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October 17, 2011Physiological ResearchOpen Access

Distinct Effects of Acute Pretreatment With Lipophilic and Hydrophilic Statins on Myocardial Stunning, Arrhythmias and Lethal Injury in the Rat Heart Subjected to Ischemia/Reperfusion

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Key result

Acute pretreatment with pravastatin and simvastatin significantly reduced infarct size to 10% and 27% respectively, compared to 42% in untreated control rat hearts subjected to ischemia/reperfusion.

Why the study?

Does acute pretreatment with simvastatin or pravastatin reduce myocardial stunning, arrhythmias, and lethal injury in isolated rat hearts subjected to ischemia/reperfusion?

Population

Isolated hearts from male Wistar rats subjected to 30-min global ischemia and reperfusion.

Comparison

Simvastatin or pravastatin given as components… vs Control untreated hearts perfused with perfusion…

Design

Preclinical

Follow-up

2-h reperfusion

Authors

SČSlávka ČarnickáAAAdriana AdameováMNMartina Nemčeková

Discussion

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Overview

Should not yet change clinical practice; hypothesis-generating for acute statin cardioprotection in ischemia/reperfusion.

Structured PICO

Does acute pretreatment with simvastatin or pravastatin reduce myocardial stunning, arrhythmias, and lethal injury in isolated rat hearts subjected to ischemia/reperfusion?

P
Population
Approximately 36 isolated hearts from male Wistar rats subjected to 30-minute global ischemia and 2-hour reperfusion.
I
Intervention
Simvastatin (10 micromol/l) or pravastatin (30 micromol/l) given as components of the perfusion medium 15 min prior to ischemia.
C
Comparator
Control untreated hearts perfused with perfusion medium only for an additional 15 min.
O
Outcome
Postischemic contractile dysfunction, reperfusion-induced ventricular arrhythmias, and infarct size after 30-min global ischemia and 2-h reperfusion.surrogate

Main Result

Absolute Event Rate: 10% vs 42%

p-value: p=<0.05

Differences in water solubility of statins may underlie their distinct cardioprotective effects on myocardial stunning and lethal injury induced by ischemia/reperfusion.

Limitations

  • Animal model (isolated rat hearts) which may not fully translate to human clinical settings
  • Statins were administered acutely prior to ischemia rather than as a chronic treatment

Cite This Study

Čarnická et al. (2011) studied Myocardial ischemia/reperfusion injury (n=36). Simvastatin and Pravastatin vs. Perfusion medium only (Control) was evaluated on Infarct size (percentage of left ventricular area) (p=<0.05). Acute pretreatment with pravastatin and simvastatin significantly reduced infarct size to 10% and 27% respectively, compared to 42% in untreated control rat hearts subjected to ischemia/reperfusion.

synapsesocial.com/papers/6a86f12ea810ea404bcf96e1https://doi.org/10.33549/physiolres.932232
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