Journal
REGULATORY PEPTIDES
Volume 163, Issue 1-3, Pages 37-42Publisher
ELSEVIER
DOI: 10.1016/j.regpep.2010.04.002
Keywords
Neurotensinergic system; Cholinergic muscarinic receptor; CNS membranes; SR 48692
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Funding
- CONICET
- Universidad de Buenos Aires, Argentina
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Neurotensin (NT) is a tridecapeptide distributed in central and peripheral nervous systems, which can behave as a neurotransmitter or neuromodulator at central and peripheral levels Herein we tested the potential effect of this peptide on quinuclidinyl benzilate ([H-3]-QNB) binding to muscarinic receptor in rat CNS membranes It was observed that NT decreased up to 50-70% ligand binding at 1 x 10(-7) M-1 x 10(-5) M concentration in cerebral cortex, cerebellum and striatum In the hippocampus, NT exerted a biphasic effect, behaving as a stimulator in the presence of 1 x 10(-12) M-1 x 10(-16) M concentration but as an inhibitor at 1 x 10(-8) M-1 x 10(-5) M concentration. In order to test the involvement of high-affinity NT receptor (NTS1) in NT inhibitory effect, assays were carried out in the presence of 1 x 10(-6) M NT and/or SR 48692 (Sanofi-Aventis, US, Inc), a specific antagonist for this receptor, dissolved in dimethylsulfoxide (DMSO) 10% v/v As controls, membranes incubated with DMSO and/or NT 1 x 10(-6) M plus DMSO were processed. It was found that NT + DMSO decreased [H-3]-QNB binding to cerebral cortex, cerebellum and hippocampal membranes by 49%, 32% and 53%, respectively This inhibition was not observed with the DMSO control group Membrane preincubation with 1 x 10-6 M SR 48692 failed to alter NT effect on binding SR 48692 at 1 x 10(-6) M concentration decreased the binding by 50% only in cerebral cortex membranes, suggesting a possible direct effect of the antagonist on muscarinic receptors in this area It was therefore concluded that the high-affinity NT receptor may not be involved in ligand binding Inhibition to muscarinic receptor by NT (C) 2010 Elsevier B V All rights reserved
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