Xylazine suppresses fentanyl consumption during self-administration and induces a unique sex-specific withdrawal syndrome that is not altered by naloxone in rats.

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Title: Xylazine suppresses fentanyl consumption during self-administration and induces a unique sex-specific withdrawal syndrome that is not altered by naloxone in rats.
Authors: Khatri SN; Department of Pharmacology and Nutritional Sciences, University of Kentucky., Sadek S; Department of Pharmacology and Nutritional Sciences, University of Kentucky., Kendrick PT; Department of Pharmacology and Nutritional Sciences, University of Kentucky., Bondy EO; Department of Pharmacology and Nutritional Sciences, University of Kentucky., Hong M; Department of Pharmacology and Nutritional Sciences, University of Kentucky., Pauss S; Department of Pharmacology and Nutritional Sciences, University of Kentucky., Luo D; Center for Pharmaceutical Research and Innovation, College of Pharmacy, University of Kentucky., Prisinzano TE; Center for Pharmaceutical Research and Innovation, College of Pharmacy, University of Kentucky., Dunn KE; Department of Psychiatry and Behavioral Sciences, Johns Hopkins University., Marusich JA; Center for Drug Discovery, RTI International., Beckmann JS; Department of Psychology, University of Kentucky., Hinds TD; Department of Pharmacology and Nutritional Sciences, University of Kentucky., Gipson CD; Department of Pharmacology and Nutritional Sciences, University of Kentucky.
Source: Experimental and clinical psychopharmacology [Exp Clin Psychopharmacol] 2024 Apr; Vol. 32 (2), pp. 150-157. Date of Electronic Publication: 2023 Jul 20.
Publication Type: Journal Article
Journal Info: Publisher: American Psychological Association Country of Publication: United States NLM ID: 9419066 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1936-2293 (Electronic) Linking ISSN: 10641297 NLM ISO Abbreviation: Exp Clin Psychopharmacol Subsets: MEDLINE
Database: MEDLINE Ultimate
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PubType: Academic Journal
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  Data: Xylazine suppresses fentanyl consumption during self-administration and induces a unique sex-specific withdrawal syndrome that is not altered by naloxone in rats.
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  Data: <searchLink fieldCode="AU" term="%22Khatri+SN%22">Khatri SN</searchLink>; Department of Pharmacology and Nutritional Sciences, University of Kentucky.<br /><searchLink fieldCode="AU" term="%22Sadek+S%22">Sadek S</searchLink>; Department of Pharmacology and Nutritional Sciences, University of Kentucky.<br /><searchLink fieldCode="AU" term="%22Kendrick+PT%22">Kendrick PT</searchLink>; Department of Pharmacology and Nutritional Sciences, University of Kentucky.<br /><searchLink fieldCode="AU" term="%22Bondy+EO%22">Bondy EO</searchLink>; Department of Pharmacology and Nutritional Sciences, University of Kentucky.<br /><searchLink fieldCode="AU" term="%22Hong+M%22">Hong M</searchLink>; Department of Pharmacology and Nutritional Sciences, University of Kentucky.<br /><searchLink fieldCode="AU" term="%22Pauss+S%22">Pauss S</searchLink>; Department of Pharmacology and Nutritional Sciences, University of Kentucky.<br /><searchLink fieldCode="AU" term="%22Luo+D%22">Luo D</searchLink>; Center for Pharmaceutical Research and Innovation, College of Pharmacy, University of Kentucky.<br /><searchLink fieldCode="AU" term="%22Prisinzano+TE%22">Prisinzano TE</searchLink>; Center for Pharmaceutical Research and Innovation, College of Pharmacy, University of Kentucky.<br /><searchLink fieldCode="AU" term="%22Dunn+KE%22">Dunn KE</searchLink>; Department of Psychiatry and Behavioral Sciences, Johns Hopkins University.<br /><searchLink fieldCode="AU" term="%22Marusich+JA%22">Marusich JA</searchLink>; Center for Drug Discovery, RTI International.<br /><searchLink fieldCode="AU" term="%22Beckmann+JS%22">Beckmann JS</searchLink>; Department of Psychology, University of Kentucky.<br /><searchLink fieldCode="AU" term="%22Hinds+TD%22">Hinds TD</searchLink>; Department of Pharmacology and Nutritional Sciences, University of Kentucky.<br /><searchLink fieldCode="AU" term="%22Gipson+CD%22">Gipson CD</searchLink>; Department of Pharmacology and Nutritional Sciences, University of Kentucky.
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  Data: <searchLink fieldCode="JN" term="%229419066%22">Experimental and clinical psychopharmacology</searchLink> [Exp Clin Psychopharmacol] 2024 Apr; Vol. 32 (2), pp. 150-157. <i>Date of Electronic Publication: </i>2023 Jul 20.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22American+Psychological+Association%22">American Psychological Association </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9419066 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1936-2293 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210641297%22">10641297 </searchLink><i>NLM ISO Abbreviation: </i>Exp Clin Psychopharmacol <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=37470999
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        Value: 10.1037/pha0000670
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        Text: English
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        StartPage: 150
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      – TitleFull: Xylazine suppresses fentanyl consumption during self-administration and induces a unique sex-specific withdrawal syndrome that is not altered by naloxone in rats.
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              Text: 2024 Apr
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