首页|抗炎合剂通过调控Beclin-1介导自噬减轻大鼠脓毒症急性肺损伤

抗炎合剂通过调控Beclin-1介导自噬减轻大鼠脓毒症急性肺损伤

扫码查看
目的 探讨抗炎合剂对脓毒症急性肺损伤(ALI)大鼠的保护作用及其可能机制。方法 将 40 只SD大鼠按随机数字表法分为假手术组、脓毒症ALI模型组(模型组)、3-甲基腺嘌呤(3-MA)对照组、抗炎合剂预处理组,每组 10 只。采用盲肠结扎穿孔术(CLP)建立脓毒症ALI大鼠模型;假手术组仅开腹、关腹,不给予穿孔结扎;两组均于术前连续 3d给予生理盐水灌胃和腹腔注射。3-MA对照组于制模前连续 3d给予生理盐水和自噬抑制剂3-MA 15 mg/kg腹腔注射。抗炎合剂预处理组于制模前连续3d给予抗炎合剂8。8 mL/kg灌胃[抗炎合剂组成:大黄15g(后下)、黄连15 g、黄芩12 g、厚朴12 g、败酱草30 g],并腹腔注射生理盐水。各组于术后24h取大鼠腹主动脉血处死,采用酶联免疫吸附试验(ELISA)检测血清炎症细胞因子白细胞介素(IL-1β、IL-6)水平。取肺组织,收集支气管肺泡灌洗液(BALF),采用ELISA法检测IL-1β、IL-6水平;检测肺湿/干质量(W/D)比值;苏木素-伊红(HE)染色后,光镜下观察肺组织病理学改变;采用蛋白质免疫印迹试验(Western blotting)检测肺组织自噬标志物微管相关蛋白1轻链3-Ⅱ/Ⅰ(LC3-Ⅱ/Ⅰ)和Beclin-1蛋白表达;透射电镜下观察肺组织自噬小体。结果 与假手术组比较,模型组大鼠肺组织结构破坏严重,有大量炎症细胞浸润,肺W/D比值、血清和BALF中IL-1β、IL-6水平均明显升高,LC3-Ⅱ/Ⅰ比值和Beclin-1蛋白表达均明显下调,自噬小体明显增加。3-MA对照组大鼠肺组织损伤程度较模型组更严重,肺W/D比值和血清、BALF中炎症细胞因子水平进一步升高,肺组织LC3-Ⅱ/Ⅰ比值和Beclin-1 蛋白表达仍较假手术组呈下调趋势,自噬小体较模型组减少。与模型组相比,抗炎合剂预处理组大鼠肺组织损伤明显减轻,少量炎症细胞浸润,肺W/D比值明显降低(7。07±1。02比11。33±1。85,P<0。05),血清和BALF中IL-1β、IL-6水平均明显下降[IL-1β(ng/L):血清为26。04±3。86比40。83±5。46,BALF为 17。75±2。02 比 26。86±4。32;IL-6(ng/L):血清为 91。28±10。15 比 129。44±13。05,BALF为 76。06±7。51 比120。91±7。47,均P<0。05],肺组织LC3-Ⅱ/Ⅰ比值和Beclin-1 蛋白表达显著上调[LC3-Ⅱ/Ⅰ比值:1。23±0。02 比0。60±0。02,Beclin-1 蛋白(Beclin-1/GAPDH):2。37±0。33 比 0。62±0。05,均P<0。05],且自噬小体数量明显增加。结论 抗炎合剂能改善CLP致脓毒症大鼠肺损伤,降低炎症水平,其机制可能与通过上调Beclin-1 表达介导自噬有关。
Anti-inflammatory mixture alleviates acute lung injury induced by sepsis in rats by modulating Beclin-1-mediated autophagy
Objective To investigate the protective effects of an anti-inflammatory mixture on acute lung injury(ALI)induced by sepsis in rats,as well as its possible mechanisms.Methods A total of 40 Sprague-Dawley(SD)rats were randomly divided into the sham group,septic ALI model group(model group),3-methyladenine(3-MA)control group,and anti-inflammatory mixture pretreatment group,with 10 rats in each group.Cecal ligation and perforation(CLP)was performed to reproduce a septic ALI model.The rats in the sham group only underwent opening and closing the abdomen without perforation and ligation.Both groups were given saline gavage and intraperitoneal injection for 3 consecutive days before surgery.The 3-MA control group was given intraperitoneal injection of saline and autophagy inhibitor 3-MA 15 mg/kg for 3 consecutive days before modeling.The anti-inflammatory mixture pretreatment group was given 8.8 mL/kg of anti-inflammatory mixture by gavage[the composition of anti-inflammatory mixture:rhubarb 15 g(after the next),coptis chinensis 15 g,baical skullcap root 12 g,magnoliae cortex 12 g,dahurian patrinia herb 30 g]and saline intraperitoneal injection for 3 consecutive days before modeling.The rats in each group were anesthetized 24 hours after surgery and died due to abdominal aortic blood collection.Enzyme-linked immunosorbent assay(ELISA)was used to detect the levels of serum inflammatory cytokines interleukins(IL-1β and IL-6).Lung tissue was taken and then the bronchoalveolar lavage fluid(BALF)was collected,and the levels of IL-1β and IL-6 were detected by ELISA.Lung wet/dry weight(W/D)ratio was measured.After hematoxylin-eosin(HE)staining,the histopathological changes of the lungs were observed under light microscopy.Western blotting was used to detect the expression of autophagy markers microtubule-associated protein 1 light chain 3-Ⅱ/Ⅰ(LC3-Ⅱ/Ⅰ)and Beclin-1 protein in lung tissue.Autophagosomes in lung tissue were observed with transmission electron microscopy.Results Compared with the sham group,the rats in the model group exhibited severe destruction of lung tissue structure,with significant infiltration of inflammatory cells,the lung W/D ratio and the levels of IL-1β and IL-6 in serum and BALF were significantly increased,the expressions of LC3-Ⅱ/Ⅰand Beclin-1 protein were down-regulated,the autophagosomes were more.The rats in the 3-MA control group exhibited more severe lung tissue injury as compared with the model group,the lung W/D ratio and the levels of inflammatory cytokines in serum and BALF were further increased,the expressions of LC3-Ⅱ/Ⅰand Beclin-1 protein still showed a decrease tendency as compared with the sham group,and the autophagosomes were less than that in the model group.Compared with the model group,the anti-inflammatory mixture pretreatment group showed milder lung tissue injury with a minimal amount of inflammatory cell infiltration,the lung W/D ratio was significantly reduced(7.07±1.02 vs.11.33±1.85,P<0.05),the levels of IL-1β and IL-6 in both serum and BALF were significantly decreased[IL-1β(ng/L):26.04±3.86 vs.40.83±5.46 in serum,17.75±2.02 vs.26.86±4.32 in BALF;IL-6(ng/L):91.28±10.15 vs.129.44±13.05 in serum,76.06±7.51 vs.120.91±7.47 in BALF,all P<0.05],and the ratio of LC3-Ⅱ/Ⅰand Beclin-1 protein expression were significantly increased[LC3-Ⅱ/Ⅰratio:1.23±0.02 vs.0.60±0.02,Beclin-1 protein(Beclin-1/GAPDH):2.37±0.33 vs.0.62±0.05,both P<0.05].Furthermore,an increase in the number of autophagosomes was observed.Conclusion The anti-inflammatory mixture improves lung injury in rats with sepsis induced by CLP and reduce inflammation levels,potentially through upregulation of Beclin-1-mediated autophagy.

SepsisAcute lung injuryAnti-inflammatory mixtureInflammatory factorAutophagy

陆玮兰、闫国良、沈一凡、李海涛、吴赛、翁同锐、张蕊、火艳雯

展开 >

上海中医药大学附属市中医医院重症医学科,上海 200071

脓毒症 急性肺损伤 抗炎合剂 炎症因子 自噬

上海市进一步加快中医药传承创新发展三年行动计划

ZY2021-2023-0209-11

2024

中华危重病急救医学
中华医学会

中华危重病急救医学

CSTPCD北大核心
影响因子:3.049
ISSN:2095-4352
年,卷(期):2024.36(7)