Mitochondrial Coenzyme Q Protects Sepsis-Induced Acute Lung Injury by Activating PI3K/Akt/GSK-3β/mTOR Pathway in Rats.

The aim of our study was to assess the effects of mitochondrial coenzyme Q (MitoQ) on sepsis-induced acute lung injury (ALI) and investigate its possible mechanisms. The cecal ligation and puncture (CLP) method was used to establish a septic ALI model. Rats were randomly divided into Con group, CLP...

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Publicado en:BioMed Research International pp. 1 - 10
Autores principales: Li, Ruirui, Ren, Tao, Zeng, Jianqiong
Formato: pictorial research tables/charts Journal Article
Publicado: Wiley-Blackwell 11/13/2019
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 11/13/2019
      pid: 480
      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        139642252
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        139642252
        10.1155/2019/5240898
        139642252
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        atl: Mitochondrial Coenzyme Q Protects Sepsis-Induced Acute Lung Injury by Activating PI3K/Akt/GSK-3β/mTOR Pathway in Rats.
      aug:
        au:
          Li, Ruirui
          Ren, Tao
          Zeng, Jianqiong
        affil: Department I of Critical Care Medicine, The First Affiliated Hospital of the Medical College, Shihezi University, North Second Road, Shihezi, Xinjiang Uygur Autonomous Region, 832008, China
      sug:
        subj:
          Coenzyme Q Physiology
          Mitochondria Physiology
          Acute Lung Injury Prevention and Control
          Sepsis Complications
          Phosphotransferases
          Signal Transduction
          Animal Studies
          Rats
          Comparative Studies
          Random Assignment
          Enzyme-Linked Immunosorbent Assay
          Apoptosis
          Blotting, Western
          Interleukins
          Gene Expression
          Pulmonary Edema
          Survival
          Acute Lung Injury Pathology
      ab: The aim of our study was to assess the effects of mitochondrial coenzyme Q (MitoQ) on sepsis-induced acute lung injury (ALI) and investigate its possible mechanisms. The cecal ligation and puncture (CLP) method was used to establish a septic ALI model. Rats were randomly divided into Con group, CLP group, MitoQ group, and MitoQ + LY294002 group. The survival rate of the rats was recorded, and the survival rate curve was plotted. Moreover, the ratio of wet/dry weight (W/D) in lung tissue was measured. The activity of myeloperoxidase (MPO) was measured by using the MPO colorimetric activity assay kit. The levels of high-mobility group box 1 (HMGB1) and interleukin-6 (IL-6), macrophage inflammatory protein 2 (MIP2), and keratinocyte chemoattractant (KC) were analyzed by ELISA. The histopathological changes were measured by HE staining, and the lung injury was scored. TUNEL assay was applied to detect the apoptotic cells in lung tissue. The protein expressions were detected by western blot. MitoQ increased the survival rate and alleviated pulmonary edema in septic ALI rats. In addition, MitoQ inhibited the MPO activity and decreased the levels of HMGB1 and IL-6. After treatment with MitoQ, alveolar wall edema, inflammatory cell infiltration, and red blood cell exudation were relieved. MitoQ inhibited cell apoptosis in lung tissue of septic ALI rats. Meanwhile, MitoQ treatment remarkedly increased the expression of p-Akt, p-GSK-3β, and p-mTOR but decreased Bax, caspase-3, caspase-9, Beclin-1, and LC-3II/LC-3I. The effects of MitoQ were significantly reversed by the PI3K inhibitor (LY294002). Our study demonstrated that MitoQ could protect sepsis-induced acute lung injury by activating the PI3K/Akt/GSK-3β/mTOR pathway in rats.
      pubtype: Academic Journal
      doctype:
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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