Cuzzocrea S, Zingarelli B, Gilad E, Hake P, Salzman A L, Szabó C
Children's Hospital Medical Center, Division of Critical Care, Cincinnati, OH 45229, USA.
Eur J Pharmacol. 1998 Jan 19;342(1):67-76. doi: 10.1016/s0014-2999(97)01417-9.
A cytotoxic cycle triggered by oxidant-induced DNA single strand breakage and subsequent activation of the nuclear enzyme poly (ADP-ribose) synthetase have been shown to contribute to the cellular injury during various forms of oxidant stress in vitro. The aim of the present study was to investigate the role of poly (ADP-ribose) synthetase in a model of acute local inflammation (carrageenan-induced pleurisy), where oxyradicals, nitric oxide and peroxynitrite are known to play a crucial role in the inflammatory process. The results show that the poly (ADP-ribose) synthetase inhibitor 3-aminobenzamide (given at 1-30 mg/kg) inhibits the inflammatory response (pleural exudate formation, mononuclear cell infiltration, histological injury). Moreover, 3-aminobenzamide reduces the formation of nitrotyrosine, an indicator of the formation of peroxynitrite, in the lung. The present results demonstrate that 3-aminobenzamide, presumably by inhibition of poly (ADP-ribose) synthetase, exerts potent anti-inflammatory effects. Part of the anti-inflammatory effects of 3-aminobenzamide may be related to a reduction of neutrophil recruitment into the inflammatory site.
由氧化剂诱导的DNA单链断裂引发的细胞毒性循环以及随后核酶聚(ADP - 核糖)合成酶的激活,已被证明在体外各种形式的氧化应激过程中会导致细胞损伤。本研究的目的是探讨聚(ADP - 核糖)合成酶在急性局部炎症模型(角叉菜胶诱导的胸膜炎)中的作用,在该模型中,氧自由基、一氧化氮和过氧亚硝酸盐在炎症过程中起着关键作用。结果表明,聚(ADP - 核糖)合成酶抑制剂3 - 氨基苯甲酰胺(以1 - 30 mg/kg给药)可抑制炎症反应(胸腔渗出液形成、单核细胞浸润、组织学损伤)。此外,3 - 氨基苯甲酰胺可减少肺中硝基酪氨酸的形成,硝基酪氨酸是过氧亚硝酸盐形成的指标。目前的结果表明,3 - 氨基苯甲酰胺大概通过抑制聚(ADP - 核糖)合成酶发挥强大的抗炎作用。3 - 氨基苯甲酰胺的部分抗炎作用可能与减少中性粒细胞向炎症部位募集有关。