首页|藏红花素调控miR-877-5p对氯吡格雷诱导胃黏膜上皮细胞损伤的影响

藏红花素调控miR-877-5p对氯吡格雷诱导胃黏膜上皮细胞损伤的影响

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目的 探讨藏红花素对氯吡格雷诱导的胃黏膜上皮细胞损伤的作用及分子机制。方法 将人胃黏膜上皮细胞GES-1分为对照组,模型组(0。5 mmol·L-1氯吡格雷)和藏红花素低、中、高浓度(0。1、1、10 nmol·L-1)组,另设 anti-miR-NC 组、miR-877-5p 抑制剂组、藏红花素(10 nmol·L-1)+miR-NC 组和藏红花素(10 nmol·L-1)+miR-877-5p mimic组。采用MTT法、克隆形成实验检测细胞存活率和克隆形成数,流式细胞术检测细胞凋亡,qRT-PCR检测miR-877-5p表达水平,Western blot法检测闭合蛋白(occludin)、闭锁小带蛋白(ZO-1)、p-P38蛋白表达。结果 与对照组相比,模型组细胞存活率、克隆形成数下降,凋亡率和miR-877-5p、p-P38表达升高,occludin和ZO-1表达降低(P<0。05)。与模型组相比,藏红花素中、高浓度组细胞存活率、克隆形成数增加,凋亡率和miR-877-5p、p-P38表达降低,occludin和ZO-1表达升高(P<0。05)。与anti-miR-NC组相比,miR-877-5p抑制剂组细胞存活率、克隆形成数及occludin、ZO-1表达增加,凋亡率和miR-877-5p、p-P38表达降低(P<0。05)。与藏红花素+miR-NC组相比,藏红花素+miR-877-5p mimic组胃黏膜上皮细胞存活率、克隆形成数及occludin、ZO-1表达下降,凋亡率和miR-877-5p、p-P38表达升高(P<0。05)。结论 藏红花素可能通过下调miR-877-5p抑制氯吡格雷诱导的胃黏膜上皮细胞凋亡,促进细胞增殖。
Effects of crocin on clopidogrel-induced gastric epithelial cells injury by regulating miR-877-5p
AIM To explore the effect of crocin on gastric mucosal epithelial cells injury induced by clopidogrel and the molecular mechanism.METHODS The gastric mucosal epithelial cells GES-1 were divided into control group,model group(0.5 mmol·L-1 clopidogrel),and crocin low,medium,and high concentration(0.1,1,10 nmol·L-1)groups,and additionally divided into anti-miR-NC group,miR-877-5p inhibitor group,crocin(10 nmol·L-1)+miR-NC group,crocin(10 nmol·L-1)+miR-877-5p mimic group.MTT and colony formation assays were used to detect cell survival rate and the number of colony formation.Flow cytometry was used to detect cell apoptosis.qRT-PCR was used to detect the expression level of miR-877-5p.Western blot was used to detect the expression of occludin,zonula occluden-1(ZO-1),and p-P38 protein.RESULTS Compared with the control group,the survival rate and the number of cell clone formation in model group were decreased,the apoptosis rate and the expression of miR-877-5p and p-P38 were increased,and the expressions of occludin and ZO-1 were decreased(P<0.05).Compared with the model group,the survival rate and the number of cell clone formation in the crocin medium and high concentration groups were increased,the apoptosis rate and the expression of miR-877-5p and p-P38 were decreased,and the expression of occludin and ZO-1 were increased(P<0.05).Compared with the anti-miR-NC group,the survival rate,the number of cell clone formation,and expression of occludin and ZO-1 were increased in the miR-877-5p inhibitor group,and apoptosis rate and expression of miR-877-5p and p-P38 were decreased(P<0.05).Compared with the crocin+miR-NC group,the survival rate,the number of cell clone formation,and the expression of occludin and ZO-1 were decreased in the crocin+miR-877-5p mimic group,while the apoptosis rate and the expression of miR-877-5p and p-P38 were increased(P<0.05).CONCLUSION Crocin may inhibit clopidogrel-induced apoptosis of gastric epithelial cells and promote cell proliferation by down-regulating miR-877-5p.

crocinmiR-877-5pclopidogrelgastric mucosalepithelial cellscell proliferationapoptosis

杨凌霞、王伟、刘萍、向丹

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荆门市中医医院消化内科,湖北荆门 448000

藏红花素 miR-877-5p 氯吡格雷 胃黏膜 上皮细胞 细胞增殖 细胞凋亡

2024

中国新药与临床杂志
中国药学会 上海市食品药品监督管理局科技情报研究所

中国新药与临床杂志

CSTPCD北大核心
影响因子:0.967
ISSN:1007-7669
年,卷(期):2024.43(6)
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