All Relations between Azapirones and serotonin

Publication Sentence Publish Date Extraction Date Species
Victoria B Risbrough, Jesse D Brodkin, Mark A Geye. GABA-A and 5-HT1A receptor agonists block expression of fear-potentiated startle in mice. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology. vol 28. issue 4. 2003-05-29. PMID:12655310. the gaba-a receptor agonists diazepam (3 and 6 mg/kg) and chlordiazepoxide (10 mg/kg) significantly reduced the expression of fps post-training, as did the serotonin 1a receptor partial agonist buspirone (5 and 10 mg/kg). 2003-05-29 2023-08-12 mouse
R C B Silva, N R Santos, M L Brandã. Influence of housing conditions on the effects of serotonergic drugs on feeding behavior in non-deprived rats. Neuropsychobiology. vol 47. issue 2. 2003-05-29. PMID:12707493. we have therefore examined the effects of fluoxetine, a selective 5-ht reuptake inhibitor, and gepirone, a 5-ht1a agonist, on body weight in isolated and in group-housed rats during 3 weeks of daily treatment. 2003-05-29 2023-08-12 rat
R C B Silva, N R Santos, M L Brandã. Influence of housing conditions on the effects of serotonergic drugs on feeding behavior in non-deprived rats. Neuropsychobiology. vol 47. issue 2. 2003-05-29. PMID:12707493. from the data obtained in this study, it is suggested that increased 5-ht transmission produced by fluoxetine during chronic administration seems to be crucial for the appetite-regulating action of 5-ht, and this hypophagic effect does not seem to be dependent on the activation of 5-ht1a receptors since it was not shared by gepirone. 2003-05-29 2023-08-12 rat
R C B Silva, N R Santos, M L Brandã. Influence of housing conditions on the effects of serotonergic drugs on feeding behavior in non-deprived rats. Neuropsychobiology. vol 47. issue 2. 2003-05-29. PMID:12707493. the hyperphagic effects of chronic regimen with gepirone in isolated animals are probably due to the concurrent reduction of the 5-ht transmission caused by this anxiogenic condition at the earlier stages of treatment. 2003-05-29 2023-08-12 rat
Jens Malmkvist, Steffen W Hansen, Birthe M Damgaar. Effect of the serotonin agonist buspirone on behaviour and hypothalamic-pituitary-adrenal axis in confident and fearful mink. Physiology & behavior. vol 78. issue 2. 2003-05-20. PMID:12576120. effect of the serotonin agonist buspirone on behaviour and hypothalamic-pituitary-adrenal axis in confident and fearful mink. 2003-05-20 2023-08-12 Not clear
Jens Malmkvist, Steffen W Hansen, Birthe M Damgaar. Effect of the serotonin agonist buspirone on behaviour and hypothalamic-pituitary-adrenal axis in confident and fearful mink. Physiology & behavior. vol 78. issue 2. 2003-05-20. PMID:12576120. two groups of 2-year-old confident (n=12) and fearful (n=12) female mink were given the serotonin (5-ht) 1a receptor agonist buspirone (1.25 mg/kg/day), whereas two other groups of 2-year-old confident (n=12) and fearful (n=12) female mink were given saline, continuously for 5 weeks via osmotic minipumps. 2003-05-20 2023-08-12 Not clear
Moemen Dannaw. Possible serotonin syndrome after combination of buspirone and St John's Wort. Journal of psychopharmacology (Oxford, England). vol 16. issue 4. 2003-05-19. PMID:12503845. possible serotonin syndrome after combination of buspirone and st john's wort. 2003-05-19 2023-08-12 Not clear
Alan D Feiger, Jon F Heiser, Ram K Shrivastava, Kenneth J Weiss, Ward T Smith, J M A Sitsen, Michael Gibertin. Gepirone extended-release: new evidence for efficacy in the treatment of major depressive disorder. The Journal of clinical psychiatry. vol 64. issue 3. 2003-05-09. PMID:12716264. to assess the efficacy and tolerability of the 5-ht(1a) agonist gepirone in extended-release formulation (gepirone-er) versus placebo in patients with major depressive disorder. 2003-05-09 2023-08-12 Not clear
Jian-Hui Liang, Xu-Hua Wang, Rui-Ke Liu, Hong-Lei Sun, Xiang-Feng Ye, Ji-Wang Zhen. Buspirone-induced antinociception is mediated by L-type calcium channels and calcium/caffeine-sensitive pools in mice. Psychopharmacology. vol 166. issue 3. 2003-05-07. PMID:12552360. previous studies have shown that buspirone, a partial 5-ht(1a) receptor agonist, produces antinociceptive effects in rats and mice; ca(2+) plays a critical role as a second messenger in mediating nociceptive transmission. 2003-05-07 2023-08-12 mouse
Bernadette Astier, Laura Lambás Señas, Fabienne Soulière, Patricia Schmitt, Nadia Urbain, Nicolas Rentero, Lionel Bert, Luc Denoroy, Bernard Renaud, Monique Lesourd, Carmen Muñoz, Guy Chouve. In vivo comparison of two 5-HT1A receptors agonists alnespirone (S-20499) and buspirone on locus coeruleus neuronal activity. European journal of pharmacology. vol 459. issue 1. 2003-04-30. PMID:12505530. the aim of the present study was to compare, in chloral-hydrate anaesthetized rats, the alpha(2)-adrenergic properties of the selective 5-ht(1a) receptor agonist, alnespirone (s-20499), with those of buspirone, a 5-ht(1a) receptor agonist exhibiting potent alpha(2)-adrenoceptor antagonist properties via its principal metabolite, 1-(2-pyrimidinyl)-piperazine. 2003-04-30 2023-08-12 rat
Jingyuan Chen, Changpeng Shen, Emanuel Melle. 5-HT1A receptor-mediated regulation of mitogen-activated protein kinase phosphorylation in rat brain. European journal of pharmacology. vol 452. issue 2. 2003-04-02. PMID:12354565. other 5-ht(1a) receptor agonists (buspirone, gepirone and ipsapirone) also reduced phospho-erk1/2 levels in hippocampus. 2003-04-02 2023-08-12 rat
Takashi Nakayama, Tetsuya Suhara, Yoshiro Okubo, Tetsuya Ichimiya, Fumihiko Yasuno, Jun Maeda, Akihiro Takano, Tomoyuki Saijo, Kazutoshi Suzuk. In vivo drug action of tandospirone at 5-HT1A receptor examined using positron emission tomography and neuroendocrine response. Psychopharmacology. vol 165. issue 1. 2003-03-20. PMID:12474116. tandospirone is a selective 5-hydroxytryptamine (ht)(1a) receptor agonist and is clinically used as an anxiolytic in japan. 2003-03-20 2023-08-12 human
A Siniscalchi, D Rodi, S Cavallini, S Marino, L Ferraro, L Beani, C Bianch. Effects of cholecystokinin tetrapeptide (CCK(4)) and of anxiolytic drugs on GABA outflow from the cerebral cortex of freely moving rats. Neurochemistry international. vol 42. issue 1. 2003-02-11. PMID:12441172. and the 5-ht(1a) agonist buspirone (3mg/kg, i.p.) 2003-02-11 2023-08-12 rat
Agnieszka Zahorodna, Krzysztof Tokarski, Maria Bija. Imipramine but not 5-HT(1A) receptor agonists or neuroleptics induces adaptive changes in hippocampal 5-HT(1A) and 5-HT(4) receptors. European journal of pharmacology. vol 443. issue 1-3. 2003-01-27. PMID:12044792. we studied the effects of repeated treatment with imipramine, the 5-ht(1a) receptor agonists 8-hydroxy-2(di-n-propylamino)tetralin (8-oh-dpat) and buspirone, and the neuroleptics haloperidol and clozapine on the sensitivity of rat hippocampal ca1 neurons to 5-ht(1a)- and 5-ht(4) receptor activation. 2003-01-27 2023-08-12 rat
Heather J Chial, Michael Camilleri, Duane Burton, George Thomforde, Kevin W Olden, Debra Stephen. Selective effects of serotonergic psychoactive agents on gastrointestinal functions in health. American journal of physiology. Gastrointestinal and liver physiology. vol 284. issue 1. 2003-01-23. PMID:12488239. participants received one of four regimens in a randomized, double-blind manner: buspirone, a 5-ht(1a) receptor agonist (10 mg twice daily); paroxetine, a selective serotonin reuptake inhibitor (20 mg daily); venlafaxine-xr, a selective serotonin and norepinephrine reuptake inhibitor (75 mg daily); or placebo for 11 days. 2003-01-23 2023-08-12 human
Yutaka Masuda, Yusuke Akagawa, Yasuo Hishikaw. Effect of serotonin 1A agonist tandospirone on depression symptoms in senile patients with dementia. Human psychopharmacology. vol 17. issue 4. 2003-01-16. PMID:12404687. effect of serotonin 1a agonist tandospirone on depression symptoms in senile patients with dementia. 2003-01-16 2023-08-12 Not clear
C K Olsen, S Hogg, M D S Lapi. Tonic immobility in guinea pigs: a behavioural response for detecting an anxiolytic-like effect? Behavioural pharmacology. vol 13. issue 4. 2002-12-24. PMID:12218506. compounds that reduced ti include the serotonin (5-ht) releaser fenfluramine, the 5-ht(1a) receptor agonists 8-hydroxy-2-(di-n-propylamino)tetralin (8-oh-dpat) and buspirone, the 5-ht(2c/2b) receptor antagonist sb206553, the 5-ht(2a) receptor antagonist mdl 100.151 -- but only at doses thought also to inhibit 5-ht(2c) receptors--the noradrenaline (na) reuptake inhibitor desipramine, the benzodiazepine inverse agonist fg-7142, the alpha(2)-adrenergic receptor antagonist yohimbine, the neurokinin (nk)(1) receptor antagonist l-733.060, and the nk(2) receptor antagonist sr-48968. 2002-12-24 2023-08-12 Not clear
Klaas P Zuideveld, Jasna Rusiç-Pavletiç, Hugo J Maas, Lambertus A Peletier, Piet H Van der Graaf, Meindert Danho. Pharmacokinetic-pharmacodynamic modeling of buspirone and its metabolite 1-(2-pyrimidinyl)-piperazine in rats. The Journal of pharmacology and experimental therapeutics. vol 303. issue 3. 2002-12-24. PMID:12438536. the results of this analysis show that buspirone and 1-pp behave as partial 5-hydroxytryptamine(1a) agonists in vivo and that following intravenous administration the amount of 1-pp formed is too small to contribute to the hypothermic effect. 2002-12-24 2023-08-12 rat
Franco Borsini, Kennett Evans, Kathryn Jason, Frank Rohde, Barbara Alexander, Stephan Pollentie. Pharmacology of flibanserin. CNS drug reviews. vol 8. issue 2. 2002-11-25. PMID:12177684. the effects of flibanserin on adenylyl cyclase are different from those of buspirone and 8-oh-dpat, two other purported 5-ht(1a) receptor agonists. 2002-11-25 2023-08-12 Not clear
Alicia M Crissman, James M O'Donnel. Effects of antidepressants in rats trained to discriminate centrally administered isoproterenol. The Journal of pharmacology and experimental therapeutics. vol 302. issue 2. 2002-08-29. PMID:12130722. the serotonin uptake inhibitor fluoxetine, the atypical antidepressants buspirone and trazodone, and the novel, putative antidepressants n(g)-nitro-l-arginine and n-acetyl-l-tryptophan 3,5-bis benzyl ester failed to substitute for isoproterenol at the dose ranges tested. 2002-08-29 2023-08-12 rat