Literature DB >> 27806662

Galantamine and Environmental Enrichment Enhance Cognitive Recovery after Experimental Traumatic Brain Injury But Do Not Confer Additional Benefits When Combined.

Patricia B de la Tremblaye1,2, Corina O Bondi1,2,3,4,5, Naima Lajud1,2,6, Jeffrey P Cheng1,2, Hannah L Radabaugh1,2, Anthony E Kline1,2,4,5,7,8.   

Abstract

Environmental enrichment (EE) enhances cognition after traumatic brain injury (TBI). Galantamine (GAL) is an acetylcholinesterase inhibitor that also may promote benefits. Hence, the aims of this study were to assess the efficacy of GAL alone (standard [STD] housing) and in combination with EE in adult male rats after TBI. The hypothesis was that both therapies would confer motor, cognitive, and histological benefits when provided singly, but that their combination would be more efficacious. Anesthetized rats received a controlled cortical impact or sham injury, then were randomly assigned to receive GAL (1, 2, or 3 mg/kg; intraperitoneally [i.p.]) or saline vehicle (VEH; 1 mL/kg; i.p.) beginning 24 h after surgery and once daily for 21 days (experiment 1). Motor (beam-balance/walk) and cognitive (Morris water maze [MWM]) assessments were conducted on post-operative Days 1-5 and 14-19, respectively. Cortical lesion volumes were quantified on Day 21. Sham controls were better versus all TBI groups. No differences in motor function or lesion volumes were observed among the TBI groups (p > 0.05). In contrast, GAL (2 mg/kg) enhanced MWM performance versus VEH and GAL (1 and 3 mg/kg; p < 0.05). In experiment 2, GAL (2 mg/kg) or VEH was combined with EE and the data were compared with the STD-housed groups from experiment 1. EE alone enhanced motor performance over the VEH-treated and GAL-treated (2 mg/kg) STD-housed groups (p < 0.05). Moreover, both EE groups (VEH or GAL) facilitated spatial learning and reduced lesion size versus STD + VEH controls (p < 0.05). No additional benefits were observed with the combination paradigm, which does not support the hypothesis. Overall, the data demonstrate that EE and once daily GAL (2 mg/kg) promote cognitive recovery after TBI. Importantly, the combined therapies did not negatively affect outcome and thus this therapeutic protocol may have clinical utility.

Entities:  

Keywords:  Morris water maze; acetylcholinesterase inhibitors (AChEIs); beam-walking; behavior; controlled cortical impact (CCI); functional recovery; galantamine; hippocampus; learning and memory; traumatic brain injury

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Year:  2016        PMID: 27806662      PMCID: PMC5397275          DOI: 10.1089/neu.2016.4790

Source DB:  PubMed          Journal:  J Neurotrauma        ISSN: 0897-7151            Impact factor:   5.269


  105 in total

1.  Time-dependent changes in rat brain cholinergic receptor expression after experimental brain injury.

Authors:  S Leigh Verbois; Stephen W Scheff; James R Pauly
Journal:  J Neurotrauma       Date:  2002-12       Impact factor: 5.269

2.  Environmental enrichment-mediated functional improvement after experimental traumatic brain injury is contingent on task-specific neurobehavioral experience.

Authors:  Ann N Hoffman; Rebecca R Malena; Brian P Westergom; Pallavi Luthra; Jeffrey P Cheng; Haris A Aslam; Ross D Zafonte; Anthony E Kline
Journal:  Neurosci Lett       Date:  2007-12-04       Impact factor: 3.046

Review 3.  The effectiveness of donepezil for cognitive rehabilitation after traumatic brain injury: a systematic review.

Authors:  Javier Ballesteros; Itziar Güemes; Nora Ibarra; José I Quemada
Journal:  J Head Trauma Rehabil       Date:  2008 May-Jun       Impact factor: 2.710

4.  Effects of cholinergic enhancing drugs on cholinergic transporters in the brain and peripheral blood lymphocytes of spontaneously hypertensive rats.

Authors:  Daniele Tomassoni; Assia Catalani; Carlo Cinque; Maria Antonietta Di Tullio; Seyed Khosrow Tayebati; Angela Cadoni; Innocent Ejike Nwankwo; Enea Traini; Francesco Amenta
Journal:  Curr Alzheimer Res       Date:  2012-01       Impact factor: 3.498

5.  Chronic treatment of old rats with donepezil or galantamine: effects on memory, hippocampal plasticity and nicotinic receptors.

Authors:  C A Barnes; J Meltzer; F Houston; G Orr; K McGann; G L Wenk
Journal:  Neuroscience       Date:  2000       Impact factor: 3.590

Review 6.  Unraveling the attentional functions of cortical cholinergic inputs: interactions between signal-driven and cognitive modulation of signal detection.

Authors:  Martin Sarter; Michael E Hasselmo; John P Bruno; Ben Givens
Journal:  Brain Res Brain Res Rev       Date:  2005-02

7.  Reduced evoked release of acetylcholine in the rodent neocortex following traumatic brain injury.

Authors:  C E Dixon; X Ma; D W Marion
Journal:  Brain Res       Date:  1997-02-21       Impact factor: 3.252

8.  Galantamine is an allosterically potentiating ligand of neuronal nicotinic but not of muscarinic acetylcholine receptors.

Authors:  Marek Samochocki; Anja Höffle; Andreas Fehrenbacher; Ruth Jostock; Jürgen Ludwig; Claudia Christner; Martin Radina; Marion Zerlin; Christoph Ullmer; Edna F R Pereira; Hermann Lübbert; Edson X Albuquerque; Alfred Maelicke
Journal:  J Pharmacol Exp Ther       Date:  2003-03-20       Impact factor: 4.030

9.  A combined therapeutic regimen of buspirone and environmental enrichment is more efficacious than either alone in enhancing spatial learning in brain-injured pediatric rats.

Authors:  Christina M Monaco; Kory M Gebhardt; Sarah M Chlebowski; Kaitlyn E Shaw; Jeffrey P Cheng; Jeremy J Henchir; Margaret F Zupa; Anthony E Kline
Journal:  J Neurotrauma       Date:  2014-09-29       Impact factor: 5.269

Review 10.  The cholinergic hypothesis of cognitive impairment caused by traumatic brain injury.

Authors:  David B Arciniegas
Journal:  Curr Psychiatry Rep       Date:  2003-10       Impact factor: 5.285

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  10 in total

1.  Post-Injury Administration of Galantamine Reduces Traumatic Brain Injury Pathology and Improves Outcome.

Authors:  Jing Zhao; Michael J Hylin; Nobuhide Kobori; Kimberly N Hood; Anthony N Moore; Pramod K Dash
Journal:  J Neurotrauma       Date:  2017-12-18       Impact factor: 5.269

2.  Spontaneous recovery after controlled cortical impact injury is not impeded by intermittent administration of the antipsychotic drug risperidone.

Authors:  Lauren J Carlson; Gina C Bao; Sonya Besagar; Jacob B Leary; Hannah L Radabaugh; Corina O Bondi; Anthony E Kline
Journal:  Neurosci Lett       Date:  2018-06-06       Impact factor: 3.046

3.  Chronic treatment with galantamine rescues reversal learning in an attentional set-shifting test after experimental brain trauma.

Authors:  Ihuoma Njoku; Hannah L Radabaugh; Melissa A Nicholas; Lindsay A Kutash; Darik A O'Neil; Ian P Marshall; Jeffrey P Cheng; Anthony E Kline; Corina O Bondi
Journal:  Exp Neurol       Date:  2019-01-31       Impact factor: 5.330

Review 4.  Elucidating opportunities and pitfalls in the treatment of experimental traumatic brain injury to optimize and facilitate clinical translation.

Authors:  Patricia B de la Tremblaye; Darik A O'Neil; Megan J LaPorte; Jeffrey P Cheng; Joshua A Beitchman; Theresa Currier Thomas; Corina O Bondi; Anthony E Kline
Journal:  Neurosci Biobehav Rev       Date:  2017-05-30       Impact factor: 8.989

5.  Rehabilitative Success After Brain Trauma by Augmenting a Subtherapeutic Dose of Environmental Enrichment With Galantamine.

Authors:  Patricia B de la Tremblaye; Jody L Wellcome; Benjamin Wells de Witt; Jeffrey P Cheng; Elizabeth R Skidmore; Corina O Bondi; Anthony E Kline
Journal:  Neurorehabil Neural Repair       Date:  2017-11-12       Impact factor: 3.919

6.  Comparable impediment of cognitive function in female and male rats subsequent to daily administration of haloperidol after traumatic brain injury.

Authors:  Kristin E Free; Anna M Greene; Corina O Bondi; Naima Lajud; Patricia B de la Tremblaye; Anthony E Kline
Journal:  Exp Neurol       Date:  2017-07-08       Impact factor: 5.330

7.  Intermittent Administration of Haloperidol after Cortical Impact Injury Neither Impedes Spontaneous Recovery Nor Attenuates the Efficacy of Environmental Enrichment.

Authors:  Gina C Bao; Isabel H Bleimeister; Lydia A Zimmerman; JoDy L Wellcome; Peter J Niesman; Hannah L Radabaugh; Corina O Bondi; Anthony E Kline
Journal:  J Neurotrauma       Date:  2019-01-09       Impact factor: 5.269

8.  A combined therapeutic regimen of citalopram and environmental enrichment ameliorates attentional set-shifting performance after brain trauma.

Authors:  Heather M Minchew; Hannah L Radabaugh; Megan L LaPorte; Kristin E Free; Jeffrey P Cheng; Corina O Bondi
Journal:  Eur J Pharmacol       Date:  2021-05-15       Impact factor: 5.195

9.  Additive Effects of Environmental Enrichment and Ketamine on Neuropathic Pain Relief by Reducing Glutamatergic Activation in Spinal Cord Injury in Rats.

Authors:  W L Tai; L Sun; H Li; P Gu; E A Joosten; C W Cheung
Journal:  Front Neurosci       Date:  2021-03-22       Impact factor: 4.677

10.  Positive allosteric modulation of the α7 nicotinic acetylcholine receptor as a treatment for cognitive deficits after traumatic brain injury.

Authors:  David J Titus; Timothy Johnstone; Nathan H Johnson; Sidney H London; Meghana Chapalamadugu; Derk Hogenkamp; Kelvin W Gee; Coleen M Atkins
Journal:  PLoS One       Date:  2019-10-03       Impact factor: 3.240

  10 in total

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