首页|莫西沙星对肺炎支原体肺炎小鼠肺损伤的作用研究

莫西沙星对肺炎支原体肺炎小鼠肺损伤的作用研究

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目的 探讨莫西沙星(Moxi)下调长链非编码RNA生长抑制特异性基因(lncRNA GAS5)通过非受体型蛋白酪氨酸激酶(JAK)/信号传导及转录激活蛋白(STAT)信号通路对肺炎支原体肺炎的保护作用.方法 将BALB/c小鼠随机分为对照组、模型组、实验组和联合组.模型组、实验组和联合组小鼠用鼻滴肺炎支原体菌液的方法建立肺炎支原体肺炎模型.实验组和联合组腹腔注射100 mg·kg-1莫西沙星治疗;在此基础上,联合组尾静脉注射过表达质粒pc-GAS5,对照组和模型组均腹腔注射等量的0.9%NaCl.用酶联免疫吸附试验法检测小鼠血清中白细胞介素-1β(IL-1β)和IL-6水平,用生化法检测小鼠血清中超氧化物歧化酶(SOD)水平,用实时荧光定量聚合酶链反应法检测小鼠肺组织中 lncRNA GAS5的表达水平,用蛋白质印迹法检测小鼠肺组织中 B淋巴细胞瘤-2基因(Bcl-2)、JAK2和STAT3的表达水平.结果 对照组、模型组和实验组血清中IL-1β含量分别为(64.03±14.19)、(254.85±63.79)和(157.46±42.93)pg·mL-1,IL-6 含量分别为(22.61±5.01)、(184.14±39.50)和(132.64±25.47)pg·mL-1,SOD 活性分别为(50.38±11.75)、(28.17±6.71)和(37.67±8.09)U·mL-1,肺组织中lncRNA GAS5相对表达水平分别为1.00±0.16、3.78±0.69和2.41±0.54;对照组、模型组、实验组和联合组肺组织中Bcl-2蛋白相对表达水平分别为1.00±0.17、0.65±0.14、0.82±0.16和0.62±0.13,磷酸化 JAK2/JAK2 比值分别 为 1.00±0.20、4.98±1.01、2.13±0.52和 4.21±0.92,磷酸化 STAT3/STAT3 比值分别为 1.00±0.18、3.77±0.78、2.65±0.64和3.49±0.75.模型组的上述指标与对照组相比,在统计学上差异均有统计学意义(P<0.05,P<0.001);实验组的上述指标与模型组相比,在统计学上差异均有统计学意义(P<0.05,P<0.01,P<0.001);联合组的上述指标与实验组相比,在统计学上差异均有统计学意义(P<0.05,P<0.001).结论 莫西沙星能够有效改善肺炎支原体肺炎小鼠肺组织形态,调节炎症因子水平和氧化应激损伤,可能是通过下调lncRNA GAS5影响细胞凋亡和JAK/STAT通路的蛋白表达来实现的.
Effects of moxifloxacin in reducing lung injury in mice with Mycoplasma pneumoniae pneumonia
Objective To investigate the protective effect of moxifloxacin(Moxi)on Mycoplasma pneumoniae pneumonia by down-regulating long non-coding RNA growth inhibition specific gene(lncRNA GAS5)through non-receptor protein tyrosine kinase(JAK)/signaling and transcriptional activator protein(STAT)signaling pathways.Methods BALB/c mice were randomly divided into control group,model group,experimental group and combined group.Mice in model group,experimental group and combined group were treated with nasal drops of Mycoplasma pneumoniae fluid to establish Mycoplasma pneumoniae pneumonia model.By intraperitoneal injection of the experimental group and the combined group of 100 mg·kg-1 moxifloxacin treatment;on the basis,the overexpressed plasmid pc-GAS5 was injected into the tail vein of the combined group.The control group and model group were injected with the same amount of 0.9%NaCl intraperitoneally.The serum levels of interleukin-1 β(IL-1β)and IL-6 were detected by enzyme-linked immunosorbent assay(ELISA);the serum levels of superoxide dismutase(SOD)were detected by biochemical method;and the expression of lncRNA GAS5 in lung tissue was detected by real-time fluorescence quantitative polymerase chain reaction;the protein expression levels of B-cell lymphoma-2(Bcl-2),JAK2 and STAT3 in mouse lung were detected by Western blot.Results The serum IL-1 β content in control group,model group and experimental group were(64.03±14.19),(254.85±63.79)and(157.46±42.93)pg·mL-1,respectively;IL-6 contents were(22.61±5.01),(184.14±39.50)and(132.64±25.47)pg·mL-1;SOD activities were(50.38±11.75),(28.17±6.71)and(37.67±8.09)U·mL-1,respectively;the relative expression levels of lncRNA GAS5 in lung tissues were 1.00±0.16,3.78±0.69 and 2.41±0.54,respectively.The relative expression levels of Bcl-2 protein in control group,model group,experimental group and combined group were 1.00±0.17,0.65±0.14,0.82±0.16 and 0.62±0.13,respectively;phospherylated JAK2/JAK2 ratios were 1.00±0.20,4.98±1.01,2.13±0.52 and 4.21±0.92,respectively;phospherylated STAT3/STAT3 ratios were 1.00±0.18,3.77±0.78,2.65±0.64 and 3.49±0.75,respectively.Compared with the control group,the above indexes in the model group had statistical significance(P<0.05,P<0.001).The above indexes in the experimental group were statistically significant compared with those in the model group(P<0.05,P<0.01,P<0.001).There were significant differences between combined group and experimental group(P<0.05,P<0.001).Conclusion Moxifloxacin can effectively improve the lung tissue morphology of mice with Mycoplasma pneumoniae pneumonia,regulate the levels of inflammatory factors and oxidative stress damage,and affect apoptosis and JAK/STAT pathway protein expression by down-regulating lncRNA GAS5.

moxifloxacinlong non-coding RNA growth arrest specific 5apoptosisJanus kinasesignal transducer and activator of transcriptionMycoplasma pneumoniae pneumonia

郭晓华、祝伟、张倩

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济南市第四人民医院检验科,山东济南 250031

济南市第四人民医院呼吸内科,山东济南 250031

莫西沙星 长链非编码RNA生长抑制特异性基因 凋亡 非受体型蛋白酪氨酸激酶 信号传导和转录激活蛋白 肺炎支原体肺炎

2024

中国临床药理学杂志
中国药学会

中国临床药理学杂志

CSTPCD北大核心
影响因子:1.91
ISSN:1001-6821
年,卷(期):2024.40(19)