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1.
Oncol Res ; 20(1): 31-7, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-23035363

RESUMO

Electrochemotherapy has been widely used for the treatment of solid tumors, although the underlying mechanism remains unclear. We aimed to investigate the effects of energy controllable steep pulse (ECSP) on the regulation of tumor growth and apoptosis in rats implanted with Walker 256 carcinosarcoma cells. A rat tumor model was established by injection of Walker 256 carcinosarcoma cells into the inguinal area. H&E staining, transmission electron microscopy, and the TUNEL assay were used to detect apoptosis. Concanavalin A-induced lymphocyte transformation and MTT assays were used to assess lymphocyte proliferation. ELISA was used to determine serum cytokine levels. After 2 weeks of ECSP treatment, tumor growth in rats was effectively suppressed, while tumor cell apoptosis was significantly induced compared to the control tumor group. Moreover, ECSP treatment enhanced proliferation and activation of lymphocytes and natural killer (NK) cells. Serum IL-2 and IFN-gamma levels were significantly decreased, and IL-4 and 1-10 levels dramatically increased in rats with control tumors compared to rats without tumors and lacking treatment (p < 0.05). In contrast, ECSP treatment increased IL-2 and IFN-gamma levels, but reduced IL-4 and IL-10 levels to normal values. Moreover, ECSP also increased TNF-alpha production, possibly from peritoneal microphages. Our current study demonstrates that ECSP treatment is able to effectively reduce tumors in rats via induction of apoptosis and activation of the rat antitumor immune response. These data provide insightful information for the future application of ECSP-based electrochemotherapy in clinical trials against solid tumors.


Assuntos
Apoptose/efeitos dos fármacos , Carcinoma 256 de Walker/tratamento farmacológico , Eletroquimioterapia/métodos , Neovascularização Patológica/tratamento farmacológico , Evasão Tumoral/imunologia , Análise de Variância , Animais , Carcinoma 256 de Walker/imunologia , Carcinoma 256 de Walker/patologia , Citocinas/imunologia , Eletroquimioterapia/instrumentação , Campos Eletromagnéticos , Feminino , Células Matadoras Naturais/imunologia , Linfócitos/imunologia , Masculino , Neovascularização Patológica/prevenção & controle , Ratos , Ratos Wistar
2.
Yao Xue Xue Bao ; 39(9): 711-5, 2004 Sep.
Artigo em Chinês | MEDLINE | ID: mdl-15606019

RESUMO

AIM: To synthesize four water-soluble metal porphyrins [5, 10, 15, 20-tetra[4-(4'-pyridine-1) butyloxy phenyl] metalloporphyrins bromide, metal = Zn (I), Cu (II), Mn (III) and Co (IV)] as analogous enzyme having two anti-active oxygen functions. METHODS: The first function, scavenging O2-, has been proved by using riboflavine-methionine photoreduction methods. The second function, scavenging H2O2, has been demonstrated by using the oxidating Vit C. The third function, scavenging HO*, has been demonstrated by using Fenton reaction. The complexes were measured by the mice liver homogenate technique of mice. RESULTS: Four model compounds could scavenge O2- in the concentration range of 1.0 x 10(-5) - 1.0 x 10(-6) mol x L(-1), decompose H2O2 in the concentration of 1.5 x 10(-6) - 1.0 x 10(-6) mol x L(-1), scavenge HO* in the concentration of 2.0 x 10(-8) - 1.0 x 10(-8) mol x L(-1). All showed that they had obvious action of decreasing the lipid peroxidation in the concentration of 1.0 x 10(-7) mol x L(-1). CONCLUSION: All above-mentioned complexes were considered to be qualified analogous enzymes of anti-active oxygen.


Assuntos
Sequestradores de Radicais Livres/síntese química , Metaloporfirinas/síntese química , Espécies Reativas de Oxigênio/metabolismo , Animais , Cobalto , Cobre , Sequestradores de Radicais Livres/farmacologia , Peróxido de Hidrogênio/metabolismo , Radical Hidroxila/metabolismo , Técnicas In Vitro , Peroxidação de Lipídeos/efeitos dos fármacos , Fígado/metabolismo , Malondialdeído/metabolismo , Manganês , Metaloporfirinas/farmacologia , Camundongos , Zinco
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