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Ticagrelor protects the heart against reperfusion injury and improves remodeling after myocardial infarction
Yumei Ye1, Gilad D Birnbaum1, Jose R Perez-Polo1
1From the Department of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston (Y.Y., J.R.P.-P., M.K.N., Y.B.); Section of Cardiology, Baylor College of Medicine, Houston, TX (G.D.B., Y.B.); and AstraZeneca R&D, Mölndal, Sweden (S.N.).
Insights
Ticagrelor, but not clopidogrel, reduces infarct size and improves heart function after ischemia. This P2Y12 inhibitor offers cardioprotection through adenosine signaling, unlike clopidogrel.
Area of Science:
- Cardiovascular Pharmacology
- Myocardial Ischemia-Reperfusion Injury
Background:
- Ticagrelor, a P2Y12 receptor antagonist, also inhibits adenosine uptake.
- Previous studies suggest ticagrelor pretreatment limits infarct size.
- The acute and long-term effects of ticagrelor versus clopidogrel on infarct size and cardiac function remain to be fully elucidated.
Purpose of the Study:
- To investigate the acute effects of ticagrelor and clopidogrel on myocardial infarct size.
- To explore the potential long-term effects of these agents on cardiac function following ischemia-reperfusion injury.
- To compare the mechanisms underlying the cardioprotective effects of ticagrelor and clopidogrel.
Main Methods:
- Rats underwent a 30-minute ischemia followed by 24-hour reperfusion.
- Agents were administered either acutely before reperfusion or chronically for 4 weeks.
- Infarct size, cardiac function (left ventricular ejection fraction), apoptosis, fibrosis, and inflammatory markers were assessed.
Main Results:
- Ticagrelor significantly reduced infarct size dose-dependently and improved left ventricular ejection fraction with acute, chronic, or combined treatment.
- Clopidogrel showed no significant effect on infarct size or cardiac function.
- Ticagrelor increased myocardial adenosine levels, enhanced pro-survival signaling pathways (Akt, eNOS, ERK1/2), decreased apoptosis and fibrosis, and modulated inflammatory responses, effects not observed with clopidogrel.
Conclusions:
- Ticagrelor, administered acutely before reperfusion, provides significant protection against ischemia-reperfusion injury.
- Both acute and chronic ticagrelor treatments, as well as their combination, improve long-term heart function.
- Despite similar P2Y12 inhibition, clopidogrel lacks the cardioprotective effects observed with ticagrelor, highlighting the role of adenosine-mediated pathways.
Objective:
In addition to P2Y12 receptor antagonism, ticagrelor inhibits adenosine cell uptake. Prior data show that 7-day pretreatment with ticagrelor limits infarct size. We explored the acute effects of ticagrelor and clopidogrel on infarct size and potential long-term effects on heart function.
Approach And Results:
Rats underwent 30-minute ischemia per 24-hour reperfusion. (1) Ticagrelor (10 or 30 mg/kg) or clopidogrel (12.5 mg/kg) was given via intraperitoneal injection 5 minutes before reperfusion. (2) Rats received ticagrelor acute (intraperitoneal; 30 mg/kg), chronic (oral; 300 mg/kg per day) for 4 weeks starting 1 day after reperfusion or the combination (acute+chronic). Another group received clopidogrel (intraperitoneal [12.5 mg/kg]+oral [62.5 mg/kg per day]) for 4 weeks. (1) Ticagrelor dose-dependently reduced infarct size, 10 mg/kg (31.5%±1.8%; P<0.001) and 30 mg/kg (21.4%±2.6%; P<0.001) versus control (45.3±1.7%), whereas clopidogrel had no effect (42.4%±2.6%). Ticagrelor, but not clopidogrel, increased myocardial adenosine levels, increased phosphorylation of Akt, endothelial NO synthase, and extracellular-signal-regulated kinase 1/2 4 hours after reperfusion and decreased apoptosis. (2) After 4 weeks, left ventricular ejection fraction was reduced in the vehicle-treated group (44.8%±3.5%) versus sham (77.6%±0.9%). All ticagrelor treatments improved left ventricular ejection fraction, acute (69.5%±1.6%), chronic (69.2%±1.0%), and acute+chronic (76.3%±1.2%), whereas clopidogrel had no effect (37.4%±3.7%). Ticagrelor, but not clopidogrel, attenuated fibrosis and decreased collagen-III mRNA levels 4 weeks after ischemia/reperfusion. Ticagrelor, but not clopidogrel, attenuated the increase in proinflammatory tumor necrosis factor-α, interleukin-1β, and interleukin-18, and increased anti-inflammatory 15-epi-lipoxin-A4 levels.
Conclusions:
Ticagrelor, but not clopidogrel, administered just before reperfusion protects against reperfusion injury. This acute treatment or chronic ticagrelor for 4 weeks or their combination improved heart function, whereas clopidogrel, despite achieving a similar degree of platelet inhibition, had no effect.
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