QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

This Article Full Text Full Text (PDF) All Versions of this Article: jpet.107.124958v1 322/3/1286    most recent Submit a response Alert me when this article is cited Alert me when eLetters are posted Alert me if a correction is posted Citation Map Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Lindström, E. Articles by Vauquelin, G. Search for Related Content PubMed PubMed Citation Articles by Lindström, E. Articles by Vauquelin, G.

CELLULAR AND MOLECULAR

Neurokinin 1 Receptor Antagonists: Correlation between in Vitro Receptor Interaction and in Vivo Efficacy

AstraZeneca R&D, Mölndal, Sweden (E.L., B.v.M., I.P., I.A., A.U., E.K., R.M., A.N., J.d.V.); and Department of Molecular and Biochemical Pharmacology, Vrije Universiteit Brussel, Brussels, Belgium (G.V.)

We compared the neurokinin 1 receptor (NK₁R) antagonists aprepitant, CP-99994 [(2S,3S)-3-(2-methoxybenzylamino)-2-phenylpiperidine], and ZD6021 [3-cyano-N-((2S)-2-(3,4-dichlorophenyl)-4-[4-[2-(methyl-(S)-sulfinyl)phenyl]piperidino]butyl)-N-methyl]napthamide]] with respect to receptor interactions and duration of efficacy in vivo. In Ca²⁺ mobilization assays (fluorometric imaging plate reader), antagonists were applied to human U373MG cells simultaneously with or 2.5 min before substance P (SP). In reversibility studies, antagonists were present for 30 min before washing, and responses to SP were repeatedly measured afterward. The compounds were administered i.p. to gerbils, and the gerbil foot tap (GFT) response was monitored at various time points. The NK₁R receptor occupancy for aprepitant was determined in striatal regions. Levels of compound in brain and plasma were measured. Antagonists were equipotent at human NK₁R and acted competitively with SP. After preincubation, aprepitant and ZD6021 attenuated the maximal responses, whereas CP-99994 only shifted the SP concentration-response curve to the right. The inhibitory effect of CP-99994 was over within 30 min, whereas for ZD6021, 50% inhibition still persisted after 60 min. Aprepitant produced maximal inhibition lasting at least 60 min. CP-99994 (3 µmol/kg) inhibited GFT by 100% 15 min after administration, but the effect declined rapidly together with brain levels thereafter. The efficacy of ZD6021 (10 µmol/kg) lasted 4 h and correlated well with brain levels. Aprepitant (3 µmol/kg) inhibited GFT and occupied striatal NK₁R by 100% for >48 h despite that brain levels of compound were below the limit of detection after 24 h. Slow functional reversibility is associated with long-lasting in vivo efficacy of NK₁R antagonists, whereas the efficacy of compounds with rapid reversibility is reflected by their pharmacokinetics.

Address correspondence to: Dr. Bengt von Mentzer, Astra Zeneca, Molecular Pharmacology, Kärragatan 5, 431 83 Mölndal, Sweden. E-mail: bengt.mentzer{at}astrazeneca.com

This article has been cited by other articles:

				J. Xu, F. Xu, and E. Barrett Metalloelastase in lungs and alveolar macrophages is modulated by extracellular substance P in mice Am J Physiol Lung Cell Mol Physiol, July 1, 2008; 295(1): L162 - L170. [Abstract] [Full Text] [PDF]