文章摘要
冯静,李莉.丹酚酸 A对脂多糖诱导人肾小球系膜细胞凋亡的作用机制研究[J].安徽医药,2022,26(7):1287-1291.
丹酚酸 A对脂多糖诱导人肾小球系膜细胞凋亡的作用机制研究
Mechanism of salvianolic acid A on lipopolysaccharide-induced apoptosis of human glomerular mesangial cells
  
DOI:10.3969/j.issn.1009-6469.2022.07.004
中文关键词: 丹参  肾小球系膜细胞  细胞凋亡  丹酚酸 A  脂多糖  磷脂酰肌醇 3激酶( PI3K)/蛋白激酶 B(AKT)/哺乳动物雷帕霉素靶蛋白(mTOR)信号通路
英文关键词: Salvia miltiorrhiza  Mesangial cells  Apoptosis  Salvianolic acid A  Lipopolysaccharide  Phosphatidylinositol-3 (PI3K)/protein kinase (AKT)/mammalian target of rapamycin (mTOR) signaling pathway
基金项目:海南省医药卫生科研基金资助项目( 18A200051)
作者单位
冯静 海口市人民医院全科医学科海南海口 570208 
李莉 海南医学院第一附属医院血液净化科海南海口 570100 
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中文摘要:
      目的探究丹酚酸 A对脂多糖(lipopolysaccharide,LPS)诱导人肾小球系膜细胞凋亡的作用机制。方法该研究起止时间为 2018年 5月至 2019年 5月。购买华拓生物生产的 HGMC人肾小球系膜细胞,分为 A组、 B组、 C组、 D组、 E组五组, A组细胞不添加任何药物, B组、 C组、 D组、 E组细胞均加入 10 mg/L LPS培养, 1h后 C组、 D组、 E组分别加入低剂量丹酚酸 A(10 mg/L)、中剂量丹酚酸 A(20 mg/L)、高剂量丹酚酸 A(40 mg/L)处理 24 h后做后续试验。检测细胞增殖、凋亡、细胞周期分布以及磷脂酰肌醇 3激酶(PI3K)/蛋白激酶 B(protein kinase,AKT)/哺乳动物雷帕霉素靶蛋白(mTOR)信号通路指标表达量。结果与 A组相比, B组细胞凋亡率、 G0/G1期细胞分布率降低, S期、 G2/M期细胞分布率升高;与 B组相比, C组、 D组、 E组 G0/G1期细胞分布率、细胞凋亡率升高, S期、 G2/M期细胞分布率降低;与 C组相比, D组、 E组细胞凋亡率、 G0/G1期细胞分布率升高, S期、 G2/M期细胞分布率降低(均 P<0.05);与 D组相比, E组细胞凋亡率(37.59±4.62)%、G0/G1期细胞分布率(86.95±11.62)%升高, S期、 G2/M期细胞分布率分别为
英文摘要:
      Objective To explore the mechanism of salvianolic acid A on lipopolysaccharide (LPS)-induced apoptosis of human glo-merular mesangial cells (HGMCs).Methods The study period was from May 2018 to May 2019. The HGMCs were purchased fromHuatuo Biotechnology and divided into five groups: A group, B group, C group, D group and E group. The cells in group A did not addany drugs, and 10 mg/L LPS was added to the B, C, D and E groups. One hour later, groups C, D, and E were treated with low-dose sal-vianolic acid A (10 mg/L), medium-dose salvianolic acid A (20 mg/L) and high-dose salvianolic acid A (40 mg/L) for 24 h, respectively.Cell proliferation, apoptosis, cell cycle distribution and the expression of phosphatidylinositol-3 (PI3K)/protein kinase (AKT)/mammali-an target of rapamycin (mTOR) signaling pathway indicators were detected.Results Compared with group A, the apoptosis rate and the distribution rate of cells in G0/G1 phase in group B decreased, while the distribution rate of cells in S phase and G2/M phase in-creased.Compared with group B, the distribution rate of cells in G0/G1 phase and apoptosis rate in groups C, D, and E increased andthe distribution rate of cells in S phase and G2/M phase decreased. Compared with group C, the apoptosis rate and the distribution rateof cells in G0/G1 phase in groups D and E increased, and the distribution rate of cells in S phase and G2/M phase decreased (All P< 0.05). Compared with group D, the apoptotic rate of cells in group E was (37.59±4.62)%, and the distribution rate of cells in G0/G1phase was (86.95±11.62)%, and the distribution rates of cells in S phase and G2/M phase were (10.23±1.03)% and (4.26±1.03)%, re-spectively (P < 0.05). Compared with group A, the cell proliferation rate, p-PI3K, p-AKT, p-mTOR, caspase-3, and B-cell lymphoma/ leukemia-2 (Bcl-2) were increased, and the expression of B-cell lymphoma/leukemia-associated protein X (Bax) was decreased (P < 0.05). Compared with group B, the cell proliferation rate and p-PI3K, p-AKT, p-mTOR, caspase-3 and Bcl-2 expression in groups C, D, and E decreased, while the expression of Bax increased (P < 0.05). Compared with group C, the cell proliferation rate and p-PI3K, p-AKT, p-mTOR, caspase-3 and Bcl-2 expression in groups D and E decreased, while the expression of Bax increased (P < 0.05). Com-pared with group D of the 12 h proliferation rate, the expression of p-PI3K, p-Akt, p-mTOR, caspase-3, Bcl-2 and Bax [(26.12±2.25)%,(0.49±0.28), (0.87±0.45), (0.59±0.25), (0.88±0.12), (1.25±0.20) and (0.87±0.12)], Group E were (19.02±1.06)%, (0.25±0.11), (0.32±0.15), (0.25±0.12), (0.54±0.12), (0.42±0.22), and (1.59±0.22), respectively (P < 0.05).Conclusions Salvianolic acid A may regulate the apoptosis-related proteins caspase-3, Bcl-2 and Bax by promoting the inactivation of the PI3K/AKT/mTOR signaling pathway and play a role in promoting LPS-induced apoptosis of human glomerular mesangial cells, inhibiting proliferation, and inhibiting apoptosis.The role of arresting cell cycle progression.
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