Objective: To investigate the effect of selective phosphodiesterase (PDE) 4 inhibitors on nuclear factor kappa B (NF-κB), tumor necrosis factor-α (TNFα) and interleukin-8 (IL-8) secreted by peripheral blood mononuclear cells (PBMCs) in patients diagnosed as rheumatoid arthritis with interstitial lung disease (RA-ILD).
Methods: PBMCs isolated from 15 healthy volunteers (group A) and 20 patients with untreated active RA-ILD (group B) were cultured in vitro. PBMCs from healthy subjects were considered as normal control.
HMGB3 overexpression has been reported in a variety of human cancers. However, the role of HMGB3 in human non-small cell lung cancer (NSCLC) remains unclear. In this study, the HMGB3 expression was examined at mRNA and protein levels by quantitative real-time reverse transcriptase-polymerase chain reaction (qRT-PCR), Western blotting, and immunohistochemistry in NSCLC tissues and adjacent non-cancerous tissues.
View Article and Find Full Text PDFGuang Pu Xue Yu Guang Pu Fen Xi
August 2006
Guang Pu Xue Yu Guang Pu Fen Xi
February 2002
In this paper, the decomposition method of sulfur and the determination of trace arsenic in sulfur by GFAAS with La(NO3)3-Ni(NO3)2 matrix modifier were studied in detail. The decomposition of sulfur with mixed acid HNO3-HClO4 by controlled temperature electrothermal method or pressure crucible method was efficient and safe. The sensitivity of the determination of arsenic with La(NO3)3-Ni(NO3)2 matrix modifier was higher than with Ni(NO3)2 or Mg(NO3)2 matrix modifiers.
View Article and Find Full Text PDFGuang Pu Xue Yu Guang Pu Fen Xi
October 2002
In this paper, the method of determining arsenic and selenium in the industrial sulphur sample has been studied. Carbon tetrachloride-boromine was used to dissolve the sulphur sample in classical methods, which is complex and harmful, and a little arsenic and selenium will be lost. In this paper, nitric acid and perchloric acid were used to dissolve the sulphur sample, which was simple, and scarcely arsenic and selenium were lost.
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