Muscle fiber viability, a novel method for the fast detection of ischemic muscle injury in rats

• Published in: PloS one 2014-01, Vol.9 (1), p.e84783-e84783
• Main Authors: Turóczi, Zsolt, Arányi, Péter, Lukáts, Ákos, Garbaisz, Dávid, Lotz, Gábor, Harsányi, László, Szijártó, Attila
• Format: Article
• Language: English
• Subjects: Abdomen; Animals; Aorta; Biology; Clinical medicine; Damage assessment; Diagnostic systems; Experiments; Glutaraldehyde; Injuries; Ischemia; Ischemia - pathology; Ischemia - physiopathology; Laboratory animals; Male; Medicine; Methods; Microcirculation; Morphology; Muscle Fibers, Skeletal - pathology; Muscle Fibers, Skeletal - ultrastructure; Muscles; Musculoskeletal system; NADH; NADH Tetrazolium Reductase - metabolism; Nicotinamide adenine dinucleotide; Occlusion; Perfusion; Rats; Rats, Wistar; Reductase; Reperfusion; Reperfusion Injury - pathology; Reperfusion Injury - physiopathology; Rodents; Surgery; Systematic review; Tissue Survival; Viability
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0084783

Acute lower extremity ischemia is a limb- and life-threatening clinical problem. Rapid detection of the degree of injury is crucial, however at present there are no exact diagnostic tests available to achieve this purpose. Our goal was to examine a novel technique - which has the potential to accurately assess the degree of ischemic muscle injury within a short period of time - in a clinically relevant rodent model. Male Wistar rats were exposed to 4, 6, 8 and 9 hours of bilateral lower limb ischemia induced by the occlusion of the infrarenal aorta. Additional animals underwent 8 and 9 hours of ischemia followed by 2 hours of reperfusion to examine the effects of revascularization. Muscle samples were collected from the left anterior tibial muscle for viability assessment. The degree of muscle damage (muscle fiber viability) was assessed by morphometric evaluation of NADH-tetrazolium reductase reaction on frozen sections. Right hind limbs were perfusion-fixed with paraformaldehyde and glutaraldehyde for light and electron microscopic examinations. Muscle fiber viability decreased progressively over the time of ischemia, with significant differences found between the consecutive times. High correlation was detected between the length of ischemia and the values of muscle fiber viability. After reperfusion, viability showed significant reduction in the 8-hour-ischemia and 2-hour-reperfusion group compared to the 8-hour-ischemia-only group, and decreased further after 9 hours of ischemia and 2 hours of reperfusion. Light- and electron microscopic findings correlated strongly with the values of muscle fiber viability: lesser viability values represented higher degree of ultrastructural injury while similar viability results corresponded to similar morphological injury. Muscle fiber viability was capable of accurately determining the degree of muscle injury in our rat model. Our method might therefore be useful in clinical settings in the diagnostics of acute ischemic muscle injury.