J. Lannergren et al., Vacuole formation in fatigued skeletal muscle fibres from frog and mouse: effects of extracellular lactate, J PHYSL LON, 526(3), 2000, pp. 597-611
1. Isolated, living muscle fibres from either Xenopus or mouse were observe
d in a confocal microscope and t-tubules were visualized with sulforhodamin
e B. Observations were made before and after fatiguing stimulation. In addi
tion, experiments were performed on fibres observed in an ordinary light mi
croscope with dark-field illumination
2. In Xenopus fibres, recovering after fatigue, t-tubules started to show d
ilatations 2-5 min post-fatigue. These swellings increased in size over the
next 10-20 min to form vacuoles. After 2-3 h of recovery the appearance of
the fibres was again normal and force production, which had been markedly
depressed 10-40 min post-fatigue, was close to control. Vacuoles were not o
bserved in mouse fibres, fatigued with the same protocol and allowed to rec
over.
3. In Xenopus fibres, fatigued in normal Ringer solution and allowed to rec
over in Ringer solution with 30-50 mM L-lactate substituting for chloride (
lactate-Ringer), the number and size of vacuoles were markedly reduced. Als
o, force recovery was significantly faster. Replacement of chloride by meth
yl sulphate or glucuronate had no effect on vacuolation.
4. Resting Xenopus fibres exposed to 50 mar lactate-Ringer and transferred
to normal Ringer solution displayed vacuoles within 5-10 min, but to a smal
ler extent than after fatigue. Vacuolation was not associated with marked f
orce reduction.
5. Mouse fibres, fatigued in 50 mM lactate-Tyrode (L-lactate substituting f
or chloride in Tyrode solution) and recovering in normal Tyrode solution, d
isplayed vacuoles for a limited period post-fatigue. Vacuolation had no eff
ect on force production.
6. The results are consistent with the view that lactate, formed during fat
igue, is transported into the t-tubules where it attracts water and causes
t-tubule swelling and vacuolation. This vacuolation may be counteracted in
vivo due to a gradual extracellular accumulation of lactate during fatigue.