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. 2021 Dec 29;11(1):78. doi: 10.3390/antiox11010078

Table 3.

EVs as target (pharmacological modulation of plasma EVs).

Extracellular Vesicles as a Therapeutic Target (Therapeutical Approach)
Drugs Species EVs Levels (Plasma)
↑: Increase
↓: Decrease
Diseases Beneficial Effect References
Antioxidants Human Inflammatory pathologies: atherosclerosis, CKD, CVD, CVD associated-CKD
Hemostasia disorders
Aging
Improved endothelial function
↓ evolution of chronic disease (CVD associated-CKD)
[158,185,195]
Antioxidants Human Atherosclerosis
Diabetic patients
Dyslipidaemic patients
↓ endothelial injury
↓ platelet activation
[187]
Erythropoietin therapy Human
(endothelial EVs)
CKD in the end-stage ↓ shear stress [201]
Anti-atherosclerotic drugs
(angiotensin-II receptor antagonists or blockers)
Human Hypertension patients ↓ endothelial injury
↓ coagulation
↓ inflammation
[196,202]
Statins Human CVD
(the process of atherogenesis)
↓ cholesterol
↓ vascular inflammation
↓ platelet aggregation
[187,203]
Simvastatin + Losartan Human
(monocyte-, endothelial- and platelet-EVs)
Patients with hypertension
Patients with type 2 diabetes
↓ cholesterol
↓ endothelial injury
↓ coagulation
↓ inflammation
[187]
Peroxisome proliferator-activated receptor (PPAR) activators Human
(platelet-derived EVs)
DyslipidaemiaType 2 diabetes Anti-inflammatory properties [187]
Antiplatelet drugs (Aspirin, Clopidogrel) Human
(platelet- and endothelial-derived EVs)
Coronary disease ↓ platelet aggregation [187,202]
Angiotensin-converting enzyme (ACE) inhibitors (Irbesartan) Human atherosclerosis ↑ endothelial progenitor cells [181]