[return to list
Jay  Hirsh
Degree(s): Ph.D.
Graduate School: California Institute of Technology
Primary Appointment: Professor of Biology
Research Interests:
Molecular genetics; development and function of neurotransmitter-synthesizing neurons in Drosophila

Email Address: jh6u@virginia.edu


Biomedical Sciences Graduate Program(s)
  • Neuroscience
  • Molecular Cell and Developmental Biology

  • Research Description

    My laboratory is using the fruit fly, Drosophila melanogaster, as a model system for studying the molecular genetics of responsiveness to cocaine and other drugs of abuse. We have shown that exposure to aerosolized free base cocaine induces multiple reflexive motor responses that resemble cocaine induced behaviors in vertebrates, and also resemble dopamine agonist induced behaviors previously observed in decapitated flies (Yellman et al, 1997). Furthermore, Drosophila develop behavioral sensitization to intermittent doses of cocaine. Sensitization has been linked to the addictive processes in vertebrates, and it is of great interest to understand the basic mechanisms leading to sensitization in a simple model system. Our results suggest that the pathways leading to cocaine induced responses are evolutionarily conserved between Drosophila and higher vertebrates, and that this genetically tractable animal can be used as a new model system to help determine the biological mechanisms underlying these processes. Recent studies are uncovering some unexpected gene products and small molecules involved in sensitization in flies. We have found that regulated production of the trace amine tyramine is essential for the development of sensitization (McClung & Hirsh, 1999). In addition, we have found that a subset of genes essential for fly circadian functions are required for sensitization (Andretic et al, 1999). Given the conservation of structure and function of these circadian genes in animals from flies to higher vertebrates, there is a strong likelihood of conserved functions for these genes in modulating drug responses across evolution. Ongoing studies are aimed at further elucidating the mechanisms and genes involved in modulating sensitization and drug responsiveness. PLEASE NOTE: Funded Postdoctoral position available to work on the above studies. Contact Jay for further information.


    Selected Publications
  • Sang Ki Park, Ying Cai, Rebecca George, Florence Friggi-Grelin, Serge Birman and Jay Hirsh (2006) Cell type-specific limitation on in vivo serotonin storage following ectopic expression of the Drosophila serotonin transporter, dSERT. J Neurobiology, in press.
  • Shannon (Cole) Hardie, J. Hirsh (2005) An Improved Method For The Separation And Detection Of Biogenic Amines In Adult Drosophila Brain Extracts By High Performance Liquid Chromatography, J. Neurosci Methods, in press.
  • Kazuhiko Kume, Shoen Kume, Sang Ki Park, Jay Hirsh and F. Rob Jackson Dopamine is a key regulator of arousal in the fruit fly. J Neuroscience (2005) 25, 7377-7384.
  • Shannon H. Cole, Ginger E. Carney, Colleen A. McClung, Stacey S. Willard, Barbara J. Taylor, Jay Hirsh (2005) Two functional but non-complementing Drosophila tyrosine decarboxylase genes: Distinct roles for neural tyramine and octopamine in female fertility. J Biol Chem, (2005) 280; 14948-14955.
  • PubMed Listings for this Faculty Member

  • Intranet Profile
    [To add/update Intranet profile information, read these instructions.]

    Contact Information
      Office Address: PO Box 400328, Gilmer Hall, 262, 
      Office Phone: +1 434-982-5608, +1 434-982-5607
      Fax Phone: +1 434-982-5626
      Home Phone: +1 434-295-9985

    Other Websites for this mentor:
    http://minerva.acc.virginia.edu/%7Ebiology/Fac/HIRSH.html

    (Find Out How to Update Your Faculty Profile)