Page last updated: 2024-08-23

eedq and prazosin

eedq has been researched along with prazosin in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19902 (33.33)18.7374
1990's4 (66.67)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Blanc, G; Glowinski, J; Hervé, D; Tassin, JP; Trovero, F1
Nowak, G; Zak, J1
Biggio, G; Giorgi, O1
Enna, SJ; Nomura, S; Pilc, A; Vetulani, J1
Chiu, AT; Timmermans, PB; Wong, PC1
Quartermain, D; Rosengarten, H; Stone, EA; Yeretsian, J; Zhang, Y1

Other Studies

6 other study(ies) available for eedq and prazosin

ArticleYear
In vivo partial inactivation of dopamine D1 receptors induces hypersensitivity of cortical dopamine-sensitive adenylate cyclase: permissive role of alpha 1-adrenergic receptors.
    Journal of neurochemistry, 1992, Volume: 59, Issue:1

    Topics: Adenylyl Cyclases; Adrenergic alpha-Antagonists; Animals; Autoradiography; Benzazepines; Binding Sites; Corpus Striatum; Dopamine; Drug Resistance; Frontal Lobe; Male; Prazosin; Quinolines; Rats; Rats, Inbred Strains; Receptors, Adrenergic, alpha; Receptors, Dopamine; Receptors, Dopamine D1

1992
The turnover of rat cortical alpha 1-adrenoceptors is not modified by repeated electroconvulsive treatment.
    Journal of neurochemistry, 1991, Volume: 56, Issue:6

    Topics: Adrenergic alpha-Antagonists; Animals; Cerebral Cortex; Electroshock; Male; Osmolar Concentration; Prazosin; Quinolines; Rats; Rats, Inbred Strains; Receptors, Adrenergic, alpha

1991
Selective unilateral inactivation of striatal D1 and D2 dopamine receptor subtypes by EEDQ: turning behavior elicited by D2 dopamine receptor agonists.
    Brain research, 1990, Nov-12, Volume: 533, Issue:1

    Topics: 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine; Animals; Corpus Striatum; Dopamine Agents; Dopamine Antagonists; Ergolines; Ketanserin; Male; Motor Activity; Prazosin; Quinolines; Quinpirole; Raclopride; Radioligand Assay; Rats; Rats, Inbred Strains; Receptors, Dopamine; Receptors, Dopamine D1; Receptors, Dopamine D2; Rotation; Salicylamides; Yohimbine

1990
An in vivo procedure for the selective inactivation of rat brain cerebral cortical alpha-adrenoceptors using N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ).
    Brain research, 1989, Jul-24, Volume: 493, Issue:1

    Topics: Adrenergic alpha-Antagonists; Animals; Cell Membrane; Cerebral Cortex; Clonidine; Cyclic AMP; Dihydroalprenolol; Inositol Phosphates; Isoproterenol; Male; Norepinephrine; Prazosin; Quinolines; Rats; Rats, Inbred Strains; Receptors, Adrenergic, alpha; Yohimbine

1989
Alpha-1 adrenoceptor-induced Ca++ movements in rat aorta: antagonism by phenoxybenzamine and N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline.
    The Journal of pharmacology and experimental therapeutics, 1987, Volume: 243, Issue:2

    Topics: Adrenergic alpha-Antagonists; Animals; Aorta; Calcium; Dose-Response Relationship, Drug; Male; Nifedipine; Phenoxybenzamine; Potassium; Prazosin; Quinolines; Rats; Rats, Inbred Strains; Receptors, Adrenergic, alpha; Vasoconstriction

1987
Brain alpha 1-adrenergic neurotransmission is necessary for behavioral activation to environmental change in mice.
    Neuroscience, 1999, Volume: 94, Issue:4

    Topics: Adrenergic alpha-Agonists; Adrenergic alpha-Antagonists; Adrenergic beta-Antagonists; Animals; Behavior, Animal; Brain; Dopamine Agonists; Environment; Injections, Intraperitoneal; Injections, Intraventricular; Male; Mice; Prazosin; Quinolines; Receptors, Adrenergic, alpha; Synaptic Transmission

1999