Mu opioid receptor availability in people with psychiatric disorders who died by suicide: a case control study

BMC Psychiatry. 2012 Aug 28:12:126. doi: 10.1186/1471-244X-12-126.

Abstract

Background: Mu 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.

Methods: Mu 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).

Conclusions: 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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Bipolar Disorder / genetics
  • Bipolar Disorder / metabolism*
  • Brain / metabolism*
  • Case-Control Studies
  • Depressive Disorder, Major / genetics
  • Depressive Disorder, Major / metabolism*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Receptors, Opioid, mu / genetics
  • Receptors, Opioid, mu / metabolism*
  • Schizophrenia / genetics
  • Schizophrenia / metabolism*
  • Suicide*

Substances

  • Receptors, Opioid, mu