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作 者:李春霖 李时超 贾英田 李建 赵鲲鹏[4] 税丕先 LI Chun-lin;LI Shi-chao;JIA Ying-tian;LI Jian;ZHAO Kun-peng;SHUI Pi-xian(Southwest Medical University,Luzhou,Sichuan 646000,China;Anorectal Dept,Affiliated Hospital of Traditional Chinese Medicine of Southwest Medical University,Luzhou,Sichuan 646000,China;Pharmaceutical Dept,Affiliated Hospital of Traditional Chinese Medicine of Southwest Medical University,Luzhou,Sichuan 646000,China;Clinical College of Gansu University of Traditional Chinese Medicine,Lanzhou 734000,China)
机构地区:[1]西南医科大学,四川泸州646000 [2]西南医科大学附属中医医院肛肠科,四川泸州646000 [3]西南医科大学附属中医医院药学部,四川泸州646000 [4]甘肃中医药大学临床学院,甘肃兰州734000
出 处:《中国药理学通报》2023年第5期938-945,共8页Chinese Pharmacological Bulletin
基 金:四川省中医药管理局科学技术研究专项(No 2020JC0137)。
摘 要:目的探讨黄连素调控JAK/STAT信号通路对溃疡性结肠炎(ulcerative colitis,UC)小鼠结肠上皮细胞和外周血中性粒细胞(peripheral blood neutrophils,PMN)凋亡的影响。方法葡聚糖硫酸钠(dextran sulfact sodium,DSS)法构建UC小鼠模型,随机分为对照组、UC组、黄连素低、中、高剂量组和阳性药物组(美沙拉嗪肠溶片组),另将小鼠随机分为UC组、黄连素高剂量组、AG490组、黄连素高剂量+AG490组。比较各组血清肿瘤坏死因子α(TNF-α)、白介素6(IL-6)水平和结肠上皮细胞凋亡、PMN凋亡情况,Western blot检测结肠组织凋亡相关、JAK/STAT信号通路相关蛋白表达情况。结果黄连素各剂量组以及阳性药物组血清TNF-α、IL-6水平、结肠上皮细胞凋亡率、Fas、FasL、Bax、caspase-3、p-JAK2/JAK2、p-STAT3/STAT3蛋白表达明显低于UC组(P<0.05),且随黄连素剂量增加逐渐降低(P<0.05);黄连素各剂量组以及阳性药物组PMN凋亡率、Bcl-2蛋白表达明显高于UC组(P<0.05),且随黄连素剂量增加逐渐升高(P<0.05);AG490能逆转黄连素上述作用(P<0.05)。结论黄连素可通过调控JAK/STAT信号通路抑制UC小鼠结肠上皮细胞凋亡,促进PMN凋亡,进而发挥治疗UC的作用。Aim To analyze the effects of berberine on the apoptosis of colon epithelial cells and polymorphonuclear neutrophils(PMNs)in mice with ulcerative colitis(UC)by regulating JAK/STAT signaling pathway.Methods The UC mouse models were established by dextran sulfate sodium(DSS)method and were randomly divided into control group,UC group,low-dose,middle-dose and high-dose berberine groups and positive drug group(mesalazine enteric-coated tablet group).In addition,the mice were randomly divided into UC group,high-dose berberine group,AG490 group,and high-dose berberine+AG490 group.Levels of serum tumor necrosis factorα(TNF-α)and interleukin 6(IL-6)and colon epithelial cell apoptosis and PMN apoptosis were compared among the groups.Western blot was used to detect the expressions of colon tissue apoptosis-related and JAK/STAT signaling pathway-related proteins.Results The levels of serum TNF-αand IL-6,apoptosis rate of colon epithelial cell and protein expressions of Fas,FasL,Bax,caspase-3,p-JAK2/JAK2 and p-STAT3/STAT3 in each dose berberine group and positive drug group were significantly lower than those in UC group(P<0.05),and the above indicators in berberine groups were reduced gradually(P<0.05).The PMN apoptosis rate and Bcl-2 protein expression were significantly higher in each dose berberine group and positive drug group than those in UC group(P<0.05),and the two indicators increased gradually in berberine groups(P<0.05).AG490 could reverse the above effects of berberine(P<0.05).Conclusions Berberine can inhibit the apoptosis of colon epithelial cell and promote the apoptosis of PMN in UC mice by regulating the JAK/STAT signaling pathway,and then play a role in the treatment of UC.
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