TY - JOUR
T1 - Brain Cannabinoid CB2 Receptor in Schizophrenia
AU - Ishiguro, Hiroki
AU - Horiuchi, Yasue
AU - Ishikawa, Maya
AU - Koga, Minori
AU - Imai, Keiko
AU - Suzuki, Yoshimi
AU - Morikawa, Miyuki
AU - Inada, Toshiya
AU - Watanabe, Yuichiro
AU - Takahashi, Makoto
AU - Someya, Toshiyuki
AU - Ujike, Hiroshi
AU - Iwata, Nakao
AU - Ozaki, Norio
AU - Onaivi, Emmanuel S.
AU - Kunugi, Hiroshi
AU - Sasaki, Tsukasa
AU - Itokawa, Masanari
AU - Arai, Makoto
AU - Niizato, Kazuhiro
AU - Iritani, Shyuji
AU - Naka, Izumi
AU - Ohashi, Jun
AU - Kakita, Akiyoshi
AU - Takahashi, Hitoshi
AU - Nawa, Hiroyuki
AU - Arinami, Tadao
N1 - Funding Information:
This work was supported by KAKENHI (Grant Nos. 20390098 and 20023006 ) and a grant from Japan Science and Technology . Australian human brain tissues were received from the New South Wales (NSW) Tissue Resource Centre and/or the Prince of Wales Medical Research Institute Tissue Resource Centre which is supported by the National Health and Medical Research Council of Australia , The University of Sydney , Prince of Wales Medical Research Institute , Neuroscience Institute of Schizophrenia and Allied Disorders , National Institute of Alcohol Abuse and Alcoholism and NSW Department of Health . American tissue/fluid specimens were obtained from the Human Brain and Spinal Fluid Resource Center, VA West Los Angeles Healthcare Center, 11301 Wilshire Boulevard, Los Angeles, California 90073, which is sponsored by NINDS/NIMH , National Multiple Sclerosis Society , and Department of Veterans Affairs . Dr. Hiroki Ishiguro had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
PY - 2010/5/15
Y1 - 2010/5/15
N2 - Background: Neural endocannabinoid function appears to be involved in schizophrenia. Two endocannabinoid receptors, CB1 and CB2, are found in the brain and elsewhere in the body. We investigated roles of CB2 in schizophrenia. Materials and Methods: An association study was performed between tag single nucleotide polymorphisms (SNPs) in the CNR2 gene encoding the CB2 receptor and schizophrenia in two independent case-control populations. Allelic differences of associated SNPs were analyzed in human postmortem brain tissues and in cultured cells. Prepulse inhibition and locomotor activity in C57BL/6JJmsSlc mice with CB2 receptor antagonist AM630 administration was examined. Results: The analysis in the first population revealed nominally significant associations between schizophrenia and two SNPs, and the associations were replicated in the second population. The R63 allele of rs2501432 (R63Q) (p = .001), the C allele of rs12744386 (p = .005) and the haplotype of the R63-C allele (p = 5 × 10-6) were significantly increased among 1920 patients with schizophrenia compared with 1920 control subjects in the combined population. A significantly lower response to CB2 ligands in cultured CHO cells transfected with the R63 allele compared with those with Q63, and significantly lower CB2 receptor mRNA and protein levels found in human brain with the CC and CT genotypes of rs12744386 compared with TT genotype were observed. AM630 exacerbated MK-801- or methamphetamine-induced disturbance of prepulse inhibition and hyperactivity in C57BL/6JJmsSlc mice. Conclusions: These findings indicate an increased risk of schizophrenia for people with low CB2 receptor function.
AB - Background: Neural endocannabinoid function appears to be involved in schizophrenia. Two endocannabinoid receptors, CB1 and CB2, are found in the brain and elsewhere in the body. We investigated roles of CB2 in schizophrenia. Materials and Methods: An association study was performed between tag single nucleotide polymorphisms (SNPs) in the CNR2 gene encoding the CB2 receptor and schizophrenia in two independent case-control populations. Allelic differences of associated SNPs were analyzed in human postmortem brain tissues and in cultured cells. Prepulse inhibition and locomotor activity in C57BL/6JJmsSlc mice with CB2 receptor antagonist AM630 administration was examined. Results: The analysis in the first population revealed nominally significant associations between schizophrenia and two SNPs, and the associations were replicated in the second population. The R63 allele of rs2501432 (R63Q) (p = .001), the C allele of rs12744386 (p = .005) and the haplotype of the R63-C allele (p = 5 × 10-6) were significantly increased among 1920 patients with schizophrenia compared with 1920 control subjects in the combined population. A significantly lower response to CB2 ligands in cultured CHO cells transfected with the R63 allele compared with those with Q63, and significantly lower CB2 receptor mRNA and protein levels found in human brain with the CC and CT genotypes of rs12744386 compared with TT genotype were observed. AM630 exacerbated MK-801- or methamphetamine-induced disturbance of prepulse inhibition and hyperactivity in C57BL/6JJmsSlc mice. Conclusions: These findings indicate an increased risk of schizophrenia for people with low CB2 receptor function.
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U2 - 10.1016/j.biopsych.2009.09.024
DO - 10.1016/j.biopsych.2009.09.024
M3 - Article
C2 - 19931854
AN - SCOPUS:77951620284
SN - 0006-3223
VL - 67
SP - 974
EP - 982
JO - Biological Psychiatry
JF - Biological Psychiatry
IS - 10
ER -