A. Kharbangar et al., Effect of cisplatin on mitochondrial protein, glutathione, and succinate dehydrogenase in Dalton lymphoma-bearing mice, CELL BIOL T, 16(6), 2000, pp. 363-373
Cisplatin treatment of tumor-bearing mice resulted a significant decrease o
f protein in the tissues studied (liver, kidney, and Dalton lymphoma) and a
lso in their mitochondrial fractions. As compared to respective tissues, th
e protein decrease was noted to be more conspicuous in their mitochondrial
fractions. Similarly, mitochondrial glutathione also decreased significantl
y in the tissues. However, succinate dehydrogenase activity was selectively
decreased in the kidney and Dalton lymphoma cells, whereas in liver it rem
ained almost unchanged. An increase in serum urea concentration and kidney
mitochondrial lipid peroxidation was also observed after cisplatin treatmen
t. It is suggested that the cisplatin-induced biochemical changes in mitoch
ondria involving mitochondrial protein, glutathione, and succinate dehydrog
enase could be the important potent cellular sites contributing to toxicity
/cytotoxicity after cisplatin treatment.