NMDA receptor subunits change in the prefrontal cortex of pure-opioid and multi-drug abusers: a post-mortem study

• Published in: European archives of psychiatry and clinical neuroscience 2019-04, Vol.269 (3), p.309-315
• Main Authors: Daneshparvar, Hamidreza, Sadat-Shirazi, Mitra-Sadat, Fekri, Monir, Khalifeh, Solmaz, Ziaie, Ali, Esfahanizadeh, Nasrin, Vousooghi, Nasim, Zarrindast, Mohammad-Reza
• Format: Article
• Language: English
• Subjects: Addictions; Addicts; Adult; Autopsy; Drug abuse; Drug addiction; Glutamic acid receptors (ionotropic); Humans; Male; Medicine; Medicine & Public Health; N-Methyl-D-aspartic acid receptors; Narcotics; Nerve Tissue Proteins - metabolism; Neurosciences; Neurotransmitters; Opioid receptors; Original Paper; Prefrontal cortex; Prefrontal Cortex - metabolism; Prefrontal Cortex - pathology; Psychiatry; Receptors, N-Methyl-D-Aspartate - metabolism; Substance-Related Disorders - metabolism; Substance-Related Disorders - pathology; Western blotting
• ISSN: 0940-1334; 1433-8491
• DOI: 10.1007/s00406-018-0900-8

Addiction is a chronic relapsing disorder and is one of the most important issues in the world. Changing the level of neurotransmitters and the activities of their receptors, play a major role in the pathophysiology of substance abuse disorders. It is well-established that N -methyl- d -aspartate receptors (NMDARs) play a significant role in the molecular basis of addiction. NMDAR has two obligatory GluN1 and two regionally localized GluN2 subunits. This study investigated changes in the protein level of GluN1, GluN2A, and GluN2B in the prefrontal cortex of drug abusers. The medial prefrontal cortex (mPFC), lateral prefrontal cortex (lPFC), and orbitofrontal cortex (OFC) were dissected from the brain of 101 drug addicts brains and were compared with the brains of non-addicts ( N  = 13). Western blotting technique was used to show the alteration in NMDAR subunits level. Data obtained using Western blotting technique showed a significant increase in the level of GluN1 and GluN2B, but not in GluN2A subunits in all the three regions (mPFC, lPFC, and OFC) of men whom suffered from addiction as compared to the appropriate controls. These findings showed a novel role for GluN1, GluN2B subunits, rather than the GluN2A subunit of NMDARs, in the pathophysiology of addiction and suggested their role in the drug-induced plasticity of NMDARs.