Mj. Tipton et al., SUBSTRATE UTILIZATION DURING EXERCISE AND SHIVERING, European journal of applied physiology and occupational physiology, 76(1), 1997, pp. 103-108
It is generally assumed that exercise and shivering are analogous proc
esses with regard to substrate utilisation and that, as a consequence,
exercise can be used as a model for shivering. In the present study,
substrate utilisation during exercise and shivering at the same oxygen
consumption ((V) over dotO(2)) were compared. Following an overnight
fast, eight male subjects undertook a 2-h immersion in cold water, des
igned to evoke three different intensities of shivering. At least 1 we
ek later they undertook a 2-h period of bicycle ergometry during which
the exercise intensity was varied to match the (V) over dotO(2) recor
ded during shivering. During both activities hepatic glucose output (H
GO), the rate of glucose utilisation (Rd), blood glucose, plasma insul
in, free fatty acid (FFA) and beta-hydroxybutyrate (B-HBA) concentrati
ons were measured. The (V) over dotO(2) measured during the different
levels of shivering averaged 0.49 l . min(-1) (level 1: low), 0.6 l mi
n(-1) (level 2: low-moderate), and 0.9 l min(-1) (level 3: moderate),
and corresponded closely to the levels measured during exercise. HGO a
nd Rd were greater (P < 0.05) during exercise than during shivering at
the same (V) over dotO(2) (9.5% and 14.7%, respectively). The average
(SD) HGO during level 3 exercise was 3.0 (0.91) mg . k(-1) . min(-1)
compared to 2.76 (1.0) mg . kg(-1) . min(-1) during shivering. The val
ues for Rd were 3.06 (0.98) mg . kg(-1) . min(-1) during level 3 exerc
ise and 2.68 (0.82) mg . kg(-1) . min(-1) during shivering. Blood gluc
ose levels did not differ between conditions, averaging 5.4 (0.3) mmol
. l(-1) over all levels of shivering and 5.2 (0.3) mmol . l(-1) durin
g exercise. Plasma FFA and B-HBA were higher (P < 0.01) during shiveri
ng than during corresponding exercise (12.3% and 33.3%, respectively).
FFA averaged 0.61 (0.2) mmol . l(-1) over all levels of shivering and
0.47 (0.16) mmol . I-1 during exercise. The figures for B-HBA were 0.
44 (0.13) mmol . l(-1) during all levels of shivering and 0.32 (0.1) m
mol . l(-1) during exercise. Plasma insulin was higher (P < 0.05) duri
ng level 2 and 3 shivering compared to corresponding exercise; at thes
e levels the average value for plasma insulin was 95.9 (21.9) pmol . l
(-1) during shivering and 80.6 (16.1) pmol . l(-1) during exercise. On
the basis of the present findings it is concluded that, with regard t
o substrate utilisation, shivering and exercise of up to 2 h duration
should not be regarded as analogous processes.