The cannabinoid receptor, in addition to being the initial site of action for the abuse drug marijuana, serves important physiological roles in pain perception and motor coordination. The overall goal of this project is to understand the molecular mechanisms of regulation of the neuronal cannabinoid receptor (CB1). It has been well established that tolerance develops to the effects of cannabinoids. We have evidence that alterations in levels of the cannabinoid receptor occur during tolerance. Therefore, specific aim 1 will examine the regulation of the cannabinoid receptor during chronic exposure to cannabinoids in transfected cells.
This aim will address post-transcriptional regulation of the CB1 receptor by utilizing CH0 cells transfected with CB1 receptor cDNA. These cell lines facilitate the study of drug effects on receptor levels, receptor localization and alterations in signal transduction. The studies proposed in specific aim 2 address transcriptional and post-transcriptional regulation of the endogenous cannabinoid receptor. These studies are conducted in neuronal cell lines and primary culture in which receptors are not overexpressed, and although CB1 receptor binding cannot be easily assessed, change in CB1 gene expression can be studied. Cerebellar neurons in primary culture will be studied since they can form synapses and thus mimic normal neuronal relationships.
Specific aim 3 will address the regulation of the CB1 receptor gene in an in vivo system. These studies will complement in specific aim 4 which is to characterize the gene for the mouse brain cannabinoid receptor and identify elements in the gene which may be responsible for regulation of receptor expression. Although the mouse is one of the primary animal models for the study of cannabinoids, the sequence of the gene encoding this receptor has not been elucidated. We have cloned the mouse brain cannabinoid receptor gene from a genomic library, and will characterize the 5' and 3' regions of this gene to determine regulatory regions. Understanding the molecular mechanisms underlying the regulation of the neuronal cannabinoid receptor will contribute significantly to our knowledge of this receptor at which marijuana and the endogenous cannabinoids act. This, in turn, may lead to a better understanding of marijuana abuse in humans.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA009978-02
Application #
2517964
Study Section
Human Development Research Subcommittee (NIDA)
Program Officer
Colvis, Christine
Project Start
1996-09-30
Project End
2000-12-31
Budget Start
1997-09-01
Budget End
1998-12-31
Support Year
2
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Virginia Commonwealth University
Department
Pharmacology
Type
Schools of Medicine
DUNS #
City
Richmond
State
VA
Country
United States
Zip Code
23298
Soroceanu, Liliana; Murase, Ryuichi; Limbad, Chandani et al. (2013) Id-1 is a key transcriptional regulator of glioblastoma aggressiveness and a novel therapeutic target. Cancer Res 73:1559-69
McAllister, Sean D; Murase, Ryuichi; Christian, Rigel T et al. (2011) Pathways mediating the effects of cannabidiol on the reduction of breast cancer cell proliferation, invasion, and metastasis. Breast Cancer Res Treat 129:37-47
Zhao, Pingwei; Leonoudakis, Dmitri; Abood, Mary E et al. (2010) Cannabinoid receptor activation reduces TNFalpha-induced surface localization of AMPAR-type glutamate receptors and excitotoxicity. Neuropharmacology 58:551-8
Scotter, Emma L; Abood, Mary E; Glass, Michelle (2010) The endocannabinoid system as a target for the treatment of neurodegenerative disease. Br J Pharmacol 160:480-98
Marcu, Jahan P; Christian, Rigel T; Lau, Darryl et al. (2010) Cannabidiol enhances the inhibitory effects of delta9-tetrahydrocannabinol on human glioblastoma cell proliferation and survival. Mol Cancer Ther 9:180-9
Kapur, Ankur; Samaniego, Patrick; Thakur, Ganesh A et al. (2008) Mapping the structural requirements in the CB1 cannabinoid receptor transmembrane helix II for signal transduction. J Pharmacol Exp Ther 325:341-8
McAllister, Sean D; Christian, Rigel T; Horowitz, Maxx P et al. (2007) Cannabidiol as a novel inhibitor of Id-1 gene expression in aggressive breast cancer cells. Mol Cancer Ther 6:2921-7
Anavi-Goffer, Sharon; Fleischer, Daniel; Hurst, Dow P et al. (2007) Helix 8 Leu in the CB1 cannabinoid receptor contributes to selective signal transduction mechanisms. J Biol Chem 282:25100-13
Kapur, Ankur; Hurst, Dow P; Fleischer, Daniel et al. (2007) Mutation studies of Ser7.39 and Ser2.60 in the human CB1 cannabinoid receptor: evidence for a serine-induced bend in CB1 transmembrane helix 7. Mol Pharmacol 71:1512-24
Gehani, Neal C; Nalwalk, Julia W; Razdan, Raj K et al. (2007) Significance of cannabinoid CB1 receptors in improgan antinociception. J Pain 8:850-60

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