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生酮饮食可诱导自噬以减轻博来霉素诱导的小鼠模型肺纤维化。

Ketogenic diet induces autophagy to alleviate bleomycin-induced pulmonary fibrosis in murine models.

作者信息

Mu En, Wang Jinli, Chen Liang, Lin Shuirong, Chen Jieming, Huang Xiaoming

机构信息

Department of Critical Care Medicine, Baoan Central Hospital of Shenzhen, The Fifth Affiliated Hospital of Shenzhen University, Shenzhen, People's Republic of China.

出版信息

Exp Lung Res. 2021 Feb;47(1):26-36. doi: 10.1080/01902148.2020.1840667. Epub 2020 Oct 29.

Abstract

Ketogenic diet (KD) has been identified as an effective strategy in treating multiple diseases. KD is capable of inducing autophagy which is an important therapeutic target for pulmonary fibrosis (PF). This study aimed to investigate the effect of KD treatment on PF progression. Intratracheal instillation of bleomycin (BLM, 5 mg/kg) to establish PF model in male Kunming mice fed either KD or standard diet. The survival of mice was recorded every day for 3 weeks. The pulmonary tissues were weighed on day 21 and the pulmonary index was calculated. The histopathological changes of pulmonary tissues were analyzed by hematoxylin and eosin staining and Masson staining, and the collagen deposition by hydroxyproline assay. Then the content of proinflammatory factors in pulmonary tissues was measured using enzyme-linked immunosorbent assay, and the expression of profibrogenic cytokines, autophagy markers and PI3K/AKT/mTOR pathway-related proteins in pulmonary tissues using western blotting or immunohistochemistry. KD treatment significantly restored the BLM-induced increase of pulmonary index and had a tendency to increase the survival rate of PF mice. Furthermore, KD treatment restored the BLM-induced damage of alveolar structure, infiltration of inflammatory cells and collagen deposition and decreased hydroxyproline content. In addition, the BLM-induced secretion of tumor necrosis factor-alpha, interleukin-6 and interleukin-1β and expression of transforming growth factor β1, phospho-Smad2/3, connective tissue growth factor, α-smooth muscle actin and collagen type III alpha 1 chain were inhibited by KD. KD treatment also up-regulated the expression of light chain 3 II/I and Beclin1 and down-regulated the expression of p62, phospho-AKT, phospho-mTOR and phospho-p70S6K, suggesting that KD induced autophagy and suppressed the BLM-induced activation of PI3K/AKT/mTOR signaling pathway. These findings indicate that KD can alleviate PF by regulating autophagy and PI3K/AKT/mTOR signaling pathway, which provides a novel therapeutic strategy for PF.

摘要

生酮饮食(KD)已被确定为治疗多种疾病的有效策略。KD能够诱导自噬,而自噬是肺纤维化(PF)的一个重要治疗靶点。本研究旨在探讨KD治疗对PF进展的影响。通过气管内注入博来霉素(BLM,5mg/kg),在喂食KD或标准饮食的雄性昆明小鼠中建立PF模型。连续3周每天记录小鼠的存活情况。在第21天称量肺组织重量并计算肺指数。通过苏木精-伊红染色和Masson染色分析肺组织的组织病理学变化,并用羟脯氨酸测定法检测胶原沉积。然后使用酶联免疫吸附测定法测量肺组织中促炎因子的含量,并用蛋白质印迹法或免疫组织化学法检测肺组织中促纤维化细胞因子、自噬标志物和PI3K/AKT/mTOR信号通路相关蛋白的表达。KD治疗显著恢复了BLM诱导的肺指数升高,并倾向于提高PF小鼠的存活率。此外,KD治疗恢复了BLM诱导的肺泡结构损伤、炎性细胞浸润和胶原沉积,并降低了羟脯氨酸含量。此外,KD抑制了BLM诱导的肿瘤坏死因子-α、白细胞介素-6和白细胞介素-1β的分泌以及转化生长因子β1、磷酸化Smad2/3、结缔组织生长因子、α-平滑肌肌动蛋白和III型胶原α1链的表达。KD治疗还上调了轻链3 II/I和Beclin1的表达,下调了p62、磷酸化AKT、磷酸化mTOR和磷酸化p70S6K的表达,表明KD诱导了自噬并抑制了BLM诱导的PI3K/AKT/mTOR信号通路的激活。这些发现表明,KD可以通过调节自噬和PI3K/AKT/mTOR信号通路来减轻PF,这为PF提供了一种新的治疗策略。

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