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Rezaie F, Ghafouri Khosroshahi A, Larki-Harchegani A, Nourian A, Khosravi H. Hydroalcoholic Sumac Extract as a Protective Agent Against X-Ray-Induced Pulmonary Fibrosis. rbmb.net 2024; 13 (2) :231-242
URL: http://rbmb.net/article-1-1368-en.html
Department of Medicinal Chemistry, School of Pharmacy, Hamadan University of Medical Sciences, Hamadan, Iran.
Abstract:   (494 Views)
Background: X-ray exposure can result in acute or chronic damage to lung tissue, leading to pneumonitis and fibrosis. Given the potent antioxidant properties of sumac, this study investigates the impact of hydroalcoholic sumac extract on X-ray-induced pulmonary fibrosis in rats.

Methods: In this experimental study, 36 rats were randomly divided into six groups of six rats each. The treatment and sham groups received intraperitoneal administration of the extract daily for one week before exposure to X-ray radiation. On the seventh day, all rats except those in group 3 were exposed to 2 Gy of 6 MV X-rays using an electro-linear accelerator. Lung tissue was subsequently removed to assess the subacute effects of the extract. Data analysis involved independent sample t-tests and one-way ANOVA using SPSS 26.

Results: A single dose of X-rays significantly increased oxidative stress and lung tissue damage in rats. However, rats receiving vitamin C and hydroalcoholic sumac extract at two different doses (100 and 400 mg/kg intraperitoneally) positively improved lung damage and decreased antioxidant parameters.

Conclusion: The findings demonstrate that hydroalcoholic sumac extract can mitigate oxidative stress and enhance lung repair following X-ray radiation exposure.
Full-Text [PDF 542 kb]   (141 Downloads)    
Type of Article: Original Article | Subject: Biochemistry
Received: 2024/04/9 | Accepted: 2024/06/23 | Published: 2025/01/4

References
1. Raghu G, Remy-Jardin M, Myers JL, Richeldi L, Ryerson CJ, Lederer DJ, et al. Diagnosis of idiopathic pulmonary fibrosis. An official ATS/ERS/JRS/ALAT clinical practice guideline. Am J Respir Crit Care Med. 2018;198(5):e44-68. [DOI:10.1164/rccm.201807-1255ST] [PMID]
2. Duchemann B, Annesi-Maesano I, Jacobe de Naurois C, et al. Prevalence and incidence of interstitial lung diseases in a multi-ethnic county of Greater Paris. Eur Respir J. 2017; 50: 1602419. [DOI:10.1183/13993003.02419-2016] [PMID]
3. Fois AG, Paliogiannis P, Sotgia S, Mangoni AA, Zinellu E, Pirina P, et al. Evaluation of oxidative stress biomarkers in idiopathic pulmonary fibrosis and therapeutic applications: a systematic review. Respiratory research. 2018;19(1):51. [DOI:10.1186/s12931-018-0754-7] [PMID] []
4. Kinnula VL, Fattman CL, Tan RJ, Oury TD. Oxidative stress in pulmonary fibrosis: a possible role for redox modulatory therapy. Am J Respir Crit Care Med. 2005;172:417-422. [DOI:10.1164/rccm.200501-017PP] [PMID] []
5. Mohammad MK, Mohamed MI, Zakaria AM, Abdul Razak HR, Saad WM. Watermelon (Citrullus lanatus (Thunb.) Matsum. and Nakai) juice modulates oxidative damage induced by low dose X-ray in mice. BioMed research international. 2014;2014:512834. [DOI:10.1155/2014/512834] [PMID] []
6. Abid SH, Malhotra V, Perry MC. Radiation-induced and chemotherapy-induced pulmonary injury. Curr Opin Oncol. 2001 Jul;13(4):242-8. [DOI:10.1097/00001622-200107000-00006] [PMID]
7. Bolourani S, Brenner M, Wang P. The interplay of DAMPs, TLR4, and proinflammatory cytokines in pulmonary fibrosis. J Mol Med (Berl). 2021;99(10):1373-1384. [DOI:10.1007/s00109-021-02113-y] [PMID] []
8. Para AE, Bezjak A, Yeung IW, Van Dyk J, Hill RP. Effects of genistein following fractionated lung irradiation in mice. Radiother Oncol. 2009;92(3):500-10. [DOI:10.1016/j.radonc.2009.04.005] [PMID]
9. Mehrabani M, Goudarzi M, Mehrzadi S, Siahpoosh A, Mohammadi M, Khalili H, Malayeri A. Crocin: a protective natural antioxidant against pulmonary fibrosis induced by bleomycin. Pharmacol Rep. 2020;72(4):992-1001. [DOI:10.1007/s43440-019-00023-y] [PMID]
10. Kosar M, Bozan B, Temelli F, Baser KH. Antioxidant activity and phenolic composition of sumac (Rhus coriaria L.) extracts. Food Chem. 2007;103(3):952-9. [DOI:10.1016/j.foodchem.2006.09.049]
11. Hosseini S, Ramezan Y, Arab S. A comparative study on physicochemical characteristics and antioxidant activity of sumac (Rhus coriaria L.), cumin (Cuminum cyminum), and caraway (Carum carvil) oils. J Food Me:as char:act. 2020;14(6):3175-83. [DOI:10.1007/s11694-020-00561-7]
12. Nozza E, Melzi G, Marabini L, Marinovich M, Piazza S, Khalilpour S, et al. Rhus coriaria L. fruit extract prevents UV-A-induced genotoxicity and oxidative injury in human microvascular endothelial cells. Antioxidants. 2020;9(4):292. [DOI:10.3390/antiox9040292] [PMID] []
13. Ashcroft T, Simpson JM, Timbrell V. Simple method of estimating severity of pulmonary fibrosis on a numerical scale. J Clin Pathol. 1988;41(4):467-70. [DOI:10.1136/jcp.41.4.467] [PMID] []
14. Raghu G, Collard HR, Egan JJ, Martinez FJ, Behr J, Brown KK, et al. An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management. Am J Resp Critiic Care Med. 2011;183(6):788-824. [DOI:10.1164/rccm.2009-040GL] [PMID] []
15. Inghilleri S, Morbini P, Campo I, Zorzetto M, Oggionni T, Pozzi E, Luisetti M. Erratum to "factors influencing oxidative imbalance in pulmonary fibrosis: an immunohistochemical study". Pulm Med. 2011;2011:515608. https://doi.org/10.1155/2011/421409 [DOI:10.1155/2011/515608]
16. Ding Q, Luckhardt T, Hecker L, Zhou Y, Liu G, Antony VB, et al. New insights into the pathogenesis and treatment of idiopathic pulmonary fibrosis. Drugs. 2011;71(8):981-1001. [DOI:10.2165/11591490-000000000-00000] [PMID] []
17. Hecker L. Mechanisms and consequences of oxidative stress in lung disease: therapeutic implications for an aging populace. Am J Physiol Lung Cell Mol Physiol. 2018;314(4):L642-53. [DOI:10.1152/ajplung.00275.2017] [PMID] []
18. Macagno F, Varone F, Leone PM, Mari PV, Panico L, Berardini L, Richeldi L. New treatment directions for IPF: current status of ongoing and upcoming clinical trials. Expert Rev Respir Med. 2017;11(7):533-548. [DOI:10.1080/17476348.2017.1335601] [PMID]
19. Veith C, Drent M, Bast A, van Schooten FJ, Boots AW. The disturbed redox-balance in pulmonary fibrosis is modulated by the plant flavonoid quercetin. Toxicol Appl Pharmacol. 2017;336:40-48. [DOI:10.1016/j.taap.2017.10.001] [PMID]
20. Weiss JF, Landauer MR. Protection against ionizing radiation by antioxidant nutrients and phytochemicals. Toxicology. 2003;189(1-2):1-20. [DOI:10.1016/S0300-483X(03)00149-5] [PMID]
21. Pehlivan FE. Vitamin C: An antioxidant agent. Vitamin C. 2017;2:23-35. [DOI:10.5772/intechopen.69660]
22. Lee YH, Kim YS, Lee SN, Lee HC, Oh SJ, Kim SJ, et al. Interstitial lung change in pre-radiation therapy computed tomography is a risk factor for severe radiation pneumonitis. Cancer Res Treat. 2015;47:676-86. [DOI:10.4143/crt.2014.180] [PMID] []
23. Miglioretti DL, Johnson E, Williams A, Greenlee RT, Weinmann S, Solberg LI, et al. The use of computed tomography in pediatrics and the associated radiation exposure and estimated cancer risk. JAMA Pediatr. 2013;167(8):700-7. [DOI:10.1001/jamapediatrics.2013.311] [PMID] []
24. Jang SS, Kim HG, Lee JS, Han JM, Park HJ, Huh GJ, Son CG. Melatonin reduces X-ray radiation-induced lung injury in mice by modulating oxidative stress and cytokine expression. Int J Radiat Biol. 2013;89(2):97-105. [DOI:10.3109/09553002.2013.734943] [PMID]
25. Homma S, Azuma A, Taniguchi H, Ogura T, Mochiduki Y, Sugiyama Y, et al. Efficacy of inhaled N-acetylcysteine monotherapy in patients with early stage idiopathic pulmonary fibrosis. Respirology. 2012;17(3):467-77. [DOI:10.1111/j.1440-1843.2012.02132.x] [PMID]
26. Hagiwara SI, Ishii Y, Kitamura S. Aerosolized administration of N-acetylcysteine attenuates lung fibrosis induced by bleomycin in mice. Am J Respir Crit Care Med. 2000;162(1):225-31. [DOI:10.1164/ajrccm.162.1.9903129] [PMID]
27. Mohammad MK, Mohamed MI, Zakaria AM, Abdul Razak HR, Saad WM. Watermelon (Citrullus lanatus (Thunb.) Matsum. and Nakai) juice modulates oxidative damage induced by low dose X-ray in mice. Biomed Res Int. 2014;2014:512834. [DOI:10.1155/2014/512834] [PMID] []
28. Alsamri H, Athamneh K, Pintus G, Eid AH, Iratni R. Pharmacological and Antioxidant Activities of Rhus coriaria L. (Sumac). Antioxidants (Basel). 2021;10(1):73. [DOI:10.3390/antiox10010073] [PMID] []
29. Ahmed Mobasher M, Galal El-Tantawi H, Samy El-Said K. Metformin Ameliorates Oxidative Stress Induced by Diabetes Mellitus and Hepatocellular Carcinoma in Rats. Rep Biochem Mol Biol. 2020;9(1):115-128. [DOI:10.29252/rbmb.9.1.115] [PMID] []
30. Mahmoudivar S, Zarredar H, Asadi M, Zafari V, Hashemzadeh S, Farzaneh R, Asvadi Kermani T. Serum miR-23 and miR-150 Profiles as Biomarkers for Predicting Recurrence following Surgical Intervention in Colorectal Cancer Patients. Rep Biochem Mol Biol. 2024;12(4):540-549. [DOI:10.61186/rbmb.12.4.540] [PMID] []
31. Azmoonfar R, Khosravi H, Rafieemehr H, Mirzaei F, Dastan D, Ghiasvand MR, et al. Radioprotective effect of Malva sylvestris L. against radiation-induced liver, kidney and intestine damages in rat: A histopathological study. Biochem Biophys Rep. 2023;34:101455. [DOI:10.1016/j.bbrep.2023.101455] [PMID] []

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