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Acute Caffeine and Coconut Oil Intake, Isolated or Combined, Does Not Improve Running Times of Recreational Runners: A Randomized, Placebo-Controlled and Crossover Study

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The aim was to evaluate the effect of caffeine (CAF) and extra virgin coconut oil (CO), isolated or combined, on running performance in runners. Methods: A randomized, placebo-controlled, and crossover study was conducted with thirteen recreational runners aged 18–40. All volunteers performed a 1600 m time trial at a 400 m track, each ingesting four different substances: (1) placebo (water), (2) decaffeinated coffee plus isolated CAF (DECAF + CAF), (3) decaffeinated coffee plus isolated CAF plus soy oil (DECAF + CAF + SO), and (4) decaffeinated coffee plus isolated CAF plus extra virgin coconut oil (DECAF + CAF + CO). The substances were ingested 60 min before the trials, the order of the situations was randomized, and there were one-week intervals between them. At the end of the trials, the Borg scale was applied to evaluate the rating of perceived exertion (RPE) and the time was measured. Results: Our data did not show differences in running time among the trials (placebo: 7.64 ± 0.80, DECAF + CAF: 7.61 ± 1.02, DECAF + CAF + SO: 7.66 ± 0.89, and DECAF + CAF + CO: 7.58 ± 0.74 min; p = 0.93), nor RPE (placebo: 6.15 ± 2.03, DECAF + CAF: 6.00 ± 2.27, DECAF + CAF + SO: 6.54 ± 2.73, and DECAF + CAF + CO: 6.00 ± 2.45 score; p = 0.99). Lactate concentrations (placebo: 6.23 ± 2.72, DECAF + CAF: 4.43 ± 3.77, DECAF + CAF + SO: 5.29 ± 3.77, and DECAF + CAF + CO: 6.17 ± 4.18 mmol/L; p = 0.55) also was not modified. Conclusion: Our study shows that ingestion of decaffeinated coffee with the addition of isolated CAF and extra virgin CO, either isolated or combined, does not improve 1600 m running times, nor influence RPE and lactate concentrations in recreational runners. Thus, combination of coffee with CO as a pre-workout supplement seems to be unsubstantiated for a short-distance race.
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nutrients
Article
Acute Caeine and Coconut Oil Intake, Isolated or
Combined, Does Not Improve Running Times of
Recreational Runners: A Randomized,
Placebo-Controlled and Crossover Study
Gabrielle de Lima Borba 1, Julianne Soares de Freitas Batista 1, Ludmilla Marques Queiroz Novais 1,
Myrnzzia Beatriz Silva 1, João Batista da Silva Júnior 1, Paulo Gentil 2, Ana Clara Baretto Marini 1,
Bruna Melo Giglio 1and Gustavo Duarte Pimentel 1, *
1Laboratory of Research in Clinical Nutrition and Sports (Labince), Faculty of Nutrition, Federal University
of Goiás, Rua 227, Quadra 68 s/n, Setor Leste Universitário, Goiânia 74605080, GO, Brazil
2College of Physical Education and Dance, Federal University of Goiás, Goiânia 74605080, GO, Brazil
*Correspondence: gupimentel@yahoo.com.br; Tel.: +55-062-3209-6270
Received: 3 June 2019; Accepted: 17 July 2019; Published: 20 July 2019


Abstract:
The aim was to evaluate the eect of caeine (CAF) and extra virgin coconut oil (CO), isolated
or combined, on running performance in runners. Methods: A randomized, placebo-controlled,
and crossover study was conducted with thirteen recreational runners aged 18–40. All volunteers
performed a 1600 m time trial at a 400 m track, each ingesting four dierent substances: (1) placebo
(water), (2) decaeinated coee plus isolated CAF (DECAF +CAF), (3) decaeinated coee plus
isolated CAF plus soy oil (DECAF +CAF +SO), and (4) decaeinated coee plus isolated CAF plus
extra virgin coconut oil (DECAF +CAF +CO). The substances were ingested 60 min before the
trials, the order of the situations was randomized, and there were one-week intervals between them.
At the end of the trials, the Borg scale was applied to evaluate the rating of perceived exertion (RPE)
and the time was measured. Results: Our data did not show dierences in running time among the
trials (placebo: 7.64
±
0.80, DECAF +CAF: 7.61
±
1.02, DECAF +CAF +SO: 7.66
±
0.89, and DECAF
+CAF +CO: 7.58
±
0.74 min; p=0.93), nor RPE (placebo: 6.15
±
2.03, DECAF +CAF: 6.00
±
2.27,
DECAF +CAF +SO: 6.54
±
2.73, and DECAF +CAF +CO: 6.00
±
2.45 score; p=0.99). Lactate
concentrations (placebo: 6.23
±
2.72, DECAF +CAF: 4.43
±
3.77, DECAF +CAF +SO: 5.29
±
3.77,
and DECAF +CAF +CO: 6.17
±
4.18 mmol/L; p=0.55) also was not modified.
Conclusion
: Our
study shows that ingestion of decaeinated coee with the addition of isolated CAF and extra virgin
CO, either isolated or combined, does not improve 1600 m running times, nor influence RPE and
lactate concentrations in recreational runners. Thus, combination of coee with CO as a pre-workout
supplement seems to be unsubstantiated for a short-distance race.
Keywords: coee; caeine; coconut oil; nutrients; running; performance
1. Introduction
Dietary supplements are widely used with the purpose of improving physical performance and
preventing fatigue [
1
]. Among the supplements, caeine (CAF, 1,3,7-trimethylxanthine) is one of the
most consumed ergogenics in the world, and can be found in many foods and beverages, such as
chocolate, teas, guarana, and coee [
2
]. CAF has been studied because of its apparent positive eects
in endurance sports [
3
5
]. During exercise, CAF can reduce the use of the glycogen and increase the
release of free fatty acids [
6
,
7
], which might delay fatigue and increase endurance. The ergogenic
potential of CAF might also be observed in the cellular matrix, where it acts as a competitive antagonist
Nutrients 2019,11, 1661; doi:10.3390/nu11071661 www.mdpi.com/journal/nutrients
Nutrients 2019,11, 1661 2 of 9
against adenosine receptors, releasing calcium to skeletal muscle, which is able to maximize the
strength for muscular contractions [8,9].
Coconut oil (CO), in turn, is a saturated fat composed of about 50% medium chain fatty acids
or medium chain triglycerides (MCT), namely lauric acid (C 12:0) and caprylic acid (C 8:0) [
10
].
However, less than 30% of lauric acid is released to the liver to be used as an energy source [
11
].
Fatty acids provide rapid energy availability and contain approximately 8–9 kcal per gram; however,
because its structure contains many carbon atoms attached to oxygen, there is greater diculty in
oxidization [
12
]. Although no evidence demonstrated that pre-workout supplementation of long
chain and medium chain fatty acids, as well as conjugated linoleic acid, has any eect on endurance
performance [
13
,
14
], a recent study showed that four weeks (30 mL/d) of virgin CO associated with
a single bout of moderate-intensity cycling in young adults was able to increase popliteal artery
endothelial-dependent dilation, but did not change the post exercise-mediated hyperemia, nor plasma
total antioxidant capacity [
15
]. Additionally, an isoenergetic ketogenic diet containing CO did not
aect the run-to-exhaustion at 70% VO2max in men [
16
]. Although CAF is reported to positively
eect physical performance [
3
,
8
], it is not fully understood whether or not CAF combined with extra
virgin CO improves running time in humans. Likewise, it is unknown if this combination leads to an
ergogenic eect.
Therefore, knowing the potential ergogenic eect of CAF, and that the pre-workout mix of CAF
with extra virgin CO has been used in clinical practice without scientific evidence, we hypothesized
that ingestion of decaeinated coee (DECAF) with CAF, but not with CO could improve running
time. Thus, this study aimed to evaluate the eect of CAF and extra virgin CO, isolated or combined,
on the running time in recreational runners.
2. Methods
2.1. Subjects and Recruitment
Thirty healthy recreational runners aged 18 to 40 initially volunteered to participate in the
study. The volunteers were invited through social medial and by word of mouth. The exclusion
criteria involved those who ran less than two times per week; having renal, cardiovascular, or hepatic
diseases; being pregnant; having dietary restrictions; or currently using dietary supplements or
anti-inflammatory medications. After removing a number of candidates based on the exclusion
criteria, thirteen (8M/5F) volunteers were selected (Figure 1). All the runners signed a written consent
that was approved by the Research Ethics Committee of the Federal University of Goias under the
number 010883/2018.
After signing a written consent, the volunteers replied the initial anamneses one week before the
familiarization test. This anamnesis consisted of body composition assessment, frequency of CAF
consumption and habitual food intake evaluation.
Nutrients 2018, 10, x FOR PEER REVIEW 2 of 9
antagonist against adenosine receptors, releasing calcium to skeletal muscle, which is able to
maximize the strength for muscular contractions [8,9].
Coconut oil (CO), in turn, is a saturated fat composed of about 50% medium chain fatty acids or
medium chain triglycerides (MCT), namely lauric acid (C 12:0) and caprylic acid (C 8:0) [10].
However, less than 30% of lauric acid is released to the liver to be used as an energy source [11]. Fatty
acids provide rapid energy availability and contain approximately 8–9 kcal per gram; however,
because its structure contains many carbon atoms attached to oxygen, there is greater difficulty in
oxidization [12]. Although no evidence demonstrated that pre-workout supplementation of long
chain and medium chain fatty acids, as well as conjugated linoleic acid, has any effect on endurance
performance [13,14], a recent study showed that four weeks (30 mL/d) of virgin CO associated with
a single bout of moderate-intensity cycling in young adults was able to increase popliteal artery
endothelial-dependent dilation, but did not change the post exercise-mediated hyperemia, nor
plasma total antioxidant capacity [15]. Additionally, an isoenergetic ketogenic diet containing CO did
not affect the run-to-exhaustion at 70% VO2max in men [16]. Although CAF is reported to positively
effect physical performance [3,8], it is not fully understood whether or not CAF combined with extra
virgin CO improves running time in humans. Likewise, it is unknown if this combination leads to an
ergogenic effect.
Therefore, knowing the potential ergogenic effect of CAF, and that the pre-workout mix of CAF
with extra virgin CO has been used in clinical practice without scientific evidence, we hypothesized
that ingestion of decaffeinated coffee (DECAF) with CAF, but not with CO could improve running
time. Thus, this study aimed to evaluate the effect of CAF and extra virgin CO, isolated or combined,
on the running time in recreational runners.
2. Methods
2.1. Subjects and Recruitment
Thirty healthy recreational runners aged 18 to 40 initially volunteered to participate in the study.
The volunteers were invited through social medial and by word of mouth. The exclusion criteria
involved those who ran less than two times per week; having renal, cardiovascular, or hepatic
diseases; being pregnant; having dietary restrictions; or currently using dietary supplements or anti-
inflammatory medications. After removing a number of candidates based on the exclusion criteria,
thirteen (8M/5F) volunteers were selected (Figure 1). All the runners signed a written consent that
was approved by the Research Ethics Committee of the Federal University of Goias under the number
010883/2018.
Figure 1. Flow diagram of study.
After signing a written consent, the volunteers replied the initial anamneses one week before the
familiarization test. This anamnesis consisted of body composition assessment, frequency of CAF
consumption and habitual food intake evaluation.
Figure 1. Flow diagram of study.
Nutrients 2019,11, 1661 3 of 9
2.2. Study Design
A randomized, placebo-controlled, and crossover design was conducted at the same time each
day (~7 to 9 a.m.), to avoid possible circadian interferences. The study was conducted over a five-week
period. In the first week, the volunteers did a five-minute warm-up and, after resting for 3–5 min,
performed practice laps of 1600 m on the 400 m circuit where the time trial test would later take
place to familiarize themselves with the track. On the day of the practice laps, the volunteers
were instructed to run in the shortest possible time and the runner’s order was randomized using
https://www.randomizer.org. During the second to fifth weeks, the trials were performed with the
ingestion of dierent pre-test substances.
The volunteers were instructed not to do vigorous physical activities for a period of 24 h, and not
to consume foods and beverages containing CAF in their composition (such as coee, chocolate, mat
é
,
guaran
á
powder and soft drinks) and alcohol in the 48 h preceding the trials. In addition, they were
strongly encouraged to maintain the same dietary and physical activity habits in order to avoid possible
discrepancies in energy balance.
The tests were conducted in a randomized, crossover and placebo-controlled manner on the
weekend (Saturday or Sunday).
The experimental tests consisted of four groups: (1) placebo: who receive 100 mL of warm water;
(2) DECAF +CAF: decaeinated coee with 100 mL of warm water plus 6 mg/kg of CAF isolated;
(3) DECAF +CAF +SO: decaeinated coee with 100 mL of warm water plus 6 mg/kg of CAF plus
15 g soy oil; and (4) DECAF +CAF +CO: decaeinated coee with 100 mL of warm water plus 6 mg/kg
of CAF plus 15 g of extra virgin CO. All trials were separated by a one-week interval.
2.3. Supplementation
Administration of CAF anhydrous (6 mg/kg) was provided by the manipulation pharmacy and
the amount was adjusted according to the weight of each runner [
17
,
18
]. The corresponding amount of
CAF was weighed on an analytical balance (Shimadzu Automatic Digital Analytical Balance, ATX124;
Kyoto, Japan) and kept in aluminium foil packets that were organized and identified by a qualified
individual that was not participating in the research.
The extra virgin CO (Copra Alimentos, Macei
ó
, Alagoas, Brazil, lot 792711818) and the refined
SO (Leve, Imcopa
®
, Arauc
á
ria, Paran
á
, lot c1017) were odorless and flavorless to minimize any bias,
or identification, on the part of the participants in the study. SO was used because it presents improved
palatability, similar to that of CO [
10
]. The amount of both oils of 15 g is equivalent to 16.5 mL. At the
time of the supplement manipulation, 20 mL syringes were used to better determine the amount of
either CO or SO.
Supplements were administered in unmarked containers and handled by a qualified individual
who was not involved in the research, so researchers and runners would not know which supplements
would be given. The DECAF coee (DECAF coee with water) was prepared 30 min prior to being
ingested and standardized to be served using the same amount of coee grinds (36 g coee grinds in
1
2
L
of mineral water) kept at ~45–40
C and stored in bottles until the moment of the tests. The hot water
trial was used for the placebo group, as in previous studies [
19
,
20
]. All substances, either containing
DECAF coee and oil (experimental groups) or only warm water (placebo groups), were ingested
60 min before participants started their time trial. Additionally, volunteers were questioned about
which supplement they believed to have received.
2.4. Evaluation of Food Sources of Caeine and Dietary Intake
The frequency of consumption of food sources of CAF was obtained using a previously-published
adapted questionnaire [21].
Dietary intake was obtained using the 24 h food recall applied throughout the trials. From the
total of six food recalls recorded, two were performed during participant recruitment (anamnesis
Nutrients 2019,11, 1661 4 of 9
application), one in the first time trial test, one in last week of the time trial tests, and two others on
weekdays (in contrast to the normal time trial tests, which were held on the weekend).
The 24 h food recall was applied by a trained nutritionist. We obtained data about serving sizes,
frequency and daily total calorie, carbohydrate, protein, lipids and water intake. For food intake
analysis, DietPro
®
software (version 5.8, Viçosa, Minas Gerais, Brazil) was used. The volunteers were
encouraged to maintain their habitual food consumption during the whole experimental period.
2.5. Running Trials
On the day of the trials, the participants woke up after eight hours of rest and were instructed to
ingest their habitual breakfast without caeine-sourced foods. After one hour, the volunteers went to
the race track.
After supplementation, volunteers were instructed to remain in a resting state for 50–55 min.
Approximately 5 min prior to the tests, a warm-up consisting of stretches and light walking was
done. Then, 60 min after supplementation, the 1600 m time trial test on the 400 m outdoor race track
commenced. The volunteers were instructed to run in the shortest possible time and this was recorded
(in minutes) using a stopwatch.
There were no dierences (p>0.05) in the climatic features during the four days of data collection
(temperature on first day: 20.5, second: 19.71, third: 20.8, and fourth: 19.8
C, and relative humidity on
first day: 54.0, second: 56.3, third: 54.0, and fourth: 61.1), as well as no dierence in humidity.
2.6. Anthropometry, Blood Lactate, and Rating of Perceived Eort (RPE) Assessment
The anthropometric evaluation consisted of body weight, height, body mass index, and waist
circumference. Moreover, skinfolds of the thighs, pectorals, supra iliac, and triceps were measured for
calculation of body fat percentage [22,23].
Blood was collected from the finger at baseline and immediately after the tests. Lactate concentrations
were determined using a portable lactate analyzer (Accutrend Plus, Roche
®
, Mannheim, Germany).
The rating of perceived effort (RPE) was taken immediately after the trials using the Borg scale [24].
2.7. Statistical Analyses
The sample size was determined using the G*Power
®
software version 3.1.9.2. The priori analysis
of variance (ANOVA) test was used for repeated measurements, with 5% alpha error, 95% beta, and
eect power of 0.75, resulting in a minimum sample of 13 volunteers. Shapiro–Wilk test was performed
to check the normality of the variables and values were expressed as means
±
standard deviation.
Paired t-test was used to compare the food intake. ANOVA two-way was used to compare the eects
of time x intervention of blood lactate concentrations. ANOVA one-way was performed to compare the
delta of time trial performance and RPE score. Eect sizes were calculated using Cohen’d following
the scale for interpretation <0.50 (small);
0.50 to <0.80 (medium);
0.80 (large). SPSS version 21.0 and
Prism version 5.0 were used to perform the statistical analyses and graphs, respectively. The level of
significance was set at 5% (p<0.05).
3. Results
The volunteers’ characteristics are described in Table 1. They were young, eutrophic, and with
normal waist circumference and body fat percentage. There was no dierence between the two
first trials compared with the two last trials for calories, macronutrients, amino acids, and water
consumption (p>0.05) (Table 2).
CAF was sourced mainly from the following: caeinated coee (85%), black tea (54%), soft drinks
(54%), and chocolate (46%), and no volunteers reported ingesting guaran
á
powder, nor CAF alone.
The weekly consumption of food/beverage sources containing CAF included the following: CAF coee
(4.18 times) >black tea (2.66 times) >chocolate (2.60 times) >soft drink (2.14 times). Therefore, all of
the participants are moderate CAF consumers.
Nutrients 2019,11, 1661 5 of 9
Table 1. Characteristics of volunteers.
Variables Mean ±SD
Age (years) 28.46 ±5.63
Body mass index (kg/m2)23.58 ±3.90
Waist circumference (cm) 75.88 ±11.24
Body fat (%) 16.19 ±6.00
Table 2. Food intake among the volunteers.
Nutrients Initial Final p
Calories (kcal) 2439.28 ±948.33 2298.50 ±672.15 0.666
Calories (kcal/kg) 35.48 ±9.78 35.04 ±10.90 0.915
Carbohydrate (%) 47.64 ±7.77 51.59 ±17.06 0.455
Carbohydrate (g) 282.29 ±107.88 288.68 ±100.64 0.877
Protein (%) 20.19 ±3.69 20.67 ±5.93 0.807
Protein (g) 120.64 ±51.67 117.47 ±50.43 0.876
Isoleucine (g) 3.02 ±1.93 3.16 ±2.04 0.862
Leucine (g) 5.41 ±3.37 5.77 ±3.74 0.797
Valine (g) 3.51 ±2.28 3.57 ±2.21 0.954
Lipids (%) 32.72 ±5.81 33.06 ±9.27 0.913
Lipids (g) 92.23 ±48.02 82.15 ±26.42 0.858
Water intake (L) 2.10 ±1.01 2.06 ±0.82 0.856
Values are expressed in means ±standard deviation.
Blood lactate concentrations at pre- and post-test were not dierent between trials (placebo:
0.91
±
0.36 to 7.14
±
2.84, DECAF +CAF: 1.00
±
0.50 to 5.43
±
3.88, DECAF +CAF +SO: 0.95
±
0.27 to
6.24
±
3.86, and DECAF +CAF +CO: 1.12
±
0.51 to 7.28
±
4.00; ptime <0.001, ptime
×
intervention
p>0.05
), nor when evaluated using the delta values (placebo: 6.23
±
2.72, DECAF +CAF: 4.43
±
3.77,
DECAF +CAF +SO: 5.29
±
3.77, and DECAF +CAF +CO: 6.17
±
4.18 nmol/L; p=0.55, with small
eect size between the groups) (Figure 2).
Nutrients 2018, 10, x FOR PEER REVIEW 5 of 9
CAF was sourced mainly from the following: caffeinated coffee (85%), black tea (54%), soft
drinks (54%), and chocolate (46%), and no volunteers reported ingesting guaraná powder, nor CAF
alone. The weekly consumption of food/beverage sources containing CAF included the following:
CAF coffee (4.18 times) > black tea (2.66 times) > chocolate (2.60 times) > soft drink (2.14 times).
Therefore, all of the participants are moderate CAF consumers.
Table 2. Food intake among the volunteers.
Nutrients Initial Final p
Calories (kcal) 2439.28 ± 948.33 2298.50 ± 672.15 0.666
Calories (kcal/kg) 35.48 ± 9.78 35.04 ± 10.90 0.915
Carbohydrate (%) 47.64 ± 7.77 51.59 ± 17.06 0.455
Carbohydrate (g) 282.29 ± 107.88 288.68 ± 100.64 0.877
Protein (%) 20.19 ± 3.69 20.67 ± 5.93 0.807
Protein (g) 120.64 ± 51.67 117.47 ± 50.43 0.876
Isoleucine (g) 3.02 ± 1.93 3.16 ± 2.04 0.862
Leucine (g) 5.41 ± 3.37 5.77 ± 3.74 0.797
Valine (g) 3.51 ± 2.28 3.57 ± 2.21 0.954
Lipids (%) 32.72 ± 5.81 33.06 ± 9.27 0.913
Lipids (g) 92.23 ± 48.02 82.15 ± 26.42 0.858
Water intake (L) 2.10 ± 1.01 2.06 ± 0.82 0.856
Values are expressed in means ± standard deviation.
Blood lactate concentrations at pre- and post-test were not different between trials (placebo: 0.91
± 0.36 to 7.14 ± 2.84, DECAF + CAF: 1.00 ± 0.50 to 5.43 ± 3.88, DECAF + CAF + SO: 0.95 ± 0.27 to 6.24 ±
3.86, and DECAF + CAF + CO: 1.12 ± 0.51 to 7.28 ± 4.00; p time < 0.001, p time × intervention p > 0.05),
nor when evaluated using the delta values (placebo: 6.23 ± 2.72, DECAF + CAF: 4.43 ± 3.77, DECAF +
CAF + SO: 5.29 ± 3.77, and DECAF + CAF + CO: 6.17 ± 4.18 nmol/L; p = 0.55, with small effect size
between the groups) (Figure 2).
Figure 2. Delta of lactate concentrations. ES: effect size (small).
RPE did not show any difference between the trials at the end of the trial (placebo: 6.15 ± 2.03,
DECAF + CAF: 6.00 ± 2.27, DECAF + CAF + SO: 6.54 ± 2.73, and DECAF + CAF + CO: 6.00 ± 2.45 score;
p = 0.99) (Figure 3A). No difference in running time was found (placebo: 7.64 ± 0.80, DECAF + CAF:
7.61 ± 1.02, DECAF + CAF + SO: 7.66 ± 0.89, and DECAF + CAF + CO: 7.58 ± 0.74 min; p = 0.93, with
small effect size between the groups) (Figure 3B).
Figure 2. Delta of lactate concentrations. ES: eect size (small).
Nutrients 2019,11, 1661 6 of 9
RPE did not show any dierence between the trials at the end of the trial (placebo: 6.15
±
2.03,
DECAF +CAF: 6.00
±
2.27, DECAF +CAF +SO: 6.54
±
2.73, and DECAF +CAF +CO: 6.00
±
2.45 score;
p=0.99) (Figure 3A). No dierence in running time was found (placebo: 7.64
±
0.80,
DECAF +CAF:
7.61
±
1.02, DECAF +CAF +SO: 7.66
±
0.89, and DECAF +CAF +CO: 7.58
±
0.74 min; p=0.93, with
small eect size between the groups) (Figure 3B).
Figure 3.
Rating of perceived exertion (RPE) (
A
) and time trial (
B
) performance at the end of running.
ES: eect size (small).
All volunteers correctly indicated the ingestion of placebo-water (n=13), 92.3% DECAF +CAF
(
n=12)
, 53.8% DECAF +CAF +SO (n=7), and 46.1% DECAF +CAF +CO (n=6) (p=0.0004).
Overall, correct identifications were made 73% of the time.
4. Discussion
To our knowledge, this is the first study to examine the ergogenic eects of pre-workout coee
ingestion combined with CO on running time in recreational runners. On the basis of our findings,
a mixture of DECAF coee with isolated CAF or extra virgin CO, either isolated or combined, does not
improve 1600 m running times, nor change blood lactate concentrations and RPE.
Among the ergogenic properties of CAF is the increase in time trial performance, through
mechanisms of central and peripheral action [
25
]. However, similar to the present study, two previous
studies showed that DECAF coee plus isolated CAF did not improve endurance performance [
26
,
27
],
suggesting that other components of coee can aect the ergogenic eect of CAF alone [27].
Contrary to our findings, previous studies showed that both CAF coee (containing 5 mg/kg)
or isolated CAF (5 mg/kg) is able to enhance endurance performance in cycling [
28
], and that CAF
coee improves 5 km time trial performance on the treadmill compared with DECAF coee [
29
].
However, one of our previous studies found no dierence in time trial performance in 800 m trials when
comparing the eects of CAF coee versus DECAF coee [
5
]. Thus, one hypothesis for inconsistencies
between studies may be related to how the CAF is administered, either isolated/alone or in a CAF
coee form.
In the present study, we did not find any dierence in 1600 m performance between the
consumption of placebo (water) compared with DECAF coee plus isolated CAF. Similarly, a previous
study also did not find any dierence on endurance performance when comparing DECAF coee
versus the other three groups (either DECAF coee plus isolated CAF or placebo) [
27
]. Although our
data did not evaluate the blood CAF levels, Graham et al. [
27
] suggest that absence of an ergogenic
eect may be independent of blood caeine, paraxanthine, and theophylline concentrations, reinforcing
Nutrients 2019,11, 1661 7 of 9
the idea that the administration procedure (vehicle) appears to modify the ergogenic response of CAF.
Likewise, other studies that combine DECAF coee and isolated CAF or CAF coee or isolated CAF
alone require further investigation.
Church et al. 2015 [
29
] investigated the eects of CAF coee or DECAF coee ingested prior to a
5 km run on a treadmill, and no changes in blood lactate between trials were found. The findings of
Church et al. 2015 [
29
] are in agreement with the present study, as we did not observe any dierences
in the blood lactate concentrations between groups. In addition, the lack of modification in lactate
concentrations has already been found in previous work of our group [
5
], when testing the eects of
CAF coee compared with DECAF coee on 1600 m running performance. Similar findings were
reported by another group that also analyzed the eects of consumption of CAF coee and isolated
CAF alone on participants that ran to exhaustion [10].
Considering that high intensity exercise increased blood lactate concentrations [
30
] and the reduced
consumption of fatty acids during exercise, we hypothesized that increases in lactate concentrations
are time-dependent, but not those of fatty acids, as we used a short-term running protocol. In addition,
pre-workout supplementation with long chain and medium chain fatty acids and conjugated linoleic
acid does not produce an ergogenic eect [
13
,
14
]. Therefore, pre-exercise supplementation with fatty
acids does not make sense in clinical practice.
Additionally, young adults that consume CO do not experience a change in total plasma antioxidant
capacity following a bout of moderate-intensity cycling exercise [
15
] Likewise, it was found in rats
that CO supplementation, with or without exercise, enhanced blood triacylglycerol and VLDL-c
concentrations [
31
]. Therefore, lipid supplements did not seem to be a healthy option. Regarding
performance, a recent study observed in men that a ketogenic diet containing CO did not change
run-to-exhaustion with a 70% VO2max in men [16].
A previous study showed that theophylline, present in coee, can also inhibit adenosine receptors
and increase carbohydrate oxidation during a 30 min cycling exercise [
32
]. Thus, in the present study,
theophylline may have influenced a greater availability of carbohydrates and lactate and, consequently,
a greater energy supply in the trials, which may explain the non-eect of the additional energy supply
from either CO or SO. However, the placebo group received only water and, when compared with the
DECAF coee group, no ergogenic eect was reported. Thus, we suggested that breakfast prior to
races may have indicated that extra calories negatively impacted the running performance among the
groups, despite CAF or CO.
In the present study, we observed that the type of oil, whether SO or CO, did not influence
palatability, as the volunteers were not able to distinguish them. Additionally, the taste identification
of the oils was minimized, as the CO is unscented and tasteless, triggering many volunteers to not be
able to identify the oil type when mixed with the coee.
One important finding in the present study was that most of the participants were able to correctly
identify the substances they took. Previous studies suggested that the placebo eect might be an
important mediator of CAF ergogenic eects [
33
,
34
]. Therefore, precise identification of placebo may
have been associated with an absence of improvement in performance in some runners.
Although the CAF ergogenic eect (3 and 6 mg/kg) on 30.6
C and 50% relative humidity led to
performance loss [
35
], our study done in cooler environmental conditions (range 19.7–20.8
C) did
not aect the running time. Therefore, it is unlikely that climatic conditions led to dehydration and
dropping performance in all trials. In addition, one of our previous studies found no dierence in
sweating rate between acute CAF and placebo supplementations [36].
Some limitations must be acknowledged. First, the small number of participants; therefore, the
data should be interpreted with caution. Second, we are unable to measure the blood CAF and its
metabolites concentrations; thus, we can not to confirm that all participants achieved similar amounts of
CAF and its metabolites following the race. Third, although temperature and humidity were measured,
wind speed was not; thus, we recognize that this could have hampered the running performance.
Nutrients 2019,11, 1661 8 of 9
5. Conclusions
Our study shows that the consumption of DECAF coee with CAF and CO, isolated or combined,
does not improve 1600 m running time, influence RPE, nor lactate concentrations in recreational runners.
Thus, combination of coee with CO as a pre-workout supplement seems to be unsubstantiated for a
short-distance race.
Author Contributions:
G.d.L.B., J.S.d.F.B., L.M.Q.N., M.B.S., J.B.d.S.J., P.G., A.C.B.M., B.M.G., and G.D.P. collected
data, data analyses, interpretation, and drafted the manuscript. All authors read and approved the final version.
Funding: This research received no external funding.
Acknowledgments:
We would like to thank the Patr
í
cia Barreto Lobo, Alexandre Soares, and Vanessa Alves de
Araújo for assistance during the collection data.
Conflicts of Interest: The authors declare no conflict of interest.
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2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access
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(CC BY) license (http://creativecommons.org/licenses/by/4.0/).
... In the 21 studies included in this systematic review [7,[23][24][25][26]30,34,35,[42][43][44][45][46][47][48][49][50][51][52][53][54], there was a total sample of 254 participants, including 220 men, 19 women and 15 participants with no information about gender. The participants were all runners, of which 167 were categorized as amateur and 87 were categorized as trained runners. ...
... All studies were crossover randomized controlled trials. A total of 18 studies [7,[23][24][25][26]30,35,42,43,45,46,[48][49][50][51][52][53][54] provided caffeine in liquid or capsule form, with doses normalized by participants' body mass. In these studies, the doses of caffeine administered ranged from 3 to 9 mg/kg. ...
... The general data of the experiments included in this systematic review are depicted in Table 2. Figure 2 displays the categorization for each RoB 2 item for each included study. Regarding selection bias, we judged only one study [53] as low risk because it reported the appropriate method of participant randomization sequences. We defined all other studies as unclear because none provided sufficient information for this item. ...
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... In view of the critical analysis of the study's evidence, a satisfactory internal validity of the study was possible with adequate randomization, with guaranteed allocation secrecy and adequate blinding scheme. Study 4 by Borba et al., 27 which randomized 13 runners in order to assess the effect of caffeine (CAF) and extra virgin coconut oil (CO), alone or combined, on running performance in runners, demonstrated that the intake of decaffeinated coffee with the addition of isolated CAF and extra virgin CO, isolated or combined, did not improve the running times of 1600 m, nor did it influence the concentrations of protein electrophoresis (EPR) and lactate in recreational runners. ...
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Coffee is one of the most consumed beverages in the world and it can improve insulin sensitivity, stimulating glucose uptake in skeletal muscle when adequate carbohydrate intake is observed. The aim of this review is to analyze the effects of coffee and coffee components on muscle glycogen metabolism. A literature search was conducted according to PRISMA and seven studies were included. They explored the effects of coffee components on various substances and signaling proteins. In one of the studies with humans, caffeine was shown to increase glucose levels, Ca2+/calmodulin-dependent protein kinase (CaMK) phosphorylation, glycogen resynthesis rates and glycogen accumulation after exercise. After intravenous injection of caffeine in rats, caffeine increased adenosine monophosphate-activated protein kinase (AMPK) and acetyl-CoA carboxylase (ACC) phosphorylation, and glucose transport. In in vitro studies caffeine raised AMPK and ACC phosphorylation, increasing glucose transport activity and reducing energy status in rat muscle cells. Cafestol and caffeic acid increased insulin secretion in rat beta-cells, and glucose uptake into human muscle cells. Caffeic acid also increased AMPK and ACC phosphorylation, reducing the energy status and increasing glucose uptake in rat muscle cells. Chlorogenic acid did not show any positive or negative effect. The findings from the current review must be taken with caution due to the limited number of studies on the subject. In conclusion, various coffee components had a neutral or positive role in the metabolism of glucose and muscle glycogen, whilst no detrimental effect was described. Coffee beverages should be tested as an option for athlete's glycogen recovery.
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Purpose: We investigated the effect of a 31-d ketogenic diet (KD) on submaximal exercise capacity and efficiency. Methods: A repeated-measures, crossover study with preintervention and postintervention outcomes was conducted in eight trained male endurance athletes (maximal oxygen uptake (V[Combining Dot Above]O2max), 59.4 ± 5.2 mL⋅kg⋅min). Participants ingested their habitual diet (HD) (43% ± 8% carbohydrate and 38% ± 7% fat) or an isoenergetic KD (4% ± 1% carbohydrate and 78% ± 4% fat) from days 0 to 31 (P < 0.001). On days -2 and 29, participants undertook a fasted graded metabolic test (~25 min), and on days 0 and 31, participants completed a run-to-exhaustion trial at 70% of their V[Combining Dot Above]O2max (~12.9 km⋅h) after the ingestion of a high-carbohydrate meal (2 g⋅kg) or an isoenergetic low-carbohydrate, high-fat meal, with carbohydrate (~55 g⋅h) or isoenergetic fat (coconut oil) supplementation during exercise. Results: Training load did not differ between trials, and there was no effect of diet on V[Combining Dot Above]O2max (all, P > 0.05). The KD impaired exercise efficiency, particularly at >70% V[Combining Dot Above]O2max, as evident by oxygen uptake that could not be explained by shifts in RER and increased energy expenditure (all, P < 0.05). However, exercise efficiency was maintained on a KD when exercising at <60% V[Combining Dot Above]O2max (all, P > 0.05). There was no effect of diet on time-to-exhaustion (237 ± 44 min (pre-HD) vs 231 ± 35 min (post-HD), P = 0.44; 239 ± 27 min (pre-KD) vs 219 ± 53 min (post-KD), P = 0.36). Conclusion: A 31-d KD can preserve submaximal exercise capacity in trained endurance athletes; however, endurance variability increases.
Article
Virgin coconut oil (VCO) is high in antioxidants, which reduces reactive oxygen species-induced conversion of vascular endothelial-derived nitric oxide (NO) to toxic peroxynitrite. As such, flow-mediated dilation (FMD, a surrogate marker of NO bioavailability) and exercise-mediated hyperemia may be enhanced following VCO treatment. Animal research support these findings but direct assessments of FMD after short-term VCO use in humans is unknown. We tested the hypotheses that a 4-week VCO supplement (30 ml·day-1) would improve popliteal artery(PA) FMD and the hyperemic response to aerobic exercise. Thirty-four young adults were divided into VCO (n=19, 9F, 22±2 years, 24±3 kg·m-2), and control (CON: n=15, 7F, 24±2 years, 24±3 kg·m-2) groups. PA-FMD and blood flow were assessed via high-resolution duplex ultrasonography (Vivid i, GE Healthcare). PA blood flow was measured at rest and for 5-minutes following a 10-minute bout of moderate-intensity (60% heart rate reserve) cycling exercise. Total PA blood volume was calculated as the integral of the 5-minute post-exercise PA blood flow response. After 4 weeks, PA-FMD increased (p=0.04)following VCO supplementation (4.9±0.9% to 5.5±1.2%) with no change (p>0.9) in the CON group(5.7±2.1% to 5.8±1.9%). There were no differences (both, p>0.28) in the post-exercise total PA blood volume response in either group (VCO: 495±355ml to 598±384ml; CON: 562±362ml to 488±229ml). Short-term VCO supplementation does not alter aerobic exercise-mediated blood flow responses in young adults. However, the augmented popliteal FMD response observed in the VCO supplement group indicates that short-term VCO supplementation improves vascular endothelial function in young, healthy adults
Article
This study sought to investigate the effect of oral caffeine supplementation on sweat rate and blood pressure in ballet dancers. A double-blind study with placebo control was conducted with nine professional ballet dancers (average age: 28.5 ± 8.8 years). Oral caffeine supplementation (400 mg per dancer, 6.3 mg/kg, range: 4.9 to 8.6 mg/kg) was ingested one hour before a ballet session that was 5 hours in length. After 3 days a second 5-hour session was performed prior to which a placebo was given to the participants. Body weight, sweat rate, and blood pressure were measured before and after each session. Student's t-tests and ANOVAs were used to assess statistical differences. Results were considered significant at p < 0.05. It was found that acute caffeine supplementation did not change any of the variables when compared to placebo.
Article
Purpose: Although the effect of caffeine in thermoneutral or cool environmental conditions has generally shown performance benefits, its efficacy in hot, humid conditions is not as well known. The purpose of this study was to further examine the effect of caffeine ingestion on endurance running performance in the heat. Methods: Ten trained endurance runners (6 males; mean±SD age 26±9 years, height 176.7±5.1 cm, mass 72.1±8.7 kg) came to the lab for four visits. The first was a VO2max test to determine cardiorespiratory fitness; the final three visits were 10km runs in an environmental chamber at 30.6°C and 50% RH under different conditions: 3 mg·kg-1 body mass (low caffeine dosage), 6 mg·kg-1 (moderate dosage), and a placebo. Repeated-measures ANOVAs were used to determine the effect of condition on 10km time, heart rate (HR), core temperature (CT), rating of perceived exertion (RPE) and thermal sensation (TS). Results: There was no difference in 10km time between the placebo (53.2±8.0 min.), 3 mg·kg-1 (53.4±8.4) and 6 mg·kg-1 (52.7±8.2) conditions (p=.575, ηp2=.060). There was not a main effect of average HR (p=.406, ηp2=.107), RPE (p=.151, ηp2=.189) or TS (p=.286, ηp2=.130). There was a significant interaction for CT (p=.025, ηp2=.170); the moderate dosage caffeine condition showed a higher rate of rise in CT (0.26±0.08 ˚C·km-1 vs. 0.20±0.06 and 0.19±0.10 in the low caffeine and placebo conditions, respectively). Conclusion: The results support previous research showing a thermogenic effect of caffeine, as the moderate dosage condition led to a greater rate of heat storage and no performance benefits.
Article
It is well established that the consumption of medium-chain triglycerides (MCT) can increase satiety and reduce food intake. Many media articles promote the use of coconut oil for weight loss advocating similar health benefits to that of MCT. The aim of this study was to examine the effect of MCT oil compared to coconut oil and control oil on food intake and satiety. Following an overnight fast, participants consumed a test breakfast smoothie containing 205 kcal of either (i) MCT oil (ii) coconut oil or (iii) vegetable oil (control) on three separate test days. Participants recorded appetite ratings on visual analogue scales and were presented with an ad libitum lunch meal of preselected sandwiches 180 min after consumption of the breakfast. The results showed a significant difference in energy and macronutrient intakes at the ad libitum meal between the three oils with the MCT oil reducing food intake compared to the coconut and control oil. Differences in food intake throughout the day were found for energy and fat, with the control having increased food intake compared to the MCT and coconut. The MCT also increased fullness over the three hours after breakfast compared to the control and coconut oils. The coconut oil was also reported as being less palatable than the MCT oil. The results of this study confirm the differences that exist between MCT and coconut oil such that coconut oil cannot be promoted as having similar effects to MCT oil on food intake and satiety.