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DO THE NONCAFFEINE INGREDIENTS OF ENERGY

DRINKS AFFECT METABOLIC RESPONSES TO HEAVY


EXERCISE?
ROBERT W. PETTITT, JOLYNNE D. NIEMEYER, PATRICK J. SEXTON, AMANDA LIPETZKY, AND
STEVEN R. MURRAY
Department of Human Performance, Minnesota State University, Mankato, Minnesota

ABSTRACT INTRODUCTION

D
Pettitt, RW, Niemeyer, JD, Sexton, PJ, Lipetzky, A, and espite the lack of scientific evidence for the
Murray, SR. Do the noncaffeine ingredients of energy drinks performance-enhancing effects of energy drinks
affect metabolic responses to heavy exercise? J Strength Cond (EDs), their popularity is impressive, with Red
Res 27(7): 19941999, 2013Energy drinks (EDs) such as Bull (RB) reporting sales exceeding 500 million
Red Bull (RB) are marketed to enhance metabolism. Secondary
cases in a single year (16). Energy drinks are marketed to
boost energy or metabolism, and such marketing is persuasive
ingredients of EDs (e.g., taurine) have been purported to
among competitive athletes (16). For instance, one group (10)
improve time trial performance; however, little research exists
reported that 72.9% of the 203 athletes surveyed consumed
on how such secondary ingredients affect aerobic metabolism
EDs with the primary reason being to enhance energy dur-
during heavy exercise. The purpose of this study was to inves- ing practice. Thus, sales and survey findings indicate that
tigate the effect of the secondary ingredients of RB on aerobic EDs are used for a performance-enhancing benefit.
metabolism during and subsequent to heavy exercise. In double- The claims for the ergogenic effects of the secondary
blind, counterbalanced, and crossover fashion, 8 recreationally (i.e., noncaffeine) ingredients of EDs, such as taurine and
trained individuals completed a graded exercise test to deter- B vitamins, by manufacturers are ambiguous. For instance,
mine the gas exchange threshold (GET). Subjects returned on 2 Red Bull markets that its secondary ingredients boost energy
separate occasions and ingested either a 245 ml serving of RB (16). Such a claim would imply RB ingestion would positively
or a control (CTRL) drink with the equivalent caffeine before affect aerobic metabolism. To date, the literature on these
engaging in two 10-minute constant-load cycling bouts, at an secondary ingredients and exercising metabolism is limited.
intensity equivalent to GET, with 3 minutes of rest between The isolated effects of taurine can reportedly enhance vascular
reactivity (20) along with muscular contractility (1,13,26),
bouts. Accumulated liters of O2 (10 minutes) were higher for
whereas B vitamins may support aerobic metabolism directly
the first bout (17.1 6 3.5 L) vs. the second bout (16.7 6 3.5 L)
(25). Furthermore, when these secondary ingredients are stud-
but did not differ between drinks. Similarly, excess postexercise
ied in combination, investigators have reported enhanced
oxygen consumption was higher after the initial bout (RB mean,
cycling time trial performances (12,17); however, noncaffei-
2.6 6 0.85 L; CTRL mean, 2.9 6 0.90 L) vs. the second bout nated RB has been reported not to enhance exhaustive
(RB mean, 1.5 6 0.85 L; CTRL mean, 1.9 6 0.87 L) but did not performance (7). There is simply a paucity of research dem-
differ between drinks. No differences occurred between drinks onstrating any positive metabolic effects of the secondary in-
for measures of heart rate or rating of perceived exertion. These gredients during submaximal exercise.
results indicate that the secondary ingredients contained in a sin- Energy drinks also are marketed to enhance recovery (16);
gle serving of RB do not augment aerobic metabolism during or yet, there is little research on if (or how) EDs may influence
subsequent to heavy exercise. short-term postexercise metabolism. Caffeine, the primary
active ingredient of EDs, may enhance utilization of free
KEY WORDS EPOC, gas exchange threshold, oxygen uptake, fatty acids at lower levels of metabolic demand (22), thereby,
taurine augmenting the rate of return to resting postexercise homeo-
stasis. Such an effect from the secondary ingredients is
unknown. Therefore, the purpose of this study was to exam-
Address correspondence to Robert W. Pettitt, robert.pettitt@mnsu.edu. ine if the noncaffeinated ingredients of RB affected heavy
27(7)/19941999 exercise and postexercise metabolism using intensities
Journal of Strength and Conditioning Research corresponding heavy exercise (i.e., at or exceeding the gas
2013 National Strength and Conditioning Association exchange threshold [GET]) (6).
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METHODS derive excess postexercise oxygen consumption (EPOC).


Experimental Approach to the Problem
V CO2 and V O2 data were divided to calculate the respiratory
A double-blind, counterbalanced, placebo-controlled, exchange ratio (RER). Ratings of perceived exercise (RPEs),
2-period within-subject, crossover experimental design was on a 620 scale (4), were obtained at the conclusion of each
used. A convenience sample of apparently healthy adults constant-load exercise bout.
(N = 8) completed a graded exercise test (GXT) to deter-
mine GET and maximum oxygen uptake (V O2max). On 2 Dietary Intake Screenings. Dietary intake can influence expired
additional visits, subjects completed 2 consecutive constant- gas analysis measurements. Because controlling for dietary
load cycling bouts at GET for 10 minutes, with 3-minute factors increases the accuracy of indirect calorimetric meas-
recovery in between bouts. Heart rate and expired gas urements, the subjects were interviewed about their use of
exchange were evaluated during exercise and 3 minutes sub- EDs and other supplements and drugs, along with a log of
sequent to each bout. We selected a heavy exercise intensity their food intake for 24 hours preceding each exercise bout.
because pervious studies have used longer-duration trials Food intake was input into a commercial dietary software
(12,17). Subjects consumed either blinded RB or a control program (Diet Analysis Plus, version 7.0; Wadsworth, Inc.,
(CTRL) drink while on another day consumed the opposite. New York, NY, USA) to help verify that the macronutrient
The CTRL drink contained identical calories and caffeine to intake was not different between the RB and CTRL trials.
RB; that is, we aimed to investigate any effects of the sec- The subjects were instructed to eat how they normally
ondary ingredients, beyond those of caffeine, on metabolism would for each day of the experiment to reduce disparities of
during and subsequent to heavy exercise. liver and muscle glycogen concentrations (19). The subjects
also self-reported their compliance with prior instructions to
Subjects
refrain from consuming food and beverages containing alco-
A convenience sample of 5 men and 3 women (age = 23 6 2
hol, caffeine, supplements, prescription, and nonprescription
years; body mass = 73.6 6 9.9 kg; height = 177.3 6 6.4 cm)
drugs for 48 hours before exercise. In particular, the half-life
volunteered for this study. The studys procedures were preap-
of caffeine is approximately 46 hours (14); therefore, our
proved by the host institution review board on human subjects,
48-hour washout period was adequate. Finally, the subjects
and informed consent was obtained. Men and women were
were asked to refrain from exercising 24 hours before each
included for generalizability of results and not for statistical anal-
data collection day.
ysis of sex differences. All subjects engaged in at least 150 minutes
of aerobic exercise per week. Exclusion criteria included any
Handling and Administration of the Experimental Drinks. The
reported history of serious medical illnesses or orthopedic
volume for both drinks was 245 ml (8.3 oz), the standard
injuries. Each subject indicated that he or she was not a regular
single serving size for RB. The control drink (ginger ale) was
user of EDs. Specifically, each subject noted that he or she pre-
modified with the addition of dry ingredients to equal 3.1 g of
viously had tried EDs, but none drank them on a regular basis.
sugar and 76 mg of caffeine (A&C Chemicals LTD, Montreal,
Procedures Quebec, Australia). Key secondary ingredients of RB include
Equipment and Metabolic Measurements. As indicated, a GXT taurine (1,000 mg), glucuronolactone (625 mg), and a volume
was determined preliminarily for each subject via cycle
ergometry. An electronically braked friction ergometer (Lode
Excalibur Sport Cycle Ergometer, Groningen, the Netherlands)
was fitted to each subjects stature and riding comfort. A cali-
brated metabolic analyzer (MedGraphics, Minneapolis, MN,
USA) and heart rate monitor (Polar Instruments, Inc., Oulu,
Finland) were used to gather dependent variables for this study.
A custom GXT was performed to determine GET and the
power-evoking GET (WGET) (21). In brief, gradation was
estimated to yield a 10-minute GXT from a series of regres-
sion equations, and the test was terminated when cadence
decreased below preferred cadence for more than 5 seconds
(3 subjects selected 60 rpm and 5 subjects selected 70 rpm).
Gas exchange threshold was determined using the V-slope
method (3), and power was interpolated with the presump-
tion of a 1-minute delay in gas exchange.
For each constant-load exercise bout, expired air, volumes,
and fractional concentrations of O2 and CO2 were sampled, Figure 1. Oxygen uptake during and after exercise for the Red Bull and
breath-by-breath, and averaged to 15 seconds. Integrated control drink trials (mean 6 SD).
values (sum of 15 seconds averaged values) were used to

VOLUME 27 | NUMBER 7 | JULY 2013 | 1995

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Noncaffeine Ingredients and Exercise Metabolism

the independent variable of the


drink (2 levels: RB vs. CTRL)
TABLE 1. Dietary intake for the Red Bull (RB) and control drink trials, mean 6 SD.
and the independent variable
Variable RB Control t p of time. A 2 3 2 model was
used to test accumulated V O2
Daily expenditure (kcal) 1,957 6 425 1,862 6 600 0.38 0.72
for bout 1 and bout 2 and
Fat (g) 70 6 31 64 6 27 0.54 0.61
Carbohydrate (g) 232 6 73 246 6 81 0.43 0.68 the EPOC values subsequent
Protein (g) 109 6 38 82 6 36 1.48 0.18 to these bouts, respectively.
A 2 3 4 model was used to
evaluate heart rate at 2 time
points during exercise (5 and
10 minutes). A similar 2 3 6
of B vitamins exceeding the minimum recommended daily model was used for RER values (see Results for justification
intake. Volume for the CTRL drink was measured with of time period). Paired t-tests were used to compare 24-hour
a graduated cylinder, and the dry ingredients were mea- recall values of the RB with the CTRL trials for total kilo-
sured with a digital scale (TE212; Sartorius, Goettingen, calories, fat, carbohydrate, and protein intake, respectively.
Germany). We did not officially conduct taste testing under The Mann-Whitney U-test was used to compare between-
controlled study; however, the additional ingredients to the trial RPEs for each bout. Level of significance for rejecting
ginger ale altered the taste profile to where it tasted the null hypothesis was set at p , .05. Data are expressed in
remarkably similar to RB, as we noted during pilot testing. mean 6 SD.
The trials were double blinded such that neither the sub-
jects nor the investigators associated directly with data col- RESULTS
lection were aware of the drink consumed. Both drinks A V O2 slow component with a delayed steady state was
were served in a black covered plastic coffee mug. Half of observed for the RB and CTRL trials (Figure 1). These data
the subjects received RB first and the CTRL drink second, indicate that the subjects achieved the desired heavy exercise
whereas the order was reversed for the other half of the domain (i.e., intensities exceeded the GET) (18). Dietary
subjects. Both drinks were consumed 35 minutes before recall records indicated no differences (p . 0.05) existed in
a 5-minute cycle ergometer warm-up at an intensity of the total energy intake and proportion of macronutrients
50% WGET. The time frame for ingestion of the drinks (Table 1); thus, diet was unlikely a confounding factor for
was determined as optimum for maximizing bioavailability the following results.
of caffeine (14), an ingredient purported to enhance the Summary statistics for accumulated exercising oxygen
effect of secondary ingredients in EDs (12,17) (N.B., we uptake and EPOC appear in Table 2. Accumulated oxygen
were unaware of any data on the bioavailability of second- uptake was higher for the first bout (17.1 6 3.5 L) compared
ary ingredients at the time of this study). No additional with the second bout (16.7 6 3.5 L) (F = 5.91, p , 0.05);
drinks were permitted during the exercise trials. however, no differences were observed between the RB and
CTRL trials (F = 0.00, p . 0.05). Similarly, EPOC was higher
Statistical Analyses after the initial bout (RB mean, 2.6 6 0.85 L; CTRL mean,
Separate 2-way analyses of variance (ANOVAs) with 2.9 6 0.90 L) compared with the second bout (RB mean, 1.5 6
repeated measures were used to test for differences between 0.85 L; CTRL mean, 1.9 6 0.87 L) (F = 5.98, p = 0.04);
however, no differences were
observed between the RB and
CTRL trials (F = 0.57, p . 0.05).
TABLE 2. Stability of exercising and postexercising oxygen uptake
Accumulated oxygen meas-
measurements.*
urements between the first and
Bout 1 (L) Bout 2 (L) second bouts were remarkably
Variable Mean 6 SD Mean 6 SD ICC (a) SEM (L) CV (%) consistent for the RB and
CTRL trials, respectively
Exercising V O2 (L)
CTRL 17.0 6 3.8 16.8 6 4.0 0.99 0.35 2.5 (Table 2). Conversely, EPOC
RB 17.1 6 3.5 16.7 6 3.2 0.97 0.53 2.7 was more variable in compari-
EPOC son with exercising V O2. Inges-
CTRL 2.95 6 0.90 1.90 6 0.87 0.77 0.43 22.4 tion of RB did not seem to alter
RB 2.65 6 0.85 1.46 6 0.85 0.85 0.33 25.0 the individual EPOC responses.
*ICC = intraclass correlation coefficient; CV = coefficient variance; RB = Red Bull. For both trials, RER
decreased abruptly at the onset
of exercise reaching steady
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Figure 4. Rating of perceived exertion (RPE) after the initial (filled bars)
and the second (open bars) cycling bouts in the Red Bull and control
drink trials.

Figure 2. Respiratory exchange ratio (RER) during and after exercise for time (F = 0.73, p = 0.58) were observed for heart rate. Sim-
the Red Bull and control drink trials. *Significant between-trial main effect ilarly, no differences in RPE occurred between the first bouts
(p , 0.05).
(z = 1.12, p = 0.26) or the second bouts (z = 1.57, p = 0.12)
(Figure 4).

state at approximately 3 minutes of exercise (Figure 2). Peak DISCUSSION


values of RER occurred at 2 minutes postexercise for each Investigators using animal models have reported that
bout; therefore, time points at 5 and 10 minutes during exer- taurine, a main secondary ingredient in EDs, can augment
cise and 2 minutes postexercise were selected for the the sustainability of force during repetitive skeletal muscle
ANOVA (2 3 6 model). On average (i.e., main effect), contractions (1,13,26). Research on humans, engaged in rig-
RER was higher (F = 7.97, p = 0.03) during the RB trial in orous exercise, has supported such claims, with 2 indepen-
comparison with the CTRL trial. dent laboratories observing improved time trial cycling
Heart rate, relative to exercise time, increased linearly for performances after subjects ingesting taurine-containing
both constant-load exercise trials (Figure 3). Neither main EDs (12,17). Athletes, however, also consume EDs for
effects (F = 0.00, p = 0.95) between trials nor main effects for energy during practice (10); yet, little research is available
to support the efficacy of EDs to augment metabolism dur-
ing heavy exercise. The primary finding of this study was
that a single serving of the secondary ingredients found in
RB, one of the more popular EDs (16), does not augment
aerobic metabolism during, or subsequent to, heavy exercise.
As indicated, subjects in this study cycled at an intensity
that was sufficient to evoke a V O2 slow component. The V O2
slow component is a phenomenon attributed largely to the
recruitment of inefficient type II muscle fibers (11). An atten-
uation of the V O2 slow component denotes enhanced mito-
chondrial efficiency typically brought about by training
adaptations (8,9,18). The marketed benefit of secondary
ingredients in EDs is to boost metabolism; however, such
a claim lacks scientific support. Our results indicate that
ingestion of the secondary ingredients, found in a single serv-
ing of RB, evoked no discernible benefit on aerobic metab-
olism during heavy exercise.
With lower energy demands, caffeine has been suggested
to enhance free fatty acid utilization (22), although other
Figure 3. Heart rate response during the Red Bull and control drink authors (15) have more recently disputed such claims. The
trials. secondary ingredients of EDs, augmented by caffeine, have
been marketed to enhance recovery. Our findings indicate

VOLUME 27 | NUMBER 7 | JULY 2013 | 1997

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Noncaffeine Ingredients and Exercise Metabolism

that the secondary ingredients for a single serving of RB do an ergogenic effect, although the precise mechanisms for
not augment EPOC subsequent to heavy exercise. The why remain unclear (12,17).
kinetics of the initial bout produced the expected increase In conclusion, athletes consume EDs not only before
on accumulated O2 and decrease in EPOC for the second major events but also for boosting energy during practice.
bouts (5,23). The ingestion of the secondary ingredients in The present study revealed that the secondary ingredients
RB did not seem to influence O2 kinetic differences between found in a single serving of RB had no augmenting affects on
the 2 bouts (Figure 1). aerobic metabolism during or subsequent to exercise inten-
A tendency for greater nonmetabolic CO2 production sities analogous to day-to-day practice (i.e., heavy exercise).
during and subsequent to exercise, as evidenced by higher Future research should examine different doses of the
RER values (Figure 2), was observed for the RB trial. Such secondary ingredients in EDs while controlling for differ-
a change occurred independent of changes in V O2 or heart ences in carbonation as a confounding variable possibly
rate (Figure 4). Greater hydrogen ion production and buff- influencing expired VCO2 values.
ering could have occurred presumably during the RB exer-
cise trial, exhibiting a deleterious effect on metabolism. Such ACKNOWLEDGMENT
differences, although statistically different, were negligible in Support was provided by the College of Graduate Studies
effect size. An equally plausible explanation for the RER and Research at Minnesota State University, Mankato.
findings may be that carbonation differed between the
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