Publication:
Inhibitory effect of agmatine on naloxone-precipitated abstinence syndrome in morphine dependent rats

dc.contributor.authorsAricioglu-Kartal, F.; Uzbay, I. T.
dc.date.accessioned2022-03-15T11:10:15Z
dc.date.accessioned2026-01-11T15:56:36Z
dc.date.available2022-03-15T11:10:15Z
dc.date.issued1997
dc.description.abstractEffects of agmatine, which is an endogenous polyamine metabolite formed by decarboxylation of L-arginine, were investigated on the morphine abstinence syndrome in rats. Two pellets containing 75 mg morphine base (total 150 mg) were implanted subcutaneously on the back of rats. Seventy-two hours after morphine implantation, agmatine sulphate (20, 30 and 40 mg/kg) or saline was injected intraperitoneally. Forty-five min later, naloxone (2 mg/kg) was injected intraperitoneally to induce precipitated withdrawal. Immediately after naloxone injection, rats were observed for 15 min, and abstinence syndrome signs, which included jumping, wet dog shake, writhing, defecation, ptosis, teeth chattering and diarrhea were counted or rated. Agmatine attenuated all of the signs of the morphine abstinence syndrome dose dependently and significantly. Our results suggest that agmatine prevents naloxone-precipitated abstinence syndrome in morphine dependent rats; thus, this drug may be beneficial in the treatment of opioid dependence.
dc.identifier.doi10.1016/s0024-3205(97)00801-1
dc.identifier.issn0024-3205
dc.identifier.pubmedPMID: 9365224
dc.identifier.urihttps://hdl.handle.net/11424/248633
dc.language.isoeng
dc.relation.ispartofLife Sciences
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectAnimals
dc.subjectMale
dc.subjectRats
dc.subjectRats, Wistar
dc.subjectBehavior, Animal
dc.subjectMorphine Dependence
dc.subjectNaloxone
dc.subjectSubstance Withdrawal Syndrome
dc.subjectAgmatine
dc.titleInhibitory effect of agmatine on naloxone-precipitated abstinence syndrome in morphine dependent rats
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage1781
oaire.citation.startPage1775
oaire.citation.titleLife Sciences
oaire.citation.volume18

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