Ashwagandha根提取物通过抑制ACE和MAPK信号通路减轻油酸诱导的ali /ARDS大鼠模型的炎症反应

K. Koc
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摘要

Ashwagandha (Withania somniferous)是民间医学中最重要的植物之一,被广泛用于治疗各种疾病。急性肺损伤(ALI)和急性呼吸窘迫综合征(ARDS)被定义为由于低氧血症和肺泡损伤继发于剧烈炎症而突然发生的呼吸衰竭。本研究旨在评价Ashwagandha对油酸诱导的ALI/ARDS大鼠模型的作用。为此,将动物分为3组:对照组、油酸(50 μl kg - 1,静脉注射)、Ashwagandha (500 mg/kg,口服)+油酸。在服用单剂量油酸之前,每天服用Ashwagandha,持续两周。末次给药24 h后,用七氟醚处死各组动物,评价肺功能。ELISA法测定大鼠肺组织中丝裂原活化蛋白激酶(MAPK)水平、髓过氧化物酶(MPO)、谷胱甘肽(GSH)、超氧化物歧化酶(SOD)、总氧化状态(TOS)、血管紧张素转换酶(ACE)活性。与模型组比较,阿什瓦甘达给药组大鼠MAPK、MPO、TOS水平均显著提高。此外,Ashwagandha显著提高了GSH和SOD的活性,降低了ACE的活性。因此,Ashwagandha可能作为一种潜在的天然资源,用于减轻油酸引起的急性肺损伤。
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Ashwagandha root extract attenuates inflammation in Oleic acid induced-ALI/ARDS rat model via inhibition of ACE and MAPK signaling pathways
Ashwagandha (Withania somniferous) is one of the most important plants of folk medicine and is widely used to treat various diseases. Acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) are defined as a respiratory failure that abruptly develops due to hypoxemia with alveolar injury secondary to intense inflammation. The present study was focused on evaluating the activity of Ashwagandha against Oleic Acid-Induced ALI/ARDS in a rat model. For this purpose, the animals were divided into the following three groups: Control, Oleic acid (50 μl kg−1, i.v. injection), Ashwagandha (500 mg/kg, orally) + Oleic acid. Ashwagandha was given daily for two weeks before a single dose of the Oleic acid. 24 hours after the last application, all the group animals were sacrificed by sevoflurane, and their lung was evaluated. The levels of Mitogen-activated protein kinases (MAPK), and the activities of myeloperoxidase (MPO), glutathione (GSH), superoxide dismutase (SOD), total oxidant status (TOS), and angiotensin-converting enzyme (ACE) were determined in lung tissues by ELISA. Compared with the model group, there was a significantly improving in the levels of MAPK, MPO, and TOS in the Ashwagandha administration group. Moreover, Ashwagandha markedly increased the activities of GSH and SOD, and decreased the activity of ACE. Therefore, Ashwagandha may be used as a potential natural resource for mitigating acute lung injury caused by Oleic acid.
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