ABSTRACT
It has been suggested that venous ischemia is more injurious to tissue viability than
is arterial ischemia of equivalent duration. The precise mechanism of tissue damage
due to venous ischemia is still not well-determined. Current research has shown that
it is multifactorial, and that lipid peroxides, prostanoid metabolism, and a free
radical mechanism are the major contributors. Vitamins A and E are lipid-soluble vitamins
that have been suggested to be successful in the treatment of arterial ischemia/reperfusion
injury due to their antioxidant properties. In the present study, the authors examined
the protective effects of vitamins A and E pretreatment on reperfusion injury induced
by venous occlusion of rat epigastric island flaps based on an epigastric artery and
vein pedicle.
In the first part of the study, to determine critical ischemia time, epigastric island
skin flaps (3 × 6 cm) were elevated on their vascular pedicles in 40 male Sprague
Dawley rats. Total venous occlusion of the skin flap was produced by ligating all
draining veins and clamping the epigastric vein. Arterial inflow was left intact.
Rats were randomly assigned to five groups (n=8) for 2, 5, 7, 9, and 10 hr of venous
ischemia. Despite the occurrence of widespread reperfusion injury, reflow was established
(p<0.005) at 9 hr. In the second part of the study, 20 rats were randomly divided into
four groups (n=5). The effects of vitamins A and E following 9 hr ischemia/reperfusion
injury were examined. Rats were pretreated with vitamin E, vitamin A and vitamins
A+E for 5 days. At the end of the fifth day, each rat had undergone an epigastric
island skin flap and venous occlusion, as described above. Mean surviving flap area
(percent) and plasma lipid peroxides (TBARs), total thiol content (t-SH), glutathione
peroxidase (Gpx), and superoxide dismutase (SOD) were determined for each rat.
Results suggest that, in the prevention of venous ischemia/reperfusion injury, vitamin
A and vitamin E are not effective when used as single agents; however, when used in
combination, they significantly increase surviving flap area by a synergistic effect.
KEYWORD
Venous ischemia reperfusion injury - vitamin A - vitamin E