Health Science Journal

Keywords

Antioxidant supplement; Erythrocyte membrane; Aerobic capacity; Running economy

Introduction

Oxidative stress plays a role in the immune system by killing bacteria or viruses, but it is also reported to be involved in numerous diseases, such as cardiovascular disease and cancer, as well as in aging [1,2]. Reactive oxygen is produced in excess as a result of transient, hyperintense exercise [3], and it has an oxidizing effect on healthy cells, which creates the source of diseases. The human body has two mechanisms to eliminate reactive oxygen in order to prevent oxidative stress occurring in this way: antioxidants and antioxidant enzymes. Antioxidants are substances that remove reactive oxygen by reacting directly with it, and can be ingested in food or as supplements. Antioxidant enzymes are proteins produced within the body, which act as catalysts. Active ingestion of antioxidants, which remove reactive oxidants, has been suggested as a way to prevent disease by increasing the body’s antioxidative capacity.

Carotenoids are a generic term for natural dyes biosynthesized in plants. Carotenoids may be broadly categorized into carotenes and xanthophylls [4]. While carotenes are highly hydrophobic, xanthophylls are highly hydrophilic and have a high affinity for the cellular membrane. Also, compared with carotenes, there are many more xanthophylls with high antioxidative capacity, and out of all the carotenoids, it is therefore considered particularly important to ingest xanthophylls actively. The human body is incapable of biosynthesizing carotenoids, the main source of which is green and yellow vegetables. Red paprika has a characteristic carotenoid composition of 90% xanthophylls and 10% carotenes, and is therefore an excellent source of xanthophylls [5]. For this reason, among the naturally-occurring antioxidants, we focused on xanthophylls derived from red paprika (paprika xanthophylls). Paprika xanthophylls contain high concentrations of seven types of xanthophylls, including capsanthin and capsorubin, which are rare components characteristic of red paprika, and β-cryptoxanthin, which is useful for the prevention of lifestylerelated diseases.

Nishino et al. [6] reported that the capsanthin and capsorubin contained in paprika xanthophylls demonstrate elimination activity against not only singlet oxygen, but also hydroxy radicals, which have strong oxidative capacity. They also showed that at 2 weeks after ingestion of carotenoids, the carotenoid concentration in the erythrocytes increases to 2.2 times the pre-ingestion level. It is therefore safe to say that continued ingestion of paprika xanthophylls increases the total carotenoid concentration of erythrocytes.

A plentiful supply of oxygen to the active muscles is needed during exercise. Oxygen that is taken into the body binds to hemoglobin in the erythrocytes and is transported to all parts of the body. The peripheral capillaries have such a fine diameter that erythrocytes need to change shape to pass through them; this function is known as erythrocyte deformability [7], and is related to the flexibility of the erythrocyte membrane. Damage to the erythrocyte membrane by reactive oxygen reduces erythrocyte deformability [8], which would likely be linked to a reduction in erythrocyte oxygen-carrying capacity. It has recently been reported that ingestion of lutein, a type of carotenoid, leads to the increased distribution of lutein to erythrocytes and a decrease in the quantity of fatty acid peroxides [9]. It is therefore likely that continuous ingestion of paprika xanthophylls with high antioxidative capacity leads to increased xanthophyll distribution to the erythrocytes, resulting in suppression of the damage caused by reactive oxygen and improvements in oxygen-carrying capacity. In the present study, the effects of ingestion of paprika xanthophylls on oxidative stress and respiratory metabolism during endurance exercise were investigated.

Methods

Participants

The participants were 21 male university student athletes (six rubber-ball baseball players, six short-distance track and field athletes, four racing cyclists, two lacrosse players, two cheerleaders, and one speed skater). All participants habitually exercised 5 or more days a week, and did not smoke. Compliance with the rules for research using human subjects, protection of personal data, and the ethical considerations of the present study were approved by the relevant ethics review committee. In accordance with the Declaration of Helsinki, all participants were provided verbal and written explanations of the ethical considerations of the study, and provided their written, informed consent to participate. In addition, this experiment was registered in the University Hospital Medical Information Network (UMIN) Clinical Trials Registry (UMIN000028271).

Study design

This randomized, double-blind, intergroup, comparative study was designed in accordance with the Consolidated Standards of Reporting Trials. The participants were assigned to either the paprika xanthophylls (PA) group (n=11) or the placebo (CON) group (n=10) such that there were no major differences between the groups in physical characteristics or previously measured peak oxygen consumption (VO2 peak). Study measurements were carried out before and at 4 and 8 weeks after ingesting the experimental product (Figure 1).

After the participants arrived at the laboratory, they were asked to rest in a seated position for 30 min. Next, they carried out 30 min of cycling at an intensity of 60% VO2 peak. After the exercise, they rested for 30 min while their recovery process was observed. Venous blood was collected prior to the exercise, and blood was collected twice from the fingertip, once before and once immediately after the exercise.

Experimental product

A commercial paprika xanthophylls preparation (“PapriX-oil”; Glico Nutrition Co., Ltd., Osaka, Japan) was used as the source of ripe paprika xanthophylls. Gelatin capsules containing PapriXoil (containing 4.5 mg of total xanthophylls, including 2.6 mg capsanthin and 0.4 mg β-cryptoxanthin per capsule) were used as the study drug. Gelatin capsules containing vegetable oil and caramel color so that they were indistinguishable from the study drug were used as placebo. All participants orally ingested one capsule every evening with a meal for 8 weeks.

Maximal oxygen consumption

Prior to the experiment, VO2 peak was measured in all participants using a cycle ergometer (Corival 1000S; Lode B.V., Groningen, The Netherlands) with a multistep, gradually-increasing load. After resting for 1 min, the participants warmed up with a load of 40 W. The exercise load was subsequently set to 60 W and then increased to 110 W, 150 W, and 190 W at 3-min intervals. The load was set to increase by 15 W at 1-min intervals from 12 min after the start of exercise, and exercise was continued until total exhaustion. The pedaling cadence was maintained at 60 rpm. Exercise was stopped at the point when the participant was either no longer able to maintain the cadence, the respiratory quotient (RQ) exceeded 1.2, or the maximum heart rate (HR) (220 - age in years) was exceeded.

Exercise load experiment

After resting for 1 min, warming up was carried out at an intensity of 40 W for 2 min using the cycle ergometer, and cycling was then carried out for 30 min at 60% of the previously measured VO2 peak.

Respiratory gas analysis

Respiratory gas analysis was carried out using a breath-by-breath respiratory gas metabolic monitoring system (AE310S, Minato Medical Science, Osaka, Japan). HR was measured using an electrocardiograph (BSM-240 Bedside Monitor; Nihon Kohden Corporation, Tokyo, Japan). VO2 and HR were evaluated by mean values of measurements taken at 1-min intervals.

Blood carotenoid analysis

Blood was collected to measure the carotenoid levels in the plasma and erythrocytes before and at 4 and 8 weeks after ingestion of the experimental product. Blood (10 mL) was collected in a heparin vacuum tube and left at room temperature for 30 min. It was then centrifuged (1000 × g) for 10 min at room temperature to separate the plasma and erythrocytes. The erythrocytes were washed four times in phosphate buffer solution (pH 7.2) to remove the leucocytes. Plasma and erythrocyte samples were stored at -80°C until analysis. Analysis of the carotenoid content of plasma and erythrocytes was carried out at the Research Institute for Production Development according to a previously reported method [4]. Total carotenoids was calculated from the sum of -carotene, β-carotene, lycopene, β-cryptoxanthin, 3-OHb, e-caro-3’-one, cryptocapsin, cucurbitaxanthin A, capsanthone, lutein, zeaxanthin, and capsanthin; total xanthophylls was calculated from the sum of β-cryptoxanthin, 3-OH-b, e-caro- 3’-one, cryptocapsin, cucurbitaxanthin A, capsanthone, lutein, zeaxanthin, and capsanthin.

Statistical analysis

Each item for measurement is shown as the mean ± standard deviation. Statistical processing was performed using IBM SPSS Statistics ver. 22. An unpaired t-test was used for physical characteristics. Plasma total carotenoids and total xanthophylls; Erythrocytes total carotenoids and total xanthophylls; Oxigen uptake (VO2); Heart rate (HR) were analyzed using a 2-way analysis of variance of the group (PA group and CON group) × time (blood components: Pre, 4 weeks and 8 weeks; expiratory gas: 5, 10, 15, 20, 25, 30 during exercise). Multiple comparisons were tested using the Bonferroni method. The level of statistical significance was set at p<0.05.

Results

Physical characteristics

The participants’ physical characteristics are shown in Table 1. No significant differences in age, height, body weight, body fat ratio, lean body mass, or VO2 peak were found between the two groups.

Figure 1: Effect of supplementation on VO2 and HR during endurance exercise. CON group and PA group . Values are expressed as mean ± standard deviation. *p<0.05, **p<0.01, ***p<0.001 compared with CON group.

Table 1 Physical characteristics of the participants.

Values are expressed as mean ± standard deviation. There is no significant difference.

Chronological changes of total carotenoids and total xanthophylls in erythrocytes and plasma

As shown in Table 2, significantly higher levels of erythrocyte total carotenoids were observed in the PA compared with the CON group at both 4 and 8 weeks after ingestion (4 weeks; p<0.01, 8 weeks; p<0.001). Similarly, significantly higher levels of erythrocyte total xanthophylls were observed in the PA compared with the CON group at both 4 and 8 weeks after ingestion (4 weeks; p<0.01, 8 weeks; p<0.001).

Table 2 Changes in total carotenoids and xanthophylls on erythrocyte and plasma in between groups.

Values are expressed as mean ± standard deviation. , **p<0.01, ***p<0.001 compared with CON group.

Chronological changes in oxygen consumption and heart rate during endurance exercise

Mean VO2 and HR values during exercise were calculated at 5-min intervals. At 4 weeks after ingestion, HR was significantly lower in the PA than in the CON group at 20 min, 25 min, and 30 min of exercise (p<0.05). In addition, at 8 weeks after ingestion, HR was significantly lower in the PA than in the CON group at 10 min, 15 min, 20 min, 25 min, and 30 min of exercise (p<0.01 and p<0.001).

Discussion

In the present study the effects of 8 weeks of continuous ingestion of paprika xanthophylls on oxidative stress, antioxidative capacity, and respiratory metabolism after 30 min of cycling exercise were investigated. As a results, the levels of total carotenoids and total xanthophylls in the erythrocytes showed significantly higher values in the PA than the in CON group at 4 and 8 weeks after ingestion (4 weeks; p<0.01, 8 weeks; p<0.001). At the same time, capsorubin, which is present in paprika xanthophylls, is reported to have potent antioxidative action against fatty acid peroxides [10]. And the xanthophylls characteristic of paprika xanthophylls are absorbed in particular into erythrocytes [6]. In the present study, the concentrations of carotenoids and xanthophylls in the erythrocytes were significantly higher, and erythrocyte deformability appeared to be improved in the PA group at both 4 and 8 weeks after ingestion.

It has been reported that when -tocopherol and eicosapentaenoi acid (EPA), which has antioxidative properties, is administered orally, there is an increase in the blood level of -tocopherol during and after administration and improvement in erythrocyte deformability [11,12]. In the present study, the absorption of xanthophylls into erythrocytes as a result of paprika xanthophylls ingestion was confirmed. Furthermore, EPA intake significantly decreased heart rate during bicycle exercise as compared with pre-intake heart rate [13]. Moreover, the changes in flowmediated dilation (FMD) before and after EPA intake was significantly greater compared with the placebo group [14], demonstrating that the blood vessel function in transporting oxygen improved because the blood vessels could be dilated more easily. Based on the above reports, antioxidant supplement intake improves erythrocyte deformability, thereby decreasing heart rate during exercise and enhancing the function of blood vessels that transport oxygen. In the present study, heart rate during bicycle exercise was significantly lower in the PA than in the CON group during 16-30 min of exercise at 4 weeks after intake and during 6-30 min of exercise at 8 weeks after intake. These results suggest that the intake of paprika xanthophyll, which exhibits antioxidative effects, improves erythrocyte deformability and decreases heart rate, thereby ameliorating exercise efficiency.

VO2max, which is commonly used as an index of endurance, is determined through both extrinsic and intrinsic factors. Intrinsic factors include lung ventilatory, lung diffusion, circulatory, tissue diffusion, and muscle oxygen consumption capacities, and are mainly related to oxygen transport and consumption in the body [15]. To transport as many oxygen molecules as possible to active muscles during maximum work, a large volume of blood needs to be pumped out from the heart. Athletes who perform endurance training on a daily basis have markedly greater stroke, heart, and end-diastolic volumes [16]; thus, they display high oxygen transport capacity and are known to have a higher VO2max than the general population [17]. Moreover, it has been demonstrated that a higher VO2max results in a lower resting heart rate [18]. Furthermore, blood volume, erythrocyte count, and Hb levels increase by infusing blood, leading to improved oxygen transport capacity and an increase in VO2max [19,20]. Based on these findings, increasing oxygen transport capacity by increasing stroke volume and decreasing heart rate can promote endurance performance. Even though the bicycle exercise in the present study was performed under the same protocol before intake, and at 4 and 8 weeks after intake, heart rate decreased in the PA group (4 weeks; p<0.05, 8 weeks; p<0.01, p<0.001). Therefore, paprika xanthophyll intake appears to improve erythrocyte deformability and oxygen transport capacity, thereby facilitating exercise with a low heart rate, even under the same exercise stress. These findings indicate that such intake may enhance endurance performance.

The present study has some limitations. This study is no significant differences in the levels of total carotenoids or total xanthophylls in the plasma were found between the two groups at any time point. The levels of total carotenoids and xanthophylls in the plasma are likely affected by the previous day’s meals; however, this was not controlled for in the present experiment, so this remains a topic for future investigation.

Conclusion

In conclusion, the results of the present study show that the oxygen-carrying capacity of erythrocytes increased as a result of the absorption of carotenoids, particularly xanthophylls, into the erythrocytes. This suggests that the increase in the oxygencarrying capacity of erythrocytes caused a reduction in the HR during endurance exercise, so that energy efficiency increased. From the foregoing, it is likely that the continuous ingestion of paprika xanthophylls can improve endurance.

Disclosure of Interest

The joint author, Takashi Ichihara is an employee of Ezaki Glico Co., Ltd. However, neither Ezaki Glico Co., Ltd. nor Glico Nutrition Co., Ltd. participated in the interpretation of the results or the conclusions of the study.

Acknowledgments

We also thank Dr. Takashi Maoka of the Research Institute for production Development for analyzing the blood carotenoids in this study.

Funding/support

No financial or material support of any kind was received for the work described in this article.

References

1. Kuroda J, Ago T, Matsushima S, Zhai P, Schneider MD, et al. (2010) NADPH oxidase 4 (Nox4) is a major source of oxidative stress in the failimg heart. Proc Natl Acad Sci USA 107: 15565-15570.
2. Forsey RJ, Thompson JM, Emerudh J, Hurst TL, Strindhall J, et al. (2003) Plasma cytokine profiles in elderly humans. Mech Apeing Dev 124: 487-493.
3. Pingitore A, Lima GP, Mastorci F, Quinones A, Iervasi G, et al. (2015) Exercise and oxidative stress: potential effects of antioxidant dietary strategies in sports. Nutrition 31: 916-922.
4. Maoka T (2009) Structure of carotenoid and distribution in living world. In: Carotenoid science and its application for current practical use 1: 3-14.
5. Aizawa K, Inakuma T (2007) Quantitation of carotenoids in commonly consumed vegetables in Japan. Food Sci Technol Res 13: 247-252.
6. Nishino A, Ichihara T, Takaha T, Kuriki T, Nihei H, et al. (2015) Accumulation of paprika carotenoids in human plasma and erythrocytes. J Oleo Sci 64: 1135-1142.
7. Braasch D (1971) Red cell deformability and capillary blood flow. Physiological Reviews 51: 679-701.
8. Cazzola R, Russo-Volpe S, Cervato G, Cestaro B (2003) Biochemical assessments of oxidative stress, erythrocyte membrane fluidity and antioxidant status in professional soccer players and sedentary controls. Eur J Clin Invest 33: 924-930.
9. Nakagawa K, Kiko T, Hatade K, Sookwong P, Arai H, et al. (2009) Antioxidant effect of lutein towards phospholipid hydroperoxidation in human erythrocytes. Br J Nutr 102: 1280-1284.
10. Maoka T, Goto Y, Isobe K, Fujiwara Y, Hashimoto K, et al. (2001) Antioxidative activity of capsorubin and related compounds from paprika (Capsicum annuum). J Oleo Sci 50: 663-665.
11. Ernst E, Matrai A. (1985) Influence of alpha-tocopherol (vitamin E) on the flow properties of the blood. Therapy week 35: 5701-5702.
12. Terano T, Hirai A, Hamazaki T, et al. (1983) Effect of oral administration of highly Purified eicosapentaenoic acid on platelet function, blood viscosity and red blood cell deformability in healthy human subjects. Atherosclerosis 46: 321-331.
13. Peoples GE, McLennan PL, Howa PR (2008) Fish oil heart rate and oxygen consumption during exercise. J Cardiovasc Pharmacol 52: 540-547.
14. Żebrowska A, Mizia-Stec K, Mizia M (2015) Omega-3 fatty acids supplementation improves endothelial function and maximal oxygen uptake in endurance-trained athletes. Eur J Sport Sci 15: 305-314.
15. Holmgren A (1967) Cardiorespiratory determinants of cardiovascular fitness. Can Med Ass J 96: 697-705.
16. Keul J, Dickhuth H-H, Lehmann M (1982) The athlete’s heart-haemodynamic and structure. Int J Sports Med 3: 33-43.
17. Robinson S, Edwards HT, Dill DB (1937) New Records In Human Power. Science 85: 409-410.
18. Kenney WL (1985) Parasympathetic control of resting heart rate: relationship to aerobic power. Med Sci Sports Exerc 17: 451-455.
19. Robertson RJ, Gilcher R, Metz KF (1982) Effect of induced erythrocythemia on hypoxia tolerance during physical exercise. J Appl Physiol Respir Environ Exerc Physiol 52: 490-495.
20. Spriet LL, Gledhill N, Froese AB (1986) Effect of graded erythrocythemia on cardiovascular and metabolic responses to exercise. J Appl Physiol 61: 1942-1948.