Repurposing Cilostazol for Raynaud's Phenomenon.

Cardiovascular disease Cold-induced vasoconstriction Raynaud's phenomenon cilostazol digital ischemia drug repurposing

Journal

Current medicinal chemistry
ISSN: 1875-533X
Titre abrégé: Curr Med Chem
Pays: United Arab Emirates
ID NLM: 9440157

Informations de publication

Date de publication:
2021
Historique:
received: 30 04 2020
revised: 16 07 2020
accepted: 21 07 2020
pubmed: 4 9 2020
medline: 28 5 2021
entrez: 4 9 2020
Statut: ppublish

Résumé

Raynaud 's Phenomenon (RP) results from exaggerated cold-induced vasoconstriction. RP patients suffer from vasospastic attacks and compromised digital blood perfusion leading to a triple color change at the level the fingers. Severe RP may cause ulcers and threaten tissue viability. Many drugs have been used to alleviate the symptoms of RP. These include calcium-channel blockers, cGMP-specific phosphodiesterase type 5 inhibitors, prostacyclin analogs, and angiotensin receptor blockers. Despite their variety, these drugs do not treat RP but rather alleviate its symptoms. To date, no drug for RP has been yet approved by the U.S Food and Drugs Administration. Cilostazol is a selective inhibitor of phosphodiesterase-III, originally prescribed to treat intermittent claudication. Owing to its antiplatelet and vasodilating properties, cilostazol is being repurposed as a potential drug for RP. This review focuses on the different lines of action of cilostazol serving to enhance blood perfusion in RP patients.

Identifiants

pubmed: 32881655
pii: CMC-EPUB-109647
doi: 10.2174/0929867327666200903114154
doi:

Substances chimiques

Calcium Channel Blockers 0
Cilostazol N7Z035406B

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

2409-2417

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Nehme El-Hachem (N)

Laboratory of Medical Genetics, Institute of Experimental Cardiology, National Medical Research Center of Cardiology, Beirut, Lebanon.

Manal M Fardoun (MM)

Department of Biology, American University of Beirut, Beirut, Lebanon.

Hasan Slika (H)

Department of Pharmacology and Toxicology, Faculty of Medicine, American University of Beirut, Beirut, Lebanon.

Elias Baydoun (E)

Department of Biology, American University of Beirut, Beirut, Lebanon.

Ali H Eid (AH)

Department of Pharmacology and Toxicology, Faculty of Medicine, American University of Beirut, Beirut, Lebanon.

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Classifications MeSH