Literature DB >> 8122313

Silent 5-HT1A receptor antagonists: utility as research tools and therapeutic agents.

A Fletcher1, I A Cliffe, C T Dourish.   

Abstract

The 5-hydroxytryptamine 5-HT1A receptor has been the focus of considerable research effort for over a decade. However, the definitive classification of this receptor and the full characterization of its pharmacology have awaited the development of highly selective 5-HT1A receptor antagonists. The only compounds available until recently have been either nonselective or partial 5-HT1A receptor agonists (or a combination of both). Confusion has arisen owing to the use of different pharmacological models in examining the functional activity of 5-HT1A receptor ligands. Several partial agonists display only antagonist activity in models of postsynaptic 5-HT1A receptor function, whereas their agonist properties are revealed in models of presynaptic, somatodendritic 5-HT1A autoreceptor function. In view of these considerations, the term 'silent antagonist' has been introduced to distinguish true 5-HT1A receptor antagonists from partial agonists. Allan Fletcher and colleagues review the pharmacological properties of the first selective silent 5-HT1A receptor antagonists that have been recently discovered and discuss the potential therapeutic utility of these novel compounds.

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Year:  1993        PMID: 8122313     DOI: 10.1016/0165-6147(93)90185-m

Source DB:  PubMed          Journal:  Trends Pharmacol Sci        ISSN: 0165-6147            Impact factor:   14.819


  14 in total

1.  Inhibition of opioid release in the rat spinal cord by serotonin 5-HT(1A) receptors.

Authors:  Bingbing Song; Wenling Chen; Juan Carlos G Marvizón
Journal:  Brain Res       Date:  2007-05-08       Impact factor: 3.252

2.  Alkylation of [3H]8-OH-DPAT binding sites in rat cerebral cortex and hippocampus.

Authors:  E K Nénonéné; F Radja; M Carli; N M van Gelder; S Afkhami-Dastjerdian; T A Reader
Journal:  Neurochem Res       Date:  1996-02       Impact factor: 3.996

3.  WAY-100635 is a potent dopamine D4 receptor agonist.

Authors:  Benjamin R Chemel; Bryan L Roth; Blaine Armbruster; Val J Watts; David E Nichols
Journal:  Psychopharmacology (Berl)       Date:  2006-08-17       Impact factor: 4.530

4.  Distribution of the 5-HT(1A) receptor antagonist [ (18)F]FPWAY in blood and brain of the rat with and without isoflurane anesthesia.

Authors:  Joji Tokugawa; Laura Ravasi; Toshiyuki Nakayama; Lixin Lang; Kathleen C Schmidt; Jurgen Seidel; Michael V Green; Louis Sokoloff; William C Eckelman
Journal:  Eur J Nucl Med Mol Imaging       Date:  2006-09-22       Impact factor: 9.236

Review 5.  Aggression, anxiety and vocalizations in animals: GABAA and 5-HT anxiolytics.

Authors:  K A Miczek; E M Weerts; J A Vivian; H M Barros
Journal:  Psychopharmacology (Berl)       Date:  1995-09       Impact factor: 4.530

6.  Behavioural evidence that d-fenfluramine-induced anorexia in the rat is not mediated by the 5-HT1A receptor subtype.

Authors:  S P Vickers; P G Clifton; C T Dourish
Journal:  Psychopharmacology (Berl)       Date:  1996-05       Impact factor: 4.530

7.  Clozapine functions through the prefrontal cortex serotonin 1A receptor to heighten neuronal activity via calmodulin kinase II-NMDA receptor interactions.

Authors:  Sudarshana Purkayastha; Jason Ford; Baishali Kanjilal; Souleymane Diallo; Joseph Del Rosario Inigo; Lorenz Neuwirth; Abdeslem El Idrissi; Zaghloul Ahmed; Andrzej Wieraszko; Efrain C Azmitia; Probal Banerjee
Journal:  J Neurochem       Date:  2011-12-15       Impact factor: 5.372

8.  The plant wound hormone systemin binds with the N-terminal part to its receptor but needs the C-terminal part to activate it.

Authors:  T Meindl; T Boller; G Felix
Journal:  Plant Cell       Date:  1998-09       Impact factor: 11.277

9.  Characterization of 4-(2-hydroxyphenyl)-1-[2'-[N-(2''-pyridinyl)-p-fluorobenzamido]ethyl]piperazine (p-DMPPF) as a new potent 5-HT1A antagonist.

Authors:  C Defraiteur; A Plenevaux; J Scuvée-Moreau; N Rouchet; D Goblet; A Luxen; V Seutin
Journal:  Br J Pharmacol       Date:  2007-08-20       Impact factor: 8.739

10.  Binding properties of the naturally occurring human 5-HT1A receptor variant with the Ile28Val substitution in the extracellular domain.

Authors:  M Brüss; M Bühlen; J Erdmann; M Göthert; H Bönisch
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1995-10       Impact factor: 3.000

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