Volume 11 - Articles-1400                   MEJDS (2021) 11: 21 | Back to browse issues page


XML Persian Abstract Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Etemad Z, Zohali S. The Effect of Aerobic Training and Royal Jelly Supplementation on Some Inflammatory Markers in Overweight Women. MEJDS 2021; 11 :21-21
URL: http://jdisabilstud.org/article-1-1753-en.html
1- Department of Physical Education & Sport Science, Sanandaj Branch, Islamic Azad University
2- Islamic Azad University Sanandaj Branch
Abstract:   (1582 Views)
Background & Objectives: Lifestyle changes, such as increasing physical activity and fostering a low–calorie diet are among the first interventions to reduce body fat and tackle obesity and overweight. Taking supplements, as a simple strategy combined with physical activity may reduce weight, fat, serum lipids, and possibly inflammatory factors. An effective relevant supplement is Royal Gel Supplement (RGS). Recently, using exercise and nutritional supplements to improve physical health has been welcomed; consuming oral supplements is better appreciated, because of their low cost and no adverse effects. However, using supplements, especially RGS along with exercise has ambiguous aspects; limited studies investigated the response of inflammatory markers to aerobic exercise and RJ supplementation. The present study explored the impact of an 8–week aerobic exercise plus RJS on some inflammatory markers in overweight women.
Methods: This was a quasi–experimental study with a pretest–posttest and a control group design. Thirty healthy overweight female students of the Islamic Azad University of Sanandaj City, Iran, were selected and randomly divided into (supplement+aerobic training; S+AT), (placebo+aerobic, training; P+AT), and control groups. The subjects were included in the study according to a researcher–made questionnaire and the inclusion criteria. The inclusion criteria of the study were presenting overweight per body mass index standards and not participating in training programs ≥6 months before this study. The exclusion criteria included no systemic problems, no diabetes, no acute or chronic cardiovascular diseases, not receiving pharmacotherapy for the past 3 months, and no smoking. One hour before each training session, the S+AT group received RJS (500 mg) orally in 100mg capsules. The P+AT group, like the supplement group, consumed capsules of the same form and color (containing starch powder) an hour before each training session. However, the controls received no supplement. The 8–week aerobic training was performed in 3 weekly sessions. Exercise intensity initiated with 60% of Maximal Heart Rate (MHR) in the first week; according to the principle of overload, it reached 75% of MHR by week 8. The required blood samples were obtained from the study subjects at 8 AM by a laboratory expert and CRP, TNF–α, and IL–6 were measured at pre– and post–training in a fasting state. TNF–α and IL–6 levels were determined by ELISA using the IBL kit according to the manufacturer's instructions (Sigma Aldrich). CRP level was determined by latex–amplified immunoturbidimetry method (CRPLX Roche Cobas c 501) with a dispersion coefficient of 0.1 and sensitivity of 0.3–350 mg/L (Pars Azmoon Company Kit). Considering the research design and previous studies’ data, a significance level of 0.05 was considered. The collected data were analyzed using Analysis of Covariance (ANCOVA) and Bonferroni posthoc tests in SPSS.
Results: The achieved results suggested a significant difference in IL–6 (p<0.001). Bonferroni posthoc test data revealed that in IL–6, this significant difference concerned the groups supplement with placebo (p<0.001), supplement with control (p=0.009), and placebo with control (p=0.001). There was also a significant difference in the CRP variable (p=0.030). The results of the Bonferroni posthoc test indicated that in CRP, this significant difference respected the groups supplement with placebo (p<0.001), and placebo with control (p=0.040), and supplement with control (p=0.015). Furthermore, there was a significant difference in TNF–α levels between the study groups (p=0.040). Bonferroni posthoc test data signified that this significant difference belonged to the groups supplement with placebo (p<0.001) and the supplement with control (p=0.022). Moreover, 70% of IL–6 changes were due to aerobic exercise (Partial Eta=0.70); 55.9% of CRP changes were induced by aerobic exercise (Partial Eta=0.559); 43.5% of TNF–α changes belonged to aerobic exercise (Partial Eta=0.435).
Conclusion: According to the obtained results, an 8–week aerobic training plus RJS could reduce the levels of inflammatory markers, including tumor necrosis factor–alpha, interleukin–6, and reactive protein–C.
Full-Text [PDF 572 kb]   (429 Downloads)    
Type of Study: Original Research Article | Subject: Rehabilitation

References
1. 1. Lorán P, Bayona M, Garriga CA, Serrano-Rodríguez RA. Association between cardiovascular disease and overweight and obesity among adults in Puerto Rico. Journal of Tropical Disease. 2015:S1–005. [DOI]
2. 2. Swift DL, Johannsen NM, Lavie CJ, Earnest CP, Church TS. The role of exercise and physical activity in weight loss and maintenance. Progress in Cardiovascular Diseases. 2014;56(4):441–7. [DOI]
3. 3. Kohno K, Okamoto I, Sano O, Arai N, Iwaki K, Ikeda M, et al. Royal jelly inhibits the production of proinflammatory cytokines by activated macrophages. Bioscience, Biotechnology, and Biochemistry. 2004;68(1):138–45. [DOI]
4. 4. Büyükipekçi S, Sarıtaş N, Soylu M, Mıstık S, Silici S. Effects of royal jelly and honey mixture on some hormones in young males performing maximal strength workout. Physical Education of Students. 2018;22(6):308–15. [DOI]
5. 5. Saritas N, Yildiz K, Büyükipekci S, Coskun B. Effect of different levels of royal jelly on biochemical parameters of swimmers. African Journal of Biotechnology. 2011;10(52):10718–23. [DOI]
6. 6. Mousavi SN, Jazayeri Sh, Khoshpay B, Malek M, Hosseini AF, Hosseini Sh, et al. Royal jelly decreases blood pressure, serum glucose, and interleukin-6 in patients with type 2 diabetes on an iso-caloric diet. Journal of Nutrition and Food Security. 2017;2(4):300–7. [Article]
7. 7. Banitalebi E, Mardanpour Shahrekordi Z, Kazemi AR, Bagheri L, Amani Shalamzari S, Faramarzi M. Comparing the effects of eight weeks of combined training (endurance and resistance) in different orders on inflammatory factors and adipokines among elderly females. Women's Health Bulletin. 2016;3(2):e30990. [Persian]
8. 8. Van Gemert WA, May AM, Schuit AJ, Oosterhof BY, Peeters PH, Monninkhof EM. Effect of weight loss with or without exercise on inflammatory markers and adipokines in postmenopausal women: the SHAPE-2 trial, a randomized controlled trial. Cancer Epidemiol and Biomarkers Prev. 2016;25(5):799–806. [DOI]
9. 9. Anderson SF, Kelley K, Maxwell SE. Sample-size planning for more accurate statistical power: a method adjusting sample effect sizes for publication bias and uncertainty. Psychological science. 2017;28(11):1547–62. [DOI]
10. 10. Gibson A, Wagner D, Heyward V. Advanced fitness assessment and exercise prescription. 8th edition. Champaign, Illinois: Human Kinetics; 2018.
11. 11. Etemad Z, Moradiani H, Aziz-Beigi K. Adiponectin is associated with inflammatory markers and insulin resistance following moderate-intensity circuit weight training in healthy overweight and obese men. Medicina Dello Sport. 2015;68(4):627–38.
12. 12. Wanderley FAC, Moreira A, Sokhatska O, Palmares C, Moreira P, Sandercock G, et al. Differential responses of adiposity, inflammation and autonomic function to aerobic versus resistance training in older adults. Experimental Gerontology. 2013;48(3):326–33. [DOI]
13. 13. Ghafari Gh, Bolboli L, Rajabi A, Saedmochshi S. The effect of 8 weeks aerobic training on predictive inflammatory markers of atherosclerosis and lipid profile in obese elderly women. Journal of Ilam University of Medical Sciences. 2016;23(7):144–54. [Persian] [Article]
14. 14. Tartibiyan B, Yaghobnezhad F, Mohamad Amini S, Maleki M, Abdollahzade N, Faridniya S. Relationship and response of inflammatory immune and hormonal markers to incremental exercise in pediatrics. Journal of Ilam University of Medical Sciences. 2016;24(2):139–48. [Persian] [DOI]
15. 15. Dhabhar FS. Effects of stress on immune function: the good, the bad, and the beautiful. Immunol Res. 2014;58(2-3):193–210. [DOI]
16. 16. Gowdaiah PK, Mamatha TR, Nirgude D, Hosamani PB. High sensitivity C-reactive protein in metabolic syndrome. International Journal of Advances in Medicine. 2016;3(3):607–10. [DOI]
17. 17. Ravasi AA, Gaieni A, Tolouyi Azar J. The influence of 8-week discontinuous aerobic training (3×10 min) on cardiovascular risk biomarkers in inactive obese women. Journal of Sport Biosciences. 2013;5(3):63–75. [Persian] [DOI]
18. 18. Zamanpour L, Banitalebi E, Amirhosseini SE. The effect of sprint training and combined aerobic and strength training on some inflammatory markers and insulin resistance in women with diabetes mellitus (T2dm). Iranian Journal of Diabetes and Metabolism. 2016;15(5):300–11. [Article]
19. 19. Steensberg A, Hall G, Osada T, Sacchetti M, Saltin B, Pedersen BK. Production of interleukin‐6 in contracting human skeletal muscles can account for the exercise‐induced increase in plasma interleukin‐6. The Journal of Physiology. 2000;529(1):237–42. [DOI]
20. 20. Takahashi Y, Hijikata K, Seike K, Nakano S, Banjo M, Sato Y, et al. Effects of royal jelly administration on endurance training-induced mitochondrial adaptations in skeletal muscle. Nutrients. 2018;10(11):1735. [DOI]

Add your comments about this article : Your username or Email:
CAPTCHA

Send email to the article author


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2024 CC BY-NC 4.0 | Middle Eastern Journal of Disability Studies

Designed & Developed by : Yektaweb