4.5 Article

M2/M4 muscarinic receptor binding in the anterior cingulate cortex in schizophrenia and mood disorders

Journal

BRAIN RESEARCH BULLETIN
Volume 65, Issue 5, Pages 397-403

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.brainresbull.2005.02.007

Keywords

muscarinic receptors; M2; autoradiography; bipolar; major depression

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We have previously shown a decrease in [H-3]pirenzepine binding to M1/M4 muscarinic receptors in the anterior cingulate cortex in schizophrenia but not in major depression or bipolar disorder. The present study aimed to extend these findings by examining the binding of [H-3]AF-DX 384 to M2/M4 receptors in the same cohort of subjects. Using quantitative autoradiography we measured [H-3]AF-DX 384 binding in the anterior cingulate cortex of 15 schizophrenia, 15 bipolar, 15 major depression and 15 control cases. Post-mortem tissue was obtained from the Stanley Foundation Brain Bank. [H-3]AF-DX 384 binding had a homogenous distribution amongst the layers of the anterior cingulate cortex, was higher in males than in C, females and declined with prolonged storage of tissue. An inverse correlation between [H-3]AF-DX384 binding and age of onset of the disease was observed in the schizophrenia group suggesting that the earlier the age at onset the higher the binding was. In the depression group, there was a significant effect of gender on [H-3]AF-DX 384 binding with females having lower binding in comparison to males. In the bipolar group, there was a significant inverse correlation between antipsychotic medication and [H-3]AF-DX 384 binding, suggesting that the higher the dose of medication the lower the binding was. No differences in [H-3]AF-DX 384 binding were seen between the four groups. The present results provide no evidence of M2/M4 receptor alterations in the anterior cingulate cortex in schizophrenia and affective disorders and extend the body of evidence implicating cortical M I but not M2 involvement in the pathology and pharmacotherapy of schizophrenia. (c) 2005 Published by Elsevier Inc.

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