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Updated: May 14, 2026

Assessing Autophagic Flux by Measuring LC3, p62, and LAMP1 Co-localization Using Multispectral Imaging Flow Cytometry
Published on: July 21, 2017
Cardiovascular autophagy: crossroads of pathology, pharmacology and toxicology
Joshua K Salabei1, Daniel J Conklin
1Department of Medicine, Diabetes and Obesity Center, University of Louisville, 580 S. Preston Street, Delia Baxter Building, Rm. 404E, Louisville, KY, 40292, USA.
Insights
Cardiovascular disease (CVD) treatments may be improved by understanding how FDA-approved drugs affect cellular autophagy. Harnessing drug-induced autophagy offers therapeutic potential for CVD management.
Area of Science:
- Biomedical Science
- Cellular Biology
- Cardiovascular Medicine
Background:
- Cardiovascular disease (CVD) is a leading global cause of mortality.
- Autophagy, a cellular recycling process, is implicated in various diseases, including CVD.
- FDA-approved drugs can induce autophagy-related side effects in the cardiovascular system.
Purpose of the Study:
- To review CVDs associated with autophagy.
- To examine FDA-approved drugs with cardiovascular autophagy-mediated side effects.
- To discuss the therapeutic potential of modulating autophagy for CVD.
Main Methods:
- Literature review of cardiovascular diseases and autophagy.
- Analysis of FDA-approved drugs and their impact on cardiovascular autophagy.
- Exploration of small molecule modulators for autophagy in CVD management.
Main Results:
- Autophagy is altered in numerous CVDs.
- Certain FDA-approved drugs induce cardiovascular side effects via autophagy.
- The role of autophagy in CVD can be adaptive or maladaptive.
Conclusions:
- Drug-induced autophagy presents both challenges and opportunities for CVD treatment.
- Careful consideration is needed to determine if autophagy modulation is beneficial.
- Small molecule autophagy modulators show promise for managing CVD progression.
Abstract:
Cardiovascular disease (CVD) remains the leading cause of death worldwide, despite the significant advances in medicine. Autophagy, a process of self-cannibalization employed by mammalian cells for the recycling of cellular contents, is altered not only in a number of CVDs, but in other diseases, as well. Many FDA-approved drugs are known to induce autophagy-mediated side effects in the cardiovascular system. In some cases, such drug-induced autophagy could be harnessed and used for treating CVD, greatly reducing the duration and cost of CVD treatments. However, because the induction of autophagy in cardiovascular targets can be both adaptive and maladaptive under specific settings, the challenge is to determine whether the changes stimulated by drug-induced autophagy are, in fact, beneficial. In this review, we surveyed a number of CVDs in which autophagy is known to occur, and we also address the role of FDA-approved drugs for which autophagy-mediated side effects occur within the cardiovascular system. The therapeutic potential of using small molecule modulators of autophagy in the management of CVD progression is discussed.
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