Neuroprotective Effects of Calycosin Against Fenpropathrin-Induced Dopaminergic Neurodegeneration in Drosophila melanogaster
Abstract
The loss of dopaminergic neurones in the substantia nigra pars compacta is a hallmark of Parkinson's disease (PD), a neurodegenerative condition. Environmental pesticide exposure, particularly to pyrethroids such as fenpropathrin (Fen), represents a significant risk factor for PD pathogenesis alongside genetic predispositions. Recently, studies have indicated that exposure to Fen may also increase the likelihood of developing PD. In this study, we validated a Drosophila melanogaster model of neurotoxicity by exposing 2-5-day-old male flied to 5 mg/L fenpropethrin (Fen) for 96 hours. Motor functions were assessed using climbing, jumping, and crawling assays, alongwith survival and pupal development studies. To investigate underlying molecular changes, protein analysis was performed through western blot to evaluatate the expression of the dopaminergic neuron marker tyrosine hydroxylase and the apoptotic marker caspase-3. Subsequently, Calycosin, an isoflavone phytoesterogen obtained from Astragalus membranaceus that has anti-inflammatory, antioxidant, and anti-apoptotic qualities, was evaluated for its neuroprotective effectiveness. Calycosin was tested at concentrations of 50, 100, and 200 µM, with 50 µM identified as the optimal dose on improved survival rates and locomotor performance. Previous studies suggest calycosin’s neuroprotective effects, but its role in fenpropathrin (Fen)-induced neurotoxicity remains unexplored. This study evaluates calycosin’s efficacy against Fen-induced neurodegeration in Drosophila melanogaster. Calycosin significantly improved motor, including a 48% increase in crawling behaviour and a 20% rise in survival rates. It reduced cleaved caspase -3 levels by 16.7%, alleviated developemental delays by 18.9%, and restored tyrosine hydroxylase expression by 44.1%, indicating protection of dopaminergic neurons. These findings demonstrate that calycosin provides significant neuroprotection against Fen-induced neurodegeneration in the Drosophila PD like model, suggesting its potential as a therapeutic intervention for pesticide-related neurodegenerative diseases.
Keywords:
calycosin, fenpropathrin, Drosophila, Parkinson's disease, Neurodegeneration, Tyrosine hydroxylaseDOI
https://doi.org/10.25004/IJPSDR.2025.170503References
Pringsheim T, Jette N, Frolkis A, Steeves TDL. The prevalence of Parkinson’s disease: A systematic review and meta‐analysis. Movement Disorders. 2014;29:1583–90. Available from: https://movementdisorders.onlinelibrary.wiley.com/doi/10.1002/mds.25945
Goldman SM. Environmental Toxins and Parkinson’s Disease. Annu Rev Pharmacol Toxicol. 2014;54:141–64. Available from:https://www.annualreviews.org/content/journals/10.1146/annurev-pharmtox-011613-135937
Przedborski S. The two-century journey of Parkinson disease research. Nat Rev Neurosci. 2017;18:251–9. Available from: https://www.nature.com/articles/nrn.2017.25
Zeng X-S, Geng W-S, Jia J-J. Neurotoxin-Induced Animal Models of Parkinson Disease: Pathogenic Mechanism and Assessment. ASN Neuro. 2018;10:175909141877743. Available from: https://www.tandfonline.com/doi/full/10.1177/1759091418777438
Santiago JA, Bottero V, Potashkin JA. Biological and Clinical Implications of Comorbidities in Parkinson’s Disease. Front Aging Neurosci. 2017;9. Available from: https://www.frontiersin.org/journals/aging-neuroscience/articles/10.3389/fnagi.2017.00394/full
Brouwer M, Huss A, van der Mark M, Nijssen PCG, Mulleners WM, Sas AMG, et al. Environmental exposure to pesticides and the risk of Parkinson’s disease in the Netherlands. Environ Int. 2017;107:100–10. Available from: https://www.sciencedirect.com/science/article/abs/pii/S0160412017300752?via%3Dihub
Ratner MH, Farb DH, Ozer J, Feldman RG, Durso R. Younger age at onset of sporadic Parkinson’s disease among subjects occupationally exposed to metals and pesticides. Interdiscip Toxicol. 2014;7:123–33. Available from: https://sciendo.com/article/10.2478/intox-2014-0017
Xiong J, Zhang X, Huang J, Chen C, Chen Z, Liu L, et al. Fenpropathrin, a Widely Used Pesticide, Causes Dopaminergic Degeneration. Mol Neurobiol. 2016;53:995–1008. Available from: https://link.springer.com/article/10.1007/s12035-014-9057-2
Tong H, Zhang X, Meng X, Lu L, Mai D, Qu S. Simvastatin Inhibits Activation of NADPH Oxidase/p38 MAPK Pathway and Enhances Expression of Antioxidant Protein in Parkinson Disease Models. Front Mol Neurosci. 2018;11. Available from: https://www.frontiersin.org/journals/molecular-neuroscience/articles/10.3389/fnmol.2018.00165/full
Feng C-W, Wen Z-H, Huang S-Y, Hung H-C, Chen C-H, Yang S-N, et al. Effects of 6-Hydroxydopamine Exposure on Motor Activity and Biochemical Expression in Zebrafish (Danio Rerio) Larvae. Zebrafish. 2014;11:227–39. Available from: https://www.liebertpub.com/doi/10.1089/zeb.2013.0950
Shukla AK, Pragya P, Chaouhan HS, Patel DK, Abdin MZ, Kar Chowdhuri D. A mutation in Drosophila methuselah resists paraquat induced Parkinson-like phenotypes. Neurobiol Aging. 2014;35:2419.e1-2419.e16. Available from: https://www.sciencedirect.com/science/article/abs/pii/S0197458014003108?via%3Dihub
Kikuchi T, Morizane A, Doi D, Magotani H, Onoe H, Hayashi T, et al. Human iPS cell-derived dopaminergic neurons function in a primate Parkinson’s disease model. Nature. 2017;548:592–6. Available from: https://www.nature.com/articles/nature23664
Naz F, Siddique YH. Drosophila melanogaster a Versatile Model of Parkinson’s Disease. CNS Neurol Disord Drug Targets. 2021;20:487–530. Available from: https://www.eurekaselect.com/article/114019
Shishtar E, Rogers GT, Blumberg JB, Au R, Jacques PF. Long-term dietary flavonoid intake and risk of Alzheimer disease and related dementias in the Framingham Offspring Cohort. Am J Clin Nutr. 2020;112:343–53. Available from: https://www.sciencedirect.com/science/article/pii/S0002916522008048?via%3Dihub
Bondonno NP, Dalgaard F, Kyrø C, Murray K, Bondonno CP, Lewis JR, et al. Flavonoid intake is associated with lower mortality in the Danish Diet Cancer and Health Cohort. Nat Commun. 2019;10:3651. Available from: https://www.nature.com/articles/s41467-019-11622-x
Fuentes-Herrera PB, Herrera-Cabrera BE, Martínez-Ayala AL, Zamilpa A, Delgado-Alvarado A. Content and Yield of L-DOPA and Bioactive Compounds of Broad Bean Plants: Antioxidant and Anti-Inflammatory Activity In Vitro. Plants. 2023;12:3918. Available from: https://www.mdpi.com/2223-7747/12/23/3918
Hack W, Gladen-Kolarsky N, Chatterjee S, Liang Q, Maitra U, Ciesla L, et al. Gardenin A treatment attenuates inflammatory markers, synuclein pathology and deficits in tyrosine hydroxylase expression and improves cognitive and motor function in A53T-α-syn mice. Biomedicine & Pharmacotherapy. 2024;173:116370. Available from: https://www.sciencedirect.com/science/article/pii/S0753332224002543?via%3Dihub
Hassan SS ul, Samanta S, Dash R, Karpiński TM, Habibi E, Sadiq A, et al. The neuroprotective effects of fisetin, a natural flavonoid in neurodegenerative diseases: Focus on the role of oxidative stress. Front Pharmacol. 2022;13. Available from: https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2022.1015835/full
Jaroonwitchawan T, Chaicharoenaudomrung N, Namkaew J, Noisa P. Curcumin attenuates paraquat-induced cell death in human neuroblastoma cells through modulating oxidative stress and autophagy. Neurosci Lett. 2017;636:40–7. Available from: https://www.sciencedirect.com/science/article/abs/pii/S0304394016308059?via%3Dihub
Wang L-Y, Yu X, Li X-X, Zhao Y-N, Wang C-Y, Wang Z-Y, et al. Catalpol Exerts a Neuroprotective Effect in the MPTP Mouse Model of Parkinson’s Disease. Front Aging Neurosci. 2019;11. Available from: https://www.frontiersin.org/journals/aging-neuroscience/articles/10.3389/fnagi.2019.00316/full
Hsu C-C, Kuo T-W, Liu W-P, Chang C-P, Lin H-J. Calycosin Preserves BDNF/TrkB Signaling and Reduces Post-Stroke Neurological Injury after Cerebral Ischemia by Reducing Accumulation of Hypertrophic and TNF-α-Containing Microglia in Rats. Journal of Neuroimmune Pharmacology. 2020;15:326–39. Available from: https://link.springer.com/article/10.1007/s11481-019-09903-9
Wang X, Zhao L. Calycosin ameliorates diabetes-induced cognitive impairments in rats by reducing oxidative stress via the PI3K/Akt/GSK-3β signaling pathway. Biochem Biophys Res Commun. 2016;473:428–34. Available from: https://www.sciencedirect.com/science/article/abs/pii/S0006291X16303370?via%3Dihub
Pan Q, Ban Y, Khan S. Antioxidant activity of calycosin against α-synuclein amyloid fibrils-induced oxidative stress in neural-like cells as a model of preventive care studies in Parkinson’s disease. Int J Biol Macromol. 2021;182:91–7. Available from: https://www.sciencedirect.com/science/article/abs/pii/S0141813021007017?via%3Dihub
Nazir A, Mukhopadhyay I, Saxena DK, Chowdhuri DK. Evaluation of the No Observed Adverse Effect Level of Solvent Dimethyl Sulfoxide in Drosophila melanogaster. Toxicol Mech Methods. 2003;13:147–52. Available from: https://www.tandfonline.com/doi/abs/10.1080/15376510309846
Aljedani DM. Effects of some insecticides (Deltamethrin and malathion) and lemongrass oil on fruit fly (drosophila melanogaster). Pakistan Journal of Biological Sciences. 2021;24:477–91. Available from: https://scialert.net/abstract/?doi=pjbs.2021.477.491
Karataş A, Bahçeci Z. Effect of cypermethrin on some developmental stages of drosophila melanogaster. Bull Environ Contam Toxicol. 2009;82:738–42. Available from: https://link.springer.com/article/10.1007/s00128-008-9604-5
Chaouhan HS, Li X, Sun KT, Wang IK, Yu TM, Yu SH, et al. Calycosin Alleviates Paraquat-Induced Neurodegeneration by Improving Mitochondrial Functions and Regulating Autophagy in a Drosophila Model of Parkinson’s Disease. Antioxidants. 2022;11. Available from: https://www.mdpi.com/2076-3921/11/2/222
Shukla AK, Pragya P, Chaouhan HS, Patel DK, Abdin MZ, Kar Chowdhuri D. A mutation in Drosophila methuselah resists paraquat induced Parkinson-like phenotypes. Neurobiol Aging. 2014;35:2419.e1-2419.e16. Available from: https://www.sciencedirect.com/science/article/abs/pii/S0197458014003108?via%3Dihub
Swank DM, Knowles AF, Suggs JA, Sarsoza F, Lee A, Maughan DW, et al. The myosin converter domain modulates muscle performance. Nat Cell Biol. 2002;4:312–7. Available from: https://www.nature.com/articles/ncb776
Jakubowski BR, Longoria RA, Shubeita GT. A high throughput and sensitive method correlates neuronal disorder genotypes to Drosophila larvae crawling phenotypes. Fly (Austin). 2012;6:303–8. Available from: https://www.tandfonline.com/doi/full/10.4161/fly.21582
Post Y, Paululat A. Muscle Function Assessment Using a Drosophila Larvae Crawling Assay. Bio Protoc. 2018;8. Available from: https://bio-protocol.org/en/bpdetail?id=2933&type=0
Nichols CD, Becnel J, Pandey UB. Methods to Assay <em>Drosophila</em> Behavior. Journal of Visualized Experiments. 2012; Available from: https://app.jove.com/t/3795/methods-to-assay-drosophila-behavior
Maitra U, Harding T, Liang Q, Ciesla L. GardeninA confers neuroprotection against environmental toxin in a Drosophila model of Parkinson’s disease. Commun Biol. 2021;4:162. Available from: https://www.nature.com/articles/s42003-021-01685-2
Gao L, Li Y, Xie H, Wang Y, Zhao H, Zhang M, et al. Effect of ethylparaben on the growth and development of Drosophila melanogaster on preadult. Environ Toxicol Pharmacol. 2020;80:103495. Available from: https://www.sciencedirect.com/science/article/abs/pii/S138266892030171X?via%3Dihub
Camus MF, Huang C, Reuter M, Fowler K. Dietary choices are influenced by genotype, mating status, and sex in Drosophila melanogaster. Ecol Evol. 2018;8:5385–93. Available from: https://onlinelibrary.wiley.com/doi/10.1002/ece3.4055
Chaouhan HS, Li X, Sun K-T, Wang I-K, Yu T-M, Yu S-H, et al. Calycosin Alleviates Paraquat-Induced Neurodegeneration by Improving Mitochondrial Functions and Regulating Autophagy in a Drosophila Model of Parkinson’s Disease. Antioxidants. 2022;11:222. Available from: https://www.mdpi.com/2076-3921/11/2/222
Maitra U, Harding T, Liang Q, Ciesla L. GardeninA confers neuroprotection against environmental toxin in a Drosophila model of Parkinson’s disease. Commun Biol. 2021;4:162. Available from: https://www.nature.com/articles/s42003-021-01685-2
Maitra U, Scaglione MN, Chtarbanova S, O’Donnell JM. Innate immune responses to paraquat exposure in a Drosophila model of Parkinson’s disease. Sci Rep. 2019;9:12714. Available from: https://www.nature.com/articles/s41598-019-48977-6
Jiao Z, Wu Y, Qu S. Fenpropathrin induces degeneration of dopaminergic neurons via disruption of the mitochondrial quality control system. Cell Death Discov. 2020;6:78. Available from: https://www.nature.com/articles/s41420-020-00313-y
Zhou ZD, Saw WT, Ho PGH, Zhang ZW, Zeng L, Chang YY, et al. The role of tyrosine hydroxylase–dopamine pathway in Parkinson’s disease pathogenesis. Cellular and Molecular Life Sciences. 2022;79:599. Available from: https://link.springer.com/article/10.1007/s00018-022-04574-x
Huang X, Liang Y, Qing Y, Chen D, Shi N. Proteasome inhibition by MG-132 protects against deltamethrin-induced apoptosis in rat hippocampus. Life Sci. 2019;220:76–83. Available from: https://www.sciencedirect.com/science/article/abs/pii/S0024320519300542?via%3Dihub
Kwon DK, Kwatra M, Wang J, Ko HS. Levodopa-Induced Dyskinesia in Parkinson’s Disease: Pathogenesis and Emerging Treatment Strategies. Cells. 2022;11:3736. Available from: https://www.mdpi.com/2073-4409/11/23/3736
Zare K, Eidi A, Roghani M, Rohani AH. The neuroprotective potential of sinapic acid in the 6-hydroxydopamine-induced hemi-parkinsonian rat. Metab Brain Dis. 2015;30:205–13. Available from: https://link.springer.com/article/10.1007/s11011-014-9604-6
Kakkar AK, Dahiya N. Management of Parkinson׳s disease: Current and future pharmacotherapy. Eur J Pharmacol. 2015;750:74–81. Available from: https://www.sciencedirect.com/science/article/abs/pii/S0014299915000631?via%3Dihub
Maan G, Sikdar B, Kumar A, Shukla R, Mishra A. Role of Flavonoids in Neurodegenerative Diseases: Limitations and Future Perspectives. Curr Top Med Chem. 2020;20:1169–94.Available from: https://www.eurekaselect.com/article/105855
Maher P. The Potential of Flavonoids for the Treatment of Neurodegenerative Diseases. Int J Mol Sci. 2019;20:3056. Available from: https://www.mdpi.com/1422-0067/20/12/3056
Maitra U, Ciesla L. Using Drosophila as a platform for drug discovery from natural products in Parkinson’s disease. Medchemcomm. 2019;10:867–79. Available from: https://pubs.rsc.org/en/content/articlelanding/2019/md/c9md00099b
Chaouhan HS, Li X, Sun K-T, Wang I-K, Yu T-M, Yu S-H, et al. Calycosin Alleviates Paraquat-Induced Neurodegeneration by Improving Mitochondrial Functions and Regulating Autophagy in a Drosophila Model of Parkinson’s Disease. Antioxidants. 2022;11:222. Available from: https://www.mdpi.com/2076-3921/11/2/222
Yang J, Jia M, Zhang X, Wang P. Calycosin attenuates MPTP‐induced Parkinson’s disease by suppressing the activation of TLR/NF‐κB and MAPK pathways. Phytotherapy Research. 2019;33:309–18. Available from: https://onlinelibrary.wiley.com/doi/10.1002/ptr.6221
Araujo SM, de Paula MT, Poetini MR, Meichtry L, Bortolotto VC, Zarzecki MS, et al. Effectiveness of γ-oryzanol in reducing neuromotor deficits, dopamine depletion and oxidative stress in a Drosophila melanogaster model of Parkinson’s disease induced by rotenone. Neurotoxicology. 2015;51:96–105. Available from: linkinghub.elsevier.com/retrieve/pii/S0161813X15001321
Lanson NA, Maltare A, King H, Smith R, Kim JH, Taylor JP, et al. A Drosophila model of FUS-related neurodegeneration reveals genetic interaction between FUS and TDP-43. Hum Mol Genet. 2011;20:2510–23. Available from: https://academic.oup.com/hmg/article-abstract/20/13/2510/2526994?redirectedFrom=fulltext
Kumar PP, Bawani SS, Anandhi DU, Prashanth KVH. Rotenone mediated developmental toxicity in Drosophila melanogaster. Environ Toxicol Pharmacol. 2022;93:103892. Available from: https://www.sciencedirect.com/science/article/abs/pii/S1382668922000850?via%3Dihub
Podder S, Roy S. Study of the changes in life cycle parameters of Drosophila melanogaster exposed to fluorinated insecticide, cryolite. Toxicol Ind Health. 2015;31:1341–7. Available from: https://journals.sagepub.com/doi/10.1177/0748233713493823
Sharma A, Mishra M, Shukla AK, Kumar R, Abdin MZ, Chowdhuri DK. Organochlorine pesticide, endosulfan induced cellular and organismal response in Drosophila melanogaster. J Hazard Mater. 2012;221–222:275–87. Available from: https://www.sciencedirect.com/science/article/abs/pii/S0304389412004360?via%3Dihub
Gao L, Li Y, Xie H, Wang Y, Zhao H, Zhang M, et al. Effect of ethylparaben on the growth and development of Drosophila melanogaster on preadult. Environ Toxicol Pharmacol. 2020;80:103495. Available from: https://www.sciencedirect.com/science/article/abs/pii/S138266892030171X?via%3Dihub
Wongchum N, Dechakhamphu A. Xanthohumol prolongs lifespan and decreases stress-induced mortality in Drosophila melanogaster. Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology. 2021;244:108994. Available from: https://www.sciencedirect.com/science/article/abs/pii/S1532045621000211?via%3Dihub
Bonilla-Ramirez L, Jimenez-Del-Rio M, Velez-Pardo C. Low doses of paraquat and polyphenols prolong life span and locomotor activity in knock-down parkin Drosophila melanogaster exposed to oxidative stress stimuli: Implication in autosomal recessive juvenile Parkinsonism. Gene. 2013;512:355–63. Available from: https://www.sciencedirect.com/science/article/abs/pii/S0378111912012292?via%3Dihub
Yamada M, Kida K, Amutuhaire W, Ichinose F, Kaneki M. Gene disruption of caspase-3 prevents MPTP-induced Parkinson’s disease in mice. Biochem Biophys Res Commun. 2010;402:312–8. Available from: https://www.sciencedirect.com/science/article/abs/pii/S0006291X10018747?via%3Dihub
Wang L-Y, Yu X, Li X-X, Zhao Y-N, Wang C-Y, Wang Z-Y, et al. Catalpol Exerts a Neuroprotective Effect in the MPTP Mouse Model of Parkinson’s Disease. Front Aging Neurosci. 2019;11. Available from: https://www.frontiersin.org/journals/aging-neuroscience/articles/10.3389/fnagi.2019.00316/full
White JB, Beckford J, Yadegarynia S, Ngo N, Lialiutska T, d’Alarcao M. Some natural flavonoids are competitive inhibitors of caspase-1, -3, and -7 despite their cellular toxicity. Food Chem. 2012;131:1453–9. Available from: https://www.sciencedirect.com/science/article/abs/pii/S0308814611014592?via%3Dihub
Soares JJ, Rodrigues DT, Gonçalves MB, Lemos MC, Gallarreta MS, Bianchini MC, et al. Paraquat exposure-induced Parkinson’s disease-like symptoms and oxidative stress in Drosophila melanogaster: Neuroprotective effect of Bougainvillea glabra Choisy. Biomedicine & Pharmacotherapy. 2017;95:245–51. Available from: https://www.sciencedirect.com/science/article/abs/pii/S0753332217320437?via%3Dihub
Chen H, Xu J, Lv Y, He P, Liu C, Jiao J, et al. Proanthocyanidins exert a neuroprotective effect via ROS/JNK signaling in MPTP induced Parkinson’s disease models in�vitro and in�vivo. Mol Med Rep. 2018; Available from: https://www.spandidos-publications.com/10.3892/mmr.2018.9509
Ma J, Gao S-S, Yang H-J, Wang M, Cheng B-F, Feng Z-W, et al. Neuroprotective Effects of Proanthocyanidins, Natural Flavonoids Derived From Plants, on Rotenone-Induced Oxidative Stress and Apoptotic Cell Death in Human Neuroblastoma SH-SY5Y Cells. Front Neurosci. 2018;12. Available from: https://www.frontiersin.org/journals/neuroscience/articles/10.3389/fnins.2018.00369/full
Zhou ZD, Saw WT, Ho PGH, Zhang ZW, Zeng L, Chang YY, et al. The role of tyrosine hydroxylase–dopamine pathway in Parkinson’s disease pathogenesis. Cellular and Molecular Life Sciences. 2022;79:599. Available from: https://link.springer.com/article/10.1007/s00018-022-04574-x
Khan W, Priyadarshini M, A. Zakai H, A. Kamal M, Alam Q. A Brief Overview of Tyrosine Hydroxylase and α-Synuclein in the Parkinsonian Brain. CNS Neurol Disord Drug Targets. 2012;11:456–62. Available from: https://www.eurekaselect.com/article/43344
Huang D, Xu J, Wang J, Tong J, Bai X, Li H, et al. Dynamic Changes in the Nigrostriatal Pathway in the MPTP Mouse Model of Parkinson’s Disease. Parkinsons Dis. 2017;2017:1–7. Available from: https://onlinelibrary.wiley.com/doi/10.1155/2017/9349487
Jiao Z, Wu Y, Qu S. Fenpropathrin induces degeneration of dopaminergic neurons via disruption of the mitochondrial quality control system. Cell Death Discov. 2020;6:78. Available from: https://www.nature.com/articles/s41420-020-00313-y
Pan Q, Ban Y, Khan S. Antioxidant activity of calycosin against α-synuclein amyloid fibrils-induced oxidative stress in neural-like cells as a model of preventive care studies in Parkinson’s disease. Int J Biol Macromol. 2021;182:91–7. Available from: https://www.sciencedirect.com/science/article/abs/pii/S0141813021007017?via%3Dihub
Wang Y, Ren Q, Zhang X, Lu H, Chen J. Neuroprotective Mechanisms of Calycosin Against Focal Cerebral Ischemia and Reperfusion Injury in Rats. Cellular Physiology and Biochemistry. 2018;45:537–46. Available from: https://karger.com/cpb/article/45/2/537/74453/Neuroprotective-Mechanisms-of-Calycosin-Against
Published
Abstract Display: 137
PDF Downloads: 53 How to Cite
Issue
Section
Copyright (c) 2025 Saba Afsheen, Mohammad Mumtaz Alam, Suhel Parvez

This work is licensed under a Creative Commons Attribution 4.0 International License.

