Complementary Medicine Journal (CMJA)

Volume 15, Issue 4

Original Article

Response of Oxidative Stress Indices to Jujube Fruit Supplementation along with Endurance Exercise after a Session of Intense Exercise in Inactive Women

Omid Mohammaddoost1*, Mitra Madadi Jaberi2, Sohila Moghadam Eftekhari2

Assistant Professor, Exercise Physiology Department, Faculty of Education and Psychology, University of Sistan and Baluchestan, Zahedan, Iran

Master’s Student, Faculty of Educational Sciences and Psychology, University of Sistan and Baluchestan, Zahedan, Iran

* Corresponding author: Omid Mohammaddoost, Exercise Physiology Department, Faculty of Education and Psychology, University of Sistan and Baluchestan, Zahedan, Iran. Email: Mo.omid@ped.usb.ac.ir

DOI: 10.22034/cmja.15.4.290

Received: 15 January 2025 | Accepted: 07 February 2026

How to Cite This Article: Mohammaddoost O, Madadi Jaberi M, Moghadam Eftekhari S. Response of Oxidative Stress Indices to Jujube Fruit Supplementation along with Endurance Exercise after a Session of Intense Exercise in Inactive Women. Complement Med J. 2026;15(4):290–300. DOI: 10.22034/cmja.15.4.290

Abstract

Introduction and Objective: Intense physical activity can damage cellular structures and may increase resting oxidative-stress indicators, reflecting impaired cell-membrane function. Creatine kinase (CK), lactate dehydrogenase (LDH), malondialdehyde (MDA), and blood lactate are relevant indicators of muscle damage and metabolic response. This study investigated the effects of eight weeks of jujube-fruit supplementation, endurance training, and their combination on these indicators in inactive women following an intense exercise session.

Materials and Methods: This semi-experimental study used a pre-test/post-test design. Forty healthy, inactive female students from the University of Sistan and Baluchestan were purposefully recruited after written informed consent and randomly allocated to four groups (n=10 each): endurance training plus jujube, endurance training, jujube, and control/placebo. Participants in the jujube groups consumed 0.4 g of jujube per kilogram of body weight daily, divided between morning and evening, for eight weeks. The training groups exercised three days per week. Sessions included a 10-minute warm-up and 30 minutes of treadmill exercise at 55–75% of heart-rate reserve, progressing from 50% during weeks 1–2 to 75% during weeks 7–8. An intense exercise test was performed before and after the intervention. Blood was sampled before and after the test. CK and LDH were measured by optical spectroscopy, MDA by spectrophotometry, and blood lactate using a lactometer. Data were analyzed in SPSS version 25 using Shapiro–Wilk, one-way ANOVA, Tukey post hoc comparisons, and paired t-tests; p<0.05 was considered significant.

Results: Body weight and BMI did not differ significantly over the eight-week program (p=0.12), whereas time to exhaustion changed significantly (p=0.01). Resting blood lactate decreased significantly in the endurance-training, combined-intervention, and jujube-only groups compared with baseline (p=0.03, p=0.00, and p=0.01, respectively). CK, LDH, and MDA did not change significantly from pre-test values. After the intervention, blood lactate differed significantly among the four groups (p=0.02). Tukey comparisons indicated differences between each intervention group (groups 1, 2, and 3) and the control group (p<0.05), while the other pairwise comparisons were not significant (p>0.05). Between-group differences were not significant for LDH (p=0.37), MDA (p=0.11), or CK (p=0.06).

Conclusion: Eight weeks of endurance training and/or jujube consumption were associated with changes in blood-lactate responses, with the combined intervention showing a greater effect after intense exercise than either intervention alone. The program did not produce significant changes in CK, LDH, or MDA. Endurance training may therefore not have altered cell-membrane function as reflected by these markers, while jujube consumption may have helped limit potential oxidative-stress-related membrane damage. Further research is needed to confirm these findings.

Keywords: Blood lactate; Creatine kinase; Endurance training; Jujube fruit; Intense activity; Inactive women; Lactate dehydrogenase; Malondialdehyde

Introduction and Objective

Intense physical activity damages cellular structures, especially in muscle tissue [1]. Free radicals can damage tissues through oxidative mechanisms, inactivating enzymes and damaging nucleic acids, proteins, and lipid membranes [1]. Reactive oxygen species are potentially harmful and contribute to oxidative tissue damage during prolonged aerobic activity. Muscle damage is associated with the release of creatine kinase (CK) and lactate dehydrogenase (LDH), whose blood levels are used as biomarkers. During intense exercise, endogenous antioxidant enzymes may not fully prevent muscle damage; antioxidant supplementation is one possible protective strategy [24].

In recent years, researchers have examined herbal products and naturally occurring antioxidants for the prevention and treatment of various conditions [25]. Jujube (Ziziphus jujuba) contains antioxidant compounds, including phenolic compounds, fatty acids, beta-carotene, and alpha-tocopherol [27, 26]. However, the effects of antioxidant supplements on physical health and athletic performance remain unclear, particularly in individuals undertaking strenuous aerobic exercise. Given the limited and inconsistent evidence regarding jujube consumption and oxidative stress after intense exercise, this study investigated the effects of endurance training and jujube-fruit consumption on CK, LDH, MDA, and blood lactate in inactive women after intense exercise.

Materials and Methods

This semi-experimental study enrolled 40 healthy, inactive female students from the University of Sistan and Baluchestan. Participants were volunteers recruited purposefully and conveniently from the female student population. They completed written consent and a medical-sports awareness questionnaire and received an explanation of the study procedures. Participants were randomly assigned to four groups: [1] endurance training, [2] endurance training plus jujube, [3] jujube consumption, and [4] control.

Blood lactate was measured in milligrams per deciliter using a lactate meter and a Vallancet kit. Serum MDA was determined by reaction with thiobarbituric acid using spectrophotometry at 532 nm [37]. Before intense exercise, 5 mL of blood was collected from the forearm vein while participants were seated and resting. Serum CK and LDH were measured by optical spectroscopy in a medical diagnostic laboratory.

After a 10-minute warm-up, participants completed an intense exercise test on an ergometer (Tuntury E433, Finland). They pedaled for 5 minutes at 60 revolutions per minute (RPM) and 50 W; the workload was then increased by 25 W every 5 minutes until the participant could no longer maintain 60 RPM. Time to exhaustion was recorded, and a second blood sample was collected while participants were seated.

Groups 1 and 2 then completed aerobic exercise three days per week for eight weeks. Each session included a 10-minute warm-up and 30 minutes of treadmill exercise at 55–75% of heart-rate reserve (HRR), calculated using the Karvonen method. Intensity was 50% during the first two weeks, 55% in week 3, 60% in week 4, 65% in week 5, 70% in week 6, and 75% during the final two weeks [38]. Exercise intensity was monitored using a Polar T31 heart-rate monitor (Finland). Cool-down consisted of five minutes of slow pedaling and stretching.

Participants in groups 2 and 3 consumed 0.4 g of jujube fruit per kilogram of body weight twice daily (morning and evening) for eight weeks [39]. Participants in groups 3 and 4 were asked to avoid regular physical activity and maintain their usual diet. At the end of week 8, the initial intense exercise test was repeated and blood samples and lactate measurements were obtained before and after exercise.

Statistical Analysis. The Shapiro–Wilk test was used to assess normality. One-way analysis of variance and Tukey post hoc tests were used to compare the four groups at rest and after intense exercise. Paired t-tests were used to assess within-group changes. Analyses were performed using SPSS version 25. Statistical significance was set at p<0.05.

Results

Analysis of variance showed no significant difference in participants’ weight and body mass index before and after the eight-week program (p=0.12). A significant difference was observed in time to exhaustion (p=0.01). Paired t-test results showed that blood lactate decreased significantly in the endurance-training, endurance-training-plus-jujube, and jujube-consumption groups compared with pre-test values (p=0.03, p=0.00, and p=0.01, respectively). CK, LDH, and MDA did not change significantly compared with pre-test values.

After the eight-week program, lactate values differed significantly among the four groups (p=0.02). No significant between-group differences were observed for LDH (p=0.37), MDA (p=0.11), or CK (p=0.06). Tukey post hoc analysis showed significant differences in lactate between groups 1, 2, and 3 and the control group (p<0.05); no significant differences were observed among the other groups (p>0.05).

Discussion

The findings indicate that jujube consumption combined with endurance training, endurance training alone, and jujube consumption alone were each associated with significant reductions in blood lactate at rest. The post-intervention lactate response differed among groups, with the intervention groups differing from the control group. Following the intense exercise bout, the significant difference was reported only between the combined-intervention group and the control group, suggesting that the combined intervention may have a greater effect on post-exercise blood lactate than either intervention alone.

Combined jujube consumption and aerobic exercise did not significantly affect resting serum CK or prevent its increase after intense exercise, consistent with previous findings [43]. The intervention also did not produce a significant difference in resting or post-exercise LDH. The article discusses antioxidant actions of fruit phenolic compounds, beta-carotene, and jujube constituents, including electron donation and inhibition of xanthine oxidase activity, as possible mechanisms for reducing oxidative stress [39]. The authors suggest that endurance training did not measurably alter cell-membrane function in this study, whereas jujube consumption may have helped prevent potential membrane damage. Further studies are needed.

Conclusion

The results suggest that jujube consumption together with endurance training significantly affects blood-lactate levels in inactive women. Lactate levels in the endurance-training-plus-jujube and jujube-only groups differed from those in the control group, while comparisons with the endurance-training group were not significant. After intense exercise, the combined intervention showed a significant difference only compared with control. The endurance-training program did not significantly change CK, LDH, or MDA. Jujube may help reduce the effects of exercise-related oxidative stress and protect cell membranes, but further research is required.

Tables

Table 1. Participants’ demographic and anthropometric characteristics

Variable

Study group
n=10

Standard deviation±Mean
Pre-test

Standard deviation±Mean
Post-test

Within-group test
(Paired t-test)

Within-group test
(Paired t-test)

Between-group test
(One-way ANOVA)

Between-group test
(One-way ANOVA)

Variable

Study group
n=10

Standard deviation±Mean
Pre-test

Standard deviation±Mean
Post-test

Value
t

Significance

Value
f

Significance

Age
(years)

Training

2.95 ±21.07

-----

---

---

---

---

Age
(years)

Training + Jujube

3.07 ±21.01

-----

---

---

---

---

Age
(years)

Consumption Jujube

3.03 ±23.08

-----

---

---

---

---

Age
(years)

Control

3.08±22.22

-----

---

---

---

---

Height
(cm)

Training

3.11 ±174.98

-----

---

---

---

---

Height
(cm)

Training + Jujube

2.93 ±176.43

-----

---

---

---

---

Height
(cm)

Consumption Jujube

2.21 ±178.85

-----

---

---

---

---

Height
(cm)

Control

2.34 ±178.78

-----

---

---

---

---

Weight
(kg)

Training

3.08 ±67.98

2.39 ± 66.59

0.42

0.08

11.76

0.12

Weight
(kg)

Training + Jujube

2.44 ±73.83

2.74 ± 72.82

2.38

0.09

11.76

0.12

Weight
(kg)

Consumption Jujube

3.01 ±78.02

3.10 ± 78.76

1.74

0.14

11.76

0.12

Weight
(kg)

Control

2.95 ±78.99

2.95 ±78.99

3.09

0.21

11.76

0.12

BMI
(kg/m2)

Training

3.04 ±23.82

3.48 ± 22.83

1.47

0.09

1.36

0.11

BMI
(kg/m2)

Training + Jujube

2.72 ±23.97

2.26 ± 22.97

3.28

0.09

1.36

0.11

BMI
(kg/m2)

Consumption Jujube

2.83 ±24.88

2.83 ± 24.88

2.74

1.14

1.36

0.11

BMI
(kg/m2)

Control

2.72 ±24.16

3.07 ±24.19

1.99

1.11

1.36

0.11

Time to exhaustion
(min)

Training

1.75 ±25.01

1.08 ±30.01

1.47

0.04*

0.05

0.01*

Time to exhaustion
(min)

Training + Jujube

2.40 ±24.13

1.44 ±29.22

5.48

0.03*

0.05

0.01*

Time to exhaustion
(min)

Consumption Jujube

1.41 ±26.15

0.55 ±26.05

2.74

0.14

0.05

0.01*

Time to exhaustion
(min)

Control

1.37 ±25.22

0.19 ±23.28

3.99

0.11

0.05

0.01*

Table 2. Changes in blood lactate and oxidative-stress indicators

Variable

Study group
n=10

Standard deviation±Mean
Pre-test

Standard deviation±Mean
Post-test

Within-group test
(Paired t-test)

Within-group test
(Paired t-test)

Between-group test
(One-way ANOVA)

Between-group test
(One-way ANOVA)

Variable

Study group
n=10

Standard deviation±Mean
Pre-test

Standard deviation±Mean
Post-test

Value
t

Significance

Value
f

Significance

Blood lactate
(mg/dL)

Training

2.95 ±14.99

1.55 ±12.65

0.432

0.039*

3.57

0.02*

Blood lactate
(mg/dL)

Training +Jujube

3.21 ±15.19

2.95 ±12.99

0.472

0.008*

3.57

0.02*

Blood lactate
(mg/dL)

Consumption Jujube

2.91 ±14.76

2.87 ±13.09

1.86

0.015*

3.57

0.02*

Blood lactate
(mg/dL)

Control

3.05 ±14.99

2.95 ±14.89

0.021

0.984

3.57

0.02*

LDH
(U/L)

Training

5.95 ±115.19

3.95 ±114.79

5.48

0.453

2.60

0.06

LDH
(U/L)

Training +Jujube

3.75±114.19

4.72±115.19

6.20

0.321

2.60

0.06

LDH
(U/L)

Consumption Jujube

4.95 ±116.19

4.44 ±117.19

1.96

0.081

2.60

0.06

LDH
(U/L)

Control

5.73 ±117.19

4.73 ±116.99

0.307

0.760

2.60

0.06

CK
(U/L)

Training

45.73±312.33

55.12±313.13

2.74

0.083

1.06

0.37

CK
(U/L)

Training +Jujube

55.23±315.19

45.23±315.25

0.684

0.402

1.06

0.37

CK
(U/L)

Consumption Jujube

45.33±314.21

32.33±313.21

2.40

0.088

1.06

0.37

CK
(U/L)

Control

35.73±315.29

45.73±317.29

0.093

0.684

1.06

0.37

MDA
(nmol/L)

Training

1.21 ±3.19

1.11 ±3.39

3.99

0.21

2.05

0.11

MDA
(nmol/L)

Training +Jujube

1.32 ±3.12

1.32 ±2.99

4.38

0.11

2.05

0.11

MDA
(nmol/L)

Consumption Jujube

1.27 ±2.89

0.96±2.69

3.78

0.075

2.05

0.11

MDA
(nmol/L)

Control

1.45 ±3.11

1.25 ±3.23

4.57

0.591

2.05

0.11

Ethical Considerations

Compliance with Ethical Guidelines

All participants were examined by a physician before entering the study and were granted permission to participate. Written informed consent was obtained, confirming voluntary and informed participation in exercise sessions and supplement consumption. The authors state that the principles of the Declaration of Helsinki were observed throughout the study.

Funding

This study was carried out with the financial and executive support of the University of Sistan and Baluchestan.

Authors’ Contributions

All authors actively and equally participated in the design, implementation, data analysis, and writing of this manuscript.

Conflicts of Interest

The authors declared that no conflicts of interest were involved.

Acknowledgments

The authors thank all study participants, the University’s Vice Chancellor for Research, the professors of the Department of Sport Sciences, and all students who assisted with the research.

References

  1. Banerjee AK, Mandal A, Chanda D, Chakraborti S. Oxidant, antioxidant and physical exercise. Mol Cell Biochem. 2003;253(1-2):307-12. doi: 10.1023/a:1026032404105 pmid
  2. Ismaeel A, Holmes M, Papoutsi E, Panton L, Koutakis P. Resistance training, antioxidant status, and antioxidant supplementation. Int J Sport Nutr Exerc Metab. 2019;29(5):539-47. doi: 10.1123/ijsnem.2018-0339 pmid
  3. Mousavirad T, Khoshnavaz l. Investigating the role of exercise on nervous pressure, mental and physical health and presenting an exercise program from the perspective of professors and students of Alborz University. Stu & Res in Beh Sci 2019;)1(1: 25-47.
  4. Soslu R, Özer Ö, Çuvalcioglu IC. The effects of core training on basketball athletes' antioxidant capacity. J Edu Train Stud. 2018;6(11):128-34. doi: 10.11114/jets.v6i11.3454
  5. Viña J, Gomez-Cabrera MC, Lloret A, Marquez R, Miñana JB, Pallardó FV, et al. Free radicals in exhaustive physical exercise: mechanism of production, and protection by antioxidants. IUBMB Life. 2000;50(4-5):271-7. doi: 10.1080/713803729 pmid
  6. Sacheck JM, Blumberg JB. Role of vitamin E and oxidative stress in exercise. Nutr. 2001;17(10):809-14. doi: doi: 10.1016/s0899-9007(01)00639-6 pmid
  7. Spriet LL, Howlett RA, Heigenhauser GJ. An enzymatic approach to lactate production in human skeletal muscle during exercise. Med Sci Sports Exerc. 2000;32(4):756-63. doi: doi: 10.1097/00005768-200004000-00007 pmid
  8. Maughan RJ, Burke LM, Dvorak J, Larson-Meyer DE, Peeling P, Phillips SM, et al. IOC consensus statement: dietary supplements and the high-performance athlete. Int J Sport Nutr Exerc Metab. 2018;28(2):104-25. doi: 10.1123/ijsnem.2018-0020 pmid
  9. Keikha AA, Ghofrani M, Helalizadeh M. Effects of twoweeks colostrum supplementation on muscle injury indices and lipid peroxidation following an acute resistance activity session in wrestlers. J Appl Heal. 2019;6(2):1-8. [Persian] doi: 10.22049/jassp.2019.26548.1218
  10. Mohammadi H, Afzalpour ME, Ievary SHA. Response of creatine kinase and lactate dehydrogenase enzymes to rest interval between sets and set-repetition configuration during bouts of eccentric exercise. Interv Med Appl Sci. 2018;10(2):83-6. doi: 10.1556/1646.10.2018.09 pmid
  11. Saengsirisuwan V, Phadungkij S, Pholpramool C. Renal and liver functions and muscle injuries during training and after competitionin thai boxers. Br J Sports Med. 1998;32(4):304-8. doi: 10.1136/bjsm.32.4.304 pmid
  12. Nameni F, Kashefi M, Lari AA. The effect of heating on the relationship between CK and LDH in the recovery period of female athletes, Olympics. 2004;4(28):97-107. [Persian] Link
  13. Irandoust K, Taheri M, Chtourou H, Nikolaidis PT, Rosemann T, Knechtle B. Effect of time-of-day-exercise in group settings on level of mood and depression of former elite male athletes. Int J Environ Res Public Health. 2019;16(19):3541. doi: 10.3390/ijerph16193541 pmid
  14. Rugbeer N, Constantinou D, Torres G. Comparison of high-intensity training versus moderate-intensity continuous training on cardiorespiratory fitness and body fat percentage in persons with overweight or obesity: a systematic review and meta-analysis of randomized controlled trials. J Phys Act Health. 2021;18(5):610-23. doi: 10.1123/jpah.2020-0335 pmid
  15. Zhang K, Zhang Q, Jiang H, Du J, Zhou C, Yu S, et al. Impact of aerobic exercise on cognitive impairment and oxidative stress markers in methamphetamine-dependent patients. Psychiatry Res. 2018;266:328-33. doi: 10.1016/j.psychres.2018.03.032 pmid
  16. Inoue K, Fujie S, Kurose S, Miyauchi T, Sanada K, Kimura Y, et al. Relationships between circulating irisin levels, cardiorespiratory fitness, and cardiometabolic risk: a cross-sectional study in Japanese adults. Am J Physiol Heart Circ Physiol. 2023;325(6):1318-24. doi: 10.1152/ajpheart.00573.2023 pmid
  17. Ghorbanian B, Yousef S. The effect of incremental interval endurance training with Portulaca supplementation on the antioxidant biological indices and oxidative stress in non-active girls. J Sport Biosci. 2019;11(2):131-46. [Persian] doi: 10.22059/jsb.2019.257146.1269
  18. Shahidi F, Shakeri C, Delfani Z. The effect of eight weeks interval aerobic exercise and consumption of green tea supplementation on oxidative stress indices of inactive young girls. Razi J Med Sci. 2019;25(11):72-8. [Persian] Link
  19. Attarzadeh Hosseini SR, Moazzami M, Farahati S, Bahremand M, Sadegh Eghbali F. Effects of high-intensity interval training versus moderateintensity continuous training on the total antioxidant capacity, malondialdehyde, and superoxide dismutase in obese/overweight middleaged women. Iran J Endocrinol Metab. 2020;22(3):207-13. Link
  20. Fakhri F, Shakeryan S, Fakhri S, Alizadeh A. The effect of 6 weeks of high intensity interval training (HIIT) with nano-curcumin supplementation on factors related to cardiovascular disease in inactive overweight girls. KAUMSJ(FEYZ). 2020;24(2):181-9. [Persian] Link
  21. Mardani A, Abednatanzi H, Gholami M, Ghazalian F, Azizbeigi K. Effect of intensity sequence of resistance training on some antioxidants factors and Malondialdehyde plasma in over weight men. Sci J Rehab Med. 2022;10(6):1258-69. doi: 10.32598/SJRM.10.6.13
  22. Masompor M, Vahidian M, Mohammaddoost O. Evaluation of the effects of six weeks of TRX exercise and curcumin on muscle injury indicators in female athletes. Health Res J. 2021;6(3):253-61. doi: 10.52547/hrjbaq.6.3.253
  23. Javadikia M, Yazdi AB, Khajei R, Abadi MR. The effect of 8 weeks high-intensity interval training and portulaca oleracea supplement on serum level of TAC, MDA, CRP, TNF-α in rats with non-alcoholic fatty liver disease. Complement Med J. 2023;12(4):13-21. [Persian] doi: 10.61186/cmja.12.4.13
  24. Tofighi A, Babaei S, Mollazadeh P. The effect of 6 weeks of aerobic training with chlorella consumption on lipid peroxidation indices and total antioxidant capacity of inactive obese men following exhaustive activity. Jundishapur Sci Med J. 2021;19(6):591-604. doi: 10.22118/jsmj.2021.252796.2250
  25. Shadkam T, Nazarali P, Bijeh N. The effect of aerobic exercises combined with curcuma longa supplementation on cardiovascular inflammatory indexes and body composition in sedentary women. J Sport Biosci. 2016;8(2):193-206. [Persian] doi: 10.22059/jsb.2016.59095
  26. Zhang H, Jiang L, Ye S, Ye Y, Ren F. Systematic evaluation of antioxidant capacities of the ethanolic extract of different tissues of jujube (Ziziphus jujuba Mill.) from China. J Food Chem Toxicol. 2010;48:1461-5. doi: doi: 10.1016/j.fct.2010.03.011 pmid
  27. San B, Yildirim AN. Phenolic, alpha-tocopherol, beta-carotene and fatty acid composition of four promising jujube (Ziziphus jujuba Miller) selections. J Food Compos Analysis. 2010;23(7):706-10. doi: doi: 10.1016/j.jfca.2010.02.008
  28. Jaydari F, Johari H, Taati M, Asadian P, Alirezaei M, Sheikhzadeh F. The effects of fruit extract on catalase activity and lipid peroxidation in the heart and erythrocytes of rats following chronic ethanol consumption. Int J Vet Res. 2011;3(2):179-83. Link
  29. Cao B. Experimental study on anti-exercise fatigue effect of Jujube polysaccharide. Food Sci. 2008;29:571-4. Link
  30. Fangling D, Cailian L. Effect of Jujube polysaccharide on some biochemical indicators of mouse's blood. J Jil Inst Phys Educat. 2008;6-24. Link
  31. Goli-Malekabadi N, Asgary S, Rashidi B, Rafieian-Kopaei M, Ghannadian M, Hajian S, et al. The protective effects of Ziziphus vulgaris L. fruits on biochemical and histological abnormalities induced by diabetes in rats. J Complement Integ Med. 2014;11(3):171-7. doi: 10.1515/jcim-2014-0010 pmid
  32. Fakhri S, Shakeryan S, Alizadeh A, Shahryari A. Effect of 6 weeks of high intensity interval training with nano curcumin supplement on antioxidant defense and lipid peroxidation in overweight girlsclinical trial. Iran J Diabetes Obes. 2020;11(3):173-80. doi: 10.18502/ijdo.v11i3.2606
  33. Mohammad-Sadeghipour M, Afsharinasab M, Mohamadi M, Mahmoodi M, Falahati-Pour SK, Hajizadeh MR. The effects of hydro-alcoholic extract of Fenugreek Seeds on the lipid profile and oxidative stress in fructose-fed rats. J Obes Metab Syndr. 2020;29(3):198-207. doi: 10.7570/jomes19051 pmid
  34. Fernández-Lázaro D, Mielgo-Ayuso J, Seco Calvo J, Córdova Martínez A, Caballero García A, Fernandez-Lazaro CI. Modulation of exerciseinduced muscle damage, inflammation, and oxidative markers by curcumin supplementation in a physically active population: a systematic review. Nutr. 2020;12(2):501. doi: 10.3390/nu12020501 pmid
  35. Hirata BKS, Pedroso AP, Machado MMF, Neto NIP, Perestrelo BO, de Sá RDCC, et al. Ginkgo biloba extract modulates the retroperitoneal fat depot proteome and reduces oxidative stress in diet-induced obese rats. Front Pharmacol. 2019;10:686. doi: doi: 10.3389/fphar.2019.00686 pmid
  36. Olszowy-Tomczyk M, Wianowska D. Antioxidant properties of selected flavonoids in binary mixtures—considerations on myricetin, kaempferol and quercetin. Int J Mol Sci. 2023;24(12):10070. doi: doi: 10.3390/ijms241210070 pmid
  37. Jahangard A, Hamedinia M, Hosseini kakhk A, Jafari A, Salehzadeh, K. Effect of short-term garlic extract supplementation on oxidative stress indices during rest and induced-exercise exhaustion in male soccer players. Iran J Endocrinol Metab. 2013;15(1):78-85. [Persian] Link
  38. Mirzaei B, Demirci A, Mehrabani J. Interactive effect of vitamin E supplementation and aerobic exercise on the LDH, CK, blood lactate of non-athletic men after helpless activity. Olympic. 2007;2(38): 29-39. [Persian]
  39. Afzalpour MA, Rezazadeh A, Abtahi Ivari H. Effects of Ziziphus Jujube on total antioxidant capacity and lipid peroxidation in young women after an intensive resistance exercise session.. Sport Biomotor Sci. 2014;6(11):16-26. [Persian] Link
  40. El Abed K, Rebai H, Bloomer RJ, Trabelsi K, Masmoudi L, Zbidi A, et al. Antioxidant status and oxidative stress at rest and in response to acute exercise in judokas and sedentary men. J Strength Cond Res. 2011;25(9):2400-9. doi: doi: 10.1519/JSC.0b013e3181fc5c35 pmid
  41. Inayama T, Kumagi Y, Sakanen M, Saito M, Matsnda M. Plasma protein-bound sulfhydryl group oxidation in humans following a full marathon race. Lif Sci. 1996;59(7):573-8. doi: doi: 10.1016/0024-3205(96)00338-4 pmid
  42. Niess AM, Sommer M, Schneider M, Angres C, Tschositsch K, Golly IC, et al. Physical exercise-induced expression of inducible nitric oxide synthase and heme oxygenase-1 in human leukocytes: effects of RRR-alpha-tocopherol supplementation. Antioxid Redox Signal. 2000;2(1):113-26. doi: doi: 10.1089/ars.2000.2.1-113 pmid
  43. Piercy RJ, Hinchcliff KW, DiSilverstro RA, Reinhart GA, Baskin CR, Hayek MG, et al. Effects of dietary supplements containing antioxidants on attenuation of muscle damage in exercising sled dogs. Am J Vet Res. 2000;61(11):1438-45. doi: doi: 10.2460/ajvr.2000.61.1438 pmid
  44. Cannon JG, Orencole SF, Fielding RA, Meydani M, Meydani SN, Fiatarone MA, et al. Acute phase respanse in exeecise: intraction of age and Vitamin E on neutrophils and muscle enzyme release. Am J Physiol. 1990;259:1214-9. doi: doi: 10.1152/ajpregu.1990.259.6.R1214 pmid
  45. Mousavi SM, Nourshahi M, Ghara Khanlou RE, Hedayati M, Akbarnejad A. The acute effect of HMB-FA supplement and sport activity on some factors that influence hypertrophy and muscle damage in inactive men. J Sport Biosci. 2021;13(3):285-300. doi: 10.22059/jsb.2018.265762.1310
  46. Helgheim I, Heltland O, Nilsson S, Ingjer F, Stromme SB. The effects of vitamin E on serum enzyme levels following heavy exercise. Eur J Appl Physiol Occup Physiol. 1979;40:283-9. doi: doi: 10.1007/BF00421520 pmid
  47. Itoh H, Ohkuwa T, Yamazaki Y, Shimoda T, Wakayama A, Tamura S, et al. Vitamin E supplementation attenuates leakage of enzymes following 6 successive days of running training. Int J Sports Med. 2000;21(5):369-74. doi: doi: 10.1055/s-2000-3777 pmid
  48. Taati M, Alirezaei M, Meshkatalsadat MH, Rasoulian B, Kheradmand A, Neamati Sh. Antioxidant effects of aqueous fruit extract of Ziziphus jujuba on ethanol-induced oxidative stress in the rat testes. J Vet Res. 2011;34:39-45. [Persian] Link
  49. Bell PG, Walshe IH, Davison GW, Stevenson E, Howatson G. Montmorency cherries reduce the oxidative stress and inflammatory responses to repeated days high-intensity stochastic cycling. J Nutr. 2014;6(2):829-43. doi: doi: 10.3390/nu6020829 pmid
  50. Belviran M, Gökbel H, Okudan N, BaOaral K. Effects of grape seed extract supplementation on exercise- induced oxidative stress in rats. Br J Nutr. 2012;108(2):249-56. doi: 10.1017/S0007114511005496 pmid
  51. Shadmanfard A, Nemati A, Naghizadeh B, Mazani M. The effect of pomegranate juice supplementation on oxidative stress following exhaustive exercise in young healthy males. J Iran Chem Soc. 2012;12(5):77-86. [Persian] Link
  52. Atashak S, Niloofari A, Azizbaygi K. The effect of blackberry extract on the total antioxidant capacity and lipid peroxidation after acute resistance exercise in obese men. J Food Technol Nutr. 2014;42(2):55. [Persian] Link
  53. Jowko E, Sacharuk J, Balasinska B, Wilczak J, Charmas M, Ostaszewski P, et al. Effect of a single dose of Green Tea polyphenols on the mlood markers of exercise-induced oxidative stress in soccer players. Int J Sport Nutr Exerc Metab. 2012;22:486-96. doi: 10.1123/ijsnem.22.6.486 pmid
  54. Jafari A, Zekri R, Dehghan Gh, Malekirad AA. Effect of short-term garlic extract supplementation on oxidative stress and inflammatory indices in non-athlete men after an aerobic exercise. J Cell Tissue. 2011;2(1):25-33. [Persian] Link
  55. Jabbari S, Kargarfard M. Short-term effect of Quercetin supplementation on inflammatory and oxidative stress indices of active individuals after intense exercise. J App Health Stud Sport Physiol. 2021;8(1):36-43. [Persian] doi: 10.22049/jahssp.2021.27237.1351

Copyright © The Author(s). Published under the journal’s stated open-access license.