Caffeine 1995
Caffeine 1995
Analyses
Pre-experimental protocol
Expired gas samples were analyzed every 20sec for fractions
Each subject visited the laboratory before the start of the actual of 0, and C02with an on-line system (Sensormedics 2900. Sen-
study and performed an incremental V0,max test on an elec- sormedics Cooperation, USA). The blood samples were mixed
tromagnetically braked cycle ergometer (Lode Excalibur. with EDTA to prevent clotting and were centrifuged immedi-
Groningen. The Netherlands) to determine maximal power ately. Plasma was frozen in liquid N, and stored at - 20'C until
output (Wmax) and maximal oxygen uptake (VOzmax) (21). further analysis. The urine samples were also stored at - 20'C.
The mean V0,max for the group and mean Wmax are shown
in Table 1. The [FFA] was determined with an in vitro enzymatic method
for quantification of the IFFA] in plasma (Wako NEFAC kit;
instructions to thesubjects Wako Chemicals. Germany). The analyses were carried out
with a Cobas-Bio semi-automated centrifugal spectrophoto-
The subjects were instructed to maintain their normal training meter. This apparatus was also used for quantification of the
program during the study and were asked to incorporate the glycerol concentration by standard enzymatic method. Caf-
experimental test into their training program as a hard work feine concentrations in urine were determined using an HPLC
out. The subjects were asked to refrain from training 24 h method (18).
before the test. A diary was kept to record food consumption
and activities during the three days before the first test. The Data anolysis
subjects were asked to eat and train before the following tests
as they had done before the first test to minimize variation in Data are presented as meankstandard deviation (SD). Data of
glycogen concentration in muscle and liver cells. An almost all subjects were available between - 60 and 35 rnin and these
similar procedure has been shown to result in similar pretest were used for statistical analysis. Data of the moment of ex-
glycogen concentrations (23). During these three pre-testing haustion (EXH)and during recovery (REC)were also analyzed.
days subjects were asked to refrain from caffeine consumption
(coffee/tea/chocolate(milk)/cola). as was done in the studies of An analysis of variance (ANOVA)with repeated measurements
Graham et al. and Spriet and colleagues (14.27). to make sore was used for statistical analysis of the response differences be-
that no caffeine was present in the body before the exercise tween four dosages of caffeine. When significant differences
test. All subjects were caffeine users invaryinggradations. Five were found ( p i 0.05) the Scheffe F-test was used to test for
subjects consumed between 100-250 rng caffeine per day and differences between pairs of dosages. Pearson correlation
four subjects consumed above 250 mg caffeine per day. coefficient (r) was calculated for relation between the dosage
of caffeine and post-exercise urinary caffeine concentration.
Experimental protocol
Results
Subjects performed the four endurance tests over four succes-
sive weeks. Day of the weekand time ofday were kept constant Time to exhaustion differed significantly among the caffeine
in each [Link] tests differed only in the amount of caf- and placebo tests. The endurance performance was signifi-
The Effect of Different Dosages of Caffeine on Endurance Performance Time Int. 1. Sports Med. 16 (1995)
Table 2 The individual endurance time data for the four different con-
ditions in minutes and seconds. Mean and standard deviations of the
four tests of the nine subjects are presented, too.
Subjects Omg 5mg 9rng 13mg
1 36.05 42.47 51.50 37.55
2 52.47 85.1 5 65.00 59.30
'p < 0.05 placebo 3 56.55 63.20 73.10 79.12
versus cdfeine
4 45.20 52.10 64.40 58.33
5 35.25 66.20 57.45 70.54
6 66.38 73.25 76.49 69.47
7 40.57 44.50 40.55 46.48
8 57.15 57.17 66.47 66.35
9 28.34 35.05 33.17 36.20
Fig. 1 Endurance performances with different caffeine concentra-
tions. The cycling time (min) is averaged for 9 subjects. The caffeine mean 47 58 59 58
performances were significantly better than the placebo performance. SD 13 11 12 12
No significant differences among the caffeine tests were found.
-
-
-
Orng
2
m 2000 Fig. 2 Free fatty acid
la00 1800 rw (FFA) concentrations
1600 16w 3 9 mg during the 4 exercise
. .1
14M) 5 I-t 13 mg tests.
MH: exhaustion
g , , -B
-- m
12W
REC: recovery
d I lox 2
y.
Y Bcm 803
MX) 600
4W 400
p < 0.05 placebo
2W 2 0
versus caffeine
0 0
- 60 o 5 10 15 25 35 EX H REC time (mid
1 10 min I10 min I 1 15 min I
2 REC: recovery
-$E!
3,
a
L
-8 200
100
p c 0.05 placebo
versus caffeine
0
-61) 0 5 10 15 25 35 EXH
I10 min I10 min I 1 15min I
cantly increased (average 27%) when caffeine was ingested nificantly higher after caffeine ingestion during the whole test
compared to the placebo test (Fig. 1).Among t h e caffeine tests and after the exercise test. The similarity of glycerol concen-
no significant differences in cycling time were found. In- trations after caffeine intake is shown in Fig.3. [The concen-
dividual endurance performances are shown in Table 2. trations for the three caffeine concentrations are almost the
same and therefore only one line is seen.]
Sixty minutes after caffeine ingestion ( t = 0 min) FFA concen-
trations were significantly different from placebo (Fig.2). The caffeine concentrations in urine following exercise showed
Duringthe first 15 rnin of exercise significantly higher FFAcon- a significant linear relationship with t h e amount of caffeine in-
centrations were found in all caffeine tests compared to gested before exercise ( r = 0.65) (p < 0.001). The mean urinary
placebo. No differences in FFA concentrations were found be- caffeine concentration obtained after exercise was 4.8k 1.8,8.9
tween the caffeine dosages. Similar to the FFA concentrations. f 5.2 and 14.9f6.9 C L ml-'~ for 5, 9 and 13m g CAF. kg BW-'.
the glycerol concentrations were significantly higher 60min The individual urinary caffeine concentrations after exercise
after caffeine ingestion (Fig.3) compared to placebo. Unlike the are shown in Fig.4 for the different caffeine dosages.
FFA concentrations, the glycerol concentrations remained sig-
*-'=
Int. I. S~ortsMed. 16 (1995) W. I. Posmon, M. A van Book,A. E. leukendrup. A. de Haan
suggested to be especially effective in the first 15 min of exer- performed after caffeine consumption were easier to carry out
cise, because glycogenolysis is normally v e y high in this pe- than after placebo consumption.
riod (11). A simultaneous down-regulation of the CHO-meta-
bolism (2) could result in glycogen-sparing which was also Side effects of caffeine intake
shown by Spriet et dl. (27). In the present study FFA and glyc-
erol concentrations in blood were increased after caffeine in- The known side effects of caffeine like dizziness. headache,
gestion which is in agreement with previous tindings in other tremor. hunger sensations. insomnia and diuresis (4.17.20)
caffeine studies (8,13.27). A n increased lipolysis is implicated were reported during and after the test. especially for the 9
in the mechanism of action. In this study no dose-response re- and 13mg CAF. kg BW-' dosages, but disappeared within a few
lationship for FFA and glycerol was found. hours.
The lipolysis might be increased via a direct or indirect caffeine In conclusion, an ergogenic effect of caffeine is found for all
effect. The cellular mechanisms of caffeine action were recently caffeine dosages [Link] cyclingtime increased on aver-
reviewed by Dodd et al. (12). The most probable cellular mech- age 27 % for all caffeine dosages. In the dose range investigated
anism of caffeine is inhibition of adenosine receptors, thereby no dose-response relation was found. A maximal beneficial
reducing the inhibition of lipolysis by adenosine. Lindinger et effect of caffeine was already found with 5 mg CAF. kg BW-I.
al. (22) suggested that the ergogenic effect of caffeine was At this dosage all subjects had urinary caffeine concentrations
caused by attenuation in plasma [I<+] during exercise. Main- below the doping limit of the IOC.
tenance of membrane potential by Na-K pump activity may
contribute to the stimulating effect of caffeine. Acknowledgements
times resulting in different moments of urine sampling after on metabolism and exercise performance. Med Sci Sports Exerc
exercise. Within 15 minutes after finishing the test urine was 10: 155-158.1978.
[Link] might affect the amount of caffeine measured in Costill D. L.. Fink W. J., Getchell L H.. Ivy J. L. Witzmann F. A.:
Lipid metabolism in skeletal muscle ofendurance-trained males
urine. The acceptability of using urinary caffeine concentra-
and females.J Appl Physiol 47: 787, 1979.
tions for competition screening has been questioned because l o Clarckson P. M.: Nutritional ergogenic aids: Caffeine. 1ntJSports
of the variation in concentration measured after exercise (10). Nutr 3: 103-111, 1993.
The doping limir of the 10C could be reached by ingesting 8 Dyck D. J., Putman C. T..Heigenhauser C. J. F.. Hultman E.. Spriet
cups of coffee (100 [Link]-'), indicating that athletes have to L. L.: Enhanced FFA availability decreases muscle glycogenolysis
refrain from caffeine consumption before competition, be- during intense aerobic cycling. Physiologist 35: 191, 1992.
cause the ergogenic drug could otherwise be measured in a l2 Dodd 5. L, Herb R. A.. Powers 5. I(.: Caffeine and exercise per-
urine sample. formance. An update. Sports Med 15: 14-23. 1993.
l 3 Essig D., Costill D. [Link] Handel P.J.: Effects of caffeine ingestion
Caffeine consumption not only affects substrate metabolism. on utilization of muscle glycogen and lipid during leg ergometer
jt is also known to effect mood and feelings of perceived exer- cycling. lntJ Sports Med 1: 86-90. 1980.
tion. In this study too, subjects reported that the exercise tests
i b ^ y sInt.]. Sports Med. 16 (1995) W,j. Posmon, M. A. von Book. A. E, jeukendrup. A. de Haan
'4 Graham T. E., Spriet L. L: Performance and metabolic responses Corresponding Author
to a high caffeine dose during prolonged exercise.] Appl Physiol
71 : 2292 - 2298,1991. W. J. Pasman
' 5 Handel P. V.: Caffeine. In 'Ergogenic Aids in Sport'. Williams M. Department of Human Biology
(ed), Champaign. Ill. Human Kinetics, 1983, Chapter 5. pp University of Limburg
128- 163. [Link] 616
' 6 Hickson R. C.. Remie M. J.. Conlee R. K., Winder W. W.. Holloszy NL-6200 MD Maastricht
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and carbohydrate feedings on endurance performance. Med Sci
Sports Exerc 11: 6-11, 1979.
l8 I.S.0 report - 10095. Coffee, determination of caffeine contents
- Methods of using HPLC. 60,first ed 01.15,1992.
l9 James E J.: Caffeine and Health. Academic Press. Norfolk, 1991.
Knapik J. J., Jones B. H., Toner M. M.. Daniels W. L. Evans W. 1.:
lnfluence of caffeine on serum substrate changes during running
in trained and untrained individuals. In: Biochemistry of Exer-
cise. Icnuttgen H. G., Vogel H.,Poortmans (eds), Champaign, Ill.,
Human Kinetics, 1983, pp 514-519.
21 Kuipers H.: Variability of Physiological Responses to Exercise.
Haarlem, de Vrieseborch: 1983, pp 19-22.