Further evidence for differential affinity states of the serotonin1A receptor in rat hippocampus
暂无分享,去创建一个
Rémi Quirion | R. Quirion | R. Mongeau | S. Welner | B. Suranyi-Cadotte | Raymond Mongeau | Sharon A. Welner | Barbara E. Suranyi-Cadotte
[1] S. Maayani,et al. Inhibition of forskolin-stimulated adenylate cyclase activity by 5-HT receptor agonists. , 1985, European journal of pharmacology.
[2] R. Heikkila. Ascorbate-induced lipid peroxidation and the binding of [3H]dihydroalprenolol. , 1983, European journal of pharmacology.
[3] M. Wood,et al. [3H]8‐OH‐DPAT labels the 5‐Hydroxytryptamine uptake recognition site and the 5‐HT1A binding site in the rat striatum , 1988, The Journal of pharmacy and pharmacology.
[4] M. Caron,et al. Effector coupling mechanisms of the cloned 5-HT1A receptor. , 1989, The Journal of biological chemistry.
[5] B. Bacon,et al. Guanyl nucleotide interactions with dopaminergic binding sites labeled by [3H]spiroperidol in human caudate and putamen: guanyl nucleotides enhance ascorbate-induced lipid peroxidation and cause an apparent loss of high affinity binding sites. , 1988, Molecular pharmacology.
[6] J. Glowinski,et al. Identification of presynaptic serotonin autoreceptors using a new ligand: 3H-PAT , 1983, Nature.
[7] M. Hekman,et al. Receptor Modification and Receptor Disposition in Membranes , 1987 .
[8] J. Bockaert,et al. Pharmacology of 5-hydroxytryptamine-1A receptors which inhibit cAMP production in hippocampal and cortical neurons in primary culture. , 1988, Molecular pharmacology.
[9] Y. Kitamura,et al. Uncoupling of Rat Cerebral Cortical α2‐Adrenoceptors from GTP‐Binding Proteins by N‐Ethylmaleimide , 1987, Journal of neurochemistry.
[10] C. Finch,et al. Effects of radioligand oxidation and ascorbate‐induced lipid peroxidation on serotonin‐1 receptor assay: Use of ascorbate and ethylenediamine tetraacetic acid buffers to prevent (3H)‐5‐HT binding artifacts , 1988, Journal of neuroscience research.
[11] F. Artaud,et al. Biochemical evidence for the 5-HT agonist properties of PAT (8-hydroxy-2-(di-n-propylamino)tetralin) in the rat brain. , 1984, European journal of pharmacology.
[12] R. Ciaranello,et al. Differential inactivation and G protein reconstitution of subtypes of [3H]5-hydroxytryptamine binding sites in brain. , 1988, Molecular pharmacology.
[13] M. Hamon,et al. [3H]8‐Hydroxy‐2‐(Di‐n‐Propylamino)Tetralin Binding to Pre‐ and Postsynaptic 5‐Hydroxytryptamine Sites in Various Regions of the Rat Brain , 1985, Journal of neurochemistry.
[14] R. Lefkowitz,et al. A ternary complex model explains the agonist-specific binding properties of the adenylate cyclase-coupled beta-adrenergic receptor. , 1980, The Journal of biological chemistry.
[15] O. H. Lowry,et al. Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.
[16] H. V. Van Tol,et al. Cloning, functional expression, and mRNA tissue distribution of the rat 5-hydroxytryptamine1A receptor gene. , 1990, The Journal of biological chemistry.
[17] B. Vallee,et al. [36] Reactions with N-ethylmaleimide and p-mercuribenzoate. , 1972, Methods in enzymology.
[18] P. Hochstein,et al. Dual Effects of Ascorbate on Serotonin and Spiperone Binding in Rat Cortical Membranes , 1983, Journal of neurochemistry.
[19] R. Lefkowitz,et al. Multiple reactive sulfhydryl groups modulate the function of adenylate cyclase coupled beta-adrenergic receptors. , 1979, Molecular pharmacology.
[20] A. Herbet,et al. Characteristics of central 5-HT receptors and their adaptive changes following intracerebral 5,7-dihydroxytryptamine administration in the rat. , 1978, Molecular pharmacology.
[21] J. Bockaert,et al. Serotonin 5-HT1 receptors mediate inhibition of cyclic AMP production in neurons. , 1986, European journal of pharmacology.
[22] S. Peroutka. 5-Hydroxytryptamine receptor subtypes: molecular, biochemical and physiological characterization , 1988, Trends in Neurosciences.
[23] Y. Vladimirov,et al. The increase of phospholipid bilayer rigidity after lipid peroxidation , 1977, FEBS letters.
[24] W. Lovenberg,et al. Chronic MAO A and MAO B inhibition decreases the 5-HT1A receptor-mediated inhibition of forskolin-stimulated adenylate cyclase. , 1988, European journal of pharmacology.
[25] H. Schoemaker,et al. [3H]8-OH-DPAT labels the serotonin transporter in the rat striatum. , 1986, European journal of pharmacology.
[26] S H Snyder,et al. Multiple serotonin receptors: differential binding of [3H]5-hydroxytryptamine, [3H]lysergic acid diethylamide and [3H]spiroperidol. , 1979, Molecular pharmacology.
[27] R. Floyd,et al. Hydroxyl free radical formation from hydrogen peroxide by ferrous iron-nucleotide complexes. , 1983, Biochemistry.
[28] M. Hamon,et al. Physical evidence of the coupling of solubilized 5-HT1A binding sites with G regulatory proteins. , 1990, Biochemical pharmacology.
[29] D. Middlemiss,et al. 8-Hydroxy-2-(di-n-propylamino)-tetralin discriminates between subtypes of the 5-HT1 recognition site. , 1983, European journal of pharmacology.
[30] M. Hamon,et al. The GTP‐Insensitive Component of High‐Affinity [3H]8‐Hydroxy‐2‐(Di‐n‐Propylamino)tetralin Binding in the Rat Hippocampus Corresponds to an Oxidized State of the 5‐Hydroxytryptamine1A Receptor , 1991, Journal of neurochemistry.
[31] J. Ieni,et al. The 5-HT1A receptor probe [3H]8-OH-DPAT labels the 5-HT transporter in human platelets. , 1988, Life sciences.
[32] G A McPherson,et al. A practical computer-based approach to the analysis of radioligand binding experiments. , 1983, Computer programs in biomedicine.
[33] S. Peroutka,et al. Modulation of 5‐Hydroxytryptamine1A Receptor Density by Nonhydrolyzable GTP Analogues , 1990, Journal of neurochemistry.
[34] S. Peroutka,et al. Pharmacological Differentiation and Characterization of 5‐HT1A, 5‐HT1B, and 5‐HT1C Binding Sites in Rat Frontal Cortex , 1986, Journal of neurochemistry.
[35] D. Middlemiss,et al. Stereoselective blockade at the 5-HT autoreceptor and inhibition of radioligand binding to central 5-HT recognition sites by the optical isomers of methiothepin , 1986, Neuropharmacology.