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Biomed Environ Sci ; 32(1): 11-21, 2019 Jan.
Article in English | MEDLINE | ID: mdl-30696535

ABSTRACT

OBJECTIVE: A strain of Aspergillus niger (A. niger), capable of releasing bound phenolic acids from wheat bran, was isolated. This strain was identified by gene sequence identification. The antioxidant and anti-inflammatory capacity of ferulic acid released from wheat bran by this A. niger strain (FA-WB) were evaluated. METHODS: Molecular identification techniques based on PCR analysis of specific genomic sequences were conducted; antioxidant ability was examined using oxygen radical absorbance capacity (ORAC), cellular antioxidant activity (CAA) assays, and erythrocyte hemolysis assays. RAW264.7 cells were used as a model to detect anti-inflammatory activity. RESULTS: The filamentous fungal isolate was identified to be A. niger. ORAC and CAA assay showed that FA-WB had better antioxidant activity than that of the ferulic acid standard. The erythrocyte hemolysis assay results suggested that FA-WB could attenuate AAPH-induced oxidative stress through inhibition of reactive oxy gen species (ROS) generation. FA-WB could significantly restore the AAPH-induced increase in intracellular antioxidant enzyme activities to normal levels as well as inhibit the intracellular malondialdehyde formation. TNF-a, IL-6, and NO levels indicated that FA-WB can inhibit the inflammation induced by lipopolysaccharide (LPS). CONCLUSION: Ferulic acid released from wheat bran by a new strain of A. niger had good anti-inflammatory activity and better antioxidant ability than standard ferulic acid.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Antioxidants/pharmacology , Aspergillus niger/metabolism , Coumaric Acids/pharmacology , Dietary Fiber/microbiology , Animals , Anti-Inflammatory Agents/metabolism , Antioxidants/metabolism , Aspergillus niger/genetics , Aspergillus niger/isolation & purification , Coumaric Acids/metabolism , DNA, Fungal/analysis , Erythrocytes/drug effects , Erythrocytes/metabolism , Fermentation , Hep G2 Cells , Humans , Interleukin-6/metabolism , Lipopolysaccharides/pharmacology , Mice , RAW 264.7 Cells , Sheep , Tumor Necrosis Factor-alpha/metabolism
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