Results 191 to 200 of about 38,715 (223)
cAMP-PKA/EPAC signaling pathways: crucial regulators of lipid homeostasis. [PDF]
Chen C, Gao H, Tian Q, Cao J.
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Signaling by intracellular β<sub>2</sub>-adrenergic receptors regulates AMPA receptor trafficking and synaptic plasticity. [PDF]
Lee B +20 more
europepmc +1 more source
Opposite kinetics of L-leucine and L-phenylalanine induced insulin release studies with the perfused rat pancreas [PDF]
Landgraf, R. +3 more
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Cirrhotic cardiomyopathy: pathophysiology, assessment, and implications for liver transplantation. [PDF]
Gill M +4 more
europepmc +1 more source
Further Insights Into Anticholinergic Action Informed by Japanese Anticholinergic Risk Scale. [PDF]
Mogi M +4 more
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Canadian Journal of Physiology and Pharmacology, 1977
The effect of neuronal-uptake inhibitors on the guanethidine-induced inhibition of responses of rabbit vas deferens to transmural stimulation was investigated. The twitch and sustained reponses were inhibited by about 70% by 1.2 × 10−5 M guanethidine.
D M Paton
exaly +3 more sources
The effect of neuronal-uptake inhibitors on the guanethidine-induced inhibition of responses of rabbit vas deferens to transmural stimulation was investigated. The twitch and sustained reponses were inhibited by about 70% by 1.2 × 10−5 M guanethidine.
D M Paton
exaly +3 more sources
Acta Physiologica Scandinavica, 1969
AbstractVarious nucleotides and metabolic inhibitors have been tested on the release, reuptake and net uptake of noradrenaline (NA) in isolated splenic nerve granules. Cytidine, inosine, and uridine triphosphate facilitated uptake of NA to a similar degree as adenosine diphosphate but less than adenosine triphosphate.
U S von Euler, F Lishajko
exaly +3 more sources
AbstractVarious nucleotides and metabolic inhibitors have been tested on the release, reuptake and net uptake of noradrenaline (NA) in isolated splenic nerve granules. Cytidine, inosine, and uridine triphosphate facilitated uptake of NA to a similar degree as adenosine diphosphate but less than adenosine triphosphate.
U S von Euler, F Lishajko
exaly +3 more sources
Developmental Biology, 1989
Tricyclic antidepressants in combination with in vitro clonal analysis of quail neural crest cells were used to examine the role the norepinephrine uptake mechanism might play in the development of adrenergic neural crest derivatives. Norepinephrine (NE) uptake inhibitors blocked expression of the adrenergic phenotype by neural crest cells.
exaly +3 more sources
Tricyclic antidepressants in combination with in vitro clonal analysis of quail neural crest cells were used to examine the role the norepinephrine uptake mechanism might play in the development of adrenergic neural crest derivatives. Norepinephrine (NE) uptake inhibitors blocked expression of the adrenergic phenotype by neural crest cells.
exaly +3 more sources
Napamezole, an alpha-2 adrenergic receptor antagonist and monoamine uptake inhibitor in vitro.
The Journal of Pharmacology and Experimental Therapeutics, 1990Napamezole (2-[3,4-dihydro-2-naphthalenyl)methyl]-4,5-dihydro-1H- imidazole-monohydrochloride) is a selective alpha-2 adrenergic receptor antagonist and a monoamine re-uptake inhibitor in vitro. The alpha adrenergic antagonist activity of napamezole was determined in vitro in rat brain receptor binding assay using [3H]clonidine and [3H]prazosin for ...
M H, Perrone +3 more
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Journal of Neurochemistry, 1993
Abstract: The aim of this study was to evaluate the effect of citalopram, a second generation antidepressant agent producing no β‐down‐regulation, on the receptors and second messenger systems related to noradrenergic transmission in the cerebral cortex of the rat.
I, Nalepa, J, Vetulani
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Abstract: The aim of this study was to evaluate the effect of citalopram, a second generation antidepressant agent producing no β‐down‐regulation, on the receptors and second messenger systems related to noradrenergic transmission in the cerebral cortex of the rat.
I, Nalepa, J, Vetulani
openaire +2 more sources

