previously, tetrabutylhydroperoxide (t-BOOH) shrinks hepatocytes by release
of cellular K+, The hyperpolarization, the increase of K+ selectivity, and
the Ba2+ sensitivity of K+ release have been taken as evidence of activati
on of K+As shown previously, tetrabutylhydroperoxide (t-BOOH) shrinks hepat
ocytes by release of cellular K+, The hyperpolarization, the increase of K selectivity, and the Ba2+ sensitivity of K+ release have been taken as evi
dence of activation of K+ channels, To further define the ion channels invo
lved, patch-clamp studies have been performed on rat hepatocytes. The data
show that 0.1 mmol/l t-BOOH inhibits an inwardly rectifying K+ channel and
simultaneously activates a 35-pS K+ channel, It is suggested that the activ
ation of the latter channel population contributes to the observed KC relea
se of hepatocytes following exposure to t-BOOH. channels, To further define
the ion channels involved, patch-clamp studies have been performed on rat
hepatocytes. The data show that 0.1 mmol/l t-BOOH inhibits an inwardly rect
ifying K+ channel and simultaneously activates a 35-pS K+ channel, It is su
ggested that the activation of the latter channel population contributes to
the observed KC release of hepatocytes following exposure to t-BOOH.