[1. S. Hasani-Ranjbar, B. Larijani and M. Abdollahi, A systematic review of the potential herbal sources of future drugs effective in oxidant-related diseases, Inflamm. Allergy Drug Targets 8 (2009) 2-10.10.2174/187152809787582561]Search in Google Scholar
[2. C. H. Oliveira, M. E. A. Moraes, M. O. Moraes, F. A. F. Bezerra, E. Abib and G. De Nucci, Clinical toxicology study of an herbal medicinal extract of Paullinia cupana, Trichilia catigua, Ptychopetalum olacoides and Zingiber officinalis (Catuama) in healthy volunteers, Phytother. Res. 19 (2005) 54-57; DOI: 10.1002/ptr.1484.10.1002/ptr.1484]Search in Google Scholar
[3. M. G. Pizzolatti, A. F. Venson, A. S. Júnior, E. F. A. Smânia and R. Braz-Filho, Two epimeric flavalignans from Trichilia catigua (Meliaceae) with antimicrobial activity, Z. Naturforsch. C 57 (2002) 483-488.10.1515/znc-2002-5-614]Search in Google Scholar
[4. W. Tang, H. Hioki, K. Harada, M. Kubo and Y. Fukuyama, Antioxidant phenylpropanoid-substituted epicatechins from Trichilia catigua, J. Nat. Prod. 70 (2007) 2010-2013; DOI: 10.1021/np0703895.10.1021/np0703895]Search in Google Scholar
[5. S. Venkatesh, M. Deecaraman, R. Kumar, M. B. Shamsi and R. Dada, Role of reactive oxygen species in the pathogenesis of mitochondrial DNA (mtDNA) mutation in male infertility, Indian J. Med. Res. 129 (2009) 127-137.]Search in Google Scholar
[6. R. L. Puntel, D. H. Roos, D. Grotto, S. C. Garcia, C. W. Nogueira and J. B. Rocha, Antioxidant properties of Krebs cycle intermediates against malonate prooxidant activity in vitro: a comparative study using the colorimetric method and HPLC analysis to determine malondialdehyde in rat brain homogenates, Life Sci. 81 (2007) 51-62; DOI: 10.1016/j.lfs.2007.04.023.10.1016/j.lfs.2007.04.023]Search in Google Scholar
[7. A. H. Laghari, S. Memon, A. Nelofar, K. M. Khan and A. Yasmin, Determination of free phenolic acids and antioxidant activity of methanolic extracts obtained from fruits and leaves of Chenopodium album, Food. Chem. 126 (2011) 1850-1855; DOI: 10.1016/j.foodchem.2010.11.165.10.1016/j.foodchem.2010.11.165]Search in Google Scholar
[8. R. L. Puntel, D. H. Roos, V. Folmer, C. W. Nogueira, A. Galina, M. Aschner and J. B. T. Rocha, Mitochondrial dysfunction induced by different organochalchogens is mediated by thiol oxidation and is not dependent on the classical mitochondrial permeability transition pore opening, Toxicol. Sci. 117 (2010) 133-143; DOI: 10.1093/toxsci/kfq185.10.1093/toxsci/kfq185]Search in Google Scholar
[9. O. H. Lowry, N. J. Rosebrough, A. L. Farr and R. J. Randall, Protein measurement with the Folin phenol reagent, J. Biol. Chem. 193 (1951) 265-275.10.1016/S0021-9258(19)52451-6]Search in Google Scholar
[10. Y. S. Velioglu, G. Mazza, L. Gao and B. D. Oomah, Antioxidant activity and total phenolics in selected fruits, vegetables and grain products, J. Agric. Food Chem. 46 (1998) 4113-4117; DOI: 10.1021/jf9801973.10.1021/jf9801973]Search in Google Scholar
[11. C. Nencini, A. Menchiari, G. G. Franchi and L. Micheli, In vitro antioxidant activity of some Italian Allium species, Plant Food Hum. Nutr. 66 (2011) 11-16; DOI: 10.1007/s11130-010-0204-2.10.1007/s11130-010-0204-221290188]Search in Google Scholar
[12. A. A. Boligon, P. R. Pereira, A. C. Feltrin, M. M. Machado, V. Janoyik, J. B. T. Rocha and M. L. Athayde, Antioxidant activities of flavonol derivatives from the leaves and stem bark of Scutia buxifolia Reiss, Biores. Technol. 100 (2009) 6592-6598; DOI: 10.1016/j.biortech.2009.03.091.10.1016/j.biortech.2009.03.09119666219]Search in Google Scholar
[13. H. Kiliçgün and D. Altiner, Correlation between antioxidant effect mechanisms and polyphenol content of Rosa canina, Pharmacogn. Mag. 23 (2010) 238-241; DOI: 10.4103/0973-1296.66943.10.4103/0973-1296.66943295038920931086]Search in Google Scholar
[14. P. A. Omololu, J. B. T. Rocha and I. J. Kade, Attachment of rhamnosyl glucoside on quercetin confers potent iron-chelating ability on its antioxidant properties, Exp. Toxicol. Pathol. 63 (2011) 249-255; DOI: 10.1016/j.etp.2010.01.002.10.1016/j.etp.2010.01.00220122821]Search in Google Scholar
[15. M. J. Hansson, R. Månsson, S. Morota, H. Uchino, T. Kallur, T. Sumi, N. Ishii, M. Shimazu, M. F. Keep, A. Jegorov and E. Elmér, Calcium-induced generation of reactive oxygen species in brain mitochondria is mediated by permeability transition, Free Radical Biol. Med. 45 (2008) 284-294; DOI: 10.1016/j.freeradbiomed.2008.04.021.10.1016/j.freeradbiomed.2008.04.02118466779]Search in Google Scholar
[16. C. Wagner, A. P. Vargas, D. H. Roos, A. F. Morel, M. Farina, C. W. Nogueira, M. Aschner and J. B. Rocha, Comparative study of quercetin and its two glycoside derivatives quercitrin and rutin against methylmercury (MeHg)-induced ROS production in rat brain slices, Arch. Toxicol. 84 (2010) 89-97; DOI: 10.1007/s00204-009-0482-3.10.1007/s00204-009-0482-319902180]Search in Google Scholar
[17. F. Sedlic, A. Sepac, D. Pravdic, A. K. S. Camara, M. Bienengreber, A. K. Brzezinska, T. Wakatsuki and Z. J. Bosnjak, Mitochondrial depolarization underlies delay in permeability transition by preconditioning with isoflurane: roles of ROS and Ca2+, Am. J. Physiol. Cell Physiol. 299 (2010) C506-C515; DOI: 10.1152/ajpcell.00006.2010.10.1152/ajpcell.00006.2010292864020519447]Search in Google Scholar