Over the last decades, several lifestyle modifications and therapeutic approaches have been employed for preventing and treating cardiovascular diseases (CVDs), which remain the leading cause of death worldwide. Because of the impact of CVDs, their molecular mechanisms and long-term side effects are under continuous investigation. To date, the contribution provided by both small and large animal models has been fundamental to improve the knowledge related to the diagnosis and the treatment of CVDs. The ideal experimental model should reproduce, as much as possible, the aspect or aspects of disease being investigated, keeping in mind the complexity of human CVDs and that several factors, such as genetics and environment, strongly influence cardiovascular physiopathology; therefore, a single experimental model cannot fully recapitulate a specific CVD. In cardiovascular disease research, different models of atherothrombotic disease, coronary heart disease (CHD), abdominal aortic aneurysm, heart failure (HF) secondary to ischemia/reperfusion, valvular heart disease, dilated or hypertensive cardiomyopathy, metabolic syndrome, and chemotherapy are employed. For instance, animal models are essential in the preclinical evaluation of therapeutic approaches to CHD and HF to assess ischemic pre-post and remote conditioning strategies and pharmacological treatments. These include vector-mediated cardiac gene delivery and stem cell therapy to prevent cardiac damage and stimulate cardiac repair, as well as cardioprotective strategies utilizing microvesicles, exosomes, and other cellular and molecular agents. This methods collection aims to expand the understanding of these experimental protective approaches for reducing the gap between the pre-clinical and clinical settings for the development of new therapeutic interventions for human CVDs.
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Cited by 14
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2021
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Gábor B Brenner*1,2, Zoltán Giricz*1,2, Rita Garamvölgyi3,4, András Makkos1, Zsófia Onódi1, Nabil V Sayour1, Tamás G Gergely1, Tamás Baranyai1, Örs Petneházy3,4, Dénes Kőrösi3, Gergő P. Szabó3, Hajnalka Vago5, Zsófia Dohy5, Csilla Czimbalmos5, Béla Merkely5, Swetlana Boldin-Adamsky6, Elena Feinstein6, Iván G Horváth7, Péter Ferdinandy1,2
1Department of Pharmacology and Pharmacotherapy, Semmelweis University, 2Pharmahungary Group, 3Diagnostic, Radiation Oncology, Research and Teaching Center, Moritz Kaposi Somogy County Teaching Hospital, 4Faculty of Agricultural and Environmental Sciences, Kaposvar University, 5Heart and Vascular Center, Semmelweis University, 6Quark Pharmaceuticals, Inc, 7Heart Institute, Medical School, University of Pécs
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Cited by 1
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2021
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Manuel Lasch1,2,3, Mykhailo Vladymyrov4, Dominic van den Heuvel1,5, Philipp Götz1,3, Elisabeth Deindl1,3, Hellen Ishikawa-Ankerhold1,5
1Walter-Brendel-Centre of Experimental Medicine, University Hospital, Ludwig-Maximilians-Universität München, 2Department of Otorhinolaryngology, Head & Neck Surgery, University Hospital, Ludwig-Maximilians-Universität München, 3Biomedical Center, Institute of Cardiovascular Physiology and Pathophysiology, Faculty of Medicine, Ludwig-Maximilians-Universität München, 4TKI, University of Bern, 5Department of Internal Medicine I and Cardiology, University Hospital, Ludwig-Maximilians-Universität München
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Cited by 11
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2022
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Michelle Mendiola Pla1, Amy Evans2, Franklin H. Lee3, Yuting Chiang1, Muath Bishawi1, Andrew Vekstein1, Lillian Kang1, Diego Zapata4, Ryan Gross3, Alexis Carnes2, Lynden E. Gault5, Julie A. Balko6, Desiree Bonadonna2, Sam Ho5, Paul Lezberg7, Benjamin S. Bryner1, Jacob N. Schroder1, Carmelo A. Milano1, Dawn E. Bowles3
1Division of Cardiothoracic Surgery, Department of Surgery, Duke University, 2Perfusion Services, Duke University, 3Division of Surgical Sciences, Department of Surgery, Duke University, 4Division of Laboratory Animal Resources, Duke University, 5Gift of Hope Organ and Tissue Donor Network, 6College of Veterinary Medicine, North Carolina State University, 7TransMedics, Inc