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Lack of effect of different pain-related manipulations on opioid self-administration, reinstatement of opioid seeking, and opioid choice in rats.
Reiner, David J; Townsend, E Andrew; Orihuel, Javier; Applebey, Sarah V; Claypool, Sarah M; Banks, Matthew L; Shaham, Yavin; Negus, S Stevens.
Afiliação
  • Reiner DJ; Behavioral Neuroscience Branch, IRP/NIDA/NIH, Baltimore, MD, USA. david.reiner@nih.gov.
  • Townsend EA; NIGMS, Bethesda, MD, USA. david.reiner@nih.gov.
  • Orihuel J; Department of Pharmacology and Toxicology, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
  • Applebey SV; Behavioral Neuroscience Branch, IRP/NIDA/NIH, Baltimore, MD, USA.
  • Claypool SM; Behavioral Neuroscience Branch, IRP/NIDA/NIH, Baltimore, MD, USA.
  • Banks ML; Behavioral Neuroscience Branch, IRP/NIDA/NIH, Baltimore, MD, USA.
  • Shaham Y; Department of Pharmacology and Toxicology, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
  • Negus SS; Behavioral Neuroscience Branch, IRP/NIDA/NIH, Baltimore, MD, USA.
Psychopharmacology (Berl) ; 238(7): 1885-1897, 2021 Jul.
Article em En | MEDLINE | ID: mdl-33765177
ABSTRACT
RATIONALE AND

OBJECTIVE:

Pain-related factors increase the risk for opioid addiction, and pain may function as a negative reinforcer to increase opioid taking and seeking. However, experimental pain-related manipulations generally do not increase opioid self-administration in rodents. This discrepancy may reflect insufficient learning of pain-relief contingencies or confounding effects of pain-related behavioral impairments. Here, we determined if pairing noxious stimuli with opioid self-administration would promote pain-related reinstatement of opioid seeking or increase opioid choice over food.

METHODS:

In Experiment 1, rats self-administered fentanyl in the presence or absence of repeated intraplantar capsaicin injections in distinct contexts to model context-specific exposure to cutaneous nociception. After capsaicin-free extinction in both contexts, we tested if capsaicin would reinstate fentanyl seeking. In Experiment 2, rats self-administered heroin after intraperitoneal (i.p.) lactic acid injections to model acute visceral inflammatory pain. After lactic acid-free extinction, we tested if lactic acid would reinstate heroin seeking. In Experiment 3, we tested if repeated i.p. lactic acid or intraplantar Complete Freund's Adjuvant (CFA; to model sustained inflammatory pain) would increase fentanyl choice over food.

RESULTS:

In Experiments 1-2, neither capsaicin nor lactic acid reinstated opioid seeking after extinction, and lactic acid did not increase heroin-induced reinstatement. In Experiment 3, lactic acid and CFA decreased reinforcement rate without affecting fentanyl choice.

CONCLUSIONS:

Results extend the range of conditions across which pain-related manipulations fail to increase opioid seeking in rats and suggest that enhanced opioid-addiction risk in humans with chronic pain involves factors other than enhanced opioid reinforcement and relapse.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Dor / Reforço Psicológico / Medição da Dor / Comportamento de Escolha / Comportamento de Procura de Droga / Analgésicos Opioides Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Psychopharmacology (Berl) Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Dor / Reforço Psicológico / Medição da Dor / Comportamento de Escolha / Comportamento de Procura de Droga / Analgésicos Opioides Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Psychopharmacology (Berl) Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos