Nan Li, Yang Yi, Jun Chen, Yue Huang, Jichao Peng, Zhao Li, Ying Wang, Jiadong Zhang, Chaoqun Xu, Haoran Liu, Jinghua Li, Xiaoran Liu
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Superoxide dismutase, malondialdehyde, reactive oxygen species and nitric oxide (NO) fluorescence were examined to detect the level of oxidative stress in HPMECs. The levels of TNF‑α, IL‑1β and IL‑6 were assessed using an ELISA. Transwell and Cell Counting Kit‑8 assays were performed to detect the migration and proliferation of the cells. The pathological changes in lung tissues and blood vessels were examined by haematoxylin and eosin staining. Evans blue staining was used to detect pulmonary microvascular permeability. Western blotting was performed to detect target protein levels. Immunofluorescence and immunohistochemical staining were used to detect the expression levels of target proteins in HPMECs and lung tissues. AH2QDS inhibited inflammatory responses in lung tissues and HPMECs, and promoted the proliferation and migration of HPMECs. In addition, AH2QDS reduced pulmonary microvascular permeability by upregulating the levels of vascular endothelial‑cadherin, zonula occludens‑1 and CD31, thereby attenuating pathological changes in the lungs in rats. Finally, these effects may be related to the suppression of the phosphatidylinositol‑3‑kinase (PI3K)/protein kinase B (AKT)/endothelial‑type NO synthase (eNOS) signalling pathway in endothelial cells. In conclusion, AH2QDS ameliorated PQ‑induced ALI by improving alveolar endothelial barrier disruption via modulation of the PI3K/AKT/eNOS signalling pathway, which may be an effective candidate for the treatment of PQ‑induced ALI.</p>","PeriodicalId":14086,"journal":{"name":"International journal of molecular medicine","volume":"54 1","pages":""},"PeriodicalIF":5.7000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11188976/pdf/","citationCount":"0","resultStr":"{\"title\":\"Anthrahydroquinone‑2,6‑disulfonate attenuates PQ‑induced acute lung injury through decreasing pulmonary microvascular permeability via inhibition of the PI3K/AKT/eNOS pathway.\",\"authors\":\"Nan Li, Yang Yi, Jun Chen, Yue Huang, Jichao Peng, Zhao Li, Ying Wang, Jiadong Zhang, Chaoqun Xu, Haoran Liu, Jinghua Li, Xiaoran Liu\",\"doi\":\"10.3892/ijmm.2024.5387\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In paraquat (PQ)‑induced acute lung injury (ALI)/ acute respiratory distress syndrome, PQ disrupts endothelial cell function and vascular integrity, which leads to increased pulmonary leakage. Anthrahydroquinone‑2,6‑disulfonate (AH2QDS) is a reducing agent that attenuates the extent of renal injury and improves survival in PQ‑intoxicated Sprague‑Dawley (SD) rats. The present study aimed to explore the beneficial role of AH2QDS in PQ‑induced ALI and its related mechanisms. A PQ‑intoxicated ALI model was established using PQ gavage in SD rats. Human pulmonary microvascular endothelial cells (HPMECs) were challenged with PQ. Superoxide dismutase, malondialdehyde, reactive oxygen species and nitric oxide (NO) fluorescence were examined to detect the level of oxidative stress in HPMECs. The levels of TNF‑α, IL‑1β and IL‑6 were assessed using an ELISA. Transwell and Cell Counting Kit‑8 assays were performed to detect the migration and proliferation of the cells. The pathological changes in lung tissues and blood vessels were examined by haematoxylin and eosin staining. Evans blue staining was used to detect pulmonary microvascular permeability. Western blotting was performed to detect target protein levels. Immunofluorescence and immunohistochemical staining were used to detect the expression levels of target proteins in HPMECs and lung tissues. AH2QDS inhibited inflammatory responses in lung tissues and HPMECs, and promoted the proliferation and migration of HPMECs. In addition, AH2QDS reduced pulmonary microvascular permeability by upregulating the levels of vascular endothelial‑cadherin, zonula occludens‑1 and CD31, thereby attenuating pathological changes in the lungs in rats. Finally, these effects may be related to the suppression of the phosphatidylinositol‑3‑kinase (PI3K)/protein kinase B (AKT)/endothelial‑type NO synthase (eNOS) signalling pathway in endothelial cells. 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引用次数: 0
摘要
在百草枯(PQ)诱导的急性肺损伤(ALI)/急性呼吸窘迫综合征中,PQ会破坏内皮细胞功能和血管完整性,从而导致肺渗漏增加。2,6-二磺酸蒽醌(AH2QDS)是一种还原剂,可减轻PQ中毒的Sprague-Dawley(SD)大鼠的肾损伤程度并提高其存活率。本研究旨在探讨 AH2QDS 在 PQ 诱导的 ALI 中的有益作用及其相关机制。通过给 SD 大鼠灌胃 PQ,建立了 PQ 致 ALI 模型。人肺微血管内皮细胞(HPMECs)受到 PQ 的挑战。通过检测超氧化物歧化酶、丙二醛、活性氧和一氧化氮荧光来检测 HPMECs 的氧化应激水平。用酶联免疫吸附法评估 TNF-α、IL-1β 和 IL-6 的水平。采用 Transwell 和细胞计数试剂盒-8 检测细胞的迁移和增殖。用血红素和伊红染色法检测肺组织和血管的病理变化。埃文斯蓝染色用于检测肺微血管的通透性。用 Western 印迹法检测目标蛋白水平。免疫荧光和免疫组化染色用于检测目标蛋白在HPMECs和肺组织中的表达水平。AH2QDS可抑制肺组织和HPMECs的炎症反应,促进HPMECs的增殖和迁移。此外,AH2QDS还能通过上调血管内皮-粘连蛋白、闭塞带-1和CD31的水平来降低肺微血管的通透性,从而减轻大鼠肺部的病理变化。最后,这些作用可能与抑制内皮细胞中磷脂酰肌醇-3-激酶(PI3K)/蛋白激酶 B(AKT)/内皮型 NO 合酶(eNOS)信号通路有关。总之,AH2QDS通过调节PI3K/AKT/eNOS信号通路改善肺泡内皮屏障的破坏,从而改善了PQ诱导的ALI,可能是治疗PQ诱导的ALI的有效候选药物。
Anthrahydroquinone‑2,6‑disulfonate attenuates PQ‑induced acute lung injury through decreasing pulmonary microvascular permeability via inhibition of the PI3K/AKT/eNOS pathway.
In paraquat (PQ)‑induced acute lung injury (ALI)/ acute respiratory distress syndrome, PQ disrupts endothelial cell function and vascular integrity, which leads to increased pulmonary leakage. Anthrahydroquinone‑2,6‑disulfonate (AH2QDS) is a reducing agent that attenuates the extent of renal injury and improves survival in PQ‑intoxicated Sprague‑Dawley (SD) rats. The present study aimed to explore the beneficial role of AH2QDS in PQ‑induced ALI and its related mechanisms. A PQ‑intoxicated ALI model was established using PQ gavage in SD rats. Human pulmonary microvascular endothelial cells (HPMECs) were challenged with PQ. Superoxide dismutase, malondialdehyde, reactive oxygen species and nitric oxide (NO) fluorescence were examined to detect the level of oxidative stress in HPMECs. The levels of TNF‑α, IL‑1β and IL‑6 were assessed using an ELISA. Transwell and Cell Counting Kit‑8 assays were performed to detect the migration and proliferation of the cells. The pathological changes in lung tissues and blood vessels were examined by haematoxylin and eosin staining. Evans blue staining was used to detect pulmonary microvascular permeability. Western blotting was performed to detect target protein levels. Immunofluorescence and immunohistochemical staining were used to detect the expression levels of target proteins in HPMECs and lung tissues. AH2QDS inhibited inflammatory responses in lung tissues and HPMECs, and promoted the proliferation and migration of HPMECs. In addition, AH2QDS reduced pulmonary microvascular permeability by upregulating the levels of vascular endothelial‑cadherin, zonula occludens‑1 and CD31, thereby attenuating pathological changes in the lungs in rats. Finally, these effects may be related to the suppression of the phosphatidylinositol‑3‑kinase (PI3K)/protein kinase B (AKT)/endothelial‑type NO synthase (eNOS) signalling pathway in endothelial cells. In conclusion, AH2QDS ameliorated PQ‑induced ALI by improving alveolar endothelial barrier disruption via modulation of the PI3K/AKT/eNOS signalling pathway, which may be an effective candidate for the treatment of PQ‑induced ALI.
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