Synaptic mechanism underlying serotonin modulation of transition to cocaine addiction

Author:

Li Yue12ORCID,Simmler Linda D.12ORCID,Van Zessen Ruud12,Flakowski Jérôme13ORCID,Wan Jin-Xia42ORCID,Deng Fei142ORCID,Li Yu-Long142ORCID,Nautiyal Katherine M.3ORCID,Pascoli Vincent14ORCID,Lüscher Christian1235ORCID

Affiliation:

1. Department of Basic Neurosciences, Medical Faculty, University of Geneva, CH-1211 Geneva, Switzerland.

2. IDG McGovern Institute for Brain Research, Peking University, Beijing 100871, China.

3. Department of Psychological and Brain Sciences, Dartmouth College, Hanover, NH 03755, USA.

4. State Key Laboratory of Membrane Biology, Peking University School of Life Sciences, Beijing 100871, China.

5. Clinic of Neurology, Department of Clinical Neurosciences, Geneva University Hospital, CH-1211 Geneva, Switzerland.

Abstract

Prevention of compulsive cocaine taking Over time, about 20% of chronic cocaine users lose control and become addicted. There are indications that the differential efficacy of the brain serotonin (5-HT) system may be involved in the vulnerability to drug addiction. However, the relevant circuits and underlying cellular processes remain elusive. Li et al . discovered a synaptic mechanism in mice that underlies the modulatory role of 5-HT in reducing the likelihood of transition to compulsion and eventually addiction (see the Perspective by Miyazaki and Miyazaki). Cocaine binds to 5-HT transporters to block 5-HT reuptake. The elevated extracellular 5-HT activates 5-HT 1B receptors and causes presynaptic depression of a projection from the orbitofrontal cortex to the dorsal striatum. These changes reduce the likelihood of inducing postsynaptic potentiation at these synapses, which ultimately drives compulsion. —PRS

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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