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Department of Health and Human Performance (J.D.A., J.M.) Louisiana State University, Baton Rouge, Louisiana
Western Carolina University and Department of Kinesiology (J.D.A., A.G.N., M.W.) Louisiana State University, Baton Rouge, Louisiana
Address reprint requests to: Jason D. Allen, Department of Kinesiology, H. P. Long Field House, Louisiana State University, Baton Rouge, LA 70803-7101
| ABSTRACT |
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Methods: Twenty men and eight women (age=23.2±3.2 years, height=175.8±8.6 cm; weight=75.2±15.3 kg) were randomly assigned to either a Panax ginseng or placebo group for a period of 3 weeks in a double blind design. Prior to and following treatment the subjects performed a symptom limited graded exercise test on a Schwinn Airdyne ergometer. The data were analyzed using an analysis of variance.
Results: No significant treatment effect was observed for the dependent variables of VO2, exercise time, workload, plasma lactate and hematocrit at peak levels, or for heart rate and rate of perceived exertion at 150 watts, 200 watts and peak.
Conclusions: The results of this study do not support an ergogenic effect on peak aerobic exercise performance following a 3-week supplementation period of 200 mg 7% Panax ginseng in healthy young adults with moderate exercise capacities and unrestricted diets.
Key words: ginseng, VO2max, aerobic, performance, supplement, ergogenic aid
| INTRODUCTION |
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Panax (Chinese or Korean) ginseng is often proposed to increase maximal exercise capacity (VO2peak) and enhance performance [57]. In contrast, other research has failed to find an ergogenic effect following ginseng supplementation [1011]. The absence of compelling research demonstrating the ability of ginseng to consistently enhance physical performance in humans may be due to the variability in the quality of the supplement [1] and/or different methods of study. Interestingly, there is a lack of information regarding the effects of ginseng supplementation on young healthy adults. Such research is necessary given that much of the ginseng advertising campaign is directed at this demographic group. In fact, approximately 40% of the 5 to 6 million Americans who are currently taking this supplement would be considered healthy young adults.
Therefore, the purpose of this study was to determine the short term effects (21 days) of 200 mg (7% standardized) Panax ginseng supplementation vs. placebo on peak aerobic exercise performance in healthy young adults. The specific aims were to determine the short term effects of ginseng on VO2peak, total exercise time (T), and work load (Wk), heart rate (HR), ratings of perceived exertion (RPE), plasma lactate, and hematocrit during a symptom limited graded exercise test (SL-GXT).
| MATERIALS AND METHODS |
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Participants were instructed in the use of the Borg [15] rate of perceived exertion (RPE) scale, and to indicate when they were approximately 1 minute from exhaustion, prior to performing a symptom-limited graded exercise test (SL-GXT) using a Schwinn Air-Dyne Ergometric Exerciser. The protocol was continuous with increments of 50 Watts (W) every 2 minutes until voluntary exhaustion. During the final minute of each stage and upon test termination HR and RPEs were obtained. During the final minute a nose clip was placed on the participants and, using a two-way valve, a 30-second sample of expired air was collected into a 100 liter (L) collection bag. Ventilations were measured using an American Meter Company gas meter. Gas fractions were determined using an Ametek Infra-red carbon dioxide (CO2) gas analyzer followed by an Ametek oxygen (O2) analyzer. All instruments were calibrated prior to testing, and all gas sample data corrected to standard temperature, pressure, dry values (STPD). Upon termination of the test the subjects were allowed an active cool down.
In addition to ventilatory and gas measures, blood samples were obtained 3 minutes after termination of the test. The procedure for this was to clean the finger and test surface with a Spongette Alcohol Wipe. The participants finger was then pierced (perpendicular to the finger print lines) using a Microtainer sterilized disposable blood lancet and the blood collected in three disposable 30T1 capillary tubes. The capillary tubes were then placed in an IEC/MB Micro Hematocrit centrifuge for 4 minutes to separate the cells from the plasma. Hematocrit levels were read from one of the capillary tubes using a Damon/IEC Division Micro-Capillary Reader. The plasma from the individuals capillary tubes was pipetted into individualized, labeled test tubes and stored on ice. Lactate reagents and standards were prepared in accordance with the manual procedures outlined in Sigma Diagnostics Lactate Procedure number 735 [16] and control solutions prepared in accordance with Sigma Diagnostics Metabolite Control catalog numbers S3005 and S3006 instructions. A Bausch and Lomb Spectronic 20 spectrophotometer set at 540 nanometers was used for the quantitative, enzymatic determination of the lactate in the plasma. The resultant data was converted to millimoles/liter (mmol/l).
Ginseng Supplementation.
The ginseng used in this study was a commercially manufactured standardized 200 mg dosage of 7% Panax ginseng. The placebo was manufactured to be identical in appearance and content, minus the ginseng. Participants were instructed to take one tablet each morning 30 minutes prior to eating breakfast, and not to modify their regular dietary practices for the duration of the testing period.
Retesting (Visit Two).
Following 21 days of Panax ginseng or placebo supplementation the participants were retested using procedures identical to the baseline tests.
Analysis of Data
Means and standard deviations were determined for the demographic and anthropometric data (age, height, weight). To determine within and between group differences and a repeated measures analysis of variance (ANOVA) was performed on the variables of VO2peak, T, WKpeak, HR and RPE at 150 W, 200 W and peak, and plasma lactate and hematocrit at peak to determine differences among and within the two treatment groups. Additionally an analysis of covariance (ANCOVA) was performed on the variables of VO2peak and HRpeak, using the pretreatment score as the covariate. The alpha level was set at 0.05 for all statistical analyses.
| RESULTS |
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Significant between group differences for VO2peak and HRpeak were noted prior to, and after supplementation. Despite this a within group ANOVA did not reveal a significant treatment or interaction effect for any of the variables observed. Similarly, the covariate analyses found a nonsignificant treatment effect, as illustrated in Figs. 13. Fig. 1 illustrates that increases in VO2peak found post supplementation were similar for both treatment groups. Although the ginseng group were able to perform slightly longer post supplementation, as seen in Fig. 2, this was not significant. Fig. 3 shows the HR responses of the two groups pre and post treatment.
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| DISCUSSION |
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In contrast, several studies have reported positive results following ginseng supplementation (Table 2). Von Ardenne and Klemm [6], observed improvements in the relative arterial pO2 levels of the blood within 2 hours of ingesting ginseng, which reached significance at 3 weeks. High dosages of ginseng have often been used to investigate its effects. McNaughton et al [5], gave 1000 mg per day dosage for 6 weeks with 30 subjects in a randomized triple crossover design using placebo, Russian, or Chinese ginseng groups. They found an increase in VO2peak and in HR recovery time with only the Chinese ginseng. Their findings are difficult to place into context within the literature due to a failure to report any actual data or to employ a control group.
Although the 200 mg dosage and 7% strength of the supplementation used in the current study, is lower than in some other studies, it is still considerably higher than most commercially available dosages (100200 mg/4% per day). Additionally, although ginseng is thought to be relatively safe, long-term use or high dosages have been reported to cause adverse reactions including, sleeplessness, euphoria, agitation, insomnia, nervousness, hypertension, diarrhea, edema and mastalgia [4]. Studies most relative to the dosage and administration period of this research have reported no ill effects for the treatment condition [5,6,7].
The current data extends previous findings [7,10,11] which refute a significant ergogenic effect in subjects with high exercise capacities. Pieralisi, Ripari, and Vecchiet [7], suggested the metabolic and physiological responses of ginseng ingestion resemble those occurring due to aerobic endurance training and may partly explain the generally poorer response results found in aerobically trained individuals. Pieralisi [7] gave Geriatric Pharmacon G115 capsules to 50 healthy male sports teachers 21 to 47 years old in a double blind, randomized, crossover study. They found significant decreases in HR, VO2, VE, and plasma lactate levels with ginseng supplementation vs. placebo at stage four of the Bruce [17], treadmill protocol (4.2 mph/16% gradient, approximate VO2 of 47 ml/kg/minute). Interpretation of the data is difficult because values for VO2 reported for maximal workload are different to those reported for maximal O2 consumption by up to 22%. The reasons for these discrepancies are unclear in the text. Despite this, if the O2 consumption at each subjects maximal workload is considered, there was a difference between subjects with pretreatment VO2peak levels below 60 ml/kg/minute and those above this level. No significant difference was found in the higher performance group. In the post-exercise period significantly lower values were measured for VO2, VCO2, VE, plasma lactate, and HR in the subjects receiving the ginseng preparation. The conclusions of the research by Pieralisi [7] are not supported by this paper because the untrained, healthy, young adults in this study showed no significant response to ginseng treatment (only one subject in this group had a VO2peak greater than 60 ml/kg/minute).
| CONCLUSIONS |
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Until standardization of the products and research on large numbers of subjects is incorporated, the mechanisms of effect, if any, for ginseng cannot be explained. Future research must concentrate on testing varying standardized levels of ginsenosides with subjects of different age groups, and fitness levels.
| ACKNOWLEDGMENTS |
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Received December 1, 1997. Accepted April 1, 1998.
| REFERENCES |
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