首页> 美国卫生研究院文献>other >Radiation Mitigating Properties of Intranasally Administered KL4 Surfactant in a Murine Model of Radiation-Induced Lung Damage
【2h】

Radiation Mitigating Properties of Intranasally Administered KL4 Surfactant in a Murine Model of Radiation-Induced Lung Damage

机译:在辐射诱发的肺损伤的小鼠模型中鼻内施用的KL4表面活性剂的辐射缓解特性。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

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, KL4 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 KL4 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 (LD50 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 KL4 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. KL4 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.
机译:核反应堆事故或故意的恐怖行动可能会暴露于电离辐射中,这是一个重大的公共卫生问题。肺特别容易受到来自外部来源的辐射诱发的伤害或来自放射性尘埃的放射性颗粒吸入的伤害。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。由于事先不太可能出现放射线暴露警告,因此需要采取医学对策(MCM)来减轻辐射诱发的肺部疾病,这种情况可在照射后数小时或数天在大规模伤亡中使用,以预防早期和晚期肺部损伤。在这项研究中,KL4表面活性剂(光敏剂)被评估为靶向胸腔照射的特征明确的小鼠模型中的放射缓解剂,因为它对早期(几周)和晚期(18周)肺损伤都有影响。在这里,在单次13.5 Gy剂量的胸腔照射(LD50剂量)后24小时,每天两次向C57BL / 6小鼠鼻腔内施用120 mg / kg KL4表面活性剂的总磷脂(使肺内吸入药物)。进行了早期和慢性阶段(分别在照射后2周,4周和18周)的评估。评价小鼠的动脉血氧合减少以及早期和慢性肺和全身炎症,肺纤维化和氧化应激的证据。通过执行肺功能/呼吸动力学并测量支气管肺泡灌洗液(BALF)的细胞蛋白含量以及肺和血浆中细胞因子,8-异前列腺素F2α,羟脯氨酸的水平以及评估肺组织学来进行分析。这项研究的结果表明,鼻腔内递送KL4表面活性剂能够保持肺功能,这一点已通过足够的动脉血氧饱和度和减少的肺部炎症和氧化应激得以证明。总白蛋白计数和绝对中性粒细胞计数在BALF中降低,血浆促炎细胞因子水平和氧化应激的生物标志物也降低。 KL4表面活性剂是一种有希望的,有针对性的MCM,可减轻有针对性的胸腔照射后对肺组织的伤害,并且有可能被开发为广谱,多用途的MCM,以对抗可能引起肺损伤的化学,生物,放射或核威胁因子。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号