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Delta/mu opioid receptor interactions in operant conditioning assays of pain-depressed responding and drug-induced rate suppression: assessment of therapeutic index in male Sprague Dawley rats.
Cone, Katherine; Lanpher, Janell; Kinens, Abigail; Richard, Philomena; Couture, Sarah; Brackin, Rebecca; Payne, Emily; Harrington, Kylee; Rice, Kenner C; Stevenson, Glenn W.
Afiliação
  • Cone K; Department of Psychology, University of New England, Biddeford, ME, 04005, USA.
  • Lanpher J; Department of Psychology, University of New England, Biddeford, ME, 04005, USA.
  • Kinens A; Department of Psychology, University of New England, Biddeford, ME, 04005, USA.
  • Richard P; Department of Psychology, University of New England, Biddeford, ME, 04005, USA.
  • Couture S; Department of Psychology, University of New England, Biddeford, ME, 04005, USA.
  • Brackin R; Department of Psychology, University of New England, Biddeford, ME, 04005, USA.
  • Payne E; Department of Psychology, University of New England, Biddeford, ME, 04005, USA.
  • Harrington K; Department of Psychology, University of New England, Biddeford, ME, 04005, USA.
  • Rice KC; Drug Design and Synthesis Section, Molecular Targets and Medications Branch, National Institute on Drug Abuse and National Institute on Alcohol Abuse and Alcoholism, Rockville, MD, 20850, USA.
  • Stevenson GW; Department of Psychology, University of New England, Biddeford, ME, 04005, USA. gstevenson@une.edu.
Psychopharmacology (Berl) ; 235(5): 1609-1618, 2018 05.
Article em En | MEDLINE | ID: mdl-29572653
RATIONALE AND OBJECTIVES: Although delta/mu receptor interactions vary as a function of behavioral endpoint, there have been no assessments of these interactions using assays of pain-depressed responding. This is the first report of delta/mu interactions using an assay of pain-depressed behavior. METHODS: A mult-cycle FR10 operant schedule was utilized in the presence of (nociception) and in the absence of (rate suppression) a lactic acid inflammatory pain-like manipulation. SNC80 and methadone were used as selective/high efficacy delta and mu agonists, respectively. Both SNC80 and methadone alone produced a dose-dependent restoration of pain-depressed responding and dose-dependent response rate suppression. Three fixed ratio mixtures, based on the relative potencies of the drugs in the nociception assay, also produced dose-dependent antinociception and sedation. Isobolographic analysis indicated that all three mixtures produced supra-additive antinociceptive effects and simply additive sedation effects. CONCLUSIONS: The therapeutic index (TI) inversely varied as a function of amount of SNC80 in the mixture, such that lower amounts of SNC80 produced a higher TI, and larger amounts produced a lower TI. Compared to literature using standard pain-elicited assays, the orderly relationship between SNC80 and TI reported here may be a unique function of assessing pain-depressed behavior.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dor / Receptores Opioides delta / Receptores Opioides mu / Condicionamento Operante / Índice Terapêutico Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dor / Receptores Opioides delta / Receptores Opioides mu / Condicionamento Operante / Índice Terapêutico Idioma: En Ano de publicação: 2018 Tipo de documento: Article