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一种新型的 SOD 模拟物,Mn(III)邻-N-正丁氧基乙基吡啶基卟啉,兼具优异的效力、亲脂性和低毒性。

A new SOD mimic, Mn(III) ortho N-butoxyethylpyridylporphyrin, combines superb potency and lipophilicity with low toxicity.

机构信息

Department of Radiation Oncology, Duke University Medical Center, NC 27710, USA.

出版信息

Free Radic Biol Med. 2012 May 1;52(9):1828-34. doi: 10.1016/j.freeradbiomed.2012.02.006. Epub 2012 Feb 13.

Abstract

The Mn porphyrins of k(cat)(O(2)(.-)) as high as that of a superoxide dismutase enzyme and of optimized lipophilicity have already been synthesized. Their exceptional in vivo potency is at least in part due to their ability to mimic the site and location of mitochondrial superoxide dismutase, MnSOD. MnTnHex-2-PyP(5+) is the most studied among lipophilic Mn porphyrins. It is of remarkable efficacy in animal models of oxidative stress injuries and particularly in central nervous system diseases. However, when used at high single and multiple doses it becomes toxic. The toxicity of MnTnHex-2-PyP(5+) has been in part attributed to its micellar properties, i.e., the presence of polar cationic nitrogens and hydrophobic alkyl chains. The replacement of a CH(2) group by an oxygen atom in each of the four alkyl chains was meant to disrupt the porphyrin micellar character. When such modification occurs at the end of long alkyl chains, the oxygens become heavily solvated, which leads to a significant drop in the lipophilicity of porphyrin. However, when the oxygen atoms are buried deeper within the long heptyl chains, their excessive solvation is precluded and the lipophilicity preserved. The presence of oxygens and the high lipophilicity bestow the exceptional chemical and physical properties to Mn(III) meso-tetrakis(N-n-butoxyethylpyridinium-2-yl)porphyrin, MnTnBuOE-2-PyP(5+). The high SOD-like activity is preserved and even enhanced: log k(cat)(O(2)(.-))=7.83 vs 7.48 and 7.65 for MnTnHex-2-PyP(5+) and MnTnHep-2-PyP(5+), respectively. MnTnBuOE-2-PyP(5+) was tested in an O(2)(.-) -specific in vivo assay, aerobic growth of SOD-deficient yeast, Saccharomyces cerevisiae, where it was fully protective in the range of 5-30 μM. MnTnHep-2-PyP(5+) was already toxic at 5 μM, and MnTnHex-2-PyP(5+) became toxic at 30 μM. In a mouse toxicity study, MnTnBuOE-2-PyP(5+) was several-fold less toxic than either MnTnHex-2-PyP(5+) or MnTnHep-2-PyP(5+).

摘要

已合成 Mn 卟啉,其对过氧阴离子(O(2)(.-))的催化活性与超氧化物歧化酶相当,且具有优化的亲脂性。其在体内的卓越功效至少部分归因于其模拟线粒体超氧化物歧化酶(MnSOD)的位置和位点的能力。MnTnHex-2-PyP(5+)是脂溶性 Mn 卟啉中研究最多的一种。它在氧化应激损伤的动物模型中具有显著的疗效,特别是在中枢神经系统疾病中。然而,当以高单剂量和多剂量使用时,它会变得有毒。MnTnHex-2-PyP(5+)的毒性部分归因于其胶束性质,即存在带正电荷的极性氮原子和疏水性烷基链。在每个烷基链中的两个 CH(2)基团被氧原子取代,旨在破坏卟啉的胶束性质。当这种修饰发生在长烷基链的末端时,氧原子被大量溶剂化,导致卟啉的亲脂性显著下降。然而,当氧原子埋藏在长庚基链内部更深时,它们的过度溶剂化被阻止,亲脂性得以保留。氧的存在和高亲脂性赋予 Mn(III)meso-四(N-正丁氧基乙基吡啶-2-基)卟啉,MnTnBuOE-2-PyP(5+) 特殊的化学和物理性质。保持并甚至增强了类似 SOD 的高活性:log k(cat)(O(2)(.-))=7.83 与 MnTnHex-2-PyP(5+)和 MnTnHep-2-PyP(5+)相比,分别为 7.48 和 7.65。MnTnBuOE-2-PyP(5+)在 O(2)(.-) 特异性体内测定、超氧化物歧化酶缺陷酵母酿酒酵母的需氧生长中进行了测试,在 5-30 μM 范围内,它完全具有保护作用。MnTnHep-2-PyP(5+)在 5 μM 时已经有毒,而 MnTnHex-2-PyP(5+)在 30 μM 时变得有毒。在小鼠毒性研究中,MnTnBuOE-2-PyP(5+)的毒性比 MnTnHex-2-PyP(5+)或 MnTnHep-2-PyP(5+)低几倍。

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