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Sulfonylurea - Pharmacology |  | Sulfonylurea - Pharmacology: Encyclopedia II - Sulfonylurea - Pharmacology |  |
Sulfonylurea - Method of action.
Sulfonylureas bind to an ATP-dependent K+ channel on the cell membrane of pancreatic beta cells. This inhibits a tonic, hyperpolarizing outflux of potassium, which causes the electric potential over the membrane to become more positive. This depolarization opens voltage-gated Ca2+ channels. The rise in intracellular calcium leads to increased fusion of insulin granulae with the cell membrane, and t ...
See also:Sulfonylurea, Sulfonylurea - Drugs in this class, Sulfonylurea - Chemistry, Sulfonylurea - Pharmacology, Sulfonylurea - Method of action, Sulfonylurea - Pharmacokinetics, Sulfonylurea - Uses, Sulfonylurea - Side-effects and cautions, Sulfonylurea - History |  | | Sulfonylurea, Sulfonylurea - Chemistry, Sulfonylurea - Drugs in this class, Sulfonylurea - History, Sulfonylurea - Method of action, Sulfonylurea - Pharmacokinetics, Sulfonylurea - Pharmacology, Sulfonylurea - Side-effects and cautions, Sulfonylurea - Uses, diabetes mellitus, metformin, thiazolidinediones |  | |
|  |  | Sulfonylurea: Encyclopedia II - Sulfonylurea - Pharmacology
Sulfonylurea - Pharmacology
Sulfonylurea - Method of action
Sulfonylureas bind to an ATP-dependent K+ channel on the cell membrane of pancreatic beta cells. This inhibits a tonic, hyperpolarizing outflux of potassium, which causes the electric potential over the membrane to become more positive. This depolarization opens voltage-gated Ca2+ channels. The rise in intracellular calcium leads to increased fusion of insulin granulae with the cell membrane, and therefore increased secretion of (pro)insulin.
There is some evidence that sulfonylureas also sensitize β-cells to glucose, that they limit glucose production in the liver, that they decrease lipolysis (breakdown and release of fatty acids by adipose tissue) and decrease clearance of insulin by the liver.
Sulfonylurea - Pharmacokinetics
Various sulfonylureas have different pharmacokinetics. The choice depends on the propensity of the patient to develop hypoglycemia - long-acting sulfonylureas with active metabolites can induce hypoglycemia. They can, however, help achieve glycemic control when tolerated by the patient. The shorter-acting agents may not control blood sugar levels adequately.
Due to varying half-life, some drugs have to be taken twice (tolbutamide) or three times a day rather than once (glimepiride). The short-acting agents may have to be taken about 30 minutes before the meal, to ascertain maximum efficacy when the food leads to increased blood glucose levels.
Some sulfonylureas are metabolised by liver metabolic enzymes (cytochrome P450) and inducers of this enzyme system (such as the antibiotic rifampicin) can therefore increase the clearance of sulfonylureas. In addition, because some sulfonylureas are bound to plasma proteins, use of drugs that also bind to plasma proteins can release the sulfonylureas from their binding places, leading to increased clearance.
Other related archives1990s, ATP, Ca, Chlorpropamide, Glibenclamide, Glimepiride, Glipizide, K, Tolazamide, Tolbutamide, adipose tissue, antibiotics, antidiabetic drugs, beta cells, cytochrome P450, depolarization, dextrose, diabetes mellitus, diabetes of pregnancy, fatty acids, headache, hypoglycemia, insulin, intravenous, liver, metformin, obese, pancreas, phenyl, rifampicin, sulfonamide, teratogenic, thiazolidinedione, thiazolidinediones
 Adapted from the Wikipedia article "Pharmacology", under the G.N U Free Docmentation License. Please also see http://en.wikipedia.org/wiki |
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