Lobeglitazone

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Lobeglitazone is a thiazolidinedione class antidiabetic drug used in the management of type 2 diabetes mellitus. It functions primarily as an insulin sensitizer, improving the body's response to insulin without increasing the secretion of insulin from the pancreas.

Mechanism of Action[edit | edit source]

Lobeglitazone works by activating the peroxisome proliferator-activated receptor gamma (PPAR-γ), a type of nuclear receptor found in adipose tissue, skeletal muscle, and the liver. Activation of PPAR-γ leads to increased transcription of insulin-responsive genes involved in the control of glucose and lipid metabolism. This results in improved insulin sensitivity, reduced blood glucose levels, and better overall glycemic control.

Clinical Use[edit | edit source]

Lobeglitazone is indicated for the treatment of type 2 diabetes mellitus in adults. It is often prescribed when diet, exercise, and other antidiabetic medications do not provide adequate glycemic control. The drug is typically administered orally.

Side Effects[edit | edit source]

Common side effects of lobeglitazone include:

Contraindications[edit | edit source]

Lobeglitazone is contraindicated in patients with:

Pharmacokinetics[edit | edit source]

Lobeglitazone is well absorbed from the gastrointestinal tract and undergoes extensive metabolism in the liver. It is primarily excreted via the urine and feces.

Research and Development[edit | edit source]

Lobeglitazone is a relatively new drug in the thiazolidinedione class, and ongoing research is focused on its long-term efficacy and safety profile. Studies are also being conducted to explore its potential benefits in other metabolic disorders.

See Also[edit | edit source]

References[edit | edit source]

External Links[edit | edit source]


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Contributors: Prab R. Tumpati, MD