文章摘要
刘莉,王莹莹,井郁陌.丙泊酚对高糖诱导的人肾小球系膜细胞氧化应激和炎症反应的影响[J].安徽医药,2024,28(6):1087-1091.
丙泊酚对高糖诱导的人肾小球系膜细胞氧化应激和炎症反应的影响
Effects of propofol on high glucose-induced oxidative stress and inflammatory responses in human mesangial cells
  
DOI:10.3969/j.issn.1009-6469.2024.06.006
中文关键词: 二异丙酚  高糖  人肾小球系膜细胞  氧化应激  炎症反应
英文关键词: Propofol  High glucose  Human glomerular mesangial cells  Oxidative stress  Inflammatory response
基金项目:河北省卫生健康委员会计划项目( 20191278)
作者单位
刘莉 河北省沧州中西医结合医院麻醉与围术期医学科河北沧州 061001 
王莹莹 河北省沧州中西医结合医院麻醉与围术期医学科河北沧州 061001 
井郁陌 河北省沧州中西医结合医院麻醉与围术期医学科河北沧州 061001 
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中文摘要:
      目的探讨丙泊酚对高糖诱导的人肾小球系膜细胞损伤的影响。方法该研究于 2021年 3月至 2022年 3月进行。体外培养人肾小球系膜细胞,采用 30 mol/L葡萄糖诱导建立人肾小球系膜细胞细胞损伤模型,用丙泊酚浓度 10、20、40 μmol/L处理细胞,细胞分为对照组、高糖组、高糖 +低、中、高剂量丙泊酚组。酶联免疫吸附测定( ELISA)检测超氧化物歧化酶( SOD)、谷胱甘肽过氧化物酶( GSH-PX)、丙二醛、活性氧、白细胞介素( IL)-10、肿瘤坏死因子 α(TNF-α)IL-1β表达;蛋白质印迹法检测诱导型一氧化氮合酶( iNOS)、细胞间黏附分子 -1(ICAM-1)、单核细胞趋化蛋白 -1(MCP-1)、 IL-10、TNF-α、IL-1β蛋白表达。结果高糖组的丙二醛[( 16.7±1.7)mmol/L比( 3.8±0.4)mmol/L]、活性氧[( 9.6±0.9)μg/L比( 3.5±0.3)μg/L]、 IL-10[( 65.3±6.9)ng/L比(26.9±3.2)ng/L]、 TNF-α[( 105.6±10.9)ng/L比( 42.8±4.8)ng/L]和 IL-1β[( 79.7±8.2)ng/L比( 31.2±3.6)ng/L]明显高于对照组; iNOS、ICAM-1、MCP-1、IL-10、TNF-α、IL-1β蛋白表达明显高于对照组; SOD、GSH-Px明显低于对照组,均 P<0.05。高糖 +低剂量丙泊酚组、高糖 +中剂量丙泊酚组、高糖 +高剂量丙泊酚组的丙二醛、活性氧、 IL-10、TNF-α和 IL-1β明显低于高糖组; iNOS、 ICAM-1、MCP-1、IL-10、TNF-α、IL-1β蛋白表达明显低于高糖组,均 P<0.05;SOD、GSH-Px明显高于高糖组,均 P<0.05。结论丙泊酚能减轻高糖诱导的人肾小球系膜细胞氧化应激和炎症反应,发挥保护肾脏的作用。
英文摘要:
      Objective To investigate the effect of propofol on human glomerular mesangial cell injury induced by high glucose.Meth ods The study was conducted from March 2021 to March 2022. Human glomerular mesangial cells were cultured in vitro, and the 30mol/L glucose concentration was used to induce a human glomerular mesangial cell injury model, and the cells were treated with propofol concentrations of 10, 20, and 40 μmol/L. The cells were divided into control (Con) group, high glucose (HG) group, high glucose+propofol low, medium and high dose (HG+propofol-L, HG+propofol-M, HG+propofol-H) groups. ELISA method to detect superoxide dis mutase (SOD), glutathione peroxidase (GSH-PX), malondialdehyde, reactive oxygen species, interleukin-10 (IL-10) the expression of tu mor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β); Western blotting method to detect the inducible type nitric oxide synthase (iNOS), intercellular adhesion molecule-1 (ICAM-1), monocyte chemoattractant protein-1 (MCP-1), IL-10, TNF-α and IL-1β protein ex pression. Results HG group malondialdehyde [(16.7±1.7) mmol/L vs. (3.8±0.4) mmol/L], malondialdehyde [(9.6±0.9) μg/L vs. (3.5± 0.3) μg/L], IL-10 [(65.3±6.9) ng/L vs. (26.9±3.2) ng/L], TNF-α [(105.6±10.9) ng/L vs. (42.8±4.8) ng/L] and IL-1β [(79.7±8.2) ng/L vs. (31.2±3.6) ng/L] were significantly higher than those in Con group; iNOS, ICAM-1, MCP-1, IL-10, TNF-α, IL-1β the expression of pro tein were significantly higher than that of Con group; SOD and GSH-Px were significantly lower than that of Con group (all P<0.05). The malondialdehyde, malondialdehyde, IL-10, TNF-α and IL-1β of the HG+propofol-L group, HG+propofol-M group, and HG+propofol-H group were significantly lower than those of the HG group; iNOS, ICAM-1, MCP-1, IL-10, TNF-α, IL-1β protein expression was signifi cantly higher than that of Con group (P<0.05); SOD and GSH-Px were significantly higher than that of the HG group, the rest are P< 0.05.Conclusion Propofol can reduce the oxidative stress and inflammation of human glomerular mesangial cells induced by high glucose, and play a role in protecting the kidneys.
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