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活性氧在喹诺酮类抗菌剂诱导的光毒性中的作用。

Participation of reactive oxygen species in phototoxicity induced by quinolone antibacterial agents.

作者信息

Umezawa N, Arakane K, Ryu A, Mashiko S, Hirobe M, Nagano T

机构信息

Faculty of Pharmaceutical Sciences, University of Tokyo, Japan.

出版信息

Arch Biochem Biophys. 1997 Jun 15;342(2):275-81. doi: 10.1006/abbi.1997.0124.

Abstract

To elucidate the mechanism of phototoxicity induced as a side effect by some of the new quinolone antibiotics, we studied sparfloxacin (SPFX), lomefloxacin, enoxacin, ofloxacin, and ciprofloxacin. We first examined the photosensitized formation of reactive oxygen species such as singlet oxygen (1O2) and superoxide anion (O2-) mediated by the new quinolones. Although a large number of studies have been reported, there is no direct evidence that these drugs generate reactive oxygen species. We employed a near-infrared emission spectrometer to detect 1O2-specific emission (1268 nm), and the nitroblue tetrazolium reduction method to detect O2-. All the quinolones investigated in this study were found to produce 1O2. Four drugs, but not SPFX, produced O2-. We also examined photodynamic DNA strand-breaking activity as a possible mechanism to explain the participation of reactive oxygen species in the phototoxicity of the drugs. All the drugs exhibited photodynamic DNA strand-breaking activity. The inhibitory effect of scavengers of reactive oxygen species indicated that the main active species was 1O2. The DNA strand-breaking activity was correlated not with the 1O2-forming ability, but with the affinity of the drugs for DNA. This result may be due to the short lifetime of 1O2. These data suggested that the phototoxicity of the new quinolones was related to DNA damage caused by reactive oxygen species, especially 1O2.

摘要

为阐明某些新型喹诺酮类抗生素作为副作用引起的光毒性机制,我们研究了司帕沙星(SPFX)、洛美沙星、依诺沙星、氧氟沙星和环丙沙星。我们首先检测了由新型喹诺酮类介导的活性氧如单线态氧(1O2)和超氧阴离子(O2-)的光敏形成。尽管已有大量研究报道,但尚无直接证据表明这些药物能产生活性氧。我们采用近红外发射光谱仪检测1O2特异性发射(1268nm),并用氮蓝四唑还原法检测O2-。本研究中所研究的所有喹诺酮类药物均被发现能产生1O2。四种药物(但不包括SPFX)能产生O2-。我们还检测了光动力DNA链断裂活性,作为解释活性氧参与药物光毒性的一种可能机制。所有药物均表现出光动力DNA链断裂活性。活性氧清除剂的抑制作用表明主要活性物质是1O2。DNA链断裂活性与1O2形成能力无关,而与药物对DNA的亲和力有关。这一结果可能是由于1O2的寿命较短。这些数据表明新型喹诺酮类药物的光毒性与活性氧尤其是1O2引起的DNA损伤有关。

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