急性呼吸窘迫综合征(ARDS)模型C57BL/6Y小鼠吸入leytrigin可提高SIRT1基因的表达水平

IF 0.1 Q4 MEDICINE, GENERAL & INTERNAL
N. S. Ogneva, L. A. Taboyakova, O. V. Alimkina, N. V. Petrova
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引用次数: 0

摘要

本文介绍了一种急性呼吸窘迫综合征(ARDS)模型C57BL/6Y小鼠肺吸入给药的方法。使用俄罗斯FMBA生物医学技术科学中心开发的欧姆龙COMP AIR NE-C24 Kids压缩吸入器进行吸入,该吸入器带有喷嘴,可同时给药于几只小鼠。采用α-半乳糖神经酰胺(α-半乳糖神经酰胺,剂量为1 μg/只小鼠)和大肠杆菌脂多糖(LPS,剂量为300 μg/只小鼠)的顺序给药,建立ARDS模型。LPS给药30分钟后,实验组小鼠吸入Leytragin药物,对照组小鼠吸入生理盐水。吸入后,收集生物材料(肺组织),通过RT- PCR评估SIRT1基因的表达,作为药物成功渗透到肺组织的标志。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhalation Administration of Leytragin to C57BL/6Y Mice in an ARDS Model Increases the Expression Level of SIRT1 Gene
This paper describes a technique for inhalation administration of Leutragin into the lungs of C57BL/6Y mice in a model of acute respiratory distress syndrome (ARDS). Inhalations were carried out using an OMRON COMP AIR NE-C24 Kids compression inhaler with a nozzle for simultaneous administration to several mice, developed at the Scientific Center of Biomedical Technologies of FMBA of Russia. Modeling of ARDS was carried out by sequential administration of α-galactosylceramide, inhaled at a dose of 1 μg/mouse, and, following 24 hours, a combination of E. coli lipopolysaccharide (LPS) at a dose of 300 μg/mouse. Thirty minutes after the administration of LPS, inhalation administration of the Leytragin drug was carried out to mice in the experimental group and normal saline in the control group. After inhalation, a biomaterial (lung tissue) was collected to evaluate the expression of the SIRT1 gene by RT- PCR as a marker of successful penetration of the drug into the lung tissue.
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来源期刊
Avances en Biomedicina
Avances en Biomedicina MEDICINE, GENERAL & INTERNAL-
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