Pharmacoepigenetics of the role of DNA methylation in μ-opioid receptor expression in different human brain regions

Author:

Knothe Claudia1,Oertel Bruno G2,Ultsch Alfred3,Kettner Mattias4,Schmidt Peter Harald5,Wunder Cora4,Toennes Stefan W4,Geisslinger Gerd12,Lötsch Jörn12

Affiliation:

1. Institute of Clinical Pharmacology, Goethe – University, Theodor-Stern-Kai 7, 60590 Frankfurt am Main, Germany

2. Fraunhofer Institute for Molecular Biology & Applied Ecology IME, Project Group Translational Medicine & Pharmacology TMP, Theodor-Stern-Kai 7, 60590 Frankfurt am Main, Germany

3. DataBionics Research Group, University of Marburg, Hans-Meerwein-Straße, 35032 Marburg, Germany

4. Institute of Legal Medicine, Goethe - University, Kennedyallee 104, 60596 Frankfurt am Main, Germany

5. Institute of Legal Medicine, Saarland University, Building 80.2, 66421, Homburg, Saar, Germany

Abstract

Aim: Exposure to opioids has been associated with epigenetic effects. Studies in rodents suggested a role of varying degrees of DNA methylation in the differential regulation of μ-opioid receptor expression across the brain. Methods: In a translational investigation, using tissue acquired postmortem from 21 brain regions of former opiate addicts, representing a human cohort with chronic opioid exposure, μ-opioid receptor expression was analyzed at the level of DNA methylation, mRNA and protein. Results & conclusion: While high or low μ-opioid receptor expression significantly correlated with local OPRM1 mRNA levels, there was no corresponding association with OPRM1 methylation status. Additional experiments in human cell lines showed that changes in DNA methylation associated with changes in μ-opioid expression were an order of magnitude greater than differences in brain. Hence, different degrees of DNA methylation associated with chronic opioid exposure are unlikely to exert a major role in the region-specificity of μ-opioid receptor expression in the human brain.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Genetics

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