Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Elisabeth Kühberger"'
Autor:
Christa Firbas, Laura Brandt, Brigitte Litschauer, Ghazaleh Gouya, Safoura Sheik-Rezaei, Stefan Weisshaar, Günther Nirnberger, Laura Moser, Ulrike Bauer, Michael Wolzt, Gabriele Fischer, Elisabeth Kühberger
Publikováno v:
British Journal of Clinical Pharmacology
Aims Oral opioid preparations combined with naloxone are intended to induce a transient acute withdrawal syndrome to avoid intravenous misuse. This trial aimed to establish an appropriate morphine–naloxone dose ratio for an abuse‐deterrent oral o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d060fea64a5296900cb2bbbbcdd45069
https://doi.org/10.1111/bcp.14271
https://doi.org/10.1111/bcp.14271
Publikováno v:
British Journal of Pharmacology. 113:1289-1294
1 Experiments were designed to analyse the requirement of myoendothelial junctions by bradykinin-induced endothelium-dependent relaxations resistant to NG-nitro-L-arginine (L-NOARG) and indo-methacin in porcine coronary arteries. 2 Rings of porcine c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb3d8c832aaf45bf5b056d9e45d32947
https://doi.org/10.1111/j.1476-5381.1994.tb17138.x
https://doi.org/10.1111/j.1476-5381.1994.tb17138.x
Publikováno v:
Europe PubMed Central
Purified cromakalim trans enantiomers were tested for their ability to antagonize three specific mechanisms of smooth muscle activation, i.e., depolarization-induced Ca2+ entry through voltage-gated channels, agonist-induced Ca2+ entry, and agonist-i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::358e0cc26801747a2be17a20be1e7221
https://doi.org/10.1097/00005344-199306000-00015
https://doi.org/10.1097/00005344-199306000-00015
Publikováno v:
European Journal of Pharmacology. 200:25-33
In order to identify the receptor subtype responsible for acetylcholine (ACh)-induced relaxation of bovine coronary artery, we determined the affinity of six subtype-selective muscarinic antagonists and compared them with affinity estimates obtained
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e3ad29135431b7de3f1ba181216bb2d
https://doi.org/10.1016/0014-2999(91)90661-9
https://doi.org/10.1016/0014-2999(91)90661-9
Publikováno v:
European Journal of Pharmacology. 196:247-255
The nature of the muscarinic receptor subtype mediating contraction of the endothelimn-denuded bovine coronary artery was investigated in vitro by functional measurements and radioligand binding studies. The acetylcholine (ACh)-induced isotonic contr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c93a5cfcc39f5190f92fb60315cd483c
https://doi.org/10.1016/0014-2999(91)90437-u
https://doi.org/10.1016/0014-2999(91)90437-u
Publikováno v:
British journal of pharmacology. 106(3)
1. One aim of this paper is to show an alternative approach for the determination of antagonist affinity estimates, KB and pA2, by construction and evaluation of antagonist dose-response curves (DRCs), using the curve-fitting programme, ALLFIT. 2. Pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a660d0fcd9364f82538b0b8cdf2163c
https://pubmed.ncbi.nlm.nih.gov/1504755
https://pubmed.ncbi.nlm.nih.gov/1504755
Publikováno v:
European journal of pharmacology. 187(2)
The aim of this study was to characterize muscarinic receptors of the bovine coronary artery by means of a combination of mechanical relaxation and contraction responses and radioligand binding data. Fresh helical strips of bovine coronary artery wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95981ce38e2753ea20f2af389cafc636
https://pubmed.ncbi.nlm.nih.gov/2272358
https://pubmed.ncbi.nlm.nih.gov/2272358
Publikováno v:
European Journal of Pharmacology. 183:2135
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e26f0fe5859cfc4f881c9181be5f3c8c
https://doi.org/10.1016/0014-2999(90)93656-b
https://doi.org/10.1016/0014-2999(90)93656-b