Tiger Fern Leaves Juice Attenuates Arsenic‐Induced Neurobehavioral and Hepatic Disorders in Mice
DOI:
https://doi.org/10.54536/ijvmas.v3i1.6891Keywords:
Antioxidants, Arsenic, Cognition, Liver, MiceAbstract
Age-related arsenic poisoning is a worldwide environmental health issue linked to neurobehavioral dysfunction and acute liver dysfunction, which is mainly mediated by oxidative stress and disruption of antioxidant activities. Natural plants present positive protective strategies, but the neuroprotective or hepatoprotective effects of tiger fern leaves juice (TFJ) have not been studied yet. The paper tested the neurobehavioral changes and hepatic toxicity of arsenic induced by tiger fern leaves juice in mice. Thirty-six adult Swiss albino male mice were randomly placed in six groups (n = 6/group), and orally fed for 28 days with distilled water (control), sodium arsenite (10 mg/kg), TFJ (5 or 10 mL/kg), or arsenic mixed with TFJ. Neurobehavioral evaluations were the Morris water maze, elevated plus maze and rotarod evaluations. The level of hepatic oxidative stress was assessed through malondialdehyde (MDA), superoxide dismutases (SOD), and catalases (CAT) activities. The liver functioning was evaluated by means of the serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP) levels. Arsenic exposure significantly deteriorated cognitive and motor activity, and it raised escape latency in the Morris water maze by around 108 per cent and hepatic lipid peroxidation by around 190 per cent, as well as antioxidant enzyme activities. The co-administration of tiger fern leaf juice was of significant effect in inhibiting these effects; the escape latency was attenuated by as much as 46%, lipid peroxidation by about 55%, and the antioxidant status was restored in a dose-dependent manner. Also, TFJ treatment had significant ameliorating effects on the increased serum liver enzyme levels, which are factors of hepatic functioning. Tiger fern leaves juice has a vigorous neuroprotective and hepatoprotective activity against the toxicity caused by arsenic, which is probably due to its antioxidant and cytoprotective properties. TFJ can be a good natural therapeutic candidate to treat the arsenic-related neurobehavioral and hepatic disorders.
References
Al-Dalahmeh, Y., Al-Bataineh, N., Al-Balawi, S. S., Lahham, J. N., Al-Momani, I. F., Al-Sheraideh, M. S., Mayyas, A. S., Abu Orabi, S. T., & Al-Qudah, M. A. (2022). LC-MS/MS Screening, Total Phenolic, Flavonoid and Antioxidant Contents of Crude Extracts from Three Asclepiadaceae Species Growing in Jordan. Molecules, 27(3), 859. https://www.mdpi.com/1420-3049/27/3/859
Biswas, S., Banna, H. U., Jahan, M., Anjum, A., Siddique, A. E., Roy, A., Nikkon, F., Salam, K. A., Haque, A., Himeno, S., Hossain, K., & Saud, Z. A. (2020). In vivo evaluation of arsenic-associated behavioural and biochemical alterations in F(0) and F(1) mice. Chemosphere, 245, 125619. https://doi.org/10.1016/j.chemosphere.2019.125619
Chang, C. Y., Guo, H. R., Tsai, W. C., Yang, K. L., Lin, L. C., Cheng, T. J., & Chuu, J. J. (2015). Subchronic Arsenic Exposure Induces Anxiety-Like Behaviors in Normal Mice and Enhances Depression-Like Behaviors in the Chemically Induced Mouse Model of Depression. Biomed Res Int, 2015, 159015. https://doi.org/10.1155/2015/159015
Cheng, L., Zhang, Y., Lv, M., Huang, W., Zhang, K., Guan, Z., Feng, X., Yang, Y., Gao, Y., & Liu, X. (2024). Impaired learning and memory in male mice induced by sodium arsenite was associated with MMP-2/MMP-9-mediated blood-brain barrier disruption and neuronal apoptosis. Ecotoxicol Environ Saf, 285, 117016. https://doi.org/10.1016/j.ecoenv.2024.117016
Chu, F., Yang, W., Li, Y., Lu, C., Jiao, Z., Bu, K., Liu, Z., Sun, H., & Sun, D. (2023). Subchronic Arsenic Exposure Induces Behavioural Impairments and Hippocampal Damage in Rats. Toxics, 11(12). https://doi.org/10.3390/toxics11120970
Clemente-Suárez, V. J., Martín-Rodríguez, A., Beltrán-Velasco, A. I., Rubio-Zarapuz, A., Martínez-Guardado, I., Valcárcel-Martín, R., & Tornero-Aguilera, J. F. (2025). Functional and Therapeutic Roles of Plant-Derived Antioxidants in Type 2 Diabetes Mellitus: Mechanisms, Challenges, and Considerations for Special Populations. Antioxidants, 14(6), 725. https://www.mdpi.com/2076-3921/14/6/725
Dey, T., Ghosh, A., Mishra, S., Pal, P. K., Chattopadhyay, A., Pattari, S. K., & Bandyopadhyay, D. (2020). Attenuation of arsenic induced high fat diet exacerbated oxidative stress mediated hepatic and cardiac injuries in male Wistar rats by piperine involved antioxidative mechanisms. Food and Chemical Toxicology, 142, 111477. https://doi.org/https://doi.org/10.1016/j.fct.2020.111477
Dutta, A., Phukan, B. C., Roy, R., Bhattacharya, P., Kumar, D., & Borah, A. (2025). Arsenic Exposure Induces Cognitive Impairment in Mice with Increased Acetylcholinesterase Activity and Inflammation in the Cortex and Hippocampus: Implications for Alzheimer’s Disease. Curr Alzheimer Res. https://doi.org/10.2174/0115672050390649250904100840
El-Saadony, M. T., Saad, A. M., Mohammed, D. M., Alkafaas, S. S., Abd El-Mageed, T. A., Fahmy, M. A., Ezzat Ahmed, A., Algopishi, U. B., Abu-Elsaoud, A. M., Mosa, W. F. A., AbuQamar, S. F., & El-Tarabily, K. A. (2025). Plant bioactive compounds: extraction, biological activities, immunological, nutritional aspects, food application, and human health benefits-A comprehensive review. Front Nutr, 12, 1659743. https://doi.org/10.3389/fnut.2025.1659743
Flora, S. J. (1999). Arsenic-induced oxidative stress and its reversibility following combined administration of N-acetylcysteine and meso 2,3-dimercaptosuccinic acid in rats. Clin Exp Pharmacol Physiol, 26(11), 865-869. https://doi.org/10.1046/j.1440-1681.1999.03157.x
Ganie, S. Y., Javaid, D., Hajam, Y. A., & Reshi, M. S. (2024). Arsenic toxicity: sources, pathophysiology and mechanism. Toxicology Research, 13(1), tfad111.
Ghorbani-Nejad, B., Baghani, M., Hasaruyieh, N. A., Jamshidi, M., Poudineh, L., Karami-Mohajeri, S., Rahimzadegan, M., & Ahmadi, J. (2025). Aminoguanidine attenuates arsenic-induced hepatic oxidative stress: Dose-dependent effects in a mouse model. Toxicol Rep, 15, 102136. https://doi.org/10.1016/j.toxrep.2025.102136
Hu, Y., Li, J., Lou, B., Wu, R., Wang, G., Lu, C., Wang, H., Pi, J., & Xu, Y. (2020). The Role of Reactive Oxygen Species in Arsenic Toxicity. Biomolecules, 10(2). https://doi.org/10.3390/biom10020240
Islam, K., Haque, A., Karim, M. R., Fajol, A., Hossain, M. E., Salam, K., Ali, N., Saud, Z., Rahman, M., Rahman, M., Karim, R., Sultana, P., Hossain, M., Akhand, A., Mandal, A., & Miyat, H. (2011). Dose-response relationship between arsenic exposure and the serum enzymes for liver function tests in the individuals exposed to arsenic: a cross sectional study in Bangladesh. Environmental Health, 10.
Islam, Z., Islam, J., Tony, S. R., Anjum, A., Ferdous, R., Roy, A. K., Hossain, S., Salam, K. A., Nikkon, F., Hossain, K., & Saud, Z. A. (2022). Mulberry leaves juice attenuates arsenic-induced neurobehavioral and hepatic disorders in mice. Food Sci Nutr, 10(12), 4360-4370. https://doi.org/10.1002/fsn3.3028
Jomova, K., Jenisova, Z., Feszterova, M., Baros, S., Liska, J., Hudecova, D., Rhodes, C. J., & Valko, M. (2011). Arsenic: toxicity, oxidative stress and human disease. Journal of applied toxicology, 31(2), 95-107.
Oliveira, T. S. d. C., Gusmão, J. V. F., Rigolon, T. C. B., Wischral, D., Campelo, P. H., Martins, E., & Stringheta, P. C. (2025). Bioactive Compounds and the Performance of Proteins as Wall Materials for Their Encapsulation. Micro, 5(3), 36. https://www.mdpi.com/2673-8023/5/3/36
Rai, V., Mishra, J., Mandrah, K., Somendu, Roy, S., & Bandyopadhyay, S. (2017). Arsenic Induces Hippocampal Neuronal Apoptosis and Cognitive Impairments via an Up-Regulated BMP2/Smad-Dependent Reduced BDNF/TrkB Signaling in Rats. Toxicological sciences : an official journal of the Society of Toxicology, 159, 137-158. https://doi.org/10.1093/toxsci/kfx124
Reddy, A. R. T., Mahadik, S. R., Choudhary, K., Pothuraju, N., Singh, S., Murti, K., Ramalingam, P., & Kumar, N. (2025). Neuro-inflammation Induced by Arsenic: An Insight into Mechanisms and Pathways Involved. Biol Trace Elem Res. https://doi.org/10.1007/s12011-025-04717-8
Roy, A., More, P., Prasad, S., Chouhan, K., & Ghatuary, S. (2025). A Review on Phytochemical Constitutions and Pharmacological activities of Acrostichum Aureum. International Journal of Innovations in Science, Engineering And Management. https://doi.org/10.69968/ijisem.2025v4i2432-438
Rudrapal, M., Khairnar, S. J., Khan, J., Dukhyil, A. B., Ansari, M. A., Alomary, M. N., Alshabrmi, F. M., Palai, S., Deb, P. K., & Devi, R. (2022). Dietary Polyphenols and Their Role in Oxidative Stress-Induced Human Diseases: Insights Into Protective Effects, Antioxidant Potentials and Mechanism(s) of Action. Front Pharmacol, 13, 806470. https://doi.org/10.3389/fphar.2022.806470
Sequeira, S. L., Silk, J. S., Ladouceur, C. D., Hanson, J. L., Ryan, N. D., Morgan, J. K., McMakin, D. L., Kendall, P. C., Dahl, R. E., & Forbes, E. E. (2021). Association of Neural Reward Circuitry Function With Response to Psychotherapy in Youths With Anxiety Disorders. Am J Psychiatry, 178(4), 343-351. https://doi.org/10.1176/appi.ajp.2020.20010094
Teitsdottir, U. D., Darreh-Shori, T., Lund, S. H., Jonsdottir, M. K., Snaedal, J., & Petersen, P. H. (2022). Phenotypic Displays of Cholinergic Enzymes Associate With Markers of Inflammation, Neurofibrillary Tangles, and Neurodegeneration in Pre- and Early Symptomatic Dementia Subjects. Front Aging Neurosci, 14, 876019. https://doi.org/10.3389/fnagi.2022.876019
Tyler, C. R., & Allan, A. M. (2014). The Effects of Arsenic Exposure on Neurological and Cognitive Dysfunction in Human and Rodent Studies: A Review. Curr Environ Health Rep, 1(2), 132-147. https://doi.org/10.1007/s40572-014-0012-1
Vázquez Cervantes, G. I., González Esquivel, D. F., Ramírez Ortega, D., Blanco Ayala, T., Ramos Chávez, L. A., López-López, H. E., Salazar, A., Flores, I., Pineda, B., & Gómez-Manzo, S. (2023). Mechanisms associated with cognitive and behavioral impairment induced by arsenic exposure. Cells, 12(21), 2537.
Xiong, L., Huang, J., Gao, Y., Gao, Y., Wu, C., He, S., Zou, L., Yang, D., Han, Y., Yuan, Q., Zheng, Z., & Hu, G. (2021). Sodium arsenite induces spatial learning and memory impairment associated with oxidative stress and activates the Nrf2/PPARγ pathway against oxidative injury in mice hippocampus. Toxicol Res (Camb), 10(2), 277-283. https://doi.org/10.1093/toxres/tfab007
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