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1.
Braz. j. med. biol. res ; 47(6): 445-451, 06/2014. graf
Article in English | LILACS | ID: lil-709443

ABSTRACT

Current studies find that degenerated cartilage endplates (CEP) of vertebrae, with fewer diffusion areas, decrease nutrient supply and accelerate intervertebral disc degeneration. Many more apoptotic cells have been identified in degenerated than in normal endplates, and may be responsible for the degenerated grade. Previous findings suggest that inhibition of apoptosis is one possible approach to improve disc regeneration. It is postulated that inhibition of CEP cell apoptosis may be responsible for the regeneration of endplates. Caspase-3, involved in the execution phase of apoptosis, is a candidate for regulating the apoptotic process. In the present study, CEP cells were incubated in 1% fetal bovine serum. Activated caspases were detected to identify the apoptotic pathway, and apoptosis was quantified by flow cytometry. Lentiviral caspase-3 short hairpin RNA (shRNA) was employed to study its protective effects against serum deprivation. Silencing of caspase-3 expression was quantified by reverse transcription-polymerase chain reaction and Western blots, and inhibition of apoptosis was quantified by flow cytometry. Serum deprivation increased apoptosis of rat CEP cells through activation of a caspase cascade. Lentiviral caspase-3 shRNA was successfully transduced into CEP cells, and specifically silenced endogenous caspase-3 expression. Surviving cells were protected by the downregulation of caspase-3 expression and activation. Thus, lentiviral caspase-3 shRNA-mediated RNAi successfully silenced endogenous caspase-3 expression, preventing inappropriate or premature apoptosis.


Subject(s)
Animals , Cattle , Apoptosis/physiology , /metabolism , Chondrocytes/metabolism , Lentivirus/genetics , RNA Interference/physiology , Starvation/metabolism , Blotting, Western , Cartilage/metabolism , Caspase 9/metabolism , /metabolism , Flow Cytometry , Genetic Vectors/metabolism , Microscopy, Fluorescence , Primary Cell Culture , Propidium , Rats, Sprague-Dawley , Reverse Transcriptase Polymerase Chain Reaction , Serum/physiology , Transfection
2.
Arq. bras. med. vet. zootec ; 60(6): 1329-1337, dez. 2008. ilus, graf, tab
Article in Portuguese | LILACS | ID: lil-506541

ABSTRACT

Avaliou-se o efeito da adição de diferentes tipos e concentrações de soro sobre o desenvolvimento e a sobrevivência de folículos ovarianos pré-antrais (FOPA) caprinos in vitro. Além disso, verificou-se a relação entre as concentrações de nitrito presentes no meio de cultivo e a viabilidade folicular. Cada par ovariano foi dividido em 29 fragmentos, sendo um destinado ao controle. Os fragmentos foram cultivados por um ou sete dias em meio essencial mínimo suplementado (MEM+) ou MEM+ com diferentes concentrações (10 ou 20 por cento) de soro fetal bovino (SFB), soro de cabra em estro (SCE) ou soro de cabra em diestro (SCD). Na análise morfológica após sete dias, apenas o tratamento com 10 por cento de SFB apresentou percentual de FOPA normais similar ao MEM+ (P>0,05). A análise ultra-estrutural dos folículos cultivados por sete dias com MEM+ ou MEM+ com 10 por cento de SFB mostrou danos oocitários, porém células da granulosa normais. A análise do meio de cultivo revelou correlação positiva entre a viabilidade folicular e a produção de nitrito. A suplementação com soro não melhorou a viabilidade de FOPA e a concentração de nitrito no meio de cultivo funcionou como um indicador da viabilidade das células da granulosa de FOPA caprinos cultivados in vitro.


The effect of the addition of different types and concentrations of sera on the viability and development of caprine preantal follicles (PAF) in vitro cultured was analyzed. In addition, it was evaluated the correlation between nitrite concentrations in culture medium and folicular viability. Each ovarian pair was divided in 29 fragments and one was used as control. The fragments were cultured for one or seven days in minimal essential medium (MEM+) or MEM+ with different concentrations of (10 or 20 percent) bovine fetal serum (BFS), estrous goat serum (EGS), or diestrous goat serum (DGS). After seven days, the morphological analysis showed that only the treatment with 10 percent BFS maintained the percentage of normal PAF similar to MEM+ (P>0.05). The ultrastructural analysis of follicles cultured for seven days in MEM+ or MEM+ with 10 percent BFS showed some oocyte damage, although the granulosa cells were normal. Analysis of culture medium revealed a positive correlation between follicular viability and nitrite production. Supplementation with serum did not improve the viability of PAF and nitrite levels in culture medium served as an indicator of viability of granulose cells from caprine PAF in vitro cultured.


Subject(s)
Animals , Female , Goats/physiology , Fertilization in Vitro/adverse effects , Fertilization in Vitro/methods , Ovarian Follicle/anatomy & histology , Ovarian Follicle/ultrastructure , Tissue Survival , Serum/physiology
3.
Arq. bras. med. vet. zootec ; 59(2): 541-542, abr. 2007. tab
Article in English | LILACS | ID: lil-455777

ABSTRACT

Colheu-se uma amostra de sangue de um albatroz Thalassarche chlororhynchos (Gmelin, 1789), recolhido pela Polícia do Meio Ambiente de Ubatuba, SP, para análises da bioquímica do soro. O objetivo dessas análises foi o de apontar possíveis alterações dos parâmetros bioquímicos, visando facilitar futuras casas para reabilitação de aves. Nenhuma anormalidade foi encontrada e o animal morreu após três dias da captura.


Subject(s)
Blood Chemical Analysis/methods , Birds/blood , Serum/physiology
4.
Arq. bras. med. vet. zootec ; 59(2): 543-546, abr. 2007. graf
Article in Portuguese | LILACS | ID: lil-455778

ABSTRACT

The present study had the objective of defining the culture conditions, optimizing the maintenance and expansion of an IDE-8 cell line in Brazil, with the aim to propose its use as a model for in vitro infection and multiplication of Brazilian strains of rickettsia and other hemoparasites. The supplementation of IDE-8 cells with two distinct fetal bovine sera (a Brazilian and an imported) was evaluated. Culture media were changed weekly and subcultures were carried out every 15 days. The development of cultures and subcultures was evaluated by the percentage of viability and cellular morphology. The results indicate that the imported SFB can be replaced by the Brazilian SFB one, as no significant differences (P<0.05) were seen among culture viabilities.


Subject(s)
Cattle , Ticks/cytology , Cell Count/methods , Serum/physiology
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