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Effect of Trans-resveratrol on Rotenone-induced Cytotoxicity in Human Breast Adenocarcinoma Cells


Affiliations
1 A.R. Al-Jeraisy Chair for DNA Research, College of Science, King Saud University, Riyadh, Saudi Arabia
2 King Abdullah Institute for Nanotechnology, King Saud University, Riyadh, Saudi Arabia
3 Department of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia
4 Department of Microbiology, Faculty of Agricultural Sciences, AMU, Aligarh, India
     

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Rotenone, a botanical insecticide is known to cause apoptosis in various cell types. Trans-resveratrol, a natural phytophenol present in red grapes and wine, is also well documented for its antioxidant, anti-inflammatory, anti-mutagenic, and anticarcinogenic activities. Therefore, the present investigations were carried out to assess the protective effect of trans-resveratrol against rotenone-induced cell death in human breast adenocarcinoma (MCF-7) cells. MCF-7 cells were exposed with various concentrations of rotenone for 24 h, and the loss in percent cell viability was evaluated by MTT [3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide] and neutral red uptake (NRU) assays. A significant decrease in percent cell viability in MCF-7 cells was observed at 50 µM and above concentrations of rotenone, as compared to untreated control. Furthermore, various concentrations (5, 10, and 25 µΜ) of trans-resveratrol were used to see its protective role on cell viability in rotenone-induced cell death in MCF-7 cells. Pre- or post- treatment of trans-resveratrol for 24 h was given to the cells. The data exhibited a significant dose dependent increase in the percent cell viability under pre- and post-treatment conditions. However, post-treatment of trans-resveratrol for 24 h after rotenone exposure to the cells was relatively less effective. Overall, the results suggest that trans-resveratrol significantly protects MCF-7 cells from rotenone-induced cell death. This model can be used as an effective and economical alternative to animal models for screening the antioxidant activity of a variety of natural compounds/drugs.

Keywords

Cytotoxicity, MCF--7 cells, rotenone, trans-resveratrol
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  • Effect of Trans-resveratrol on Rotenone-induced Cytotoxicity in Human Breast Adenocarcinoma Cells

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Authors

M. A. Siddiqui
A.R. Al-Jeraisy Chair for DNA Research, College of Science, King Saud University, Riyadh, Saudi Arabia
Q. Saquib
A.R. Al-Jeraisy Chair for DNA Research, College of Science, King Saud University, Riyadh, Saudi Arabia
M. Ahamed
King Abdullah Institute for Nanotechnology, King Saud University, Riyadh, Saudi Arabia
J. Ahmad
A.R. Al-Jeraisy Chair for DNA Research, College of Science, King Saud University, Riyadh, Saudi Arabia
A. A. Al-Khedhairy
Department of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia
F. M. Abou-Tarboush
Department of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia
J. Musarrat
Department of Microbiology, Faculty of Agricultural Sciences, AMU, Aligarh, India

Abstract


Rotenone, a botanical insecticide is known to cause apoptosis in various cell types. Trans-resveratrol, a natural phytophenol present in red grapes and wine, is also well documented for its antioxidant, anti-inflammatory, anti-mutagenic, and anticarcinogenic activities. Therefore, the present investigations were carried out to assess the protective effect of trans-resveratrol against rotenone-induced cell death in human breast adenocarcinoma (MCF-7) cells. MCF-7 cells were exposed with various concentrations of rotenone for 24 h, and the loss in percent cell viability was evaluated by MTT [3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide] and neutral red uptake (NRU) assays. A significant decrease in percent cell viability in MCF-7 cells was observed at 50 µM and above concentrations of rotenone, as compared to untreated control. Furthermore, various concentrations (5, 10, and 25 µΜ) of trans-resveratrol were used to see its protective role on cell viability in rotenone-induced cell death in MCF-7 cells. Pre- or post- treatment of trans-resveratrol for 24 h was given to the cells. The data exhibited a significant dose dependent increase in the percent cell viability under pre- and post-treatment conditions. However, post-treatment of trans-resveratrol for 24 h after rotenone exposure to the cells was relatively less effective. Overall, the results suggest that trans-resveratrol significantly protects MCF-7 cells from rotenone-induced cell death. This model can be used as an effective and economical alternative to animal models for screening the antioxidant activity of a variety of natural compounds/drugs.

Keywords


Cytotoxicity, MCF--7 cells, rotenone, trans-resveratrol