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Vol. 54, No. 4, 2006 
Editor's Choice -- Free Access

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Original Paper

Neuropsychobiological Evidence for the Functional Presence and Expression of Cannabinoid CB2 Receptors in the Brain
Emmanuel S. Onaivi

Department of Biology, William Paterson University, Wayne, N.J., USA

Address of Corresponding Author

Neuropsychobiology 2006;54:231-246 (DOI: 10.1159/000100778)


 goto top of outline Key Words

  • CB2 cannabinoid receptor
  • CB2 gene
  • CB2 polyclonal antibody
  • CB2 knockout mice
  • CB2 electron micrograph from brain neurons

 goto top of outline Abstract

For over a decade, until recently, it was thought that marijuana acts by activating brain-type cannabinoid receptors called CB1, and that a second type called CB2 cannabinoid receptor was found only in peripheral tissues. Neuronal CB2 receptors in the brain had been controversial. We reported the discovery and functional presence of CB2 cannabinoid receptors in the mammalian brain that may be involved in depression and drug abuse and this was supported by reports of identification of neuronal CB2 receptors that are involved in emesis. RT-PCR, immunoblotting, hippocampal cultures, immunohistochemistry, transmission electron microscopy, and stereotaxic techniques with behavioral assays were used to determine the functional expression of CB2 cannabinoid receptors in the rat brain and mouse brain exposed to chronic mild stress or treated with abused drugs. RT-PCR analyses supported the expression of brain CB2 receptor transcripts at levels much lower than those of CB1 receptors. In situ hybridization revealed CB2 mRNA in cerebellar neurons of wild-type but not of CB2 knockout mice. Abundant CB2 receptor immunoreactivity (iCB2) in neuronal and glial processes was detected in the brain. The effect of direct CB2 antisense oligonucleotide injection into the brain and treatment with JWH015 in motor function and plus-maze tests also demonstrated the functional presence of CB2 cannabinoid receptors in the central nervous system. In humans, there was a high incidence of Q63R polymorphism in the CB2 gene in Japanese alcoholics and depressed subjects. Contrary to the prevailing view that CB2 cannabinoid receptors are restricted to peripheral tissues and predominantly in immune cells, we demonstrated that CB2 cannabinoid receptors and their gene transcripts are widely distributed in the brain. This multifocal expression of iCB2 in the brain suggests that CB2 receptors may play broader roles than previously anticipated and may therefore be exploited as new targets in the treatment of depression and substance abuse.

Copyright © 2006 S. Karger AG, Basel


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 goto top of outline Author Contacts

Emmanuel S. Onaivi, PhD
Department of Biology
William Paterson University
Wayne, NJ 07470 (USA)
Tel. +1 973 720 3453, Fax +1 973 720 2338, E-Mail Onaivie@wpunj.edu


 goto top of outline Article Information

Received: January 2, 2006
Accepted after revision: December 17, 2006
Published online: March 15, 2007
Number of Print Pages : 16
Number of Figures : 7, Number of Tables : 0, Number of References : 64


 goto top of outline Publication Details

Neuropsychobiology (International Journal of Experimental and Clinical Research in Biological Psychiatry, Pharmacopsychiatry, Biological Psychology/Pharmacopsychology and Pharmacoelectroencephalography)

Vol. 54, No. 4, Year 2006 (Cover Date: April 2007)

Journal Editor: Strik, W. (Bern)
ISSN: 0302-282X (print), 1423-0224 (Online)

For additional information: http://www.karger.com/NPS


 goto top of outline Drug Dosage / Copyright

Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in goverment regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug. Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher or, in the case of photocopying, direct payment of a specified fee to the Copyright Clearance Center.

   


copyright  © 2009 S. Karger AG, Basel
  Last update: 4/4/2007