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1.
Microb Ecol ; 68(4): 871-80, 2014 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-25004996

RESUMEN

The previous studies all focus on the effect of probiotics and antibiotics on infection after liver transplantation. Here, we focus on the effect of gut microbiota alteration caused by probiotics and antibiotics on hepatic damage after allograft liver transplantation. Brown-Norway rats received saline, probiotics, or antibiotics via daily gavage for 3 weeks. Orthotopic liver transplantation (OLT) was carried out after 1 week of gavage. Alteration of the intestinal microbiota, liver function and histopathology, serum and liver cytokines, and T cells in peripheral blood and Peyer's patch were evaluated. Distinct segregation of fecal bacterial diversity was observed in the probiotic group and antibiotic group when compared with the allograft group. As for diversity of intestinal mucosal microbiota and pathology of intestine at 2 weeks after OLT, antibiotics and probiotics had a significant effect on ileum and colon. The population of Lactobacillus and Bifidobacterium in the probiotic group was significantly greater than the antibiotic group and the allograft group. The liver injury was significantly reduced in the antibiotic group and the probiotic group compared with the allograft group. The CD4/CD8 and Treg cells in Peyer's patch were decreased in the antibiotic group. The intestinal Treg cell and serum and liver TGF-ß were increased markedly while CD4/CD8 ratio was significantly decreased in the probiotic group. It suggested that probiotics mediate their beneficial effects through increase of Treg cells and TGF-ß and deduction of CD4/CD8 in rats with acute rejection (AR) after OLT.


Asunto(s)
Bacterias/efectos de los fármacos , Rechazo de Injerto , Intestinos/microbiología , Trasplante de Hígado , Hígado/fisiopatología , Alimentación Animal/análisis , Animales , Antibacterianos/administración & dosificación , Bacterias/genética , Bacterias/crecimiento & desarrollo , ADN Bacteriano/genética , ADN Bacteriano/metabolismo , Dieta , Suplementos Dietéticos/análisis , Masculino , Microbiota/genética , Microbiota/fisiología , Datos de Secuencia Molecular , Filogenia , Probióticos/administración & dosificación , ARN Ribosómico 16S/genética , ARN Ribosómico 16S/metabolismo , Ratas , Análisis de Secuencia de ADN
2.
Zhongguo Zhong Yao Za Zhi ; 33(3): 292-5, 2008 Feb.
Artículo en Chino | MEDLINE | ID: mdl-18536469

RESUMEN

OBJECTIVE: To investigate the effects of Paecilomyces cicadae polysaccharide (PCPS) on the immunological function of aged rats in vivo. METHOD: The young and old rats were administered with normal saline as control groups, and the rats from test group were sc given 50, 100, 200 mg x kg(-1) x d(-1) dosage of PCPS for 3 weeks. The phagocytizing rate and index of PMphi, AMphi to S. aureas were observed, and the colorimetric MTI was used to analyze the proliferative activity of spleenocytes which had been stimulated with ConA or LPS. We also inspected the ability varing of ACP, LDH, ARG of spleen, and observed the ultramicro structure of spleen under the SEM. RESULT: The phagocytosis of Mphi was lower in aged group than that in young' s group, and the proliferative activity of spleenocytes was lower too. The activities of ACP, LDH, ARG of spleen were extremely decreased (P < 0.01) in aged rats as well. The proliferative activity and phagocytotic rate were both extremely increased in PCPS groups (P < 0.01), and the mitochondrion and endoplasmic reticulum of spleen were accrementition as well (P < 0.01). CONCLUSION: PCPS could enhance the phagocytizing function of PMphi, AMphi of aged rats in vivo, and strengthen the immune function of spleen and its proliferative activity as well. Then the immunity of aged rats could be improved. The PCPS may be an anti-aging agent.


Asunto(s)
Hypocreales/química , Inmunidad/efectos de los fármacos , Polisacáridos/farmacología , Animales , Hypocreales/aislamiento & purificación , Masculino , Microscopía Electrónica de Transmisión , Distribución Aleatoria , Ratas , Ratas Sprague-Dawley , Bazo/efectos de los fármacos , Bazo/ultraestructura
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