Cl. Overend et al., Altered cardiac sarcoplasmic reticulum function of intact myocytes of rat ventricle during metabolic inhibition, CIRCUL RES, 88(2), 2001, pp. 181-187
Changes in the behavior of the sarcoplasmic reticulum (SR) in rat ventricul
ar myocytes were investigated under conditions of metabolic inhibition usin
g laser-scanning confocal microscopy to measure intracellular Ca2+ and the
perforated patch-clamp technique to measure SR Ca2+ content. Metabolic inhi
bition had several effects on SR function, including reduced frequency of s
pontaneous releases of Ca2+ (sparks and waves of Ca2+-induced Ca2+ release)
, increased SR Ca2+ content (79.4+/-5.7 to 115.2+/-6.6 mu mol/L cell volume
[mean+/-SEM; P<0.001]), and, after a wave of Ca2+ release, slower reuptake
of Ca2+ into the SR (rate constant of fall of Ca2+ reduced from 8.5+/-1.1
s(-1) in control to 5.2+/-0.4 s(-1) in metabolic inhibition [P<0.01]). Inhi
bition of L-type Ca2+ channels with Cd2+ (100 mu mol/L) did not reproduce t
he effects of metabolic inhibition on spontaneous Ca2+ sparks. These result
s are evidence of inhibition of both Ca2+ release and reuptake mechanisms.
Reduced frequency of release could be attributable to either of these effec
ts, but the increased SR Ca2+ content at the time of reduced frequency of s
pontaneous release of Ca2+ shows that the dominant effect of metabolic inhi
bition is to inhibit release of Ca2+ from the SR, allowing the accumulation
of greater than normal amounts of Ca2+ In the context of ischemia, this ex
tra accumulation of Ca2+ would present a risk of potentially arrhythmogenic
, spontaneous release of Ca2+ on reperfusion of the tissue.