Sato Emiko, Kato Masatoshi, Kohno Masahiro, Niwano Yoshimi
New Industry Creation Hatchery Center, Tohoku University, Sendai, Japan.
Int J Dermatol. 2007 Nov;46(11):1185-7. doi: 10.1111/j.1365-4632.2007.03338.x.
Clindamycin phosphate (CLDMP) is effective against Gram-positive and anaerobic bacteria, and is known to have anti-inflammatory properties.
To further study the anti-inflammatory properties of CLDMP, we examined the scavenging effects on superoxide anion and hydroxyl radical using an electron spin resonance (ESR) spin trapping method.
In a hypoxanthine-xanthine oxidase reaction system, CLDMP did not scavenge superoxide anion. In a Fenton reaction system, however, CLDMP reduced the level of hydroxyl radical, and the scavenging activity of CLDMP against hydroxyl radical was more potent than that of mannitol. As the concentration which inhibits the formation of hydroxyl radical by 50% (IC(50)) of CLDMP was changed by the addition of a 10-fold amount of a spin trapping agent, 5,5-dimethyl-1-pyrroline-N-oxide, it is strongly suggested that CLDMP scavenges hydroxyl radical directly.
This is the first report of the direct scavenging effect of CLDMP on hydroxyl radical, and the effect may improve the inflammatory response caused by invading bacteria.
磷酸克林霉素(CLDMP)对革兰氏阳性菌和厌氧菌有效,且已知具有抗炎特性。
为进一步研究CLDMP的抗炎特性,我们采用电子自旋共振(ESR)自旋捕获法检测了其对超氧阴离子和羟基自由基的清除作用。
在次黄嘌呤 - 黄嘌呤氧化酶反应体系中,CLDMP不清除超氧阴离子。然而,在芬顿反应体系中,CLDMP降低了羟基自由基水平,且CLDMP对羟基自由基的清除活性比甘露醇更强。由于通过添加10倍量的自旋捕获剂5,5 - 二甲基 - 1 - 吡咯啉 - N - 氧化物改变了CLDMP抑制羟基自由基形成50%(IC50)时的浓度,强烈提示CLDMP直接清除羟基自由基。
这是关于CLDMP对羟基自由基直接清除作用的首次报道,该作用可能改善由入侵细菌引起的炎症反应。