Nateglinide: Difference between revisions

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[[Category:Antidiabetic drugs]]
[[Category:Antidiabetic drugs]]
[[Category:Meglitinides]]
[[Category:Meglitinides]]
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File:Nateglinide.svg|Nateglinide
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Latest revision as of 01:45, 20 February 2025

An oral antidiabetic medication


Nateglinide
INN
Drug class
Routes of administration
Pregnancy category
Bioavailability
Metabolism
Elimination half-life
Excretion
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CAS Number
PubChem
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Nateglinide is an oral antidiabetic drug used in the management of type 2 diabetes mellitus. It belongs to the class of medications known as meglitinides, which stimulate the pancreas to release insulin.

Mechanism of Action[edit]

Nateglinide works by closing the ATP-sensitive potassium channels in the beta cells of the pancreas. This action leads to the opening of calcium channels, resulting in an influx of calcium ions and subsequent release of insulin. The drug is particularly effective in controlling postprandial blood glucose levels.

Pharmacokinetics[edit]

Nateglinide is rapidly absorbed from the gastrointestinal tract and has a quick onset of action. It is metabolized primarily in the liver by the cytochrome P450 enzyme system, particularly CYP2C9 and CYP3A4. The drug has a short half-life, which minimizes the risk of hypoglycemia.

Clinical Use[edit]

Nateglinide is indicated for the treatment of type 2 diabetes mellitus in conjunction with diet and exercise. It is often used in combination with other antidiabetic agents such as metformin or thiazolidinediones.

Side Effects[edit]

Common side effects of nateglinide include:

Contraindications[edit]

Nateglinide is contraindicated in patients with:

Administration[edit]

Nateglinide is administered orally, typically taken before meals to optimize its effect on postprandial glucose levels.

Related pages[edit]