Please use this identifier to cite or link to this item: https://apo.ansto.gov.au/dspace/handle/10238/5177
Title: Paranoid schizophrenia is characterized by increased cannabinoid CB1 receptor binding in the dorsolateral prefrontal cortex.
Authors: Dalton, VS
Long, LE
Weickert, C S
Zavitsanou, K
Keywords: Receptors
Cerebral cortex
Rats
Autoradiography
Density
Brain
Issue Date: 1-Jul-2011
Publisher: Nature Publishing Group
Citation: Dalton, V. S., Long, L. E., Weickert, C. S., & Zavitsanou, K. (2011). Paranoid schizophrenia is characterized by increased cannabinoid CB1 receptor binding in the dorsolateral prefrontal cortex. Neuropsychopharmacology, 36 (8), 1620-1630. doi:10.1038/npp.2011.43
Abstract: A number of studies suggest a dysregulation of the endogenous cannabinoid system in schizophrenia (SCZ). In the present study, we examined cannabinoid CB1 receptor (CB1R) binding and mRNA expression in the dorsolateral prefrontal cortex (DLPFC) (Brodmann's area 46) of SCZ patients and controls, post-mortem. Receptor density was investigated using autoradiography with the CB1R ligand [3H] CP 55 940 and CB1R mRNA expression was measured using quantitative RT-PCR in a cohort of 16 patients with paranoid SCZ, 21 patients with non-paranoid SCZ and 37 controls matched for age, post-mortem interval and pH. All cases were obtained from the University of Sydney Tissue Resource Centre. Results were analyzed using one-way analysis of variance (ANOVA) and post hoc Bonferroni tests and with analysis of covariance (ANCOVA) to control for demographic factors that would potentially influence CB1R expression. There was a main effect of diagnosis on [3H] CP 55 940 binding quantified across all layers of the DLPFC (F(2,71)=3.740, p=0.029). Post hoc tests indicated that this main effect was due to patients with paranoid SCZ having 22% higher levels of CB1R binding compared with the control group. When ANCOVA was employed, this effect was strengthened (F(2,67)=6.048, p=0.004) with paranoid SCZ patients differing significantly from the control (p=0.004) and from the non-paranoid group (p=0.016). In contrast, no significant differences were observed in mRNA expression between the different disease subtypes and the control group. Our findings confirm the existence of a CB1R dysregulation in SCZ and underline the need for further investigation of the role of this receptor particularly in those diagnosed with paranoid SCZ. © 2011, Nature Publishing Group.
Gov't Doc #: 5282
URI: http://dx.doi.org/10.1038/npp.2011.43
http://apo.ansto.gov.au/dspace/handle/10238/5177
ISSN: 0893-133X
Appears in Collections:Journal Articles

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