Abstract
To analyze the role of Nrf2-ARE signaling pathway in the regulation of the acute phase of pilocarpine-induced epilepsy in juvenile rats by Tatarinow Sweetflag Extract (TSE). One hundred and twenty SPF-grade Wistar male rats were were divided into five groups by random number table method, namely, normal group, model group, low-dose TSE group, high-dose TSE group, low-dose TSE + Nrf2 inhibitor Brusatol group (low-dose TSE + BRU group), and high-dose TSE + Nrf2 inhibitor Brusatol group (high-dose TSE + BRU group), with 20 rats in each group. The success rate of modelling in the model group, low-dose TSE group, high-dose TSE group, low-dose TSE + BRU group, high-dose TSE + BRU group were 60.00% (12/20), 65.00% (13/20), 65.00% (13/20), 70.00% (14/20), and 70.00% (14/20), respectively, showing no significant difference (P > 0.05). The latency and incidence of class IV and V, discharge amplitude as well as frequency of rats in the low- and high-dose TSE groups were lower than those in the model group (P < 0.05); the lipid peroxide and malondialdehyde concentrations in hippocampal tissues in the low- and high-dose TSE groups were lower than those in the model group (P < 0.05); The Nrf2, NQO-1 and HO- 1 protein and mRNA expression levels were increased in the low- and high-dose TSE groups compared with the model group (P < 0.05). The therapeutic effect of TSE in rats with acute epilepsy was satisfactory, and its mechanism of action may be related to activation of Nrf2-ARE signaling pathway to reduce the degree of oxidative stress.
Similar content being viewed by others
Data Availability
All data generated or used during the study appear in the submitted article.
References
Chen, J. F., & Zhang, M. E. H. (2017). Effects of sodium valproate extended-release tablets on oxidative stress system and cognitive function in epileptic patients. Journal of Hainan Medical College, 23, 841–843.
Kwan, P., Schachter, S. C., & Brodie, M. J. (2011). Drug-resistant epilepsy. New England Journal of Medicine, 365, 919–926.
Williams-Karnesky, R. L., Sandau, U. S., Lusardi, T. A., Lytle, N. K., Farrell, J. M., Pritchard, E. M., et al. (2013). Epigenetic changes induced by adenosine augmentation therapy prevent epileptogenesis. The Journal of Clinical Investigation, 123, 3552–3563.
Xi, X., Yang, J., Song, C., & Pu, Y. (2018). Effects of methionine vitamin B_1 injection on oxidative stress in patients with epilepsy. Journal of Brain and Nervous Diseases, 6, 232–235.
Zhao, J. W., & Cheng, J. M. (2015). Comparative pharmacodynamic study of anticonvulsant effects of 18 single herbal extracts. Journal of Integrative Medicine and Cardiovascular Diseases, 7, 593–596.
Lin, C., & An, H. (2014). Study on the pharmacological effects of Acorus calamus on the central nervous system. Journal of Changchun University of Traditional Chinese Medicine, 30, 230–233.
Ming, J., Ye, J., Zhang, Y., Yang, X., Shao, X., Qiang, J., et al. (2019). Effects of curcumin on growth performance, oxidative stress resistance and expression of nuclear factor erythroid 2-related factor 2/antioxidant responsive element signaling pathway-related genes in grass carp (Ctenopharyngodon idella). Chinese Journal of Animal Nutrition, 31, 809–823.
Gan, N., Yin, F., Kong, H., Ma, Y., Peng, J., & Wu, L. (2013). Interaction of IL-1β and NF-κB in a model of chronic medial temporal lobe epilepsy. Journal of Neuroanatomy, 29, 637–643.
Arbuckle JL (2010). IBM SPSS Amos 19.0 User’s Guide. Crawfordville: Amos Development Corporation.
Ghelani, H., Chapala, M., & Jadav, P. (2016). Diuretic and antiurolithiatic activities of an ethanolic extract of Acorus calamus L. rhizome in experimental animal models. Journal of Traditional and Complementary Medicine, 6, 431–436.
Rahamooz Haghighi, S., Asadi, M. H., Akrami, H., & Baghizadeh, A. (2017). Anti-carcinogenic and anti-angiogenic properties of the extracts of Acorus calamus on gastric cancer cells. Avicenna J Phytomed, 7, 145–156.
Reddy, S., Rao, G., Shetty, B., & Hn, G. (2015). Effects of Acorus calamus rhizome extract on the neuromodulatory system in restraint stress male rats. Turkish Neurosurgery, 25, 425–431.
Ibadullaeva, G., Pichkhadze, G., Ustenova, G., Tikhonova, S., Grudko, V., Bevz, N. Y., et al. (2015). Chemical composition of the CO2-extract of Acorus Calamus obtained under subcritical conditions. Pharmaceutical Chemistry Journal, 49, 388–392.
Zanoli, P., Avallone, R., & Baraldi, M. (1998). Sedative and hypothermic effects induced by β-asarone, a main component of Acorus calamus. Phytotherapy Research: An International Journal Devoted to Pharmacological and Toxicological Evaluation of Natural Product Derivatives, 12, S114–S116.
Dutra, M. R. H., Feliciano, Rd. S., Jacinto, K. R., Gouveia, T. L. F., Brigidio, E., Serra, A. J., et al. (2018). Protective role of UCP2 in oxidative stress and apoptosis during the silent phase of an experimental model of epilepsy induced by pilocarpine. Oxidative medicine and cellular longevity, 2018, 1–12.
Yahata, T., & Hamaoka, K. (2017). Oxidative stress and Kawasaki disease: How is oxidative stress involved from the acute stage to the chronic stage? Rheumatology, 56, 6–13.
Carretón, E., Cerón, J. J., Martínez-Subiela, S., Tvarijonaviciute, A., Caro-Vadillo, A., & Montoya-Alonso, J. A. (2017). Acute phase proteins and markers of oxidative stress to assess the severity of the pulmonary hypertension in heartworm-infected dogs. Parasites & vectors, 10, 165–171.
Bhuyan, P., Patel, D. C., Wilcox, K. S., & Patel, M. (2015). Oxidative stress in murine Theiler’s virus-induced temporal lobe epilepsy. Experimental Neurology, 271, 329–334.
Reddy, A. J., Dubey, A. K., Handu, S. S., Sharma, P., Mediratta, P. K., Ahmed, Q. M., et al. (2018). Anticonvulsant and antioxidant effects of Musa sapientum stem extract on acute and chronic experimental models of epilepsy. Pharmacognosy Research, 10, 49.
Gopcevic, K., Rovcanin, B., Kekic, D., Milasinovic, D., Kocic, G., & Stojanovic, I. (2017). Gelatinases A and B and antioxidant enzyme activity in the early phase of acute myocardial infarction. Folia Biologica, 63, 20.
Funding
This study was supported by the Guiding project of Liaoning Natural Science Foundation (No. 2019-ZD-0802).
Author information
Authors and Affiliations
Contributions
GJ, ZW, WZ, GL designed the study, performed the research and analyzed the data. GL contributed new methods. GJ wrote the paper.
Corresponding author
Ethics declarations
Conflict of Interest
The authors declare that they have no conflict of interest.
Ethics Approval
Every procedure was approved by the Animal Care and Use Committee of the First Affiliated Hospital of Jinzhou Medical University.
Consent to Participate
Not applicable.
Consent to Publish
Not applicable.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Jin, G., Wang, Z., Zhou, W. et al. The Role of Nrf2-ARE Signaling Pathway and Tatarinow Sweetflag Extract to Regulate the Acute Phase of Pilocarpine-Induced Epilepsy in Juvenile Rats. Mol Biotechnol (2023). https://doi.org/10.1007/s12033-023-00911-y
Received:
Accepted:
Published:
DOI: https://doi.org/10.1007/s12033-023-00911-y