A M Laporte
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Explore the profile of A M Laporte including associated specialties, affiliations and a list of published articles.
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35
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626
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Recent Articles
1.
Radja F, Laporte A, Daval G, Verge D, Gozlan H, Hamon M
Neurochem Int
. 2010 May;
18(1):1-15.
PMID: 20504669
The autoradiographic technique is the most relevant approach for the visualization at the light microscope level of the different classes (5-HT(1A), 5-HT(1B), 5-HT(1C), 5-HT(1D), 5-HT(2) and 5-HT(3)) of receptors for...
2.
Ahnaou A, Laporte A, Ballet S, Escourrou P, Hamon M, Adrien J, et al.
Eur J Neurosci
. 2000 Dec;
12(12):4496-504.
PMID: 11122360
Cholinergic and PACAPergic systems within the oral pontine reticular nucleus (PnO) play a critical role in REM sleep generation in rats. In this present work, we have investigated whether REM...
3.
Le Poul E, Boni C, Hanoun N, Laporte A, Laaris N, Chauveau J, et al.
Neuropharmacology
. 2000 Feb;
39(1):110-22.
PMID: 10665824
Quantification of receptor binding sites and their encoding mRNAs, and electrophysiological recordings, were used to assess central serotonin (5-HT) neurotransmission in rats 24 h after a 2-3 week treatment with...
4.
Evrard A, Laporte A, Chastanet M, Hen R, Hamon M, Adrien J
Eur J Neurosci
. 1999 Dec;
11(11):3823-31.
PMID: 10583471
The characteristics of the spontaneous firing of serotoninergic neurons in the dorsal raphe nucleus and its control by serotonin (5-hydroxytryptamine, 5-HT) receptors were investigated in wild-type and 5-HT1B knock-out (5-HT1B-/-)...
5.
Laaris N, Le Poul E, Laporte A, Hamon M, Lanfumey L
Neuroscience
. 1999 Jul;
91(3):947-58.
PMID: 10391473
Extracellular and intracellular recording techniques were used to assess possible changes in the functional properties of 5-hydroxytryptamine-1A receptors in brain slices prepared from rats subjected to different stress paradigms. Whereas...
6.
Bourgin P, Ahnaou A, Laporte A, Hamon M, Adrien J
Neuroscience
. 1999 Mar;
89(1):291-302.
PMID: 10051236
In rats, rapid eye movement sleep can be induced by microinjection of either the cholinergic agonist carbachol or the neuropeptide vasoactive intestinal peptide into the oral pontine reticular nucleus. Possible...
7.
Antunes Bras J, Laporte A, Benoliel J, Bourgoin S, Mauborgne A, Hamon M, et al.
J Neurochem
. 1999 Feb;
72(2):858-67.
PMID: 9930763
Because cholecystokinin (CCK) acts as a "functional" endogenous opioid antagonist, it has been proposed that changes in central CCKergic neurotransmission might account for the relative resistance of neuropathic pain to...
8.
Corradetti R, Laaris N, Hanoun N, Laporte A, Le Poul E, Hamon M, et al.
Br J Pharmacol
. 1998 Mar;
123(3):449-62.
PMID: 9504386
1. The aim of the present work was to characterize the 5-hydroxytryptamine1A (5-HT1A) antagonistic actions of (-)-pindolol and WAY 100635 (N-(2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl)-N-(2-pyridinyl) cyclohexane carboxamide). Studies were performed on 5-HT1A receptors located...
9.
Fabre V, Boni C, Mocaer E, Lesourd M, Hamon M, Laporte A
Eur J Pharmacol
. 1998 Jan;
337(2-3):297-308.
PMID: 9430429
Determination of the optimal assay conditions for the specific binding of a tritiated derivative of the novel potential anxiolytic drug alnespirone (S-20499, (+)-4-[N-(5-methoxy-chroman-3-yl)-N-propylamino]butyl-8-azaspiro-( 4,5)-decane-7,9-dione) allowed the demonstration that this radioligand...
10.
Lanfumey L, Laporte A, MARTIN P, Hamon M, Gozlan H
Eur J Pharmacol
. 1997 Apr;
323(2-3):137-48.
PMID: 9128832
Biochemical and electrophysiological approaches were used to assess possible changes in 5-HT1A receptors in the rat brain after long-term treatment with an anxiolytic benzodiazepine. Rats were treated with diazepam (2...