Differentiation by in vitro treatment of lidocaine-epinephrine and prilocaine-felypressine in neutrophils

被引:8
作者
Azuma, Y [1 ]
Wang, PL [1 ]
Shinohara, M [1 ]
Ohura, K [1 ]
机构
[1] Osaka Dent Univ, Dept Pharmacol, Hirakata, Osaka 5731121, Japan
关键词
lidocaine-epinephrine; prilocaine-felypressine; neutrophil; epinephrine; superoxide dismutase;
D O I
10.1016/S0165-2478(01)00221-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Neutrophils are often the first cells of the immune system to encounter an invader, such as bacteria and fungi. Lidocaine-epinephrine induced transient potentiation of the production of superoxide anion; while prilocaine-felypressine induced persistent inhibition of the production in neutrophils. Moreover, lidocaine-epinephrine inhibited the production of hydrogen peroxide in spite that it potentiated the production of superoxide anion, while prilocaine-felypressine inhibited the production of hydrogen peroxide as well as superoxide anion. By contrast, lidocaine-epinephrine and prilocaine-felypressine are both effective in significantly inhibiting adhesion and phagocytosis. Using flow cytometric analysis, both local anesthetics were found to be effective in inhibiting the expression of Mac-1 (CD11b/CD18) in neutrophils. These results suggest that lidocaine-epinephrine and prilocaine-felypressine differentially modulate the production of superoxide anion, and could similarly inhibit adhesion, phagocytosis, and the production of hydrogen peroxide by neutrophils. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:151 / 158
页数:8
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