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Department of Physiology, McGill University, Montreal, Quebec, Canada H3G 1Y6
Received 14 January 1997; accepted in final form 21 April 1997.
Saiki, Chikako, and Jacopo P. Mortola. Effect of
2,4-dinitrophenol on the hypometabolic response to hypoxia of conscious adult rats. J. Appl. Physiol. 83(2):
537-542, 1997.
During acute hypoxia, a hypometabolic response is
commonly observed in many newborn and adult mammalian species. We
hypothesized that, if hypoxic hypometabolism were entirely a regulated
response with no limitation in O2
availability, pharmacological uncoupling of the oxidative
phosphorylation should raise O2
consumption
(
O2) by
similar amounts in hypoxia and normoxia. Metabolic, ventilatory, and
cardiovascular measurements were collected from conscious rats in air
and in hypoxia, both before and after intravenous injection of the
mitochondrial uncoupler 2,4-dinitrophenol (DNP). In hypoxia (10%
O2 breathing, 60% arterial
O2 saturation),
O2, as measured by an
open-flow technique, was less than in normoxia (~80%). Successive
DNP injections (6 mg/kg, 4 times) progressively increased
O2 in both normoxia and
hypoxia by similar amounts. Body temperature slightly increased in
normoxia, whereas it did not change in hypoxia. The DNP-stimulated
O2 during hypoxia could
even exceed the control normoxic value. A single DNP injection (17 mg/kg iv) had a similar metabolic effect; it also resulted in
hypotension and a drop in systemic vascular resistance. We conclude
that pharmacological stimulation of
O2 counteracts the
O2 drop determined by
hypoxia and stimulates
O2
not dissimilarly from normoxia. Hypoxic hypometabolism is likely to
reflect a regulated process of depression of thermogenesis, with no
limitation in cellular O2
availability.
cellular hypoxia; hypoxic ventilatory response; oxidative phosphorylation; oxygen consumption; uncoupling agents
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