Different effects on the responses of functional pre- and postsynaptic 5-HT1A receptors by repeated treatment of rats with the 5-HT1A receptor agonist 8-OH-DPAT (Q34558558)

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scientific article published on February 1, 1990

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English	Different effects on the responses of functional pre- and postsynaptic 5-HT1A receptors by repeated treatment of rats with the 5-HT1A receptor agonist 8-OH-DPAT	scientific article published on February 1, 1990

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scholarly article

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Europe PubMed Central

3 August 2017

Different effects on the responses of functional pre- and postsynaptic 5-HT1A receptors by repeated treatment of rats with the 5-HT1A receptor agonist 8-OH-DPAT (English)

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10.1016/0028-3908(90)90047-U

https://api.crossref.org/works/10.1016/0028-3908(90)90047-U

30 October 2022

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10.1016/0028-3908(90)90047-U

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30 October 2022

author name string

Rényi L

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Angeby-Möller K

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Europe PubMed Central

3 August 2017

L. G. Larsson

1

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1691832

30 October 2022

L. Rényi

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30 October 2022

S. B. Ross

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30 October 2022

B. Svensson

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30 October 2022

K. Angeby-Möller

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30 October 2022

language of work or name

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30 October 2022

publication date

1 February 1990

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number of pages

7

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full work available at URL

https://api.elsevier.com/content/article/PII:002839089090047U?httpAccept=text/xml

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10.1016/0028-3908(90)90047-U

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https://api.elsevier.com/content/article/PII:002839089090047U?httpAccept=text/plain

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10.1016/0028-3908(90)90047-U

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Neuropharmacology

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Europe PubMed Central

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Europe PubMed Central

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Europe PubMed Central

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85-91

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A G protein couples serotonin and GABAB receptors to the same channels in hippocampus.

1

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8-Hydroxy-2-(di-n-propylamino)tetralin, a new centrally acting 5-hydroxytryptamine receptor agonist

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10.1016/0028-3908(90)90047-U

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Piperazine derivatives including the putative anxiolytic drugs, buspirone and ipsapirone, are agonists at 5-HT1A receptors negatively coupled with adenylate cyclase in hippocampal neurons

3

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5-HT1A receptor agonists inhibit carbachol-induced stimulation of phosphoinositide turnover in the rat hippocampus.

4

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Para-chlorophenylalanine prevents feeding induced by the serotonin agonist 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT).

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Inhibition of forskolin-stimulated adenylate cyclase activity by 5-HT receptor agonists

6

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A behavioural and biochemical study in mice and rats of putative selective agonists and antagonists for 5-HT1 and 5-HT2 receptors

9

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[3H]8-hydroxy-2-(di-n-propylamino)tetralin binding to pre- and postsynaptic 5-hydroxytryptamine sites in various regions of the rat brain.

10

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Biochemical evidence for the 5-HT agonist properties of PAT (8-hydroxy-2-(di-n-propylamino)tetralin) in the rat brain

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5-Hydroxytryptamine1A receptors are linked to a Gi-adenylate cyclase complex in rat hippocampus.

12

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Hypothermia in the rat induced by the potent serotoninergic agent 8-OH-DPAT

13

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The 5-HT 1A receptor agonist, 8-OH-DPAT, preferentially activates cell body 5-HT autoreceptors in rat brain in vivo

15

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Hypothermia induced by the putative 5-HT1A agonists LY165163 and 8-OH-DPAT is not prevented by 5-HT depletion.

16

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Single administration of 5-HT1A agonists decreases 5-HT1A presynaptic, but not postsynaptic receptor-mediated responses: relationship to antidepressant-like action

17

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5-HT1A-receptors mediate stimulation of adenylate cyclase in rat hippocampus.

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8-Hydroxy-2-(di-n-propylamino)-tetralin discriminates between subtypes of the 5-HT1 recognition site

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LIGAND: A versatile computerized approach for characterization of ligand-binding systems

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Pharmacological Differentiation and Characterization of 5-HT1A, 5-HT1B, and 5-HT1C Binding Sites in Rat Frontal Cortex

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The involvement of subtypes of the 5-HT1 receptor and of catecholaminergic systems in the behavioural response to 8-hydroxy-2-(di-n-propylamino)tetralin in the rat.

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Presynaptic 5-HT autoreceptors on serotonergic cell bodies and/or dendrites but not terminals are of the 5-HT1A subtype.

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10.1016/0028-3908(90)90047-U

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Europe PubMed Central

3 August 2017

1 reference

Europe PubMed Central

3 August 2017

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