Effect of lidocaine on LPS-induced NF-KB activity in rat peritoneal macrophages
Huanliang Wang, Changqing Zhou, Ye Ting, Wang Chun-ling, Liang Li, Zhang Li, Lei Wei-fu
Abstract
Huanliang Wang, Changqing Zhou, Ye Ting, Wang Chun-ling, Liang Li, Zhang Li, Lei Wei-fu
Abstract
Objective To investigate the effect of lidocaine on the LPS-induced NF-kB activity in rat peritoneal macrophages. Methods The peritoneal macrophages obtained from male Wistar rats were placed in 12- well plates at 2 × 10 6 cell/ml after being cultured for 3 days. Each well contained 1 ml of cell suspension. The cells were randomized into control group (group C), LPS group and 3 LPS + lidocaine group S (group LL1,2,3 ) (n = 10 wells each) . In group LPS and LL1,2,3 , the cells were exposed to LPS 100 ng/ml. In group LL1,2,3 the cells were exposed to lidocaine 2, 20 200 kg/ml respectively in addition to LPS 100 ng/ml. After being incubated for 24 h, the HMGB1 concentration in the supematant (by ELISA) and HMGB1 mRNA expression (by RT-PCR) and NF-kB activity in the cells were measured. Results LPS significantly increased HMGB1 concentration, HMGB1 mRNA expression and NF-kB activity in the supernatant. Lidocaine treatment significantly attenuated the LPS-induced increase in HMGB1 concentration HMGB1 mRNA expression and NF-kB activity in a dose-dependent manner. Conclusion Lidocaine can inhibit NF-kB activity in the rat peritoneal macrophages and in turn inhibit the synthesis and release of HMGB1. Key words: Lidocaine ; NF- kappa B ; Endotoxemia ; Macrophages
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Objective To investigate the effect of lidocaine on the LPS-induced NF-kB activity in rat peritoneal macrophages. Methods The peritoneal macrophages obtained from male Wistar rats were placed in 12- well plates at 2 × 10 6 cell/ml after being cultured for 3 days. Each well contained 1 ml of cell suspension. The cells were randomized into control group (group C), LPS group and 3 LPS + lidocaine group S (group LL1,2,3 ) (n = 10 wells each) . In group LPS and LL1,2,3 , the cells were exposed to LPS 100 ng/ml. In group LL1,2,3 the cells were exposed to lidocaine 2, 20 200 kg/ml respectively in addition to LPS 100 ng/ml. After being incubated for 24 h, the HMGB1 concentration in the supematant (by ELISA) and HMGB1 mRNA expression (by RT-PCR) and NF-kB activity in the cells were measured. Results LPS significantly increased HMGB1 concentration, HMGB1 mRNA expression and NF-kB activity in the supernatant. Lidocaine treatment significantly attenuated the LPS-induced increase in HMGB1 concentration HMGB1 mRNA expression and NF-kB activity in a dose-dependent manner. Conclusion Lidocaine can inhibit NF-kB activity in the rat peritoneal macrophages and in turn inhibit the synthesis and release of HMGB1. Key words: Lidocaine ; NF- kappa B ; Endotoxemia ; Macrophages
Key concepts: HMGB1, Lidocaine, Messenger RNA, Chemistry, Pharmacology, Molecular biology, Suspension culture, Lidocaine Hydrochloride