Show simple item record

dc.contributor.authorRadin, Daniel Pierce
dc.contributor.authorZhong, Sheng
dc.contributor.authorCerne, Rok
dc.contributor.authorShoaib, Mohammed
dc.contributor.authorWitkin, Jeffrey M.
dc.contributor.authorLippa, Arnold
dc.contributor.editorSchifano, Fabrizio
dc.date.accessioned2024-03-25T13:34:03Z
dc.date.available2024-03-25T13:34:03Z
dc.date.issued2024-02-26
dc.identifier.citationRadin , D P , Zhong , S , Cerne , R , Shoaib , M , Witkin , J M , Lippa , A & Schifano , F (ed.) 2024 , ' Low-Impact Ampakine CX1739 Exerts Pro-Cognitive Effects and Reverses Opiate-Induced Respiratory Depression in Rodents ' , Future Pharmacology , vol. 4 , no. 1 , 4010012 , pp. 173-187 . https://doi.org/10.3390/futurepharmacol4010012
dc.identifier.issn2673-9879
dc.identifier.otherJisc: 1815080
dc.identifier.otherpublisher-id: futurepharmacol-04-00012
dc.identifier.urihttp://hdl.handle.net/2299/27643
dc.description© 2024 The Author(s). Licensee MDPI, Basel, Switzerland. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY), https://creativecommons.org/licenses/by/4.0/
dc.description.abstractAMPA-glutamate receptors (AMPARs) are expressed throughout the CNS and mediate the majority of fast excitatory synaptic transmission. Ampakines are orally available small molecules that bind allosterically to AMPARs and enhance excitatory currents elicited by the endogenous agonist glutamate. In preclinical studies, ampakines are effective in ameliorating symptoms in a battery of neurodegenerative and neuropsychiatric diseases in which excitatory transmission is compromised. However, the development of ampakines as medicines was slowed by the emergence of neurotoxicity and seizures in rodents due to some ampakines. Here, we describe the preclinical pharmacology of a novel ampakine, N-methyl-N-(tetrahydro-2H-pyran-4-yl)benzo[c][1,2,5] oxadiazole-5-carboxamide (CX1739), that does not induce seizures in animals or humans at efficacious doses. CX1739 dose-dependently enhanced long-term potentiation in vivo in rats, a process thought to be a molecular substrate of learning and memory. Correspondingly, CX1739 dose-dependently enhanced performance in assays that probed multiple aspects of cognition—the novel object recognition test, the win shift radial arm maze, and the five-choice serial reaction time task in rats. CX1739 also abrogated amphetamine-induced locomotor activity, demonstrating that it may be given in conjunction with stimulants for pro-cognitive gains while mitigating the side effects of stimulant-based ADHD medications. CX1739 also rapidly reversed opioid-induced respiratory depression. While efficacy in these tests occurred at doses of 0.03–18 mg/kg, there were no adverse events detected in safety studies in rats up to 2000 mg/kg. These preclinical findings suggest that CX1739 can be translated safely into the clinical setting to potentially treat dementia, neuropsychiatric disorders, and the life-threatening complication of opiate-induced suppression of endogenous inspiratory breathing rhythms.en
dc.format.extent15
dc.format.extent3613026
dc.language.isoeng
dc.relation.ispartofFuture Pharmacology
dc.subjectopiate-induced respiratory depression
dc.subjectLTP
dc.subjectAMPA receptor
dc.subjectADHD
dc.subjectampakine
dc.subjecthyperactivity
dc.titleLow-Impact Ampakine CX1739 Exerts Pro-Cognitive Effects and Reverses Opiate-Induced Respiratory Depression in Rodentsen
dc.contributor.institutionCentre for Health Services and Clinical Research
dc.contributor.institutionPsychopharmacology, Drug Misuse and Novel Psychoactive Substances Unit
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionDepartment of Clinical, Pharmaceutical and Biological Science
dc.description.statusPeer reviewed
rioxxterms.versionofrecord10.3390/futurepharmacol4010012
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record