Therapeutic effect of Tymasin plus in experimental model of cerebral ischemia

Document Type : Original Article

Authors

1 Department of Basic sciences, Faculty of Veterinary Medicine, Semnan University, Semnan, Iran.

2 Division of Physiology, Department of Basic sciences, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran.

3 Department of basic sciences, Faculty of Veterinary Medicine, Semnan University, Semnan. Iran

4 Department of clinical sciences, Faculty of Veterinary Medicine, Semnan University, Semnan, Iran

5 Department of pathobiology, Faculty of Veterinary Medicine, Semnan University, Semnan, Iran.

Abstract

Acute ischemic brain damage, which is caused by the reduction of blood supply to the brain or the blockage of cerebral vessels, is one of the important causes of death, disability, and behavioral and cognitive disorders in humans all over the world. Tymasin Plus(TP) is an Iranian herbal medicine manufactured by Medin Pharma for some respiratory diseases in humans. In this study, the effect of the mentioned drug on spatial memory and explorative behavior of laboratory animals after experimental cerebral ischemia was investigated. 24 male Wistar rats were divided into 4 experimental groups including control, ischemic, recipients of 0.5 ml and 1 ml of TP. Animals in the control group were not subjected to any intervention. In order to create experimental temporary cerebral ischemia in the ischemic and TP administrated groups, surgery was done on rats and then the ischemic group received normal saline and the TP administrated groups received the mentioned drug. Spatial memory was investigated using Morris Water Maze test, exploratory behavior via open field test and rat brains were examined histopathologically. The results of Morris water Maze and open field tests as well as histopathological results, showed significant differences between the ischemic and control groups. The TP administrated groups compared with ischemic group had significant differences in terms of Morris Water Maze test (1 ml TP administrated group) and histopathological evaluations. Based on the results of this research, it can be concluded that TP has therapeutic effect on the cerebral ischemic induced spatial memory impairment and also has neuroprotective effect.
 

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Al-Majed, A. A., Al-Omar, F. A., & Nagi, M. N. (2006). Neuroprotective effects of thymoquinone against transient forebrain ischemia in the rat hippocampus. European Journal of Pharmacology, 543(1–3), 40–47. https://doi.org/10.1016/j.ejphar.2006.05.033
Andersen, M. B., Zimmer, J., & Sams-Dodd, F. (1999). Specific behavioral effects related to age and cerebral ischemia in rats. Pharmacology Biochemistry and Behavior, 64, 673–682. https://doi.org/10.1016/S0091-3057(99)00125-5
Bachevalier, J., & Meunier, M. (1996). Cerebral ischemia: Are the memory deficits associated with hippocampal cell loss? Hippocampus, 6(5), 553–560. https://doi.org/10.1002/(SICI)1098-1063(1996)6:5<553: AID-HIPO14>3.0.CO;2-3
Bromley-Brits, K., Deng, Y., & Song, W. (2011). Morris water maze test for learning and memory deficits in Alzheimer's disease model mice. Journal of Visualized Experiments, 53, e2920. https://doi.org/10.3791/2920
Broughton, B. R., Reutens, D. C., & Sobey, C. G. (2009). Apoptotic mechanisms after cerebral ischemia. Stroke, 40, 331–339. https://doi.org/10.1161/STROKEAHA.108.531632
Escobar, I., Xu, J., Jackson, C. W., & Perez-Pinzon, M. A. (2019). Altered neural networks in the Papez Circuit: Implications for cognitive dysfunction after cerebral ischemia. Journal of Alzheimer's Disease, 67, 425–446. https://doi.org/10.3233/JAD-180891
Lucas, S. M., Rothwell, N. J., & Gibson, R. M. (2006). The role of inflammation in CNS injury and disease. British Journal of Pharmacology, 147(S1), S232–S240. https://doi.org/10.1038/sj.bjp.0706400
Rabiei, Z., Mokhtari, S., Asgharzade, S., Gholami, M., Rahnama, S., & Rafieian-Kopaei, M. (2015). Inhibitory effect of Thymus vulgaris extract on memory impairment induced by scopolamine in rat. Asian Pacific Journal of Tropical Biomedicine, 5(10), 845–851. https://doi.org/10.1016/j.apjtb.2015.07.008
Setorki, M., & Mirzapoor, S. (2017). Evaluation of Thymus vulgaris extract on hippocampal injury induced by transient global cerebral ischemia and reperfusion in rat. Zahedan Journal of Research in Medical Sciences, 19(11), e9604. https://doi.org/10.5812/zjrms.9604
Shi, H., & Liu, K. J. (2007). Cerebral tissue oxygenation and oxidative brain injury during ischemia and reperfusion. Frontiers in Bioscience, 12, 13–26. https://doi.org/10.2741/2031
Vannucci, R. C., Towfighi, J., & Vannucci, S. J. (2004). Secondary energy failure after cerebral hypoxia–ischemia in the immature rat. Journal of Cerebral Blood Flow & Metabolism, 24, 1090–1097. https://doi.org/10.1097/01.WCB.0000130866.37074.D1
Warner, D. S., Sheng, H., & Batinić-Haberle, I. (2004). Oxidants, antioxidants and the ischemic brain. Journal of Experimental Biology, 207, 3221–3231. https://doi.org/10.1242/jeb.01022
Zaghlool, S. S., Abo-Seif, A. A., Rabeh, M. A., Abdelmohsen, U. R., & Messiha, B. A. (2019). Gastro-protective and antioxidant potential of Althaea officinalis and Solanum nigrum on pyloric ligation/indomethacin-induced ulceration in rats. Antioxidants, 8(11), 512. https://doi.org/10.3390/antiox8110512
Zavari, F., & Karimzadeh, F. (2017). A review on the behavioral tests for learning and memory assessments in rat. The Neuroscience Journal of Shefaye Khatam, 5(2), 110–124. https://doi.org/10.29252/shefa.5.2.110