Results 241 to 250 of about 169,266 (282)
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Interaction between serotonin uptake inhibitors and alpha-2 adrenergic heteroreceptors in the rat hypothalamus.

Journal of Pharmacology and Experimental Therapeutics, 1990
The effectiveness of presynaptic receptor agonists to inhibit the electrically evoked release of [3H]monoamines from brain slices is attenuated in the presence of blockade of neuronal uptake for the serotonin (5-HT) and the norepinephrine (NE) systems ...
P. Blier, A. Galzin, Salomon Z. Langer
semanticscholar   +1 more source

Potency of Inhibitors for γ-Aminobutyric Acid Uptake by Mouse Brain Subcellular Particles at 0°

Molecular Pharmacology, 1975
Binding of γ-amino[14C]butyric acid by sucellular particles of mouse brain homogenates at 0° is apparently due to action of the specific transport system for GABA.
R. Olsen, J. Bayless, M. Ban
semanticscholar   +1 more source

CHROMEN-2-ONE DERIVATIVES AND THEIR USE AS MONOAMINE NEUROTRANSMITTER RE-UPTAKE INHIBITORS

2012
The present applications discloses novel 8-aza-bicyclo[3.2.1]oct-3-yloxy)-chromen-2-one derivatives and their use as monoamine neurotransmitter re-uptake inhibitors. In other aspects the applications discloses the use of these compounds in a method for therapy and to pharmaceutical compositions comprising the compounds of the invention.
NEUROSEARCH AS   +3 more
openaire   +1 more source

Trafficking-dependent and -independent pathways of neurotransmitter transporter regulation differentially involving p38 mitogen-activated protein kinase revealed in studies of insulin modulation of norepinephrine transport in SK-N-SH cells.

Journal of Pharmacology and Experimental Therapeutics, 2001
Presynaptic, cocaine- and antidepressant-sensitive norepinephrine (NE) transporters (NETs) dictate levels of extracellular NE after vesicular release. Recent studies suggest that G protein-coupled receptors linked to protein kinase C (PKC) down-regulate ...
S. Apparsundaram   +3 more
semanticscholar   +1 more source

A pharmacological review of competitive inhibitors and substrates of high-affinity, sodium-dependent glutamate transport in the central nervous system.

Current pharmaceutical design, 1999
The acidic amino acid L-glutamate acts as both a primary excitatory neurotransmitter and a potential neurotoxin within the mammalian central nervous system. Functionally juxtaposed between these neurophysiological and pathological actions are an assorted
R. Bridges, M. Kavanaugh, A. Chamberlin
semanticscholar   +1 more source

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