Publication:
Alteration of cholinergic pressor and antinociceptive responses in rats pretreated with the cholinergic toxin AF64A

dc.contributor.authorsTellioğlu, T.; Erin, N.; Akin, S. B.; Berkman, K.; Oktay, S.
dc.date.accessioned2022-03-15T11:23:02Z
dc.date.accessioned2026-01-10T19:16:10Z
dc.date.available2022-03-15T11:23:02Z
dc.date.issued1998
dc.description.abstract1. In the present study, the pressor and antinociceptive effects of physostigmine and oxotremorine were investigated in rats injected with AF64A intracerebroventricularly. 2. Physostigmine (50-100 micrograms/kg, i.v.)-induced pressor responses were significantly lower in AF64A-injected rats compared with saline-injected animals, whereas oxotremorine (20-80 micrograms/kg, i.v.)-induced responses were found to be similar to those seen in the saline group. 3. The physostigmine (100 micrograms/kg, s.c.)-induced antinociceptive effect was totally abolished by AF64A treatment, but that of oxotremorine (30 micrograms/kg, s.c.) remained unchanged at the tail-flick test. 4. The results of this study present functional evidence for AF64A-produced substantial loss of cholinergic neurons involved in the regulation of blood pressure and nociception but not in postsynaptic muscarinic receptors.
dc.identifier.doi10.1016/s0306-3623(97)00298-x
dc.identifier.issn0306-3623
dc.identifier.pubmedPMID: 9522170
dc.identifier.urihttps://hdl.handle.net/11424/249896
dc.language.isoeng
dc.relation.ispartofGeneral Pharmacology
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectFemale
dc.subjectAnimals
dc.subjectMale
dc.subjectRats
dc.subjectCholine
dc.subjectPain Measurement
dc.subjectRats, Sprague-Dawley
dc.subjectAvoidance Learning
dc.subjectCholinesterase Inhibitors
dc.subjectPhysostigmine
dc.subjectMuscarinic Agonists
dc.subjectOxotremorine
dc.subjectAnalgesia
dc.subjectAziridines
dc.subjectMaze Learning
dc.subjectNeuromuscular Blocking Agents
dc.titleAlteration of cholinergic pressor and antinociceptive responses in rats pretreated with the cholinergic toxin AF64A
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage531
oaire.citation.startPage525
oaire.citation.titleGeneral Pharmacology
oaire.citation.volume4

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