Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Elizabeth P. Faison"'
Autor:
Katherine Lipschutz, Allan I. Goldberg, John D. Irvin, E B Nelson, David A Shapiro, Michael A. Weber, Elizabeth P. Faison
Publikováno v:
Clinical Pharmacology and Therapeutics. 55:346-352
Two hundred eighty-six patients with mild to moderate hypertension who had untreated diastolic blood pressure while seated of 95 to 115 mm Hg were randomized to receive placebo or once-daily doses of 2.5, 5, or 10 mg of the dihydropyridine calcium ch
Autor:
D B Snavely, R L Byyny, Elizabeth P. Faison, E B Nelson, J H Pratt, Allan I. Goldberg, Michael A. Weber
Publikováno v:
Archives of Internal Medicine. 155:405
Background: Losartan potassium, the first nonpeptide selective blocker of angiotensin II at the ATI receptor, has been shown to exhibit clinical antihypertensive effects. The aim of the present study was to characterize the efficacy and duration of a
Autor:
Tom Dobbins, Hans R. Brunner, Bengt E. Karlberg, Lawrence E. Ramsay, Richard S. Irwin, Yves Lacourcière, E B Nelson, D B Snavely, Elizabeth P. Faison
Publikováno v:
Journal of Hypertension. 12:1387
ObjectiveTo compare the incidence of cough in patients with a history of angiotensin converting enzyme (ACE) inhibitor-related cough who received losartan [a type 1 angiotensin II (Ang II) receptor antagonist], lisinopril (an ACE inhibitor) or hydroc
Publikováno v:
European Journal of Pharmacology. 102:169-173
The vasodilator profile of synthetic atrial natriuretic factor (ANF) was characterized using isolated vascular preparations. Nanomolar concentrations of ANF relaxed rabbit aortic rings contracted by serotonin, histamine, methoxamine or angiotensin II
Autor:
Edward H. Blaine, Ruth F. Nutt, S F Brady, M A Napier, Elizabeth P. Faison, Raymond J. Winquist, Richard L. Vandlen, L A Heinel, Georg Albers-Schönberg, T. A. Lyle
Publikováno v:
Proceedings of the National Academy of Sciences. 81:5946-5950
Membranes from rabbit aorta and from rabbit and rat kidney cortex possess high-affinity (Kd = 10(-10) M) specific binding sites for atrial natriuretic factor (ANF). Similar high-affinity sites are present in an established cell line from pig kidney,
Autor:
Robert M. Rapoport, Raymond J. Winquist, Elizabeth P. Faison, Ferid Murad, Scott A. Waldman, Karen Schwartz
Publikováno v:
Proceedings of the National Academy of Sciences. 81:7661-7664
A 26 amino acid synthetic peptide fragment of atrial natriuretic factor (ANF) relaxed isolated rabbit aortic segments in which the endothelium was either intact or functionally destroyed. The relaxations were temporally associated with increases in l
Publikováno v:
Neuroscience letters. 34(3)
Rats that have been chronically exposed to neuroleptic drugs exhibit an enhanced stereotypic response to dopaminergic agonists, and it has been suggested that this phenomenon is a useful animal model of tardive dyskinesia. Administration of MK-771, a
Autor:
Scott A. Waldman, Elizabeth P. Baskin, Raymond J. Winquist, Robert M. Rapoport, Ferid Murad, Elizabeth P. Faison
Publikováno v:
European journal of pharmacology. 120(1)
The effects of atriopeptins I and II on relaxation and cyclic GMP levels were studied on rat and rabbit aortas. Atriopeptin I was 2- and 100-fold less potent than atriopeptin II in causing relaxation of rat and rabbit aortas, respectively. The atriop
Autor:
Elizabeth P. Baskin, Raymond J. Winquist, Richard L. Vandlen, Mary A. Napier, Elizabeth P. Faison, Karen E. Arcuri, Maureen E. Keegan
Publikováno v:
Clinical and experimental hypertension. Part A, Theory and practice. 7(5-6)
Characterization of the vascular pharmacology and receptor binding of atrial natriuretic factor (ANF) has been achieved utilizing a synthetic peptide which contains the sequence and biological activity of ANF. The synthetic ANF (sANF) relaxes aortic
Autor:
Raymond J. Winquist, Patricia K. Lumma, Gregory J. Kaczorowski, Mayme J. Trumble, Baldwin John J, David A. Claremon, Seth A. Rosenthal, Elizabeth P. Faison, Graham M. Smith, David E. McClure
Publikováno v:
Journal of medicinal chemistry. 30(4)
The pharmacological activity of rigid analogues of 1,4-dihydropyridine calcium entry antagonists 9-16 is demonstrated by dose-dependent inhibition of the calcium contraction in depolarized rat aortic strips and by a [3H]nitrendipine binding assay in