مطالعات کاربردی علوم زیستی در ورزش

مطالعات کاربردی علوم زیستی در ورزش

اثر هشت هفته تمرین تناوبی با شدت بالا و مصرف گالیک اسید بر SIRT1 و miR-9-5P در بافت کلیه موش‌‌های صحرایی در معرض کادمیوم

نوع مقاله : مقاله پژوهشی

نویسندگان
1 گروه ﺗﺮﺑﯿﺖ بدنی، واﺣﺪ ﺑﺮوﺟﺮد، دانشگاه آزاد اسلامی، ﺑﺮوﺟﺮد، اﯾﺮان
2 گروه ﺗﺮﺑﯿﺖ بدنی، واﺣﺪ ﺑﺮوﺟﺮد، دانشگاه آزاد اﺳﻼﻣی، ﺑﺮوﺟﺮد، اﯾﺮان
3 گروه ﻓﯿﺰﯾﻮﻟﻮژی ورزشی، واﺣﺪ ﻣﺮودﺷﺖ، دانشگاه آزاد اسلامی، ﻣﺮودﺷﺖ، اﯾﺮان
4 گروه تربیت بدنی، واحد زﻧﺠﺎن، دانشگاه آزاد اسلامی، زﻧﺠﺎن، اﯾﺮان
چکیده
زمینه و هدف: آسیب به بافت کلیه متعاقب سمیت ناشی از کادمیوم از مشکلات اساسی جوامع بشری است. اگرچه نقش تمرین ورزشی و آنتی‌‌اکسیدان‌‌ها در بافت کلیه بررسی شده است، اما اثر همزمان هشت هفته تمرین تناوبی با شدت بالا (HIIT) و مصرف گالیک اسید (GA) بر سیرتوئین 1 (SIRT1) و miR-9-5p در بافت کلیه موش‌‌های صحرایی در معرض کادمیوم (Cd) هدف این تحقیق بود. روش تحقیق: تعداد 42 سر موش صحرایی نر نژاد اسپراگو-داولی با سن هشت تا نه ماه و وزن 250 تا 270 گرم به‌‌طور تصادفی به گروه‌‌های کنترل سالم (HC)، کنترل، دریافت Cd، شم (Sham)، Cd+GA، Cd+HIIT و Cd+HIIT+GA تقسیم شدند. گروه‌‌های مصرف Cd روزانه پنج میلی‌گرم به ازای هر کیلوگرم وزن بدن Cd را در آب آشامیدنی دریافت نمودند. گروه‌‌های مصرف مکمل روزانه mg/kg 20 GA حل شده در طعم دهنده غذا و آب مصرف نمودند. گروه‌‌های تمرین نیز به‌‌‌مدت هشت هفته، سه جلسه در هفته و هر جلسه تمرینات HIIT را با شدت 80 تا 110 درصد حداکثر اکسیژن مصرفی انجام دادند. سطوح بیان ژنی miR-9-5p و SIRT1 به روش ریل تایم پی‌سی‌آر اندازه گیری شد. برای تجزیه و تحلیل داده‌‌ها از آزمون تحلیل واریانس یک‌طرفه همراه با آزمون تعقیبی توکی در سطح معنی‌‌داری 05/0>p استفاده شد. یافته‌‌ها: بیان ژن miR-9-5p و SIRT1 در گروه Cd+GA (001/0=p)، Cd+HIIT (001/0=p) و Cd+HIIT+GA (001/0=p) بیشتر از گروه Cd بود؛ ضمن آن که این دو متغیر در گروه Cd+HIIT+GA بیشتر از گروه‌‌های Cd+GA (001/0=p) و Cd+HIIT (001/0=p) بودند. از طرف دیگر، بیان ژن SIRT1 در گروه Cd+HIIT+GA کمتر از گروه Cd+HIIT (02/0=p) بود. نتیجه‌‌گیری: به‌‌نظر می‌‌رسد HIIT و مصرف GA هم به تنهایی و هم به‌‌طور همزمان، می‌‌توانند در تعدیل بیان ژن‌‌های SIRT1 و miR-9-5p شوند که در بیوژنزیس میتوکندریایی و کاهش آپوپتوزیس نقش دارند؛ ضمن آن که ترکیب تمرین تناوبی با شدت بالا و مصرف گالیک اسید در تعدیل بیان این ژن‌‌ها به مراتب موثر‌‌تر از اثر هر کدام به تنهایی می‌باشد.
کلیدواژه‌ها

عنوان مقاله English

The effect of 8 weeks of high-intensity interval training and gallic acid consumption on Sirtuin-1 and miR-9-5P expression in kidney tissue of rats exposed to cadmium

نویسندگان English

Maryam zarei 1
Ahmad Hemmatfar 2
seyed ali hosseini 3
arash sameni 4
1 Department of Physical Education and Exercise Science, Bo. C., Islamic Azad University, Borujerd, Iran
2 Department of Physical Education and Exercise Science, Bo. C., Islamic Azad University, Borujerd, Iran
3 Department of Exercise Physiology, Marv.C, Islamic Azad University, Marvdasht, Iran
4 Department of Physical Education and Exercise Science, Za.C., Islamic Azad University, Zanjan, Iran
چکیده English

Extended Abstract
Background and Aim: Cadmium (Cd)-induced kidney injury is a major public health concern due to its widespread environmental exposure and nephrotoxic effects. Cadmium accumulation in renal tissue can impair kidney function by inducing oxidative stress, inflammation, and cellular damage. In contrast, growing evidence suggests that regular physical exercise exerts protective effects on kidney health by improving protein metabolism, enhancing tubular reabsorption, and maintaining iron and urea homeostasis. In addition to exercise, naturally occurring dietary antioxidants have been shown to exert beneficial effects on the function of various organs. Among these antioxidants, gallic acid (GA), also known as 3,4,5-trihydroxybenzoic acid, is a naturally occurring polyphenolic compound found in a variety of fruits and plant-derived foods, including walnuts, sumac, hazelnuts, tea leaves, and oak. Owing to its potent antioxidant and anti-inflammatory properties, GA has attracted considerable attention as a potential therapeutic agent for reducing cadmium-induced tissue damage.
Although the independent effects of exercise and antioxidant supplementation on kidney tissue have been investigated, limited information is available regarding their combined effects on molecular pathways associated with cadmium-induced nephrotoxicity. Therefore, the present study aimed to investigate the combined effects of eight weeks of high-intensity interval training (HIIT) and gallic acid supplementation on the expression of SIRT1 and miR-9-5p in the kidney tissue of cadmium-exposed rats.
Materials and Methods: This experimental study employed a posttest-only design with a control group. A total of 42 male Sprague–Dawley rats, aged 8–9 months and weighing 250–270 g, were obtained from the Pasteur Institute Laboratory Animal Breeding and Reproduction Center. The sample size was determined based on previous studies using a similar experimental design, in which seven animals were allocated to each of six experimental groups, resulting in a total sample of 42 rats. Following purchase, the animals were transferred to the Exercise Physiology Laboratory of the Bitaran Research Center and allowed to acclimatize to the laboratory environment for one week under standard housing conditions. All experimental procedures were conducted in accordance with the ethical guidelines for the care and use of laboratory animals and were approved by the Biomedical Research Ethics Committee of the Islamic Azad University, Borujerd Branch (Approval No. IR.IAU.B.REC.1403.094). After the acclimatization period, the rats were randomly assigned to six groups (n=7 per group): healthy control (HC), cadmium (Cd), sham, Cd + gallic acid (GA), Cd + high-intensity interval training (HIIT), and Cd + HIIT + GA. Cadmium chloride was purchased from Sigma-Aldrich (USA). A dose equivalent to 5 mg/kg body weight was prepared daily by dissolving the appropriate amount of cadmium in the drinking water of the designated groups, allowing the animals to receive the required dose through voluntary water consumption. Gallic acid (GA; Sigma-Aldrich, USA; Catalog No. 27645) was administered at a dose of 20 mg/kg body weight per day. The required amount of GA was dissolved in a food and water flavoring solution to facilitate oral administration. Before the intervention, rats assigned to the exercise groups underwent a one-week familiarization period consisting of five treadmill-running sessions at a speed of 8 m/min for 5 min per session. Subsequently, the HIIT protocol was performed for eight weeks, with three sessions per week. Before initiating the training program, each rat’s maximum running speed was determined using the incremental treadmill test developed by Bedford et al. (1979) and subsequently standardized by Lindberg and colleagues. The HIIT program consisted of treadmill running at an intensity corresponding to 80–110% of maximal oxygen uptake (VO₂max), with exercise intensity and duration adjusted according to the experimental protocol. Data were analyzed using one-way analysis of variance (ANOVA) followed by Tukey’s post hoc test for multiple comparisons. Statistical significance was established at p<0.05.
Results: The Shapiro–Wilk test confirmed that all study variables were normally distributed. One-way analysis of variance (ANOVA) revealed significant differences among the experimental groups in the expression of miR-9-5p (F=261.31, p<0.001) and SIRT1 (F=272.97, p<0.001). Tukey’s post hoc analysis showed no significant difference in miR-9-5p expression between the healthy control (HC) and sham groups (p=0.47, MD=−0.05). Compared with the HC group, miR-9-5p expression was significantly reduced in the cadmium (Cd) group (p<0.001, MD=0.61). In contrast, miR-9-5p expression was significantly increased in the Cd + GA (p<0.001, MD=−0.54), Cd + HIIT (p<0.001, MD=−0.48), and Cd + HIIT + GA (p<0.001, MD=−1.15) groups compared with the Cd group. No significant difference was observed between the Cd + GA and Cd + HIIT groups (p=0.51, MD=−0.05). However, the Cd + HIIT + GA group exhibited significantly higher miR-9-5p expression than both the Cd + GA (p<0.001, MD=−0.60) and Cd + HIIT (p<0.001, MD=−0.66) groups (Figure 1). Similarly, no significant difference in SIRT1 expression was observed between the HC and sham groups (p=0.42, MD=−0.05). Cadmium exposure significantly reduced SIRT1 expression compared with the HC group (p<0.001, MD=−0.91). Treatment with GA (p<0.001, MD=−0.69), HIIT (p<0.001, MD=−0.63), and their combination (p<0.001, MD=−0.72) significantly increased SIRT1 expression compared with the Cd group. No significant differences were found between the Cd + GA and Cd + HIIT groups (p=0.31) or between the Cd + GA and Cd + HIIT + GA groups (p=0.83). However, SIRT1 expression was significantly higher in the Cd + HIIT + GA group than in the Cd + HIIT group (p=0.02, MD=0.09) (Figure 1).
Conclusion: The findings of the present study suggest that both high-intensity interval training (HIIT) and gallic acid (GA) attenuate cadmium-induced renal injury by modulating molecular pathways associated with oxidative stress and cellular protection. HIIT may enhance the endogenous antioxidant defense system through activation of the NRF2 signaling pathway, thereby increasing the expression and activity of antioxidant enzymes such as superoxide dismutase (SOD), glutathione peroxidase (GPx), and reduced glutathione (GSH). In addition, HIIT may improve mitochondrial function, promote mitochondrial biogenesis, enhance cellular energy metabolism, and inhibit apoptosis through SIRT1- and SIRT3-dependent signaling pathways. Exercise may also suppress inflammatory responses by modulating macrophage polarization and inhibiting TLR2 and NF-κB signaling.
Gallic acid appears to exert nephroprotective effects through complementary antioxidant and anti-inflammatory mechanisms. In addition to directly scavenging reactive oxygen species, GA may inhibit NF-κB, NADPH oxidase, and myeloperoxidase activity, reduce lipid peroxidation and nitric oxide production, suppress pro-inflammatory cytokines such as interleukin-6 (IL-6), and promote SIRT1-mediated mitochondrial biogenesis. Collectively, these molecular adaptations may contribute to the preservation of renal cellular integrity during cadmium exposure. The present findings further indicate that the combined administration of HIIT and GA produced greater beneficial effects on SIRT1 and miR-9-5p expression than either intervention alone. This enhanced response may be attributed to the simultaneous activation of endogenous antioxidant defenses, attenuation of oxidative stress and inflammatory signaling, improvement of mitochondrial homeostasis, and coordinated regulation of SIRT1 and miR-9-5p. Therefore, the combination of HIIT and GA may represent a promising strategy for mitigating cadmium-induced renal injury, although further mechanistic and clinical studies are required to confirm these findings.
Ethical Considerations: It should be noted that all ethical principles regarding the use of laboratory animals in this study were observed under the supervision of the Ethics Committee for Biomedical Research at the Islamic Azad University, Borujerd Branch (approval code: IR.IAU.B.REC.1403.094).
Compliance with Ethical Guidelines: The research followed the ethical standards of the Declaration of Helsinki and institutional guidelines.
Funding: No funding.
Conflicts of Interest: The authors declare no conflicts of interest regarding the publication of this study.

کلیدواژه‌ها English

Exercise
Gallic Acid
SIRT1
miR-9-5p
Kidney
Cadmium
1. Zhang K, Long M, Dong W, Li J, Wang X, Liu W, Huang Q, Ping Y, Zou H, Song R, Liu G, Ran D, Liu Z. Cadmium induces kidney iron deficiency and chronic kidney injury by interfering with the iron metabolism in rats. International Journal of Molecular Sciences. 2024 Jan 7;25(2):763. https://doi.org/10.3390/ijms25020763. PMID: 38255838; PMCID: PMC10815742.
2. Abbaszadeh M, Pakdel H, Barakeh S, Pakdel A. Association between cadmium exposure and risk of chronic kidney disease; a systematic review and meta-analysis. Journal of Renal Injury Prevention. 2024; x(x): e32254.  https://doi.org/10.34172/jrip.2024.32254 
3. Dong W, Zhang K, Wang X, Li J, Zou H, Yuan Y, Gu J, Zhu J, Liu G, Liu Z, Song R. SIRT1 alleviates Cd nephrotoxicity through NF-κB/p65 deacetylation-mediated pyroptosis in rat renal tubular epithelial cells. The Science of the Total Environment. 2024 Jun 15; 929:172392.  https://doi.org/10.2139/ssrn.4768608 
4. Liu Y, Lin X, Hao Z, Yu M, Tang Y, Teng X, Sun W, Kang L. Cadmium exposure caused cardiotoxicity in common carps (Cyprinus carpio L.): miR-9-5p, oxidative stress, energetic impairment, mitochondrial division/fusion imbalance, inflammation, and autophagy. Fish Shellfish Immunology. 2023 Jul; 138:108853.  https://doi.org/10.1016/j.fsi.2023.108853 
5. Zhang D, Liu J, Liu J, Fatima M, Yang L, Qin Y, Li W, Sun Z, Yang B. Exercise antagonizes cadmium-caused liver and intestinal injury in mice via Nrf2 and TLR2/NF-κB signalling pathway. Ecotoxicology and Environmental Safety. 2025 Apr 1; 294:118100.  https://doi.org/10.1016/j.ecoenv.2025.118100 
6. Delshad A, Salimi F, Valipour S. The effect of physical activity along with the consumption of hydroalcoholic extract of date pollen on the expression of some microRNAs in cadmium-induced toxicity in rat kidney tissue. Medical Journal of Tabriz University of Medical Sciences. 2024;46(2):165-174. [In Persian].  https://doi.org/10.34172/mj.2024.023 
7. Deng X, Liu D, Li M, He J, Fu Y. Physical activity can reduce the risk of blood cadmium and blood lead on stroke: Evidence from NHANES. Toxicology and Applied Pharmacology. 2024 Feb; 483:116831.  https://doi.org/10.1016/j.taap.2024.116831 
8. Sadat Hosseini N, Shirazpour S, Sepehri G, Dabiri S, Meymandi MS. High-intensity interval training alleviates ethanol-induced renal damage: A study on inflammation, oxidative stress, and histopathological changes in rats. Drug and Alcohol Dependence Reports. 2025 Feb 6; 14:100320.  https://doi.org/10.1016/j.dadr.2025.100320 
9. Tucker PS, Briskey DR, Scanlan AT, Coombes JS, Dalbo VJ. High intensity interval training favourably affects antioxidant and inflammation mRNA expression in early-stage chronic kidney disease. Free Radical Biology & Medicine. 2015 Dec; 89:466-72.  https://doi.org/10.1016/j.freeradbiomed.2015.07.162 
10. Alejolowo O O, Elias A O, Eseagwu O S, Nwonuma C O, Osemwegie O O. Gallic acid modulates oxido-inflammatory response in acrylamide-induced hepato-renal toxicity. Scientific African, 2024; 23, e02024.‏ https://doi.org/10.1016/j.sciaf.2023.e02024
11. Ojo OA, Rotimi DE, Ojo AB. Gallic acid abates cadmium chloride toxicity via alteration of neurotransmitters and modulation of inflammatory markers in Wistar rats. Scientific Report. 2023; 13, 1577. https://doi.org/10.1038/s41598-023-28893-6
12. Sundaresan S, John S, Paneerselvam G, Andiapppan R, Christopher G, Selvam GS. Gallic acid attenuates cadmium mediated cardiac hypertrophic remodelling through upregulation of Nrf2 and PECAM-1signalling in rats. Environmental Toxicology and Pharmacology. 2021 Oct; 87: 103701.  https://doi.org/10.1016/j.etap.2021.103701 
13. Hiratsuka H, Satoh Si, Satoh M, Nishijima M, Katsuki Y, Suzuki J, et al. Tissue distribution of cadmium in rats given minimum amounts of cadmium-polluted rice or cadmium chloride for 8 months. Toxicology and Applied Pharmacology. 1999 Oct 15; 160(2): 183-91.  https://doi.org/10.1006/taap.1999.8768 
14. Bedford TG, Tipton CM, Wilson NC, Oppliger RA, Gisolfi CV. Maximum oxygen consumption of rats and its changes with various experimental procedures. Journal of Applied Physiology: Respiratory, Environmental and Exercise Physiology. 1979 Dec; 47(6):1278-83.  https://doi.org/10.1152/jappl.1979.47.6.1278 
15. Momeni L, Fathi Moghadam H, Hosseini S, Nikbakht M. Interactive effects of endurance training and selenium consumption on the intrinsic apoptosis pathway in the liver tissue of cadmium-exposed rats. Journal of Nutritional Sciences and Dietetics. 2020; 5(3-4). https://doi.org/10.5812/modernc.96468 
16. Alruhaimi RS, Hassanein EHM, Bin-Jumah MN, Mahmoud AM. Cadmium-induced lung injury is associated with oxidative stress, apoptosis, and altered SIRT1 and Nrf2/HO-1 signaling; protective role of the melatonin agonist agomelatine. Naunyn-Schmiedeberg’s Archives of Pharmacology. 2024 Apr; 397(4): 2335-2345.  https://doi.org/10.1007/s00210-023-02754-5 
17. Wen S, Xu M, Zhang W, Song R, Zou H, Gu J, Liu X, Bian J, Liu Z, Yuan Y. Cadmium induces mitochondrial dysfunction via SIRT1 suppression-mediated oxidative stress in neuronal cells. Environmental Toxicology. 2023 Mar; 38(4): 743-753.  https://doi.org/10.1002/tox.23724 
18. Liu J, Qu W, Kadiiska MB. Role of oxidative stress in cadmium toxicity and carcinogenesis. Toxicology and Applied Pharmacology. 2009 Aug 1; 238(3): 209-14.  https://doi.org/10.1016/j.taap.2009.01.029 
19. Tsangaris GT, Tzortzatou-Stathopoulou F. Cadmium induces apoptosis differentially on immune system cell lines. Toxicology. 1998 Jul 3; 128(2): 143-50.  https://doi.org/10.1016/s0300-483x(98)00032-8
20. Liu J, Zuo X, Han J, Dai Q, Xu H, Liu Y, Cui S. MiR-9-5p inhibits mitochondrial damage and oxidative stress in AD cell models by targeting GSK-3. Bioscience, Biotechnology, and Biochemistry. 2020 Nov; 84(11): 2273-2280. https://doi.org/10.1080/09168451.2020.1797469 
21. Minigalieva I A, Shabardina L V, Ryabova Y V, Panov V G, Kungurtseva A K,  Sakhautdinova R R. (2024). Experimental study of toxic effects of cadmium against background of physical exercise. Hygiene and Sanitation, 103(8): 895-905.‏  https://doi.org/10.47470/0016-9900-2024-103-8-895-905 
22. Azhdari A, Hosseini S A, Farsi S. Antioxidant effect of high intensity interval training on cadmium-induced cardiotoxicity in rats. Gene Cell Tissue. 2019; 6(3):e94671. https://doi.org/10.5812/gct.94671
23. Ghajari H, Hosseini SA, Farsi S. The effect of endurance training along with cadmium consumption on Bcl-2 and Bax gene expressions in heart tissue of rats. Annals of Military and Health Sciences Research. 2019; 17(1): e86795. https://doi.org/10.5812/amh.86795
24. Humayun Fard H, Hosseini S A, Azarbayjani M A, Nikbakht M. Antiapoptotic effects of continuous training and selenium consumption on the liver tissue of cadmium- exposed rats. Middle East Journal of Rehabilitation and Health Studies. 2019; 6(3): e91278. https://doi.org/10.5812/mejrh.91278
25. Adebayo A A, Ademosun A O, Oboh G. Gallic acid abrogates cadmium-induced neurochemical changes and cognitive deficits in Wistar rat. Nutrire, 2023; 48(1):30.‏  https://doi.org/10.1186/s41110-023-00216-9 
26. Amini N, Badavi M, Mard SA, Dianat M, Moghadam MT. The renoprotective effects of gallic acid on cisplatin-induced nephrotoxicity through anti-apoptosis, anti-inflammatory effects, and downregulation of lncRNA TUG1. Naunyn-Schmiedeberg’s Archives of Pharmacology. 2022 Jun; 395(6):691-701.  https://doi.org/10.1007/s00210-022-02227-1 
27. Ahmadvand H, Yalameha B, Adibhesami G, Nasri M, Naderi N, Babaeenezhad E, Nouryazdan N. The protective role of gallic acid pretreatment n renal ischemia-reperfusion injury in rats. Reports of Biochemistry & Molecular Biology. 2019 Apr; 8(1): 42-48.  https://doi.org/10.1590/1678-4324-2020200131 
28. Ranjbar K, Matin Homaie H, Azarbayjani M A, Piri, M. The effect of gallic acid supplement and resistance exercise on the bio-markers of liver in intoxicated male rats of anabolic steroid. Medical Laboratory Journal, 2020; 14(1): 44-49.‏  https://doi.org/10.29252/mlj.14.1.44 
29. Akbari M, Moradi L, Alizadeh R, Abbasi Daloii A. Investigating the effects of endurance training and gallic acid on Annexin-5 and caspase-3 of cardiac tissue in male wistar rats undergoing boldenone. Complementary Medicine Journal. 2018; 8(2): 2279-92.‏
30. Yu L, Tian D, Su Z. Gallic acid alleviates exercise-induced muscle damage by inhibiting mitochondrial oxidative stress and ferroptosis. Journal of Translational Medicine, 2025; 23, 30. https://doi.org/10.1186/s12967-024-06042-5