B Sofia Beas1, Barry Setlow1,2, Jennifer L Bizon3,4. 1. Department of Neuroscience, University of Florida College of Medicine, McKnight Brain Institute, PO Box 100244, Gainesville, FL, 32610-0244, USA. 2. Department of Psychiatry, University of Florida College of Medicine, Gainesville, FL, USA. 3. Department of Neuroscience, University of Florida College of Medicine, McKnight Brain Institute, PO Box 100244, Gainesville, FL, 32610-0244, USA. bizonj@ufl.edu. 4. Department of Psychiatry, University of Florida College of Medicine, Gainesville, FL, USA. bizonj@ufl.edu.
Abstract
RATIONALE: The ability to adjust response strategies when faced with changes in the environment is critical for normal adaptive behavior. Such behavioral flexibility is compromised by experimental disruption of cortical GABAergic signaling, as well as in conditions such as schizophrenia and normal aging that are characterized by cortical hyperexcitability. The current studies were designed to determine whether stimulation of GABAergic signaling using the GABA(B) receptor agonist baclofen can facilitate behavioral flexibility. METHODS: Male Fischer 344 rats were trained in a set-shifting task in which they learned to discriminate between two response levers to obtain a food reward. Correct levers were signaled in accordance with two distinct response rules (rule 1: correct lever signaled by a cue light; rule 2: correct lever signaled by its left/right position). The order of rule presentation varied, but they were always presented sequentially, with the trials and errors to reach criterion performance on the second (set shift) rule providing the measure of behavioral flexibility. Experiments determined the effects of the GABA(B) receptor agonist baclofen (intraperitoneal, 0, 1.0, 2.5, and 4.0 mg/kg) administered acutely before the shift to the second rule. RESULTS: Baclofen enhanced set-shifting performance. Control experiments demonstrated that this enhancement was not simply due to improved discrimination learning, nor was it due to impaired recall of the initial discrimination rule. CONCLUSIONS: The results demonstrate that baclofen can facilitate behavioral flexibility, suggesting that GABA(B) receptor agonists may have utility for treating behavioral dysfunction in neuropsychiatric disorders.
RATIONALE: The ability to adjust response strategies when faced with changes in the environment is critical for normal adaptive behavior. Such behavioral flexibility is compromised by experimental disruption of cortical GABAergic signaling, as well as in conditions such as schizophrenia and normal aging that are characterized by cortical hyperexcitability. The current studies were designed to determine whether stimulation of GABAergic signaling using the GABA(B) receptor agonist baclofen can facilitate behavioral flexibility. METHODS: Male Fischer 344 rats were trained in a set-shifting task in which they learned to discriminate between two response levers to obtain a food reward. Correct levers were signaled in accordance with two distinct response rules (rule 1: correct lever signaled by a cue light; rule 2: correct lever signaled by its left/right position). The order of rule presentation varied, but they were always presented sequentially, with the trials and errors to reach criterion performance on the second (set shift) rule providing the measure of behavioral flexibility. Experiments determined the effects of the GABA(B) receptor agonist baclofen (intraperitoneal, 0, 1.0, 2.5, and 4.0 mg/kg) administered acutely before the shift to the second rule. RESULTS:Baclofen enhanced set-shifting performance. Control experiments demonstrated that this enhancement was not simply due to improved discrimination learning, nor was it due to impaired recall of the initial discrimination rule. CONCLUSIONS: The results demonstrate that baclofen can facilitate behavioral flexibility, suggesting that GABA(B) receptor agonists may have utility for treating behavioral dysfunction in neuropsychiatric disorders.
Entities:
Keywords:
Baclofen; Behavioral flexibility; GABA(B) receptor; Prefrontal cortex; Set shifting
Authors: Dennis R Sparta; Nanna Hovelsø; Alex O Mason; Pranish A Kantak; Randall L Ung; Heather K Decot; Garret D Stuber Journal: J Neurosci Date: 2014-03-05 Impact factor: 6.167
Authors: James C Garbutt; Alexei B Kampov-Polevoy; Robert Gallop; Linda Kalka-Juhl; Barbara A Flannery Journal: Alcohol Clin Exp Res Date: 2010-11 Impact factor: 3.455
Authors: M J Gandal; J Sisti; K Klook; P I Ortinski; V Leitman; Y Liang; T Thieu; R Anderson; R C Pierce; G Jonak; R E Gur; G Carlson; S J Siegel Journal: Transl Psychiatry Date: 2012-07-17 Impact factor: 6.222
Authors: Paulo Jannuzzi Cunha; Priscila Dib Gonçalves; Mariella Ometto; Bernardo Dos Santos; Sergio Nicastri; Geraldo F Busatto; Arthur Guerra de Andrade Journal: Front Psychiatry Date: 2013-10-21 Impact factor: 4.157
Authors: Luis A Natividad; Michael Q Steinman; Sarah A Laredo; Cristina Irimia; Ilham Y Polis; Robert Lintz; Matthew W Buczynski; Rémi Martin-Fardon; Marisa Roberto; Loren H Parsons Journal: Addict Biol Date: 2017-09-22 Impact factor: 4.280
Authors: Caesar M Hernandez; Lauren M Vetere; Caitlin A Orsini; Joseph A McQuail; Andrew P Maurer; Sara N Burke; Barry Setlow; Jennifer L Bizon Journal: Neurobiol Aging Date: 2017-09-05 Impact factor: 4.673
Authors: D Sinclair; R Featherstone; M Naschek; J Nam; A Du; S Wright; K Pance; O Melnychenko; R Weger; S Akuzawa; M Matsumoto; S J Siegel Journal: eNeuro Date: 2017-03-01
Authors: Abbi R Hernandez; Caesar M Hernandez; Keila Campos; Leah Truckenbrod; Quinten Federico; Brianna Moon; Joseph A McQuail; Andrew P Maurer; Jennifer L Bizon; Sara N Burke Journal: Front Aging Neurosci Date: 2018-12-03 Impact factor: 5.750
Authors: Joseph A McQuail; B Sofia Beas; Kyle B Kelly; Caesar M Hernandez; Jennifer L Bizon; Charles J Frazier Journal: Neuropharmacology Date: 2021-07-15 Impact factor: 5.273
Authors: Bastien Ribot; Aymar de Rugy; Nicolas Langbour; Anne Duron; Michel Goillandeau; Thomas Michelet Journal: Front Hum Neurosci Date: 2022-01-04 Impact factor: 3.169