ethacrynic acid has been researched along with Cystic Fibrosis in 5 studies
Ethacrynic Acid: A compound that inhibits symport of sodium, potassium, and chloride primarily in the ascending limb of Henle, but also in the proximal and distal tubules. This pharmacological action results in excretion of these ions, increased urinary output, and reduction in extracellular fluid. This compound has been classified as a loop or high ceiling diuretic.
etacrynic acid : An aromatic ether that is phenoxyacetic acid in which the phenyl ring is substituted by chlorines at positions 2 and 3, and by a 2-methylidenebutanoyl group at position 4. It is a loop diuretic used to treat high blood pressure resulting from diseases such as congestive heart failure, liver failure, and kidney failure. It is also a glutathione S-transferase (EC 2.5.1.18) inhibitor.
Cystic Fibrosis: An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION.
Excerpt | Relevance | Reference |
---|---|---|
"We demonstrate previously that fibroblasts from cystic fibrosis (CF) patients are significantly more resistant to the toxic effects of ouabain than normal human fibroblasts are." | 3.65 | Increased dexamethasone resistance of cystic fibrosis fibroblasts. ( Breslow, JL; Davidson, RL; Epstein, J, 1977) |
"The ouabain-sensitive and the ethacrynic acid-sensitive sodium efflux from erythrocytes of patients with cystic fibrosis are both decreased." | 3.64 | Red-cell transport defect in patients with cystic fibrosis and in their parents. ( Balfe, JW; Cole, C; Welt, LG, 1968) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (80.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (20.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Chung, WJ | 1 |
Goeckeler-Fried, JL | 1 |
Havasi, V | 1 |
Chiang, A | 1 |
Rowe, SM | 1 |
Plyler, ZE | 1 |
Hong, JS | 1 |
Mazur, M | 1 |
Piazza, GA | 1 |
Keeton, AB | 1 |
White, EL | 1 |
Rasmussen, L | 1 |
Weissman, AM | 1 |
Denny, RA | 1 |
Brodsky, JL | 1 |
Sorscher, EJ | 1 |
Whitman, V | 1 |
Stern, RC | 1 |
Bellet, P | 1 |
Doershuk, CF | 1 |
Liebman, J | 1 |
Boat, TF | 1 |
Borkat, G | 1 |
Matthews, LW | 1 |
Epstein, J | 1 |
Breslow, JL | 1 |
Davidson, RL | 1 |
Balfe, JW | 1 |
Cole, C | 1 |
Welt, LG | 1 |
Duffy, MJ | 1 |
5 other studies available for ethacrynic acid and Cystic Fibrosis
Article | Year |
---|---|
Increasing the Endoplasmic Reticulum Pool of the F508del Allele of the Cystic Fibrosis Transmembrane Conductance Regulator Leads to Greater Folding Correction by Small Molecule Therapeutics.
Topics: Alleles; Benzoates; Cells, Cultured; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regu | 2016 |
Studies on cor pulmonale in cystic fibrosis: I. Effects of diuresis.
Topics: Acid-Base Equilibrium; Adolescent; Adult; Blood Pressure; Carbon Dioxide; Cardiac Catheterization; C | 1975 |
Increased dexamethasone resistance of cystic fibrosis fibroblasts.
Topics: Aminopterin; Biological Transport; Cell Survival; Cells, Cultured; Colchicine; Cystic Fibrosis; Dexa | 1977 |
Red-cell transport defect in patients with cystic fibrosis and in their parents.
Topics: Adenosine Triphosphatases; Biological Transport, Active; Counseling; Cystic Fibrosis; Erythrocytes; | 1968 |
Letter: Na+ transport defect in cystic fibrosis.
Topics: Adenosine Triphosphatases; Biological Transport; Cystic Fibrosis; Erythrocytes; Ethacrynic Acid; Fib | 1974 |