Increased muscle glycogen content is associated with increased capacity torespond to T-system depolarisation in mechanically skinned skeletal musclefibres from the rat
M. Barnes et al., Increased muscle glycogen content is associated with increased capacity torespond to T-system depolarisation in mechanically skinned skeletal musclefibres from the rat, PFLUG ARCH, 442(1), 2001, pp. 101-106
The ability of mechanically skinned muscle fibres from the rat to respond t
o T-system depolarisation was studied ill relation to muscle glycogen conte
nt. Muscle glycogen was altered by incubating extensor digitorum longus (ED
L) muscles in Krebs solution without glucose or in Krebs solution with gluc
ose (10 mM) and insulin (20 U(.)1(-1)). The glycogen content of muscles sto
red without glucose was rather stable between 30 and 480 min (11.27 +/-0.39
mu mol(.)g(-1)), while the muscles stored with glucose and insulin maintai
ned an elevated and stable level of glycogen (23.48 +/-1.67 mu mol.g(-1)) b
etween 100 and 360 mill. Single mechanically skinned fibres from paired mus
cles, incubated in either glucose-free Krebs or in Krebs with glucose and i
nsulin, were subjected to cycles of T-system depolarisation-repolarisation
in a controlled environment (8 mM ATP, 10 mM creatine phosphate, 1 mM Mg2+,
pH 7.10) and the force response was monitored until the force had declined
to 50% of the maximum response (50% rundown). Fibres from muscles with a h
igher glycogen content reached 50% rundown after a larger number of depolar
isations and displayed consistently larger average response capacity values
, calculated as the sum of the force responses to 50% rundown divided by th
e maximum Ca2+-activated force response in that fibre. Thus skinned fibres
originating from muscles with a higher glycogen content have an increased a
bility to respond to T-system depolarisation when the effect of metabolite
accumulation is minimised and the function of glycogen acting as an energy
source is by-passed. This provides direct support to the hypothesis that gl
ycogen has a protective role in maintaining fibre excitability.