dc.creatorQueiroz M.L.S.
dc.creatorda Rocha M.C.
dc.creatorTorello C.O.
dc.creatorde Souza Queiroz J.
dc.creatorBincoletto C.
dc.creatorMorgano M.A.
dc.creatorRomano M.R.
dc.creatorParedes-Gamero E.J.
dc.creatorBarbosa C.M.V.
dc.creatorCalgarotto A.K.
dc.date2011
dc.date2015-06-30T20:38:18Z
dc.date2015-11-26T14:52:24Z
dc.date2015-06-30T20:38:18Z
dc.date2015-11-26T14:52:24Z
dc.date.accessioned2018-03-28T22:04:27Z
dc.date.available2018-03-28T22:04:27Z
dc.identifier
dc.identifierFood And Chemical Toxicology. , v. 49, n. 11, p. 2934 - 2941, 2011.
dc.identifier2786915
dc.identifier10.1016/j.fct.2011.06.056
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-80053565969&partnerID=40&md5=721e009415156757254a20dbd2f244c7
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/108739
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/108739
dc.identifier2-s2.0-80053565969
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1254815
dc.descriptionChlorella vulgaris (CV) was examined for its modulating effects on the reduction induced by lead (Pb) on the numbers of marrow hematopoietic stem cells (HSCs) (c-Kit +Lin -), granulocyte-macrophage progenitors (Gr1 +Mac1 +) and total bone marrow cellularity. In mice gavage-treated daily with 50mg/kg dose of CV for 10days, concomitant to a continuous offering of 1300ppm lead acetate in drinking water, the treatment with the algae recovered the significantly reduced numbers of these cell populations to control values. As CV may have a myelostimulating effect through the induction of cytokines, we evaluated its modulating effects on the production of IL-1α, TNF-α, IFN-γ, IL-10 and IL-6. Our results demonstrated that lead significantly impairs the production of IFN-γ, IL-1α and TNF-α and increases the production of IL-10 and IL-6 and that these effects are successfully modulated by the CV treatment. The activity of NK cells, reduced in Pb-exposed animals, was raised to levels higher than those of controls in the exposed group treated with CV. Treatment with the algae also stimulated the production of IFN-γ, IL-1α, TNF-α and NK cells activity in normal mice. In addition, zinc bone concentrations, reduced in lead-exposed mice, were partially, but significantly, reversed by the treatment with CV. © 2011 Elsevier Ltd.
dc.description49
dc.description11
dc.description2934
dc.description2941
dc.descriptionApasheva, L.M., Gusareva, E.V., Kulinich, A.V., Study of the role of thiols in determining the radiosensitivity of various strains of Chlorella vulgaris (1972) Radiobiology, 12, pp. 904-906
dc.descriptionBarry, P.S., Letter: lead levels in blood (1975) Nature, 258, p. 775
dc.descriptionBellinger, D.C., Lead (2004) Pediatrics, 113, pp. 1016-1022
dc.descriptionBincoletto, C., Queiroz, M.L.S., The effect of lead on the bone marrow stem cells of mice infected with Listeria monocytogenes (1996) Vet. Hum. Toxicol., 38, pp. 186-190
dc.descriptionBishayi, B., Sengupta, M., Synergism in immunotoxicology effects due to repeated combined administration of lead and arsenic in mice (2006) Int. Immunopharmacol., 6, pp. 454-464
dc.descriptionBlakley, B.K., Archer, D.L., Mitogen stimulation of lymphocytes exposed to lead (1982) Toxicol. Appl. Pharmacol., 62, pp. 183-189
dc.descriptionBrewer, G.J., Hill, G.M., Dick, R.D., Interactions of trace elements: clinical significance (1985) J. Am. Coll. Nutr., 4, pp. 33-38
dc.descriptionCervi, L., MacDonald, A.S., Kane, C., Cutting edge: dendritic cells coupled with microbial and helminth antigens undergo modified maturation, segregate the antigens to distinct intracellular compartments, and concurrently induce microbe-specific Th1 and helminth-specific Th2 responses (2004) J. Immunol., 172, pp. 2016-2020
dc.descriptionChen, S., Golemboski, K.A., Sanders, F.S., Persistent effect of in utero meso-2,3-dimercaptosuccinic acid (DMSA) on immune function and lead-induced immunotoxicity (1999) Toxicology, 132, pp. 67-79
dc.descriptionChoi, J.W., Kim, S.K., Association between blood lead concentrations and body iron status in children (2003) Arch. Dis. Child., 88, pp. 791-792
dc.descriptionCobbett, C., Goldsbrough, P., Phytochelatins and metallothioneins: roles in heavy metal detoxification and homeostasis (2002) Annu. Rev. Plant Biol., 53, pp. 159-182
dc.descriptionDantas, D.C.M., Queiroz, M.L.S., Effects of Chlorella vulgaris on bone marrow progenitor cells of mice infected with Listeria monocytogenes (1999) Int. J. Immunopharmacol., 21, pp. 499-508
dc.descriptionDantas, D.C., Kaneno, R., Queiroz, M.L., The effects of Chlorella vulgaris in the protection of mice infected with Listeria monocytogenes. Role of natural killer cells (1999) Immunopharmacol. Immunotoxicol., 21, pp. 609-619
dc.descriptionDietert, R.R., Piepenbrink, M.S., Lead and immune function (2006) Crit. Rev. Toxicol., 36, pp. 359-385
dc.descriptionDomen, J., Weissman, I.L., Self-renewal, differentiation or death: regulation and manipulation of hematopoietic stem cell fate (1999) Mol. Med. Today, 5, pp. 201-208
dc.descriptionElenkov, I.J., Papanicolaou, D.A., Wilder, R.L., Modulatory effects of glucocorticoids and catecholamines on human interleukin-12 and interleukin-10 production: clinical implications (1996) Proc. Assoc. Am. Phys., 108, pp. 374-381
dc.descriptionElenkov, I.J., Wilder, R.L., Chrousos, G.P., The sympathetic nerve-an integrative interface between two supersystems: the brain and the immune system (2000) Pharmacol. Rev., 52, pp. 595-638
dc.descriptionFaith, R.E., Luster, M.I., Kimmel, C.A., Effect of chronic developmental lead exposure on cell-mediated immune functions (1979) Clin. Exp. Immunol., 35, pp. 413-420
dc.descriptionGurer, H., Ercal, N., Can antioxidants be beneficial in the treatment of lead poisoning? (2000) Free Radic. Biol. Med., 29, pp. 927-945
dc.descriptionHaeger-Aronsen, B., Schutz, A., Antagonistic effect in vivo of zinc on inhibition of delta-aminolevulinic acid dehydratase by lead (1976) Arch. Environ. Health, 31, pp. 215-220
dc.descriptionHasegawa, T., Yohikai, Y., Okuda, M., Accelerated restoration of the leukocyte number and augmented resistance against Escherichia coli in cyclophosphamide-treated rats orally administered with a hot water extract of Chlorella vulgaris (1990) Int. J. Immunopharmacol., 12, pp. 883-891
dc.descriptionHasegawa, T., Okuda, M., Nomoto, K., Augmentation of the resistance against Listeria monocytogenes by oral administration of a hot water extract of Chlorella vulgaris in mice (1994) Immunopharmacol. Immunotoxicol., 16, pp. 191-202
dc.descriptionHasegawa, T., Kimura, Y., Hiromatsu, K., Effect of hot water extract of Chlorella vulgaris on cytokine expression patterns in mice with murine acquired immunodeficiency syndrome after infection with Listeria monocytogenes (1997) Immunopharmacology, 35, pp. 273-282
dc.descriptionHasegawa, T., Noda, K., Kumamoto, S., Chlorella vulgaris culture supernatant (CVS) reduces psychological stress-induced apoptosis in thymocytes of mice (2000) Int. J. Immunopharmacol., 22, pp. 877-885
dc.descriptionHemdan, N.Y.A., Emmrich, F., Adham, K., Dose-dependent modulation of the in vitro cytokine production of human immune competent cells by lead salts (2005) Toxicol. Sci., 86, pp. 75-83
dc.descriptionHeo, Y., Lee, W.T., Lawrence, D.A., Differential effects of lead and camp on development and activities of Th1- and Th2-lymphocytes (1998) Toxicol. Sci., 43, pp. 172-185
dc.descriptionHeyworth, C.M., Whetton, A.D., Nicholls, S.E., Stem cell factor directly stimulates the development of enriched granulocyte-macrophage colony-forming cells and promotes the effects of other colony-stimulating factors (1992) Blood, 80, pp. 2230-2236
dc.descriptionHorwitz, W., (2005) Official Methods of Analysis of the Association of Official Analytical Chemists, pp. 15-18. , AOAC, Gaithersburg, Maryland
dc.descriptionIbusuki, K., Minamishima, Y., Effects of Chlorella vulgaris extract on murine 659 cytomegalovirus infections (1990) Nat. Immun. Cell. Growth Regul., 9, pp. 121-128
dc.descriptionJamieson, J.A., Taylor, C.G., Weiler, H.A., Marginal zinc deficiency exacerbates bone lead accumulation and high dietary zinc attenuates lead accumulation at the expense of bone density in growing rats (2006) Toxicol. Sci., 92, pp. 286-294
dc.descriptionJarup, L., Hazards of heavy metal contamination (2003) Br. Med. Bull., 68, pp. 167-182
dc.descriptionJusto, G.Z., Silva, M.R., Queiroz, M.L.S., Effects of the Green algae Chlorella vulgaris on the response of the host hematopoietic system to intraperitoneal Ehrlich ascites tumor transplantation in mice (2001) Immunopharmacol. Immunotoxicol., 23, pp. 119-132
dc.descriptionJusto, G.Z., Durán, N., Queiroz, M.L., Natural killer cell activity, lymphocyte proliferation, and cytokine profile in tumor-bearing mice treated with MAPA, a magnesium aggregated polymer from Aspergillus oryzae (2003) Immunopharmacol. Immunotoxicol., 25, pp. 305-319
dc.descriptionKim, S., Iizuka, K., Aguila, H.L., In vivo natural killer cell activities revealed by natural killer cell-deficient mice (2000) Proc. Natl. Acad. Sci. USA, 97, pp. 2731-2736
dc.descriptionKing, L.E., Fraker, P.J., Zinc deficiency in mice alters myelopoiesis and hematopoiesis (2002) J. Nutr., 132, pp. 3301-3307
dc.descriptionKishikawa, H., Song, R., Laurence, A., Interleukin-12 promoters enhanced resistance to Listeria monocytogenes infection of Pb-exposed mice (1997) Toxicol. Appl. Pharmacol., 147, pp. 180-189
dc.descriptionKonishi, F., Tanaka, K., Himeno, K., Antitumor effect induced by a hot water extract of Chlorella vulgaris (CE): resistance to meth A tumor growth mediated by CE-induced polymorphonuclear leukocytes (1985) Cancer Immunol. Immunother., 19, pp. 73-78
dc.descriptionKonishi, F., Tanaka, K., Kumamoto, S., Enhanced resistance against Escherichia coli infection by subcutaneous administration of the hot-water extract of Chlorella vulgaris in cyclophosphamide-treated mice (1990) Cancer Immunol. Immunother., 32, pp. 1-7
dc.descriptionKonishi, F., Mitsuyama, M., Okuda, M., Protective effect of an acidic glycoprotein obtained from culture of Chlorella vulgaris against myelossuppression by 5-fluorouracil (1996) Cancer Immunol. Immunother., 42, pp. 268-274
dc.descriptionKowolenko, M., Tracy, L., Lawrence, D., Early effects of lead on bone marrow cells responsiveness in mice challenged with Listeria monocytogenes (1991) Fundam. Appl. Toxicol., 17, pp. 75-82
dc.descriptionKumamoto, S., Ando, Y., Yamada, A., Oral administration of hot water extracts of Chlorella vulgaris reduces IgE production against milk casein in mice (1999) Int. J. Immunoparmacol., 21, pp. 311-323
dc.descriptionLarsson, J., Karlsson, S., The role of Smad signaling in hematopoiesis (2005) Oncogene, 24, pp. 5676-5692
dc.descriptionLópez, C.E., Castro, J.M., Gonzáles, V., Determination of metal ions in algal solution samples by capillary electrophoresis (1998) J. Chromatogr. Sci., 36, pp. 352-356
dc.descriptionLyman, S.D., Jacobsen, S.E., C-kit ligand and Flt3 ligand: stem/progenitor cell factors with overlapping yet distinct activities (1998) Blood, 91, pp. 1101-1134
dc.descriptionMcCabe, M.J., Singh, K.P., Reiners, J.J., Lead intoxication impairs the generation of a delayed type hypersensitivity response (1999) Toxicology, 139, pp. 255-264
dc.descriptionMisawa, E., Sakurai, T., Yamada, M., Effects of macrophage colony-stimulating factor and interleukin-2 administration on NK1.1(+) cells in mice (2000) Int. J. Immunopharmacol., 22, pp. 967-977
dc.descriptionMuzzioli, M., Stecconi, R., Donnini, A., Zinc improves the development of human CD34+ cell progenitors towards Natural Killer cells and induces the expression of GATA-3 transcription factor (2007) Int. J. Biochem. Cell Biol., 39, pp. 955-965
dc.descriptionNoda, K., Ohno, N., Tanaka, K., A new type of biological response modifier from Chlorella vulgaris which needs protein moiety to show an antitumour activity (1998) Phytother. Res., 12, pp. 309-319
dc.descriptionOlfert, E.D., Cross, B.M., McWilliam, A.A., (1993) Guide to the Care and Use of Experimental Animals, 1, p. 1. , Canadian Council on Animal Care, Ottawa
dc.descriptionOrange, J.S., Ballas, Z.K., Natural killer cells in human health and disease (2006) Clin. Immunol., 118, pp. 1-10
dc.descriptionPawlik-Skowronska, B., Pirszel, J., Brown, M.T., Concentrations of phytochelatins and glutathione found in natural assemblages of seedweeds depend on species and metal concentrations of the habitat (2007) Aquat. Toxicol., 20, pp. 190-199
dc.descriptionPrasad, A.S., Effects of zinc deficiency on Th1 and Th2 cytokine shifts (2000) J. Infect. Dis., 182, pp. 62-68
dc.descriptionQueiroz, M.L.S., Bincoletto, C., Valadares, M.C., Effects of Chlorella vulgaris extract on cytokines production in Listeria monocytogenes infected mice (2002) Immunopharmacol. Immunotoxicol., 24, pp. 483-496
dc.descriptionQueiroz, M.L.S., Rodrigues, A.P.O., Bincoletto, C., Protective effects of Chlorella vulgaris in lead-exposed mice infected with Listeria monocytogenes (2003) Int. Immunopharmacol., 3, pp. 889-900
dc.descriptionQueiroz, M.L., Torello, C.O., Perhs, S.M., Chlorella vulgaris up-modulation of myelossupression induced by lead: the role of stromal cells (2008) Food Chem. Toxicol., 46, pp. 3147-3154
dc.descriptionRamos, A.L., Torello, C.O., Queiroz, M.L.S., Chlorella vulgaris modulates immunomyelopoietic activity and enhances the resistance of tumor-bearing mice (2010) Nutr. Cancer., 62, pp. 1170-1180
dc.descriptionRodriguez-Garcia, I., Guil-Guerrero, J.L., Evaluation of the antioxidant activity of three microalgal species for use as dietary supplements and in the preservation of foods (2008) Food Chem., 108, pp. 1023-1026
dc.descriptionSarders, V.M., Baker, R.A., Ranner-Quinn, D.S., Differential expression of the beta2-adrenergic receptor by Th1 and Th2 clones: implications for cytokine production and B cell help (1997) J. Immunol., 158, pp. 4200-4210
dc.descriptionSchmitt, N., Anderson, T.W., Philion, J.J., Could zinc help protect children from lead poisoning? (1996) Can. Med. Assoc. J., 154, pp. 13-14
dc.descriptionSchuerwegh, A.J., Dombrecht, E.J., Stevens, W.J., Influence of pro-inflammatory (IL-1 alpha, IL-6, TNF-alpha, IFN-gamma) and anti-inflammatory (IL-4) cytokines on chondrocyte function (2003) Osteoarthritis Cartilage, 11, pp. 681-687
dc.descriptionSinicropi, M.S., Amantea, D., Caruso, A., Chemical and biological properties of toxic metals and use of chelating agents for the pharmacological treatment of metal poisoning (2010) Arch. Toxicol., 84, pp. 501-520
dc.descriptionSlaveykova, V., Wilkinson, K.J., Physicochemical aspects of lead bioaccumulation by Chlorella vulgaris (2002) Environ. Sci. Technol., 36, pp. 969-975
dc.descriptionSouza-Queiroz, J., Malacrida, S.A., Justo, G.Z., Myelopoietic response in mice exposed to acute cold/restraint stress: modulation by Chlorella vulgaris prophylactic treatment (2004) Immunopharmacol. Immunotoxicol., 26, pp. 455-467
dc.descriptionSouza-Queiroz, J., Torello, C.O., Palermo-Neto, J., Hematopoietic response of rats exposed to the impact of an acute psychophysiological stressor on responsiveness to an in vivo challenge with Listeria monocytogenes: modulation by Chlorella vulgaris prophylactic treatment (2008) Brain Behav. Immun., 22, pp. 1056-1065
dc.descriptionSpangrude, G.J., Heimfeld, S., Weissman, I.L., Purification and characterization of mouse hematopoietic stem cells (1988) Science, 241, pp. 58-62
dc.descriptionTanaka, K., Konishi, F., Himeno, K., Augmentation of anti tumor resistance by a strain of unicellular green algae, Chlorella vulgaris (1984) Cancer Immunol. Immunother., 17, pp. 90-94
dc.descriptionTanaka, K., Koga, T., Konishi, F., Augmentation of host defense by a unicellular green alga, Chlorella vulgaris, to Escherichia coli infection (1986) Infect. Immun., 53, pp. 267-271
dc.descriptionTanaka, K., Yamada, A., Noda, K., A novel glycoprotein obtained from Chlorella vulgaris strain CK22 shows antimetastatic immunopotentiation (1998) Cancer Immunol. Immunother., 45, pp. 313-320
dc.descriptionTraviesso, L., Canizares, R.O., Borja, R., Heavy metal removal by microalgae (1999) Bull. Environ. Contam. Toxicol., 62, pp. 144-151
dc.descriptionVan Den Heuvel, R.L., Leppens, H., Schoeters, G.E., Lead and catechol hematotoxicity in vitro using human and murine hematopoietic progenitor cells (1999) Cell Biol. Toxicol., 15, pp. 101-110
dc.descriptionVeglio, F., Beolchini, F., Removal of metals by biosorption: a review (1997) Hydrometallurgy, 44, pp. 301-316
dc.descriptionVijayavel, K., Anbuselvam, C., Balasubramanian, M.P., Antioxidant effect of the marine algae Chlorella vulgaris against naphthalene-induced oxidative stress in the albino rats (2007) Mol. Cell Biochem., 303, pp. 39-44
dc.descriptionVirgolini, M.B., Chen, K., Weston, D.D., Interactions of chronic lead exposure and intermittent stress: consequences for brain-catecholamine systems and associated behaviors and HPA axis function (2005) Toxicol. Sci., 87, pp. 469-482
dc.descriptionVivier, E., Tomasello, E., Baratin, M., Functions of natural killer cells (2008) Nat. Immunol., 95, pp. 503-510
dc.descriptionWesterman, M.P., Pfitzer, E., Ellis, L.D., Concentrations of lead in bone in plumbism (1965) N. Engl. J. Med., 23, pp. 1246-1250
dc.descriptionWilde, E.W., Benemann, J.R., Bioremoval of heavy metals by the use of microalgae (1993) Biotechnol. Adv., 11, pp. 781-812
dc.descriptionWinneke, G., Zinc to prevent lead poisoning (1996) Can. Med. Assoc. J., 154, pp. 1622-1623
dc.descriptionWoiciechowsky, C., Asadullah, K., Nestler, D., Sympathetic activation triggers systemic interleukin-10 release in immunodepression induced by brain injury (1998) Nat. Med., 4, pp. 808-813
dc.descriptionWong, S.L., Nakamoto, L., Wainwright, J.F., Detection of toxic organometallic complexes in waste waters using algal assays (1997) Arch. Environ. Contam. Toxicol., 32, pp. 358-366
dc.descriptionYamaguchi, M., Role of zinc in bone formation and bone resorption (1998) J. Trace Elem. Exp. Med., 11, pp. 119-135
dc.descriptionYamamoto, N., Zou, J.P., Li, X.F., Regulatory mechanisms for production of IFN-γ and TNF by antitumor T cells or macrophages in the tumor-bearing state (1995) J. Immunol., 154, pp. 2281-2290
dc.descriptionZhang, X., Okutsu, M., Kanemi, O., Effect of foot shock stress on the interferon-γ production of murine intestinal intraepithelial lymphocytes (2005) Immunol. Lett., 100, pp. 170-176
dc.descriptionZhao, X., Ren, G., Liang, L., Brief report: interferon-gamma induces expansion of Lin(-) Sca-1(+)C-Kit(+) cells (2010) Stem Cells, 28, pp. 122-126
dc.descriptionZhou, D., Kusnecov, A.W., Shurin, M.R., Exposure to physical and psychological stressors elevates plasma interleukin-6: relationship to the activation of hypothalamic-pituitary-adrenal axis (1993) Endocrinology, 133, pp. 2523-2530
dc.descriptionZwirner, N.W., Domaica, C.I., Cytokine regulation of natural killer cell effector functions (2010) Biofactors, 36, pp. 274-288
dc.languageen
dc.publisher
dc.relationFood and Chemical Toxicology
dc.rightsfechado
dc.sourceScopus
dc.titleChlorella Vulgaris Restores Bone Marrow Cellularity And Cytokine Production In Lead-exposed Mice
dc.typeArtículos de revistas


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