Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Deanna Gage"'
Autor:
Jamie Blackbourne, Dan Weinzapfel, G.Keith Matheson, Deanna Gage, Andrew Knowles, Deanne Guthrie
Publikováno v:
General Pharmacology: The Vascular System. 29:823-828
1. The effects of ipsapirone, nefazodone, tiaspirone, BMS-20661, buspirone and gepirone on the hypothalamic-pituitary-adrenal (HPA) axis were studied. These drugs were selected because they have serontonin 1A (5-HT1A) receptor-binding capability and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2894a7a7661e21d0115604416dc39c06
https://doi.org/10.1016/s0306-3623(97)00006-2
https://doi.org/10.1016/s0306-3623(97)00006-2
Autor:
Jamie Blackbourne, Deanne Guthrie, Carla Michel, Keith Matheson, Christopher Bauer, Andrew Knowles, Deanna Gage, Dan Weinzapfel
Publikováno v:
Pharmacology. 55:59-65
The effects of tandospirone, enciprazine, gepirone, buspirone (5-HT1A agents) and carvotroline (5-HT2) on hypothalamic-pituitary-adrenocortical activity (HPA) activity were studied. These drugs increased the plasma corticosterone levels in a dose-dep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b6cd7bea00a17294f61037803230adc
https://doi.org/10.1159/000139513
https://doi.org/10.1159/000139513
Publikováno v:
Neuropharmacology. 27(8)
The effects of the anxiolytic agents, buspirone and diazepam, on the hypothalamic-pituitary-adrenal axis (HPAA), indicated by changes in the concentration of corticosterone (CS) in plasma, were studied 1 2 , 1, 2, 4, 6, 8 and 24 hr after administrati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e684831febda3103da842de0ae284798
https://pubmed.ncbi.nlm.nih.gov/3216961
https://pubmed.ncbi.nlm.nih.gov/3216961
Autor:
Deanne Guthrie, Janet Rhoades, Deanna Gage-White, Gary W. White, G.K. Matheson, Vanessa Dixon
Publikováno v:
Neuropharmacology. 28(4)
It was found that gepirone and 1-(2-pyrimidinyl)-piperazine (1-PP) increased levels of corticosterone in plasma in the intact rat. Gepirone was more potent and more efficacious than its metabolite, 1-PP. The ED50 was 6.4 μmol/kg for gepirone and 65.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbfe4e2ae7a65b7c61244fe3cf3b94f8
https://pubmed.ncbi.nlm.nih.gov/2747846
https://pubmed.ncbi.nlm.nih.gov/2747846