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Oxygen tension-independent protection against hypoxic cell killing in rat liver by low sodium
Author(s) -
Andrea Ferrigno,
Laura Giuseppina Di Pasqua,
Clarissa Berardo,
Veronica Siciliano,
Plinio Richelmi,
Mariapia Vairetti
Publication year - 2017
Publication title -
european journal of histochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.754
H-Index - 42
eISSN - 2038-8306
pISSN - 1121-760X
DOI - 10.4081/ejh.2017.2798
Subject(s) - trypan blue , chemistry , hypoxia (environmental) , sodium , tbars , staining , oxygen , microbiology and biotechnology , biochemistry , cell , biology , pathology , lipid peroxidation , medicine , oxidative stress , organic chemistry

The role of Na+ in hypoxic injury was evaluated by a time-course analysis of damage in isolated livers perfused with N2-saturated buffer containing standard (143 mM) or low (25 mM) Na+ levels. Trypan blue uptake was used to detect non-viable cells. Under hypoxia with standard-Na+, trypan blue uptake began at the border between pericentral areas and periportal regions and increased in the latter zone; using a low-Na+ buffer, no trypan blue zonation occurred but a homogenous distribution of dye was found associated with sinusoidal endothelial cell (SEC) staining. A decrease in hyaluronic acid (HA) uptake, index of SEC damage, was observed using a low-Na+ buffer. A time dependent injury was confirmed by an increase in LDH and TBARS levels with standard-Na+ buffer. Using low-Na+ buffer, SEC susceptibility appears elevated under hypoxia and hepatocytes was protected, in an oxygen independent manner.

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