Phosphodiesterase inhibitors

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Overview[edit | edit source]

A phosphodiesterase inhibitor is a drug that blocks one or more of the five subtypes of the enzyme phosphodiesterase (PDE), therefore preventing the inactivation of the intracellular second messengers, cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP), by the respective PDE subtype(s).

History[edit | edit source]

These multiple forms or subtypes of phosphodiesterase were initially isolated from rat brain by Uzunov and Weiss in 1972^[1] and were soon afterward shown to be selectively inhibited by a variety of drugs in brain and other tissues. ^[2][3] The potential for selective phosphodisterase inhibitors to be used as therapeutic agents was predicted as early as 1977 by Weiss and Hait.^[4] This prediction has now come to pass in a variety of fields.

Classification[edit | edit source]

Non-selective phosphodiesterase inhibitors[edit | edit source]

1. the minor stimulant caffeine
2. the bronchodilator theophylline
3. IBMX (3-isobutyl-1-methylxanthine): used as investigative tool in pharmacological research

PDE1-selective inhibitors[edit | edit source]

1. Vinpocetine

PDE2-selective inhibitors[edit | edit source]

1. EHNA

PDE3-selective inhibitors[edit | edit source]

1. Enoximone and milrinone: used clinically for short-term treatment of cardiac failure. These drugs mimic sympathetic stimulation and increase cardiac output.
   PDE3 is sometimes referred to as cGMP-inhibited phosphodiesterase.

PDE4-selective inhibitors[edit | edit source]

1. Mesembrine: an alkaloid present in the herb Sceletium tortuosum
2. Rolipram: used as investigative tool in pharmacological research
3. Ibudilast, a neuroprotective and bronchodilator drug used mainly in the treatment of asthma and stroke, inhibits PDE-4 to the greatest extent, but also shows significant inhibition of other PDE subtypes, and so can be viewed either as a selective PDE-4 inhibitor or a non-selective phosphodiesterase inhibitor depending on the dose used.

PDE4 is the major cAMP-metabolizing enzyme found in inflammatory and immune cells. PDE4 inhibitors have proven potential as anti-inflammatory drugs especially in airway diseases. They suppress the release of inflammatory signals, e.g., cytokines, and inhibit the production of reactive oxygen species. PDE4 inhibitors have a high therapeutic and commercial potential as non-steroidal disease controllers in inflammatory airway diseases such as asthma, COPD and rhinitis. PDE4 inhibitors may have an antidepressant action^[5] and have also recently been proposed for use as antipsychotic medications.^[6][7]

PDE5-selective inhibitors[edit | edit source]

1. Sildenafil, tadalafil and vardenafil; and the newer ones, udenafil and avanafil: selectively inhibit (PDE5), which is cGMP-specific and responsible for the degradation of cGMP in the corpus cavernosum. These phosphodiesterase inhibitors are used primarily as remedies for erectile dysfunction, as well as having some other medical applications such as treatment of pulmonary hypertension.

References[edit | edit source]

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