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Center for Perinatal Biology, School of Medicine, Loma Linda University, Loma Linda, California 92350; and Department of Pediatrics, School of Medicine, University of Auckland, Auckland, New Zealand
Received 19 May 1995; accepted in final form 6 August 1996.
Ball, Karen T., Tania R. Gunn, Peter D. Gluckman, and Gordon
G. Power. Suppressive action of endogenous adenosine on ovine
fetal nonshivering thermogenesis. J. Appl.
Physiol. 81(6): 2393-2398, 1996.
Nonshivering
thermogenesis is not initiated when the fetal sheep is cooled in utero
but appears to require the removal of an inhibitor of placental origin
at birth. To test whether adenosine is such an inhibitor, we examined
the effect of the adenosine antagonist theophylline on the initiation
of nonshivering thermogenesis during sequential cooling, ventilation, and umbilical cord occlusion in utero. Theophylline (18 mg/kg bolus and
0.6 mg · kg
1 · min
1
thereafter) was infused for 90 min before and 90 min after cord occlusion. Theophylline enhanced the nonshivering thermogenic free
fatty acid (FFA) and glycerol responses before cord occlusion, raising
FFA concentrations 99% to 415 ± 60 µeq/l
(P < 0.01) and glycerol levels 87%
to 526 ± 135 µmol/l (P < 0.05). These FFA (P < 0.001) and
glycerol (P < 0.05) concentrations
were significantly greater than the corresponding period during the
birth-simulation control. Umbilical cord occlusion did not alter FFA
levels but induced a 41% rise in glycerol concentrations to 774 ± 203 µmol/l (P < 0.05). The
increases in nonshivering thermogenic indexes after the administration
of the adenosine-receptor antagonist suggest that the quiescent state
of ovine fetal brown adipose tissue may result, in part, from the tonic
inhibitory actions of adenosine and that a decrease in adenosine
concentrations enhances nonshivering thermogenesis. However, the
further rise after umbilical cord occlusion suggests that at least one
other inhibitor of placental origin inhibits nonshivering thermogenesis
before birth.
brown adipose tissue; placenta; A1-receptor antagonist
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