Please use this identifier to cite or link to this item:
Title: Do gabapentin or pregabalin directly modulate the µ receptor?
Authors: Murnion, Bridin ;Manandhar, P.;Grimsey, N.L.;Connor, M.;Santiago, M.
Affliation: Central Coast Local Health District
Issue Date: Apr-2021
Source: 9:e11175
Journal title: PeerJ
Department: Drug & Alcohol
Abstract: Abstract Background Pregabalin and gabapentin improve neuropathic pain symptoms but there are emerging concerns regarding their misuse. This is more pronounced among patients with substance use disorder, particularly involving opioids. Co-ingestion of gabapentinoids with opioids is increasingly identified in opioid related deaths, however, the molecular mechanism behind this is still unclear. We have sought to determine whether pregabalin or gabapentin directly modulates acute μ receptor signaling, or μ receptor activation by morphine. Methods The effects of pregabalin and gabapentin were assessed in HEK 293 cells stably transfected with the human μ receptor. Their effect on morphine induced hyperpolarization, cAMP production and ERK phosphorylation were studied using fluorescent-based membrane potential assay, bioluminescence based CAMYEL assay and ELISA assay, respectively. Pregabalin/gabapentin effects on morphine-induced hyperpolarization were also investigated in AtT20 cells. Results Pregabalin or gabapentin (1 µM, 100 µM each) did not activate the µ receptor or affect K channel activation or ERK phosphorylation produced by morphine. Neither drug affected the desensitization of K channel activation produced by prolonged (30 min) application of morphine. Gabapentin (1 µM, 100 µM) and pregabalin (1 µM) did not affect inhibition of forskolin-stimulated cAMP production by morphine. However, pregabalin (100 µM) potentiated forskolin mediated cAMP production, although morphine still inhibited cAMP levels with a similar potency to control.
DOI: 10.7717/peerj.11175
ISSN: 2167-8359
Publicaton type: Journal Article
Keywords: Drug and Alcohol
Appears in Collections:Health Service Research

Show full item record

Page view(s)

checked on Jun 3, 2023

Google ScholarTM



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.