TY - JOUR
T1 - Inhaled drugs of abuse enhance serotonin-3 receptor function
AU - Lopreato, Gregory F.
AU - Phelan, Rachel
AU - Borghese, Cecilia M.
AU - Beckstead, Michael J.
AU - Mihic, S. John
N1 - Funding Information:
The authors wish to thank Drs. David Julius and Tina Machu for kindly providing the 5-HT 3A receptor subunit cDNAs used in this study. This research was supported by NIH grant 5R01AA11525 (to S.J.M.), an individual NRSA fellowship 1F31AA05605 (to M.J.B.) and a postdoctoral fellowship from Alcohol Training Grant 5T32AA007471 to the University of Texas at Austin (to G.F.L.). Support was also provided by the Texas Commission on Alcohol and Drug Abuse (to S.J.M.).
PY - 2003/5/1
Y1 - 2003/5/1
N2 - Despite the prevalence of their use, little is currently known of the molecular mechanisms of action of inhaled drugs of abuse. Recent studies have shown effects on NMDA, GABAA and glycine receptors in vitro, suggesting that inhalants may exert at least some of their pharmacological effects on ligand-gated ion channels. Enhancement of serotonin-3 receptor function has been shown to play a role in the reinforcing properties of drugs of abuse. We tested the hypothesis that the commonly abused inhaled agents 1,1,1-trichloroethane, trichloroethylene, and toluene enhance serotonin-3 receptor function. All three inhalants significantly and reversibly potentiated, in a dose-dependent manner, serotonin-activated currents mediated by mouse serotonin-3A receptors expressed in Xenopus oocytes. Our findings add the serotonin-3 receptor to the growing list of molecular targets commonly affected by both inhalants and classic CNS depressants such as ethanol and the volatile anesthetics.
AB - Despite the prevalence of their use, little is currently known of the molecular mechanisms of action of inhaled drugs of abuse. Recent studies have shown effects on NMDA, GABAA and glycine receptors in vitro, suggesting that inhalants may exert at least some of their pharmacological effects on ligand-gated ion channels. Enhancement of serotonin-3 receptor function has been shown to play a role in the reinforcing properties of drugs of abuse. We tested the hypothesis that the commonly abused inhaled agents 1,1,1-trichloroethane, trichloroethylene, and toluene enhance serotonin-3 receptor function. All three inhalants significantly and reversibly potentiated, in a dose-dependent manner, serotonin-activated currents mediated by mouse serotonin-3A receptors expressed in Xenopus oocytes. Our findings add the serotonin-3 receptor to the growing list of molecular targets commonly affected by both inhalants and classic CNS depressants such as ethanol and the volatile anesthetics.
KW - Electrophysiology
KW - Inhalants
KW - Serotonin-3 receptor
KW - Xenopus oocytes
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U2 - 10.1016/S0376-8716(02)00330-7
DO - 10.1016/S0376-8716(02)00330-7
M3 - Article
C2 - 12681521
AN - SCOPUS:0037402029
VL - 70
SP - 11
EP - 15
JO - Drug and Alcohol Dependence
JF - Drug and Alcohol Dependence
SN - 0376-8716
IS - 1
ER -