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经鼻给药的KL表面活性剂在辐射诱导的肺损伤小鼠模型中的辐射减轻特性

Radiation Mitigating Properties of Intranasally Administered KL Surfactant in a Murine Model of Radiation-Induced Lung Damage.

作者信息

Christofidou-Solomidou Melpo, Pietrofesa Ralph A, Arguiri Evguenia, Koumenis Constantinos, Segal Robert

机构信息

a  Division of Pulmonary, Allergy, and Critical Care Medicine and the Department of Medicine, University of Pennsylvania, Perelman School of Medicine, Philadelphia, Pennsylvania, 19104.

b  Department of Radiation Oncology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, Pennsylvania, 19104.

出版信息

Radiat Res. 2017 Nov;188(5):491-504. doi: 10.1667/RR14686.1. Epub 2017 Sep 6.

Abstract

The threat of exposure to ionizing radiation from a nuclear reactor accident or deliberate terrorist actions is a significant public health concern. The lung is particularly susceptible to radiation-induced injury from external sources or inhalation of radioactive particles from radioactive fallout. Radiation-induced lung disease can manifest with an acute radiation pneumonitis and/or delayed effects leading to pulmonary fibrosis. As prior warning of radiation exposure is unlikely, medical countermeasures (MCMs) to mitigate radiation-induced lung disease that can be given in mass-casualty situations many hours or days postirradiation are needed to prevent both early and late lung damage. In this study, KL surfactant (lucinactant) was evaluated as a radiation mitigator in a well-characterized mouse model of targeted thoracic radiation exposure, for its effect on both early (several weeks) and late (18 weeks) lung damage. Here, 120 mg/kg total phospholipid of KL surfactant was administered twice daily intranasally, (enabling intrapulmonary inhalation of drug) to C57BL/6 mice 24 h after a single 13.5 Gy dose of thoracic irradiation (LD dose). Both early and chronic phase (2 and 4 weeks and 18 weeks postirradiation, respectively) assessments were performed. Mice were evaluated for evidence of reduced arterial blood oxygenation and early and chronic lung and systemic inflammation, lung fibrosis and oxidative stress. Analysis was done by performing lung function/respiration dynamics and measuring cellular protein content of bronchoalveolar lavage fluid (BALF), and levels of cytokines, 8-iso-prostaglandin F2α, hydroxyproline in lung and plasma, along with evaluating lung histology. The results of this study showed that intranasal delivery of KL surfactant was able to preserve lung function as evidenced by adequate arterial oxygen saturation and reduced lung inflammation and oxidative stress; total white count and absolute neutrophil count was decreased in BALF, as were plasma pro-inflammatory cytokine levels and biomarker of oxidative stress. KL surfactant is a promising MCM for mitigation of lung tissue damage after targeted, thoracic irradiation and has the potential to be developed as a broad-spectrum, multi-use MCM against chemical, biological, radiological or nuclear threat agents with potential to cause lung injury.

摘要

核反应堆事故或蓄意恐怖行动导致的电离辐射暴露威胁是一个重大的公共卫生问题。肺部特别容易受到外部来源的辐射损伤或吸入放射性沉降物中的放射性颗粒的影响。辐射诱发的肺部疾病可表现为急性放射性肺炎和/或导致肺纤维化的延迟效应。由于不太可能有辐射暴露的预先警告,因此需要在辐射后数小时或数天的大规模伤亡情况下能够给予的医学对策(MCM)来减轻辐射诱发的肺部疾病,以预防早期和晚期肺部损伤。在本研究中,在一个特征明确的靶向胸部辐射暴露小鼠模型中,评估了KL表面活性剂(路西那肽)作为辐射缓解剂对早期(数周)和晚期(18周)肺部损伤的影响。在此,在单次13.5 Gy剂量的胸部照射(LD剂量)后第24小时,将120 mg/kg总磷脂的KL表面活性剂通过鼻内给药(使药物能够在肺内吸入)给予C57BL/6小鼠。分别在早期和慢性期(照射后2周和4周以及18周)进行评估。评估小鼠动脉血氧合降低以及早期和慢性肺部及全身炎症、肺纤维化和氧化应激的证据。通过进行肺功能/呼吸动力学分析以及测量支气管肺泡灌洗液(BALF)中的细胞蛋白含量、肺和血浆中的细胞因子、8-异前列腺素F2α、羟脯氨酸水平,并评估肺组织学来进行分析。本研究结果表明,鼻内给予KL表面活性剂能够维持肺功能,这表现为动脉血氧饱和度充足以及肺部炎症和氧化应激减轻;BALF中的白细胞总数和绝对中性粒细胞计数降低,血浆促炎细胞因子水平和氧化应激生物标志物也降低。KL表面活性剂是一种有前景的MCM,可减轻靶向胸部照射后的肺组织损伤,并且有潜力被开发成为一种针对有潜力导致肺损伤的化学、生物、放射或核威胁剂的广谱、多用途MCM。

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