H. Matsumoto et al., SMOOTH-MUSCLE STRETCH-ACTIVATED PHOSPHOLIPASE-C ACTIVITY, American journal of physiology. Cell physiology, 37(2), 1995, pp. 458-465
Rabbit aortic muscles were stretched from a holding length of 0.6 maxi
mum length (L(max)) to lengths as great as 1.0 L(max) and the new leng
th maintained. When muscles were stretched to 1.0 L(max) inositol 1,4,
5-trisphosphate [Ins(1,4,5)P-3] and inositol 1,4-bisphosphate [Ins(1,4
)P-2] contents were increased at 375 ms (uncorrected for freezing time
) poststretch to 209 +/- 27 and 139.8 +/- 12% (SE), respectively, of c
ontrol values. Increases in Ins(1,4,5)P-3 and Ins(1,4)P-2 contents rea
ched an apparent maximum at similar to 500 ms, i.e., to 243.7 +/- 15.8
and 180.9 +/- 16.2% of control, and were decreased to near control le
vels at 1,700 ms poststretch. The stretch threshold for phospholipase
C (PLC) activation was 0.85 L(max). The latency to onset of PLC activa
tion, correcting for the time for freezing, was 275 to 375 ms. Maximal
PLC activity was 91 pmol.s(-1).100 nmol total lipid P-i(-1), which co
rresponded to 10% of total phosphatidylinositol bisphosphate being hyd
rolyzed per second. The mechanism of stretch-activated PLC activity in
volved influx of Ca2(+) via gadolinium-sensitive ion channels, but not
via nifedipine-sensitive ion channels.