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Protective Effects of Taraxacum Officinale Leaf Extract Against Hydrogen Peroxide-Induced Oxidative Stress in Drosophila Melanogaster Larvae

Year 2025, Volume: 14 Issue: 4, 2032 - 2051, 31.12.2025
https://doi.org/10.17798/bitlisfen.1674538

Abstract

This study investigated the protective effects of Taraxacum officinale leaf extract against hydrogen peroxide-induced oxidative stress in Drosophila melanogaster larvae. T. officinale leaves collected from the Çorum-Amasya region were dried and extracted with ethanol. Synchronized third instar D. melanogaster larvae were divided into six groups: control group, oxidative stress group, three test groups with different extract concentrations (1%, 2%, 4%), and a positive control group (ascorbic acid). Larval mortality was monitored at 24, 48, and 72 hours, and antioxidant enzyme activities (SOD, CAT, GPx) were measured at 48 hours. Results showed that mortality rates significantly increased in the oxidative stress group compared to the control group, while mortality decreased in a dose-dependent manner in the extract-treated groups. Biochemical analyses revealed that antioxidant enzyme activities were significantly elevated in the extract-treated groups compared to the stress group. The highest activity increase was observed in the group treated with 4% extract. These findings demonstrate that T. officinale extract has protective effects against oxidative stress in D. melanogaster larvae and strengthens the antioxidant defense system in a dose-dependent manner.

References

  • B. Halliwell and J. M. C. Gutteridge, “free radicals in biology and medicine,” free radicals in biology and medicine, oct. 2015, doi: 10.1093/acprof:oso/9780198717478.001.0001.
  • H. Sies and D. P. Jones, “Reactive oxygen species (ROS) as pleiotropic physiological signalling agents,” Nature Reviews Molecular Cell Biology 2020 21:7, vol. 21, no. 7, pp. 363–383, Mar. 2020, doi: 10.1038/s41580-020-0230-3.
  • I. Liguori et al., “Oxidative stress, aging, and diseases,” Clin Interv Aging, vol. 13, pp. 757–772, Jan. 2018, doi: 10.2147/cıa.s158513.
  • O. M. Ighodaro and O. A. Akinloye, “First line defence antioxidants-superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPX): Their fundamental role in the entire antioxidant defence grid,” Alexandria Journal of Medicine, vol. 54, no. 4, pp. 287–293, Dec. 2018, doi: 10.1016/j.ajme.2017.09.001.
  • K. B. Pandey and S. I. Rizvi, “Plant Polyphenols as Dietary Antioxidants in Human Health and Disease,” Oxid Med Cell Longev, vol. 2, no. 5, pp. 270–278, Jan. 2009, doi: 10.4161/oxım.2.5.9498.
  • D. M. Kasote, S. S. Katyare, M. V. Hegde, and H. Bae, “Significance of Antioxidant Potential of Plants and its Relevance to Therapeutic Applications,” Int J Biol Sci, vol. 11, no. 8, p. 982, Jun. 2015, doi: 10.7150/ıjbs.12096.
  • M. González-Castejón, F. Visioli, and A. Rodriguez-Casado, “Diverse biological activities of dandelion,” Nutr Rev, vol. 70, no. 9, pp. 534–547, Sep. 2012, doi: 10.1111/j.1753-4887.2012.00509.x.
  • K. Schütz, R. Carle, and A. Schieber, “Taraxacum—A review on its phytochemical and pharmacological profile,” J Ethnopharmacol, vol. 107, no. 3, pp. 313–323, Oct. 2006, doi: 10.1016/j.jep.2006.07.021.
  • M. Davaatseren et al., “Taraxacum official (dandelion) leaf extract alleviates high-fat diet-induced nonalcoholic fatty liver,” Food and Chemical Toxicology, vol. 58, pp. 30–36, Aug. 2013, doi: 10.1016/j.fct.2013.04.023.
  • C. Hu and D. D. Kitts, “Dandelion (Taraxacum officinale) flower extract suppresses both reactive oxygen species and nitric oxide and prevents lipid oxidation in vitro,” Phytomedicine, vol. 12, no. 8, pp. 588–597, Aug. 2005, doi: 10.1016/j.phymed.2003.12.012.
  • M. Hfaiedh, D. Brahmi, and L. Zourgui, “Hepatoprotective effect of Taraxacum officinale leaf extract on sodium dichromate-induced liver injury in rats,” Environ Toxicol, vol. 31, no. 3, pp. 339–349, Mar. 2016, doi: 10.1002/tox.22048.
  • I. O. Pfingstgraf et al., “Protective Effects of Taraxacum officinale L. (Dandelion) Root Extract in Experimental Acute on Chronic Liver Failure,” Antioxidants 2021, Vol. 10, Page 504, vol. 10, no. 4, p. 504, Mar. 2021, doi: 10.3390/antıox10040504.
  • W. P. Jiang, H. P. Hung, J. G. Lin, L. H. Chang, A. Inose, and G. J. Huang, “Taraxacum mongolicum Ameliorates DNCB-Induced Atopic Dermatitis-like Symptoms in Mice by Regulating Oxidative Stress, Inflammation, MAPK, and JAK/STAT/TSLP Signaling Pathways,” International Journal of Molecular Sciences 2025, Vol. 26, Page 6601, vol. 26, no. 14, p. 6601, Jul. 2025, doi: 10.3390/ıjms26146601.
  • U. B. Pandey and C. D. Nichols, “Human Disease Models in Drosophila melanogaster and the Role of the Fly in Therapeutic Drug Discovery,” Pharmacol Rev, vol. 63, no. 2, pp. 411–436, Jun. 2011, doi: 10.1124/PR.110.003293.
  • M. T. Paula et al., “Effects of Hg(II) Exposure on MAPK Phosphorylation and Antioxidant System in D. melanogaster,” Environ Toxicol, vol. 29, no. 6, pp. 621–630, Jun. 2014, doi: 10.1002/tox.21788.
  • Y. Dai et al., “The protective effect and bioactive compounds of Astragalus membranaceus against neurodegenerative disorders via alleviating oxidative stress in Drosophila,” The FASEB Journal, vol. 38, no. 13, p. e23727, Jul. 2024, doi: 10.1096/fj.202400390r.
  • Y. H. Siddique, G. Ara, and M. Afzal, “Estimation of lipid peroxidation induced by hydrogen peroxide in cultured human lymphocytes,” Dose-Response, vol. 10, no. 1, pp. 1–10, 2012, doi: https://doi.org/10.1093/biomet/52.3-4.591.
  • R. Hosamani and Muralidhara, “Acute exposure of Drosophila melanogaster to paraquat causes oxidative stress and mitochondrial dysfunction,” Arch Insect Biochem Physiol, vol. 83, no. 1, pp. 25–40, May 2013, doi: 10.1002/arch.21094.
  • S. Staats, K. Lüersen, A. E. Wagner, and G. Rimbach, “Drosophila melanogaster as a Versatile Model Organism in Food and Nutrition Research,” 2018. doi: 10.1021/acs.jafc.7b05900.
  • N. Johnmark and H. W. Kinyi, “Amaranth leaf extract protects against hydrogen peroxide induced oxidative stress in Drosophila melanogaster,” BMC Res Notes, vol. 14, no. 1, pp. 1–5, Dec. 2021, doi: 10.1186/s13104-021-05603-x/fıgures/3.
  • A. Vrailas-Mortimer, R. Gomez, H. Dowse, and S. Sanyal, “A survey of the protective effects of some commercially available antioxidant supplements in genetically and chemically induced models of oxidative stress in Drosophila melanogaster,” Exp Gerontol, vol. 47, no. 9, pp. 712–722, Sep. 2012, doi: 10.1016/j.exger.2012.06.016.
  • D. Altun Çolak and T. Atıcı, “Investigation Healing Effects of Isgın and Dandelion against of Doxorubicin-Induced Toxicity in D. melanogaster,” 2019.
  • T. M. Bass, R. C. Grandison, R. Wong, P. Martinez, L. Partridge, and M. D. W. Piper, “Optimization of Dietary Restriction Protocols in Drosophila,” The Journals of Gerontology: Series A, vol. 62, no. 10, pp. 1071–1081, Oct. 2007, doi: 10.1093/gerona/62.10.1071.
  • C. Hu, D. K.- Phytomedicine, and undefined 2005, “Dandelion (Taraxacum officinale) flower extract suppresses both reactive oxygen species and nitric oxide and prevents lipid oxidation in vitro,” Elsevier, vol. 12, no. 8, pp. 588–597, Aug. 2005, doi: 10.1016/j.phymed.2003.12.012.
  • V. L. Singleton and J. A. Rossi, “Colorimetry of Total Phenolics with Phosphomolybdic-Phosphotungstic Acid Reagents,” Am J Enol Vitic, vol. 16, no. 3, pp. 144–158, Jan. 1965, doi: 10.5344/ajev.1965.16.3.144.
  • C. C. Chang, M. H. Yang, H. M. Wen, and J. C. Chern, “Estimation of total flavonoid content in propolis by two complementary colometric methods,” J Food Drug Anal, vol. 10, no. 3, p. 3, Jul. 2020, doi: 10.38212/2224-6614.2748.
  • W. Brand-Williams, M. E. Cuvelier, and C. Berset, “Use of a free radical method to evaluate antioxidant activity,” LWT - Food Science and Technology, vol. 28, no. 1, pp. 25–30, Jan. 1995, doi: 10.1016/S0023-6438(95)80008-5.
  • D. J. Benford et al., “Biomarkers as predictive tools in toxicity testing,” Alternatives to Laboratory Animals, vol. 28, no. 1, pp. 119–131, 2000, doi: https://doi.org/10.1177/026119290002800104.
  • H. P. Misra and I. Fridovich, “The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase.,” Journal of Biological Chemistry, vol. 247, no. 10, pp. 3170–3175, May 1972, doi: 10.1016/s0021-9258(19)45228-9.
  • H. Aebi, “Catalase in vitro,” Methods Enzymol, vol. 105, no. C, pp. 121–126, Jan. 1984, doi: 10.1016/S0076-6879(84)05016-3.
  • L. Flohé and W. A. Günzler, “Assays of glutathione peroxidase,” Methods Enzymol, vol. 105, no. C, pp. 114–120, Jan. 1984, doi: 10.1016/S0076-6879(84)05015-1.
  • M. M. Bradford, “A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding,” Anal Biochem, vol. 72, no. 1–2, pp. 248–254, May 1976, doi: 10.1016/0003-2697(76)90527-3.
  • S. S. SHAPIRO and M. B. WILK, “An analysis of variance test for normality (complete samples),” Biometrika, vol. 52, no. 3–4, pp. 591–611, Dec. 1965, doi: 10.1093/bıomet/52.3-4.591.
  • L. H, “Robust tests for equality of variances,” Contributions to probability and statistics, pp. 278–292, 1960, Accessed: Apr. 08, 2025. [Online]. Available: https://cir.nii.ac.jp/crid/1573950400526848896
  • J. W. Tukey, “Comparing Individual Means in the Analysis of Variance,” Biometrics, vol. 5, no. 2, p. 99, Jun. 1949, doi: 10.2307/3001913.
  • E. L. Kaplan and P. Meier, “Nonparametric Estimation from Incomplete Observations,” J Am Stat Assoc, vol. 53, no. 282, pp. 457–481, 1958, doi: 10.1080/01621459.1958.10501452.
  • “VII. Mathematical contributions to the theory of evolution.—III. Regression, heredity, and panmixia,” Philosophical Transactions of the Royal Society of London. Series A, Containing Papers of a Mathematical or Physical Character, vol. 187, pp. 253–318, Dec. 1896, doi: 10.1098/rsta.1896.0007.
  • C. A. Rice-Evans, N. J. Miller, and G. Paganga, “Structure-antioxidant activity relationships of flavonoids and phenolic acids,” Free Radic Biol Med, vol. 20, no. 7, pp. 933–956, Jan. 1996, doi: 10.1016/0891-5849(95)02227-9.
  • D. Golubev et al., “Berberis vulgaris L. extract supplementation exerts regulatory effects on the lifespan and healthspan of Drosophila through its antioxidant activity depending on the sex,” Biogerontology, vol. 25, no. 3, pp. 507–528, Jun. 2024, doi: 10.1007/s10522-023-10083-6/metrıcs.
  • F. Diab et al., “Supplementation with Thymbra spicata extract ameliorates lifespan, body-weight gain and Paraquat-induced oxidative stress in Drosophila melanogaster: An age- and sex-related study,” J Funct Foods, vol. 114, p. 106078, Mar. 2024, doi: 10.1016/j.jff.2024.106078.
  • M. T. He, C. H. Park, Y. S. Shin, J. H. Kim, and E. J. Cho, “Carthamus tinctorius L. Seed and Taraxacum coreanum Attenuate Oxidative Stress Induced by Hydrogen Peroxide in SH-SY5Y Cells,” Foods 2023, Vol. 12, Page 3617, vol. 12, no. 19, p. 3617, Sep. 2023, doi: 10.3390/foods12193617.
  • Y. Yang et al., “Artemisia argyi extract exerts antioxidant properties and extends the lifespan of Drosophila melanogaster,” J Sci Food Agric, vol. 104, no. 7, pp. 3926–3935, May 2024, doi: 10.1002/jsfa.13273.
  • Y. Huang et al., “White Tea Aqueous Extract: A Potential Anti-Aging Agent Against High-Fat Diet-Induced Senescence in Drosophila melanogaster,” Foods, vol. 13, no. 24, p. 4034, Dec. 2024, doi: 10.3390/foods13244034/s1.
  • S. J. Padayatty et al., “Vitamin C as an Antioxidant: Evaluation of Its Role in Disease Prevention,” J Am Coll Nutr, vol. 22, no. 1, pp. 18–35, Feb. 2003, doi: 10.1080/07315724.2003.10719272.
  • C. A. Williams, F. Goldstone, and J. Greenham, “Flavonoids, cinnamic acids and coumarins from the different tissues and medicinal preparations of Taraxacum officinale,” Phytochemistry, vol. 42, no. 1, pp. 121–127, May 1996, doi: 10.1016/0031-9422(95)00865-9.
  • J. A. Johnson et al., “The Nrf2–ARE Pathway,” Ann N Y Acad Sci, vol. 1147, no. 1, pp. 61–69, Dec. 2008, doi: 10.1196/annals.1427.036.
  • Q. Ma, “Role of Nrf2 in oxidative stress and toxicity,” Annu Rev Pharmacol Toxicol, vol. 53, no. Volume 53, 2013, pp. 401–426, Jan. 2013, doi: 10.1146/annurev-pharmtox-011112-140320/1.
  • M. C. Wang, D. Bohmann, and H. Jasper, “JNK Extends Life Span and Limits Growth by Antagonizing Cellular and Organism-Wide Responses to Insulin Signaling,” Cell, vol. 121, no. 1, pp. 115–125, Apr. 2005, doi: 10.1016/j.cell.2005.02.030.
  • A. O. Adedara, G. N. Bressan, M. M. dos Santos, R. Fachinetto, A. O. Abolaji, and N. V. Barbosa, “Antioxidant responses driven by Hesperetin and Hesperidin counteract Parkinson’s disease-like phenotypes in Drosophila melanogaster,” Neurotoxicology, vol. 101, pp. 117–127, Mar. 2024, doi: 10.1016/j.neuro.2024.02.006.
  • S. Kalra, H. Sachdeva, A. Bhushan Pant, and G. Singh, “Acorus calamus Linn.: A novel neuroprotective approach for traumatic brain injury in Drosophila melanogaster,” Brain Res, vol. 1836, p. 148953, Aug. 2024, doi: 10.1016/j.braınres.2024.148953.
  • D. A. Omoboyowa, E. A. Agboola, D. S. Bodun, S. T. Akinsulure, S. Belahcene, and D. AlFahad, “Antioxidant Potential of Curculigo pilosa Rhizome Extracts in Hydrogen Peroxide Induced Oxidation In Vivo,” Journal of Angiotherapy, vol. 9, no. 1, pp. 1–15, Jan. 2025, doi: 10.25163/angıotherapy.9110134.
  • Y. Zhu, M. Wang, J. Zhu, X. Zhang, X. Ye, and J. Chen, “Protective effects of Chinese bayberry pomace wine against oxidative stress on Drosophila melanogaster,” Food Research International, vol. 194, p. 114885, Oct. 2024, doi: 10.1016/j.foodres.2024.114885.
  • J. Karpac and H. Jasper, “Metabolic homeostasis: HDACs take center stage,” Cell, vol. 145, no. 4, pp. 497–499, May 2011, doi: 10.1016/j.cell.2011.04.017.
  • C. Li et al., “Antioxidant peptides from Lateolabrax japonicus to protect against oxidative stress injury in Drosophila melanogaster via biochemical and gut microbiota interaction assays,” Food Science and Human Wellness, vol. 14, no. 7, Jul. 2025, doi: 10.26599/fshw.2024.9250154.
There are 54 citations in total.

Details

Primary Language English
Subjects Genotoxicity and Cytotoxicity, Genetics (Other)
Journal Section Research Article
Authors

Mehmet Fidan 0000-0001-9016-6730

Submission Date April 11, 2025
Acceptance Date October 14, 2025
Publication Date December 31, 2025
Published in Issue Year 2025 Volume: 14 Issue: 4

Cite

IEEE M. Fidan, “Protective Effects of Taraxacum Officinale Leaf Extract Against Hydrogen Peroxide-Induced Oxidative Stress in Drosophila Melanogaster Larvae”, Bitlis Eren Üniversitesi Fen Bilimleri Dergisi, vol. 14, no. 4, pp. 2032–2051, 2025, doi: 10.17798/bitlisfen.1674538.

Bitlis Eren University
Journal of Science Editor
Bitlis Eren University Graduate Institute
Bes Minare Mah. Ahmet Eren Bulvari, Merkez Kampus, 13000 BITLIS