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Zhongguo Dang Dai Er Ke Za Zhi ; 13(7): 573-6, 2011 Jul.
Artigo em Chinês | MEDLINE | ID: mdl-21752326

RESUMO

OBJECTIVE: This study examined the effects of maternal deficiency of folic acid during pregnancy on pulmonary development and protein A (SP-A) expression in newborn rats in order to explore the possible mechanism of lung developmental disorders. METHODS: Thirty-six adult Sprague-Dawley female rats were randomly assigned into two groups: control and study (n=18). The study and the control groups were fed with fodder containing folic acid or not respectively. Two weeks later, the female rats in the two groups copulated with normal male rats. Newborn rats were sacrificed at 1, 7 and 14 days after birth (8 pups at each time point). Lung sections were stained with hematoxylin and eosin for histological examination. SP-A expression of protein and mRNA were determined by immunohistochemistry and real-time quantitative RT-PCR, respectively. RESULTS: The newborn rats from the study group showed damaged lung tissue structures. The mean optical density of type II cells with positive expression of SP-A decreased significantly from 1 to 14 days in newborn rats of the study group compared with the control newborn rats (P<0.05). The real-time quantitative RT-PCR showed that the expression of lung SP-A mRNA also decreased significantly from 1 to 14 days in newborn rats of the study group compared with control newborn rats (P<0.05). CONCLUSIONS: Maternal deficiency of folic acid during pregnancy can decrease the expression of SP-A in lung tissues of newborn rats, which might lead to the disorder of lung development maturation.


Assuntos
Deficiência de Ácido Fólico/metabolismo , Pulmão/embriologia , Complicações na Gravidez/metabolismo , Proteína A Associada a Surfactante Pulmonar/análise , Animais , Animais Recém-Nascidos , Feminino , Imuno-Histoquímica , Masculino , Gravidez , Proteína A Associada a Surfactante Pulmonar/genética , RNA Mensageiro/análise , Ratos , Ratos Sprague-Dawley , Reação em Cadeia da Polimerase Via Transcriptase Reversa
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