Effectiveness of various regimens of systemic anti-inflammatory therapy with glucocorticoids in the development of acute LPS-induced lung damage in the experiment
- 作者: Salukhov V.V.1, Voloshin N.I.1, Shperling M.I.1
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隶属关系:
- Military Medical Academy
- 期: 卷 41, 编号 2 (2022)
- 页面: 111-116
- 栏目: Original articles
- URL: https://journals.rcsi.science/RMMArep/article/view/104619
- DOI: https://doi.org/10.17816/rmmar104619
- ID: 104619
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详细
BACKGROUND: When studying new and effective methods of treating acute respiratory distress syndrome, an immunogenic model of lung injury occupies a special place. To date, the search for the optimal strategy and regimen for the use of glucocorticoids in the development of acute respiratory distress syndromе is relevant.
AIM: The article evaluates the effectiveness of various schemes of systemic anti-inflammatory therapy with glucocorticoids in an experimental model of acute LPS-induced lung injury.
MATERIALS AND METHODS: The study was conducted on 100 outbred male rats. Acute lung injury was modeled using an experimental model of direct acute lung injury by a single intratracheal injection of lipopolysaccharide (LPS) from the cell wall of the bacterium Salmonella enterica (Sigma-Aldrich) at a dose of LD50 (20 mg/kg). All animals were divided into groups (20 each): 1 — intact rats; 2 — control group (LPS + saline); 3 — LPS + dexamethasone 0.52 mg/kg (small doses); 4 — LPS + dexamethasone 1.71 mg/kg (average doses); 5 — LPS + dexamethasone 8 mg/kg (high doses). The drugs were administered intraperitoneally once a day for 3 days. Dexamethasone doses were calculated using the interspecies dose transfer method using a factor that takes into account differences in body surface area.
RESULTS: It has been established that an experimental model based on the endotracheal administration of S. enterica leads to the development of mortality from pulmonary causes. According to a preclinical study, the systemic use of low doses of dexamethasone (0.52 mg/kg) was found to be better than higher doses (1.71 mg/kg, 8 mg/kg) in the treatment of acute LPS-induced lung injury.
作者简介
Vladimir Salukhov
Military Medical Academy
Email: vlasaluk@yandex.ru
ORCID iD: 0000-0003-1851-0941
SPIN 代码: 4531-6011
Scopus 作者 ID: 55804184100
Vladimir V. Salukhov, M.D., D.Sc. (Medicine), Associate Professor
俄罗斯联邦, Saint PetersburgNikita Voloshin
Military Medical Academy
Email: nikitavoloshin1990@gmail.com
ORCID iD: 0000-0002-3880-9548
SPIN 代码: 6061-4342
postgraduate student of Therapy of Doctors Improvement Department
俄罗斯联邦, Saint PetersburgMaxim Shperling
Military Medical Academy
编辑信件的主要联系方式.
Email: mersisaid@yandex.ru
ORCID iD: 0000-0002-3274-2290
SPIN 代码: 7658-7348
Scopus 作者 ID: 57215661145
Researcher ID: ABC-3170-2021
M.D., clinical resident of Therapy of Doctors Improvement Department
俄罗斯联邦, Saint Petersburg参考
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- Yubero S, Manso MA, Ramudo L, et al. Dexamethasone down-regulates the inflammatory mediators but fails to reduce the tissue injury in the lung of acute pancreatitis rat models. Pulmonary pharmacology and therapeutics. 2012;25(4):319–324. doi: 10.1016/j.pupt.2012.05.009
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