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Ashish Kushwaha,
Ritik Srivastava,
Arun K. Maurya,
Lalit Bisht,
Arvind Negi,
Kirti Kumari,
Mohit Pal,
Shipra Omar,
Abhishek Chauhan,
- Assistant Professors, Department of Pharmacy, The JB Institute of Technology College of Pharmacy, Dehradun, Uttarakhand, India
- Assistant Professors, Department of Pharmacy, The JB Institute of Technology College of Pharmacy, Dehradun, Uttarakhand, India
- Professors, Department of Pharmacy, The JB Institute of Technology College of Pharmacy, Dehradun, Uttarakhand, India
- Professors, Department of Pharmacy, The JB Institute of Technology College of Pharmacy, Dehradun, Uttarakhand, India
- Professors, Department of Pharmacy, The JB Institute of Technology College of Pharmacy, Dehradun, Uttarakhand, India
- Assistant Professors, Department of Pharmacy, The JB Institute of Technology College of Pharmacy, Dehradun, Uttarakhand, India
- Assistant Professors, Department of Pharmacy, The JB Institute of Technology College of Pharmacy, Dehradun, Uttarakhand, India
- Assistant Professor, Department of Pharmacy Practice, School of Pharmaceutical Sciences, Shri Guru Ram Rai University, Dehradun, Uttarakhand, India
- Assistant Professor, Department of Pharmacy, Keshri chand Subharti Institute of Pharmacy, Dehradun, Uttarakhand, India
Abstract
Myrmecodia platytyrea, commonly known as the ant plant, is a medicinal epiphyte traditionally used in Southeast Asia for its purported health benefits, including anti-inflammatory, antioxidant, antimicrobial, and anticancer activities. Its tuber contains abundant secondary metabolites, including flavonoids, tannins, phenolic compounds, and saponins. While these phytochemicals are generally associated with therapeutic effects, the biological activity of Myrmecodia extracts varies depending on the type of extract, dosage, and route of administration. In contrast to the commonly assumed anti-inflammatory properties of many plant-derived compounds, recent studies indicate that some aqueous extracts can produce unexpected or harmful effects under certain disease conditions. The influence of Myrmecodia platytyrea tuber extract on neuroinflammation remains largely unexplored. Methods: Astrocyte cytotoxicity was assessed using the MTT assay. The impact of MPAE at concentrations between 0.025 and 0.5 mg/mL was evaluated on reactive oxygen species (ROS) generation and the secretion of pro-inflammatory cytokines (TNF-α, IL-1β, and IL-6) in astrocyte cultures stimulated with Fe₂SO₄, H₂O₂, and LPS. Results: MPAE exhibited no cytotoxic effects on astrocytes under baseline conditions. However, it failed to confer protection against oxidative or inflammatory stress induced by Fe₂SO₄, H₂O₂, or LPS. In contrast, MPAE treatment led to increased astrocyte death and elevated ROS and cytokine levels in a dose-dependent fashion. Conclusion: While MPAE does not exhibit inherent cytotoxicity, its ability to amplify neuroinflammation in vitro raises important safety concerns—particularly for elderly individuals using this plant to alleviate inflammatory symptoms. These findings underline the necessity for further in-depth research to assess its safety and therapeutic potential before considering it for neurodegenerative disease treatment.
Keywords: Astrocytes, neuroinflammation, oxidative stress, pro-oxidant, Myrmecodia platytyrea
Ashish Kushwaha, Ritik Srivastava, Arun K. Maurya, Lalit Bisht, Arvind Negi, Kirti Kumari, Mohit Pal, Shipra Omar, Abhishek Chauhan. Neuroinflammation Is Aggravated by the Aqueous Extract of Myrmecodia Platytyrea Tuber. International Journal of Brain Sciences. 2026; 03(01):-.
Ashish Kushwaha, Ritik Srivastava, Arun K. Maurya, Lalit Bisht, Arvind Negi, Kirti Kumari, Mohit Pal, Shipra Omar, Abhishek Chauhan. Neuroinflammation Is Aggravated by the Aqueous Extract of Myrmecodia Platytyrea Tuber. International Journal of Brain Sciences. 2026; 03(01):-. Available from: https://journals.stmjournals.com/ijbs/article=2026/view=237743
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- Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods. 1983;65(1–2):55–63. [Crossref].
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- Altamura S, Muckenthaler MU. Iron toxicity in diseases of aging: Alzheimer’s disease, Parkinson’s disease and atherosclerosis. J Alzheimers Dis. 2009;16(4):879–95. [Crossref].
- Jomová K, Hudecova L, Lauro P, Simunkova M, Alwasel SH, Alhazza IM, et al. A switch between antioxidant and prooxidant properties of the phenolic compounds myricetin, morin, 3’,4’-dihydroxyflavone, taxifolin and 4-hydroxy-coumarin in the presence of copper (II) ions: a spectroscopic, absorption titration and DNA damage study. 2019;24(23):4335–45. [Crossref].
- DeTure MA, Dickson DW. The neuropathological diagnosis of Alzheimer’s disease. Mol Neurodegener. 2019;14(1):32–42. [Crossref].
- Mizaton HH, Maisarah MZ, Nik H, Mohd K, Ibtisam AW, Adam A. Anti-inflammatory and anti-hyperlipidaemic activities of Myrmecodia platytyrea tuber: the in vitro studies. Malays J Med Health Sci. 2022;92–101.
- Kurutas EB. The importance of antioxidants which play the role in cellular response against oxidative/nitrosative stress: current state. Nutr J. 2016;15(1):71–82. [Crossref]
- Lin HJ, Wang X, Shaffer KM, Sasaki CY, Ma W. Characterization of H₂O₂-induced acute apoptosis in cultured neural stem/progenitor cells. FEBS Lett. 2004;570(1):102–6. [Crossref]
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- Cragg GM, Newman DJ. Natural products: a continuing source of novel drug leads. Biochim Biophys Acta. 2013;1830(6):3670–95. [Crossref].
- Zhang W, Xiao D, Mao Q, Xia H. Role of neuroinflammation in neurodegeneration development. Signal Transduct Target Ther. 2023;8(1):267–77. [Crossref].
- Solleiro-Villavicencio H, Rivas-Arancibia S. Effect of chronic oxidative stress on neuroinflammatory response mediated by CD4+ T cells in neurodegenerative diseases. Front Cell Neurosci. 2018;12:114–24. [Crossref].
- Cioffi F, Adam RHI, Broersen K. Molecular mechanisms and genetics of oxidative stress in Alzheimer’s disease. J Alzheimers Dis. 2019;72(4):981–1017. [Crossref].
- Halliwell B. Oxidative stress and neurodegeneration: where are we now? J Neurochem. 2006;97(6):1634–58. [Crossref].
- Suh SW, Gum ET, Hamby AM, Chan PH, Swanson RA. Hypoglycemic neuronal death is triggered by glucose reperfusion and activation of neuronal NADPH oxidase. J Clin Invest. 2007;117(4):910–8. [Crossref].
- Chen Y, Qin C, Huang J, Tang X, Liu C, Huang K, et al. The role of astrocytes in oxidative stress of central nervous system: a mixed blessing. Cell Prolif. 2020;53(3):e12781. [Crossref].
- Li N, Zhang X, Dong H, Zhang S, Sun J, Qian Y. Lithium ameliorates LPS-induced astrocytes activation partly via inhibition of toll-like receptor 4 expression. Cell Physiol Biochem. 2016;38(2):714–25. [Crossref].
- Colombo E, Farina C. Astrocytes: key regulators of neuroinflammation. Trends Immunol. 2016;37(9):608–20. [Crossref].
- Garland EF, Hartnell IJ, Boche D. Microglia and astrocyte function and communication: what do we know in humans? Front Neurosci. 2022;16:824888. [Crossref].
- Phatnani H, Maniatis T. Astrocytes in neurodegenerative disease. Cold Spring Harb Perspect Biol. 2015;7(6):a020628. [Crossref].
- Farina C, Aloisi F, Meinl E. Astrocytes are active players in cerebral innate immunity. Trends Immunol. 2007;28(3):138–45. [Crossref].
- Linnerbauer M, Wheeler MA, Quintana FJ. Astrocyte crosstalk in CNS inflammation. 2020;108(4):608–22. [Crossref].
- Bhat R, Crowe EP, Bitto A, Moh M, Katsetos CD, Garcia FU, et al. Astrocyte senescence as a component of Alzheimer’s disease. PLoS One. 2012;7(9):e45069. [Crossref].
- Jiwaji Z, Hardingham GE. Good, bad, and neglectful: astrocyte changes in neurodegenerative disease. Free Radic Biol Med. 2022;182:93–9. [Crossref].
- Roesslein M, Hirsch C, Kaiser JP, Krug HF, Wick P. Comparability of in vitro tests for bioactive nanoparticles: a common assay to detect reactive oxygen species as an example. Int J Mol Sci. 2013;14(12):24320–37. [Crossref].
- Franklin H, Clarke BE, Patani R. Astrocytes and microglia in neurodegenerative diseases: lessons from human in vitro models. Prog Neurobiol. 2021;200:101973. [Crossref].
- Agatonovic-Kustrin S, Morton DW, Adam A, Mizaton HH, Zakaria H. High-performance thin-layer chromatographic methods in the evaluation of the antioxidant and anti-hyperglycemic activity of Myrmecodia platytyrea as a promising opportunity in diabetes treatment. J Chromatogr A. 2017;1530:192–6. [Crossref].
- Ju A, Cho Y, Kim BR, Lee S, Le HT, Vuong HL, et al. Anticancer effects of methanol extract of Myrmecodia platytyrea leaves against human hepatocellular carcinoma cells via inhibition of ERK and STAT3 signaling pathways. Int J Oncol. 2018;52:201–10. [Crossref].
- Hasan MH, Zakaria H, Wahab IA, Ponto T, Adam A. Myrmecodia platytyrea methanol tuber extract ameliorates hyperglycemia in STZ-induced diabetic Sprague-Dawley male rats. Indones J Pharm. [Crossref].
- Agatonovic-Kustrin S, Morton DW, Mizaton HH, Zakaria H. The relationship between major polyphenolic acids and stigmasterol to antioxidant activity in different extracts of Myrmecodia platytyrea. South Afr J Bot. 2018;115:94–9. [Crossref].
- Haris NFM, Hasan MKN, Wahab IA, Hasan MH, Ponto T, Adam A. Compounds from the antioxidant active fraction of platytyrea. J Health Sci. 2016;14(1):23–9. [Crossref].
- Ayaz M, Sadiq A, Junaid M, Ullah F, Ovais M, Ullah I, et al. Flavonoids as prospective neuroprotectants and their therapeutic propensity in aging associated neurological disorders. Front Aging Neurosci. 2019;11:155–65. [Crossref].
- Bakoyiannis I, Daskalopoulou A, Pergialiotis V, Perrea D. Phytochemicals and cognitive health: are flavonoids doing the trick? Biomed Pharmacother. 2019;109:1488–97. [Crossref].
- de Andrade Teles RB, Diniz TC, Costa Pinto TC, de Oliveira Júnior RG, Gama ESM, de Lavor ÉM, et al. Flavonoids as therapeutic agents in Alzheimer’s and Parkinson’s diseases: a systematic review of preclinical evidences. Oxid Med Cell Longev. 2018;2018:7043213. [Crossref].
- Nn A. A review on the extraction methods use in medicinal plants, principle, strength and limitation. Med Aromat Plants. 2015;4:1–6. [Crossref].
- Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods. 1983;65(1–2):55–63. [Crossref].
- Figueroa D, Asaduzzaman M, Young F. Real time monitoring and quantification of reactive oxygen species in breast cancer cell line MCF-7 by 2’,7’-dichlorofluorescin diacetate (DCFDA) assay. J Pharmacol Toxicol Methods. 2018;94(Pt 1):26–33. [Crossref].
- Sajjadi SE, Ghanadian M, Haghighi M, Mouhebat L. Cytotoxic effect of Cousinia verbascifolia Bunge against OVCAR-3 and HT-29 cancer cells. J HerbMed Pharmacol. 2015;4:15–9.
- Pandey AK, Tripathi S. Concept of standardization, extraction and pre phytochemical screening strategies for herbal drug. J Pharmacogn Phytochem. 2014;2:115–9.
- Zhang QW, Lin LG, Ye WC. Techniques for extraction and isolation of natural products: a comprehensive review. Chin Med. 2018;13:20–30. [Crossref].
- Altamura S, Muckenthaler MU. Iron toxicity in diseases of aging: Alzheimer’s disease, Parkinson’s disease and atherosclerosis. J Alzheimers Dis. 2009;16(4):879–95. [Crossref].
- Jomová K, Hudecova L, Lauro P, Simunkova M, Alwasel SH, Alhazza IM, et al. A switch between antioxidant and prooxidant properties of the phenolic compounds myricetin, morin, 3’,4’-dihydroxyflavone, taxifolin and 4-hydroxy-coumarin in the presence of copper (II) ions: a spectroscopic, absorption titration and DNA damage study. 2019;24(23):4335–45. [Crossref].
- DeTure MA, Dickson DW. The neuropathological diagnosis of Alzheimer’s disease. Mol Neurodegener. 2019;14(1):32–42. [Crossref].
- Mizaton HH, Maisarah MZ, Nik H, Mohd K, Ibtisam AW, Adam A. Anti-inflammatory and anti-hyperlipidaemic activities of Myrmecodia platytyrea tuber: the in vitro studies. Malays J Med Health Sci. 2022;92–101.
- Kurutas EB. The importance of antioxidants which play the role in cellular response against oxidative/nitrosative stress: current state. Nutr J. 2016;15(1):71–82. [Crossref]
- Lin HJ, Wang X, Shaffer KM, Sasaki CY, Ma W. Characterization of H₂O₂-induced acute apoptosis in cultured neural stem/progenitor cells. FEBS Lett. 2004;570(1):102–6. [Crossref]
- Rahal A, Kumar A, Singh V, Yadav B, Tiwari R, Chakraborty S, et al. Oxidative stress, prooxidants, and antioxidants: the interplay. Biomed Res Int. 2014;2014:761264. [Crossref]
- Granzotto A, Zatta P. Resveratrol and Alzheimer’s disease: message in a bottle on red wine and cognition. Front Aging Neurosci. 2014;6:95–105. [Crossref]
- Halliwell B. Are polyphenols antioxidants or pro-oxidants? What do we learn from cell culture and in vivo studies? Arch Biochem Biophys. 2008;476(2):107–12.
- Hinojosa AE, Caso JR, García-Bueno B, Leza JC, Madrigal JL. Dual effects of noradrenaline on astroglial production of chemokines and pro-inflammatory mediators. J Neuroinflammation. 2013;10:81–92.
- Zhou XY, Liu J, Xu ZP, Fu Q, Wang PQ, Zhang H. Dexmedetomidine inhibits the lipopolysaccharide-stimulated inflammatory response in microglia through the pathway involving TLR4 and NF-κB. Kaohsiung J Med Sci. 2019;35(12):750–6.
- Tong W, Chen X, Song X, Chen Y, Jia R, Zou Y, et al. Resveratrol inhibits LPS-induced inflammation through suppressing the signaling cascades of TLR4-NF-κB/MAPKs/IRF3. Exp Ther Med. 2020;19(3):1824–34.
- Jazvinšćak Jembrek M, Oršolić N, Mandić L, Sadžak A, Šegota S. Anti-oxidative, anti-inflammatory and antiapoptotic effects of flavonols: targeting Nrf2, NF-κB and p53 pathways in neurodegeneration. Antioxidants (Basel). 2021;10(10):1628–39.
- Hussain T, Tan B, Yin Y, Blachier F, Tossou MC, Rahu N. Oxidative stress and inflammation: what polyphenols can do for us? Oxid Med Cell Longev. 2016;2016:7432797.
- Panche AN, Diwan AD, Chandra SR. Flavonoids: an overview. J Nutr Sci. 2016;5:e47.
- Othman RA, Moghadasian MH. Beyond cholesterol-lowering effects of plant sterols: clinical and experimental evidence of anti-inflammatory properties. Nutr Rev. 2011;69(7):371–82.
- Simunkova M, Alwasel SH, Alhazza IM, Jomova K, Kollar V, Rusko M, et al. Management of oxidative stress and other pathologies in Alzheimer’s disease. Arch Toxicol. 2019;93(9):2491–513.
- Engida AM, Faika S, Nguyen-Thi BT, Ju YH. Analysis of major antioxidants from extracts of Myrmecodia pendans by UV/visible spectrophotometer, liquid chromatography/tandem mass spectrometry, and high-performance liquid chromatography/UV techniques. J Food Drug Anal. 2015;23(2):303–9.
- Bouayed J, Bohn T. Exogenous antioxidants—Double-edged swords in cellular redox state: health beneficial effects at physiologic doses versus deleterious effects at high doses. Oxid Med Cell Longev. 2010;3(4):228–37.
- Pizzino G, Irrera N, Cucinotta M, Pallio G, Mannino F, Arcoraci V, et al. Oxidative stress: harms and benefits for human health. Oxid Med Cell Longev. 2017;2017:8416763.
- Biswas SK. Does the interdependence between oxidative stress and inflammation explain the antioxidant paradox? Oxid Med Cell Longev. 2016;2016:5698931.
- Eghbaliferiz S, Iranshahi M. Prooxidant activity of polyphenols, flavonoids, anthocyanins and carotenoids: updated review of mechanisms and catalyzing metals. Phytother Res. 2016;30(9):1379–91.

International Journal of Brain Sciences
| Volume | 03 |
| 01 | |
| Received | 13/09/2025 |
| Accepted | 24/09/2025 |
| Published | 31/01/2026 |
| Publication Time | 140 Days |
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