{Reference Type}: Journal Article
{Title}: Protective role of alpha-lipoic acid against rhabdomyolysis-induced acute kidney injury in rats.
{Author}: Nouripour S;Mehri S;Aminifard T;Hosseini A;Khajavi Rad A;Jafarian A;Hosseinzadeh H;
{Journal}: Iran J Basic Med Sci
{Volume}: 27
{Issue}: 8
{Year}: 2024
{Factor}: 2.532
{DOI}: 10.22038/IJBMS.2024.74864.16252
{Abstract}: <B>UNASSIGNED: </B>Rhabdomyolysis, a potentially life-threatening condition, occurs when myoglobin is released from damaged muscle cells, leading to acute kidney injury (AKI). Alpha lipoic acid (ALA), an organosulfur compound known for its anti-oxidant and anti-inflammatory properties, was examined in this study for its potential impact on rhabdomyolysis-induced AKI in rats.<BR><B>UNASSIGNED: </B>Six groups of rats were included in the study, with each group consisting of six rats (n=6): Control, rhabdomyolysis, rhabdomyolysis treated with different doses of ALA (5, 10, and 20 mg/kg), and ALA alone (20 mg/kg) groups. Rhabdomyolysis was induced by intramuscular injection of glycerol on the first day of the experiment, while ALA was administered intraperitoneally for four consecutive days. Renal function parameters, oxidative stress markers, and histological changes in the kidneys were evaluated. Western blot analysis was performed to measure the levels of neutrophil gelatinase-associated lipocalin (NGAL) and tumor necrosis factor-alpha (TNF-α) proteins.<BR><B>UNASSIGNED: </B>A significant increase in serum urea, creatinine, renal malondialdehyde, NGAl, and TNF-α protein levels was observed in glycerol-injected rats. In addition, a significant decrease in glutathione was recorded. Compared to the rhabdomyolysis group, treatment with ALA recovered kidney histological and biochemical abnormalities.<BR><B>UNASSIGNED: </B>Results suggest that rhabdomyolysis-induced AKI is associated with increased oxidative stress and inflammation. Treatment with ALA improved kidney histological abnormalities and reduced oxidative stress markers in rats. Therefore, ALA may have a potential protective effect against rhabdomyolysis-induced AKI.