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Sevoflurane suppresses tumour necrosis factor-α-induced inflammatory responses in small airway epithelial cells after anoxia/reoxygenation  K. Watanabe,

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Presentation on theme: "Sevoflurane suppresses tumour necrosis factor-α-induced inflammatory responses in small airway epithelial cells after anoxia/reoxygenation  K. Watanabe,"— Presentation transcript:

1 Sevoflurane suppresses tumour necrosis factor-α-induced inflammatory responses in small airway epithelial cells after anoxia/reoxygenation  K. Watanabe, C. Iwahara, H. Nakayama, K. Iwabuchi, T. Matsukawa, K. Yokoyama, K. Yamaguchi, Y. Kamiyama, E. Inada  British Journal of Anaesthesia  Volume 110, Issue 4, Pages (April 2013) DOI: /bja/aes469 Copyright © 2013 The Author(s) Terms and Conditions

2 Fig 1 Effects of sevoflurane on TNF-α-induced IL-6, IL-8, and MCP-1 gene expression in SAEC. SAEC were stimulated by TNF-α (0, 5, 10, 50 ng ml−1) under A/R conditions without (blue bar) or with 1.1 vol% (green bar) or 2.2 vol% (red bar) sevoflurane. Levels of IL-6 (a), IL-8 (b), and MCP-1 (c) gene expression were measured by quantitative real-time RT–PCR. The data were normalized relative to β-actin as an internal control and are presented as mean (sd); n=3 per group. *P<0.05, **P<0.01, ***P<0.001, ****P< for the comparison between A/R and A/R+sevo. British Journal of Anaesthesia  , DOI: ( /bja/aes469) Copyright © 2013 The Author(s) Terms and Conditions

3 Fig 2 Effects of sevoflurane on TNF-α (50 ng ml−1)-induced production of IL-6 and IL-8 in SAEC. Concentrations of IL-6 (a) and IL-8 (b) in cell supernatants were measured by ELISA. Data are presented as mean (sd); n=3 per group. ****P< for the comparison between A/R and A/R+sevo. British Journal of Anaesthesia  , DOI: ( /bja/aes469) Copyright © 2013 The Author(s) Terms and Conditions

4 Fig 3 Effect of sevoflurane on TNF-a-induced activation of p65 NF-κB. (a) The effect of sevoflurane on nuclear translocation of p65 NF-κB was analysed by immunoblotting. (b) Band density was measured by densitometric analysis. Data were normalized relative to lamin C as an internal control, and are presented as mean (sd) of three independent experiments. **P < 0.01 for the comparison between A/R and A/R+sevo. (c–e) Levels of NFKB1, NFKBIA, and NFKBIE gene expression were measured by quantitative real-time RT-PCR. Data were normalized relative to β-actin as an internal control. Black and white bars represent the experiments without and with sevoflurane, respectively. Data are presented as mean (sd); n = 3 per group. *P < 0.05 for the comparison between A/R and A/R+sevo. British Journal of Anaesthesia  , DOI: ( /bja/aes469) Copyright © 2013 The Author(s) Terms and Conditions

5 Fig 4 Effect of sevoflurane on mitochondrial integrity in TNF-α-stimulated SAEC. (a) SAEC were stained with JC-1 and analysed by flow cytometry. Ordinate: mitochondrial membrane potential (Δψm). CCCP, carbonyl cyanide 3-chlorophenylhydrazone (a reagent that causes rapid depolarization of Δψm). (b) To account for variations in mitochondrial volume, the ratio of FL2/FL1 shown in (a) was calculated. Each bar represents the mean (sd) of three experiments. British Journal of Anaesthesia  , DOI: ( /bja/aes469) Copyright © 2013 The Author(s) Terms and Conditions


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