دوره 30، شماره 139 - ( 11-1400 )                   جلد 30 شماره 139 صفحات 145-138 | برگشت به فهرست نسخه ها


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Ziamajidi N, Abbasalipourkabir R, Lotfi F, Goodarzi M T. Aqueous Garlic Extract Alleviates Oxidative Stress and Inflammation in Retinal Tissue of Rats with Diabetes Type 2. J Adv Med Biomed Res 2022; 30 (139) :138-145
URL: http://journal.zums.ac.ir/article-1-6346-fa.html
Aqueous Garlic Extract Alleviates Oxidative Stress and Inflammation in Retinal Tissue of Rats with Diabetes Type 2. Journal of Advances in Medical and Biomedical Research. 1400; 30 (139) :138-145

URL: http://journal.zums.ac.ir/article-1-6346-fa.html


چکیده:   (88144 مشاهده)

Background and Objective: Retinopathy is a common difficulty in diabetic subjects. Hyperglycemia damages the tissues through stimulation of oxidative stress and inflammation. Since the antioxidant function of garlic has been proven, in the current report the activity of aqueous garlic extract (AGE) upon the oxidative stress and inflammation in the retinal substances of rats with diabetes was investigated.
Materials and Methods: 24 male Wistar rats were distributed in 4 groups: the healthy rats,  the rats with diabetes (DM2),the garlic- treated rats with diabetes (DM2+AGE), and the garlic- treated healthy rats (AGE). After the treatment was finished, oxidative stress, total antioxidant capacity (TAC), total oxidant status (TOS), oxidative stress index (OSI), thiol group (SH), and lipid peroxidation (LPO) were assayed. For the evaluation of inflammation, mRNA and protein levels of transforming growth factor beta-2 (TGF-β2) and interleukin-1 beta (IL-1β) were measured in retinal homogenates using real-time PCR and ELISA, correspondingly.
Results: In  the DM2 rats, TAC and thiol group diminished (p<0.05 and p<0.001, respectively), whereas TOS and LPO increased (p<0.01 and p<0.001, correspondingly) compared to the control rats. In the DM2+AGE rats TAC and thiol group increased (p<0.01 and p<0.05, correspondingly), whereas TOS and LPO diminished (p<0.05 and p<0.001, correspondingly) compared with DM2 rats. The gene expression and protein concentrations of TGF-β2 and IL-1β increased in  the DM2 rats compared to the healthy group, whereas these parameters decreased in the DM2+AGE rats compared to the untreated rats with diabetes (p<0.001).
Conclusion: The findings revealed the antioxidant and anti-inflammatory results of garlic extract. Thus, garlic extract could be beneficial for lessening diabetes-induced retinopathy.

متن کامل [PDF 355 kb]   (47135 دریافت)    
نوع مطالعه: مقاله پژوهشی | موضوع مقاله: Pharmacology
دریافت: 1399/10/8 | پذیرش: 1400/3/15 | انتشار: 1400/11/11

فهرست منابع
1. Care D. Diagnosis and classification of diabetes mellitus. Diabetes care. 2006.
2. Chawla A, Chawla R, Jaggi S. Microvasular and macrovascular complications in diabetes mellitus: distinct or continuum? Indian J Endocrinol Metab. 2016;20(4):546. [DOI:10.4103/2230-8210.183480] [PMID] [PMCID]
3. Robles-Rivera RR, Castellanos-González JA, Olvera-Montaño C, et al. Adjuvant therapies in diabetic retinopathy as an early approach to delay its progression: the importance of oxidative stress and inflammation. Oxid Med Cell Longevity. 2020;2020. [DOI:10.1155/2020/3096470] [PMID] [PMCID]
4. Song S, Yu X, Zhang P, Dai H. Increased levels of cytokines in the aqueous humor correlate with the severity of diabetic retinopathy. J Diabet Complicat. 2020;34(9):107641. [DOI:10.1016/j.jdiacomp.2020.107641] [PMID]
5. Bonfiglio V, Platania CBM, Lazzara F, et al. TGF-β serum levels in diabetic retinopathy patients and the role of anti-VEGF therapy. Int J Molec Sci. 2020;21(24):9558. [DOI:10.3390/ijms21249558] [PMID] [PMCID]
6. Lingappan K. NF-κB in oxidative stress. Current opinion in toxicology. 2018;7:81-6. [DOI:10.1016/j.cotox.2017.11.002] [PMID] [PMCID]
7. Choudhury H, Pandey M, Hua CK, et al. An update on natural compounds in the remedy of diabetes mellitus: A systematic review. J Trad Complement Med. 2018;8(3):361-76. [DOI:10.1016/j.jtcme.2017.08.012] [PMID] [PMCID]
8. Ai X, Yu P, Hou Y, et al. A review of traditional Chinese medicine on treatment of diabetic retinopathy and involved mechanisms. Biomed Pharmacother. 2020;132:110852. [DOI:10.1016/j.biopha.2020.110852] [PMID]
9. Bayan L, Koulivand PH, Gorji A. Garlic: a review of potential therapeutic effects. Avicenna J Phytomed. 2014;4(1):1.
10. Ghasemi A, Khalifi S, Jedi S. Streptozotocin-nicotinamide-induced rat model of type 2 diabetes. Acta Physiologica Hungarica. 2014;101(4):408-20. [DOI:10.1556/APhysiol.101.2014.4.2] [PMID]
11. Benzie IF, Strain JJ. The ferric reducing ability of plasma (FRAP) as a measure of "antioxidant power": the FRAP assay. Analytic Biochem. 1996;239(1):70-6. [DOI:10.1006/abio.1996.0292] [PMID]
12. Erel O. A new automated colorimetric method for measuring total oxidant status. Clin Biochem. 2005;38(12):1103-11. [DOI:10.1016/j.clinbiochem.2005.08.008] [PMID]
13. Sedlak J, Lindsay RH. Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman's reagent. Analytic Biochem. 1968;25:192-205. [DOI:10.1016/0003-2697(68)90092-4]
14. Kurokawa Y, Takamura N, Matsuoka C, et al. Comparative studies on lipid peroxidation in the kidney of rats, mice, and hamsters and on the effect of cysteine, glutathione, and diethyl maleate treatment on mortality and nephrotoxicity after administration of potassium bromate. J Am College Toxicol. 1987;6(4):489-501. [DOI:10.3109/10915818709075694]
15. Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2− ΔΔCT method. Methods. 2001;25(4):402-8. [DOI:10.1006/meth.2001.1262] [PMID]
16. Kumari S, Panda S, Mangaraj M, Mandal M, Mahapatra P. Plasma MDA and antioxidant vitamins in diabetic retinopathy. Indian J Clin Biochem. 2008;23(2):158-62. [DOI:10.1007/s12291-008-0035-1] [PMID] [PMCID]
17. Mancino R, Di Pierro D, Varesi C, et al. Lipid peroxidation and total antioxidant capacity in vitreous, aqueous humor, and blood samples from patients with diabetic retinopathy. Molec Vision. 2011;17:1298.
18. Kirboga K, Ozec AV, Kosker M, et al. The association between diabetic retinopathy and levels of ischemia-modified albumin, total thiol, total antioxidant capacity, and total oxidative stress in serum and aqueous humor. J Ophthalmol. 2014;2014. [DOI:10.1155/2014/820853] [PMID] [PMCID]
19. Rangasamy S, McGuire PG, Das A. Diabetic retinopathy and inflammation: novel therapeutic targets. Middle East African J Ophthalmol. 2012;19(1):52. [DOI:10.4103/0974-9233.92116] [PMID] [PMCID]
20. Anwar MM, Meki A-RM. Oxidative stress in streptozotocin-induced diabetic rats: effects of garlic oil and melatonin. Compar Biochem Physiol Part A: Molec Integrat Physiol. 2003;135(4):539-47. [DOI:10.1016/S1095-6433(03)00114-4]
21. Al-brakati AY. Protective effect of garlic against diabetic retinopathy in adult albino rats. Res J Pharmaceut Biol Chem Sci. 2016;7(5):2748-59.
22. Shouk R, Abdou A, Shetty K, Sarkar D, Eid AH. Mechanisms underlying the antihypertensive effects of garlic bioactives. Nutr Res. 2014;34(2):106-15. [DOI:10.1016/j.nutres.2013.12.005] [PMID]
23. Kowluru RA, Chan P-S. Oxidative stress and diabetic retinopathy. Experiment Diabet Res. 2007;2007. [DOI:10.1155/2007/43603] [PMID] [PMCID]
24. Saika S. TGF β pathobiology in the eye. Laboratory Investigat. 2006;86(2):106-15. [DOI:10.1038/labinvest.3700375] [PMID]
25. Kowluru RA, Kanwar M. Effects of curcumin on retinal oxidative stress and inflammation in diabetes. Nutr Metab. 2007;4(1):8. [DOI:10.1186/1743-7075-4-8] [PMID] [PMCID]
26. Liu J, Bhuvanagiri S, Qu X. The protective effects of lycopus lucidus turcz in diabetic retinopathy and its possible mechanisms. Artificial Cells, Nanomed, Biotechnol. 2019;47(1):2900-8. [DOI:10.1080/21691401.2019.1640230] [PMID]
27. Moon SW, Shin YU, Cho H, Bae SH, Kim HK. Effect of grape seed proanthocyanidin extract on hard exudates in patients with non-proliferative diabetic retinopathy. Medicine. 2019;98(21). [DOI:10.1097/MD.0000000000015515] [PMID] [PMCID]
28. Gupta SK, Kumar B, Nag TC, et al. Effects of Trigonella foenum-graecum (L.) on retinal oxidative stress, and proinflammatory and angiogenic molecular biomarkers in streptozotocin-induced diabetic rats. Molec Cell Biochem. 2014;388(1-2):1-9. [DOI:10.1007/s11010-013-1893-2] [PMID]
29. Keiss H-P, Dirsch VM, Hartung T, et al. Garlic (Allium sativum L.) modulates cytokine expression in lipopolysaccharide-activated human blood thereby inhibiting NF-κB activity. J Nutrition. 2003;133(7):2171-5. [DOI:10.1093/jn/133.7.2171] [PMID]

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