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通过使用超氧化物触发的过硫化物前药治疗来减轻细胞氧化应激。

Alleviating Cellular Oxidative Stress through Treatment with Superoxide-Triggered Persulfide Prodrugs.

机构信息

Department of of Chemistry, Virginia Tech Center for Drug Discovery, Macromolecules Innovation Institute, Virginia Tech, Blacksburg, VA, 24061, USA.

出版信息

Angew Chem Int Ed Engl. 2020 Sep 14;59(38):16698-16704. doi: 10.1002/anie.202006656. Epub 2020 Jul 23.

Abstract

Overproduction of superoxide anion (O ), the primary cellular reactive oxygen species (ROS), is implicated in various human diseases. To reduce cellular oxidative stress caused by overproduction of superoxide, we developed a compound that reacts with O to release a persulfide (RSSH), a type of reactive sulfur species related to the gasotransmitter hydrogen sulfide (H S). Termed SOPD-NAC, this persulfide donor reacts specifically with O , decomposing to generate N-acetyl cysteine (NAC) persulfide. To enhance persulfide delivery to cells, we conjugated the SOPD motif to a short, self-assembling peptide (Bz-CFFE-NH ) to make a superoxide-responsive, persulfide-donating peptide (SOPD-Pep). Both SOPD-NAC and SOPD-Pep delivered persulfides/H S to H9C2 cardiomyocytes and lowered ROS levels as confirmed by quantitative in vitro fluorescence imaging studies. Additional in vitro studies on RAW 264.7 macrophages showed that SOPD-Pep mitigated toxicity induced by phorbol 12-myristate 13-acetate (PMA) more effectively than SOPD-NAC and several control compounds, including common H S donors.

摘要

超氧阴离子 (O ) 的过度产生是主要的细胞活性氧 (ROS),与各种人类疾病有关。为了减轻由超氧过度产生引起的细胞氧化应激,我们开发了一种与 O 反应释放过硫化物 (RSSH) 的化合物,过硫化物是与气体递质硫化氢 (H S) 相关的活性硫物种。这种过硫化物供体被称为 SOPD-NAC,它与 O 特异性反应,分解生成 N-乙酰半胱氨酸 (NAC) 过硫化物。为了增强过硫化物向细胞的传递,我们将 SOPD 基序与短的自组装肽 (Bz-CFFE-NH ) 缀合,制成超氧响应性过硫化物供体肽 (SOPD-Pep)。SOPD-NAC 和 SOPD-Pep 都将过硫化物/H S 传递到 H9C2 心肌细胞,并通过定量体外荧光成像研究证实降低了 ROS 水平。对 RAW 264.7 巨噬细胞的进一步体外研究表明,SOPD-Pep 比 SOPD-NAC 和几种对照化合物(包括常见的 H S 供体)更有效地减轻了佛波醇 12-肉豆蔻酸 13-乙酸酯 (PMA) 诱导的毒性。

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