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纯锰(III)5,10,15,20-四(4-苯甲酸)卟啉(MnTBAP)在水性体系中并非超氧化物歧化酶模拟物:作为实验治疗学和生物学中一种监督机制的构效关系实例

Pure manganese(III) 5,10,15,20-tetrakis(4-benzoic acid)porphyrin (MnTBAP) is not a superoxide dismutase mimic in aqueous systems: a case of structure-activity relationship as a watchdog mechanism in experimental therapeutics and biology.

作者信息

Rebouças Júlio S, Spasojević Ivan, Batinić-Haberle Ines

机构信息

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

出版信息

J Biol Inorg Chem. 2008 Feb;13(2):289-302. doi: 10.1007/s00775-007-0324-9. Epub 2007 Nov 29.

Abstract

Superoxide is involved in a plethora of pathological and physiological processes via oxidative stress and/or signal transduction pathways. Superoxide dismutase (SOD) mimics have, thus, been actively sought for clinical and mechanistic purposes. Manganese(III) 5,10,15,20-tetrakis(4-benzoic acid)porphyrin (MnTBAP) is one of the most intensely explored "SOD mimics" in biology and medicine. However, we show here that this claimed SOD activity of MnTBAP in aqueous media is not corroborated by comprehensive structure-activity relationship studies for a wide set of Mn porphyrins and that MnTBAP from usual commercial sources contains different amounts of noninnocent trace impurities (Mn clusters), which inhibited xanthine oxidase and had SOD activity in their own right. In addition, the preparation and thorough characterization of a high-purity MnTBAP is presented for the first time and confirmed that pure MnTBAP has no SOD activity in aqueous medium. These findings call for an assessment of the relevance and suitability of using MnTBAP (or its impurities) as a mechanistic probe and antioxidant therapeutic; conclusions on the physiological and pathological role of superoxide derived from studies using MnTBAP of uncertain purity should be examined judiciously. An unequivocal distinction between the biological effects due to MnTBAP and that of its impurities can only be unambiguously made if a pure sample is/was used. This work also illustrates the contribution of fundamental structure-activity relationship studies not only for drug design and optimization, but also as a "watchdog" mechanism for checking/spotting eventual incongruence of drug activity in chemical and biological settings.

摘要

超氧化物通过氧化应激和/或信号转导途径参与众多病理和生理过程。因此,人们一直在积极寻找超氧化物歧化酶(SOD)模拟物用于临床和机理研究。锰(III)5,10,15,20-四(4-苯甲酸)卟啉(MnTBAP)是生物学和医学领域中研究最为深入的“超氧化物歧化酶模拟物”之一。然而,我们在此表明,对于一系列锰卟啉的全面构效关系研究并未证实MnTBAP在水性介质中所宣称的超氧化物歧化酶活性,而且常规商业来源的MnTBAP含有不同量的非无害痕量杂质(锰簇),这些杂质抑制黄嘌呤氧化酶并自身具有超氧化物歧化酶活性。此外,首次报道了高纯度MnTBAP的制备及其全面表征,并证实纯MnTBAP在水性介质中没有超氧化物歧化酶活性。这些发现要求评估使用MnTBAP(或其杂质)作为机理探针和抗氧化治疗剂的相关性和适用性;对于使用纯度不确定的MnTBAP进行的研究得出的关于超氧化物生理和病理作用的结论应谨慎审视。只有使用纯样品,才能明确区分MnTBAP及其杂质所产生的生物学效应。这项工作还说明了基础构效关系研究不仅对药物设计和优化有贡献,而且作为一种“监督”机制,用于检查/发现化学和生物学环境中药物活性最终的不一致性。

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