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Inhibitory effect of lanthanum chloride on the expression of inducible nitric oxide synthase in RAW264.7 macrophages induced by lipopolysaccharide / 中华烧伤杂志
Chinese Journal of Burns ; (6): 280-283, 2007.
Article in Chinese | WPRIM | ID: wpr-347687
ABSTRACT
<p><b>OBJECTIVE</b>To explore the influence of lanthanum chloride (LaCl3) on inducible nitric oxide synthase (iNOS) expression in RAW264.7 macrophages with lipopolysaccharide (LPS) induction, and to investigate its possible mechanisms.</p><p><b>METHODS</b>The RAW264.7 macrophages were randomly divided into four groups i. e, control group (without treatment), LaCl3 group (with treatment of 2.5 micromol/L of LaCl3 for 24 hrs), LaCl3 + LPS group (with treatment of 2.5 micromol/L LaCl3 for 24h), and LPS group (with treatment of 1 mg/L LPS for 24 hrs). The iNOS protein expression was measured by immunofluorescence and Western blot. iNOS gene expression was assayed by reverse transcription-polymerase chain reaction (RT-PCR). NO production in culture supernatant was assayed by nitrate reductase method.</p><p><b>RESULTS</b>Immunofluorescence analysis showed that iNOS was located mainly in the cytoplasm. RAW264.7 cells with overexpression of iNOS accounted for 44.4%, which was obviously higher than that in LaCl3 + LPS group (11.8%, P < 0.05). There was a faint signal of FITC-labeled green tint in control group or LaCl3 group. The iNOS mRNA and protein expression, and the NO content in LPS group were significantly higher than those in control, LaCl3, and LaCl3 + LPS groups (P < 0.05).</p><p><b>CONCLUSION</b>LaCl3 can suppress LPS-induced iNOS overexpression at mRNA and protein level and reduce NO production, indicating that LaCl3 can antagonize the excessive activation of iNOS induced by LPS.</p>
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pharmacology / RNA, Messenger / Cell Line / Lipopolysaccharides / Reverse Transcriptase Polymerase Chain Reaction / Nitric Oxide Synthase Type II / Toxicity / Lanthanum / Macrophages / Metabolism Limits: Animals Language: Chinese Journal: Chinese Journal of Burns Year: 2007 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pharmacology / RNA, Messenger / Cell Line / Lipopolysaccharides / Reverse Transcriptase Polymerase Chain Reaction / Nitric Oxide Synthase Type II / Toxicity / Lanthanum / Macrophages / Metabolism Limits: Animals Language: Chinese Journal: Chinese Journal of Burns Year: 2007 Type: Article