Zobrazeno 1 - 10
of 10
pro vyhledávání: '"M. O. Den Boer"'
Autor:
Edward O McFalls, P. D. Verdouw, P.R. Saxena, L. M. A. Sassen, M. O. Den Boer, L. J. Van Woerkens, Dirk J. Duncker
Publikováno v:
British Journal of Pharmacology. 104:246-250
1. We investigated the presence of dopamine D1 receptors in the myocardium of anesthetized pigs using intravenous infusions of dopamine, alone and after alpha- and beta-adrenoceptor blockade and intracoronary infusions of the selective D1 receptor ag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa3c15973deee9429149e58192d1c30d
https://doi.org/10.1111/j.1476-5381.1991.tb12414.x
https://doi.org/10.1111/j.1476-5381.1991.tb12414.x
Publikováno v:
British Journal of Pharmacology. 100:665-667
Intravenous bolus injections of 5-hydroxytryptamine (5-HT; 3, 10 and 30 micrograms kg-1), 5-methoxytryptamine (5-MeO-T; 3, 10 and 30 micrograms kg-1), renzapride (BRL 24924; 3, 10, 30 and 100 micrograms kg-1) and isoprenaline (0.03, 0.1 and 0.3 micro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f601702a226bbd5d1b0ee8fc5fbf4a1
https://doi.org/10.1111/j.1476-5381.1990.tb14073.x
https://doi.org/10.1111/j.1476-5381.1990.tb14073.x
Autor:
M. O. Den Boer, P.R. Saxena, P. D. Verdouw, D. J. Duncker, Judith A.E. Somers, L. J. Van Woerkens, Burkhard Lachmann
Publikováno v:
Journal of applied physiology (Bethesda, Md. : 1985). 75(2)
In conscious pigs, arteriovenous anastomoses (AVAs) are in a constricted state so that < 5% of intra-atrially injected radioactive (15-microns-diam) microspheres are shunted to the lungs. Many of the anesthetic regimens frequently used in cardiovascu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51c75b81d899d5134e95d0d07fe34f24
https://pubmed.ncbi.nlm.nih.gov/8226482
https://pubmed.ncbi.nlm.nih.gov/8226482
1. Though it is well known that the antimigraine drugs ergotamine and dihydroergotamine reduce carotid arteriovenous anastomotic shunting, it is uncertain whether a 5-HT1-like receptor is responsible for this effect. Using a high dose of methiothepin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72c9d7208b8c0b1a0a621f8b1e043b60
https://europepmc.org/articles/PMC1908277/
https://europepmc.org/articles/PMC1908277/
Autor:
M. O. Den Boer, P.R. Saxena
Publikováno v:
Journal of neurology. 238
The drugs used in migraine therapy can be divided into two groups: agents that abort an established migraine attack and agents used prophylactically to reduce the number of migraine attacks. Both groups have drugs that are specific for migrainous hea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef7effab18216d870f55d82022129e21
https://pubmed.ncbi.nlm.nih.gov/1646288
https://pubmed.ncbi.nlm.nih.gov/1646288
Publikováno v:
Serotonin: Molecular Biology, Receptors and Functional Effects ISBN: 9783034872614
The tachycardic response to 5-HT in the anaesthetized pig was mimicked by the indole derivatives, 5-methoxytryptamine and α-methyl-5-HT, and, to a lesser extent, by the benzamide derivatives (in order of potency) zacopride, renzapride, cisapride, me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9f9d60ba1d6fd992153ad9a58fc1e2f
https://doi.org/10.1007/978-3-0348-7259-1_23
https://doi.org/10.1007/978-3-0348-7259-1_23
Publikováno v:
Serotonin: Molecular Biology, Receptors and Functional Effects ISBN: 9783034872614
It is well recognized that 5-HT1 -like receptors are heterogeneous and since in the radioligand studies at least four different 5-HT1 binding site subtypes (5-HT1A, 5-HT1B, 5-HT1C and 5-HT1D) have been discriminated, four such receptor sites may well
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b49c0d24f9769ede89193999376e139
https://doi.org/10.1007/978-3-0348-7259-1_18
https://doi.org/10.1007/978-3-0348-7259-1_18
Publikováno v:
European Journal of Pharmacology. 183:1275-1276
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfa7cf7ff8d3f9a6972dc2bfd505044b
https://doi.org/10.1016/0014-2999(90)94382-8
https://doi.org/10.1016/0014-2999(90)94382-8
Publikováno v:
European Journal of Pharmacology. 183:1160
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35b0febf55f886517456fdb5f6160458
https://doi.org/10.1016/0014-2999(90)94248-v
https://doi.org/10.1016/0014-2999(90)94248-v
Publikováno v:
British journal of pharmacology. 95(2)
1. The ability of the cardioselective beta-adrenoceptor antagonist bisoprolol ((+/-)-1-[4-(2-isopropoxyethoxymethyl)-phenoxy]-3-isopropyl-amino -2-propanol hemifumarate, EMD 33512) to suppress isoprenaline-induced increases in heart rate and maximal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0f0aa24bae2768be011501ca8d6de5a
https://pubmed.ncbi.nlm.nih.gov/2976288
https://pubmed.ncbi.nlm.nih.gov/2976288