, such as a protein binding site, and are using it to define potential sites of anesthetic action.
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Albino Xenopus laevis  tadpoles (stage 40–47, Nasco, Fort Atkinson, WI) were incubated for 30 min in pond water containing the fluorescent general anesthetic 1-aminoanthracene (15 μM). Immobilized tadpoles were rinsed with fresh pond water and imaged again with an Olympus IX81 fluorescence microscope (Center Valley, PA). The tadpoles were excited with ∼440 nm light and emission collected at ∼520 nm; then, we obtained regional images that were stitched together to obtain the fluorescence micrograph shown. This image shows striking preference for labeling of neuronal tissues (brain, eyes, olfactory organs, spinal cord), which is consistent with our preconceived notion of where a general anesthetic ought to be acting. Also consistent with our current ideas of anesthetics acting on ion channels and synapses in excitable tissues is the labeling of tail muscle and gut. Aside from directly visualizing binding sites for general anesthetics in a living organism, this new tool allows the dissection and validation of molecular targets far more rapidly and inexpensively than previous methods. Using approaches such as this, it should be possible to begin a campaign of target discovery to more fully understand the cellular and molecular basis of general anesthesia.
The authors thank Ashley Fiamengo, Ph.D. (Postdoctoral Fellow), and John Psonis (Undergraduate Student), both of the Department of Chemistry, University of Pennsylvania School of Arts and Sciences, Philadelphia, Pennsylvania, for help with tadpole handling and imaging experiments.
Reference
Reference
Butts CA, Xi J, Brannigan G, Saad AA, Venkatachalan SP, Pearce RA, Klein ML, Eckenhoff RG, Dmochowski IJ: Identification of a fluorescent general anesthetic, 1-aminoanthracene. Proc Natl Acad Sci USA 2009; 106:6501–6
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