Literature DB >> 8075886

Evaluation of a series of novel CCKB antagonists using a functional assay in the rat central nervous system.

P R Boden1, R D Pinnock, M C Pritchard, G N Woodruff.   

Abstract

1. Electrophysiological recordings from rat ventromedial hypothalamus (VMH) in vitro have been used to compare the effects of novel chemical entities on CCKB receptor activation in the rat central nervous system. 2. Twenty compounds from three different chemical series were evaluated for their ability to reduce pentagastrin-induced increases in action potential firing rate. 3. All twenty compounds studies were found to be CCKB antagonists, with equilibrium constants spanning a concentration-range of several orders of magnitude. The rank order for their ability to block pentagastrin responses correlated well with values obtained for their relative affinities for the mouse cortex CCKB binding site. 4. It is concluded that the VMH preparation provides a good functional correlate to binding assays in the rodent central nervous system for a structurally diverse series of CCKB antagonists.

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Year:  1994        PMID: 8075886      PMCID: PMC1910345          DOI: 10.1111/j.1476-5381.1994.tb13127.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  17 in total

1.  Cholecystokinin dipeptoid antagonists: design, synthesis, and anxiolytic profile of some novel CCK-A and CCK-B selective and "mixed" CCK-A/CCK-B antagonists.

Authors:  P R Boden; M Higginbottom; D R Hill; D C Horwell; J Hughes; D C Rees; E Roberts; L Singh; N Suman-Chauhan; G N Woodruff
Journal:  J Med Chem       Date:  1993-03-05       Impact factor: 7.446

2.  Design of potent, orally effective, nonpeptidal antagonists of the peptide hormone cholecystokinin.

Authors:  B E Evans; M G Bock; K E Rittle; R M DiPardo; W L Whitter; D F Veber; P S Anderson; R M Freidinger
Journal:  Proc Natl Acad Sci U S A       Date:  1986-07       Impact factor: 11.205

3.  Cholecystokinin decreases food intake in rats.

Authors:  J Gibbs; R C Young; G P Smith
Journal:  J Comp Physiol Psychol       Date:  1973-09

4.  Cholecystokinin octapeptide-like immunoreactivity: histochemical localization in rat brain.

Authors:  R B Innis; F M Corrêa; G R Uhl; B Schneider; S H Snyder
Journal:  Proc Natl Acad Sci U S A       Date:  1979-01       Impact factor: 11.205

5.  Biochemical and pharmacological characterization of an extremely potent and selective nonpeptide cholecystokinin antagonist.

Authors:  R S Chang; V J Lotti
Journal:  Proc Natl Acad Sci U S A       Date:  1986-07       Impact factor: 11.205

6.  Methods for drug discovery: development of potent, selective, orally effective cholecystokinin antagonists.

Authors:  B E Evans; K E Rittle; M G Bock; R M DiPardo; R M Freidinger; W L Whitter; G F Lundell; D F Veber; P S Anderson; R S Chang
Journal:  J Med Chem       Date:  1988-12       Impact factor: 7.446

7.  Evidence for the neuropeptide cholecystokinin as an antagonist of opiate analgesia.

Authors:  P L Faris; B R Komisaruk; L R Watkins; D J Mayer
Journal:  Science       Date:  1983-01-21       Impact factor: 47.728

8.  A new potent and selective non-peptide gastrin antagonist and brain cholecystokinin receptor (CCK-B) ligand: L-365,260.

Authors:  V J Lotti; R S Chang
Journal:  Eur J Pharmacol       Date:  1989-03-21       Impact factor: 4.432

9.  Potentiation of opiate analgesia and apparent reversal of morphine tolerance by proglumide.

Authors:  L R Watkins; I B Kinscheck; D J Mayer
Journal:  Science       Date:  1984-04-27       Impact factor: 47.728

10.  Effects of cholecystokinin and related peptides on neuronal activity in the ventromedial nucleus of the rat hypothalamus.

Authors:  P Boden; R G Hill
Journal:  Br J Pharmacol       Date:  1988-05       Impact factor: 8.739

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  2 in total

Review 1.  Cholecystokinin receptors.

Authors:  P Boden; M D Hall; J Hughes
Journal:  Cell Mol Neurobiol       Date:  1995-10       Impact factor: 5.046

2.  Small synthetic ligands of the cholecystokinin-B/gastrin receptor can mimic the function of endogenous peptide hormones.

Authors:  M Beinborn; C Chen; L DeMeo; E W McBride; A S Kopin
Journal:  Yale J Biol Med       Date:  1998 May-Aug
  2 in total

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