4.6 Article

Altered Signaling in CB1R-5-HT2AR Heteromers in Olfactory Neuroepithelium Cells of Schizophrenia Patients is Modulated by Cannabis Use

Journal

SCHIZOPHRENIA BULLETIN
Volume 46, Issue 6, Pages 1547-1557

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/schbul/sbaa038

Keywords

schizophrenia; antipsychotics; cognition; can nabis; human olfactory neuroepithelium

Categories

Funding

  1. DIUE de la Generalitat de Catalunya
  2. Secretaria General D'Economia i Coneixement [2014-SGR-680, 2017-SGR-1497]
  3. Instituto de Salud Carlos III, Ministerio de Ciencia e Innovacion de Espana y fondos FEDER [PI14/00210, PI18/00053]
  4. FIS-FEDER Funds, Ministerio de EconomiayCompetitividad de Espana [SAF-2017-87629-R, SAF-2015-69762-R, SAF2015-74627-JIN, PID2019-109240RB-I00]
  5. Programa de Excelencia Maria de Maeztu, Ministerio de Ciencia e Innovacion de Espana [MDM-2014-0370]
  6. Red de Trastornos Adictivos, Instituto de Salud Carlos III, Ministerio de Ciencia e Innovacion de Espana
  7. Centro de Investigacion Biomedica en Red de Salud Mental, Instituto de Salud Carlos III
  8. Centro de Investigacion Biomedica en Red de Fisiopatologia de la Obesidad y Nutricion, Instituto de Salud Carlos III
  9. Centro de Investigacion Biomedica en Red de Enfermedades Neurodegenerativas, Instituto de Salud Carlos

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Schizophrenia (SCZ) has been associated with serotonergic and endocannabinoid systems dysregulation, but difficulty in obtaining in vivo neurological tissue has limited its exploration. We investigated CB1R-5-HT2AR heteromer expression and functionality via intracellular pERK and cAMP quantification in olfactory neuroepithelium (ON) cells of SCZ patients non-cannabis users (SCZ/nc), and evaluated whether cannabis modulated these parameters in patients using cannabis (SCZ/c). Results were compared vs healthy controls non-cannabis users (HC/nc) and healthy controls cannabis users (HC/c). Further, antipsychotic effects on heteromer signaling were tested in vitro in HC/nc and HC/c. Results indicated that heteromer expression was enhanced in both SCZ groups vs HC/nc. Additionally, pooling all 4 groups together, heteromer expression correlated with worse attentional performance and more neurological soft signs (NSS), indicating that these changes may be useful markers for neurocognitive impairment. Remarkably, the previously reported signaling properties of CB1R-5-HT2AR heteromers in ON cells were absent, specifically in SCZ/nc treated with clozapine. These findings were mimicked in cells from HC/nc exposed to clozapine, suggesting a major role of this antipsychotic in altering the quaternary structure of the CB1R-5-HT2AR heteromer in SCZ/nc patients. In contrast, cells from SCZ/c showed enhanced heteromer functionality similar to HC/c. Our data highlight a molecular marker of the interaction between antipsychotic medication and cannabis use in SCZ with relevance for future studies evaluating its association with specific neuropsychiatric alterations.

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