From Surf Wiki (app.surf) — the open knowledge base
Dipyridamole
Anticoagulant drug
Anticoagulant drug
| Drugs.com =
| elimination_half-life = α phase: 40 min, β phase: 10 hours
Dipyridamole, sold under the brand name Persantine among others, is an antiplatelet drug of the nucleoside transport inhibitor and PDE3 inhibitor class that inhibits blood clot formation when given chronically and causes blood vessel dilation when given at high doses over a short time.
Medical uses
- Dipyridamole is used to dilate blood vessels in people with peripheral arterial disease and coronary artery disease.
- Dipyridamole has been shown to lower pulmonary hypertension without significant drop of systemic blood pressure.
- It inhibits proliferation of smooth muscle cells in vivo and modestly increases unassisted patency of synthetic arteriovenous hemodialysis grafts.
- Cyclic adenosine monophosphate impairs platelet aggregation and also causes arteriolar smooth muscle relaxation. Chronic therapy did not show significant drop of systemic blood pressure.
- It inhibits the replication of mengovirus RNA.
- It can be used for myocardial stress testing as an alternative to exercise-induced stress methods such as treadmills.
- It is an experimental agent used for the treatment of restless leg syndrome, conditionally recommended by the American Academy of Sleep Medicine as a second-line treatment (conditional recommendation, low certainty of evidence).
Stroke
A combination of dipyridamole and aspirin (acetylsalicylic acid/dipyridamole) is FDA-approved for the secondary prevention of stroke and has a bleeding risk equal to that of aspirin use alone.
However, it is not licensed as monotherapy for stroke prophylaxis, although a Cochrane review suggested that dipyridamole may reduce the risk of further vascular events in patients presenting after cerebral ischemia.
A triple therapy of aspirin, clopidogrel, and dipyridamole has been investigated, but this combination led to an increase in adverse bleeding events.
Interactions
Due to its action as a phosphodiesterase inhibitor, dipyridamole is likely to potentiate the effects of adenosine. This occurs by blocking the nucleoside transporter (ENT1) through which adenosine enters erythrocyte and endothelial cells.
According to Association of Anaesthetists of Great Britain and Ireland 2016 guidelines, dipyridamole is considered to not cause risk of bleeding when receiving neuroaxial anaesthesia and deep nerve blocks. It does not therefore require cessation prior to anaesthesia with these techniques, and can continue to be taken with nerve block catheters in place.
Overdose
Dipyridamole overdose can be treated with aminophylline or caffeine which reverses its dilating effect on the blood vessels. Symptomatic treatment is recommended, possibly including a vasopressor drug. Gastric lavage should be considered. Since dipyridamole is highly protein bound, dialysis is not likely to be of benefit.
Mechanisms of action
Dipyridamole has two known effects, acting via different mechanisms of action:
- Dipyridamole inhibits the phosphodiesterase enzymes that normally break down cAMP (increasing cellular cAMP levels and blocking the platelet aggregation, response to ADP) and/or cGMP.
- Dipyridamole inhibits the cellular reuptake of adenosine into platelets, red blood cells, and endothelial cells, leading to increased extracellular concentrations of adenosine.
References
References
- (May 1979). "Pharmacokinetics of dipyridamole". Acta Pharmacologica et Toxicologica.
- "Aggrenox (aspirin/extended-release dipyridamole) Capsules. Full Prescribing Information". Boehringer Ingelheim Pharmaceuticals, Inc..
- (May 2009). "Effect of dipyridamole plus aspirin on hemodialysis graft patency". The New England Journal of Medicine.
- (September 2005). "Dipyridamole reversibly inhibits mengovirus RNA replication". Journal of Virology.
- (January 2025). "Treatment of restless legs syndrome and periodic limb movement disorder: an American Academy of Sleep Medicine clinical practice guideline". Journal of Clinical Sleep Medicine.
- (January 1994). "pH-related changes in the absorption of dipyridamole in the elderly". Pharmaceutical Research.
- (July 2005). "Dipyridamole bioavailability in subjects with reduced gastric acidity". Journal of Clinical Pharmacology.
- "Persantin Retard 200mg - Summary of Product Characteristics (SPC)". Electronic Medicines Compendium (EMC).
- (2009). "Stockley's Drug Interactions". The Pharmaceutical Press.
- (July 2007). "Dipyridamole for preventing stroke and other vascular events in patients with vascular disease". The Cochrane Database of Systematic Reviews.
- (August 2008). "A randomised controlled trial of triple antiplatelet therapy (aspirin, clopidogrel and dipyridamole) in the secondary prevention of stroke: safety, tolerability and feasibility". PLOS ONE.
- (October 2005). "Role of adenosine and nitric oxide on the mechanisms of action of dipyridamole". Stroke.
- AAGBI Guidelines Neuraxial and Coagulation June 2016
- (March 2015). "A review of traditional and novel oral anticoagulant and antiplatelet therapy for dermatologists and dermatologic surgeons". Journal of the American Academy of Dermatology.
This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.
Ask Mako anything about Dipyridamole — get instant answers, deeper analysis, and related topics.
Research with MakoFree with your Surf account
Create a free account to save articles, ask Mako questions, and organize your research.
Sign up freeThis content may have been generated or modified by AI. CloudSurf Software LLC is not responsible for the accuracy, completeness, or reliability of AI-generated content. Always verify important information from primary sources.
Report