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:: Volume 28, Issue 3 (August-September 2024) ::
Feyz Med Sci J 2024, 28(3): 253-260 Back to browse issues page
The effect of aerobic exercise and aqueous garlic extract on markers of cardiac mitochondrial biogenesis in diabetic rats
Masoumeh Ebrahimpour , Saqqa Farajtabar Behrestaq *
Department of Physical Education and Sport Sciences, Qaemshahr Branch, Islamic Azad University, Qaemshahr, Iran , farajtabarp@yahoo.com
Abstract:   (624 Views)
Background and Aim: Exercise induces various adaptations, including increased antioxidant capacity, enhanced mitochondrial size, and improved insulin signaling. The present study aimed to investigate the effects of aerobic exercise along with aqueous garlic extract consumption on markers of cardiac mitochondrial biogenesis in diabetic rats.
Methods: In this experimental study, 40 male Wistar rats (5 weeks old, weighing 162.1 ± 15.2 grams) were obtained from the Pasteur Institute. Eight rats were assigned to the healthy control group (CN). The remaining 32 rats were rendered diabetic through a single intraperitoneal injection of streptozotocin (60 mg/kg) and were randomly divided into four groups: diabetes (DM), diabetes + exercise (TDM), diabetes + garlic (GDM), and diabetes + exercise + garlic (TGDM). The exercise groups underwent an aerobic exercise program on a treadmill for 8 weeks. Additionally, each rat received 1 milliliter of garlic extract (0.4 g per 100 g of body weight) via gavage daily. Changes in the expression of PGC-1α and Nrf2 genes were measured in heart tissue using real-time PCR.
Results: Induction of diabetes resulted in a significant decrease in PGC-1α (P=0.0001) and Nrf2 (P=0.0001) gene expression compared to the control group. In the TDM group, PGC-1α and Nrf2 expressions significantly increased (P=0.038 and P=0.031, respectively), as did those in the GDM group (P=0.036 and P=0.025, respectively) compared to the DM group. However, the combined intervention of exercise and garlic supplementation did not yield significant improvements compared to each intervention alone regarding PGC-1α and Nrf2 expression (P< 0.05).
Conclusion: Both garlic supplementation and exercise may inhibit streptozotocin-induced cardiac damage by upregulating the PGC-1α and Nrf2 pathways. Further studies are warranted to explore this area more comprehensively.
Keywords: Aerobic exercise, Garlic, PGC-1α, Nrf2, Diabetes
Full-Text [PDF 442 kb]   (308 Downloads)    
Type of Study: Research | Subject: medicine, paraclinic
Received: 2024/05/30 | Revised: 2024/09/8 | Accepted: 2024/07/7 | Published: 2024/08/31
References
1. Cai X, Zhang Y, Li M, Wu JH, Mai L, Li J, Yang Y, Hu Y, Huang Y. Association between prediabetes and risk of all cause mortality and cardiovascular disease: updated meta-analysis. BMJ. 2020; 370: m2297. doi: 10.1136/bmj.m2297. PMID: 32669282; PMCID: PMC7362233.
2. Yang Z, Wu Y, Wang L, Qiu P, Zha W, Yu W. Prokineticin 2 (PK2) Rescues Cardiomyocytes from High Glucose/High Palmitic Acid-Induced Damage by Regulating the AKT/GSK3β Pathway In Vitro. Oxid Med Cell Longev. 2020;2020:3163629. doi: 10.1155/2020/3163629. PMID: 32509142; PMCID: PMC7251470.
3. Newsholme P, Cruzat VF, Keane KN, Carlessi R, de Bittencourt PI Jr. Molecular mechanisms of ROS production and oxidative stress in diabetes. Biochem J. 2016; 473(24): 4527-50. doi: 10.1042/BCJ20160503C. PMID: 27941030.
4. Park JE, Lee H, Rho H, Hong SM, Kim SY, Lim Y. Effect of Quamoclit angulata Extract Supplementation on Oxidative Stress and Inflammation on Hyperglycemia-Induced Renal Damage in Type 2 Diabetic Mice. Antioxidants (Basel). 2020; 9(6): 459. doi: 10.3390/antiox9060459. PMID: 32471242; PMCID: PMC7346142.
5. Bolisetty S, Jaimes EA. Mitochondria and reactive oxygen species: physiology and pathophysiology. Int J Mol Sci. 2013;14(3):6306-44. doi: 10.3390/ijms14036306. PMID: 23528859; PMCID: PMC3634422.
6. Steinbacher P, Eckl P. Impact of oxidative stress on exercising skeletal muscle. Biomolecules. 2015; 5(2):356-77. doi: 10.3390/biom5020356. PMID: 25866921; PMCID: PMC4496677.
7. Egan B, Zierath JR. Exercise metabolism and the molecular regulation of skeletal muscle adaptation. Cell Metab. 2013; 17(2):162-84. doi: 10.1016/j.cmet.2012.12.012. PMID: 23395166.
8. Gomez-Cabrera MC, Salvador-Pascual A, Cabo H, Ferrando B, Viña J. Redox modulation of mitochondriogenesis in exercise. Does antioxidant supplementation blunt the benefits of exercise training? Free Radic Biol Med. 2015; 86: 37-46. doi: 10.1016/j.freeradbiomed.2015.04.006. Epub 2015 Apr 15. PMID: 25889822.
9. Ristow M, Zarse K, Oberbach A, Klöting N, Birringer M, Kiehntopf M, Stumvoll M, Kahn CR, Blüher M. Antioxidants prevent health-promoting effects of physical exercise in humans. Proc Natl Acad Sci U S A. 2009; 106(21): 8665-70. doi: 10.1073/pnas.0903485106. Epub 2009 May 11. PMID: 19433800; PMCID: PMC2680430.
10. Taskin S, Celik H, Demiryurek S, Turedi S, Taskin A. Effects of different-intensity exercise and creatine supplementation on mitochondrial biogenesis and redox status in mice. Iran J Basic Med Sci. 2022; 25(8).
11. Kianmehr P, Azarbayjani MA, Peeri M, Farzanegi P. Synergic effects of exercise training and octopamine on peroxisome proliferator-activated receptor-gamma coactivator-1a and uncoupling protein 1 mRNA in heart tissue of rat treated with deep frying oil. Biochem Biophys Rep. 2020; 22: 100735.
12. Ziegler A, Damgaard A, Mackey A, Schjerling P, Magnusson P, Olesen A, et al. An anti-inflammatory phenotype in visceral adipose tissue of old lean mice, augmented by exercise. Sci Reports. 2019; 9(1): 1-10.
13. Botta A, Laher I, Beam J, Decoffe D, Brown K, Halder S, Devlin A, Gibson DL, Ghosh S. Short term exercise induces PGC-1α, ameliorates inflammation and increases mitochondrial membrane proteins but fails to increase respiratory enzymes in aging diabetic hearts. PLoS One. 2013; 8(8): e70248. doi: 10.1371/journal.pone.0070248. PMID: 23936397; PMCID: PMC3731348.
14. Colín-González AL, Ali SF, Túnez I, Santamaría A. On the antioxidant, neuroprotective and anti-inflammatory properties of S-allyl cysteine: An update. Neurochem Int. 2015; 89: 83-91. doi: 10.1016/j.neuint.2015.06.011. Epub 2015 Jun 26. PMID: 26122973.
15. Suzuki J-i, Kodera Y, Miki S, Ushijima M, Takashima M, Matsutomo T, et al. Anti-inflammatory action of cysteine derivative S-1-propenylcysteine by inducing MyD88 degradation. Sci Reports. 2018; 8(1): 1-10. DOI:10.1038/s41598-018-32431-0.
16. Yu L, Di W, Dong X, Li Z, Xue X, Zhang J, Wang Q, Xiao X, Han J, Yang Y, Wang H. Diallyl trisulfide exerts cardioprotection against myocardial ischemia-reperfusion injury in diabetic state, role of AMPK-mediated AKT/GSK-3β/HIF-1α activation. Oncotarget. 2017; 8(43): 74791-805. doi: 10.18632/oncotarget.20422. PMID: 29088824; PMCID: PMC5650379.
17. Chen PH, Chang CH, Lin WS, Nagabhushanam K, Ho CT, Pan MH. S-Allylcysteine Ameliorates Aging Features via Regulating Mitochondrial Dynamics in Naturally Aged C57BL/6J Mice. Mol Nutr Food Res. 2022; 66(7): e2101077. doi: 10.1002/mnfr.202101077. Epub 2022 Feb 11. PMID: 35092643.
18. Sadeghpour Firozabadi E, Abdi A, Abbassi Daloii A. Effect of Aerobic Training with Aqueous Allium sativum L on IL-17, IL-22 Expression and Insulin Resistance in Diabetic Rats. J Sport Exercise Physiol. 2023; 16(1): 1-11.
19. Soheilpour M. The effect of six weeks aerobic training and L-carnitine on apoptosis, oxidative stress indices and cardiac enzymes in diabetic rats. 2018; PHD thesis in exercise physiology, Islamic Azad University, Science and Research Branch.
20. El-Demerdash FM, Yousef MI, El-Naga NI. Biochemical study on the hypoglycemic effects of onion and garlic in alloxan-induced diabetic rats. Food Chem Toxicol. 2005; 43(1): 57-63. doi: 10.1016/j.fct.2004.08.012. PMID: 15582196.
21. El-Demerdash F, Yousef MI, El-Naga NA. Biochemical study on the hypoglycemic effects of onion and garlic in alloxan-induced diabetic rats. Food Chem Toxicol. 2005; 43(1):57-63.
22. Chae CH, Jung SL, An SH, Jung CK, Nam SN, Kim HT. Treadmill exercise suppresses muscle cell apoptosis by increasing nerve growth factor levels and stimulating p-phosphatidylinositol 3-kinase activation in the soleus of diabetic rats. J Physiol Biochem. 2011; 67(2): 235-41. doi: 10.1007/s13105-010-0068-9. Epub 2011 Jan 5. PMID: 21207218.
23. Abdi A, Mehrabani J, Haeri T, Shykholeslami Z, Mostafavian M. Protective effect of aerobic training along with Punica granatum l on cardiac injury biomarkers in women with type 2 diabetes. Iran J Nutr Sci Food Technol. 2019;13(4):1-10.
24. Rius-Pérez S, Torres-Cuevas I, Millán I, Ortega ÁL, Pérez S. PGC-1α, Inflammation, and Oxidative Stress: An Integrative View in Metabolism. Oxid Med Cell Longev. 2020; 2020: 1452696. doi: 10.1155/2020/1452696. PMID: 32215168; PMCID: PMC7085407.
25. Marín-Royo G, Rodríguez C, Le Pape A, Jurado-López R, Luaces M, Antequera A, et al. The role of mitochondrial oxidative stress in the metabolic alterations in diet-induced obesity in rats. FASEB J. 2019; 33(11): 12060-72. doi: 10.1096/fj.201900347RR. Epub 2019 Aug 1. PMID: 31370681; PMCID: PMC6902682.
26. Sahin K, Orhan C, Akdemir F, Tuzcu M, Sahin N, Yılmaz I, et al. β-Cryptoxanthin ameliorates metabolic risk factors by regulating NF-κB and Nrf2 pathways in insulin resistance induced by high-fat diet in rodents. Food Chem Toxicol. 2017; 107: 270-9. https://doi.org/10.1016/j.fct. 2017.07.008.
27. Abebe T, Mahadevan J, Bogachus L, Hahn S, Black M, Oseid E, et al. Nrf2/antioxidant pathway mediates β cell self-repair after damage by high-fat diet-induced oxidative stress. JCI Insight. 2017; 2(24): e92854. doi: 10.1172/jci.insight.92854. PMID: 29263299; PMCID: PMC5752274.
28. Zhou S, Sun W, Zhang Z, Zheng Y. The role of Nrf2-mediated pathway in cardiac remodeling and heart failure. Oxid Med Cell Longev. 2014; 2014: 260429. doi: 10.1155/2014/260429. Epub 2014 Jul 1. PMID: 25101151; PMCID: PMC4102082.
29. Pall ML, Levine S. Nrf2, a master regulator of detoxification and also antioxidant, anti-inflammatory and other cytoprotective mechanisms, is raised by health promoting factors. Sheng Li Xue Bao. 2015; 67(1): 1-18. PMID: 25672622.
30. Zoladz JA, Koziel A, Broniarek I, Woyda-Ploszczyca AM, Ogrodna K, Majerczak J, Celichowski J, Szkutnik Z, Jarmuszkiewicz W. Effect of temperature on fatty acid metabolism in skeletal muscle mitochondria of untrained and endurance-trained rats. PLoS One. 2017; 12(12): e0189456. doi: 10.1371/journal.pone.0189456. PMID: 29232696; PMCID: PMC5726737.
31. Ebrahimnezhad N, Nayebifar S, Soltani Z, Khoramipour K. High-intensity interval training reduced oxidative stress and apoptosis in the hippocampus of male rats with type 2 diabetes: The role of the PGC1α-Keap1-Nrf2 signaling pathway. Iran J Basic Med Sci. 2023; 26(11): 1313-9. doi: 10.22038/IJBMS.2023.70833.15387. PMID: 37885999; PMCID: PMC10598812.
32. Narasimhan M, Hong J, Atieno N, Muthusamy VR, Davidson CJ, Abu-Rmaileh N, et al. Nrf2 deficiency promotes apoptosis and impairs PAX7/MyoD expression in aging skeletal muscle cells. Free Radic Biol Med. 2014; 71: 402-14. doi: 10.1016/j.freeradbiomed.2014.02.023. Epub 2014 Mar 6. PMID: 24613379; PMCID: PMC4493911.
33. Done AJ, Gage MJ, Nieto NC, Traustadóttir T. Exercise-induced Nrf2-signaling is impaired in aging. Free Radic Biol Med. 2016; 96: 130-8. doi: 10.1016/j.freeradbiomed.2016.04.024. Epub 2016 Apr 22. PMID: 27109910.
34. Holmström KM, Baird L, Zhang Y, Hargreaves I, Chalasani A, Land JM, et al. Nrf2 impacts cellular bioenergetics by controlling substrate availability for mitochondrial respiration. Biol Open. 2013; 2(8): 761-70. doi: 10.1242/bio.20134853. PMID: 23951401; PMCID: PMC3744067.
35. Merry TL, Ristow M. Nuclear factor erythroid-derived 2-like 2 (NFE2L2, Nrf2) mediates exercise-induced mitochondrial biogenesis and the anti-oxidant response in mice. J Physiol. 2016; 594(18):5195-207. doi: 10.1113/JP271957. Epub 2016 May 27. PMID: 27094017; PMCID: PMC5023720.
36. Hoseinzade I, Abdi A, Abbassi Daloii A. Protective Effect of Aerobic Training and Royal Jelly on Oxidative Stress in Cardiomyocytes in Obese Rats. J Mazandaran Univ Med Sci. 2022; 31(206): 30-42.
37. Shaker M, Khamisipour G, Sadeghipour H, Zar A, Naeimi B, Akbarzadeh S. Effect of resistance training and garlic extract on insulin sensitivity/resistance and biochemical parameters in diabetic rats. Comparative Exercise Physiol. 2022;18(2):163-70. DOI:10.3920/CEP210031.
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Ebrahimpour M, Farajtabar Behrestaq S. The effect of aerobic exercise and aqueous garlic extract on markers of cardiac mitochondrial biogenesis in diabetic rats. Feyz Med Sci J 2024; 28 (3) :253-260
URL: http://feyz.kaums.ac.ir/article-1-5186-en.html


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Volume 28, Issue 3 (August-September 2024) Back to browse issues page
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