Glibenclamide, a blocker of ATP‐sensitive potassium channels, reverses endotoxin‐induced hypotension in pig

G Vanelli, SN Hussain… - … Translation and Integration, 1995 - Wiley Online Library
G Vanelli, SN Hussain, G Aguggini
Experimental Physiology: Translation and Integration, 1995Wiley Online Library
In anaesthetized, mechanically ventilated, indomethacin‐treated pigs, we infused E. coli
endotoxin (LPS, 20 micrograms kg‐1 h‐1, iv). After 150 min of endotoxaemia, 10 mg kg‐1
glibenclamide (an ATP‐sensitive K+ channel antagonist) was administered iv over 5 min.
Vascular variables were recorded before (control), after 150 min of endotoxaemia and 5, 15
and 30 min after glibenclamide infusion. Glibenclamide transiently (within 5 min) increased
systemic arterial pressure, reduced by LPS administration, without an effect on cardiac …
In anaesthetized, mechanically ventilated, indomethacin‐treated pigs, we infused E. coli endotoxin (LPS, 20 micrograms kg‐1 h‐1, i.v.). After 150 min of endotoxaemia, 10 mg kg‐1 glibenclamide (an ATP‐sensitive K+ channel antagonist) was administered i.v. over 5 min. Vascular variables were recorded before (control), after 150 min of endotoxaemia and 5, 15 and 30 min after glibenclamide infusion. Glibenclamide transiently (within 5 min) increased systemic arterial pressure, reduced by LPS administration, without an effect on cardiac output. Our data indicate that ATP‐sensitive K+ channels may play a partial role in the vascular changes due to endotoxaemia.
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