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基于新型环金属化铱(III)配合物的双光子探针用于可视化线粒体硝基还原酶并评估脓毒症诱导的肺损伤的治疗反应。

Novel cyclometalated iridium(III) complex-based two-photon probe for visualizing mitochondrial nitroreductase and assessing treatment responses in sepsis-induced lung injury.

作者信息

Liu Chaolong, Du Peng, Yuan Lu, Jiang Lin, Di Jiabin, Sun Yong

机构信息

Department of Pharmaceutics, School of Pharmacy, Qingdao University, Qingdao, 266071, China.

Department of Pharmaceutics, School of Pharmacy, Qingdao University, Qingdao, 266071, China.

出版信息

Anal Chim Acta. 2025 Oct 8;1370:344397. doi: 10.1016/j.aca.2025.344397. Epub 2025 Jul 8.

Abstract

BACKGROUND

Sepsis-induced lung injury (SILI) is an acute condition characterized by respiratory failure, with lung hypoxia as a prominent feature. Nitroreductase (NTR) is significantly upregulated during SILI, highlighting its potential as a promising biomarker for assessing the severity of SILI and monitoring therapeutic response. Molecular biology studies indicate that mitochondria serve as potential therapeutic targets for SILI. Accurate monitoring of mitochondrial NTR activity in SILI is expected to provide insights into the pathogenesis of the disease and offer valuable guidance for clinical treatment. However, reliable tools for monitoring mitochondrial NTR variations and assessing treatment responses in SILI are still lacking.

RESULTS

In this study, a mitochondria-targeting, two-photon Ir(III) complex-based probe, Cym-Ir-NTR, was designed and synthesized for accurate detection of mitochondrial NTR. Cym-Ir-NTR displayed weak luminescence due to the strong electron-withdrawing effect of the nitro group. Under hypoxic conditions, the nitro group is reduced to an amino group, yielding Cym-Ir-AMN, accompanied by significant luminescence enhancement. Molecular docking analysis indicated that Cym-Ir-NTR can be effectively catalyzed by NTR. Cym-Ir-NTR demonstrated high sensitivity, excellent selectivity, and rapid luminescence response to NTR. With its low toxicity and superior mitochondrial-targeting properties, Cym-Ir-NTR enabled successful imaging of mitochondrial NTR in living cells. Notably, leveraging Cym-Ir-NTR as an imaging probe, variations in mitochondrial NTR levels during SILI progression and the therapeutic effect of PHD inhibitors (dimethyloxalylglycine and roxadustat) on SILI were successfully monitored for the first time.

SIGNIFICANCE

These findings confirm Cym-Ir-NTR's capability as a robust imaging tool for tracking mitochondrial NTR and evaluating treatment response of SILI to drugs. Additionally, probe Cym-Ir-NTR can be used to reveal the biological roles that mitochondrial NTR plays in SILI and offer valuable guidance for the prevention and treatment of SILI.

摘要

背景

脓毒症诱导的肺损伤(SILI)是一种以呼吸衰竭为特征的急性病症,肺缺氧是其突出特点。在SILI期间,硝基还原酶(NTR)显著上调,这凸显了其作为评估SILI严重程度和监测治疗反应的有前景生物标志物的潜力。分子生物学研究表明,线粒体是SILI潜在的治疗靶点。准确监测SILI中线粒体NTR活性有望为该疾病的发病机制提供见解,并为临床治疗提供有价值的指导。然而,仍缺乏用于监测SILI中线粒体NTR变化和评估治疗反应的可靠工具。

结果

在本研究中,设计并合成了一种基于线粒体靶向、双光子铱(III)配合物的探针Cym-Ir-NTR,用于准确检测线粒体NTR。由于硝基的强吸电子作用,Cym-Ir-NTR发出微弱的荧光。在缺氧条件下,硝基被还原为氨基,生成Cym-Ir-AMN,同时荧光显著增强。分子对接分析表明,Cym-Ir-NTR可被NTR有效催化。Cym-Ir-NTR对NTR表现出高灵敏度、优异的选择性和快速的荧光响应。因其低毒性和优异的线粒体靶向特性,Cym-Ir-NTR能够成功对活细胞中的线粒体NTR进行成像。值得注意的是,利用Cym-Ir-NTR作为成像探针,首次成功监测了SILI进展过程中线粒体NTR水平的变化以及PHD抑制剂(二甲基草酰甘氨酸和罗沙司他)对SILI的治疗效果。

意义

这些发现证实了Cym-Ir-NTR作为一种强大的成像工具,可用于追踪线粒体NTR并评估SILI对药物的治疗反应。此外,探针Cym-Ir-NTR可用于揭示线粒体NTR在SILI中所起的生物学作用,并为SILI的预防和治疗提供有价值的指导。

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