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1.
BMC Vet Res ; 14(1): 1, 2018 Jan 02.
Artigo em Inglês | MEDLINE | ID: mdl-29291752

RESUMO

BACKGROUND: Silver nanoparticles (AgNP) have gained much attention in recent years due to their biomedical applications, especially as antimicrobial agents. AgNP may be used in poultry production as an alternative to the use of antibiotic growth promoter. However, little is known about the impact of oral administration of AgNP on the gut microbiota and the immune system. The aim of the present study was to investigate the effects of AgNP on growth, hematological and immunological profile as well as intestinal microbial composition in broilers challenged with Campylobacter jejuni (C. jejuni). RESULTS: AgNP did not affect the intestinal microbial profile of birds. The body weight gain and the relative weights of bursa and spleen were reduced when supplemented with AgNP. There was no difference with respect to packed cell volume. However, the plasma concentrations of IgG and IgM were lower in birds receiving AgNP compared to the non-supplemented control group. The expression of TNF-α and NF-kB at mRNA level was significantly higher in birds receiving AgNP. CONCLUSIONS: The application of AgNP via the drinking water in the concentration of 50 ppm reduced broiler growth, impaired immune functions and had no antibacterial effect on different intestinal bacterial groups, which may limit the applicability of AgNP against C. jejuni in broiler chickens.


Assuntos
Infecções por Campylobacter/veterinária , Nanopartículas Metálicas/administração & dosagem , Doenças das Aves Domésticas/prevenção & controle , Prata/administração & dosagem , Administração Oral , Animais , Infecções por Campylobacter/prevenção & controle , Campylobacter jejuni/efeitos dos fármacos , Galinhas/crescimento & desenvolvimento , Galinhas/imunologia , Galinhas/microbiologia , Microbioma Gastrointestinal/efeitos dos fármacos , Expressão Gênica , Imunoglobulina G/sangue , Imunoglobulina M/sangue , Masculino , Nanopartículas Metálicas/efeitos adversos , NF-kappa B/genética , NF-kappa B/metabolismo , Doenças das Aves Domésticas/microbiologia , RNA Mensageiro , Prata/efeitos adversos , Prata/imunologia , Fator de Necrose Tumoral alfa/genética , Fator de Necrose Tumoral alfa/metabolismo
2.
Int J Mol Sci ; 16(10): 25214-33, 2015 Oct 23.
Artigo em Inglês | MEDLINE | ID: mdl-26512645

RESUMO

Our previous studies revealed that graphene had anticancer properties in experiments in vitro with glioblastoma multiforme (GBM) cells and in tumors cultured in vivo. We hypothesized that the addition of arginine or proline to graphene solutions might counteract graphene agglomeration and increase the activity of graphene. Experiments were performed in vitro with GBM U87 cells and in vivo with GBM tumors cultured on chicken embryo chorioallantoic membranes. The measurements included cell morphology, mortality, viability, tumor morphology, histology, and gene expression. The cells and tumors were treated with reduced graphene oxide (rGO) and rGO functionalized with arginine (rGO + Arg) or proline (rGO + Pro). The results confirmed the anticancer effect of graphene on GBM cells and tumor tissue. After functionalization with amino acids, nanoparticles were distributed more specifically, and the flakes of graphene were less agglomerated. The molecule of rGO + Arg did not increase the expression of TP53 in comparison to rGO, but did not increase the expression of MDM2 or the MDM2/TP53 ratio in the tumor, suggesting that arginine may block MDM2 expression. The expression of NQO1, known to be a strong protector of p53 protein in tumor tissue, was greatly increased. The results indicate that the complex of rGO + Arg has potential in GBM therapy.


Assuntos
Antineoplásicos/farmacologia , Glioblastoma/metabolismo , Grafite/farmacologia , Animais , Antineoplásicos/química , Arginina/química , Linhagem Celular Tumoral , Proliferação de Células , Sobrevivência Celular , Embrião de Galinha , Grafite/química , NAD(P)H Desidrogenase (Quinona)/genética , NAD(P)H Desidrogenase (Quinona)/metabolismo , Neurônios/efeitos dos fármacos , Óxidos/química , Proteínas Proto-Oncogênicas c-mdm2/genética , Proteínas Proto-Oncogênicas c-mdm2/metabolismo , Proteína Supressora de Tumor p53/genética , Proteína Supressora de Tumor p53/metabolismo
3.
Int J Mol Sci ; 16(5): 9484-503, 2015 Apr 27.
Artigo em Inglês | MEDLINE | ID: mdl-25923079

RESUMO

Due to their physicochemical and biological properties, silver nanoparticles (NanoAg) have a wide range of applications. In the present study, their roles as a carrier of nutrients and an immunomodulator were tested in chicken embryos. Cysteine (Cys)+NanoAg injected embryos had smaller livers but heavier breasts on the 19th day of embryogenesis. Cys injected embryos had lower oxygen consumption compared to threonine (Thr) or NanoAg injected embryos. The energy expenditure in Thr+NanoAg, or NanoAg injected embryos was higher than Cys or Cys+NanoAg but was not different from uninjected control embryos. Relative expression of the hepatic insulin-like growth factor-I (IGF-I) gene was higher in Cys or NanoAg injected embryos after lipopolysaccharide (LPS) induction. The gene expression of hepatic tumour necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6) did not differ among amino acids, NanoAg and uninjected controls in the non-LPS groups, but increased by many folds in the LPS treated NanoAg, Cys and Cys+NanoAg groups. In LPS treated spleens, TNF-α expression was also up-regulated by NanoAg, amino acids and their combinations, but interleukin-10 (IL-10) expression was down-regulated in Thr, Cys or Thr+NanoAg injected embryos. Toll like receptor-2 (TLR2) expression did not differ in NanoAg or amino acids injected embryos; however, toll like receptor-4 (TLR4) expression was higher in all treated embryos, except for Cys+NanoAg, than in uninjected control embryos. We concluded that NanoAg either alone or in combination with amino acids did not affect embryonic growth but improved immunocompetence, indicating that NanoAg and amino acid complexes can act as potential agents for the enhancement of innate and adaptive immunity in chicken.


Assuntos
Embrião de Galinha/efeitos dos fármacos , Embrião de Galinha/imunologia , Cisteína/administração & dosagem , Regulação da Expressão Gênica no Desenvolvimento/imunologia , Nanopartículas Metálicas/química , Prata/química , Treonina/administração & dosagem , Animais , Coloides/química , Perfilação da Expressão Gênica , Sistema Imunitário , Fator de Crescimento Insulin-Like I/metabolismo , Interleucina-10/metabolismo , Lipopolissacarídeos/química , Nanotecnologia , Consumo de Oxigênio , Baço/metabolismo , Receptor 2 Toll-Like/metabolismo , Receptor 4 Toll-Like/metabolismo , Fator de Necrose Tumoral alfa/metabolismo
4.
Int J Mol Sci ; 16(3): 4838-49, 2015 Mar 03.
Artigo em Inglês | MEDLINE | ID: mdl-25741768

RESUMO

Copper is a key element affecting blood vessel growth and muscle development. However, the ions released from Cu salts are toxic. Given their specific physicochemical properties, nanoparticles of Cu (NanoCu) may have different bioactivity and affect the development of blood vessel and muscles in a different manner than Cu salts. The objective of the study was to evaluate the influence of NanoCu on embryo development and angiogenesis at the systemic and molecular level, in experiments using a chick embryo model. Fertilized chicken eggs were divided into a control group, and groups injected with a placebo, CuSO4 or NanoCu. Embryo development at the whole body level and molecular indices using an embryo chorioallantoic membrane model were measured during embryogenesis. The present study indicated for the first time that NanoCu have pro-angiogenic properties at the systemic level, to a greater degree than CuSO4 salt. The properties of NanoCu were confirmed at the molecular level, demonstrating significant effects on mRNA concentration and on mRNA gene expression of all pro-angiogenic and pro-proliferative genes measured herein.


Assuntos
Cobre/química , Desenvolvimento Embrionário/efeitos dos fármacos , Nanopartículas Metálicas/toxicidade , Neovascularização Fisiológica/efeitos dos fármacos , Animais , Embrião de Galinha , Galinhas , Membrana Corioalantoide/irrigação sanguínea , Sulfato de Cobre/química , Sulfato de Cobre/toxicidade , Nanopartículas Metálicas/química , RNA Mensageiro/metabolismo , Fator A de Crescimento do Endotélio Vascular/genética , Fator A de Crescimento do Endotélio Vascular/metabolismo
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