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Chinese Journal of Industrial Hygiene and Occupational Diseases ; (12): 199-202, 2005.
Article in Chinese | WPRIM | ID: wpr-346532

ABSTRACT

<p><b>OBJECTIVE</b>To explore the possible mechanism of heme oxygenase-1 (HO-1) induction for its protective effects on acute respiratory distress syndrome (ARDS).</p><p><b>METHODS</b>The production of HO-1 was induced by hemoglobin (Hb) injection into oleic acid (OA) induced ARDS rats. Western blot and RT-PCR techniques were used to observe the induction of HO-1 in vivo. Both the levels of tumor necrosis factor-alpha (TNF-alpha) and interleukin-8 (IL-8) in serum and bronchoalveolar lavage fluid (BALF) were measured by enzyme linked immunosorbent assay (ELISA). Combined with blood gas analysis and other indexes, the effect of HO-1 on ARDS could be clearly manifested.</p><p><b>RESULTS</b>The expression of HO-1 mRNA was increased significantly 16 h after Hb injection, and the protein expression of HO-1 was also obviously increased 24 h later (P < 0.01). The levels of TNF-alpha and IL-8 in both serum and BALF were significantly lower in Hb + OA group than in OA group (P < 0.01). Arterial blood PaO(2), oxygen saturation, and oxygenated index in Hb + OA group [(56.28 +/- 6.71) mm Hg, (79.53 +/- 5.82)%, and (258.81 +/- 29.37) mm Hg respectively] were higher than in OA group [(35.08 +/- 4.59) mm Hg, (55.80 +/- 12.76)%, and (167.86 +/- 21.94) mm Hg]. Lung wet and dry weight, and pathological changes were also improved.</p><p><b>CONCLUSION</b>The production of HO-1 was successfully induced by hemoglobin in vivo. Protective effects of HO-1 on ARDS might be related to the decreasing in inflammatory factors, such as TNF-alpha and IL-8.</p>


Subject(s)
Animals , Male , Rats , Blotting, Western , Bronchoalveolar Lavage Fluid , Chemistry , Enzyme-Linked Immunosorbent Assay , Heme Oxygenase-1 , Genetics , Hemoglobins , Pharmacology , Interleukin-8 , Metabolism , Oleic Acid , RNA, Messenger , Genetics , Rats, Sprague-Dawley , Respiratory Distress Syndrome , Metabolism , Reverse Transcriptase Polymerase Chain Reaction , Tumor Necrosis Factor-alpha , Metabolism
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