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Effects of the cannabinoid-1 receptor antagonist rimonabant on psychiatric symptoms in overweight people with schizophrenia: a randomized, double-blind, pilot study.大麻素 1 型受体拮抗剂利莫那班对超重精神分裂症患者精神症状的影响:一项随机、双盲、初步研究。
J Clin Psychopharmacol. 2011 Feb;31(1):86-91. doi: 10.1097/JCP.0b013e318204825b.
2
Increased interstitial white matter neuron density in the dorsolateral prefrontal cortex of people with schizophrenia.精神分裂症患者背外侧前额叶皮质的细胞间白质神经元密度增加。
Biol Psychiatry. 2011 Jan 1;69(1):63-70. doi: 10.1016/j.biopsych.2010.08.020. Epub 2010 Oct 25.
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Human brain weight is correlated with expression of the 'housekeeping genes' beta-2-microglobulin (β2M) and TATA-binding protein (TBP).人脑重量与“管家基因”β2-微球蛋白 (β2M) 和 TATA 结合蛋白 (TBP) 的表达相关。
Neuropathol Appl Neurobiol. 2010 Oct;36(6):498-504. doi: 10.1111/j.1365-2990.2010.01098.x.
4
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Neuropsychopharmacology. 2010 Sep;35(10):2060-71. doi: 10.1038/npp.2010.75. Epub 2010 Jun 16.
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Promoter specific alterations of brain-derived neurotrophic factor mRNA in schizophrenia.精神分裂症中脑源性神经营养因子 mRNA 的启动子特异性改变。
Neuroscience. 2010 Sep 1;169(3):1071-84. doi: 10.1016/j.neuroscience.2010.05.037. Epub 2010 May 27.
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Quantification of cerebral cannabinoid receptors subtype 1 (CB1) in healthy subjects and schizophrenia by the novel PET radioligand [11C]OMAR.新型 PET 示踪剂 [11C]OMAR 定量检测健康受试者和精神分裂症患者脑型大麻素受体 1 亚型 (CB1)
Neuroimage. 2010 Oct 1;52(4):1505-13. doi: 10.1016/j.neuroimage.2010.04.034. Epub 2010 Apr 18.
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Potential antipsychotic properties of central cannabinoid (CB1) receptor antagonists.中枢大麻素(CB1)受体拮抗剂的潜在抗精神病特性。
World J Biol Psychiatry. 2010 Mar;11(2 Pt 2):208-19. doi: 10.3109/15622970801908047.
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Selection of reference gene expression in a schizophrenia brain cohort.精神分裂症脑队列中参考基因表达的选择。
Aust N Z J Psychiatry. 2010 Jan;44(1):59-70. doi: 10.3109/00048670903393662.
9
Psychosis following anti-obesity treatment with rimonabant.使用利莫那班治疗肥胖症后出现精神病。
Obes Facts. 2008;1(2):103-5. doi: 10.1159/000122763. Epub 2008 Apr 16.
10
Risperidone treatment increases CB1 receptor binding in rat brain.利培酮治疗可增加大鼠脑内 CB1 受体结合。
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偏执型精神分裂症的特征是背外侧前额叶皮层中 CB1 受体结合增加。

Paranoid schizophrenia is characterized by increased CB1 receptor binding in the dorsolateral prefrontal cortex.

机构信息

ANSTO Life Sciences, Australian Nuclear Science and Technology Organization, Sydney, New South Wales, Australia.

出版信息

Neuropsychopharmacology. 2011 Jul;36(8):1620-30. doi: 10.1038/npp.2011.43. Epub 2011 Apr 6.

DOI:10.1038/npp.2011.43
PMID:21471953
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3138655/
Abstract

A number of studies suggest a dysregulation of the endogenous cannabinoid system in schizophrenia (SCZ). In the present study, we examined cannabinoid CB(1) receptor (CB(1)R) 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 CB(1)R ligand [(3)H] CP 55,940 and CB(1)R 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 CB(1)R expression. There was a main effect of diagnosis on [(3)H] 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 CB(1)R 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 CB(1)R dysregulation in SCZ and underline the need for further investigation of the role of this receptor particularly in those diagnosed with paranoid SCZ.

摘要

一些研究表明,精神分裂症(SCZ)患者内源性大麻素系统失调。在本研究中,我们检测了精神分裂症患者和对照组死后尸体的背外侧前额叶皮层(Brodmann 区 46)的大麻素 CB(1) 受体(CB(1)R)结合和 mRNA 表达。使用 CB(1)R 配体 [(3)H] CP 55,940 进行放射自显影来研究受体密度,并使用定量 RT-PCR 在一组 16 名偏执型 SCZ 患者、21 名非偏执型 SCZ 患者和 37 名年龄、死后间隔和 pH 值匹配的对照组中测量 CB(1)R mRNA 表达。所有病例均来自悉尼大学组织资源中心。使用单向方差分析(ANOVA)和事后 Bonferroni 检验以及协方差分析(ANCOVA)分析结果,以控制可能影响 CB(1)R 表达的人口统计学因素。[(3)H] CP 55,940 结合在 DLPFC 的所有层上的诊断存在主效应(F(2,71) = 3.740,p = 0.029)。事后检验表明,这种主要影响是由于偏执型 SCZ 患者的 CB(1)R 结合水平比对照组高 22%。当使用协方差分析时,这种效应得到了加强(F(2,67) = 6.048,p = 0.004),偏执型 SCZ 患者与对照组(p = 0.004)和非偏执型组(p = 0.016)差异显著。相比之下,不同疾病亚型和对照组之间的 mRNA 表达没有显著差异。我们的发现证实了 SCZ 中存在 CB(1)R 失调,并强调需要进一步研究该受体的作用,特别是在那些被诊断为偏执型 SCZ 的患者中。