Basic Science Tower, SUNY Stony Brook, Stony Brook, NY 11794-8651 / 631-444-3219
STATE UNIVERSITY OF NEW YORK AT STONY BROOK
Medical Scientist (M.D./Ph.D.) Training Program

Amy L. DeMarco
B.A. Colgate University, 2005

2nd Year Medical Student

Department: Medicine

Graduate Program: Will be Molecular & Cellular
    Pharmacology

Advisor: Holly Colognato, Ph.D.


Abstract (undergraduate):

Advisor: Dr. Stephen Dewey, Medical Department, Brookhaven National Laboratory

Title:
 Racemic gamma vinyl-GABA (R,S-GVG) blocks methamphetamine-triggered reinstatement of conditioned place preference

DeMarco A, Dalal RM, Pai J, Aquilina SD, Mullapudi U, Hammel C, Kothari SK, Kahanda M, Liebling CN, Patel V, Schiffer WK, Brodie JD, Dewey SL.
Medical Department, Brookhaven National Laboratory, Upton, New York 11973.

Preventing relapse poses a significant challenge to the successful management of methamphetamine (METH) dependence. Although no effective medication currently exists for its treatment, racemic gamma vinyl-GABA (R,S-GVG, vigabatrin) shows enormous potential as it blocks both the neurochemical and behavioral effects of a variety of drugs, including METH, heroin, morphine, ethanol, nicotine, and cocaine. Using the reinstatement of a conditioned place preference (CPP) as an animal model of relapse, the present study specifically investigated the ability of an acute dose of R,S-GVG to block METH-triggered reinstatement of a METH-induced CPP. Animals acquired a METH CPP following a 20-day-period of conditioning, in which they received 10 pairings of alternating METH and saline injections. During conditioning, rats were assigned to one of four METH dosage groups: 1.0, 2.5, 5.0, or 10.0 mg/kg (i.p., n = 8/group). Animals in all dosage groups demonstrated a robust and consistent CPP. This CPP was subsequently extinguished in each dosage group with repeated saline administration. Upon extinction, all groups reinstated following an acute METH challenge. On the following day, an acute dose of R,S-GVG (300 mg/kg, i.p.) was administered 2.5 h prior to an identical METH challenge. R,S-GVG blocked METH-triggered reinstatement in all four groups. Given that drug re-exposure may potentiate relapse to drug-seeking behavior, the ability of R,S-GVG to block METH-triggered reinstatement offers further support for its use in the successful management of METH dependence. Synapse 63:87-94, 2009. (c) 2008 Wiley-Liss, Inc.

Publications:
(pre-MSTP publications indicated with an *)

*DeMarco A, Dalal RM, Kahanda M, Mullapudi U, Pai J, Hammel C, Liebling CN, Patel V, Brodie JD, Schiffer WK, Dewey SL, Aquilina SD. (2008). Subchronic racemic gamma vinyl-GABA produces weight loss in Sprague Dawley and Zucker fatty rats. Synapse. Nov;62(11):870-2.

*DeMarco A, Dalal RM, Pai J, Aquilina SD, Mullapudi U, Hammel C, Kothari SK, Kahanda M, Liebling CN, Patel V, Schiffer WK, Brodie JD, Dewey SL. (2009). Racemic gamma vinyl-GABA (R,S-GVG) blocks methamphetamine-triggered reinstatement of conditioned place preference. Synapse. Feb;63(2):87-94.

 


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