Zobrazeno 1 - 10
of 130
pro vyhledávání: '"B, Fjalland"'
Autor:
B. Fjalland
Publikováno v:
Acta Pharmacologica et Toxicologica. 42:377-380
A method is described for the preparation and perfusion in vitro of isolated guinea pig lungs, 5-HT is rapidly taken up from a perfusing solution by the organ (about 70% uptake). In the concentration range 10(-7) to 5 X 10(-6) M citalopram concentrat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af9a3b732162075b4f2bfc86bcbe8ad0
https://doi.org/10.1111/j.1600-0773.1978.tb02220.x
https://doi.org/10.1111/j.1600-0773.1978.tb02220.x
Autor:
B. Fjalland
Publikováno v:
Acta Pharmacologica et Toxicologica. 33:103-112
The influence of adrenergic and serotoninergic mechanisms on gastric secretion was investigated using fistula- and pylorus-ligated rats. Secretion was increased by the tyrosine hydroxylase inhibitor α-methyltyrosine. This effect could be reversed by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a15bbf18980fd4fa82fecc4ef42cc1f8
https://doi.org/10.1111/j.1600-0773.1973.tb01513.x
https://doi.org/10.1111/j.1600-0773.1973.tb01513.x
Autor:
B. Fjalland
Publikováno v:
Acta Pharmacologica et Toxicologica. 42:73-76
Neuroleptics from various chemical groups and some amino acids were examined for GABA uptake-inhibiting properties in rat brain synaptosomes. The phenothiazine and thioxanthene neuroleptics inhibited GABA uptake by 50% in the concentration range of 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48ae028755c7252aedad148be13c18f7
https://doi.org/10.1111/j.1600-0773.1978.tb02171.x
https://doi.org/10.1111/j.1600-0773.1978.tb02171.x
Autor:
B. Fjalland
Publikováno v:
Acta Pharmacologica et Toxicologica. 35:293-299
The influence of amphetamine, apomorphine and methylphenidate on basal gastric secretion was investigated using fistula- and pylorus-ligated rats. The antisecretory effect of amphetamine was reversed by pretreating the animals with α-methyl-p-tyrosi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9690942a3d038ca2f367a7f175c78ac
https://doi.org/10.1111/j.1600-0773.1974.tb00749.x
https://doi.org/10.1111/j.1600-0773.1974.tb00749.x
Publikováno v:
European Journal of Clinical Pharmacology. 50:179-184
Concentrations of plasma neutral amino acids, i.e. threonine, serine, asparagine, glycine, alanine, citrulline, alpha-aminobutyric acid, valine, methionine, isoleucine, leucine, tyrosine, phenylalanine, and tryptophan, and serum cholesterol, were det
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a25e3b0c783226b89296c3c440e686aa
https://doi.org/10.1007/s002280050089
https://doi.org/10.1007/s002280050089
Publikováno v:
Annals of the New York Academy of Sciences. 689:593-596
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4525bd4e865fd5533549854a82d39f4d
https://doi.org/10.1111/j.1749-6632.1993.tb55601.x
https://doi.org/10.1111/j.1749-6632.1993.tb55601.x
Publikováno v:
British journal of pharmacology. 133(4)
Based on an unexpected high maximum response to piperidine-4-sulphonic acid (P4S) at human alpha1alpha6beta2gamma2 GABA(A) receptors expressed in Xenopus oocytes attempts to correlate this finding with the pharmacological profile of P4S and other GAB
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cbe594f46eb7f257be18fba5a765ae6c
https://pubmed.ncbi.nlm.nih.gov/11399671
https://pubmed.ncbi.nlm.nih.gov/11399671
Publikováno v:
Molecular pharmacology. 55(3)
Dehydroepiandrosterone sulfate (DHEAS) is a neuroactive steroid with antagonist action at gamma-aminobutyric acid type A (GABAA) receptors. Patch-clamp techniques were used to investigate DHEAS actions at GABAA receptors of the rat pituitary gland at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d8a4e6aa95e84bdeb83fcbabe2e9e14a
https://pubmed.ncbi.nlm.nih.gov/10051532
https://pubmed.ncbi.nlm.nih.gov/10051532
Publikováno v:
British journal of pharmacology. 126(1)
1. This study sought to evaluate whether the effects of acute and long-term treatment with 17-beta-estradiol on the vasomotor responses in rat aortic rings are mediated through the same mechanism. 2. Ovariectomized rats were treated daily with either
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2366dee15edf7aa69d8cd482538461c8
https://pubmed.ncbi.nlm.nih.gov/10051132
https://pubmed.ncbi.nlm.nih.gov/10051132
Autor:
B, Fjalland
Publikováno v:
Theriaca. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a9a253b2b5287f0a84e5dff6cd4d0a5c
https://pubmed.ncbi.nlm.nih.gov/11640710
https://pubmed.ncbi.nlm.nih.gov/11640710