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Updated: Feb 4, 2026

A Flow Cytometry-based Assay for Measuring Mitochondrial Membrane Potential in Cardiac Myocytes After Hypoxia/Reoxygenation
Published on: July 13, 2018
Hypoxia-inducible factor 1 signalling, metabolism and its therapeutic potential in cardiovascular disease
Maria da Luz Sousa Fialho1, Amira H Abd Jamil2, George A Stannard1
1Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK.
Insights
Cardiovascular disease (CVD) involves metabolic changes driven by hypoxia. Hypoxia-inducible factor (HIF) activation offers a potential therapeutic target for treating cardiac dysfunction and heart disease.
Area of Science:
- Cardiology
- Metabolic research
- Molecular biology
Background:
- Cardiovascular disease (CVD) is a leading cause of global mortality.
- Cardiac dysfunction in CVD is linked to altered energy metabolism.
- Hypoxia, or reduced oxygen, significantly impacts cardiac metabolism.
Purpose of the Study:
- To review cardiac energy metabolism in health and disease.
- To explore the role of hypoxia-inducible factor (HIF) in regulating cardiac metabolism.
- To assess the therapeutic potential of HIF activation for CVD.
Main Methods:
- Literature review of cardiac energy metabolism.
- Analysis of HIF signaling pathways in the heart.
- Overview of hypoxia-mimetic drug research.
Main Results:
- Hypoxia is a key driver of metabolic changes in ischemic heart disease.
- HIF-1α activation influences cardiac energy metabolism.
- Hypoxia-mimetic drugs show promise in other fields.
Conclusions:
- HIF is a potential therapeutic target for CVD.
- Systemic HIF-1α activation therapy warrants further investigation for cardiac conditions.
- Understanding metabolic regulation in the heart is crucial for CVD treatment.
Abstract:
Cardiovascular disease (CVD) accounts for the largest number of deaths worldwide, necessitating the development of novel treatments and prevention strategies. Given the huge energy demands placed on the heart, it is not surprising that changes in energy metabolism play a key role in the development of cardiac dysfunction in CVD. A reduction in oxygen delivery to the heart, hypoxia, is sensed and responded to by the hypoxia-inducible factor (HIF) and its family of proteins, by regulating the oxygen-dependent signalling cascade and subsequent response. Hypoxia is one of the main drivers of metabolic change in ischaemic disease and myocardial infarction, and we therefore suggest that HIF may be an attractive therapeutic target. In this review, we assess cardiac energy metabolism in health and disease, and how these can be regulated by HIF-1α activation. We then present an overview of research in the field of hypoxia-mimetic drugs recently developed in other treatment fields, which provide insight into the potential of systemic HIF-1α activation therapy for treating the heart.
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