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Professor Barry J Everitt Sc D, FRS, F Med Sci

Professor Barry J Everitt, Sc D, FRS, F Med Sci

Emeritus Professor of Behavioural Neuroscience

Provost, Gates Cambridge Trust

Department of Psychology
University of Cambridge
Downing Street
Cambridge CB2 3EB

Office Phone: +44 (0)1223 3 33583/(0)1223 7 65286 (Dept)/(0)1223 3 34806 (Downing College)

Research Interests

My research is in the general area of behavioural neuroscience and is concerned with the neural and psychological mechanisms underlying learning, memory and motivation. My major research focus is the neuropsychology of drug addiction and is funded by the Medical Research Council. There are several key themes to this research: (i) the impact of learning on drug addiction – both its development and its persistence. For example, individuals who initially take drugs do so voluntarily (in psychological terms it is ‘goal-directed’); subsequently, prolonged bouts of drug taking, in some individuals, result in a loss of control over drug intake and in time it becomes a compulsive habit that is extremely difficult to relinquish. We have shown that this transition from initial, voluntary drug use to the compulsive drug taking, addicted state occurs through the progressive engagement of different pavlovian and instrumental learning systems in the brain and we are continuing to investigate this issue at a cellular and systems level. (ii) Only a small proportion of individuals who take drugs go on to become addicted and they can be considered as vulnerable. Research in our laboratory has shown that behavioural impulsivity is a vulnerability characteristic for addiction: impulsive individuals more readily escalate their cocaine intake and are those most likely to develop compulsive drug seeking and taking, which persists in the face of adverse outcomes. Impulsivity, we have shown, is associated with reduced levels of the D2 subtype of dopamine receptor in a specific brain area, the nucleus accumbens. (iii) Drug cues – stimuli that have become associated with the effects of self-administered drugs through pavlovian conditioning (these include not only the paraphernalia used by drug addicts, but specific places and even people) – also exert a powerful control over addictive behaviour. These cues elicit drug craving and they can precipitate relapse to a drug-taking habit in otherwise abstinent individuals. We have studied extensively the neural systems underlying these pavlovian influences on drug seeking. (iv) When individuals retrieve drug-associated memories, for example when they are exposed to drug-associated stimuli, the retrieved memory enters a labile state from which it must be restored, or reconsolidated through a new round of protein synthesis in the brain. This means that maladaptive drug-associated memories can be disrupted when they are made labile at retrieval. In our recent research we have shown both the underlying neural and cellular mechanisms involved, and also that disrupting such maladaptive memories can prevent subsequent drug seeking and relapse. Thus, disrupting drug memories in a clinical setting might provide a future treatment for drug addiction – and also other neuropsychiatric disorders characterized by intrusive and maladaptive memories, such as post-traumatic stress disorder.


  • memory reconsolidation
  • neural and psychological basis of drug addiction
  • reconsolidation
  • learning
  • memory
  • addiction
  • cocaine

Key Publications


Everitt BJ & Robbins TW. (2013) From the ventral to the dorsal striatum: evolving views of their roles in drug addiction. Neurosci Biobehav Rev. 2013 Nov;37(9 Pt A):1946-54. doi: 10.1016/j.neubiorev.2013.02.010. PubMed PMID: 23438892.

Belin D, Belin-Rauscent A, Murray JE, Everitt BJ (2013) Addiction: failure of control over maladaptive incentive habits. Curr Opin Neurobiol. 2013 Aug;23(4):564-72. doi: 10.1016/j.conb.2013.01.025. PubMed PMID: 23452942.

Giuliano C, Robbins TW, Wille DR, Bullmore ET, Everitt BJ. (2013) Attenuation of cocaine and heroin seeking by μ-opioid receptor antagonism. Psychopharmacology (Berl). 2013 May;227(1):137-47. doi: 10.1007/s00213-012-2949-9. PubMed PMID: 23299095; PubMed Central PMCID: PMC3622002.

Willuhn I, Burgene LM, Everitt BJ & Phillips PEM. (2012) Encoding of drug cues by dopamine is under the control of a striatal hierarchy. Proc Natl Acad Sci U S A. 109(50):20703-8. doi: 10.1073/pnas.1213460109. PubMed PMID: 23184975; PubMed Central PMCID: PMC3528544.

Giuliano C, Robbins TW , Nathan PJ, Bullmore ET & Everitt BJ. (2012) Inhibition of opioid transmission at the µ-opioid receptor prevents both food seeking and binge-like eating. Neuropsychopharmacology doi: 10.1038/npp.2012.128

Murray JE, Belin D & Everitt BJ. (2012) Double dissociation of the dorsomedial and dorsolateral striatal control over the acquisition and performance of cocaine seeking. Neuropsychopharmacology 37:2456-66. doi: 10.1038/npp.2012.104.

Pelloux, Y Dilleen R, Economidou D, Theobald D & Everitt BJ. Reduced forebrain serotonin transmission is causally involved in the development of compulsive cocaine seeking.  Neuropsychopharmacology  37(11):2505-14 doi: 10.1038/npp.2012.111

Jonkman S, Pelloux Y & Everitt BJ. (2012) Differential roles of the dorsolateral and midlateral striatum in punished drug seeking. J Neuroscience 2(13):4645– 4650 • 4645

Belin, D., & Everitt, B.J. (2008). Cocaine seeking habits depend upon dopamine-dependent serial connectivity linking the ventral with the dorsal striatum. Neuron, 57 (3): 432-441.

Belin D., Mar, A.C., Dalley, J.W., Robbins, T.W., & Everitt, B.J. (2008). High impulsivity predicts the switch to compulsive cocaine seeking. Science 320(5881): 1352-1355.

Everitt, B.J., Belin, D., Economidou, D., Pelloux, Y., Dalley, J.W., & Robbins, T.W. (2008). Neural mechanisms underlying the vulnerability to develop compulsive drug seeking habits and addiction. Philosophical Transactions of the Royal Society, Lond. B Biol. Sci. 363(1507): 3125-313

Everitt BJ, Robbins TW (2005). Neural systems of reinforcement for drug addiction: from actions to habits to compulsion.  Nature Neuroscience 8: 1481-1489