Results 81 to 90 of about 1,780 (186)

New methoxy-chroman derivatives, 4[N-(5-methoxy-chroman-3-yl)N- propylamino]butyl-8-azaspiro-(4,5)-decane-7,9-dione [(+/-)-S 20244] and its enantiomers, (+)-S 20499 and (-)-S 20500, with potent agonist properties at central 5-hydroxytryptamine1A receptors

open access: yes, 1993
The potential interaction of the new methoxy-chroman derivatives: (+/-)-S 20244 (4-[N-(5-methoxy-chroman-3-yl)N-propylamino]butyl-8-azaspiro- (4,5)-decane-7,9-dione) and its enantiomers (+)-S 20499 and (-)-S 20500 with central 5-hydroxytryptamine1A (5 ...
Lanfumey, L.   +7 more
core  

Pharmacodynamic and Pharmacokinetic Studies in Rats of S-8-(2-Furyl)- and R-8-Phenyl-2-(di-n-Propylamino)Tetralin, Two Novel 5-HT1A Receptor Agonists In-vitro with Different Properties In-vivo

open access: yes, 1997
R- and S-8-(2-Furyl)- and R- and S-8-phenyl-2-(di-n-propylamino)tetralins (R- and S-LY-55 and R- and S-LY-49, respectively), novel enantiopure dipropylaminotetralins, have been screened as 5-HT1A receptor ligands.
Hong Yu   +5 more
core   +1 more source

Biochemical and electrophysiological effects of 7-OH-DPAT on the mesolimbic dopaminergic system

open access: yes, 1995
Systemic administration of the putative selective D3 receptor agonist 7-hydroxy-2-(N,N-di-n-propylamino)tetralin (7-OH-DPAT) consistently decreased extracellular dopamine and 3,4-dihydroxyphenylacetic acid (DOPAC) levels in the nucleus accumbens and ...
COLLU, MARIA   +6 more
core   +1 more source

PRESENCE OF SEROTONIN(1A) (5-HT1A) RECEPTOR MESSENGER-RNA WITHOUT BINDING OF [H-3] 8-OH-DPAT IN PERIPHERAL-BLOOD MONONUCLEAR-CELLS

open access: yes, 1995
The authors investigated the presence of serotonin receptor type 1A (5-HT1A) as labeled by the specific ligand H-3-8 hydroxy-2-(di-N-propylamino)tetralin (H-3-8-OH-DPAT) in saturation experiments, and the expression of the mRNA encoding them, in human ...
Cassano G.B.   +13 more
core   +1 more source

Dopaminergic 2-aminotetralins: Affinities for Dopamine D2-receptors, Molecular Structures, and Conformational Preferences

open access: yes, 1986
A combination of X-ray crystallography, NMR spectroscopy, and molecular mechanics (MMP2) calculations was used to determine the three-dimensional structures and conformational preferences of the enantiomers of 5-hydroxy-2-(di-n-propylamino)tetralin and ...
HACKSELL, U   +11 more
core   +1 more source

Involvement of hypothalamic serotonin in activation of the sympathoadrenomedullary system and hypothalamo-pituitary-adrenocortical axis in male Wistar rats

open access: yes, 1991
Infusion of the 5-HT1A receptor agonist, 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) (2.5-20 µg in 1 µl during 15 min), into the paraventricular nucleus of the hypothalamus (PVN) in the rat dose dependently increased plasma adrenaline and ...
Duin, Solita van,   +9 more
core   +1 more source

Effects of chronic paroxetine pretreatment on (+/-)-8-hydroxy-2-(di-n-propyl-amino)tetralin induced c-fos expression following sexual behavior.

open access: yes, 2005
Contains fulltext : 47657.pdf (Publisher’s version ) (Closed access)Chronic treatment with the selective serotonin reuptake inhibitor paroxetine impairs the functioning of 5-HT(1A) receptors involved in ejaculation.
Waldinger, M. D.   +11 more
core   +1 more source

Stimulation of serotonin-1A receptors in mammals to alleviate motion sickness and emesis induced by chemical agents

open access: yes, 1990
A method for the alleviation of both motion sickness and chemically-induced emesis is provided which includes the administration of a nontoxic, therapeutically effective amount of a composition which stimulates serotonin-1A receptors in a mammal in need ...
Lucot, James B., Crampton, George H.
core  

Serotonin and 8-OH-DPAT reduce excitatory transmission in rat hippocampal area CA1 via reduction in presumed presynaptic Ca2+ entry

open access: yes, 1995
The effect of 5-HT and its 1A receptor agonist 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) on excitatory transmission in CA1 pyramidal cells was studied.
Empson, R.M., Heinemann, U., Schmitz, D.
core   +1 more source

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