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评价通常被称为超氧化物歧化酶和过氧化氢酶模拟物的化合物在细胞模型中的作用。

Evaluation of the compounds commonly known as superoxide dismutase and catalase mimics in cellular models.

机构信息

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

Centre Interdisciplinaire de Recherche en Biologie (CIRB), CNRS UMR7241/INSERM U1050/Collège de France, 75231 Paris, Cedex 05, France; Sorbonne Université, 4 place Jussieu, 75005 Paris, France.

出版信息

J Inorg Biochem. 2021 Jun;219:111431. doi: 10.1016/j.jinorgbio.2021.111431. Epub 2021 Mar 19.

Abstract

Oxidative stress that results from an imbalance between the concentrations of reactive species (RS) and antioxidant defenses is associated with many pathologies. Superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase are among the key enzymes that maintain the low nanomolar physiological concentrations of superoxide and hydrogen peroxide. The increase in the levels of these species and their progeny could have deleterious effects. In this context, chemists have developed SOD and CAT mimics to supplement them when cells are overwhelmed with oxidative stress. However, the beneficial activity of such molecules in cells depends not only on their intrinsic catalytic activities but also on their stability in biological context, their cell penetration and their cellular localization. We have employed cellular assays to characterize several compounds that possess SOD and CAT activities and have been frequently used in cellular and animal models. We used cellular assays that address SOD and CAT activities of the compounds. Finally, we determined the effect of compounds on the suppression of the inflammation in HT29-MD2 cells challenged by lipopolysaccharide. When the assay requires penetration inside cells, the SOD mimics Mn(III) meso-tetrakis(N-(2'-n-butoxyethyl)pyridinium-2-yl)porphyrin (MnTnBuOE-2-PyP) and Mn(II) dichloro[(4aR,13aR,17aR,21aR)-1,2,3,4,4a,5,6,12,13,13a,14,15,16,17,17a,18,19,20,21,21a-eicosahydro-11,7-nitrilo-7Hdibenzo[b,h] [1,4, 7,10] tetraazacycloheptadecine-κN5,κN13,κN18,κN21,κN22] (Imisopasem manganese, M40403, CG4419) were found efficacious at 10 μM, while Mn(II) chloro N-(phenolato)-N,N'-bis[2-(N-methyl-imidazolyl)methyl]-ethane-1,2-diamine (Mn1) requires an incubation at 100 μM. This study thus demonstrates that MnTnBuOE-2-PyP, M40403 and Mn1 were efficacious in suppressing inflammatory response in HT29-MD2 cells and such action appears to be related to their ability to enter the cells and modulate reactive oxygen species (ROS) levels.

摘要

氧化应激是由于活性氧(ROS)和抗氧化防御之间的浓度不平衡引起的,与许多病理学有关。超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和谷胱甘肽过氧化物酶是维持超氧化物和过氧化氢的低纳摩尔生理浓度的关键酶之一。这些物质及其产物水平的增加可能会产生有害影响。在这种情况下,化学家们已经开发出 SOD 和 CAT 的模拟物,以在细胞受到氧化应激时补充它们。然而,这些分子在细胞中的有益活性不仅取决于它们的内在催化活性,还取决于它们在生物环境中的稳定性、细胞穿透性和细胞定位。我们使用细胞测定法来表征几种具有 SOD 和 CAT 活性的化合物,并经常在细胞和动物模型中使用。我们使用了测定化合物的 SOD 和 CAT 活性的细胞测定法。最后,我们确定了这些化合物在抑制脂多糖刺激的 HT29-MD2 细胞炎症中的作用。当测定需要穿透细胞内部时,SOD 模拟物 Mn(III)meso-四((2′-正丁氧基乙基)吡啶-2-基)卟啉(MnTnBuOE-2-PyP)和 Mn(II)二氯[(4aR,13aR,17aR,21aR)-1,2,3,4,4a,5,6,12,13,13a,14,15,16,17,17a,18,19,20,21,21a-二十氢-11,7-亚硝基-7H-二苯并[b,h][1,4,7,10]四氮杂环十七烷-κN5,κN13,κN18,κN21,κN22](Imisopasem 锰,M40403,CG4419)在 10μM 时有效,而 Mn(II)氯-N-(苯氧基)-N,N′-双[2-(N-甲基-咪唑基)甲基]乙烷-1,2-二胺(Mn1)则需要在 100μM 时孵育。因此,本研究表明,MnTnBuOE-2-PyP、M40403 和 Mn1 能有效抑制 HT29-MD2 细胞的炎症反应,这种作用似乎与其进入细胞并调节活性氧(ROS)水平的能力有关。

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