Zobrazeno 1 - 10
of 10
pro vyhledávání: '"E. J. Stack"'
Autor:
Leonard Share, David P. Brooks, Mark Pullen, E. J. Stack, Joan T. Crofton, Yi-Xin Wang, Richard M. Edwards, Ponnal Nambi
Publikováno v:
American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. 265:R1284-R1290
A possible gender difference in the antidiuretic activity of vasopressin was studied in male and female Sprague-Dawley rats. Infusion of vasopressin (3-100 pg.kg-1.min) into conscious, chronically instrumented water-loaded rats resulted in a dose-dep
Autor:
T. M. Morgan, David T. Hill, Richard M. Keenan, R. M. Edwards, J. Samanen, Catherine E. Peishoff, E. Griffin, R. G. Franz, E. J. Stack, Finkelstein Ja, Nambi Aiyar, Joseph Weinstock, E. F. Weidley, L. M. Tucker, G. R. Girard, E. H. Ohlstein, Dimitri Gaitanopoulos
Publikováno v:
ChemInform. 24
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 290(1)
The transport of the angiotensin II receptor antagonist losartan and its interaction with organic anion transport were examined in the isolated perfused rabbit proximal tubule. Losartan reversibly inhibited the secretion of para-aminohippurate (PAH)
Interaction of L-arginine analogs with L-arginine uptake in rat renal brush border membrane vesicles
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 285(3)
The dibasic amino acid, L-arginine, is a substrate for both nitric oxide synthase (NOS) and arginase and therefore, plays an important role in cell signaling and cell growth. We examined the effects of various NOS inhibitors on L-arginine transport i
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 276(1)
The angiotensin II (AII) antagonist, losartan, increases uric acid excretion when administered to humans. However, the active metabolite of losartan, EXP 3174, and other nonpeptide AII antagonists such as eprosartan and SB 203220 are devoid of uricos
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 267(3)
We characterized the endothelin (ET) receptor subtype responsible for the inhibition of vasopressin (AVP)-induced increases in osmotic water permeability (Pf) and cAMP accumulation in rat inner medullary collecting ducts (IMCD). ET-1 (10 nM) produced
Angiotensin II inhibits glomerular adenylate cyclase via the angiotensin II receptor subtype 1 (AT1)
Autor:
R M, Edwards, E J, Stack
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 266(2)
We examined the role of angiotensin II (AII) receptor subtypes in the regulation of hormone-stimulated cyclic AMP (cAMP) accumulation in isolated rat glomeruli. All inhibited cAMP formation induced by histamine, serotonin and parathyroid hormone, but
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 257(3)
The effects of calcitonin gene-related peptide (CGRP) on lumen diameter and adenylate cyclase activity in isolated intracerebral arterioles were examined. CGRP produced a concentration-dependent relaxation of spontaneous tone developed by the arterio
1. 3-Mercaptopicolinic acid (SK&F 34288) inhibited gluconeogenesis in vitro, with lactate as substrate, in rat kidney-cortex and liver slices. 2. In perfused rat livers, gluconeogenesis was inhibited when lactate, pyruvate or alanine served as substr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4656549da6ae5b37b4622973b3b43915
https://europepmc.org/articles/PMC1166224/
https://europepmc.org/articles/PMC1166224/
Autor:
N W, DiTullio, E J, Stack
Publikováno v:
Journal of lipid research. 14(5)
Mice were fed a lithogenic diet consisting of Purina chow and 0.5% dehydrocholic acid (DHA group). Controls received Purina chow. Every 2 wk for 20 wk animals were killed, and biliary phospholipid, cholesterol, and bile salt concentrations were deter