Royal Jelly Supplementation Enhances Post-Exhaustive Exercise Energy Metabolism

Research Article

Authors

DOI:

https://doi.org/10.5281/zenodo.13783567

Keywords:

Acute exhaustion exercise, Royal jelly, Muscle adaptation, Energy metabolism

Abstract

Introduction: Lactate accumulation, free radical increase and changes in the activity of regulatory enzymes in energy metabolism that occur after acute exhaustion exercise disrupt the muscle adaptation mechanism and lead to muscle damage. Royal jelly, which is considered a superfood with its cell regeneration and therapeutic effects, can compensate for the effects that occur after exercise.

Objective: In this study, the effects of royal jelly supplementation were investigated in Balb-c type mice in which an acute exhaustion exercise model was created.

Methods: Mice were randomly divided into four groups: control, royal jelly, acute exhaustion exercise, acute exhaustion exercise + royal jelly. In all groups, the levels of mitochondrial biogenesis markers Ppargc1a and TFAM, which regulate muscle adaptation, and the levels of PDHa and Slc16a1, which are effective in aerobic and anaerobic regulation, were analyzed by ELISA method.

Results: PDHa and Slc16a1 levels were statistically significant between groups (p=0.024, p=0.029, respectively), but Ppargc1a and TFAM levels were not significant between groups (p=0.087, p=0.082, respectively). It was found that PDHa, Slc16a1, Ppargc1a and TFAM levels increased in the group receiving royal jelly supplementation with acute exhaustion exercise compared to the group not receiving supplementation.

Conclusions: These findings highlight the effective potential of royal jelly in developing/improving aerobic and anaerobic respiratory pathways and in the muscle adaptation process against the impaired muscle adaptation mechanism caused by acute exhausting exercise. Based on these promising results, further research is required to explore new knowledge in exercise physiology and sports sciences.

References

Powers SK, Jackson MJ. Exercise-induced oxidative stress: cellular mechanisms and impact on muscle force production. Physiol Rev. 2008 Oct;88(4):1243-76. doi:10.1152/physrev.00031.2007

Suzuki K, Nakaji S, Yamada M, Totsuka M, Sato K, Sugawara K. Systemic inflammatory response to exhaustive exercise. Cytokine kinetics. Exerc Immunol Rev. 2002;8:6-48

Alu'datt MH, Rababah T, Obaidat MM, et al. Probiotics from Milk Fortified with Royal Jelly. J Food Saf. 2015;35:509-522

Hu H, Bezabih G, Feng M, et al. In-depth Proteome of the Hypopharyngeal Glands of Honeybee Workers Reveals Highly Activated Protein and Energy Metabolism in Priming the Secretion of Royal Jelly. Mol Cell Proteomics. 2019;18(4):606-621.

Cohen S, Nathan JA, Goldberg AL. Muscle wasting in disease: Molecular mechanisms and promising therapies. Nature Reviews Drug Discovery. 2014;14(1):58–74.

Neufer PD, Bamman MM, Muoio DM, et al. Understanding the Cellular and Molecular Mechanisms of Physical Activity-Induced Health Benefits. Cell Metabolism. 2015;22(1):4–11

Liang X, Liu L, Fu T, et al. Exercise inducible lactate dehydrogenase B regulates mitochondrial function in skeletal muscle". Journal of Biological Chemistry. 2016;291(49):25306–25318.

Park HM, Cho MH, Cho Y, Kim SY, Lee YH. Royal jelly increases endurance by enhancing mitochondrial function and muscle energy metabolism in mice. Journal of Nutritional Biochemistry. 2018;55:69-76. doi:10.1016/j.jnutbio.2018.01.001.

Gasiorowski A, Dutkiewicz J. Comprehensive rehabilitation in chronic heart failure. Ann Agric Environ Med. 2013;20:606–12.

Gayda M, Ribeiro PA, Juneau M, Nigam A. Comparison of different forms of exercise training in patients with cardiac disease: where does high-intensity interval training fit? Can J Cardiol. 2016;32:485–94. doi:10.1016/j.cjca.2016.01.017

Boule NG, Haddad E, Kenny GP, Wells GA, Sigal RJ. Effects of exercise on glycemic control and body mass in type 2 diabetes mellitus: a meta-analysis of controlled clinical trials. JAMA. 2001;286:1218–27. doi:10.1001/jama.286.10.1218

Egan B, Zierath JR. Exercise metabolism and the molecular regulation of skeletal muscle adaptation. Cell Metab. 2013;17:162–84. doi:10.1016/j.cmet.2012.12.012

Chalder M, Wiles NJ, Campbell J, et al. Facilitated physical activity as a treatment for depressed adults: randomised controlled trial. BMJ. 2012;344:e2758. doi:10.1136/bmj.e2758

Holme I, Anderssen SA. Increases in physical activity is as important as smoking cessation for reduction in total mortality in elderly men: 12 years of follow-up of the Oslo II study. Br J Sports Med. 2015;49:743–8. doi:10.1136/bjsports-2014-094522

Heinonen I, Kalliokoski KK, Hannukainen JC, Duncker DJ, Nuutila P, Knuuti J. Organ-specific physiological responses to acute physical exercise and long-term training in humans. Physiology. 2014;29:421–36. doi:10.1152/physiol.00067.2013

Taskin S, Celik T, 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):1009-1015. doi:10.22038/IJBMS.2022.65047.14321

Hellsten Y, Nyberg M. Cardiovascular Adaptations to Exercise Training. Compr Physiol. 2015;6(1):1-32. doi:10.1002/cphy.c140080

Rønnestad BR, Mujika I. Optimizing strength training for running and cycling endurance performance: A review. Scand J Med Sci Sports. 2014;24(4):603-12. doi:10.1111/sms.12104

Lim C, Nunes EA, Currier BS, McLeod JC, Thomas ACQ, Phillips SM. An Evidence-Based Narrative Review of Mechanisms of Resistance Exercise-Induced Human Skeletal Muscle Hypertrophy. Med Sci Sports Exerc. 2022;54(9):1546-1559. doi:10.1249/MSS.0000000000002929

Bonen A. The expression of lactate transporters (MCT1 and MCT4) in heart and muscle. Eur J Appl Physiol. 2001;86(1):6–11.

Spriet LL, Heigenhauser GJ. Regulation of pyruvate dehydrogenase (PDH) activity in human skeletal muscle during exercise. Exerc Sport Sci Rev. 2002;30(2):91-95. doi:10.1097/00003677-200204000-00009

Ward GR, Sutton JR, Jones NL, Toews CJ. İnsan iskelet kası pirüvat dehidrogenazının egzersizle in vivo aktivasyonu. Clin. Sci. 1982;63:87–92.

Robergs RA, Ghiasvand F, Parker D. Biochemistry of exercise-induced metabolic acidosis. Am J Physiol Regul Integr Comp Physiol. 2004;287(3): R502–16.

Halestrap AP, Marieangela C. Wilson the Monocarboxylate transporter family—role and regulation. IUBMB Life. 2012;64(2):109–19.

Hood DA, Uguccioni G, Ainshtein A, D’souza D. Mechanisms of ExerciseInduced Mitochondrial Biogenesis in Skeletal Muscle: Implications for Health and Disease. Comprehensive Physiology. 2011;1:1119–1134.

Jornayvaz FR, Shulman GI. Regulation of mitochondrial biogenesis. Essays in Biochemistry. 2010;47:1010-1042.

Takahashi Y, Hijikata K, Seike K, et al. Effects of Royal Jelly Administration on Endurance Training-Induced Mitochondrial Adaptations in Skeletal Muscle. Nutrients. 2018;10(11):1735.

Luthi JM, Howald H, Claassen H, et al. Structural changes in skeletal muscle tissue with heavy-resistance exercise. Int J Sports Med. 1986;7:123–127.

Greene NP, Nilsson MI, Washington TA, et al. Impaired exercise-induced mitochondrial biogenesis in the obese Zucker rat, despite PGC-1alpha induction, is due to compromised mitochondrial translation elongation. Am J Physiol Endocrinol Metab. 2014;306:E503–E511.

Porter C, Reidy PT, Bhattarai N, et al. Resistance exercise training alters mitochondrial function in human skeletal muscle. Med Sci Sports Exerc. 2015;47:1922–1931.

Parry HA, Roberts MD, Kavazis AN. Human Skeletal Muscle Mitochondrial Adaptations Following Resistance Exercise Training. Int J Sports Med. 2020;41(6):349-359. doi:10.1055/a-1121-7851

Flockhart M, Nilsson LC, Tais S, Ekblom B, Apró W, Larsen FJ. Excessive exercise training causes mitochondrial functional impairment and decreases glucose tolerance in healthy volunteers. Cell Metab. 2021;33(5):957-970.e6. doi:10.1016/j.cmet.2021.02.017

Larsen FJ, Schiffer TA, Ørtenblad N, et al. High-intensity sprint training inhibits mitochondrial respiration through aconitase inactivation. FASEB J. 2016;30(1):417-427. doi:10.1096/fj.15-276857

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Published

2024-09-20

How to Cite

Taşkın, S. (2024). Royal Jelly Supplementation Enhances Post-Exhaustive Exercise Energy Metabolism: Research Article. Acta Medica Ruha, 2(3), 208–215. https://doi.org/10.5281/zenodo.13783567

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Research Articles