# Angiotensin-Converting Enzyme Inhibitors and Metabolic Aging: A Drosophila Perspective

**Authors:** Denise Vecchie’, Victoria G. Faber, Patricia Jumbo-Lucioni, Robert R. H. Anholt, Trudy F. C. Mackay, Maria De Luca

PMC · DOI: 10.3390/biom15101378 · Biomolecules · 2025-09-28

## TL;DR

This paper explores how ACE inhibitors like lisinopril affect aging and metabolism using fruit flies as a model.

## Contribution

The study highlights sex- and age-specific effects of lisinopril in Drosophila, offering new insights into RAS inhibition and aging.

## Key findings

- Lisinopril shows sex- and age-specific effects on metabolic rates in Drosophila.
- Drosophila's open circulatory system makes it a useful model for studying ACE inhibition and aging.
- ACE inhibition may extend healthspan by targeting intermediary metabolism.

## Abstract

Aging is characterized by a progressive decline in physiological function that impairs performance and increases vulnerability to disease and mortality. Delaying this deterioration is key to promoting healthy aging. Age-associated functional decline is closely linked to alterations in intermediary metabolism, including disrupted lipid metabolism and impaired mitochondrial function. Counteracting these metabolic changes, particularly those affecting basal metabolic rate and energy utilization, may be a feasible strategy to extend healthspan. The Renin-Angiotensin System (RAS), which controls blood pressure through Angiotensin II, an octapeptide hormone generated from Angiotensin I by Angiotensin-Converting Enzyme (ACE), has been identified as a potential target for aging therapies. ACE inhibitors, such as the commonly prescribed vasodilator lisinopril, have been shown to exert beneficial effects on healthspan. Disentangling their systemic effects from direct cellular actions on intermediary metabolism is challenging in humans but can be pursued in model organisms. Drosophila melanogaster expresses two ortholog of mammalian ACE, Ance and Acer, which have diverged to acquire different functions. Since fundamental cellular processes are evolutionarily conserved and flies have an open circulatory system, Drosophila provides a versatile model for translational studies on ACE inhibition and aging. Recent studies in Drosophila reveal sex-, age-, and genetic background-specific effects of lisinopril on metabolic rates and aging-related organismal phenotypes. Integrating preclinical findings from Drosophila with clinical studies will be essential to define the therapeutic potential of RAS inhibition in extending lifespan and delaying aging.

## Linked entities

- **Proteins:** Ance (Angiotensin converting enzyme), Acer (Angiotensin-converting enzyme-related)
- **Chemicals:** lisinopril (PubChem CID 5362119)
- **Species:** Drosophila melanogaster (taxon 7227)

## Full-text entities

- **Genes:** Ance (Angiotensin converting enzyme) [NCBI Gene 34805] {aka ACE, BG:DS08220.3, CG8827, Dmel\CG8827, RACE, Race}, Acer (Angiotensin-converting enzyme-related) [NCBI Gene 34189] {aka ACE, CG10593, Dmel\CG10593, l(2)k07704}
- **Diseases:** impaired mitochondrial function (MESH:D028361), disrupted lipid metabolism (MESH:D052439)
- **Chemicals:** lisinopril (MESH:D017706)
- **Species:** Diptera (flies, order) [taxon 7147], Homo sapiens (human, species) [taxon 9606], Drosophila melanogaster (fruit fly, species) [taxon 7227]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12564483/full.md

## References

90 references — full list in the complete paper: https://tomesphere.com/paper/PMC12564483/full.md

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Source: https://tomesphere.com/paper/PMC12564483