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1.
R. bras. Ci. avíc. ; 23(3): eRBCA-2020-1430, 2021. tab, ilus, graf
Artigo em Inglês | VETINDEX | ID: vti-31512

Resumo

In this study, immunohistochemistry and real-time fluorescent-based quantitative PCR were used to evaluate the expression of heat shock protein (HSP) 60, HSP70, and HSP90 in the small intestine of Wenchang chicks. Compared with the control group (CK), the positive expression of HSP60 and HSP60 mRNA in the heat stress group (HS) were initially higher and subsequently lower in the duodenum (p<0.01). In the HS jejunum, the levels of HSP60 were higher (p<0.01) and the HSP60 mRNA was lower (p<0.05). Whereas the levels of HSP60 in the HS ileum were higher (p<0.05) and then lower (p<0.01), and the HSP60 mRNA was higher (p<0.01). The levels of HSP70 were higher (p<0.01) and the HSP70 mRNA was lower in the duodenum (p<0.05), while the expression of both HSP70 and HSP70 mRNA was higher in the jejunum (p<0.01) and the ileum (p<0.05) of the HS. In the HS duodenum the levels of HSP90 were lower and then higher (p<0.01), and the HSP90 mRNA was higher (p<0.01). The expression of both HSP90 and HSP90 mRNA was higher in the HS jejunum (p<0.05). The levels of HSP90 were lower while the HSP90 mRNA was higher in the HS ileum (p<0.01). These results indicate that heat stress disturbed the expression of HSP60, HSP70, and HSP90 in the small intestine of chicks.(AU)


Assuntos
Animais , Galinhas/fisiologia , Transtornos de Estresse por Calor/diagnóstico , Transtornos de Estresse por Calor/veterinária , Proteínas de Choque Térmico
2.
Rev. bras. ciênc. avic ; 23(3): eRBCA, 2021. tab, ilus, graf
Artigo em Inglês | VETINDEX | ID: biblio-1490875

Resumo

In this study, immunohistochemistry and real-time fluorescent-based quantitative PCR were used to evaluate the expression of heat shock protein (HSP) 60, HSP70, and HSP90 in the small intestine of Wenchang chicks. Compared with the control group (CK), the positive expression of HSP60 and HSP60 mRNA in the heat stress group (HS) were initially higher and subsequently lower in the duodenum (p<0.01). In the HS jejunum, the levels of HSP60 were higher (p<0.01) and the HSP60 mRNA was lower (p<0.05). Whereas the levels of HSP60 in the HS ileum were higher (p<0.05) and then lower (p<0.01), and the HSP60 mRNA was higher (p<0.01). The levels of HSP70 were higher (p<0.01) and the HSP70 mRNA was lower in the duodenum (p<0.05), while the expression of both HSP70 and HSP70 mRNA was higher in the jejunum (p<0.01) and the ileum (p<0.05) of the HS. In the HS duodenum the levels of HSP90 were lower and then higher (p<0.01), and the HSP90 mRNA was higher (p<0.01). The expression of both HSP90 and HSP90 mRNA was higher in the HS jejunum (p<0.05). The levels of HSP90 were lower while the HSP90 mRNA was higher in the HS ileum (p<0.01). These results indicate that heat stress disturbed the expression of HSP60, HSP70, and HSP90 in the small intestine of chicks.


Assuntos
Animais , Galinhas/fisiologia , Proteínas de Choque Térmico , Transtornos de Estresse por Calor/diagnóstico , Transtornos de Estresse por Calor/veterinária
3.
R. bras. Ci. avíc. ; 17(3): 287-292, jul.-set. 2015. tab, graf
Artigo em Inglês | VETINDEX | ID: vti-17101

Resumo

Intramuscular fat (IMF) content in chickens significantly contributes to meat quality. The main objective of this study was to assess the expression of calcineurin (CaN) and Ca2+/calmodulin-dependent protein kinase (CaMK) in lipogenesis in chicken muscle. Chickens were slaughtered and sampled at 4, 8, and 16 weeks of age. IMF content and the expression of CaN subunits and CaMK isoforms were measured in the thigh muscle tissue. The results showed that the IMF contents were greater at 16 weeks compared with those at 4 and 8 weeks (p 0.05). Transcription of fatty acid synthase (FAS) and fatty acid translocase CD36 (FAT/CD36) mRNA significantly increased with age, from four to 16 weeks (p 0.05). The mRNA levels of CaNB and CaMK IV were significantly lower at 16 weeks than at four weeks (p 0.05), but CaMK II mRNA levels were significantly higher than at four weeks (p 0.05). In order to evaluate the role of CaMK and CaN in adipogenesis, SV cells were incubated in standard adipogenic medium for 24 h and treated with specific inhibitor of CaMK and CaN. The expressions of CCAAT/enhancer binding protein b (C/EBPb, sterol regulatory element-binding protein 1 (SREBP1),and peroxisome proliferation-activated receptor g (PPAR)were dramatically enhanced by the CsA, CaN inhibitor (p 0.05). KN93, CaMK II inhibitor, dramatically repressed the expression of those lipogenic gene (p 0.05). These results indicated that CaN and CaMK had different effects on adipogenesis in the muscle of chickens.(AU)


Assuntos
Animais , Galinhas/anatomia & histologia , Galinhas/metabolismo , Proteínas Quinases Dependentes de Cálcio-Calmodulina/administração & dosagem , Proteínas Quinases Dependentes de Cálcio-Calmodulina/análise
4.
Rev. bras. ciênc. avic ; 17(3): 287-292, jul.-set. 2015. tab, graf
Artigo em Inglês | VETINDEX | ID: biblio-1490178

Resumo

Intramuscular fat (IMF) content in chickens significantly contributes to meat quality. The main objective of this study was to assess the expression of calcineurin (CaN) and Ca2+/calmodulin-dependent protein kinase (CaMK) in lipogenesis in chicken muscle. Chickens were slaughtered and sampled at 4, 8, and 16 weeks of age. IMF content and the expression of CaN subunits and CaMK isoforms were measured in the thigh muscle tissue. The results showed that the IMF contents were greater at 16 weeks compared with those at 4 and 8 weeks (p 0.05). Transcription of fatty acid synthase (FAS) and fatty acid translocase CD36 (FAT/CD36) mRNA significantly increased with age, from four to 16 weeks (p 0.05). The mRNA levels of CaNB and CaMK IV were significantly lower at 16 weeks than at four weeks (p 0.05), but CaMK II mRNA levels were significantly higher than at four weeks (p 0.05). In order to evaluate the role of CaMK and CaN in adipogenesis, SV cells were incubated in standard adipogenic medium for 24 h and treated with specific inhibitor of CaMK and CaN. The expressions of CCAAT/enhancer binding protein b (C/EBPb, sterol regulatory element-binding protein 1 (SREBP1),and peroxisome proliferation-activated receptor g (PPAR)were dramatically enhanced by the CsA, CaN inhibitor (p 0.05). KN93, CaMK II inhibitor, dramatically repressed the expression of those lipogenic gene (p 0.05). These results indicated that CaN and CaMK had different effects on adipogenesis in the muscle of chickens.


Assuntos
Animais , Galinhas/anatomia & histologia , Galinhas/metabolismo , Proteínas Quinases Dependentes de Cálcio-Calmodulina/administração & dosagem , Proteínas Quinases Dependentes de Cálcio-Calmodulina/análise
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