tolbutamide has been researched along with sodium azide in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (14.29) | 18.7374 |
1990's | 2 (28.57) | 18.2507 |
2000's | 3 (42.86) | 29.6817 |
2010's | 1 (14.29) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Barnett, DW; Falke, LC; Gillis, KD; Misler, S; Pressel, DM; Scharp, DW | 1 |
Falke, LC; Gillis, KD; Misler, S; Pressel, DM | 1 |
Ashford, ML; Campbell, CM; Kinsella, JM; McKay, NG | 1 |
Dickel, C; Grimmsmann, T; Herrmann, C; Rustenbeck, I | 1 |
Lee, EW; Lee, KS; Sun, XD; Wong, EH | 1 |
Chen, M; Dong, Y; Simard, JM | 1 |
Cannone, G; Carbonara, G; Cippone, V; Conte Camerino, D; Fracchiolla, G; Laghezza, A; Loiodice, F; Mele, A; Rolland, JF; Tortorella, P; Tricarico, D | 1 |
7 other study(ies) available for tolbutamide and sodium azide
Article | Year |
---|---|
Stimulus-secretion coupling in beta-cells of transplantable human islets of Langerhans. Evidence for a critical role for Ca2+ entry.
Topics: 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester; Action Potentials; Azides; Calcium; Cytosol; Electrophysiology; Glucose; Humans; In Vitro Techniques; Insulin; Insulin Secretion; Islets of Langerhans; Islets of Langerhans Transplantation; Kinetics; Membrane Potentials; Nifedipine; Potassium Chloride; Sodium Azide; Time Factors; Tolbutamide | 1992 |
'Perforated patch recording' allows long-term monitoring of metabolite-induced electrical activity and voltage-dependent Ca2+ currents in pancreatic islet B cells.
Topics: 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester; Action Potentials; Animals; Azides; Calcium Channels; Diazoxide; Electric Conductivity; Glucose; Humans; Islets of Langerhans; Membrane Potentials; Nifedipine; Rats; Sodium Azide; Tolbutamide | 1989 |
Sensitivity of Kir6.2-SUR1 currents, in the absence and presence of sodium azide, to the K(ATP) channel inhibitors, ciclazindol and englitazone.
Topics: Adenosine Triphosphate; Animals; ATP-Binding Cassette Transporters; Benzopyrans; Cell Line; Dose-Response Relationship, Drug; Female; Glyburide; Humans; Indoles; Membrane Potentials; Mice; Microinjections; Oocytes; Potassium Channels; Potassium Channels, Inwardly Rectifying; Receptors, Drug; RNA, Complementary; Sodium Azide; Sulfonylurea Receptors; Thiazoles; Thiazolidinediones; Tolbutamide; Xenopus laevis | 2000 |
Mitochondria present in excised patches from pancreatic B-cells may form microcompartments with ATP-dependent potassium channels.
Topics: Adenosine Triphosphate; Aldehydes; Animals; Antimycin A; Ascorbic Acid; Carbonyl Cyanide m-Chlorophenyl Hydrazone; Cell Compartmentation; Cell Membrane; Enzyme Inhibitors; Fluorescent Dyes; Hemiterpenes; Islets of Langerhans; Keto Acids; Mice; Mitochondria; Oligomycins; Potassium Channels; Rhodamines; Rotenone; Sodium Azide; Succinic Acid; Tetramethylphenylenediamine; Tolbutamide | 1999 |
ATP-sensitive potassium channels in freshly dissociated adult rat striatal neurons: activation by metabolic inhibitors and the dopaminergic receptor agonist quinpirole.
Topics: Action Potentials; Adenosine Triphosphate; Animals; Calcium; Corpus Striatum; Dopamine Agonists; Electric Conductivity; Female; Male; Membrane Potentials; Neurons; Potassium; Potassium Channels; Quinpirole; Rats; Rats, Sprague-Dawley; Sodium Azide; Tolbutamide | 2000 |
Functional coupling between sulfonylurea receptor type 1 and a nonselective cation channel in reactive astrocytes from adult rat brain.
Topics: Adenosine Triphosphate; Animals; Antibodies; Astrocytes; ATP-Binding Cassette Transporters; Binding, Competitive; Brain; Brain Injuries; Cell Size; Cells, Cultured; Diazoxide; Gliosis; Glyburide; Ion Channels; Membrane Potentials; Patch-Clamp Techniques; Potassium Channels; Potassium Channels, Inwardly Rectifying; Rats; Rats, Wistar; Receptors, Drug; Reverse Transcriptase Polymerase Chain Reaction; Sodium Azide; Sulfonylurea Compounds; Sulfonylurea Receptors; Tolbutamide; Trypsin | 2003 |
Structural nucleotide analogs are potent activators/inhibitors of pancreatic β cell KATP channels: an emerging mechanism supporting their use as antidiabetic drugs.
Topics: Animals; Area Under Curve; Benzoxazines; Blood Glucose; Dose-Response Relationship, Drug; Electrophysiological Phenomena; Fasting; Glucose; Glucose Tolerance Test; Glyburide; HEK293 Cells; Humans; Hypoglycemic Agents; Insulin; Insulin Secretion; Insulin-Secreting Cells; KATP Channels; Membrane Potentials; Mice; Mice, Inbred Strains; Patch-Clamp Techniques; Potassium Channels, Inwardly Rectifying; Sodium Azide; Tolbutamide | 2012 |