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Anti-Inflammatory Activity of Sanghuangporus sanghuang Mycelium

机译:桑黄菌桑黄菌丝体的抗炎活性

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Acute lung injury (ALI) is characterized by inflammation of the lung tissue and oxidative injury caused by excessive accumulation of reactive oxygen species. Studies have suggested that anti-inflammatory or antioxidant agents could be used for the treatment of ALI with a good outcome. Therefore, our study aimed to test whether the mycelium extract of Sanghuangporus sanghuang (SS-1), believed to exhibit antioxidant and anti-inflammatory properties, could be used against the excessive inflammatory response associated with lipopolysaccharides (LPS)-induced ALI in mice and to investigate its possible mechanism of action. The experimental results showed that the administration of SS-1 could inhibit LPS-induced inflammation. SS-1 could reduce the number of inflammatory cells, inhibit myeloperoxidase (MPO) activity, regulate the TLR4/PI3K/Akt/mTOR pathway and the signal transduction of NF-κB and MAPK pathways in the lung tissue, and inhibit high mobility group box-1 protein 1 (HNGB1) activity in BALF. In addition, SS-1 could affect the synthesis of antioxidant enzymes Heme oxygenase 1 (HO-1) and Thioredoxin-1 (Trx-1) in the lung tissue and regulate signal transduction in the KRAB-associated protein-1 (KAP1)uclear factor erythroid-2-related factor Nrf2/Kelch Like ECH associated Protein 1 (Keap1) pathway. Histological results showed that administration of SS-1 prior to induction could inhibit the large-scale LPS-induced neutrophil infiltration of the lung tissue. Therefore, based on all experimental results, we propose that SS-1 exhibits a protective effect against LPS-induced ALI in mice. The mycelium of S. sanghuang can potentially be used for the treatment or prevention of inflammation-related diseases.
机译:急性肺损伤(ALI)的特征是肺组织发炎和由于活性氧的过度积累而引起的氧化损伤。研究表明,抗炎药或抗氧化剂可用于治疗ALI,效果良好。因此,我们的研究旨在检验被认为具有抗氧化和抗炎特性的桑黄孢桑黄菌丝体提取物(SS-1)是否可用于抵抗脂多糖(LPS)诱导的ALI引起的过度炎症反应。调查其可能的作用机理。实验结果表明,SS-1的给药可以抑制LPS诱导的炎症。 SS-1可以减少炎症细胞的数量,抑制髓过氧化物酶(MPO)活性,调节TLR4 / PI3K / Akt / mTOR通路以及肺组织中NF-κB和MAPK通路的信号转导,并抑制高迁移率族盒子-1蛋白1(HNGB1)在BALF中的活性。此外,SS-1可能会影响肺组织中抗氧化酶血红素加氧酶1(HO-1)和硫氧还蛋白1(Trx-1)的合成,并调节KRAB相关蛋白1(KAP1)/核因子erythroid-2相关因子Nrf2 / Kelch像ECH相关蛋白1(Keap1)途径。组织学结果表明,诱导前施用SS-1可以抑制大规模LPS诱导的肺中性粒细胞浸润。因此,基于所有实验结果,我们建议SS-1对小鼠LPS诱导的ALI表现出保护作用。桑黄链球菌的菌丝体可潜在地用于治疗或预防炎症相关疾病。

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