Azemiglitazone
Azemiglitazone is a pharmaceutical compound that belongs to the class of thiazolidinediones, which are used primarily as antidiabetic drugs. These drugs function by improving insulin sensitivity in patients with type 2 diabetes mellitus.
Mechanism of Action[edit | edit source]
Azemiglitazone works by activating the peroxisome proliferator-activated receptor gamma (PPAR-γ), a type of nuclear receptor. Activation of PPAR-γ influences the transcription of various genes involved in glucose and lipid metabolism. This leads to an increase in insulin sensitivity in peripheral tissues, such as adipose tissue, skeletal muscle, and the liver.
Clinical Use[edit | edit source]
Azemiglitazone is primarily indicated for the management of type 2 diabetes mellitus. It is used to improve glycemic control in conjunction with diet and exercise. It may be used as monotherapy or in combination with other antidiabetic agents such as metformin or sulfonylureas.
Side Effects[edit | edit source]
Common side effects of azemiglitazone include:
- Weight gain
- Edema
- Increased risk of heart failure
Less common but serious side effects may include:
- Hepatotoxicity
- Increased risk of bone fractures
Contraindications[edit | edit source]
Azemiglitazone is contraindicated in patients with:
- Heart failure
- Severe hepatic impairment
- Known hypersensitivity to the drug or its components
Pharmacokinetics[edit | edit source]
Azemiglitazone is absorbed from the gastrointestinal tract and undergoes extensive metabolism in the liver. It is primarily excreted via the kidneys. The half-life of azemiglitazone allows for once-daily dosing.
Research and Development[edit | edit source]
Azemiglitazone is still under investigation in various clinical trials to better understand its efficacy and safety profile. Ongoing research aims to compare its effectiveness with other thiazolidinediones like pioglitazone and rosiglitazone.
See Also[edit | edit source]
- Thiazolidinedione
- Type 2 diabetes mellitus
- Insulin resistance
- Peroxisome proliferator-activated receptor
References[edit | edit source]
External Links[edit | edit source]
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Contributors: Prab R. Tumpati, MD