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1.
Fish Shellfish Immunol ; 39(1): 108-17, 2014 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-24795082

RESUMO

The fish gill is in direct and standing contact with the immediate external environment and, therefore, is highly vulnerable to aquatic pollutants. In this study, Prochilodus argenteus were caught at two different points in São Francisco river. The first point is located near Três Marias dam, while the second is placed downstream the Abaeté river. Chemical approaches showed the presence of metals contamination in the first point. Thus, the main goal of this study was to investigate the possible toxic effects of these contaminants and the likely use of biomarkers on fish gills. Biometric data of length and weight of fish were obtained in order to calculate the condition factor as an organismal biomarker. The histological changes in gills and alterations in mucous and rodlet cells occurrence were detected microscopically and evaluated with quantitative analyses. Myeloperoxidase (MPO) and Eosinophil Peroxidase (EPO) were also assessed in fish gill. The analysis of the water and sediment samples revealed the presence of metals at the two points. As and Cd were detected at higher concentrations at point 1. The presence of lamellar cell hyperplasia, lamellar fusion, lamellar edema and inflammatory foci varied according to the point. Additionally, mucous and rodlet cells and MPO and EPO activities showed variability according to the environmental conditions. Furthermore, with exception of lamellar hyperplasia and eosinophil peroxidase activity, all others parameters showed sex-variation responses. At the first point, male fish showed a chronical inflammation in gills due to the lowest activity of MPO and EPO, as well as low occurrence of inflammatory foci and glycoprotein secretion by mucous cells, while female fish presented an opposite pattern of response to the same environmental conditions. Therefore, we suggest the use of such biomarkers in future monitoring of aquatic systems, taking into account the sex-variation responses.


Assuntos
Caraciformes/imunologia , Caraciformes/metabolismo , Brânquias/efeitos dos fármacos , Metais/toxicidade , Poluentes Químicos da Água/toxicidade , Animais , Biomarcadores/metabolismo , Brasil , Caraciformes/anatomia & histologia , Monitoramento Ambiental , Peroxidase de Eosinófilo/metabolismo , Feminino , Brânquias/enzimologia , Brânquias/imunologia , Brânquias/patologia , Masculino , Peroxidase/metabolismo , Rios/química , Fatores Sexuais , Espectrofotometria Atômica
2.
Sci Rep ; 7: 44317, 2017 03 20.
Artigo em Inglês | MEDLINE | ID: mdl-28317860

RESUMO

Microinjection is commonly performed to achieve fish transgenesis; however, due to difficulties associated with this technique, new strategies are being developed. Here we evaluate the potential of lentiviral particles to genetically modify Nile tilapia cells to achieve transgenesis using three different approaches: spermatogonial stem cell (SSC) genetic modification and transplantation (SC), in vivo transduction of gametes (GT), and fertilised egg transduction (ET). The SC protocol using larvae generates animals with sustained production of modified sperm (80% of animals with 77% maximum sperm fluorescence [MSF]), but is a time-consuming protocol (sexual maturity in Nile tilapia is achieved at 6 months of age). GT is a faster technique, but the modified gamete production is temporary (70% of animals with 52% MSF). ET is an easier way to obtain mosaic transgenic animals compared to microinjection of eggs, but non-site-directed integration in the fish genome can be a problem. In this study, PI3Kc2α gene disruption impaired development during the embryo stage and caused premature death. The manipulator should choose a technique based on the time available for transgenic obtainment and if this generation is required to be continuous or not.


Assuntos
Animais Geneticamente Modificados , Ciclídeos/genética , Neovascularização Fisiológica/genética , Fosfatidilinositol 3-Quinases/genética , Transdução Genética/métodos , Células-Tronco Germinativas Adultas/citologia , Células-Tronco Germinativas Adultas/metabolismo , Células-Tronco Germinativas Adultas/transplante , Animais , Ciclídeos/crescimento & desenvolvimento , Ciclídeos/metabolismo , Embrião não Mamífero/irrigação sanguínea , Embrião não Mamífero/citologia , Embrião não Mamífero/metabolismo , Feminino , Regulação da Expressão Gênica no Desenvolvimento , Células Germinativas , Larva/genética , Larva/crescimento & desenvolvimento , Larva/metabolismo , Masculino , Microinjeções/métodos , Mutação , Fosfatidilinositol 3-Quinases/deficiência , Zigoto/crescimento & desenvolvimento , Zigoto/metabolismo
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