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Inapurapu, Santhipriya, Rao Kudle, Karunakar, Bodiga, Sreedhar, Lakshmi Bodiga, Vijaya. (1395). Cisplatin cytotoxicity is dependent on mitochondrial respiration in Saccharomyces cerevisiae. , 20(1), 83-89. doi: 10.22038/ijbms.2017.8099
Santhipriya Inapurapu; Karunakar Rao Kudle; Sreedhar Bodiga; Vijaya Lakshmi Bodiga. "Cisplatin cytotoxicity is dependent on mitochondrial respiration in Saccharomyces cerevisiae". , 20, 1, 1395, 83-89. doi: 10.22038/ijbms.2017.8099
Inapurapu, Santhipriya, Rao Kudle, Karunakar, Bodiga, Sreedhar, Lakshmi Bodiga, Vijaya. (1395). 'Cisplatin cytotoxicity is dependent on mitochondrial respiration in Saccharomyces cerevisiae', , 20(1), pp. 83-89. doi: 10.22038/ijbms.2017.8099
Inapurapu, Santhipriya, Rao Kudle, Karunakar, Bodiga, Sreedhar, Lakshmi Bodiga, Vijaya. Cisplatin cytotoxicity is dependent on mitochondrial respiration in Saccharomyces cerevisiae. , 1395; 20(1): 83-89. doi: 10.22038/ijbms.2017.8099

Cisplatin cytotoxicity is dependent on mitochondrial respiration in Saccharomyces cerevisiae

Iranian Journal of Basic Medical Sciences
مقاله 13، دوره 20، شماره 1، فروردین 2017، صفحه 83-89    اصل مقاله (1.09 M)
نوع مقاله: Original Article
شناسه دیجیتال (DOI): 10.22038/ijbms.2017.8099
نویسندگان
Santhipriya Inapurapu1؛ Karunakar Rao Kudle2؛ Sreedhar Bodiga3؛ Vijaya Lakshmi Bodiga* 1
1Institute of Genetics & Hospital for Genetic Diseases, Osmania University, Hyderabad, Telangana, India-500016
2Department of Biochemistry, Osmania University, Hyderabad, Telangana, India- 500007
3Department of Biochemistry, Kakatiya University, Warangal, Telangana, India -506009
چکیده
Objective(s): To understand the role of mitochondrial respiration in cisplatin sensitivity, we have employed wild-type and mitochondrial DNA depleted Rho0 yeast cells.
Materials and Methods: Wild type and Rho0 yeast cultured in fermentable and non-fermentable sugar containing media, were studied for their sensitivity against cisplatin by monitoring growth curves, oxygen consumption, pH changes in cytosol/mitochondrial compartments, reactive oxygen species production and respiratory control ratio.
Results: Wild-type yeast grown on glycerol exhibited heightened sensitivity to cisplatin than yeast grown on glucose. Cisplatin (100 μM), although significantly reduced the growth of wild- type cells, only slightly altered the growth rate of Rho0 cells. Cisplatin treatment decreased both pHcyt and pHmit to a similar extent without affecting the pH difference. Cisplatin dose-dependently increased the oxidative stress in wild-type, but not in respiration-deficient Rho0 strain. Cisplatin decreased the respiratory control ratio.
Conclusion: These results suggest that cisplatin toxicity is influenced by the respiratory capacity of the cells and the intracellular oxidative burden. Although cisplatin per se slightly decreased the respiration of yeast cells grown in glucose, it did not disturb the mitochondrial chemiosmotic gradient.
کلیدواژه‌ها
Cisplatin؛ Mitochondria؛ Oxidative phosphorylation Respiration؛ Rho0
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