Document Detail


[3H]-BIBP3226 and [3H]-NPY binding to intact SK-N-MC cells and CHO cells expressing the human Y1 receptor.
MedLine Citation:
PMID:  9879066     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We have studied the binding of [3H]-NPY and the newly developed non-peptide Y1 receptor antagonist [3H]-BIBP3226 to intact SK-N-MC cells and CHO-K1 cells transfected with the human NPY Y1 receptor gene i.e. CHO-Y1 cells. Whereas the association and dissociation of the specific [3H]-NPY binding was slow, the binding kinetics of [3H]-BIBP3226 binding was very rapid. Saturation binding of both radioligands reveal the presence of an apparently homogeneous population of high affinity binding sites in both cell lines. The corresponding equilibrium dissociation constants are similar for the two cell lines and are close to those obtained from previous competition binding experiments. The specific binding of both radioligands was completely and with high affinity displaced by BIBP3226 and its inactive (S)-enantiomer BIBP3435 was much less potent. Whilst the NPY Y1 agonists NPY, PYY and [Leu31-Pro34]-NPY completely and potently displaced [3H]-NPY binding, they could only displace 70 to 80% of the [3H]-BIBP3226 binding sites in CHO-Y1 and SK-N-MC cells. A possible explanation can be that only part of the receptors are G-protein coupled. In agreement pertussis toxin was found to reduce high affinity [3H]-NPY binding sites in CHO-Y1 cells whereas [3H]-BIBP3226 binding parameters remained unchanged.
Authors:
P M Vanderheyden; I Van Liefde; J P de Backer; G Vauquelin
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Journal of receptor and signal transduction research     Volume:  18     ISSN:  1079-9893     ISO Abbreviation:  J. Recept. Signal Transduct. Res.     Publication Date:    1998 Jul-Nov
Date Detail:
Created Date:  1999-03-12     Completed Date:  1999-03-12     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  9509432     Medline TA:  J Recept Signal Transduct Res     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  363-85     Citation Subset:  IM    
Affiliation:
Department of Protein Chemistry, Free University of Brussels (VUB), Belgium.
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MeSH Terms
Descriptor/Qualifier:
Animals
Arginine / analogs & derivatives*,  metabolism
Binding, Competitive
CHO Cells
Cricetinae
Humans
Neuroblastoma / metabolism
Neuropeptide Y / metabolism*
Receptors, Neuropeptide Y / antagonists & inhibitors,  metabolism*
Chemical
Reg. No./Substance:
0/BIBP 3226; 0/Neuropeptide Y; 0/Receptors, Neuropeptide Y; 0/neuropeptide Y-Y1 receptor; 74-79-3/Arginine

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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