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Département de Kinésiologie, Université de Montréal and Research Centre of the Centre Hospitalier de l'Université de Montréal, Montreal, Quebec, Canada H3C 3J7
The goal of the present experiment was to
measure the volume of the different compartments in liver of exercised
rats and to get some insights into the appropriate working of the
hepatic function following exercise. Hence, livers from male rats were isolated and perfused after treadmill exercise or rest. This procedure was performed on rats that were overnight semifasted (50% food restriction) or well fed. To evaluate the hepatocyte cell volume, the
multiple-indicator dilution curve technique was used after 40 min of
perfusion. Radioactive tracers for red blood cells, sucrose, and water
were used to measure liver vascular space, liver interstitial space,
and water cellular space, respectively. The hepatocyte function was
assessed by taurocholate and propanolol clearance. Oxygen consumption,
intrahepatic resistance, bile secretion, and lactate dehydrogenase
release estimated liver viability. Liver viability and hepatocyte
function were not changed following exercise either in the fed or in
the semifasted animals. As expected, liver glycogen levels were
significantly (P < 0.01) reduced in
the food-restricted rats. Consequently, liver glycogen levels following
exercise were decreased significantly
(P < 0.01) only in the fed rats.
Despite this, exercise decreased the hepatocyte water space in both
food-restricted and fed groups (~15%;
P < 0.01) without altering the
sinusoidal and interstitial space. The present data show that acute
exercise decreased the hepatocyte volume and that this volume change is not entirely linked to a decrease in hepatic glycogen level.
cell volume; liver viability; liver perfusion; hepatic clearance
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