Differential Effects
Differential Effects
CALDWELL,JAY E., ESAAHONEN,ANDUNTO NOUSIAINEN. these methods been compared as they are actually used
Differential effects of sauna-, diuretic-, and exercise-induced by athletes. Differences between separate treatments can
hypohydration. J. ~Appl. Physiol.: Respirat. Environ. Exercise modify physiological responses to hypohydration and
Physiol. 57(4): 1018-1023, 1984.-The physiological effects on explain the changes in ability to perform in a competi-
submaximal and maximal exercise of three methods commonly tion.
used by athletes for achieving rapid weight loss were determined
by measuring cardiorespiratory variables in 62 nonendurance The purpose of the present study was to examine the
athletes. A mean weight loss of 4.1% was achieved by those weight loss methods commonly practiced by Finnish
who followed either a sauna (SAU), diuretic (DIU), or exercise athletes. It was hypothesized that sauna-, diuretic-, and
(ACT) protocol, compared with the average weight loss of 1.2% exercise-induced weight reduction limit physical per-
in the control group. At maximal exercise O2 consumption, 02 formance, that this limitation is not attributable to hy-
pulse, blood lactate concentration, and work load decreased in pohydration alone, and that it also depends on the nature
SAU and DIU groups relative to the ACT group, whereas only of selected treatments. We studied the effects of these
a few differences were observed at the aerobic threshold. Weight methods on cardiorespiratory variables related to aerobic
loss achieved over a 48-h period was less detrimental to an power and endurance in wrestlers, boxers, judoka, and
athlete than was a more rapid (24-h) weight reduction achieved weight lifters.
through sauna bathing or the use of diuretics. We conclude
that not only the quantity of weight loss but also the method
itself may limit physical performance. MATERIALS AND METHODS
dehydration; aerobic threshold; training; aerobic capacity Sixty-two male athletes from four top Finnish sport
clubs (15 weight lifters, 19 wrestlers, 12 judoka, and 16
boxers) took part in the study. Th .eir anthropometric and
IT IS WELL ESTABLISHED that hypohydration limits phys- physiological measurements are presented in Table 1.
ical performance (4, 15, 22-24). This limitation appears The athletes were randomly divided into three experi-
to have both anaerobic and aerobic components, includ- mental subgroups and a control group. Base-line values
ing decrements in peak power (16),strength (1,3), lactate of these groups are expressed in Table 2. All athletes
production (24), and 02 consumption (10). It has been were asked to follow a low-calorie low-fluid diet such as
reported, however, that strength (27, 30) and aerobic they would normally consume before competition. Mem-
power (2, 16, 24), are unchanged following hypohydra- bers of the experimental groups then attempted to lose
tion. Nonetheless, except as reported in some studies 5% of their body weight by one of three prescribed
(12, 27), physical work capacity< (or endurance) is de- methods. 1) Diuretic group (DIU, n = 15). After base-
creased with increasing hypohydration. line testing each subject received furosemide (1.7 mg/kg
A variety of methods has been used to induce weight total) in two equal doses, the first 16 h and the second 4
loss: heat exposure (1, 4, 6, 22, 24), exercise (21, 24), h before follow-up testing. No electrolyte supplement
exercise during heat exposure (8, lo), diuretics (5, 22), was provided. Urine volume was measured during the
and restriction of food and water alone or in combination ensuing 24-h period. No other treatment was provided,
with the other methods (16,30). All of these methods for and the athletes were asked not to exercise. 2) Sauna
weight reduction are commonly practiced by athletes who group (SA U, n = 16). After base-line testing each athlete
are competing within weight divisions. The common had 24 h to achieve the prescribed weight loss. Sauna
denominator of these methods is hypohydration. When exposure was performed in the experimental sauna of
the various methods of hypohydration have been com- the University of Kuopio in which the temperature (at
pared, exercise has been shown to have the most unfa- head level) was maintained at 80°C and the humidity at
vorable effect because of lowered glycogen stores, ele- 50% by means of an automatic water injection system.
vated core temperature, contracted plasma volume, and The interval between the last sauna and the follow-up
altered concentrations of blood components (22). Sauna- testing was at least 2 h. 3) Active exercise group (ACT, n
and diuretic-induced hypohydration have been reported = 16). Each athlete was given 48 h to achieve the pre-
to have fewer side effects (22).Only in a few studies have scribed weight loss through increased exercise (training,
1018 0161-7567/84 $1.50 Copyright 0 1984 the American Physiological Society
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HYPOHYDRATION AND PERFORMANCE 1019
TABLE 1. Base-line anthropometric and they had not engaged in competition. During the
and physiological measurements by sport week before the tests they were asked not to change their
regular routines and to consume their usual diets. At the
Weight Wrestlers Judoka Boxers time of testing all athletes were in good health and free
Variable Lifters
(n = 15) (n = 19) (n = 12) (n = 16) of injury. All tests were conducted over a 4-wk period, so
that each club was tested on a separate weekend. All
Age 22.6 k 5.5 22.6 k 4.2 24.1 k 6.1 19.6 z!z 3.4
measurements were performed by the same persons
Yr
Ht, 173.6 ,t 8.7 172.4 ,t 6.7 174.6 ,t 6.1 177.0 ,t 6.6 throughout the study period.
cm Members of the control and exercise groups were
W. 77.2 t 12.1 72.5 It 10.0 72.7 t 7.9 66.3 t 10.0 t est ed on the afternoons of days 1 and 3, and the sauna
kg and diuretic groups were tested on the mornings of days
Fat, % 15.0 15.1 13.8 11.2
Hematocrit, % 48.6 & 2.3 48.1 t 1.8 48.4 zk 2.3 47.8 zk 2.7 2 and 3. The order of testing was as follows: underwater
Hemoglobin, 165.1 t 7.1 162.5 z!z 7.4 161.3 t 7.4 160.8 t 9.3 densitometry, anthropometry, venous blood sampling,
Vitalg/l capacity, 4.66 zk 0.74 4.87 k 0.59 4.85 & 0.43 4.78 + 0.66 muscle biopsy (weight lifters and wrestlers only), power
tests, and cycle ergometry. The details of the various
liters
‘($0 2-, bin 3.90 t 0.71 4.05 t 0.49 4.04 t 0.49 3.86 t 0.60 physiological tests are described below.
00 2-, m l* 51.1 AI 8.7 56.1 2 4.0 55.8 t 6.5 58.4 2 6.4 Anthropometry. Height and weight were determined
kg-l. min’l before the physiological testing and after the weight loss.
Pulse (max), 181.5 -c- 5.4 183.3 t 8.9 184.0 t 9.6 181.3 * 9.0 Skinfold measurements were made according to the
. _
beats/min
Aerobic 28.8 Z!E7.3 32.7 t 7.2 33.2 t 3.3 31.9 & 5.9 method of Durnin and Womersley (13) with-a Lange
threshold, skinfold caliper. Body fat percentages were interpolated
ml kg-l - l from the Durnin-Womersley tables. Vital capacity was
min-’ measured on a Godart water-seal Expirograph with the
Aerobic 56.2 t, 9.9 57.5 t 10.3 60.1 zk 8.1 54.5 & 9.9 athlete in a standing position.
threshold, %
VO 2 max
Hematology and blood chemistry. Hematocrit, hemo-
globin, and sodium and potassium concentrations were
Values are means t SD. 00 2max, maximum 02 consumption.
measured in blood obtained from a stasis-free antecubital
TABLE 2. Base-line anthropometric vein before exercise testing. Blood hematocrit (Hct) was
and physiological measurements by experimental group corrected for trapped plasma (0.96 x Hct), and hemoglo-
bin was measured by cyanohemoglobin spectrophotom-
Group etry. Changes in plasma volume were determined by the
Variable ACT SAU DIU CON
Total
(n = 62)
calculations introduced by Dill and Costill (11).Concen-
(n = 16) (n = 16) (n = 15) (n= 15) trations of sodium and potassium in serum were deter-
Age, 21.4 21.7 23.0 22.3 22.1 mined by flame photometry.
Yr t6.2 k3.0 k4.1 k6.0 24.9 A&& biopsy. Under local anesthesia (4 ml lidocaine
Ht, 172.8 177.4 174.4 172.4 174.3 without epinephrine) -50 mg of tissue were obtained
cm k 6.9 t 7.4 k 8.1 t 5.6 ‘k 7.2 from the vastus lateralis muscle using a, 1.2 x 70 mm
wt 66.6 74.1 74.1 73.7 71.5
zk 9.3 z!z 9.3 2 11.1 zk 12.0 * 10.3
Trucat biopsy needle; each sample was immediately fro-
kg
Fat, % 13.6 13.4 13.6 15.0 14.2 zen in liquid nitrogen. Glycogen was measured in glucose
Hematocrit, % 48.4 48.0 48.3 48.1 48.2 units (mmol/mg wet wt), using a photometric method
zk 2.5 k 2.3 -c- 1.9 t 2.2 zk 2.2 modified by Hultman (17).
Hemoglobin, g/l 163.8 163.2 161.9 160.8 162.5
t 7.5 t 7.2
Ergometry. Ergometry was performed on a Siemens
* 8.6 k 8.3 zk 7.8
Vital capacity, 4.36 4.94 5.03 4.85 4.79 380B cycle-ergometer in a well ventilated room. During
liters t 0.56 t 0.61 t 0.59 & 0.50 zk 0.61 the test cardiac activity was monitored continuously and
VO 2 max9 bin 3.61 4.25 4.15 3.84 3.96 the heart rate recorded at the end of every minute. Direct
k 0.61 k 0.50 t 0.38 t 0.57 zk 0.57 02 and CO2 concentrations and gas volume measure-
00 2-, ml kg-l l l 54.7 57.6 56.8 52.5 55.4
ments were made using a Mijnhardt Oxycon-2 system
mine1 k 8.5 t 5.3 k 6.7 k 5.8 I!z 6.8
Pulse (max), 181.5 182.3 183.9 182.4 182.4 and were recorded every minute. Pollowing an unloaded
beats/min k 8.9 k 7.3 t 8.4 rt 9.0 zk 8.2 period of 5 min the athletes were fitted with rubber
Aerobic threshold, 31.0 31.3 31.5 32.2 31.6 facemask assemblies for gas collection. The test began
ml kg-’ mine1 t 8.3 t 5.1 k 6.6 k 5.2 f: 6.4
l l
with a O-W load. At the end of each 1-min stage the load
Aerobic threshold, 57.1 53.9 55.4 60.8 57.0
%VO,mm k 12.0 z!r 7.6 t 9.9 t 8.3 k 9.6 was increased by 25 W until the subject complained of
fatigue or until the requisite pedal cadence (60 rpm)
Values are means & SD. ACT, active exercise group; SAU, sauna
group; DIU, diuretics group; CON, control group. 302-, maximum O2 could not be sustained. Criteria for a maximal test were
consumption. a respiratory exchange ratio (RER) > 1.0 and either a
plateau or a decrease in O2 consumption (TO,). From the
running, or swimming). 4) Control group (CON, n = 15). test data ventilation was plotted against I702 to deter-
This group continued normal training during the 48-h mine the aerobic-anaerobic transition point. The aerobic
test period. threshold was defined according to Wasserman et al.
Before the testing period all athletes had been follow- (31).
ing a regular training schedule for their respective sports, Lactate measurements. Arterialized capillary blood
samples were obtained from a fingertip before and after TABLE 4. Changes in physiological variables
the warm-up period, at the end of the 225-W stage, and at aerobic threshold after hypohydration
4 min after completion of the test. Blood was also ob-
tained from the wrestlers every 2 min during the test. ACT+
ACT SAU DIU SAU + CON
Blood lactate values determined from these samples were Variable (n = 16) (n = 16) (n = 15) DIU (n = 15)
used to corroborate the aerobic thresholds determined (n = 47)
from the expired minute ventilation vs.-V02 curves. The VO 2mart,
n&kg-‘0 0.2 -1.3c -2.8' -1.5' -1.0
concentration of lactate in blood was measured using the min-’ t3.0 k4.4 zk4.3 k4.0 k4.0
method described by Gutmann and Wahlefeld (14). Pulse, beats/min 0.8 8.3 2.4 3.8= 1.0
Statistics. Comparison of initial values of the experi- k1.0 t14.5 k11.2 kl2.2 kO.7
mental groups with those of the control group was made O2 pulse, ml/beat -o.73e -2.294d -1.31"" -1.454d -0.35
k1.26 t1.64 k1.28 k1.51 k0.78
using the two-tailed Student’s t test for groups. Compar- Ventilation, l/min 1.0 -0.4 -5.1Cvd -1.7 1.9
ison of those variables before and after the weight loss t6.2 kg.8 t8.8 k8.7 k7.0
was made using the one-tailed Student’s t tests for pairs. Respiratory rate, 0.1 0.1 -0.1 0.1 0.2
Differences were expressed as changes from the initial beats/min k0.8 - kO.6 k0.6 *0.9 20.7
Tidal volume, 0.01 -0.19= -0.18 -0.12 0
values. Comparisons between experimental groups and liters kO.19 zkO.27 k0.36 kO.29 to.30
the control group were made using one-tailed Student’s Respiratory 4.1 -4.5 -2.9 -1.2 0.5
t tests for groups and analysis of variance and covariance, efficiency, %
so that the effect of weight loss was standardized for Tidal 02, ml/beat -2.2 -1.1 -1.9 -1.6 -0.5
comparison of methods. In the tables results are ex- k4.7 k2.6 zk3.9 k4.2 k4.4
Work load, W -15.6' -15.1* -26.9'$ -19.1a -5.0
pressed as changes after the hypohydration procedures. t22.3 k28.5 t28.7 k26.6 t19.7
RER, % -6.44b -0.5 -4.gc -3.Pd 1.0
RESULTS Values are means & SD. Respiratory efficiency, tidal volume/vital
capacity; tidal 02, V02/respiratory rate; RER, respiratory exchange
Base-line measurements of the athletes after the ratio. Other abbreviations as in Table 2. aP < 0.001 after
weight loss are presented in Table 3. The experimental hypohydration. bP c 0.001 when compared with controls. "PC
groups all lost significantly more weight (2.3-3.5 kg, P c 0.01 after hypohydration. dP < 0.01 when compared with
0.001)than did the control group. The sauna and diuretic controls. *P C 0.05 after hypohydration. fP < 0.005 when
compared with controls.
groups achieved a greater weight loss than did the active
group. Those in the active group experienced no statis-
crit (5.3 and 7.2%, respectively). In the sauna group,
tically significant alterations in plasma volume, although
their concentrations of sodium in serum increased which lost weight via production of a hypotonic sweat
slightly (1.2%).On the other hand, the sauna and diuretic (9), the concentration of sodium in serum increased.
groups underwent marked decreases in plasma volume Functional vital capacity (FVC) decreased only in the
(10.3and 14.1%,respectively) and increases in hemato- diuretic group. Muscle glycogen showed no marked
changes in any of the test groups.
The changes in the physiological variables at the
TABLE 3. Changes in base-line measurements aerobic
. threshold are shown in Table 4. The values of
after hypohydration vo 2 m-9 02 pulse, and ventilation in the active exercise
group resembled those of the controls, while these vari-
ACT + ables showed significant decreases in other experimental
ACT SAU DIU SAU + CON
Variable (n = 16) (n = 16) (n = 15) DIU (n = 15) groups. The work load decreased in all exberimental
(n = 47) groups, and the respiratory exchange ratio decreased in
the active exercise and diuretic groups. The tidal volume
w kg -2.34b -3Jasb -3.1"tb -304b -O.Ba
and the exercise respiratory efficiency (the fraction of
to.8 to.8 to.8 a0:9 k1.0
Vital capacity, 0.04 -0.10 -0.27Cpd -o.13c -0.03 vital capacity used with each breath) in all test groups
liters kO.19 to.29 k0.36 kO.30 to.18 remained almost unchanged.
Aerobic threshold, -1.3 -0.1 0 -0.5 -5.9 Changes of physiological variables at maximal work
%Vo2-
Hematocrit, % 0.13 2.634b 3.6Pb 2.0Pb -0.87' intensity are shown in Table 5. Moderate decreases in
t2.45 t1.93 k2.23 *2.62 Al.46 maximal ventilation were observed in each of the exper-
Hemoglobin, g/l 1.7 10.34b 14.74b 8.74b -2.3 imental groups. The maximal frequency of respiration
zk7.9 k6.8 k8.6 k9.4 k5.6 increased slightly in all the groups but most clearly in
Plasma volume, % -0.9 -10.3b X4.1b -8.3b 3.3
Serum Na+, 1.74d 3.54b 0.6 2 04b -0.3 the controls. The decrease in tidal volume was most
mmol/l a.7 &2.5 a.9 -c-2:3 ~1.8 noticeable in the sauna and diuretic groups, and therefore
Serum K+, mmol/l 0.10 0.29" 0.14d 0.09 0.11 the decreases in VO 2 m-3 tidal 02, and 02 pulse were most
kO.35 kO.33 *0.33 to.37 kO.36 marked in these test groups. The work load in maximal
Muscle glycogen, -0.31 0.21 0.37 0.09 -1.58 exercise decreased in all experimental groups, the sauna
mm01 glucose/ -t-3.77 zk1.46 a.92 k2.48 k4.70
mg wet wt and diuretic groups having the largest reduction.
Differences beween the methods estimated by analysis
Values are means k SD. Abbreviations as in Table 2. Students t test
was used for pairs and groups. *P c 0.001 after hypohy- of covariance are summated in Table 6. The effect of
dration. bP < 0.001 when compared with controls. cP < 0.01 amount of weight reduction was eliminated, and the
after hvpohvdration. d P < 0.01 when compared with controls. differences evaluated were thus due to the methods alone.
TABLE 5. Changes in physiological variables in the sauna (P < 0.02) and diuretic (P < 0.07) groups
at maximal exercise after hypohydration when compared with the active exercise group, probably
due to different relationships between the decreases of
ACT + CON body weight and VOWm-0 Heart rate and respiratory rate
ACT SAU DIU SAU + (n = 15)
Variable (n = 16) (n=16) (n = 15) DIU did not indicate any significant difference between meth-
(n = 47) ods at maximal work intensity.
vo2 -, ml gkg-’ 1.1 -2.34b -4.5 -1 84b 2.7e
min’l
l
work intensity in the second test was probably greater duction of lactate. However, the decrease in maximal
than at the aerobic threshold. work load was less than the decrease in maximal blood
Dysfunction of thermoregulation probably plays an lactate in the experimental groups, possibly due to the
important role in the effects which we have described. exponential increase of blood lactate concentration at
The increase in core temperature during hypohydration the final stage of the exercise test.
has been attributed to plasma hyperosmolality and hy- In conclusion, it can be stated that, although the effects
povolemia (see DISCUSSION of ref. 25),which contributes of hypohydration are evident at low exercise intensities,
to a decrease in sweat rate response and cutaneous blood the full impact of hypohydration is felt at maximal work
flow. Diuretics have been reported to cause isosmotic intensity when cardiorespiratory reserves can no longer
hypovolemia (5, 21), which could elicit different physio- be tapped. A 3-5% weight loss by active exercise, diuret-
logical responses than a hyperosmotic hypovolemia (25). ics, or sauna bathing is unfavorable for the athlete pre-
It has also been shown that in hypohydrated subjects paring for competition. With respect to the effects of the
heat acclimatization decreases thermoregulatory and different treatments, measurements at maximal work
cardiovascular strain in a comfortable environment, but intensity indicated that the active exercise group did the
only cardiovascular strain decreases in hot environments best. Interaction of physical exercise and food and fluid
(25). Nadel (21) has shown that during hypohydration a restriction, which was allowed for the test groups, may
slow increase in skin blood flow begins at a higher core explain the different responses. On the other hand, the
temperature and then characteristically stops at a members in the active exercise group lost the weight in
slightly higher temperature. This thermoregulatory dys- 48 h, which allowed them more time than was available
function occurs at submaximal exercise levels and is for the subjects in the diuretic and sauna groups to
accompanied by hemoconcentration in those not accli- compensate for hypohydration-induced changes in phys-
mated to heat. Senay and Kok (26) have shown that iological responses.
hemoconcentration begins when the intensity of the
exercise exceeds about 50% of the aerobic threshold. This work was supported by a grant from the Finnish Olympic
Some differences noted after hypohydration are prob- Committee and by the Kuopio Institute of Exercise Medicine. We
express our gratitude to medical students Jarmo Heikkinen, Eija Hut-
ably not primary, e.g., the decrease in maximal lactate tunen, Raija Seuri, and Erkki Vehmanen, without whose able assistance
production. It is known that lactate production is reduced this work could not have been completed. Aija Finne performed the
when the muscle glycogen stores are diminished (18),but laboratory analyses and Raija Holopainen the graphical work. We also
in our biopsy samples glycogen content was not reduced. thank Prof. Osmo Hanninen and Dr. Esko Lansimies for reviewing the
Furthermore, there was no correlation between the level manuscript.
of glycogen in individual muscles and the maximal pro- Received 21 June 1982; accepted in final form 20 April 1984.
REFERENCES
1. BILJANI, R. L., AND K. N. SHARMA. Effect of dehydration and a total body density and its estimation from skinfold thickness:
few regimes of rehydration on human performance. Indian J. measurements on 481 men and women aged from 16 to 72 years.
Physiol. Pharmacol. 24: 255-266,198O. Br. J. Nutr. 32: 77-97, 1974.
2. BOCK, W., E. L. Fox, AND R. BOWERS. The effects of acute 14. GUTMANN, I., AND A. W. WAHLEFELD. L-(+)-lactate determina-
dehydration upon cardio-respiratory endurance. J. Sports Med. tion with lactate dehydrogenase and NAD. In: Methods of Enzy-
Phys. Fitness 7: 67-72, 1967. matic Analysis (2nd ed.), edited by H. U. Bergmeyer. New York:
3. Bosco, J. S., AND R. L. TERJUNG. Effects of progressive hypohy- Academic, 1974,1464 pp.
dration on maximal isometric strength. J. Sports Med. Phys. Fit- 15. HORSTMAN, D. H., AND S. M. HORVATH. Cardiovascular adjust-
ness 8: 81-86, 1968. ments to progressive dehydration. J. Appl. Physiol. 35: 501-504,
4. BUSKIRK, E. R., P. F. IAMPIETRO, AND D. E. BASS. Work perform- 1973.
ance after dehydration-effects of physical conditioning and heat 16. HOUSTON, M. E., D. A. MARRIN, H. J. GREEN, AND J. A. THOMP-
acclimatization. J. Appl. Physiol. 12: 189-194, 1958. SON. The effect of rapid weight loss on physiological functions in
5. CLAREMONT, A. D., D. L. COSTILL, W. FINK, AND P. VAN HANDEL. wrestlers. Phys. Sports. Med. 9: 73-78, 1981.
Heat tolerance following diuretic induced dehydration. 1Med. Sci. 17. HULTMAN, E. Muscle glycogen in man determined in needle biopsy
Sports 8: 239-243,1976. specimens- method and normal values. Stand. J. Clin. Lab. Invest.
6. COSTILL, D. L. Sweating-its composition and effects on body 19: 209-217,1967.
fluids. Ann. NY Acad. Sci. 301: 160-173,1977. 18. JACOBS, I. Lactate, muscle glycogen and exercise performance in
7. COSTILL, D. L., R.’ COT& AND W. FINK. Muscle water and electro- man. Acta Physiol. Stand. Suppl. 495: l-35,1981.
lytes following varied levels of dehydration in man. J. Appl. Physiol. 19. KINDERMANN, W., G. SIMON, AND J. KEUL. The significance of
40: 6-11,1976. the aerobic-anaerobic transition for the determination of work load
8. COSTILL, D.L., AND W. J. FINK. Plasma volume changes following intensities during endurance training. Eur. J. Appl. Physiol. Occup.
exercise and thermal dehydration. J. Appl. Physiol. 37: 521-525, Physiol. 42: 25-34,1979.
1974. 20. LOKE, J., D. A. MAHLER, AND J. A. VIRGULTO. Respiratory muscle
9. COSTILL, D. L., AND K. E. SPARKS. Rapid fluid replacement fatigue after marathon running. J. Appl. Physiol.: Respirat. Envi-
following thermal dehydration. J. Appl. Physiol. 34: 299-303,1973. ron. Exercise Physiol. 52: 821-824,1982.
10. CRAIG, F. N., AND E. G. CUMMINGS. Dehydration and muscular 21. NADEL, E. R. Circulatory and thermal regulations during exercise.
work. J. Appl. Physiol. 21: 670-674,1966. Federation Proc. 39: 1491-1497,198O.
11. DILL, D. B., AND D. L. COSTILL. Calculation of percentage changes 22. NIELSEN, B., R. KUBICA, A. BONNESEN, I. B. RASSMUSSEN, J.
in volumes of blood, plasma, and red cells in dehydration. J. Appl. STOKLOSA, AND B. WILK. Physical work capacity after dehydration
Physiol. 37: 247-248,1974. and hyperthermia: a comparison of the effect of exercise versus
12. DOSCHER, N. The effects of rapid weight loss upon the performance passive heating and sauna and diuretic dehydration. Stand. J.
of wrestlers and boxers, and upon the physical proficiency of college Sports Sci. 3: 2-10, 1981.
students. Res. Q. 15: 317-324, 1944. 23. RIBISL, P. M., AND W. G. HERBERT. Effects of rapid weight
13. DURNIN, J. V. G. A., AND J. WOMERSLEY. Body fat assessed from reduction and subsequent rehydration upon the physical working