Literature DB >> 33845073

Gabapentin attenuates somatic signs of precipitated THC withdrawal in mice.

M L Eckard1, S G Kinsey2.   

Abstract

Cannabis is the most frequently used federally illicit substance in the United States. However, there are currently no FDA-approved pharmacotherapies to mitigate the withdrawal symptoms associated with cessation in heavy users. A promising, readily available, non-cannabinoid therapy are the gabapentinoids. Although currently approved for epilepsy and neuropathic pain, gabapentinoids are increasingly used for their "off-label" efficacy in treating various psychiatric conditions and substance abuse. Gabapentin (GBP) synergizes with cannabinoid agonism in neuropathic pain models, substitutes for Δ9-tetrahydrocannabinol (THC) in drug discrimination procedures, and reduced withdrawal symptoms in an outpatient clinical trial. However, there are limited data on the biological plausibility of the therapeutic action of gabapentinoids in cannabinoid withdrawal in preclinical models. The purpose of the current study was to determine the efficacy of GBP on attenuating THC withdrawal in mice, using an array of tests targeting withdrawal-induced and withdrawal-suppressed behaviors. Separate cohorts of male and female mice were administered THC (10 mg/kg, s.c.) or vehicle for 5.5 days, and withdrawal was precipitated by the CB1 antagonist rimonabant (2 or 3 mg/kg, i.p.) on the sixth day. GBP (≥10 mg/kg) reduced somatic signs of withdrawal (i.e., paw tremors and head twitches), but had no effect in locomotor activity or conditioned place preference. GBP (50 mg/kg) also restored withdrawal-suppressed responding on a progressive ratio reinforcement schedule. However, GBP (50 mg/kg) had no effect in withdrawal-suppressed marble burying or tail suspension struggling and did not normalize the stress response induced by THC withdrawal, as indicated by plasma corticosterone. These data suggest gabapentin may be effective at treating cannabinoid withdrawal symptoms including somatic and affective symptoms but may act independently of endocrine stress activation.
Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.

Entities:  

Keywords:  Cannabis addiction; Cannabis use disorder; Drug dependence; Substance use disorders

Mesh:

Substances:

Year:  2021        PMID: 33845073      PMCID: PMC8204917          DOI: 10.1016/j.neuropharm.2021.108554

Source DB:  PubMed          Journal:  Neuropharmacology        ISSN: 0028-3908            Impact factor:   5.273


  64 in total

1.  Precipitated Δ9-THC withdrawal reduces motivation for sucrose reinforcement in mice.

Authors:  M L Eckard; K R Trexler; B T Kotson; K G Anderson; S G Kinsey
Journal:  Pharmacol Biochem Behav       Date:  2020-06-09       Impact factor: 3.533

Review 2.  The mechanisms of action of gabapentin and pregabalin.

Authors:  Graeme J Sills
Journal:  Curr Opin Pharmacol       Date:  2005-12-22       Impact factor: 5.547

3.  Withdrawal following repeated exposure to d-amphetamine decreases responding for a sucrose solution as measured by a progressive ratio schedule of reinforcement.

Authors:  A M Barr; A G Phillips
Journal:  Psychopharmacology (Berl)       Date:  1999-01       Impact factor: 4.530

4.  A proof-of-concept randomized controlled study of gabapentin: effects on cannabis use, withdrawal and executive function deficits in cannabis-dependent adults.

Authors:  Barbara J Mason; Rebecca Crean; Vivian Goodell; John M Light; Susan Quello; Farhad Shadan; Kimberly Buffkins; Mark Kyle; Murali Adusumalli; Adnan Begovic; Santosh Rao
Journal:  Neuropsychopharmacology       Date:  2012-02-29       Impact factor: 7.853

5.  THC and gabapentin interactions in a mouse neuropathic pain model.

Authors:  Nicholas Atwal; Sherelle L Casey; Vanessa A Mitchell; Christopher W Vaughan
Journal:  Neuropharmacology       Date:  2018-10-09       Impact factor: 5.250

6.  The antiepileptic agent gabapentin (Neurontin) possesses anxiolytic-like and antinociceptive actions that are reversed by D-serine.

Authors:  L Singh; M J Field; P Ferris; J C Hunter; R J Oles; R G Williams; G N Woodruff
Journal:  Psychopharmacology (Berl)       Date:  1996-09       Impact factor: 4.530

7.  Dronabinol and lofexidine for cannabis use disorder: A randomized, double-blind, placebo-controlled trial.

Authors:  Frances R Levin; John J Mariani; Martina Pavlicova; Daniel Brooks; Andrew Glass; Amy Mahony; Edward V Nunes; Adam Bisaga; Elias Dakwar; Kenneth M Carpenter; Maria A Sullivan; Jean C Choi
Journal:  Drug Alcohol Depend       Date:  2015-11-27       Impact factor: 4.492

8.  Cannabinoids inhibit N- and P/Q-type calcium channels in cultured rat hippocampal neurons.

Authors:  W Twitchell; S Brown; K Mackie
Journal:  J Neurophysiol       Date:  1997-07       Impact factor: 2.714

Review 9.  Pharmacology and mechanism of action of pregabalin: the calcium channel alpha2-delta (alpha2-delta) subunit as a target for antiepileptic drug discovery.

Authors:  Charles P Taylor; Timothy Angelotti; Eric Fauman
Journal:  Epilepsy Res       Date:  2006-11-28       Impact factor: 3.045

Review 10.  CB(1) cannabinoid receptors and their associated proteins.

Authors:  Allyn C Howlett; Lawrence C Blume; George D Dalton
Journal:  Curr Med Chem       Date:  2010       Impact factor: 4.530

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