year 18, Issue 72 (11-2019)                   J. Med. Plants 2019, 18(72): 183-191 | Back to browse issues page


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Yadegari M, Mirdar S, Hamidian G, Berenjeian Tabrizi H. Effect of the Adiantum capillus-veneris Extract on Immunohistochemical Expression of Lung Heat-Shock Proteins in Rats Exposed to Hypoxia. J. Med. Plants 2019; 18 (72) :183-191
URL: http://jmp.ir/article-1-2713-en.html
1- PhD of Exercise Physiology, Department of Exercise Physiology, Faculty of Physical Education and Sport Sciences, University of Mazandaran, Mazandaran, Iran
2- Professor, PhD of Exercise Physiology, Department of Exercise Physiology, Faculty of Physical Education and Sport Sciences,University of Mazandaran, Mazandaran, Iran
3- Assistant Professor, PhD of Histological, Department of Basic Sciences, Faculty of Veterinary Medicine, University of Tabriz, Tabriz, Iran
4- Assistant Professor, Department of Physical Education and Sport Sciences, Kazerun Branch, Islamic Azad University, Kazerun, Iran , hberenjeian@gmail.com
Abstract:   (3363 Views)
Background: Despite the traditional use of the Adiantum capillus-veneris plant, there is little evidence of its clinical effects.
Objective: The purpose of the present study was to investigate the effect of the Adiantum capillus-veneris extract on Immunohistochemical expression of Lung heat-Shock Proteins in rats exposed to hypoxia.
Methods: Twenty-four male Wistar rats (control: 8, training-hypoxia: 8, training-hypoxia-supplement: 8) without clinically evident disease were used. The rats were exposed to hypoxia environment for 3 week following 6 weeks interval training. Tweleve of the experimental samples were taken 500 ml Adiantum capillus-veneris extract per body weight (kg) in during exposure to hypoxia environment. Finally lung tissue was removed for immunohistochemistry tests of HSP70 and HSP90. To analyze of data, ANOVA test was used (α≤0.05).
Results: Expression of HSP70 and HSP90 increased significantly in hypoxia group comparison with the control group (P≤0.05). Expression of HSP70 and HSP90 protein decreased significantly in the Supplement hypoxia group comparison with the hypoxia group (P≤0.05).
Conclusion: Reduction effects of Adiantum capillus-veneris extract on expression of the parenchyma lung heat- shock protein in hypoxia conditions was observed that probably indicate decreased oxidative stress in the lung.
Full-Text [PDF 1129 kb]   (1070 Downloads)    
Type of Study: Research | Subject: Pharmacology & Toxicology
Received: 2018/07/13 | Accepted: 2018/09/2 | Published: 2019/10/28

References
1. Semenza GL. Hypoxia-inducible factors in physiology and medicine. Cell 2012; 148 (3): 399-408. [DOI:10.1016/j.cell.2012.01.021]
2. Majmundar AJ, Wong WJ and Simon MC. Hypoxia-inducible factors and the response to hypoxic stress. Molecular Cell. 2010; 40 (2): 294-309. [DOI:10.1016/j.molcel.2010.09.022]
3. Richalet J-P, Larmignat P, Poitrine E, Letournel M and Canouï-Poitrine F. Physiological risk factors for severe high-altitude illness: a prospective cohort study. American J. Respiratory and Critical Care Medicine 2012; 185 (2): 192-8. [DOI:10.1164/rccm.201108-1396OC]
4. Majmundar AJ, Wong WJ and Simon MC. Hypoxia-inducible factors and the response to hypoxic stress. Molecular Cell 2010; 40: 294-309. [DOI:10.1016/j.molcel.2010.09.022]
5. Yadegari M, Mirdar S and Hamidian G. The impact of three weeks taper in hypoxic environment on apoptotic index of Bax / Bcl2 and pulmonary alveolar epithelial cell population. 10th international conference of Tehran. 2017; 10.22089/10thconf.2017.680.
6. Yadegari M, Riahi S, Mirdar S, Hamidiyan GH, Yousefpour M and Riyahi F. Immunohistochemical detection of apoptotic factors Bax and Bcl-2 in the lung alveoli, followed by six weeks of high intensity exercise training. Daneshvar Medicine 2016; 24 (129): 31-40.
7. Yadegari M, Mirdar S and Hamidian G. The effect of high-intensity interval training on lung parenchymal and non-parenchymal structural changes. Daneshvar Medicine 2016; 23 (124): 51-60.
8. Yadegari M, Riahi S, mirdar S, Hamidiyan G and Mosadegh P. investigatingof IL-6 level and lung inflammatory cells after performing high-intensity interval training and Exposure to hypoxic environment. SJE. 2016; 18 (3): 26-36.
9. Yadegari M, Riahi S, Mirdar S, Hamidian G and Mosadegh zavaragh P. Effect of the Adiantum capillus Veneris Extract on Bax and Bcl2 Apoptotic Markers of Lung Modulation in Trained Rats and Exposed to Hypoxic Stress. Journal of Medicinal Plants 2018; 4 (64): 162-71.
10. Latchman DS. Heat shock proteins and cardiac protection. Cardiovascular Res. 2001; 51 (4): 637-46. [DOI:10.1016/S0008-6363(01)00354-6]
11. Asea AA and Pedersen BK. Heat shock proteins and whole body physiology: Springer Science & Business Media; 2009, pp: 38-45. [DOI:10.1007/978-90-481-3381-9]
12. Packer N, Pervaiz N and Hoffman-Goetz L. Does exercise protect from cognitive decline by altering brain cytokine and apoptotic protein levels? A systematic review of the literature. Exerc. Immunol. Rev. 2010; 16: 138-62.
13. Podhorska-Okolow M, Dziegiel P, Gomulkiewicz A, Kisiela D, Dolinska-Krajewska B, Jethon Z and et al. Exercise-induced apoptosis in rat kidney is mediated by both angiotensin II AT1 and AT2 receptors. 2006, 11-17.
14. Mujika I. Intense training: the key to optimal performance before and during the taper. Scandinavian J. Medicine & Science in Sports 2010; 20 (s2): 24-31. [DOI:10.1111/j.1600-0838.2010.01189.x]
15. Yuan Q, Zhang X, Liu Z, Song S, Xue P, Wang J and et al. Ethanol extract of Adiantum capillus-veneris L. suppresses the production of inflammatory mediators by inhibiting NF-κB activation. J. Ethnopharmacol. 2013; 147 (3): 603-11. [DOI:10.1016/j.jep.2013.03.046]
16. Mehdi YA SM and GholamReza HA. The effect of high-intensity interval training on lung parenchymal and non-parenchymal structural changes. Daneshvar Medicine 2016; 23 (124): 51-60.
17. Nilforoushzadeh MA, Javanmard SH, Ghanadian M, Asghari G, Jaffary F, Yakhdani AF and et al. The effects of Adiantum capillus-veneris on wound healing: An experimental in vitro evaluation. International J. Preventive Medicine 2014; 5 (10): 1261.
18. Wendakoon C, Calderon P and Gagnon D. Evaluation of selected medicinal plants extracted in different ethanol concentrations for antibacterial activity against human pathogens. J. Medicinally Active Plants 2012; 1 (2): 60-8.
19. Rajurkar N and Gaikwad K. Evaluation of phytochemicals, antioxidant activity and elemental content of Adiantum capillus veneris leaves. J. Chemical and Pharmaceutical Res. 2012; 4 (1): 365-74.
20. Schneider JP and Ochs M. Stereology of the lung. Methods in Cell Biol. 2012; 113: 257-94. [DOI:10.1016/B978-0-12-407239-8.00012-4]
21. Hofman F. Immunohistochemistry. Current Protocols in Immunol. 2002, 21.4. 1-.4. 3.
22. Di Cataldo S, Ficarra E, Acquaviva A and Macii E. Automated segmentation of tissue images for computerized IHC analysis. Computer Methods and Programs in Biomedicine 2010; 100 (1): 1-15. [DOI:10.1016/j.cmpb.2010.02.002]
23. Aoi W, Naito Y, Takanami Y, Kawai Y, Sakuma K, Ichikawa H and et al. Oxidative stress and delayed-onset muscle damage after exercise. Free Radical Biology and Medicine 2004; 37 (4): 480-7. [DOI:10.1016/j.freeradbiomed.2004.05.008]
24. Lawler HM, Underkofler CM, Kern PA, Erickson C, Bredbeck B and Rasouli N. Adipose tissue hypoxia, inflammation, and fibrosis in obese insulin-sensitive and obese insulin-resistant subjects. The Journal of Clinical Endocrinology & Metabolism 2016; 101 (4): 1422-8. [DOI:10.1210/jc.2015-4125]
25. Fisher-Wellman K and Bloomer RJ. Acute exercise and oxidative stress: a 30 year history. Dynamic Medicine 2009; 8 (1): 1. [DOI:10.1186/1476-5918-8-1]
26. Eltzschig HK and Carmeliet P. Hypoxia and inflammation. New England J. Medicine 2011; 364 (7): 656-65. [DOI:10.1056/NEJMra0910283]
27. Paulsen G, Vissing K, Kalhovde JM, Ugelstad I, Bayer ML, Kadi F and et al. Maximal eccentric exercise induces a rapid accumulation of small heat shock proteins on myofibrils and a delayed HSP70 response in humans. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 2007; 293 (2): R844-R53. [DOI:10.1152/ajpregu.00677.2006]
28. Nixon B, Bromfield EG, Cui J and De Iuliis GN. Heat Shock Protein A2 (HSPA2): Regulatory Roles in Germ Cell Development and Sperm Function. The Role of Heat Shock Proteins in Reproductive System Development and Function: Springer; 2017, pp: 67-93. [DOI:10.1007/978-3-319-51409-3_4]
29. Atalay M, Oksala NK, Laaksonen DE, Khanna S, Nakao C, Lappalainen J and et al. Exercise training modulates heat shock protein response in diabetic rats. J. Applied Physiol. 2004; 97 (2): 605-11. [DOI:10.1152/japplphysiol.01183.2003]
30. Yuan Q, Zhang X, Liu Z, Song S, Xue P, Wang J and et al. Ethanol extract of Adiantum capillus-veneris L. suppresses the production of inflammatory mediators by inhibiting NF-κB activation. J. Ethnopharmacol. 2013; 147 (3): 603-11. [DOI:10.1016/j.jep.2013.03.046]
31. Kumar A. Antioxidant effect of Adiantum capillus-veneris Linn. on human lymphocyte: an in vitro study. J. Cell and Tissue Res. 2009; 9 (2): 1899-902.
32. Jiang M-Z, Yan H, Wen Y and Li X-M. In vitro and in vivo studies of antioxidant activities of flavonoids from Adiantum capillus-veneris L. Afr. J. Pharm. Pharmacol. 2011; 5 (18): 2079-85. [DOI:10.5897/AJPP11.500]

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