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Therapeutic Methods and Therapies TCIM
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1.
Pol J Vet Sci ; 15(3): 547-52, 2012.
Article in English | MEDLINE | ID: mdl-23214377

ABSTRACT

UNLABELLED: The present study was designed to investigate the influence of Se deficiency on serum histamine concentration and the expression of histamine receptor in the jejunum of chickens. Forty neonatal chickens were randomly divided into two groups. Experimental chickens were fed a low-Se diet (0.034 mg/kg), whereas chickens in the control group were fed a diet with a Se level of 0.229 mg/kg. Ten chickens were sacrificed on days 30, 45, 60 and 75. Blood and jejunum samples were collected. Histamine concentration in the jejunum was measured by ELISA, the jejunal mast cell (MC) ultrastructure was studied by transmission electron microscopy, and the expression level of histamine H2 receptor (H2R) mRNA in the jejunum was examined using real-time PCR. RESULTS: The jejunal histamine concentration in chickens fed the low-Se diet was significantly higher than that in the control group (P < 0.01). Se deficiency induced degranulation of MC in the jejunum of chickens in the low-Se diet group; their cytoplasm was filled with fused granules and vacuoles. The expression level of jejunal H2R mRNA in chickens fed the low-Se diet was also significantly higher than that in the control group (P < 0.01). The results obtained suggest that Se deficiency stimulates MC degranulation and release of histamine, binding H2R promotes both regulation of digestion and cell proliferation while protects the jejunum from injury induced by Se deficiency.


Subject(s)
Chickens/physiology , Histamine/metabolism , Jejunum/physiology , Receptors, Histamine H2/metabolism , Selenium/deficiency , Animal Feed/analysis , Animals , Diet/veterinary , Gene Expression Regulation/physiology , Jejunum/cytology , Mast Cells/ultrastructure , RNA, Messenger/genetics , RNA, Messenger/metabolism , Receptors, Histamine H2/genetics
2.
Wei Sheng Wu Xue Bao ; 45(6): 895-9, 2005 Dec.
Article in Chinese | MEDLINE | ID: mdl-16496699

ABSTRACT

Radix Ranuncoli Ternati is clinically effective traditional Chinese medicine for multidrug resistant tuberculosis. Its active components and mechanism of action remain unsolved. Two dimensional gel electrophoresis (2-DE) was employed to address this problem. Globlal proteome of Mycobacterium tuberculosis untreated and treated with Radix Ranuncoli Ternati were compared, and 22 protein spots were found to be expressed differentially. 3 protein spots which remarkably decreased in Mycobacterium tuberculosis treated with Radix Ranuncoli Ternati were subjected to matrix assisted laser desorption ionization time of flight mass spectrometry (MALDI-TOF-MS) analysis. The data obtained from peptide mass finger printing were used for database search. The 3 protein spots in gel were identified as cysA2 (thiosulfate sulfurtransferase), tsf (elongation factor EF-Ts) and hspX (heat shock protein X). These data provide insights into the changed global protein patterns of Mycobacterium tuberculosis treated with Radix Ranuncoli Ternati and may prove useful for further study in the mechanism in how Radix Ranuncoli Ternati influence the life of Mycobacterium tuberculosis. The differentially expressed proteins may be potential novel antituberculosis drug targets.


Subject(s)
Bacterial Proteins/analysis , Medicine, Chinese Traditional , Mycobacterium tuberculosis/drug effects , Plant Extracts/pharmacology , Proteome , Antigens, Bacterial/analysis , Electrophoresis, Gel, Two-Dimensional , Mycobacterium tuberculosis/chemistry , Peptide Elongation Factor Tu/analysis , Peptide Elongation Factors/analysis , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
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