Animal models of pulmonary hypertension: Getting to the heart of the problem
- PMID: 33724447
- DOI: 10.1111/bph.15444
Animal models of pulmonary hypertension: Getting to the heart of the problem
Abstract
Despite recent therapeutic advances, pulmonary hypertension (PH) remains a fatal disease due to the development of right ventricular (RV) failure. At present, no treatments targeted at the right ventricle are available, and RV function is not widely considered in the preclinical assessment of new therapeutics. Several small animal models are used in the study of PH, including the classic models of exposure to either hypoxia or monocrotaline, newer combinational and genetic models, and pulmonary artery banding, a surgical model of pure RV pressure overload. These models reproduce selected features of the structural remodelling and functional decline seen in patients and have provided valuable insight into the pathophysiology of RV failure. However, significant reversal of remodelling and improvement in RV function remains a therapeutic obstacle. Emerging animal models will provide a deeper understanding of the mechanisms governing the transition from adaptive remodelling to a failing right ventricle, aiding the hunt for druggable molecular targets. LINKED ARTICLES: This article is part of a themed issue on Preclinical Models for Cardiovascular disease research (BJP 75th Anniversary). To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v179.5/issuetoc.
Keywords: SU5416; animal models; chronic hypoxia; monocrotaline; pulmonary artery banding; pulmonary hypertension; right ventricular failure; right ventricular hypertrophy.
© 2021 The Authors. British Journal of Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society.
References
REFERENCES
-
- Abe, K., Toba, M., Alzoubi, A., Ito, M., Fagan, K. A., Cool, C. D., Voelkel, N. F., McMurtry, I. F., & Oka, M. (2010). Formation of plexiform lesions in experimental severe pulmonary arterial hypertension. Circulation, 121, 2747-2754.
-
- Abraham, W. T., Adams, K. F., Fonarow, G. C., Costanzo, M. R., Berkowitz, R. L., Lejemtel, T. H., Cheng, M. L., Wynne, J., & ADHERE Scientific Advisory Committee and Investigators, ADHERE Study Group. (2005). In-hospital mortality in patients with acute decompensated heart failure requiring intravenous vasoactive medications: An analysis from the Acute Decompensated Heart Failure National Registry (ADHERE). Journal of the American College of Cardiology, 46, 57-64.
-
- Agarwal, S., Harter, Z. J., Krishnamachary, B., Chen, L., Nguyen, T., Voelkel, N. F., & Dhillon, N. K. (2020). Sugen-morphine model of pulmonary arterial hypertension. Pulmonary Circulation, 10, 2045894019898376.
-
- Akazawa, Y., Okumura, K., Ishii, R., Slorach, C., Hui, W., Ide, H., Honjo, O., Sun, M., Kabir, G., Connelly, K., & Friedberg, M. K. (2020). Pulmonary artery banding is a relevant model to study the right ventricular remodeling and dysfunction that occurs in pulmonary arterial hypertension. Journal of Applied Physiology, 129, 238-246.
-
- Akhavein, F., Jean St-Michel, E., Seifert, E., & Rohlicek, C. V. (2007). Decreased left ventricular function, myocarditis, and coronary arteriolar medial thickening following monocrotaline administration in adult rats. Journal of Applied Physiology, 103, 287-295.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical