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

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Authors

  • A.R. Al-Jeraisy Chair for DNA Research, College of Science, King Saud University, Riyadh ,SA
  • A.R. Al-Jeraisy Chair for DNA Research, College of Science, King Saud University, Riyadh ,SA
  • King Abdullah Institute for Nanotechnology, King Saud University, Riyadh ,SA
  • A.R. Al-Jeraisy Chair for DNA Research, College of Science, King Saud University, Riyadh ,SA
  • Department of Zoology, College of Science, King Saud University, Riyadh ,SA
  • Department of Zoology, College of Science, King Saud University, Riyadh ,SA
  • Department of Microbiology, Faculty of Agricultural Sciences, AMU, Aligarh ,IN

Keywords:

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

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 µÎœ) 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.

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Published

2018-05-18

How to Cite

Siddiqui, M. A., Saquib, Q., Ahamed, M., Ahmad, J., Al-Khedhairy, A. A., Abou-Tarboush, F. M., & Musarrat, J. (2018). Effect of <i>Trans</i>-resveratrol on Rotenone-induced Cytotoxicity in Human Breast Adenocarcinoma Cells. Toxicology International, 18(2), 105–110. Retrieved from http://www.informaticsjournals.com/index.php/toxi/article/view/21253
Received 2018-05-17
Accepted 2018-05-17
Published 2018-05-18

 

References

Lee J, Huang MS, Yang IC, Lai TC, Wang JL, Pang VF, et al. Essential roles of caspases and their upstream regulators in rotenone-induced apoptosis. Biochem Biophys Res Commun 2008;371:33-8.

Fields PG, Arnason JT, Philogene BJ, Aucoin RR, Morand P, Soucy-Breau C. Phototoxins as Insecticides and Natural Plant Defenses. Mem ent Soc Can 1991;IS9:29-38

Radad K, Rausch WD, Gille G. Rotenone induces apoptosis in MCF-7 human breast cancer cell-mediated ROS through JNK and p38 signaling. Neurochem Int 2006;49:379-86.

Deng YT, Huang HC, Lin JK. Rotenone induces apoptosis in MCF-7 human breast cancer cell-mediated ROS through JNK and p38 signaling. Mol Carcinog 2010;49:141-51.

Wang G, Qi C, Fan GH, Zhou HY, Chen SD. PACAP protects neuronal differentiated PC12 cells against the neurotoxicity induced by a mitochondrial complex I inhibitor, rotenone. FEBS Lett 2005;579:4005-11.

Armstrong JS, Hornung B, Lecane P, Jones DP, Knox SJ. Rotenoneinduced G2/M cell cycle arrest and apoptosis in a human B lymphoma cell line PW. Biochem Biophys Res Commun 2001;289:973-8.

Tada-Oikawa S, Hiraku Y, Kawanishi M, Kawanishi S. Mechanism for generation of hydrogen peroxide and change of mitochondrial membrane potential during rotenone-induced apoptosis. Life Sci 2003;73:3277-88.

Chung WG, Miranda CL, Maier CS. Epigallocatechin gallate (EGCG) potentiates the cytotoxicity of rotenone in neuroblastoma SH-SY5Y cells. Brain Res 2007;1176:133-42.

Siddiqui MA, Kashyap MP, Khanna VK, Yadav S, Al-Khedhairy AA, Musarrat J, et al. Association of dopamine DA-D2 receptor in rotenone-induced cytotoxicity in PC12 cells. Toxicol Ind Health 2010;26:533-42.

Miller NJ, Rice-Evans CA. Antioxidant activity of resveratrol in red wine. Clin Chem 1995;41:1789.

Ozkan OV, Yuzbasioglu MF, Ciralik H, Kurutas EB, Yonden Z, Aydin M, et al. Resveratrol, a natural antioxidant, attenuates intestinal ischemia/reperfusion injury in rats. Tohoku J Exp Med 2009;218:251-8.

Oh YC, Kang OH, Choi JG, Chae HS, Lee YS, Brice OO, et al. Anti-inflammatory effect of resveratrol by inhibition of IL-8 production in LPS-induced THP-1 cells. Am J Chin Med 2009;37:1203-14.

Subbiah U, Raghunathan M. Chemoprotective action of resveratrol and genistein from apoptosis induced in human peripheral blood lymphocytes. J Biomol Struct Dyn 2008;25:425-34.

Athar M, Back JH, Kopelovich L, Bickers DR, Kim AL. Multiple molecular targets of resveratrol: Anti-carcinogenic mechanisms. Arch Biochem Biophys 2009;486:95-102.

Gao ZB, Hu GY. Trans-resveratrol, a red wine ingredient, inhibits voltage-activated potassium currents in rat hippocampal neurons. Brain Res 2005;1056:68-75.

Kim HI, Kim TH, Song JH. Resveratrol inhibits Na+ currents in rat dorsal root ganglion neurons. Brain Res 2005;1045:134-41.

Gao ZB, Chen XQ, Hu GY. Inhibition of excitatory synaptic transmission by trans-resveratrol in rat hippocampus. Brain Res 2006;1111:41-7.

Zamin LL, Dillenburg-Pilla P, Argenta-Comiran R, Horn AP, Simao F, Nassif M, et al. Protective effect of resveratrol against oxygenglucose deprivation in organotypic hippocampal slice cultures: Involvement of PI3-K pathway. Neurobiol Dis 2006;24:170-82.

Siddiqui MA, Kashyap MP, Kumar V, Al-Khedhairy AA, Musarrat J, Pant AB. Protective potential of trans-resveratrol against 4-hydroxynonenal induced damage in PC12 cells. Toxicol In Vitro 2010;24:1592-8.

Zaidi SF, Ahmed K, Yamamoto T, Kondo T, Usmanghani K, Kadowaki M, et al. Effect of resveratrol on Helicobacter pyloriinduced interleukin-8 secretion, reactive oxygen species generation and morphological changes in human gastric epithelial cells. Biol Pharm Bull 2009;32:1931-5.

Robb EL, Stuart JA. Trans-Resveratrol as a neuroprotectant. Molecules 2010;15:1196-212.

Liu L, Zhang J, Su X, Mason RP. In vitro and in vivo assessment of CdTe and CdHgTe toxicity and clearance. J Biomed Nanotechnol 2008;4:524-8.

Kumar RA, Papaí¯conomou N, Lee JM, Salminen J, Clark DS, Prausnitz JM. In vitro cytotoxicities of ionic liquids: effect of cation rings, functional groups, and anions. Environ Toxicol 2009;24:388-95.

Wei RG, Zhao YX, Liu PY, Qin ZF, Yan SS, Li Y, et al. Determination of environmentally relevant exposure concentrations of polybrominated diphenyl ethers for in vitro toxicological studies. Toxicol In Vitro 2010;24:1078-85.

Musarrat J, Wilson JA. Abou-Issa H, Wani AA. O(6)-alkylguanine DNA alkyltransferase activity levels in normal, benign and malignant human female breast. Biochem Biophys Res Commun 1995;208:688-96.

Siddiqui MA, Singh G, Kashyap MP, Khanna VK, Yadav S, Chandra D, et al. Influence of cytotoxic doses of 4-hydroxynonenal on selected neurotransmitter receptors in PC-12 cells. Toxicol In Vitro 2008;22:1681-8.

Siddiqui MA, Kashyap MP, Al-Khedhairy AA, Musarrat J, Khanna VK, Yadav S, et al. Protective potential of 17{beta}-estradiol against co-exposure of 4-hydroxynonenal and 6-hydroxydopamine in PC12 cells. Hum Exp Toxicol 2011;30:860-9.

Krantic S, Mechawar N, Reix S, Quirion R. Molecular basis of programmed cell death involved in neurodegeneration. Trends Neurosci 2005;28:670-6.

Anekonda TS, Reddy PH. Neuronal protection by sirtuins in Alzheimer's disease. J Neurochem 2006;96:305-13.

Baur JA, Sinclair DA. Therapeutic potential of resveratrol: the in vivo evidence. Nat Rev Drug Discov 2006;5:493-506.

Mattson MP, Cheng A. Neurohormetic phytochemicals: Lowdose toxins that induce adaptive neuronal stress responses. Trends Neurosci 2006;29:632-9

Araki T, Sasaki Y, Milbrandt J. Increased nuclear NAD biosynthesis and SIRT1 activation prevent axonal degeneration. Science 2004;305;1010-3.

Anekonda TS. Resveratrol-a boon for treating Alzheimer's disease? Brain Res Rev 2006;52:316-26.

Sanchez L, Mitjans M, Infante MR, Vinardell MP. Assessment of the potential skin irritation of lysine-derivative anionic surfactants using mouse fibroblasts and human keratinocytes as an alternative to animal testing. Pharma Res 2004;21:1637-41.

Yoon IS, Au Q, Barber JR, Ng SC, Zhang B. Development of a high-throughput screening assay for cytoprotective agents in rotenone-induced cell death. Anal Biochem 2010;407:205-10.

Testa CM, Sherer TB, Greenamyre JT. Rotenone induces oxidative stress and dopaminergic neuron damage in organotypic substantia nigra cultures. Brain Res Mol Brain Res 2005;134:109-18.

Fato R, Bergamini C, Bortolus M, Maniero AL, Leoni S, Ohnishi T, et al. Differential effects of mitochondrial Complex I inhibitors on production of reactive oxygen species. Biochim Biophys Acta 2009;1787:384-92.

Siddiqui MA, Kashyap MP, Kumar V, Tripathi VK, Khanna VK, Yadav S, et al. Differential protection of pre-, co- and post-treatment of curcumin against hydrogen peroxide in PC12 cells. Hum Exp Toxicol 2011;30:192-8.

Gelinas S, Martinoli MG. Neuroprotective effect of estradiol and phytoestrogens on MPP+-induced cytotoxicity in neuronal PC12 cells. J Neurosci Res 2002;70:90-6.

Jang JH, Surh YJ. Protective effect of resveratrol on betaamyloidinduced oxidative PC12 cell death. Free Radic Biol Med 2003;34:1100-10.

Savaskan E, Olivieri G, Meier F, Seifritz E, Wirz-Justice A, MullerSpahn F. Red wine ingredient resveratrol protects from betaamyloid neurotoxicity. Gerontology 2003;49:380-3.

Chen J, Zhou Y, Mueller-Steiner S, Chen LF, Kwon H, Yi S, et al. SIRT1 protects against microglia-dependent amyloid-beta toxicity through inhibiting NF-kappaB signaling. J Biol Chem 2005;280;40364-74.

Raval AP, Dave KR, Perez-Pinzón MA. Resveratrol mimics ischemic preconditioning in the brain. J Cereb Blood Flow Metab 2006;26:1141-7.

Lu KT, Chiou RY, Chen LG, Chen MH, Tseng WT, Hsieh HT, et al. Neuroprotective effects of resveratrol on cerebral ischemiainduced neuron loss mediated by free radical scavenging and cerebral blood flow elevation. J Agric Food Chem 2006;54:3126-31.

Wang Q, Yu S, Simonyi A, Rottinghaus G, Sun GY, Sun AY. Resveratrol protects against neurotoxicity induced by kainic acid. Neurochem Res 2004;29:2105-12.

Ates O, Cayli S, Altinoz E, Gurses I, Yucel N, Sener M, Kocak A, Yologlu S. Neuroprotection by resveratrol against traumatic brain injury in rats. Mol Cell Biochem 2007;294;137-44.