Repurposing Cilostazol for Raynaud's Phenomenon

被引:10
作者
El-Hachem, Nehme [1 ]
Fardoun, Manal M. [2 ]
Slika, Hasan [3 ]
Baydoun, Elias [2 ]
Eid, Ali H. [3 ,4 ]
机构
[1] Natl Med Res Ctr Cardiol, Inst Expt Cardiol, Lab Med Genet, Beirut, Lebanon
[2] Amer Univ Beirut, Dept Biol, Beirut, Lebanon
[3] Amer Univ Beirut, Fac Med, Dept Pharmacol & Toxicol, POB 11-0236, Beirut, Lebanon
[4] Qatar Univ, Dept Biomed Sci, Doha, Qatar
关键词
Cardiovascular disease; cilostazol; digital ischemia; drug repurposing; Raynaud's phenomenon; Cold-induced vasoconstriction; DOUBLE-BLIND; PATHOGENESIS; ADENOSINE; ISCHEMIA; INHIBITOR; RECEPTORS; INCREASE; WILLOW; DRUGS;
D O I
10.2174/0929867327666200903114154
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:2409 / 2417
页数:9
相关论文
共 50 条
[41]   Botulinum Toxin Type A in the Treatment of Raynaud's Phenomenon [J].
Neumeister, Michael W. .
JOURNAL OF HAND SURGERY-AMERICAN VOLUME, 2010, 35A (12) :2085-2092
[42]   Raynaud’s phenomenon—an update on diagnosis, classification and management [J].
John D Pauling ;
Michael Hughes ;
Janet E Pope .
Clinical Rheumatology, 2019, 38 :3317-3330
[43]   Pathophysiology of Raynaud's phenomenon. [J].
Mourad, JJ ;
Priollet, P .
REVUE DE MEDECINE INTERNE, 1997, 18 (08) :611-617
[44]   Chromosome aberrations in Raynaud's phenomenon [J].
Porciello, G ;
Scarpato, R ;
Storino, F ;
Migliore, L ;
Ferri, C ;
Cagetti, F ;
Morozzi, G ;
Bellisai, F ;
Marcolongo, R ;
Galeazzi, M .
EUROPEAN JOURNAL OF DERMATOLOGY, 2004, 14 (05) :327-331
[45]   Homocysteine and Raynaud's phenomenon: A review [J].
Lazzerini, Pietro Enea ;
Capecchi, Pier Leopoldo ;
Bisogno, Stefania ;
Cozzalupi, Mauro ;
Rossi, Pier Carlo ;
Pasini, Franco Laghi .
AUTOIMMUNITY REVIEWS, 2010, 9 (03) :181-187
[46]   Raynaud's Phenomenon: Beware of Cancers! [J].
Aqodad, Zahida ;
Bachir, Houda ;
Alaoui, Habiba ;
Hamaz, Siham ;
Serraj, Khalid, Sr. .
CUREUS JOURNAL OF MEDICAL SCIENCE, 2021, 13 (03)
[47]   Vasodilators for primary Raynaud's phenomenon [J].
Su, Kevin Y. C. ;
Sharma, Meghna ;
Kim, Hyunjun Jonathan ;
Kaganov, Elizabeth ;
Hughes, Ian ;
Abdeen, Mohamed Hashim ;
Ng, Jennifer Hwee Kwoon .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2021, (05)
[48]   Phosphodiesterase inhibitors in Raynaud's phenomenon [J].
Levien, Terri L. .
ANNALS OF PHARMACOTHERAPY, 2006, 40 (7-8) :1388-1393
[49]   Differential diagnoses of Raynaud's phenomenon [J].
Ahrazoglu, M. ;
Moinzadeh, P. ;
Hunzelmann, N. .
DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT, 2014, 139 (20) :1064-1069
[50]   Primary and secondary Raynaud's phenomenon [J].
Distler, J. H. W. .
ZEITSCHRIFT FUR RHEUMATOLOGIE, 2008, 67 (03) :211-217