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Interaction of Risk Factors, Comorbidities, and Comedications with Ischemia/Reperfusion Injury and Cardioprotection by Preconditioning, Postconditioning, and Remote Conditioning

Journal

PHARMACOLOGICAL REVIEWS
Volume 66, Issue 4, Pages 1142-1174

Publisher

AMER SOC PHARMACOLOGY EXPERIMENTAL THERAPEUTICS
DOI: 10.1124/pr.113.008300

Keywords

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Funding

  1. British Heart Foundation [FS/10/039/28270]
  2. RoseTrees Trust
  3. German Research Foundation [DFG Schu 843/7-1, DFG Schu 843/7-2, DFG Schu 843/9-1, He 1320/18-1, He 1320/18-3]
  4. National Research Fund of Hungary [ANN 107803, K 109737]
  5. European Foundation for the Study of Diabetes
  6. National Institute for Health Research University College London Hospitals Biomedical Research Centre
  7. National Excellence Program of Hungary [TAMOP 4.2.4.A/2-11-1-2012-0001]
  8. British Heart Foundation [PG/08/013/24504] Funding Source: researchfish

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Pre-, post-, and remote conditioning of the myocardium are well described adaptive responses that markedly enhance the ability of the heart to withstand a prolonged ischemia/reperfusion insult and provide therapeutic paradigms for cardioprotection. Nevertheless, more than 25 years after the discovery of ischemic preconditioning, we still do not have established cardioprotective drugs on the market. Most experimental studies on cardioprotection are still undertaken in animal models, in which ischemia/reperfusion is imposed in the absence of cardiovascular risk factors. However, ischemic heart disease in humans is a complex disorder caused by, or associated with, cardiovascular risk factors and comorbidities, including hypertension, hyperlipidemia, diabetes, insulin resistance, heart failure, altered coronary circulation, and aging. These risk factors induce fundamental alterations in cellular signaling cascades that affect the development of ischemia/reperfusion injury per se and responses to cardioprotective interventions. Moreover, some of the medications used to treat these risk factors, including statins, nitrates, and antidiabetic drugs, may impact cardioprotection by modifying cellular signaling. The aim of this article is to review the recent evidence that cardiovascular risk factors and their medication may modify the response to cardioprotective interventions. We emphasize the critical need to take into account the presence of cardiovascular risk factors and concomitant medications when designing preclinical studies for the identification and validation of cardioprotective drug targets and clinical studies. This will hopefully maximize the success rate of developing rational approaches to effective cardioprotective therapies for the majority of patients with multiple risk factors.

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