Tryptophan depletion impairs stimulus-reward learning while methylphenidate disrupts attentional control in healthy young adults: implications for the monoaminergic basis of impulsive behaviour.

@article{citeulike:1305945, abstract = {RATIONALE: Altered serotonergic and dopaminergic function have been widely implicated in behavioural disorders associated with impulsivity and risk-taking. However, little research has addressed the specific cognitive consequences of changed monoaminergic function that might contribute to the production of impulsive behaviour. OBJECTIVES AND METHODS: We compared the effects of rapid plasma tryptophan depletion, acute doses of the mixed indirect catecholamine agonist, methylphenidate (40 mg), and acute doses of the alpha(1)/alpha(2 )agonist, clonidine (1.5 microg/kg), on aspects of visual discrimination learning involving either acquisition of altered stimulus-reward associations (i.e. updating the affective valence of exteroceptive stimuli) or the control of attention towards relevant as opposed to irrelevant stimulus dimensions. RESULTS: Relative to subjects who received placebo, subjects with reduced tryptophan exhibited a deficit in the ability to learn changed stimulus-reward associations, but were still able to shift an acquired attentional set away from a now-irrelevant stimulus dimension towards a newly relevant dimension. By contrast, subjects who received methylphenidate were able to learn effectively about changing stimulus-reward associations, but showed an enhanced ability to shift an attentional bias, in combination with slowed response times. Subjects who received clonidine showed neither of these changes. CONCLUSIONS: These results suggest that reduction in central serotonin leads to altered neuromodulation of the cortical and subcortical regions (e.g. orbitofrontal cortex, striatum and anterior temporal structures) that mediate important aspects of associative learning whereby exteroceptive stimuli acquire altered incentive motivational value. On the other hand, facilitation of catecholamine neurotransmitters may disrupt the allocation of attention between relevant and irrelevant features of the environment, perhaps through altered modulation of the dorsolateral prefrontal cortex. The implications of these results for understanding the differential neuromodulation of cognitive functions are discussed.}, address = {Departments of Experimental Psychology and Psychiatry, University of Cambridge, Cambridge, UK. robert.rogers@psychiatry.oxford.ac.uk}, author = {Rogers, R. D. and Blackshaw, A. J. and Middleton, H. C. and Matthews, K. and Hawtin, K. and Crowley, C. and Hopwood, A. and Wallace, C. and Deakin, J. F. and Sahakian, B. J. and Robbins, T. W. }, citeulike-article-id = {1305945}, issn = {0033-3158}, journal = {Psychopharmacology (Berl)}, keywords = {stimulus-reward\_learning, tryptophan\_depletion}, month = {October}, number = {4}, pages = {482--491}, posted-at = {2007-05-18 17:59:52}, priority = {2}, title = {Tryptophan depletion impairs stimulus-reward learning while methylphenidate disrupts attentional control in healthy young adults: implications for the monoaminergic basis of impulsive behaviour.}, url = {http://view.ncbi.nlm.nih.gov/pubmed/10550499}, volume = {146}, year = {1999} }

TY - JOUR ID - citeulike:1305945 L3 - citeulike-article-id:1305945 TI - Tryptophan depletion impairs stimulus-reward learning while methylphenidate disrupts attentional control in healthy young adults: implications for the monoaminergic basis of impulsive behaviour. JF - Psychopharmacology (Berl) VL - 146 IS - 4 SP - 482 EP - 491 AD - Departments of Experimental Psychology and Psychiatry, University of Cambridge, Cambridge, UK. robert.rogers@psychiatry.oxford.ac.uk SN - 0033-3158 N2 - RATIONALE: Altered serotonergic and dopaminergic function have been widely implicated in behavioural disorders associated with impulsivity and risk-taking. However, little research has addressed the specific cognitive consequences of changed monoaminergic function that might contribute to the production of impulsive behaviour. OBJECTIVES AND METHODS: We compared the effects of rapid plasma tryptophan depletion, acute doses of the mixed indirect catecholamine agonist, methylphenidate (40 mg), and acute doses of the alpha(1)/alpha(2 )agonist, clonidine (1.5 microg/kg), on aspects of visual discrimination learning involving either acquisition of altered stimulus-reward associations (i.e. updating the affective valence of exteroceptive stimuli) or the control of attention towards relevant as opposed to irrelevant stimulus dimensions. RESULTS: Relative to subjects who received placebo, subjects with reduced tryptophan exhibited a deficit in the ability to learn changed stimulus-reward associations, but were still able to shift an acquired attentional set away from a now-irrelevant stimulus dimension towards a newly relevant dimension. By contrast, subjects who received methylphenidate were able to learn effectively about changing stimulus-reward associations, but showed an enhanced ability to shift an attentional bias, in combination with slowed response times. Subjects who received clonidine showed neither of these changes. CONCLUSIONS: These results suggest that reduction in central serotonin leads to altered neuromodulation of the cortical and subcortical regions (e.g. orbitofrontal cortex, striatum and anterior temporal structures) that mediate important aspects of associative learning whereby exteroceptive stimuli acquire altered incentive motivational value. On the other hand, facilitation of catecholamine neurotransmitters may disrupt the allocation of attention between relevant and irrelevant features of the environment, perhaps through altered modulation of the dorsolateral prefrontal cortex. The implications of these results for understanding the differential neuromodulation of cognitive functions are discussed. KW - stimulus-reward_learning KW - tryptophan_depletion AU - Rogers, RD AU - Blackshaw, AJ AU - Middleton, HC AU - Matthews, K AU - Hawtin, K AU - Crowley, C AU - Hopwood, A AU - Wallace, C AU - Deakin, JF AU - Sahakian, BJ AU - Robbins, TW PY - 1999/10// UR - http://view.ncbi.nlm.nih.gov/pubmed/10550499 ER -