Tp. Whetzel et al., THE EFFECT OF ISCHEMIC PRECONDITIONING ON THE RECOVERY OF SKELETAL-MUSCLE FOLLOWING TOURNIQUET ISCHEMIA, Plastic and reconstructive surgery, 100(7), 1997, pp. 1767-1775
It has been well documented that ischemic preconditioning limits ische
mic-reperfusion injury in cardiac muscle, but the ability of ischemic
preconditioning to limit skeletal muscle injury is less clear. Previou
s reports have emphasized the beneficial effects of ischemic precondit
ioning on skeletal muscle structure and capillary perfusion but have n
ot evaluated muscle function. We investigated the morphologic and func
tional consequences of ischemic preconditioning, followed by a 2-hour
period of tourniquet ischemia on muscles in the rat hindlimb. The 2-ho
ur ischemia was imposed without preconditioning, or was preceded by th
ree brief (10 minutes on/10 minutes off) preischemic conditioning inte
rvals. We compared muscle morphology, isometric contractile function,
and muscle fatigue proper ties in predominantly fast-twitch, tibialis
anterior muscles 3 (n = 8) and 7 (n = 8) days after ischemia-reperfusi
on. Two hours of ischemia, followed by reperfusion, results in a 20 pe
rcent reduction of muscle mass (p < 0.05) and a 33 percent reduction i
n tetanic tension (p < 0.05) when compared with controls (n = 8) at 3
days. The same protocol, when preceded by ischemic preconditioning, re
sults in similar decreases in muscle mass and contractile function. Ne
uromuscular transmission was also impaired in both ischemic groups 7 d
ays after ischemia. Nerve-evoked maximum tetanic tension was 69 percen
t of the tension produced by direct muscle stimulation in the ischemia
group and 65 percent of direct tension in the ischemic preconditionin
g/ischemia group. In summary, ischemic preconditioning, using the same
protocol reported to be effective in limiting infarct size in porcine
muscle, had no significant benefit in limiting injury or improving re
covery in the ischemic rat tibialis anterior. The value of ischemic pr
econditioning in reducing imposed ischemic-repel fusion-induced functi
onal deficits in skeletal muscle remains to be demonstrated.