S. Angermuller et al., ALTERATIONS OF NA-ATPASE ACTIVITY AFTER HYPOXIA AND REOXYGENATION IN THE PERFUSED-RAT-LIVER - AN ELECTRON-MICROSCOPIC CYTOCHEMICAL STUDY(,K+), Journal of hepatology, 22(5), 1995, pp. 565-575
Background/Aims: Using the cerium technique for ultrastructural cytoch
emical studies, Na+,K+-ATPase activity was investigated in hypoxic and
reoxygenated rat liver. Methods: In the control group, the livers mer
e perfused with oxygenated hemoglobin-free Krebs-Henseleit buffer for
1 h, For hypoxia (60 min), the flow rate of the perfusate was decrease
d and oxygen was replaced by nitrogen, For reoxygenation, the liver wa
s reperfused under oxygenated conditions for 5 min after 60 min of hyp
oxia. Results: In control livers, a strong Na+,K+-ATPase activity was
detected at the basolateral membrane of hepatocytes while the apical m
embrane forming the bile canaliculi did not display any staining. In h
ypoxic livers, Na+,K+-ATPase activity had ceased in the plasma membran
e of hepatocytes. In reoxygenated livers, Na+,K+-ATPase was rapidly re
activated in the basolateral hepatic membrane. The membrane of blebs g
enerated during the hypoxic phase also showed enzyme activity, In addi
tion, a striking accumulation of reaction product could be observed in
about 10% of the apical membranes lining the bile canaliculi, Conclus
ion: The results indicate a plasticity of the Na+,K+-ATPase in hypoxic
and reoxygenated rat liver.