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基于开链配体的超氧化物歧化酶模拟物 Mn(II) 配合物的钝性、生物活性及其在肠上皮细胞中的检测。

Inertness of Superoxide Dismutase Mimics Mn(II) Complexes Based on an Open-Chain Ligand, Bioactivity, and Detection in Intestinal Epithelial Cells.

机构信息

Laboratoire des Biomolécules, LBM, Département de chimie, Ecole Normale Supérieure, PSL University, Sorbonne Université, CNRS, 75005 Paris, France.

Centre de Recherche Saint Antoine, INSERM, UMRS 938, Metabolism-Inflammation Department, 184 Rue du Faubourg Saint-Antoine, 75012 Paris, France.

出版信息

Oxid Med Cell Longev. 2022 Apr 1;2022:3858122. doi: 10.1155/2022/3858122. eCollection 2022.

Abstract

Oxidative stress is known to play a major role in the pathogenesis of inflammatory bowel diseases (IBDs), and, in particular, superoxide dismutase (SODs) defenses were shown to be weakened in patients suffering from IBDs. SOD mimics, also called SOD mimetics, as low-molecular-weight complexes reproducing the activity of SOD, constitute promising antioxidant catalytic metallodrugs in the context of IBDs. A Mn(II) complex SOD mimic (Mn1) based on an open-chain diaminoethane ligand exerting antioxidant and anti-inflammatory effects on an intestinal epithelial cellular model was shown to experience metal exchanges between the manganese center and metal ions present in the biological environment (such as Zn(II)) to some degrees. As the resulting complexes (mainly Zn(II)) were shown to be inactive, improving the kinetic inertness of Mn(II) complexes based on open-chain ligands is key to improve their bioactivity in a cellular context. We report here the study of three new Mn(II) complexes resulting from Mn1 functionalization with a cyclohexyl and/or a propyl group meant to limit, respectively, (a) metal exchanges and (b) deprotonation of an amine from the 1,2-diaminoethane central scaffold. The new manganese-based SOD mimics display a higher intrinsic SOD activity and also improved kinetic inertness in metal ion exchange processes (with Zn(II), Cu(II), Ni(II), and Co(II)). They were shown to provide anti-inflammatory and antioxidant effects in cells at lower doses than Mn1 (down to 10 M). This improvement was due to their higher inertness against metal-assisted dissociation and not to different cellular overall accumulations. Based on its higher inertness, the SOD mimic containing both the propyl and the cyclohexyl moieties was suitable for intracellular detection and quantification by mass spectrometry, quantification, that was achieved by using a C-labeled Co-based analog of the SOD mimics as an external heavy standard.

摘要

氧化应激被认为在炎症性肠病 (IBD) 的发病机制中起主要作用,特别是超氧化物歧化酶 (SOD) 的防御在患有 IBD 的患者中被证明减弱。SOD 模拟物,也称为 SOD 模拟物,作为复制 SOD 活性的低分子量配合物,在 IBD 中构成有前途的抗氧化催化金属药物。一种基于开链二氨基乙烷配体的 Mn(II) 配合物 SOD 模拟物 (Mn1),对肠上皮细胞模型表现出抗氧化和抗炎作用,被证明在一定程度上经历锰中心和生物环境中存在的金属离子(如 Zn(II))之间的金属交换。由于形成的配合物(主要是 Zn(II))是无活性的,因此提高基于开链配体的 Mn(II) 配合物的动力学惰性是提高其在细胞环境中生物活性的关键。我们在这里报告了三种新的 Mn(II) 配合物的研究,这些配合物是通过 Mn1 与环己基和/或丙基的功能化得到的,目的是分别限制(a)金属交换和(b)1,2-二氨基乙烷中心支架中氨基的去质子化。新型基于锰的 SOD 模拟物显示出更高的固有 SOD 活性,并且在金属离子交换过程中(与 Zn(II)、Cu(II)、Ni(II)和 Co(II))也具有改善的动力学惰性。与 Mn1 相比,它们在较低剂量下(低至 10 μM)在细胞中表现出抗炎和抗氧化作用。这种改善是由于它们对金属辅助解离的更高惰性,而不是不同的细胞整体积累。基于其更高的惰性,同时含有丙基和环己基部分的 SOD 模拟物适合通过质谱法进行细胞内检测和定量,通过使用 SOD 模拟物的 C 标记 Co 类似物作为外部重标准来实现定量。

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