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首页> 外文期刊>Cellular Physiology and Biochemistry >Mitochondria Targeted Peptide Attenuates Mitochondrial Dysfunction, Controls Inflammation and Protects Against Spinal Cord Injury-Induced Lung Injury
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Mitochondria Targeted Peptide Attenuates Mitochondrial Dysfunction, Controls Inflammation and Protects Against Spinal Cord Injury-Induced Lung Injury

机译:线粒体靶向肽可减轻线粒体功能障碍,控制炎症并防止脊髓损伤引起的肺损伤。

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>Background/Aims: Spinal cord injury (SCI) is a common and devastating disease, which results in systemic inflammatory response syndrome and secondary lung injury. Mitochondrial dysfunction and inflammation are closely related to lung injury in diverse disease models. No studies have demonstrated the effects of mitochondrial targeted peptide SS-31 in a mouse model of SCI-induced lung injury. Methods: Immediately after injury, mice in the treatment groups received a daily, single-dose intraperitoneal injection of SS-31 and for the next 2 days. The sham and SCI groups also received a daily single dose of vehicle (DMSO and 0.9% NaCl, 1: 3). The lung tissue of mice was examined after SCI, and tissue damage, apoptosis, inflammation, and mitochondrial dysfunction were recorded. Results: SS-31 treatment attenuated lung edema and tissue damage. Furthermore, SS-31 treatment reduced apoptosis of alveolar type II cells, the number of total macrophages and M1 macrophages, and neutrophil infiltration. Moreover, SS-31 treatment attenuated reactive oxygen species levels, reversed mitochondrial dysfunction and inhibited NLRP3 inflammasome activation. Conclusions: Collectively, our results demonstrate that SS-31 attenuates mitochondrial dysfunction, controls inflammatory responses, and alleviates the severity of lung damage in a mouse model of SCI-induced lung injury.
机译:> 背景/目的: 脊髓损伤(SCI)是一种常见的破坏性疾病,其导致全身性炎症反应综合征和继发性肺损伤。在多种疾病模型中,线粒体功能障碍和炎症与肺损伤密切相关。没有研究证明线粒体靶向肽SS-31在SCI诱导的肺损伤小鼠模型中的作用。 方法: 受伤后,治疗组的小鼠立即接受每日一次单剂量腹膜内注射SS-31的治疗,并持续2天。假手术组和SCI组也每天接受单剂媒介物(DMSO和0.9%NaCl,1:3)。 SCI后检查小鼠的肺组织,并记录组织损伤,凋亡,炎症和线粒体功能障碍。 结果: SS-31治疗可减轻肺水肿和组织损伤。此外,SS-31处理减少了II型肺泡细胞的凋亡,总巨噬细胞和M1巨噬细胞的数量以及中性粒细胞浸润。此外,SS-31治疗可减弱活性氧水平,逆转线粒体功能障碍并抑制NLRP3炎性体激活。 结论: 我们的研究结果表明,在SCI诱发的肺损伤小鼠模型中,SS-31可减轻线粒体功能障碍,控制炎症反应并减轻肺损伤的严重程度。

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