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1.
Exp Ther Med ; 12(2): 987-990, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27446309

ABSTRACT

The aim of the study was to investigate the therapeutic effect of chloride-restrictive fluid to prevent acute kidney injury (AKI) in cardiovascular patients in intensive care unit (ICU) wards. Between January 2013 and September 2014, 456 patients admitted to ICU wards following diagnosis of cardiovascular disease were recruited and randomized to receive chloride-rich (232 patients) or chloride-restrictive (224 patients) fluid. The baseline characteristics and incidence of Kidney Disease Improving Global Outcomes (KDIGO)-defined AKI was then compared. No significant difference was identified in the baseline characteristics between the two groups. The incidence of moderate-to-severe KDIGO-defined AKI was significantly decreased in patients who received chloride-restrictive fluid. In conclusion, chloride-restrictive may be a novel effective intervention in preventing KDIGO-defined AKI in cardiovascular patients in ICU wards.

2.
Int J Clin Exp Pathol ; 8(5): 5145-52, 2015.
Article in English | MEDLINE | ID: mdl-26191210

ABSTRACT

BACKGROUND: Resveratrol has demonstrated many beneficial effects against aging, including anti-inflammatory and antioxidant roles. The present study was designed to observe the effects of resveratrol on the dysfunction of dendritic cells (DCs) from COPD patients and its possible mechanism and use in the treatment for COPD. METHODS: Flow cytometry analysis was used to examine the expression of costimulatory markers CD80 and CD86 and ELISA was used to examine the secretion of IFN-α. Expression of miR-34 was examined by using real-time PCR. Expression vector of miR-34, LV3-miR-34 was also constructed and transfected into DCs to observe the effects on functions of DCs. RESULTS: The results showed that there was remarkable upregulation of CD80 and CD86 and secretion of cytokines IFN-α in DCs from COPD patients. Resveratrol displayed a dose-dependent cytotoxicity action over 10 µg/mL and pretreatment with resveratrol inhibited upregulation of CD80 and CD86 and secretion of cytokines IFN-α. Further study showed resveratrol upregulated the expression of miR-34, which inhibited the dysfunction of DCs. CONCLUSION: These proofs suggest that resveratrol inhibited dysfunction of DCs from COPD patients through promoting miR-34.


Subject(s)
Dendritic Cells/drug effects , MicroRNAs/metabolism , Pulmonary Disease, Chronic Obstructive/drug therapy , Stilbenes/pharmacology , B7-1 Antigen/metabolism , B7-2 Antigen/metabolism , Biomarkers/metabolism , Dendritic Cells/immunology , Dendritic Cells/metabolism , Dose-Response Relationship, Drug , Female , HEK293 Cells , Humans , Interferon-gamma/metabolism , Male , MicroRNAs/genetics , Middle Aged , Pulmonary Disease, Chronic Obstructive/genetics , Pulmonary Disease, Chronic Obstructive/immunology , Pulmonary Disease, Chronic Obstructive/metabolism , Resveratrol , Signal Transduction/drug effects , Transfection , Up-Regulation
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