Dipyridamole

Dipyridamole

Clinical data
Trade names	Persantine, others
AHFS/Drugs.com	Monograph
MedlinePlus	a682830
Routes of administration	By mouth, intravenous
ATC code	B01AC07 ( WHO )
Legal status
Legal status	UK: POM (Prescription only) US: ℞-only
Pharmacokinetic data
Bioavailability	37–66% [1]
Protein binding	~99%
Metabolism	Liver (glucuronidation) [2]
Elimination half-life	α phase: 40 min, β phase: 10 hours
Excretion	Biliary (95%), urine (negligible)
Identifiers
IUPAC name 2,2',2'',2'''-(4,8-di(piperidin-1-yl)pyrimido[5,4-d]pyrimidine-2,6-diyl)bis(azanetriyl)tetraethanol
CAS Number	58-32-2  Y
PubChem CID	3108
IUPHAR/BPS	4807
DrugBank	DB00975  Y
ChemSpider	2997  Y
UNII	64ALC7F90C
KEGG	D00302  Y
ChEBI	CHEBI:4653  Y
ChEMBL	ChEMBL932  Y
CompTox Dashboard (EPA)	DTXSID6040668
ECHA InfoCard	100.000.340
Chemical and physical data
Formula	C24H40N8O4
Molar mass	504.636 g·mol−1
3D model (JSmol)	Interactive image
SMILES C1CCN(CC1)C2=NC(=NC3=C2N=C(N=C3N4CCCCC4)N(CCO)CCO)N(CCO)CCO
InChI InChI=1S/C24H40N8O4/c33-15-11-31(12-16-34)23-26-20-19(21(27-23)29-7-3-1-4-8-29)25-24(32(13-17-35)14-18-36)28-22(20)30-9-5-2-6-10-30/h33-36H,1-18H2 Y Key:IZEKFCXSFNUWAM-UHFFFAOYSA-N Y
(verify)

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. ^[3]
• 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. ^[4]
• 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. ^[5]
• 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). ^[6]

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. ^[3] Dipyridamole absorption is pH-dependent and concomitant treatment with gastric acid suppressors (such as a proton pump inhibitor) will inhibit the absorption of liquid and plain tablets. ^{[7] [8] [9] [10]}

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. ^[11]

A triple therapy of aspirin, clopidogrel, and dipyridamole has been investigated, but this combination led to an increase in adverse bleeding events. ^[12]

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. ^[13]

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. ^[14]

Overdose

Dipyridamole overdose can be treated with aminophylline ^{[2] : 6} 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 ^[3] 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

1. Nielsen-Kudsk F, Pedersen AK (May 1979). "Pharmacokinetics of dipyridamole". Acta Pharmacologica et Toxicologica. 44 (5): 391–399. doi:10.1111/j.1600-0773.1979.tb02350.x. PMID   474151.
2. "Aggrenox (aspirin/extended-release dipyridamole) Capsules. Full Prescribing Information" (PDF). Boehringer Ingelheim Pharmaceuticals, Inc. Retrieved 1 December 2016.
3. Brown DG, Wilkerson EC, Love WE (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. 72 (3): 524–534. doi:10.1016/j.jaad.2014.10.027. PMID   25486915.
4. Dixon BS, Beck GJ, Vazquez MA, Greenberg A, Delmez JA, Allon M, et al. (May 2009). "Effect of dipyridamole plus aspirin on hemodialysis graft patency". The New England Journal of Medicine. 360 (21): 2191–2201. doi:10.1056/nejmoa0805840. PMC   3929400 . PMID   19458364.
5. Dipyridamole in the laboratory: Fata-Hartley CL, Palmenberg AC (September 2005). "Dipyridamole reversibly inhibits mengovirus RNA replication". Journal of Virology. 79 (17): 11062–11070. doi:10.1128/JVI.79.17.11062-11070.2005. PMC   1193570 . PMID   16103157.
6. Winkelman JW, Berkowski JA, DelRosso LM, Koo BB, Scharf MT, Sharon D, et al. (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. 21 (1): 137–152. doi: 10.5664/jcsm.11390 . PMC   11701286 . PMID   39324694.
7. Russell TL, Berardi RR, Barnett JL, O'Sullivan TL, Wagner JG, Dressman JB (January 1994). "pH-related changes in the absorption of dipyridamole in the elderly". Pharmaceutical Research. 11 (1): 136–43. doi:10.1023/a:1018918316253. hdl: 2027.42/41435 . PMID   7908130. S2CID   12877330.
8. Derendorf H, VanderMaelen CP, Brickl RS, MacGregor TR, Eisert W (July 2005). "Dipyridamole bioavailability in subjects with reduced gastric acidity". Journal of Clinical Pharmacology. 45 (7): 845–50. doi:10.1177/0091270005276738. PMID   15951475. S2CID   36579161.
9. "Persantin Retard 200mg - Summary of Product Characteristics (SPC)". Electronic Medicines Compendium (EMC). Archived from the original on 5 July 2009. Retrieved 6 February 2010.
10. Stockley I (2009). Stockley's Drug Interactions. The Pharmaceutical Press. ISBN   978-0-85369-424-3.
11. De Schryver EL, Algra A, van Gijn J (July 2007). Algra A (ed.). "Dipyridamole for preventing stroke and other vascular events in patients with vascular disease". The Cochrane Database of Systematic Reviews (3): CD001820. doi:10.1002/14651858.CD001820.pub3. PMID   17636684.
12. Sprigg N, Gray LJ, England T, Willmot MR, Zhao L, Sare GM, et al. (August 2008). Berger JS (ed.). "A randomised controlled trial of triple antiplatelet therapy (aspirin, clopidogrel and dipyridamole) in the secondary prevention of stroke: safety, tolerability and feasibility". PLOS ONE. 3 (8): e2852. Bibcode:2008PLoSO...3.2852S. doi: 10.1371/journal.pone.0002852 . PMC   2481397 . PMID   18682741.
13. Gamboa A, Abraham R, Diedrich A, Shibao C, Paranjape SY, Farley G, et al. (October 2005). "Role of adenosine and nitric oxide on the mechanisms of action of dipyridamole". Stroke. 36 (10): 2170–5. doi:10.1161/01.STR.0000179044.37760.9d. PMID   16141426. S2CID   1877425.
14. AAGBI Guidelines Neuraxial and Coagulation June 2016