Our laboratory has used assays of the gross behavior of the fruit fly, Drosophila melanogaster, to isolate mutants that alter the sensitivity of the animal to general anesthetics. To narrow the focus of this research toward mutants that directly influence anesthetic targets, we study the neural pathway involved in the visual escape response (VER) of Drosophila, which has the desired combination of simplicity and sensitivity to anesthetic agents. The placement of electrodes that activate the anesthetic-sensitive pathway indicates that the critical target lies in an oligosynaptic pathway that connects the lamina of the visual system with the giant fiber neuron in the deutocerebrum. Mutants that affect the sensitivity of this oligosynaptic pathway will be vital tools for exploring what regulates the sensitivity of the anesthetic target. We are using a minichromosome, Df(1;f)LJ9, to fashion a proper comparison between wild-type flies and those that carry a mutation in a novel locus, harA, that alters halothane sensitivity in behavioral assays. We have also undertaken the cloning of this locus. Genomic clones that cover over 200 kbp from its presumptive location have been obtained; mapping of deficiency breakpoints within these clones has confirmed and refined the position of the gene.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Intramural Research (Z01)
Project #
1Z01MH002228-11
Application #
2578708
Study Section
Special Emphasis Panel (LMB)
Project Start
Project End
Budget Start
Budget End
Support Year
11
Fiscal Year
1996
Total Cost
Indirect Cost
Name
U.S. National Institute of Mental Health
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Burg, E D; Langan, S T; Nash, H A (2013) Drosophila social clustering is disrupted by anesthetics and in narrow abdomen ion channel mutants. Genes Brain Behav 12:338-47
Peabody, Nathan C; Pohl, Jascha B; Diao, Fengqiu et al. (2009) Characterization of the decision network for wing expansion in Drosophila using targeted expression of the TRPM8 channel. J Neurosci 29:3343-53
Sandstrom, David J (2008) Isoflurane reduces excitability of Drosophila larval motoneurons by activating a hyperpolarizing leak conductance. Anesthesiology 108:434-46
Cheng, Yuzhong; Nash, Howard A (2008) Visual mutations reveal opposing effects of illumination on arousal in Drosophila. Genetics 178:2413-6
Cheng, Yuzhong; Nash, Howard A (2007) Drosophila TRP channels require a protein with a distinctive motif encoded by the inaF locus. Proc Natl Acad Sci U S A 104:17730-4
Humphrey, John A; Hamming, Kevin S; Thacker, Colin M et al. (2007) A putative cation channel and its novel regulator: cross-species conservation of effects on general anesthesia. Curr Biol 17:624-9
Yu, James X; Guan, Zhonghui; Nash, Howard A (2006) The mushroom body defect gene product is an essential component of the meiosis II spindle apparatus in Drosophila oocytes. Genetics 173:243-53
Rajaram, Shantadurga; Scott, Robert L; Nash, Howard A (2005) Retrograde signaling from the brain to the retina modulates the termination of the light response in Drosophila. Proc Natl Acad Sci U S A 102:17840-5
Sandstrom, David J; Nash, Howard (2004) Drug targets: turning the channel (on) for sedation. Curr Biol 14:R185-6
Sandstrom, David J (2004) Isoflurane depresses glutamate release by reducing neuronal excitability at the Drosophila neuromuscular junction. J Physiol 558:489-502

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