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Addictive drugs have been hypothesized to access the same neurophysiologicalmechanisms as natural learning systems. These natural learningsystems can be modeled through temporal-difference reinforcementlearning (TDRL), which requires a reward-error signal that hasbeen hypothesized to be carried by dopamine. TDRL learns topredict reward by driving that reward-error signal to zero.By adding a noncompensable drug-induced dopamine increase toa TDRL model, a computational model of addiction is constructedthat over-selects actions leading to drug receipt. The modelprovides an explanation for important aspects of the addictionliterature and provides a theoretic view-point with which toaddress other aspects.
Department of Neuroscience, 6-145 Jackson Hall, 321 Church Street SE, University of Minnesota, Minneapolis, MN 55455, USA.
Thermostable Variants of Cocaine Esterase for Long-Time Protection against Cocaine Toxicity.
D. Gao, D. L. Narasimhan, J. Macdonald, R. Brim, M.-C. Ko, D. W. Landry, J. H. Woods, R. K. Sunahara, and C.-G. Zhan (2009)
Mol. Pharmacol.
75, 318-323
|Abstract »|Full Text »|PDF »
Decision-Making Dysfunctions in Psychiatry Altered Homeostatic Processing?.
Neural signature of fictive learning signals in a sequential investment task.
T. Lohrenz, K. McCabe, C. F. Camerer, and P. R. Montague (2007)
PNAS
104, 9493-9498
|Abstract »|Full Text »|PDF »
Differential Regulation of Action Potential- and Metabotropic Glutamate Receptor-Induced Ca2+ Signals by Inositol 1,4,5-Trisphosphate in Dopaminergic Neurons.
G. Cui, B. E. Bernier, M. T. Harnett, and H. Morikawa (2007)
J. Neurosci.
27, 4776-4785
|Abstract »|Full Text »|PDF »
Previous Cocaine Exposure Makes Rats Hypersensitive to Both Delay and Reward Magnitude.
M. R. Roesch, Y. Takahashi, N. Gugsa, G. B. Bissonette, and G. Schoenbaum (2007)
J. Neurosci.
27, 245-250
|Abstract »|Full Text »|PDF »