scholarly journals Do gabapentin or pregabalin directly modulate the µ receptor?

PeerJ ◽  
2021 ◽  
Vol 9 ◽  
pp. e11175
Author(s):  
Preeti Manandhar ◽  
Bridin Patricia Murnion ◽  
Natasha L. Grimsey ◽  
Mark Connor ◽  
Marina Santiago

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. Discussion Pregabalin or gabapentin did not activate or modulate µ receptor signaling in three different assays. Our data do not support the hypothesis that gabapentin or pregabalin augment opioid effects through direct or allosteric modulation of the µ receptor. Pregabalin at a high concentration increases cAMP production independent of morphine. The mechanism of enhanced opioid-related harms from co-ingestion of pregabalin or gabapentin with opioids needs further investigation.

2017 ◽  
Vol 812 ◽  
pp. 57-63 ◽  
Author(s):  
Kenji Sakamoto ◽  
Taiyo Kuroki ◽  
Tomonori Sagawa ◽  
Hiroko Ito ◽  
Asami Mori ◽  
...  

1997 ◽  
Vol 42 (3) ◽  
pp. 317-326 ◽  
Author(s):  
Piet J Boels ◽  
Beirong Gao ◽  
Joan Deutsch ◽  
Sheila G Haworth

2000 ◽  
Vol 278 (2) ◽  
pp. L239-L244 ◽  
Author(s):  
Scott M. O'Grady ◽  
Xinpo Jiang ◽  
David H. Ingbar

In this review, we discuss evidence that supports the hypothesis that adrenergic stimulation of transepithelial Na absorption across the alveolar epithelium occurs indirectly by activation of apical Cl channels, resulting in hyperpolarization and an increased driving force for Na uptake through amiloride-sensitive Na channels. This hypothesis differs from the prevailing idea that adrenergic-receptor activation increases the open probability of Na channels, leading to an increase in apical membrane Na permeability and an increase in Na and fluid uptake from the alveolar space. We review results from cultured alveolar epithelial cell monolayer experiments that show increases in apical membrane Cl conductance in the absence of any change in Na conductance after stimulation by selective β-adrenergic-receptor agonists. We also discuss possible reasons for differences in Na-channel regulation in cells grown in monolayer culture compared with that in dissociated alveolar epithelial cells. Finally, we describe some preliminary in vivo data that suggest a role for Cl-channel activation in the process of amiloride-sensitive alveolar fluid absorption.


2010 ◽  
Vol 79 (1) ◽  
pp. 1-9 ◽  
Author(s):  
Morten Grunnet ◽  
Jennifer Abbruzzese ◽  
Frank B. Sachse ◽  
Michael C. Sanguinetti

Neuroreport ◽  
2003 ◽  
Vol 14 (2) ◽  
pp. 167-171 ◽  
Author(s):  
Pauline Cavelier ◽  
Thomas Desplantez ◽  
Huguette Beekenkamp ◽  
Jean-Louis Bossu

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