All Relations between 5-ht receptor 2 and serotonin

Publication Sentence Publish Date Extraction Date Species
C A Wilson, A J Hunte. Progesterone stimulates sexual behaviour in female rats by increasing 5-HT activity on 5-HT2 receptors. Brain research. vol 333. issue 2. 1985-07-23. PMID:2581660. it is suggested that 5-ht has a dual effect on female sexual receptivity acting via different systems, the inhibitory tract acting on 5-ht1 and the stimulatory tract on 5-ht2 receptors. 1985-07-23 2023-08-11 rat
J M Lakoski, G K Aghajania. Effects of ketanserin on neuronal responses to serotonin in the prefrontal cortex, lateral geniculate and dorsal raphe nucleus. Neuropharmacology. vol 24. issue 4. 1985-07-09. PMID:3158835. the ability of the putative serotonin2 (5-ht2) antagonist ketanserin, to alter serotonin (5-ht)-induced responses in cell firing was examined in the prefrontal cortex, the lateral geniculate nucleus and the dorsal raphe nucleus of the rat by microiontophoretic extracellular single unit recording techniques. 1985-07-09 2023-08-11 rat
J M Lakoski, G K Aghajania. Effects of ketanserin on neuronal responses to serotonin in the prefrontal cortex, lateral geniculate and dorsal raphe nucleus. Neuropharmacology. vol 24. issue 4. 1985-07-09. PMID:3158835. the observed potentiation by ketanserin of inhibitory responses to 5-ht but not those of gamma-aminobutyric acid, tryptamine or norepinephrine, recorded in the prefrontal cortex, may be consistent with the proposed interaction between ketanserin and a specific 5-ht2 binding site. 1985-07-09 2023-08-11 rat
A Metz, G M Goodwin, A R Gree. The administration of baclofen to mice increases 5-HT2-mediated head-twitch behaviour and 5-HT2 receptor number in frontal cortex. Neuropharmacology. vol 24. issue 4. 1985-07-09. PMID:4000408. it is suggested that the enhanced 5-ht2 function, following longer-term administration of baclofen is the consequence of the drug inhibiting 5-ht release in vivo, as indicated by the observations after acute administration. 1985-07-09 2023-08-11 mouse
D A Kendall, S R Nahorsk. 5-Hydroxytryptamine-stimulated inositol phospholipid hydrolysis in rat cerebral cortex slices: pharmacological characterization and effects of antidepressants. The Journal of pharmacology and experimental therapeutics. vol 233. issue 2. 1985-07-02. PMID:2987487. this response to 5-ht was blocked potently by ketanserin and other putative 5-ht2 antagonists but the overall pattern of apparent drug affinities was inconsistent with that seen at 5-ht2 sites labeled with [3h]ketanserin in cortical membranes. 1985-07-02 2023-08-11 rat
V V Petkov, V D Petkov, T Grahovska, E Konstantinov. Age-related changes in rat brain dopaminergic receptors. Acta physiologica et pharmacologica Bulgarica. vol 10. issue 4. 1985-06-27. PMID:6535368. however, considering the fact that in the cerebral cortex [3h] spiroperidol labels a subclass of serotonin receptors (5-ht2) rather than da receptors, the present results, particularly those concerning the cerebral cortex, suggest an age-related decrease also in the number of 5-ht receptors in this cerebral structure. 1985-06-27 2023-08-12 rat
G M Goodwin, A R Gree. A behavioural and biochemical study in mice and rats of putative selective agonists and antagonists for 5-HT1 and 5-HT2 receptors. British journal of pharmacology. vol 84. issue 3. 1985-06-20. PMID:2580582. radioligand binding techniques have demonstrated the existence of 5-hydroxytryptamine (5-ht) binding subtypes: 5-ht2, 5-ht1a and 5-ht1b. 1985-06-20 2023-08-11 mouse
G M Goodwin, A R Gree. A behavioural and biochemical study in mice and rats of putative selective agonists and antagonists for 5-HT1 and 5-HT2 receptors. British journal of pharmacology. vol 84. issue 3. 1985-06-20. PMID:2580582. 9 we suggest that 5-ht-induced head-twitch behaviour in mice is a useful 5-ht2 receptor model and the temperature change following 8-oh-dpat injection in rats may be a 5-ht,a model. 1985-06-20 2023-08-11 mouse
S P Olese. A calcium-dependent reversible permeability increase in microvessels in frog brain, induced by serotonin. The Journal of physiology. vol 361. 1985-06-20. PMID:3157795. pre-treatment with the 5-ht2 receptor antagonist ketanserin blocked the serotonin response completely. 1985-06-20 2023-08-11 Not clear
D Hoffmann, W Weseman. Characterization of 5-hydroxytryptamine binding sites in the plasma membrane of pig blood platelets. Journal of neural transmission. vol 61. issue 3-4. 1985-06-19. PMID:3157778. since ketanserin inhibited 5-ht induced aggregation of pig platelets (ic50 = 14.2 nm), the ketanserin binding sites can be classified as 5-ht2 receptors. 1985-06-19 2023-08-11 rat
N S Buckholtz, D X Freedman, L D Middaug. Daily LSD administration selectively decreases serotonin2 receptor binding in rat brain. European journal of pharmacology. vol 109. issue 3. 1985-06-19. PMID:3987809. [3h]lsd (3.0 nm) was used with either 30.0 nm 5-ht or 70.0 nm cinanserin to estimate 5-ht1 and 5-ht2 receptors, respectively. 1985-06-19 2023-08-11 rat
C J Garlan. Endothelial cells and the electrical and mechanical responses of the rabbit coronary artery to 5-hydroxytryptamine. The Journal of pharmacology and experimental therapeutics. vol 233. issue 1. 1985-05-23. PMID:3981453. hyperpolarization to 5-ht was not observed, even with 1 microm ketanserin (a 5-ht2 receptor antagonist) present to reduce its direct action on the smooth muscle. 1985-05-23 2023-08-11 rabbit
M L Cohen, L A Wittenaue. Relationship between serotonin and tryptamine receptors in the rat stomach fundus. The Journal of pharmacology and experimental therapeutics. vol 233. issue 1. 1985-05-23. PMID:3981465. tryptamine and serotonin (5-ht) are relatively potent contractile agonists in the rat fundus, a tissue in which contraction to 5-ht is not mediated by interaction with 5-ht1 or 5-ht2 receptors. 1985-05-23 2023-08-11 rat
R A Locock, G B Baker, R T Coutts, W G Dewhurs. Displacement of serotonin from binding sites in rat cortex: the effects of biogenic "trace" amines. Progress in neuro-psychopharmacology & biological psychiatry. vol 8. issue 4-6. 1985-05-17. PMID:6531441. the concentrations for 50 percent inhibition of binding (ic50's) to specific in vitro serotonin binding sites (5-ht1 and 5-ht2) of rat cerebral cortex were determined for the trace amines 2-phenylethylamine, m- and p-tyramine, tryptamine, and (+)- and (-)- alpha-methyltryptamine. 1985-05-17 2023-08-12 rat
R A Locock, G B Baker, R T Coutts, W G Dewhurs. Displacement of serotonin from binding sites in rat cortex: the effects of biogenic "trace" amines. Progress in neuro-psychopharmacology & biological psychiatry. vol 8. issue 4-6. 1985-05-17. PMID:6531441. the trace amines may have different functional roles as evidenced by their different degrees of displacement of serotonin at 5-ht1 and 5-ht2 binding sites in the brain. 1985-05-17 2023-08-12 rat
J L Blackshear, C Orlandi, J D Garnic, N K Hollenber. Differential large and small vessel responses to serotonin in the dog hindlimb in vivo: role of the 5HT2 receptor. Journal of cardiovascular pharmacology. vol 7. issue 1. 1985-05-16. PMID:2580149. differential large and small vessel responses to serotonin in the dog hindlimb in vivo: role of the 5ht2 receptor. 1985-05-16 2023-08-11 dog
J L Blackshear, C Orlandi, J D Garnic, N K Hollenber. Differential large and small vessel responses to serotonin in the dog hindlimb in vivo: role of the 5HT2 receptor. Journal of cardiovascular pharmacology. vol 7. issue 1. 1985-05-16. PMID:2580149. failure of ne to constrict large arteries in vivo and ketanserin antagonism of constriction produced by 5ht suggest the response to 5ht involves the 5ht2 receptor. 1985-05-16 2023-08-11 dog
M Frenken, A J Kauman. Ketanserin causes surmountable antagonism of 5-hydroxytryptamine-induced contractions of large coronary arteries of dog. Naunyn-Schmiedeberg's archives of pharmacology. vol 328. issue 3. 1985-05-15. PMID:3157065. we conclude that large coronary arteries of dog are contracted by 5-ht mainly through 5-ht2-receptors and to a smaller extent through receptors different from 5-ht2. 1985-05-15 2023-08-11 dog
P D Verdouw, H M Jennewein, J Mierau, P R Saxen. N-(3-acetylaminophenyl)piperazine hydrochloride (BEA 1654), a putative 5-HT1 agonist, causes constriction of arteriovenous anastomoses and dilatation of arterioles. European journal of pharmacology. vol 107. issue 3. 1985-05-10. PMID:3156750. the compound had a ki value of 32 nm (5-ht: 8 nm) on 5-ht1 but no or very weak affinity for 5-ht2, alpha 1- and alpha 2-adrenoceptor sites in rat cerebral cortex homogenates. 1985-05-10 2023-08-11 rat
P D Verdouw, H M Jennewein, J Mierau, P R Saxen. N-(3-acetylaminophenyl)piperazine hydrochloride (BEA 1654), a putative 5-HT1 agonist, causes constriction of arteriovenous anastomoses and dilatation of arterioles. European journal of pharmacology. vol 107. issue 3. 1985-05-10. PMID:3156750. in view of the high and selective affinity of bea 1654 to 5-ht1 binding sites, the similarity of pharmacological responses between 5-ht and bea 1654, and the ineffectiveness of antagonists of 5-ht2 and alpha-adrenergic receptors to block the ava constriction and arteriolar dilatation caused by both 5-ht and bea 1654, we conclude that these effects are mediated by 5-ht1 receptors. 1985-05-10 2023-08-11 rat