Literature DB >> 26494422

Evaluation of a Postoperative Pain-Like State on Motivated Behavior in Rats: Effects of Plantar Incision on Progressive-Ratio Food-Maintained Responding.

Emily Warner1, Rebecca Krivitsky1, Katherine Cone1, Phillip Atherton1, Travis Pitre1, Janell Lanpher1, Denise Giuvelis2, Ivy Bergquist2, Tamara King2,3, Edward J Bilsky2,3, Glenn W Stevenson1,3.   

Abstract

There has been recent interest in characterizing the effects of pain-like states on motivated behaviors in order to quantify how pain modulates goal-directed behavior and the persistence of that behavior. The current set of experiments assessed the effects of an incisional postoperative pain manipulation on food-maintained responding under a progressive-ratio (PR) operant schedule. Independent variables included injury state (plantar incision or anesthesia control) and reinforcer type (grain pellet or sugar pellet); dependent variables were tactile sensory thresholds and response breakpoint. Once responding stabilized on the PR schedule, separate groups of rats received a single ventral hind paw incision or anesthesia (control condition). Incision significantly reduced breakpoints in rats responding for grain, but not sugar. In rats responding for sugar, tactile hypersensitivity recovered within 24 hr, indicating a faster recovery of incision-induced tactile hypersensitivity compared to rats responding for grain, which demonstrated recovery at PD2. The NSAID analgesic, diclofenac (5.6 mg/kg) completely restored incision-depressed PR operant responding and tactile sensitivity at 3 hr following incision. The PR schedule differentiated between sucrose and grain, suggesting that relative reinforcing efficacy may be an important determinant in detecting pain-induced changes in motivated behavior.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  nociception; operant conditioning; pain-depressed behavior; postoperative incisional pain; preclinical pain assay; progressive ratio schedules

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Year:  2015        PMID: 26494422      PMCID: PMC4715615          DOI: 10.1002/ddr.21284

Source DB:  PubMed          Journal:  Drug Dev Res        ISSN: 0272-4391            Impact factor:   4.360


  61 in total

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