# Antioxidant enzymes, oxidative stress, and physiological aging markers in Drosophila melanogaster (Diptera: Drosophilidae): a systematic review with translational perspectives

**Authors:** Anđela Savić, Mirjana Šipovac, Aleksandra Novaković, Ljubica Vasiljević, Maja Palangetić

PMC · DOI: 10.1093/jisesa/ieag020 · 2026-03-24

## TL;DR

This paper reviews how oxidative stress and antioxidant enzymes affect aging in fruit flies, with implications for human health.

## Contribution

A systematic review of recent studies on oxidative stress and aging in Drosophila, highlighting conserved mechanisms relevant to humans.

## Key findings

- Excessive ROS production leads to oxidative stress and lipid damage in older Drosophila.
- Superoxide dismutase and catalase are key markers of oxidative homeostasis in aging studies.
- Lifespan and locomotor activity are primary physiological aging indicators in Drosophila.

## Abstract

Oxidative stress contributes to cellular damage and aging. In this study, the model organism Drosophila melanogaster Meigen 1830 was used to examine the molecular and physiological mechanisms of aging associated with oxidative stress. A systematic search and detailed analysis of scientific publications on this topic were conducted using the PubMed database. The analysis included 30 original research articles published between April 2020 and April 2025. Studies focusing primarily on upstream signaling pathways or other stress mechanisms without direct measurement of reactive oxygen species (ROS), antioxidant enzymes, or physiological aging markers were excluded. For each article, key elements were extracted, including the research topic, assessed ROS and antioxidant enzyme markers, physiological aging indicators, main experimental findings, and study conclusions. The results were classified using a descriptive frequency-based analysis of reported ROS and aging markers, as well as by the main topic and research approach of each study. Collectively, the reviewed studies indicate that excessive ROS production leads to oxidative stress and lipid damage, particularly in older individuals. The enzymes superoxide dismutase and catalase were the most commonly assessed markers and served as primary indicators of oxidative homeostasis. Lifespan and locomotor activity were identified as the main physiological aging parameters, while natural extracts and phytonutrients were the most frequently used intervention agents. These findings confirm the value of D. melanogaster as a model for aging research and support its use in identifying conserved redox mechanisms and evaluating potential interventions with translational relevance for human health.

## Linked entities

- **Proteins:** Cat (Catalase)
- **Species:** Drosophila melanogaster (taxon 7227)

## Full-text entities

- **Genes:** Prx2 (Peroxiredoxin 2) [NCBI Gene 53578] {aka 1633, CG1633, DPx-4783, DPx4783, DmTPx-1, Dmel\CG1633}, mTor (mechanistic Target of rapamycin) [NCBI Gene 47396] {aka 5092, CG5092, CT16317, CT24745, CT24817, DmTOR}, Ret (Ret oncogene) [NCBI Gene 43875] {aka CG1061, CG14396, D-ret, DRET, DRet, DmHD-59}, mth (methuselah) [NCBI Gene 38058] {aka CG6936, Dmel\CG6936}, N (Notch) [NCBI Gene 31293] {aka 1.1, 16-178, 16-55, Ax, CG3936, CT13012}, GstS1 (Glutathione S transferase S1) [NCBI Gene 36927] {aka CG8938, DmGST-2, DmGST2, DmGSTS1, DmGSTS1-1, DmGst-2}, Nox (NADPH oxidase) [NCBI Gene 5740310] {aka CG15924, CG34399, CG3896, DmNox, Dmel\CG34399, Dmel_CG15924}, Gtpx (Glutathione peroxidase homolog with thioredoxin peroxidase activity) [NCBI Gene 38413] {aka CG12013, DmGPx, DmGpx, DmPHGPx, Dmel\CG12013, GPx}, Trxr1 (Thioredoxin reductase 1) [NCBI Gene 31760] {aka 2151, CG2151, DTR, Dm-TrxR, DmTR, DmTrx}, p38b (p38b MAP kinase) [NCBI Gene 34780] {aka 186F5S, BG:DS00797.3, CG7393, D-p38, D-p38 MAPK, D-p38b}, Prx5 (Peroxiredoxin 5) [NCBI Gene 3771951] {aka CG 32920, CG 7217, CG3292, CG32920, CG7217, Dmel\CG7217}, Sod1 (Superoxide dismutase 1) [NCBI Gene 39251] {aka 24492, CG11793, Cu, Cu-Zn SOD, Cu-Zn-SOD, Cu/Zn SOD}, Keap1 (Keap1) [NCBI Gene 42062] {aka CG3962, DmKeap1, Dmel\CG3962, Keap-1, Nrf-2, dKEAP1}, InR (Insulin-like receptor) [NCBI Gene 42549] {aka 18402, CG18402, DIHR, DILR, DIR, DIRH}, foxo (forkhead box, sub-group O) [NCBI Gene 41709] {aka 3143, Afx, Akh, CG3143, DFOXO, DfoxO}, Cat (Catalase) [NCBI Gene 40048] {aka CAT1, CATA, CG6871, CT21282, Cat-A, CatA}, Su(osk)P16 (Suppressor of oskar P16) [NCBI Gene 250692] {aka P16}, Pten (Phosphatase and tensin homolog) [NCBI Gene 43991] {aka CG5671, D.PTEN, DPTEN, Dmel\CG5671, PTEN3, dPTEN}, bsk (basket) [NCBI Gene 44801] {aka Basket, CG5680, D-JNK, D-junk, DBSK/JNK, DJNK}, Akt (Akt kinase) [NCBI Gene 41957] {aka AKT-1, AKT/PKB, AKT1, Akt-1, Akt/PKB, Akt1}, Pxd (Peroxidase) [NCBI Gene 2768671] {aka CG3477, DmPO, Dmel\CG3477, Dpxd, HPX1, PO}, ROS [NCBI Gene 44175], Ace (Acetylcholine esterase) [NCBI Gene 41625] {aka ACHE, AChE, AcChE, AchE, CG17907, CHE}
- **Diseases:** systemic (MESH:D015619), cardiovascular conditions (MESH:D002318), Parkinson's disease (MESH:D010300), diabetes (MESH:D003920), mitochondrial dysfunction (MESH:D028361), atherosclerosis (MESH:D050197), neurodegeneration (MESH:D019636), developmental arrest (MESH:D006323), intestinal damage (MESH:D007410), disease (MESH:D004194), obesity (MESH:D009765), hypertension (MESH:D006973), AD (MESH:D000544), biliary conditions (MESH:D001660), chronic inflammation (MESH:D007249), acute and chronic kidney disease (MESH:D058186), Hypoxia (MESH:D000860), cancer (MESH:D009369), ocular diseases (MESH:D005128)
- **Chemicals:** chitosan (MESH:D048271), Resveratrol (MESH:D000077185), catechins (MESH:D002392), adenine (MESH:D000225), alkoxyl radicals (MESH:C059688), cytosine (MESH:D003596), cysteine sulfinic acid (MESH:C013461), zinc (MESH:D015032), Polysaccharides (MESH:D011134), NADPH (MESH:D009249), MAG-EPA (MESH:C588285), peroxyl radical (MESH:C049375), Lipid (MESH:D008055), Curcumin (MESH:D003474), manganese (MESH:D008345), polymers (MESH:D011108), O2 (-), oxygen (MESH:D010100), MDA (MESH:D008315), Phytosterols (MESH:D010840), chitin (MESH:D002686), methionine (MESH:D008715), superoxide (MESH:D013481), heavy metal (MESH:D019216), sulfur (MESH:D013455), flavonoids (MESH:D005419), stigmasterol (MESH:D013265), polyphenols (MESH:D059808), steroid hormones (MESH:D013256), H2O (MESH:D014867), copper (MESH:D003300), selenium (MESH:D012643), Quercetin (MESH:D011794), guanine (MESH:D006147), lipid hydroperoxides (MESH:D008054), GSSG (MESH:D019803), polyunsaturated fatty acids (MESH:D005231), ROS (MESH:D017382), hydroxyl radical (MESH:D017665), H2O2 (MESH:D006861), 8-oxoguanine (MESH:C024829), oils (MESH:D009821), phospholipids (MESH:D010743), GSH (MESH:D005978), cysteine (MESH:D003545), amino acid (MESH:D000596)
- **Species:** Homo sapiens (human, species) [taxon 9606], Diptera (flies, order) [taxon 7147], Drosophila melanogaster (fruit fly, species) [taxon 7227], Eleutherococcus senticosus (species) [taxon 82096], Agrocybe aegerita [taxon 5400], Lycium barbarum (Duke of Argyll's teatree, species) [taxon 112863]
- **Mutations:** A in D

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13010287/full.md

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Source: https://tomesphere.com/paper/PMC13010287