Volume 1074, Issue 1 p. 514-536

Discovery of the Presence and Functional Expression of Cannabinoid CB2 Receptors in Brain

EMMANUEL S. ONAIVI

William Paterson University, Wayne, New Jersey 07470, USA

MNB, NIDA, Baltimore, Maryland 21224, USA

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HIROKI ISHIGURO

Institute of Basic Medical Sciences, University of Tsukuba, Tsukuba Japan

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JIAN‐PING GONG

MNB, NIDA, Baltimore, Maryland 21224, USA

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SEJAL PATEL

William Paterson University, Wayne, New Jersey 07470, USA

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ALEX PERCHUK

William Paterson University, Wayne, New Jersey 07470, USA

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PAUL A. MEOZZI

William Paterson University, Wayne, New Jersey 07470, USA

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LESTER MYERS

William Paterson University, Wayne, New Jersey 07470, USA

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ZOILA MORA

William Paterson University, Wayne, New Jersey 07470, USA

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PATRICIA TAGLIAFERRO

Universidad de Buenos Aires, Buenos Aires, Argentina

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EILEEN GARDNER

William Paterson University, Wayne, New Jersey 07470, USA

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ALICIA BRUSCO

Universidad de Buenos Aires, Buenos Aires, Argentina

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BABATUNDE E. AKINSHOLA

Howard University, Washington, DC 20059, USA

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QING‐RONG LIU

MNB, NIDA, Baltimore, Maryland 21224, USA

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BRUCE HOPE

Behavioral Neuroscience Branch, NIDA, Baltimore, Maryland 21224, USA

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SHINYA IWASAKI

Institute of Basic Medical Sciences, University of Tsukuba, Tsukuba Japan

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TADAO ARINAMI

Institute of Basic Medical Sciences, University of Tsukuba, Tsukuba Japan

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LINDSEY TEASENFITZ

William Paterson University, Wayne, New Jersey 07470, USA

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GEORGE R. UHL

MNB, NIDA, Baltimore, Maryland 21224, USA

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First published: 06 September 2006
Citations: 277
Address for correspondence: Dr. Emmanuel S. Onaivi, Department of Biology, William Paterson University, Wayne, NJ 07470. Voice: 973‐720‐3453; fax: 973‐720‐2338.
 e‐mail: Onaivie@wpunj.edu

Abstract

Abstract: Two well‐characterized cannabinoid receptors (CBrs), CB1 and CB2, mediate the effects of cannabinoids and marijuana use, with functional evidence for other CBrs. CB1 receptors are expressed primarily in brain and peripheral tissues. For over a decade several laboratories were unable to detect CB2 receptors in brain and were known to be intensely expressed in peripheral and immune tissues and have traditionally been referred to as peripheral CB2 CBrs. We have reported the discovery and functional presence of CB2 cannabinoid receptors in 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. We used RT‐PCR, immunoblotting, hippocampal cultures, immunohistochemistry, transmission electron microscopy, and stereotaxic techniques with behavioral assays to determine the functional expression of CB2 CBrs in rat brain and mice brain exposed to chronic mild stress (CMS) or those 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 brain and CB2 expression was detected in neuron‐specific enolase (NSE) positive hippocampal cell cultures. 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 (CNS). Thus, contrary to the prevailing view that CB2 CBrs are restricted to peripheral tissues and predominantly in immune cells, we demonstrated that CB2 CBrs and their gene transcripts are widely distributed in the brain. This multifocal expression of CB2 immunoreactivity in brain suggests that CB2 receptors may play broader roles in the brain than previously anticipated and may be exploited as new targets in the treatment of depression and substance abuse.