Çolak Mustafa, Kalemci Serdar, Alpaydın Aylin Özgen, Karaçam Volkan, Meteoğlu Ibrahim, Yılmaz Osman, Itil Bahriye Oya
Chest Disease Department, Dokuz Eylül Üniversity, Izmir, Turkey.
Chest Diseases Department, Muğla Sıtkı Koçman University, Mugla, Turkey.
Kardiochir Torakochirurgia Pol. 2020 Jun;17(2):65-69. doi: 10.5114/kitp.2020.97259. Epub 2020 Jul 20.
Acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) are acute onset syndromes affecting the lungs, which develop for several reasons and are characterized by hypoxemia and diffuse lung infiltration. The activity of thymoquinone (TQ) is known in acute lung injury. It is considered that it could be effective in ALI/ARDS treatment by ensuring possible COX-2 inhibition.
By this study was to show the protective activity of TQ in lipopolysaccharide (LPS) induced acute lung injury.Material and methods: A total of 28 BALB/c male mice were randomized to 4 groups of 7 as the Control group, TQ group (3 mg/kg), LPS group (5 mg/kg) and TQ treatment group. TQ was administered intraperitoneally 1 hour before the intratracheal administration of LPS (5 mg/kg). The mice were sacrificed 6 hours after the LPS administration and the lungs were extracted for histopathological examination. All experimental procedures complied with the requirements of the Animal Care and Ethics Committee of Dokuz Eylul University.
When all the study groups were compared, significant differences were found between the groups in terms of the degrees of neutrophil migration ( = 0.042), intra-alveolar hemorrhage ( = 0.004) and alveolar destruction ( < 0.0006). A significant recovery was observed in the lung histopathological changes (neutrophil migration, intra-alveolar hemorrhage and alveolar destruction) in the TQ treatment group.
The results of this study showed that TQ may have a protective effect against LPS-induced acute lung injury. The possible mechanism could be considered to be cyclooxygenase 2 (COX-2) inhibition.
急性肺损伤(ALI)和急性呼吸窘迫综合征(ARDS)是影响肺部的急性发病综合征,其发病原因多样,以低氧血症和弥漫性肺浸润为特征。百里醌(TQ)在急性肺损伤中的活性是已知的。人们认为它可能通过确保对环氧合酶-2(COX-2)的抑制作用而对ALI/ARDS治疗有效。
本研究旨在显示TQ对脂多糖(LPS)诱导的急性肺损伤的保护活性。
总共28只BALB/c雄性小鼠被随机分为4组,每组7只,分别为对照组、TQ组(3mg/kg)、LPS组(5mg/kg)和TQ治疗组。在气管内给予LPS(5mg/kg)前1小时腹腔注射TQ。LPS给药6小时后处死小鼠,取出肺组织进行组织病理学检查。所有实验程序均符合多库兹埃于勒大学动物护理和伦理委员会的要求。
比较所有研究组时,发现各组在中性粒细胞迁移程度(P = 0.042)、肺泡内出血(P = 0.004)和肺泡破坏(P < 0.0006)方面存在显著差异。TQ治疗组的肺组织病理学变化(中性粒细胞迁移、肺泡内出血和肺泡破坏)有显著改善。
本研究结果表明,TQ可能对LPS诱导的急性肺损伤具有保护作用。可能的机制可认为是抑制环氧合酶2(COX-2)。