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The potent and selective α4ß2*/α6*-nicotinic acetylcholine receptor partial agonist 2-[5-[5-((S)Azetidin-2-ylmethoxy)-3-pyridinyl]-3-isoxazolyl]ethanol demonstrates antidepressive-like behavior in animal models and a favorable ADME-tox profile.
Yu, Li-Fang; Brek Eaton, J; Zhang, Han-Kun; Sabath, Emily; Hanania, Taleen; Li, Guan-Nan; van Breemen, Richard B; Whiteaker, Paul; Liu, Qiang; Wu, Jie; Chang, Yong-Chang; Lukas, Ronald J; Brunner, Dani; Kozikowski, Alan P.
Afiliación
  • Yu LF; Department of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago 833 South Wood Street, Chicago, Illinois, 60612 ; Institute of Drug Design and Development, Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, East China Normal University 366
  • Brek Eaton J; Division of Neurobiology, Barrow Neurological Institute 350 West Thomas Road, Phoenix, Arizona, 85013.
  • Zhang HK; Department of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago 833 South Wood Street, Chicago, Illinois, 60612 ; Institute of Biomedical Sciences and School of Life Sciences, East China Normal University 500 Dongchuan Road, Shanghai, 200241, China.
  • Sabath E; PsychoGenics, Inc. 765 Old Saw Mill River Road, Tarrytown, New York, 10591.
  • Hanania T; PsychoGenics, Inc. 765 Old Saw Mill River Road, Tarrytown, New York, 10591.
  • Li GN; Department of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago 833 South Wood Street, Chicago, Illinois, 60612.
  • van Breemen RB; Department of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago 833 South Wood Street, Chicago, Illinois, 60612.
  • Whiteaker P; Division of Neurobiology, Barrow Neurological Institute 350 West Thomas Road, Phoenix, Arizona, 85013.
  • Liu Q; Division of Neurobiology, Barrow Neurological Institute 350 West Thomas Road, Phoenix, Arizona, 85013 ; Division of Neurology, Barrow Neurological Institute 350 West Thomas Road, Phoenix, Arizona, 85013.
  • Wu J; Division of Neurology, Barrow Neurological Institute 350 West Thomas Road, Phoenix, Arizona, 85013.
  • Chang YC; Division of Neurobiology, Barrow Neurological Institute 350 West Thomas Road, Phoenix, Arizona, 85013.
  • Lukas RJ; Division of Neurobiology, Barrow Neurological Institute 350 West Thomas Road, Phoenix, Arizona, 85013.
  • Brunner D; PsychoGenics, Inc. 765 Old Saw Mill River Road, Tarrytown, New York, 10591 ; Department of Psychiatry, Columbia University, NYSPI 1051 Riverside Drive, New York, New York, 10032.
  • Kozikowski AP; Department of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago 833 South Wood Street, Chicago, Illinois, 60612.
Pharmacol Res Perspect ; 2(2): e00026, 2014 Apr.
Article en En | MEDLINE | ID: mdl-25505580
Preclinical and clinical studies demonstrated that the inhibition of cholinergic supersensitivity through nicotinic antagonists and partial agonists can be used successfully to treat depressed patients, especially those who are poor responders to selective serotonin reuptake inhibitors (SSRIs). In our effort to develop novel antidepressant drugs, LF-3-88 was identified as a potent nicotinic acetylcholine receptor (nAChR) partial agonist with subnanomolar to nanomolar affinities for ß2-containing nAChRs (α2ß2, α3ß2, α4ß2, and α4ß2*) and superior selectivity away from α3ß4 - (K i > 10(4) nmol/L) and α7-nAChRs (K i > 10(4) nmol/L) as well as 51 other central nervous system (CNS)-related neurotransmitter receptors and transporters. Functional activities at different nAChR subtypes were characterized utilizing (86)Rb(+) ion efflux assays, two-electrode voltage-clamp (TEVC) recording in oocytes, and whole-cell current recording measurements. In mouse models, administration of LF-3-88 resulted in antidepressive-like behavioral signatures 15 min post injection in the SmartCube® test (5 and 10 mg/kg, i.p.; about 45-min session), decreased immobility in the forced swim test (1-3 mg/kg, i.p.; 1-10 mg/kg, p.o.; 30 min pretreatment, 6-min trial), and decreased latency to approach food in the novelty-suppressed feeding test after 29 days chronic administration once daily (5 mg/kg but not 10 mg/kg, p.o.; 15-min trial). In addition, LF-3-88 exhibited a favorable profile in pharmacokinetic/ADME-Tox (absorption, distribution, metabolism, excretion, and toxicity) assays. This compound was also shown to cause no mortality in wild-type Balb/CJ mice when tested at 300 mg/kg. These results further support the potential of potent and selective nicotinic partial agonists for use in the treatment of depression.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pharmacol Res Perspect Año: 2014 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pharmacol Res Perspect Año: 2014 Tipo del documento: Article
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