Zobrazeno 1 - 10
of 271
pro vyhledávání: '"M Laubie"'
Publikováno v:
Fundamental & Clinical Pharmacology. 7:205-208
Summary— The effects of the novel antagonist S 11978 (Endo-7-[(8-methyl-8-azabicyclo[3,2,1]-3-octyl)oxycarbonyl] benzo[b] thiophene) on 5HT3 receptors were examined in N1E-115 mouse neuroblastoma x rat glioma hybrid cells, with radioligand binding
Publikováno v:
Magnetic Resonance in Chemistry. 30:1186-1195
Perindopril, the tert-butylamine salt of 1-{(2S)-2-[(1S)-(1-carbethoxybutyl)amino]-1-oxopropyl}-(2S,3aS,7aS)-perhydroindole-2-carboxylic acid, is an inhibitor of angiotensin-converting enzyme (ACE) and a new drug for the treatment of hypertension. Th
Publikováno v:
British journal of pharmacology. 122(7)
1. Saphenous vein reactivity was recorded in the anaesthetized dog by use of an ultrasonic echo-tracking device to measure the internal diameter of the vein and to calculate the venous compliance. This method was used to investigate the effects of a
Autor:
J J, Descombes, P, Mennecier, D, Versluys, V, Barou, G, de Nanteuil, M, Laubie, T J, Verbeuren
Publikováno v:
Journal of cardiovascular pharmacology. 26
Endothelin-1 (ET-1) is a powerful renal vasoconstrictor peptide that may be implicated in acute renal failure. The aim of the present study was to test the effects of the novel endothelin-converting enzyme inhibitor S 17162 (N-(2,3 dihydroxy propyl p
Autor:
Marie-Luce Bea, Mickaelle Bensoussan, Pierre Ronco, M Budisavljevic, P P Van Chuong, Pierre J. Verroust, M Laubie, Jean-Claude Dussaule
Publikováno v:
Hypertension (Dallas, Tex. : 1979). 19(4)
This article reports on the binding and the angiotensin II (Ang II) antagonistic properties of a peptide, referred to as hIIA, encoded by an RNA strand complementary to the human Ang II messenger RNA. Although Ang II and hIIA (H2N-Glu-Gly-Val-Tyr-Val
Autor:
M. Laubie, H. Schmitt
Publikováno v:
Current Medical Research and Opinion. 5:89-100
SummaryA series of experiments was carried out to investigate the comparative diuretic and natriuretic effects of indapamide and frusemide in saline loaded dogs, and the effects of indapamide on urinary diluting and concentrating mechanisms. Comparat
Publikováno v:
Journal of Medicinal Chemistry. 11:1151-1155
Publikováno v:
European Journal of Pharmacology. 6:75-82
ET 495 is a new piperazine derivative inducing complex cardiovascular changes. In dogs infusion of low doses (20 μg/kg/min i.v.) or intraduodenal administration (2 mg/kg) induced a long lasting increase in femoral blood flow and decrease in splanchn
Publikováno v:
La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris. 54(5-8)
Evidence has been found for the view that piribedil stimulates peripheral and central dopamine receptors. Piribedil stimulates the nigro-striatal pathway and has been shown to be an effective antiparkinsonian agent. The stimulation of dopamine recept
Autor:
M, Laubie
Publikováno v:
European journal of respiratory diseases. Supplement. 126
In anaesthetized, paralysed and artificially ventilated dogs, activities were recorded from the phrenic nerve and from respiratory units within the nucleus tractus solitarius (NTS) and the nucleus ambiguus (NA). Prolonged stimulation of peripheral ch