机构地区:[1]南华大学衡阳医学院附属第三医院内分泌科,湖南衡阳421900 [2]南华大学衡阳医学院附属第三医院血液净化科,湖南衡阳421900 [3]湖南中医药大学第一附属医院内分泌科,湖南长沙410021
出 处:《中国临床药理学杂志》2021年第18期2427-2432,共6页The Chinese Journal of Clinical Pharmacology
基 金:湖南省教育厅科学研究课题资助项目(18C0441)。
摘 要:目的研究红车轴草总黄酮对高糖诱导的大鼠胰岛β细胞损伤的影响,及其潜在的分子机制。方法本实验分为对照组,模型组,低、中、高剂量实验组,miR-NC组,miR-99a-3p组,anti-miR-NC,anti-miR-99a-3p组,模型+miR-NC组,模型+miR-99a-3p组,模型+si-NC组,模型+si-CD36组,高剂量实验+anti-miR-NC组和高剂量实验+anti-miR-99a-3p组。对照组给予5.5 mmol·L^(-1)葡萄糖处置;模型组给予25 mmol·L^(-1)葡萄糖处置;低、中、高剂量实验组分别给予12.5,25.0和50.0 mg·L^(-1)红车轴草总黄酮和25 mmol·L^(-1)葡萄糖处置;miR-NC组、miR-99a-3p组、anti-miR-NC组、anti-miR-99a-3p组分别转染miR-NC、miR-99a-3p、anti-miR-NC、anti-miR-99a-3p;模型+miR-NC组、模型+miR-99a-3p组、模型+si-NC组、模型+si-CD36组均给予25 mmol·L^(-1)葡萄糖处理,并分别转染miR-NC、miR-99a-3p、si-NC、si-CD36;高剂量实验+anti-miR-NC组、高剂量实验+anti-miR-99a-3p组均给予50.0 mg·L^(-1)红车轴草总黄酮+25 mmol·L^(-1)葡萄糖,并分别转染anti-miR-NC或anti-miR-99a-3p。用流式细胞术测定细胞凋亡率,用定量实时聚合酶链反应检测细胞中miR-99a-3p和CD36 mRNA的表达水平。结果模型组INS-1细胞中CD36 mRNA(2.74±0.27 vs 1.01±0.08)和细胞凋亡率[(27.63±2.71)%vs(5.69±0.58)%]均较对照组显著升高,miR-99a-3p(0.38±0.03 vs 1.00±0.09)较对照组显著降低,差异均有统计学意义(均P<0.05);与模型组比较,低、中、高剂量实验组的上述结果相反。模型+miR-99a-3p组的细胞凋亡率[(12.48±1.19)%vs(26.84±2.41)%]较模型+miR-NC组显著降低,miR-99a-3p表达量(0.79±0.07 vs 0.34±0.03)较模型+miR-NC组显著升高,差异均有统计学意义(均P<0.05)。模型+si-CD36组INS-1细胞中CD36 mRNA(1.35±0.12 vs 2.81±0.26)及细胞凋亡率[(13.54±1.32)%vs(25.87±2.52)%]均较模型+si-NC组显著降低,差异均有统计学意义(均P<0.05)。高剂量实验+anti-miR-99a-3p组INS-1细胞中miR-99a-3p(0.43±0.14 vs 0.88±0.06)较高剂量实验+anti-miObjective To investigate the effects of red clover flavonoids on the injury of rat pancreaticβcells induced by high glucose and its potential molecular mechanism.Methods This experiment was divided into control group,model group,experimental-L,-M,-H groups,miR-NC group,miR-99a-3p group,anti-miR-NC,anti-miR-99a-3p group,model+miR-NC group,model+miR-99a-3p group,model+si-NC group,model+si-CD36 group,experimental-H+anti-miR-NC group and experimental-H+anti-miR-99a-3p group.The pancreatic isletβcells in the control group were treated with 5.5 mmol·L^(-1)glucose with INS-1,the model group INS-1 cells were treated with 25 mmol·L^(-1)glucose,and the experimental-L,-M,-H groups INS-1 cells were treated with 12.5,25.0 and 50.0 mg·L^(-1)total flavonoids of red clover and 25 mmol·L^(-1)glucose treatment,miR-NC group,miR-99a-3p group,anti-miR-NC group,anti-miR-99a-3p Group INS-1 cells were treated with transfected miR-NC,miR-99a-3p,anti-miR-NC,anti-miR-99a-3p,model+miR-NC group,model+miR-99a-3p group,model+si-NC group,model+si-CD36 group INS-1 cells were treated with 25 mmol·L^(-1)glucose and transfected with miR-NC,miR-99a-3p,si-NC,siCD36,experimental-H+anti-miR-NC group,experimental-H+anti-miR-99a-3p group INS-1 cells were given 50.0 mg·L^(-1)total red clover flavonoids,25 mmol·L^(-1)glucose and transfected with anti-miR-NC or antimiR-99a-3p treatment.Flow cytometry was used to determine the rate of apoptosis,and quantitative real-time polymerase chain reaction was used to detect the levels of miR-99a-3p and CD36 mRNA in INS-1 cells.Results The levels of CD36 mRNA(2.74±0.27 vs 1.01±0.08)and apoptosis rate[(27.63±2.71)%vs(5.69±0.58)%]of INS-1 cells in the model group were significantly increased compared with the control group,while miR-99a-3p(0.38±0.03 vs 1.00±0.09)was significantly lower than that in control group(all P<0.05).Compared with the model group,the results of the experimental-L,-M,-H groups were opposite.Apoptosis rate[(12.48±1.19)%vs(26.84±2.41)%]in the model+miR-99a-3p group were significantl
关 键 词:红车轴草总黄酮 大鼠胰岛β细胞INS-1 高糖 miR-99a-3p 脂肪酸转运蛋白 损伤 凋亡
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