Effects of Herbs and High-Intensity Exercise Training on Antioxidant Properties Regarding Weight Management and Exercise-Related Variables: A Review

  • Reza Sabzevari Rad Department of Exercise Physiology Research Center, Life Style Institute, Baqiyatallah University Medical of Sciences Tehran, Tehran, Iran
  • Maryam Iman * Chemical Injuries Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran
  • Reza Bagheri Department of Exercise Physiology, Ferdowsi University of Mashhad, Mashhad, Iran http://orcid.org/0000-0003-1433-2906
  • Behzad Bazgir Department of Exercise Physiology Research Center, Life Style Institute, Baqiyatallah University Medical of Sciences Tehran, Tehran, Iran
  • Hasti Iman Department of Chemistry, Faculty of Basic Sciences, Islamic Azad University, Yadegar Emam Khomeini Branch, Tehran, Iran
Keywords: Rapid Reaction Forces, Medicinal Plants, Antioxidants, Obesity

Abstract

It has been determined that high-intensity exercise training is associated with the production of oxidative stress factors leading to a reduction in the efficiency and physical functioning of rapid reaction forces. Conversely, high levels of physical activity and coping with oxidative stress factors (using supplements) are highly suggested for rapid reaction forces. Hence, the present study sought to examine the effects of plants and high-intensity exercise on antioxidant properties associated with weight management and some related factors. The literature on this research was collected from the PubMed archive on January 31, 2019, and included the keywords, high-intensity exercise training, herb and overweight. To date, 15,000 articles have been published on the PubMed archive with the keyword 'herb', 4473 articles have been published concerning high-intensity exercise training, and 94 articles related to the present review article are categorized into two categories of complete and abstract texts. All the articles were classified according to the novelty before being examined. Rapid reaction forces need to increase physical activity in order to have better functions. Likewise, they use plants and herbal supplements owing to maintaining physical fitness, and counteract the effects of oxidative stress caused by high-intensity exercise. Consequently, a comprehensive and efficient research that would adequately indicate the side effects and the effectiveness of these plants had to be carried out. The use of herbs and supplements will depend on the purpose of the individuals, particularly rapid reaction forces. If the goal of these forces is to increase their vigilance as well as their reaction and to postpone fatigue in missions, Ginseng and caffeine are the best plants, and if they seek to maintain physical fitness and reduce body fat, green tea is the best option. Nutritional interventions and the use of supplements (antioxidant, herbal and physical activity enhancers) are effective ways of protecting rapid reaction forces against the effects of oxidative stress caused by high-intensity exercise and maintaining fitness. Remarkably, despite the positive effects of plants, the excessive consumption of these supplements induces certain side effects on the kidneys and stomach. Likewise, they should be used cautiously.

References

Riggio D. EU‐NATO cooperation and complementarity between the rapid reaction forces. The international spectator. 2003;38(3):47-60.

Ara I, Perez-Gomez J, Vicente-Rodriguez G, Chavarren J, Dorado C, Calbet J. Serum free testosterone, leptin and soluble leptin receptor changes in a 6-week strength-training programme. British journal of nutrition. 2006;96(6):1053-9.

Artinian NT, Fletcher GF, Mozaffarian D, Kris-Etherton P, Van Horn L, Lichtenstein AH, et al. Interventions to promote physical activity and dietary lifestyle changes for cardiovascular risk factor reduction in adults. A scientific statement from the American Heart Association. Circulation. 2010.

McCord S. PDR for Nonprescription Drugs and Dietary Supplements. MEDICAL REFERENCE SERVICES QUARTERLY. 2002;21(4):82-.

Belviranlı M, Gökbel H. Acute exercise induced oxidative stress and antioxidant changes. Eur J Gen Med. 2006;3(3):126-31.

Pittler M, Ernst E. Complementary therapies for reducing body weight: a systematic review. International journal of Obesity. 2005;29(9):1030.

Nagao T, Meguro S, Soga S, OTSUKA A, TOMONOBU K, FUMOTO S, et al. Tea catechins suppress accumulation of body fat in humans. Journal of Oleo Science. 2001;50(9):717-28.

He R-r, Chen L, Lin B-h, Matsui Y, Yao X-s, Kurihara H. Beneficial effects of oolong tea consumption on diet-induced overweight and obese subjects. Chinese journal of integrative medicine. 2009;15(1):34-41.

Roberts AT, de Jonge-Levitan L, Parker CC, Greenway FL. The effect of an herbal supplement containing black tea and caffeine on metabolic parameters in humans. Alternative medicine review. 2005;10(4):321.

Haaz S, Fontaine K, Cutter G, Limdi N, Perumean‐Chaney S, Allison D. Citrus aurantium and synephrine alkaloids in the treatment of overweight and obesity: an update. Obesity reviews. 2006;7(1):79-88.

Allison D, Cutter G, Poehlman E, Moore D, Barnes S. Exactly which synephrine alkaloids does Citrus aurantium (bitter orange) contain? International journal of obesity. 2005;29(4):443.

Bui LT, Nguyen DT, Ambrose PJ. Blood pressure and heart rate effects following a single dose of bitter orange. Annals of Pharmacotherapy. 2006;40(1):53-7.

Haller CA, Benowitz NL, Jacob III P. Hemodynamic effects of ephedra-free weight-loss supplements in humans. The American journal of medicine. 2005;118(9):998-1003.

Penzak SR, Jann MW, Cold JA, Hon YY, Desai HD, Gurley BJ. Seville (sour) orange juice: synephrine content and cardiovascular effects in normotensive adults. The Journal of Clinical Pharmacology. 2001;41(10):1059-63.

Pathak B, Gougeon R, Center MN. Thermic effect of Citrus aurantium in obese subjects. Curr Ther Res. 1999;60:145-51.

Henry C, Emery B. Effect of spiced food on metabolic rate. Human nutrition Clinical nutrition. 1986;40(2):165-8.

Yoshioka M, St-Pierre S, Suzuki M, Tremblay A. Effects of red pepper added to high-fat and high-carbohydrate meals on energy metabolism and substrate utilization in Japanese women. British Journal of Nutrition. 1998;80(6):503-10.

Pittler MH, Ernst E. Guar gum for body weight reduction: meta-analysis of randomized trials. The American journal of medicine. 2001;110(9):724-30.

Doi K. Effect of konjac fibre (glucomannan) on glucose and lipids. European journal of clinical nutrition. 1995;49:S190-7.

Walsh DE, Yaghoubian V, Behforooz A. Effect of glucomannan on obese patients: a clinical study. Int J Obes. 1984;8(4):289-93.

Celleno L, Tolaini MV, D'Amore A, Perricone NV, Preuss HG. A dietary supplement containing standardized Phaseolus vulgaris extract influences body composition of overweight men and women. International journal of medical sciences. 2007;4(1):45.

Looije NA, Risovic V, Stewart DJ, Debeyer D, Kutney J, Wasan KM. Disodium Ascorbyl Phytostanyl Phosphates (FM-VP4) reduces plasma cholesterol concentration, body weight and abdominal fat gain within a dietary-induced obese mouse model. J Pharm Pharm Sci. 2005;8(3):400-8.

Chevassus H, Gaillard J-B, Farret A, Costa F, Gabillaud I, Mas E, et al. A fenugreek seed extract selectively reduces spontaneous fat intake in overweight subjects. European journal of clinical pharmacology. 2010;66(5):449-55.

Li Y-J, Chen J, Li Y, Li Q, Zheng Y-F, Fu Y, et al. Screening and characterization of natural antioxidants in four Glycyrrhiza species by liquid chromatography coupled with electrospray ionization quadrupole time-of-flight tandem mass spectrometry. Journal of Chromatography A. 2011;1218(45):8181-91.

Jia J, Zhu F, Ma X, Cao ZW, Li YX, Chen YZ. Mechanisms of drug combinations: interaction and network perspectives. Nature reviews Drug discovery. 2009;8(2):111.

Kobayashi M, Fujita K, Katakura T, Utsunomiya T, Pollard RB, Suzuki F. Inhibitory effect of glycyrrhizin on experimental pulmonary metastasis in mice inoculated with B16 melanoma. Anticancer research. 2002;22(6C):4053-8.

Wang Z, Nishioka M, Kurosaki Y, Nakayama T, Kimura T. Gastrointestinal absorption characteristics of glycyrrhizin from glycyrrhiza extract. Biological and Pharmaceutical Bulletin. 1995;18(9):1238-41.

Maha M, Gazia A, Nermeen M. Effect of glabridin on the structure of ileum and pancreas in diabetic rats: a histological, immunohistochemical and ultrastructural study. Nature and Sci. 2012;10(3):78-90.

Ghasemi E, Esmaeil Afzalpour M, Saghebjoo M, Zarban A. Effects of Short-Term Green Tea Supplementation on Total Antioxidant Capacity and Lipid Peroxidation in Young Women after a Resistance Training Session. Journal of Isfahan Medical School. 2012;30(202).

Jafari A, Zekri R, Dehghan G, Malekirad A. Effect of short-term garlic extract supplementation on oxidative stress and inflammatory indices in non-athlete men after an aerobic exercise. 2011.

Aruoma OI, Spencer JP, Warren D, Jenner P, Butler J, Halliwell B. Characterization of food antioxidants, illustrated using commercial garlic and ginger preparations. Food chemistry. 1997;60(2):149-56.

Atashak S, Azarbayjani M, Piri M, Jafari A. Effects of combination of long-term ginger consumption and resistance training on lipid peroxidation and insulin resistance in obese men. Journal of Medicinal Plants. 2012;2(42):179-88.

Sellami M, Slimeni O, Pokrywka A, Kuvačić G, Hayes LD, Milic M, et al. Herbal medicine for sports: a review. Journal of the International Society of Sports Nutrition. 2018;15(1):14.

Kimoto R, Kambayashi I, Ishimura N, Nakamura T. Effect of aged garlic extract supplementation on the change of urinary 8-OHdG content during daily regular and temporary intense exercise. Hokkaido J Med Sci. 2005;10:17-26.

Mirdar S, Maleki F, Alavi Y. Moderate Caffeine dose and one Session incremental exercise effect on oxidative stress and enzymatic antioxidant status in active men. Sport Physiology. 2014;5(20):39-52.

Ranjbar A, Ghasmeinezhad S, Zamani H, Malekirad AA, Baiaty A, Mohammadirad A, et al. Antioxidative stress potential of Cinnamomum zeylanicum in humans: a comparative cross-sectional clinical study. Therapy. 2006;3(1):113-7.

Gahreman DE, Boutcher YN, Bustamante S, Boutcher SH. The combined effect of green tea and acute interval sprinting exercise on fat oxidation of trained and untrained males. Journal of exercise nutrition & biochemistry. 2016;20(1):1.

Crespy V, Williamson G. A review of the health effects of green tea catechins in in vivo animal models. The Journal of nutrition. 2004;134(12):3431S-40S.

Jówko E, Sacharuk J, Balasińska B, Ostaszewski P, Charmas M, Charmas R. Green tea extract supplementation gives protection against exercise-induced oxidative damage in healthy men. Nutrition research. 2011;31(11):813-21.

Lafay S, Jan C, Nardon K, Lemaire B, Ibarra A, Roller M, et al. Grape extract improves antioxidant status and physical performance in elite male athletes. Journal of sports science & medicine. 2009;8(3):468.

Atashak S, Niloufari A, Azizbeigi K. Effect of Extract of Blackberry on Total Antioxidant Capacity and Lipid Peroxidation after Acute Resistance Exercise in Obese Men. Journal of Food Technology. 2014:55-62.

Kim S, Park K, Chang M, Sung J. Effects of Panax ginseng extract on exercise-induced oxidative stress. Journal of Sports Medicine and Physical Fitness. 2005;45(2):178.

Lyall KA, Hurst SM, Cooney JM, Jensen DJ, Lo K, Hurst RD, et al. Short-term blackcurrant extract consumption modulates exercise-induced oxidative stress and lipopolysaccharide-stimulated inflammatory responses. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. 2009.

Prasad KN, Yang B, Dong X, Jiang G, Zhang H, Xie H, et al. Flavonoid contents and antioxidant activities from Cinnamomum species. Innovative Food Science & Emerging Technologies. 2009;10(4):627-32.

Published
2019-10-03
Section
Review Article