1 research outputs found

    Evaluation Of The Genotoxic And Antigenotoxic Effects After Acute And Subacute Treatments With Açai Pulp (euterpe Oleracea Mart.) On Mice Using The Erythrocytes Micronucleus Test And The Comet Assay

    No full text
    Açai, the fruit of a palm native to the Amazonian basin, is widely distributed in northern South America, where it has considerable economic importance. Whereas individual polyphenolics compounds in açai have been extensively evaluated, studies of the intact fruit and its biological properties are lacking. Therefore, the present study was undertaken to investigate the . in vivo genotoxicity of açai and its possible antigenotoxicity on doxorubicin (DXR)-induced DNA damage. The açai pulp doses selected were 3.33, 10.0 and 16.67. g/kg b.w. administered by gavage alone or prior to DXR (16. mg/kg b.w.) administered by intraperitoneal injection. Swiss albino mice were distributed in eight groups for acute treatment with açai pulp (24. h) and eight groups for subacute treatment (daily for 14 consecutive days) before euthanasia. The negative control groups were treated in a similar way. The results of chemical analysis suggested the presence of carotenoids, anthocyanins, phenolic, and flavonoids in açai pulp. The endpoints analyzed were micronucleus induction in bone marrow and peripheral blood cells polychromatic erythrocytes, and DNA damage in peripheral blood, liver and kidney cells assessed using the alkaline (pH >13) comet assay. There were no statistically significant differences (. p>. 0.05) between the negative control and the groups treated with the three doses of açai pulp alone in all endpoints analyzed, demonstrating the absence of genotoxic effects. The protective effects of açai pulp were observed in both acute and subacute treatments, when administered prior to DXR. In general, subacute treatment provided greater efficiency in protecting against DXR-induced DNA damage in liver and kidney cells. These protective effects can be explained as the result of the phytochemicals present in açai pulp. These results will be applied to the developmental of food with functional characteristics, as well as to explore the characteristics of açai as a health promoter. © 2009 Elsevier B.V..6951-22228Lila, M.A., Anthocyanins and human health: an in vitro investigative approach (2004) J. Biomed. Biotechnol., 5, pp. 306-313De Rosso, V.V., Mercadante, A.Z., Identification and quantification of carotenoids, by HPLC-PDA-MS/MS, from Amazonian fruits (2007) J. Agric. Food Chem., 55, pp. 5062-5072Murrieta, R.S.S., Dufour, D., Siqueira, A.D., Food consumption and subsistence in three caboclo populations on Marajo Island, Amazônia, Brazil (1999) Hum. Ecol., 27, pp. 455-475Tinoco, A.C., (2005), Açaí amazônico: novas perspectivas de negócio, Embrapa Amazônia Oriental, Belém, PA, 2005, 1 CD-ROM. Trabalho apresentado no Workshop Regional do Açaizeiro: pesquisa, produção e comercialização, Belém, PAKhayat, T.C., Comportamento do risco para doença aterosclerótica coronária na população de Inhangapí cuja base alimentar é o fruto do açaí (Euterpe oleracea), 2005, Trabalho de Conclusão de Curso. (Graduação em Medicina) - Universidade Federal do Pará, Conselho Nacional de Desenvolvimento Científico e TecnológicoOliveira, M.S.P., Carvalho, J.E.U., (2000), p. 51. , W.M.O. Nascimento, Açaí (Euterpe oleracea Mart.) Jaboticabal: FUNEPPozo-Insfran, D., Brenes, D., Talcott, S.T., Phytochemical composition and pigment stability of Açai (Euterpe oleracea Mart.) (2004) J. Agric. Food Chem., 52, pp. 1539-1545Pozo-Insfran, D., Percival, S.S., Talcott, S.T., Açai (Euterpe oleracea Mart.) polyphenolics in their glycoside and aglycone forms induce apoptosis of HL-60 leukemia cells (2006) J. Agric. Food Chem., 54, pp. 1222-1229De Rosso, V.V., Morán, F.E.V., Mercadante, A.Z., Borsarelli, C.D., Singlet oxygen quenching by anthocyanin's flavylium cations (2008) Free Radic. Res., 42, pp. 885-891Ghosh, D., Sheepens, A., Vascular action of polyphenols (2009) Mol. Nutr. Food Res., 53, pp. 322-331Rocha, A.P., Carvalho, L.C., Sousa, M.A., Madeira, S.V., Sousa, P.J., Tano, T., Schini-Kerth, V.B., Soares de Moura, R., Endothelium-dependent vasodilator effect of Euterpe oleracea Mart. (Açaí) extracts in mesenteric vascular bed of the rat (2007) Vascul. Pharmacol., 46, pp. 97-104Stevenson, D.E., Hurst, R.D., Polyphenolic phytochemicals-just antioxidants or much more? (2007) Cell. Mol. Life Sci., 64, pp. 2900-2916Weiss, R.B., The anthracyclines: will we ever find a better doxorubicin? (1992) Semin. Oncol., 19, pp. 670-686Kaklamani, V.G., Gradishar, W.J., Epirubicin versus doxorubicin: which is the anthracycline of choice for the treatment of breast cancer? (2003) Clin. Breast Cancer, 4, pp. S26-S33Pai, V.B., Nahata, M.C., Cardiotoxicity of chemotherapeutic agents: incidence, treatment and prevention (2000) Drug Saf., 22, pp. 263-302Islaih, M., Halstead, B.W., Kadura, I.A., Reid-Hubbard, J.L., Flick, F., Altizer, J.L., Thom, D.J., Watson, D.E., Relationships between genomic, cell cycle, and mutagenic responses of TK6 cells exposed to DNA damaging chemicals (2005) Mutat. Res., 578, pp. 100-116Antunes, L.M.G., Takahashi, C.S., Effects of high doses of vitamins C and E against doxorubicin-induced chromosomal damage in Wistar rat bone marrow cells (1998) Mutat. Res., 419, pp. 137-143Antunes, L.M.G., Pascoal, L.M., Bianchi, M.L.P., Dias, F.L., Evaluation of the clastogenicity and anticlastogenicity of the carotenoid bixin in human lymphocyte cultures (2005) Mutat. Res., 585, pp. 113-119Tan, H.H., Porter, A.G., DNA methyltransferase I is a mediator of doxorubicin-induced genotoxicity in human cancer cells (2009) Biochem. Biophys. Res. Commun., 382, pp. 462-467Beillerot, A., Dominguez, J.C., Kirsch, G., Bagrel, D., Synthesis and protective effects of coumarin derivatives against oxidative stress induced by doxorubicin (2008) Bioorg. Med. Chem. Lett., 18, pp. 1102-1105Spada, P.D., de Souza, G.G., Bortolini, G.V., Henriques, J.A., Salvador, M., Mutagenic, and antimutagenic activity of frozen fruits (2008) J. Med. Food, 11, pp. 144-151. , AntioxidantSingleton, V.L., Rossi, J.A., Colorimetry of total phenolics with phosphomolybdic-phosphotungstic acid reagents (1965) Am. J. Enol. Vitic., 16, pp. 144-158Zhishen, J., Mengcheng, T., Jianming, W., The determination of flavonoid contents in mulberry and their scavenging effects on superoxide radicals (1999) Food Chem., 64, pp. 555-559De Rosso, V.V., Mercadante, A.Z., HPLC-PDA-MS/MS of anthocyanins and carotenoids from dovyalis and tamarillo fruits (2007) J. Agric. Food Chem., 55, pp. 9135-9141Prahalathan, C., Selvakumar, E., Varalashmi, P., Kumarasamy, P., Saravanan, R., Salubrious effects of lipoic acid against adriamycin-induced clastogenesis and apoptosis in Wistar rat bone marrow cells (2006) Toxicology, 222, pp. 225-232MacGregor, J.T., Heddle, J.A., Hite, M., Margolin, B.H., Ramel, C., Salamone, M.F., Tia, R.R., Wild, D., Guidelines for the conduct of micronucleus assay in mammalian bone marrow erythrocyte (1987) Mutat. Res., 189, pp. 103-112Hayashi, M., MacGregor, J.T., Gatehouse, D.G., Adler, I.D., Blakey, D.H., Dertinger, S.D., Krishna, G., Sutou, S., In vivo rodent erythrocyte micronucleus assay. II. Some aspects of protocol design including repeated treatments, integration with toxicity testing, and automated scoring (2000) Environ. Mol. Mutagen., 35, pp. 234-252Waters, M.D., Brady, A.L., Stack, H.F., Brockman, H.E., Antimutagenicity profiles for some model compounds (1990) Mutat. Res., 238, pp. 57-85Tice, R.R., Agurell, E., Anderson, D., Burlinson, B., Hartmann, A., Kobayashi, H., Miyamae, Y., Sasaki, Y.F., Single cell gel/comet assay: guidelines for in vitro and in vivo genetic toxicology testing (2000) Environ. Mol. Mutagen., 35, pp. 206-221Singh, N.P., McCoy, M.T., Tice, R.R., Shneider, E.L., A simple technique for quantitation of low DNA levels of DNA damage in individual cells (1988) Exp. Cell Res., 175, pp. 181-191Collins, A.R., Ma, A.G., Duthie, S.J., The kinetics of repair of oxidative DNA damage (strand breaks and oxidised pyrimidines) in human cells (1995) Mutat. Res., 336, pp. 69-77Antunes, L.M.G., Ara, M.C.P., Mutagenicity and antimutagenicity of the main food colorings (2000) Rev. Nutr., 13, pp. 81-88Zeiger, E., What is needed for an acceptable antimutagenicity manuscript? (2007) Mutat. Res., 626, pp. 1-3Serpeloni, J.M., Bisarro dos Reis, M., Rodrigues, J., Campaner dos Santos, L., Vilegas, W., Varanda, E.A., Dokkedal, A.L., Cólus, I.M., In vivo assessment of DNA damage and protective effects of extracts from Miconia species using the comet assay and micronucleus test (2008) Mutagenesis, 23, pp. 501-507Santos, R.A., Jordão, A.A., Vannucchi, H., Takahashi, C.S., Protection of doxorubicin-induced DNA damage by sodium selenite and selenomethionine in Wistar rats (2007) Nutr. Res., 27, pp. 343-348Takeuchi, P.L., Antunes, L.M.G., Takahashi, C.S., Modulation of doxorubicin-induced clastogenesis in Wistar rat bone marrow cells by vitamin B6 (2008) Arch. Toxicol., 82, pp. 869-873Weijl, N.I., Cleton, F.J., Osanto, S., Free radicals and antioxidants in chemotherapy-induced toxicity (1997) Cancer Treat. Rev., 23, pp. 209-240Conklin, K.A., Cancer chemotherapy and antioxidants (2004) J. Nutr., 134, pp. 3201-3204Simpson, C., Herr, H., Courtville, K.A., Concurrent therapies that protect against doxorubicin-induced cardiomyopathy (2003) Clin. J. Oncol. Nurs., 8, pp. 497-501Andreadou, I., Papaefthimiou, M., Zira, A., Constantinou, M., Sigala, F., Skaltsounis, A.L., Tsantili-Kakoulidou, A., Mikros, E., Metabonomic identification of novel biomarkers in doxorubicin cardiotoxicity and protective effect of the natural antioxidant oleuropein (2009) NMR Biomed., 22, pp. 585-592Preston, R.J., Dean, B.J., Galloway, S., Holden, H., McFee, A.F., Shelby, M.D., Mammalian in vivo cytogenetic assays: analysis of chromosome aberrations in bone marrow cells (1987) Mutat. Res., 189, pp. 157-165Salvadori, D.M., Ribeiro, L.R., Oliveira, M.D., Pereira, C.A., Beçak, W., The protective effect of beta-carotene on genotoxicity induced by cyclophosphamide (1992) Mutat. Res., 265, pp. 237-244Nesslany, F., Zennouche, N., Simar-Meintiéres, S., Talahari, I., Nkili-Mbou, E.N., Marzin, D., In vivo comet assay on isolated kidney cells to distinguish genotoxic carcinogens from epigenetic carcinogens or cytotoxic compounds (2007) Mutat. Res., 630, pp. 28-41Schauss, A.G., Wu, X., Prior, R.L., Ou, B., Patel, D., Huang, D., Kababick, J.P., Phytochemical and nutrient composition of the freeze-dried amazonian palm berry, Euterpe oleracea Mart. (acai) (2006) J. Agric. Food Chem., 54, pp. 8598-8603Azevedo, L., Alves de Lima, P.L., Gomes, J.C., Stringheta, P.C., Ribeiro, D.A., Salvadori, D.M., Differential response related to genotoxicity between eggplant (Solanum melanogena) skin aqueous extract and its main purified anthocyanin (delphinidin) in vivo (2007) Food Chem. Toxicol., 45, pp. 852-858Ghosh, D., Konishi, T., Anthocyanins and anthocyanin-rich extracts: role in diabetes and eye function (2007) Asia Pac. J. Clin. Nutr., 16, pp. 200-208Pacheco-Palencia, L.A., Talcott, S.T., Safe, S., Mertens-Talcott, S., Absorption and biological activity of phytochemical-rich extracts from açai (Euterpe oleracea Mart.) pulp and oil in vitro (2008) J. Agric. Food Chem., 56, pp. 3593-3600Youdim, K.A., Shudit-hale, B., MacKinnon, S., Kalt, W., Joseph, J.A., Polyphenolics enhance red blood cell resistance to oxidative stress: in vitro and in vivo (2000) Biochim. Biophys. Acta, 1523, pp. 117-122Lichtenthäler, R., Rodrigues, R.B., Maia, J.G., Papagiannopoulos, M., Fabricius, H., Marx, F., Total oxidant scavenging capacities of Euterpe oleracea Mart. (Açaí) fruits (2005) Int. J. Food Sci. Nutr., 56, pp. 53-64Talavéra, S., Felgines, C., Texier, O., Besson, C., Gil-Izquierdo, A., Lamaison, J.L., Rémésy, C., Anthocyanin metabolism in rats and their distribution to digestive area, kidney, and brain (2005) J. Agric. Food Chem., 53, pp. 3902-3908Schauss, A.G., Wu, X., Prior, R.L., Ou, B., Huang, D., Owens, J., Agarwal, A., Shanbrom, E., Antioxidant capacity and other bioactivities of the freeze-dried Amazonian palm berry, Euterpe oleracea Mart. (acai) (2006) J. Agric. Food Chem., 54, pp. 8604-8610De Rosso, V.V., Hillebrand, S., Montilla, E.C., Bobbio, F.O., Winterhalter, P., Mercadante, A.Z., Determination of anthocyanins from acerola (Malpighia emarginata DC.) and açai (Euterpe oleracea Mart.) by HPLC-PDA and HPLC-MS (2008) J. Food Compos. Anal., 21, pp. 291-299Mertens-Talcott, S.U., Rios, J., Jilma-Stohlawetz, P., Pacheco-Palencia, L.A., Meibohm, B., Talcott, S.T., Derendorf, H., Pharmacokinetics of anthocyanins and antioxidant effects after the consumption of anthocyanin-rich açai juice and pulp (Euterpe oleracea Mart.) in human healthy volunteers (2008) J. Agric. Food Chem., 56, pp. 7796-780
    corecore