Abstract
BackgroundMu opioid receptors have previously been shown to be altered in people with affective disorders who died as a result of suicide. We wished to determine whether these changes were more widespread and independent of psychiatric diagnoses.MethodsMu receptor levels were determined using [3 H]DAMGO binding in BA24 from 51 control subjects; 38 people with schizophrenia (12 suicides); 20 people with major depressive disorder (15 suicides); 13 people with bipolar disorder (5 suicides) and 9 people who had no history of psychiatric disorders but who died as a result of suicide. Mu receptor levels were further determined in BA9 and caudate-putamen from 38 people with schizophrenia and 20 control subjects using [3 H]DAMGO binding and, in all three regions, using Western blots. Data was analysed using one-way ANOVAs with Bonferroni’s Multiple Comparison Test or, where data either didn’t approximate to a binomial distribution or the sample size was too small to determine distribution, a Kruskal-Wallis test with Dunn’s Multiple Comparison Test.Results[3 H]DAMGO binding density was lower in people who had died as a result of suicide (p<0.01). People with schizophrenia who had died as a result of suicide had lower binding than control subjects (p<0.001), whilst people with bipolar disorder (non- suicide) had higher levels of binding (p<0.05). [3 H]DAMGO binding densities, but not mu protein levels, were significantly decreased in BA9 from people with schizophrenia who died as a result of suicide (p<0.01).ConclusionsOverall these data suggest that mu opioid receptor availability is decreased in the brains of people with schizophrenia who died as a result of suicide, which would be consistent with increased levels of endogenous ligands occupying these receptors.
Highlights
Mu opioid receptors have previously been shown to be altered in people with affective disorders who died as a result of suicide
Overall these data suggest that mu opioid receptor availability is decreased in the brains of people with schizophrenia who died as a result of suicide, which would be consistent with increased levels of endogenous ligands occupying these receptors
[3 H]DAMGO Binding in BA24 and suicide [3 H]DAMGO binding was homogenous across BA24 an integrated measure was taken across all cortical laminae
Summary
Mu opioid receptors have previously been shown to be altered in people with affective disorders who died as a result of suicide. OPRM were reported to be increased in the frontal cortex and caudate [13] from people who had died as a result of suicide compared to those from age and sex matched control subjects One of these studies [12] only included people with depression among those who had died by suicide, whilst the second study predominantly consisted of people with undetermined diagnoses or depression (one subject had schizophrenia) [13]. It is not clear if there is an interaction between psychiatric disorder and OPRM in people who died by suicide. A decreased binding affinity was reported for the pre- and post-central gyri from people who died as a result of suicide [14]
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