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Sökning: id:"swepub:oai:DiVA.org:liu-101855" > 3-(4-Chloro-2-morph...

3-(4-Chloro-2-morpholin-4-yl-thiazol-5-yl)-8-(1-ethylpropyl)-2,6-dimethyl-imidazo[1,2-b]pyridazine : a novel brain-penetrant, orally available corticotropin-releasing factor receptor 1 antagonist with efficacy in animal models of alcoholism

Gehlert, Donald R. (författare)
Eli Lilly and Company, Indianapolis, IN, USA
Cippitelli, Andrea (författare)
National Institute on Alcohol Abuse and Alcoholism, NIH; Bethesda, MD, USA
Thorsell, Annika (författare)
National Institute on Alcohol Abuse and Alcoholism, NIH; Bethesda, MD, USA
visa fler...
Lê, Anh Dzung (författare)
University of Toronto, Canada
Hipskind, Philip A (författare)
Eli Lilly and Company, Indianapolis, IN, USA
Hamdouchi, Chafiq (författare)
Eli Lilly and Company, Indianapolis, IN, USA
Lu, Jianliang (författare)
Eli Lilly and Company, Indianapolis, IN, USA
Hembre, Erik J. (författare)
Eli Lilly and Company, Indianapolis, IN, USA
Cramer, Jeffrey (författare)
Eli Lilly and Company, Indianapolis, IN, USA
Song, Min (författare)
Eli Lilly and Company, Indianapolis, IN, USA
McKinzie, David (författare)
Eli Lilly and Company, Indianapolis, IN, USA
Morin, Michelle (författare)
Eli Lilly and Company, Indianapolis, IN, USA
Ciccocioppo, Roberto (författare)
University of Camerino, Italy
Heilig, Markus (författare)
National Institute on Alcohol Abuse and Alcoholism, NIH; Bethesda, MD, USA
visa färre...
 (creator_code:org_t)
Society for Neuroscience, 2007
2007
Engelska.
Ingår i: Journal of Neuroscience. - : Society for Neuroscience. - 0270-6474 .- 1529-2401. ; 27:10, s. 2718-2726
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • We describe a novel corticotropin-releasing factor receptor 1 (CRF1) antagonist with advantageous properties for clinical development, and its in vivo activity in preclinical alcoholism models. 3-(4-Chloro-2-morpholin-4-yl-thiazol-5-yl)-8-(1-ethylpropyl)-2,6-dimethyl-imidazo[1,2-b]pyridazine (MTIP) inhibited 125I-sauvagine binding to rat pituitary membranes and cloned human CRF1 with subnanomolar affinities, with no detectable activity at the CRF2 receptor or other common drug targets. After oral administration to rats, MTIP inhibited 125I-sauvagine binding to rat cerebellar membranes ex vivo with an ED50 of approximately 1.3 mg/kg and an oral bioavailability of 91.1%. Compared with R121919 (2,5-dimethyl-3-(6-dimethyl-4-methylpyridin-3-yl)-7-dipropylamino-pyrazolo[1,5-a]pyrimidine) and CP154526 (N-butyl-N-ethyl-4,9-dimethyl-7-(2,4,6-trimethylphenyl)-3,5,7-triazabicyclo[4.3.0]nona-2,4,8,10-tetraen-2-amine), MTIP had a markedly reduced volume of distribution and clearance. Neither open-field activity nor baseline exploration of an elevated plus-maze was affected by MTIP (1-10 mg/kg). In contrast, MTIP dose-dependently reversed anxiogenic effects of withdrawal from a 3 g/kg alcohol dose. Similarly, MTIP blocked excessive alcohol self-administration in Wistar rats with a history of dependence, and in a genetic model of high alcohol preference, the msP rat, at doses that had no effect in nondependent Wistar rats. Also, MTIP blocked reinstatement of stress-induced alcohol seeking both in postdependent and in genetically selected msP animals, again at doses that were ineffective in nondependent Wistar rats. Based on these findings, MTIP is a promising candidate for treatment of alcohol dependence.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

Nyckelord

alcoholism; drug seeking; self-administration; relapse; stress; CRF

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ref (ämneskategori)
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