机构地区:[1]济宁医学院药学院,日照276826 [2]烟台大学药学院,山东大学先进用药系统与生物技术药物协同创新中心,烟台264005 [3]济宁医学院护理学院,济宁272067
出 处:《济宁医学院学报》2025年第1期19-26,共8页Journal of Jining Medical University
基 金:cx2021134济宁医学院大学生创新训练计划项目(2021-ZXJK-08山东省人文社会科学课题)。
摘 要:目的 探究银杏达莫预处理对大鼠小肠缺血-再灌注损伤的影响及相关机制。方法 采用结扎肠系膜上动脉模拟大鼠小肠缺血-再灌注损伤模型,根据随机数字表法将36只Wistar大鼠随机分为假手术组(Sham组),小肠缺血-再灌注模型组(I/R组),银杏达莫干预组(Gin组),每组12只。建模前7d Gin组按3.6mL/1kg给药量进行腹腔注射,一天一次,连续7d, Sham组、I/R组注射等剂量生理盐水。苏木素-伊红(HE)染色观察细胞状态,天狼星红染色和Masson染色观察胶原纤维;血液生化检测血清中超氧化物歧化酶(SOD)和丙二醛(MDA)含量变化;免疫组化检测小肠组织中白介素6(IL-6)、白介素10(IL-10)、Bcl-相关X蛋白(Bax)、B细胞淋巴瘤/白血病-2(Bcl-2)的蛋白表达变化;聚合酶链式反应(PCR)检测Bax、Bcl-2的mRNA表达水平;免疫印迹法(Western blot)检测小肠组织中Smad蛋白(Smad)和Bcl-2,Bax的蛋白表达水平。结果 与Sham组相比,I/R组小肠组织中SOD活性[(125.34±59.58)U/L]降低(P<0.05),MDA含量[(6.24±0.73)U/L]增加(P<0.05);与I/R组相比,Gin组小肠组织中SOD活性[(262.62±22.57)U/L]增强(P<0.05),MDA含量[(2.88±0.74)U/L]降低(P<0.05)。Sham组小肠黏膜结构正常,绒毛完整,I/R组可见大量裸露绒毛,绒毛出现水肿,脱落受损严重,并且有炎性细胞浸润现象,Gin组小肠绒毛结构破坏较轻,可见黏膜轻微水肿和轻微脱落,损伤较轻;天狼星红和Masson染色发现I/R组中胶原纤维较Sham组明显增多,Gin组中的胶原纤维较I/R组有所减轻;免疫组化结果显示,I/R组IL-6、IL-10、Bax、Bcl-2阳性面积占比[(32.24±7.07)%、(10.23±1.63)%、(40.35±7.07)%、(24.64±8.04)%]均高于Sham组[(4.24±1.31)%、(3.77±0.91)%、(2.35±0.87)%、(3.25±0.87)%](P<0.05),Gin组IL-6、Bax阳性面积[(10.23±0.71)%、(6.71±1.41)%]低于I/R组(P<0.05),IL-10、Bcl-2阳性面积[(32.24±8.16)%、(48.40±7.07)%]均高于I/R组(P<0.05);与Sham组相比,I/R组大鼠小肠组织中Bax、Bcl-2、Akt、Smad Objective To explore the effect of Ginkgodamol preconditioning on small intestine ischemia-reperfu-sion injury in rats and its related mechanism.Methods A rat small intestine ischemia-reperfusion injury model was simulated by ligating superior mesenteric artery.According to the random number table,36 Wistar rats were randomly divided into normal group(Sham group),small intestine ischemia-reperfusion model group(I/R group)and Ginkgo-damol intervention group(Gin group),with 12 rats in each group.Seven days before modeling,the Ginkgodamol(Gin)group was injected intraperitoneally at a dosage of 3.6mL/1000g once a day for seven days,while the Sham group and I/R group were injected with the same dose of normal saline.HEmatoxylin-eosin(HE)staining was used to observe the cell state,while Sirius red staining and Masson staining were used to observe the collagen fibers.The contents of superoxide dismutase(SOD)and malondialdehyde(MDA)in serum were detected by blood biochemistry.Immunohisto-chemistry was used to detect the protein expression changes of interleukin-6(IL-6),interleukin-10(IL-10),Bcl-related X protein(Bax)and B-cell lymphoma/leukemia-2(Bcl-2)in small intestine.The mRNA expression levels of Bax and Bcl-2 were detected by polymerase chain reaction(PCR).Western blot was used to detect the protein expression levels of Smad,Bcl-2 and Bax in small intestine.Results Compared with Sham group,the SOD activity(125.34±59.58)u/L in I/R group decreased(P<0.05),and the MDA content(6.24±0.73)u/L increased(P<0.05).Compared with I/R group,SOD activity(262.62±22.57)u/L in small intestine of Gin group was increased(P<0.05),while MDA content(2.88±0.74)u/L was decreased(P<0.05).The results of HE staining showed that the intestinal mucosal structure in Sham group was normal,and the villi were intact.In I/R group,a large number of exposed villi were seen,and the villi were edema,shedding and damaged seriously,and inflammatory cells infiltrated.In Gin group,the structural damage of intestinal villi was light,and the mucosal edema
关 键 词:银杏达莫 小肠缺血-再灌注 TGF-Β/SMAD PI3K/Akt
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