医学分子生物学杂志 ›› 2023, Vol. 20 ›› Issue (6): 493-499.doi: 10.3870/j.issn.1672-8009.2023.06.005

• 论著 • 上一篇    下一篇

褪黑素通过 JAK2 / STAT3 信号通路对糖尿病大鼠肺缺血再灌注损伤的作用机制研究 #br#


  

  1. 河北省定州市人民医院 1麻醉科2药剂科 河北省定州市, 073000
  • 出版日期:2023-11-30 发布日期:2023-12-28
  • 基金资助:
    河北省医学科学研究课题 (No. 20210971)

Effect of Melatonin on Pulmonary Ischemia-reperfusion Injury in Diabetic Rats through JAK2 / STAT3 Signaling Pathway #br#

  1. 1Department of Anesthesiology,2 Department of Pharmacy, Peoples Hospital of Dingzhou, Dingzhou, Hebei, 073000, China
  • Online:2023-11-30 Published:2023-12-28

摘要: 目的 探讨褪黑素对糖尿病 (diabetes mellitus, DM) 大鼠肺缺血/ 再灌注 (I / R) 损伤的作用及其潜在分子机制方法 将大鼠随机分为对照 + 假手术组 (Control + Sham )、 糖尿病 + 假手术组 ( DM + Sham )、 对照 + 缺血再灌注组 (Control + IR )、 糖尿病 + 缺血再灌注组 (DM + IR )、 糖尿病 + 缺血再灌注 + 褪黑素组 (DM + IR + MT ), 每组 8 检测各组大鼠的肺组织湿重/ 干重 ( W / D) 比值; 苏木精-伊红染色检测各组大鼠肺组织病理学变化; 检测各组大鼠肺组织中氧化应激因子谷胱甘肽过氧化物酶(glutathione peroxidase, GSH-PX) 活性总抗氧化能力 (total antioxidant capacity, T-AOC) 水平超氧化物歧化酶 (superoxide dismutase, SOD) 活性和丙二醛 ( malondialdehyde, MDA) 活性; ELISA 实验检测炎症因子 IL-1β、 IL-6 TNF-α 的浓度; 蛋白质印迹法检测各组大鼠肺组织中 p-JAK2 p-STAT3 蛋白水平结果 Control + Sham 组比较, Control + IR 组中 W / D 比值升高, 肺泡间隔和间隙水肿, 间质增厚, 肺泡内出血和白细胞浸润, 肺损伤评分较高, GSH-PX、 SOD、 T-AOC 活性降低, MDA 水平升高, 炎症因子 IL- 1β、 IL-6、 TNF-α 水平升高, p-JAK2 p-STAT3 蛋白水平升高 ( P< 0. 05)。 DM + Sham 组和 DM + IR 组的上述指标进一步升高, 其中 DM + IR 组的差异性更显著DM + IR 组比较, DM + IR + ME 组中 W / D 比值显著降低, 肺组织损伤明显减轻, 肺损伤评分降低, GSH-PX、 SOD、 T-AOC 活性显著升高, MDA 水平显著降低, IL-1β、 IL-6、 TNF-α 水平显著降低, p-JAK2 p-STAT3 蛋白水平降低 ( P< 0. 05)。 结论 褪黑素通过降低氧化应激和炎症水平从而减轻糖尿病大鼠的肺 I / R 损伤, 其机制可能与 JAK2 / STAT3 信号通路有关

关键词:

褪黑素, 糖尿病, 肺缺血再灌注损伤, JAK2 / STAT3 信号通路, 氧化应激

Abstract: Objective To investigate the effect of melatonin on lung ischemia / reperfusion (I /R) injury in diabetes mellitus ( DM) rats and its underlying molecular mechanism. Methods Rats were randomly divided into Control + Sham operation group (Control + Sham group), diabetes +Sham operation group ( DM + Sham group), Control + ischemia-reperfusion group ( Control + IRgroup), diabetes + ischemia-reperfusion group (DM + IR group), diabetes + ischemia-reperfusion +melatonin group (DM + IR + MT group), 8 rats in each group. The wet / dry weight ratio ( W / D)was measured in each group. Hematoxylin-eosin (HE) staining was used to detect the pathologicalchanges of lung tissues in each group. The activity of oxidative stress factor glutathione peroxidase(GSH-PX), superoxide dismutase ( SOD) and malondialdehyde ( MDA), and the level of totalantioxidant capacity (T-AOC) were detected in the lung tissues of rats in each group. The levels ofinflammatory cytokines interleukin-1β (IL-1β), interleukin-6 (IL-6) and tumor necrosis factor-α(TNF-α) were detected by ELISA. The expression levels of p-JAK2 and p-STAT3 were detected by Western blotting. Results Compared with those in the Control + Sham group, the ratio of W/ D wasincreased, the alveolar septum and space edema, the interstitial thickening, and the alveolar hemorrhage and leukocyte infiltration were found, the lung injury score was higher, the activities of GSH-Px, SOD and T-AOC were decreased, and the level of MDA was increased, the levels of IL- 1β, IL-6 and TNF-a were increased, and the expression levels of p-JAK2 and p-STAT3 were increased in the Control + IR group (P< 0. 05). The above indexes were further increased in the DM+ sham group and the DM + IR group, and the difference was more significant in the DM + IR group. Compared with those in the DM + IR group, the ratio of W/ D was significantly decreased, the injuries in the lung tissue were significantly reduced, the lung injury score was decreased, the activities of GSH-Px, SOD and T-AOC were increased, and the level of MDA was decreased, the levels of IL-1β, IL-6 and TNF-α were decreased, and the expression levels of p-JAK2 and pSTAT3 were decreased in the DM + IR + ME group (P< 0. 05). Conclusion Melatonin attenuatedlung I / R injury the diabetic rats by reducing oxidative stress and inflammation, and its mechanism could be related to the JAK2 / STAT3 signaling pathway.

Key words:

melatonin, diabetes, lung ischemia / reperfusion injury, JAK2 / STAT3 signaling pathway, oxidative stress

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