Cilostamide
Cilostamide is a phosphodiesterase inhibitor specifically targeting phosphodiesterase 3 (PDE3). It was first developed in the 1980s and has been studied for various medical applications, particularly in the treatment of cardiovascular diseases and diabetes.
Pharmacology[edit | edit source]
Cilostamide works by inhibiting the action of PDE3, an enzyme that breaks down cyclic adenosine monophosphate (cAMP) in cells. By preventing the breakdown of cAMP, Cilostamide increases the levels of this molecule in cells, which can have various effects depending on the specific type of cell. In cardiac muscle cells, for example, increased cAMP levels can lead to increased contractility.
Medical Applications[edit | edit source]
Cilostamide has been studied for use in several different medical applications. One of the most prominent of these is in the treatment of cardiovascular diseases. By increasing the contractility of cardiac muscle cells, Cilostamide can potentially improve heart function in patients with conditions such as heart failure.
In addition to its potential use in treating cardiovascular diseases, Cilostamide has also been studied for use in treating diabetes. In this context, the drug's ability to increase cAMP levels in cells can potentially improve the body's ability to regulate blood sugar levels.
Side Effects[edit | edit source]
Like all drugs, Cilostamide can have side effects. These can include nausea, vomiting, and diarrhea. In some cases, the drug can also cause more serious side effects such as arrhythmia.
See Also[edit | edit source]
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Contributors: Prab R. Tumpati, MD