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1.
Chinese Journal of Pediatrics ; (12): 136-140, 2012.
Artigo em Chinês | WPRIM | ID: wpr-356322

RESUMO

<p><b>OBJECTIVE</b>To investigate the impact of sodium nitroprusside (a nitric oxide donor) in the ductus arteriosus in preterm rabbits on hydrogen sulfide (H(2)S)-cystathionine-γ-lyase (CSE) system.</p><p><b>METHODS</b>For 16 Japanese white rabbits pregnant for 21 days were randomly divided into four groups, each of the following groups had 4 rabbits: control group, intraperitoneal injection of sodium nitroprusside 1 mg/kg, 2.5 mg/kg, and 5.0 mg/kg groups. The rabbits in control group had a peritoneal puncture with a simple hollow needle, and those in the other groups were given corresponding dose of intraperitoneal injection of sodium nitroprusside at gestational age 23 and 25 days, respectively. At gestational age 26 days the fetuses of the pregnant rabbits were removed surgically, and 28 fetal rabbits were obtained from the control group, 27 from the sodium nitroprusside small dose group, 29 from the medium dose group, and 26 from the large dose group. The fetal heart blood sample of 1 ml was taken from each fetus, and immediately after sampling the arterial ductal tissues were dissected. Fetal rabbit plasma proteins hydrogen sulfide content was determined by using de-protein method, and real time quantitative RT-PCR was used for determination of arterial tissue CSE gene and western-blotting was used for measuring protein expression of CSE.</p><p><b>RESULTS</b>In control group hydrogen sulfide content of fetal rabbits plasma (55.68 ± 6.57) µmol/L and arterial tissue CSE mRNA expression was 1.07 ± 4.12; the parameters in intraperitoneal injection of sodium nitroprusside group 1 mg/kg were (60.02 ± 6.09) µmol/L and 3.46 ± 0.18; in intraperitoneal injection of sodium nitroprusside group 2.5 mg/kg, were (64.71 ± 7.12) µmol/L and 10.95 ± 0.22; and in intraperitoneal injection of sodium nitroprusside group 1 mg/kg were (70.63 ± 8.07) µmol/L and 19.56 ± 0.17. Comparison between small dose group and control group, medium dose group and small dose group, high dose group and medium dose group showed that the above data were significantly different P < 0.05, with the injection of sodium nitroprusside CSE protein expression increased gradually with increasing doses.</p><p><b>CONCLUSION</b>Sodium nitroprusside showed an enhancing effect on preterm CSE-H(2)S system in rabbit ductus arteriosus in a certain range of concentration in a dose-dependent manner.</p>


Assuntos
Animais , Feminino , Gravidez , Coelhos , Cistationina gama-Liase , Sangue , Canal Arterial , Metabolismo , Sulfeto de Hidrogênio , Sangue , Óxido Nítrico , Sangue , Nitroprussiato , Farmacologia
2.
Acta Academiae Medicinae Sinicae ; (6): 242-245, 2002.
Artigo em Chinês | WPRIM | ID: wpr-301882

RESUMO

<p><b>OBJECTIVE</b>To clone a novel gene relative to blood glucose regulation.</p><p><b>METHODS</b>Rat modes of autonomous regulation of blood glucose was made by intra jugular vein to right atrium injection of high concentration of glucose solution, and the control rats were injected with 0.9%NaCl both before skeletal muscles were separated for gene analysis. The differentially expressed fragments were identified by differential display technology (DDRT-PCR). After slot blot and Northern blot analysis, the artificial positive fragments were excluded and the true EST (expression sequence tag) differentially expressed was obtained. These positive EST were used as probes to screen cDNA library of rat skeletal muscle.</p><p><b>RESULTS</b>A novel full-length cDNA, named as Fang-2 was obtained. GenBank Accession No. was AF399874. Fang-2 was found rat homologue of human troponin T by blast software (NCBI). It shared 78% identical nucleotides, which showed the family proteins were conservative. After high concentration of glucose stimulation of rats, the expression of Fang-2 was down-regulated.</p><p><b>CONCLUSIONS</b>A novel gene relative to blood glucose regulation was cloned from rat skeletal muscle. The gene can regulate blood glucose level by effect certain mechanisms unknown yet with down-regulation expression.</p>


Assuntos
Animais , Masculino , Ratos , Sequência de Aminoácidos , Sequência de Bases , Glicemia , Metabolismo , Clonagem Molecular , DNA Complementar , Perfilação da Expressão Gênica , Modelos Animais , Dados de Sequência Molecular , Músculo Esquelético , Metabolismo , Ratos Sprague-Dawley , Troponina T , Genética
3.
Acta Academiae Medicinae Sinicae ; (6): 611-615, 2002.
Artigo em Chinês | WPRIM | ID: wpr-278127

RESUMO

<p><b>OBJECTIVE</b>To observe the characteristics and difference of gene expression in the pituitary adenomas and para-tumor normal pituitary tissues.</p><p><b>METHODS</b>Using serial analysis of gene expression (SAGE), two SAGE libraries were generated. Forty clones from each SAGE library were sequenced, and the results were analyzed by SAGE2000 software and compared with the SAGE map at NCBI.</p><p><b>RESULTS</b>A total of 655 gene tags, representing 43 genes, were extracted from the 40 sequence files of the para-tumor normal pituitary tissues and 737 gene tags, representing 53 genes, were extracted from the 40 sequence files of the pituitary adenomas. Of these tags, 13 were not reported before. The genes related to pituitary hormone secretion and energy metabolism were highly expressed in the two kinds of tissues. Some growth factors and cytokines were also expressed, including those involved in the immunological system. But there were also much difference of gene expression in the two tissues. Thirty-one and five tags were only detected in para-tumor normal pituitary tissues and pituitary adenomas, respectively.</p><p><b>CONCLUSIONS</b>Genes involved in hormones secretion and energy metabolism were highly expressed in the pituitary adenomas and para-tumor normal pituitary tissues. Many growth factors and cytokines were also expressed in pituitary. There was also much difference of gene expression in the two kinds of tissues. SAGE can be used not only in understanding the quantity information of gene expression, but also in finding new genes.</p>


Assuntos
Humanos , Adenoma , Genética , Metabolismo , Sequência de Bases , Clonagem Molecular , Etiquetas de Sequências Expressas , Expressão Gênica , Perfilação da Expressão Gênica , Métodos , Regulação Neoplásica da Expressão Gênica , Biblioteca Gênica , Dados de Sequência Molecular , Análise de Sequência com Séries de Oligonucleotídeos , Hipófise , Metabolismo , Neoplasias Hipofisárias , Genética , Metabolismo
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