[1]韩莎莎,尹丹,李跃峰,等.连翘苷通过调控CTRP3表达对高糖诱导的人视网膜血管内皮细胞损伤的影响及其机制研究[J].眼科新进展,2024,44(5):354-359.[doi:10.13389/j.cnki.rao.2024.0069]
 HAN Shasha,YIN Dan,LI Yuefeng,et al.Effect of phillyrin on high glucose-induced injury of human retinal vascular endothelial cells by regulating complement C1q/tumor necrosis factor-related protein-3 expression and its mechanism[J].Recent Advances in Ophthalmology,2024,44(5):354-359.[doi:10.13389/j.cnki.rao.2024.0069]
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连翘苷通过调控CTRP3表达对高糖诱导的人视网膜血管内皮细胞损伤的影响及其机制研究/HTML
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《眼科新进展》[ISSN:1003-5141/CN:41-1105/R]

卷:
44卷
期数:
2024年5期
页码:
354-359
栏目:
实验研究
出版日期:
2024-04-30

文章信息/Info

Title:
Effect of phillyrin on high glucose-induced injury of human retinal vascular endothelial cells by regulating complement C1q/tumor necrosis factor-related protein-3 expression and its mechanism
作者:
韩莎莎尹丹李跃峰叶琴
053000 河北省衡水市,衡水市人民医院眼科(韩莎莎,尹丹,李跃峰);350004 福建省福州市,福建医科大学附属第一医院眼科(叶琴)
Author(s):
HAN Shasha1YIN Dan1LI Yuefeng1YE Qin2
1.Department of Ophthalmology, Hengshui People’s Hospital ,Hengshui 053000,Hebei Province,China
2.Department of Ophthalmology, the First Affiliated Hospital of Fujian Medical University,Fuzhou 350004,Fujian Province,China
关键词:
连翘苷高糖人视网膜血管内皮细胞补体C1q/肿瘤坏死因子相关蛋白3氧化应激细胞凋亡
Keywords:
phillyrin high glucose retinal vascular endothelial cells complement C1q/tumor necrosis factor-related protein-3 oxidative stress cell apoptosis
分类号:
R774
DOI:
10.13389/j.cnki.rao.2024.0069
文献标志码:
A
摘要:
目的 比较不同剂量连翘苷(PHN)对高糖(HG)诱导的人视网膜血管内皮细胞损伤的影响,并分析其对补体C1q/肿瘤坏死因子相关蛋白3(CTRP3)表达的调控作用及可能的作用机制。
方法 采用HG培养人视网膜血管内皮细胞并建立细胞损伤模型(HG组)。HG+PHN-L组、HG+PHN-M组、HG+PHN-H组人视网膜血管内皮细胞分别用1 μmol·L-1、10 μmol·L-1、100 μmol·L-1PHN处理后进行HG诱导。HG+pcDNA组、HG+pcDNA-CTRP3组分别用pcDNA、pcDNA-CTRP3转染至人视网膜血管内皮细胞后进行HG诱导。HG+PHN-H+sh-NC组、HG+PHN-H+sh-CTRP3组分别用sh-NC、sh-CTRP3转染后,用100 μmol·L-1 PHN处理HG诱导的人视网膜血管内皮细胞。检测细胞丙二醛(MDA)、超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-Px)水平。采用流式细胞术检测细胞凋亡率。采用实时荧光定量聚合酶链反应(qRT-PCR)、Western blot分别检测B淋巴细胞瘤-2(Bcl-2)、Bcl-2相关蛋白(Bax)、CTRP3蛋白表达水平。
结果 与Con组比较,HG组细胞凋亡率、MDA水平、Bax蛋白水平均升高,SOD、GSH-Px、Bcl-2蛋白、CTRP3 mRNA及蛋白水平均降低(均为P<0.05)。与HG组比较,HG+PHN-L组、HG+PHN-M组、HG+PHN-H组细胞凋亡率、MDA水平、Bax蛋白水平均降低,且HG+PHN-H组<HG+PHN-M组<HG+PHN-L组(均为P<0.05),SOD、GSH-Px、Bcl-2蛋白、CTRP3 mRNA及蛋白水平均升高,且HG+PHN-H组>HG+PHN-M组>HG+PHN-L组(均为P<0.05)。与HG+pcDNA组比较,HG+pcDNA-CTRP3组细胞凋亡率、MDA水平、Bax蛋白水平均降低,SOD、GSH-Px、CTRP3蛋白、Bcl-2蛋白水平均升高(均为P<0.05)。与HG+PHN-H+sh-NC组比较,HG+PHN-H+sh-CTRP3组细胞凋亡率、MDA水平、Bax蛋白水平均升高,SOD水平、GSH-Px水平、CTRP3蛋白、Bcl-2蛋白水平均降低(均为P<0.05)。
结论 PHN可减轻HG诱导的人视网膜血管内皮细胞损伤,其作用机制可能与上调CTRP3表达有关。
Abstract:
Objective To compare the effects of different doses of phillyrin (PHN) on the injury of human retinal vascular endothelial cells (RVECs) induced by high glucose (HG) and analyze its regulatory effect on the expression of complement C1q/tumor necrosis factor-related protein-3 (CTRP3) and its possible mechanism.
Methods RVECs were cultured with HG to establish cell injury models (HG group). RVECs in the HG+PHN-L group, HG+PHN-M group, and HG+PHN-H group were treated with 1 μmol·L-1, 10 μmol·L-1, and 100 μmol·L-1 PHN, respectively, followed by HG induction. RVECs in the HG+pcDNA group and HG+pcDNA-CTRP3 group were transfected with pcDNA and pcDNA-CTRP3, respectively, followed by HG induction. RVECs in the HG+PHN-H+sh-NC group and HG+PHN-H+sh-CTRP3 group were transfected with sh-NC and sh-CTRP3, respectively, then induced by HG and treated with 100 μmol·L-1 PHN. The levels of malondialdehyde (MDA), superoxide dismutase (SOD), and glutathione peroxidase (GSH-Px) were measured. Cell apoptosis was detected by flow cytometry. The expression levels of B-cell lymphoma-2 (Bcl-2), Bcl-2-associated X (Bax) and CTRP3 protein were determined by quantitative real-time polymerase chain reaction (qRT-PCR) and Western blot, respectively.
Results Compared with the Con group, the cell apoptosis rate and the levels of MDA and Bax protein in the HG group increased, while the levels of SOD, GSH-Px, Bcl-2 protein, CTRP3 mRNA and protein decreased (all P<0.05). Compared with the HG group, the cell apoptosis rate and the levels of MDA and Bax protein in the HG+PHN-L, HG+PHN-M, and HG+PHN-H groups decreased (HG+PHN-H group < HG+PHN-M group < HG+PHN-L group), while the levels of SOD, GSH-Px, Bcl-2 protein, CTRP3 mRNA and protein increased (HG+PHN-H group > HG+PHN-M group > HG+PHN-L group) (all P<0.05). Compared with the HG+pcDNA group, the cell apoptosis rate and the levels of MDA and Bax protein in the HG+pcDNA-CTRP3 group decreased, while the levels of SOD, GSH-Px, CTRP3 protein, and Bcl-2 protein increased (all P<0.05). Compared with the HG+PHN-H+sh-NC group, the HG+PHN-H+sh-CTRP3 group showed an increase in the cell apoptosis rate and the levels of MDA and Bax protein and a decrease in the levels of SOD, GSH-Px, CTRP3 protein, and Bcl-2 protein (all P<0.05).
Conclusion PHN can alleviate HG-induced damage to RVECs, which may be related to the upregulation of the CTRP3 expression.

参考文献/References:

[1] 孔慧,崔彦.CD40-ATP-P2 X7/NLRP3炎症信号通路在糖尿病视网膜病变中的作用研究进展[J].眼科新进展,2021,41(9):879-882.
KONG H,CUI Y.Research progress on the role of CD40-ATP-P2 X7/NLRP3 inflammatory signaling pathway in diabetes retinopathy[J].Rec Adv Ophthalolmol,2021,41(9):879-882.
[2] XIE H,ZHANG C Y,LIU D D,YANG Q,TANG L,WANG T Q,et al.Erythropoietin protects the inner blood-retinal barrier by inhibiting microglia phagocytosis via Src/Akt/cofilin signalling in experimental diabetic retinopathy[J].Diabetologia,2021,64(1):211-225.
[3] OUYANG H,DU A,ZHOU L,ZHANG T,LU B,WANG Z,et al.Chlorogenic acid improves diabetic retinopathy by alleviating blood-retinal-barrier dysfunction via inducing Nrf2 activation[J].Phytother Res,2022,36(3):1386-1401.
[4] LIU K,GAO X,HU C,GUI Y,GUI S,NI Q,et al.Capsaicin ameliorates diabetic retinopathy by inhibiting poldip2-induced oxidative stress[J].Redox Biol,2022,56(1):102460-102470.
[5] JIANG Q,WEI D,HE X,GAN C,LONG X,ZHANG H.Phillyrin prevents neuroinflammation-induced blood-brain barrier damage following traumatic brain injury via altering microglial polarization[J].Front Pharmacol,2021,12(1):719823-719833.
[6] PEHLIVAN V,GURSU M F,CITAK O,ONALAN E,YAKAR B,DONDER E.Evaluation of serum ANGPTL8/betatrophin and cartonectin/CTRP3 levels in diabetic and non-diabetic retinopathy[J].J Coll Physicians Surg Pak,2023,33(1):66-72.
[7] 刘珣,李丹,王海凤,杨蕙頔.白藜芦醇通过circACTR2/miR-186-5p对高糖诱导的视网膜血管内皮细胞损伤的影响[J].解放军医药杂志,2022,34(2):7-11.
LIU X,LI D,WANG H F,YANG H Y.The effect of resveratrol on high glucose induced damage to retinal endothelial cells through circACTR2/miR-186-5p[J].Med Pharm J Chin PLA,2022,34(2):7-11.
[8] 武国利,张宁,马竞.连翘苷通过调控miR-483-3p对oxLDL诱导的血管平滑肌细胞损伤的影响[J].中国药师,2022,25(12):2108-2112.
WU G L,ZHANG N,MA J.The effect of Forsythia suspensa glycoside on oxLDL induced vascular smooth muscle cell injury by regulating miR-483-3p[J].Chin Pharmacist,2022,25(12):2108-2112.
[9] 杨洁,朱晓敏,胡子毅,张会民,冯子龙.糖尿病视网膜病变患者血清转化生长因子-β水平变化及其在监测抗VEGF药物治疗效果中的作用[J].眼科新进展,2021,41(12):1158-1163.
YANG J,ZHU X M,HU Z Y,ZHANG H M,FENG Z L.Serum transforming growth factor in patients with diabetes retinopathy- β Horizontal changes and their role in monitoring the therapeutic effect of anti VEGF drugs[J].Rec Adv Ophthalmol,2021,41(12):1158-1163.
[10] LONG L,LI Y,YU S,LI X,HU Y,LONG T,et al.Scutellarin prevents angiogenesis in diabetic retinopathy by downregulating VEGF/ERK/FAK/Src pathway signaling[J].J Diabetes Res,2019,19(2):421-431.
[11] TANG K,QIN W,WEI R,JIANG Y,FAN L,WANG Z,et al.Ginsenoside Rd ameliorates high glucose-induced retinal endothelial injury through AMPK-STRT1 interdependence[J].Pharmacol Res,2022,179(1):106123-106133.
[12] CHEN S,ZHANG S,WU H,ZHANG D,YOU G,YOU J,et al.Protective effect of phillyrin against cerebral ischemia/reperfusion injury in rats and oxidative stress-induced cell apoptosis and autophagy in neurons[J].Bioengineered,2022,13(3):7940-7950.
[13] JIANG Q,CHEN J,LONG X,YAO X,ZOU X,YANG Y,et al.Phillyrin protects mice from traumatic brain injury by inhibiting the inflammation of microglia via PPARγ signaling pathway[J].Int Immunopharmacol,2020,79(1):106083-106093.
[14] ZHANG D,QI B,LI D,FENG J,HUANG X,MA X,et al.Phillyrin relieves lipopolysaccharide-induced AKI by protecting against glycocalyx damage and inhibiting inflammatory responses[J].Inflammation,2020,43(2):540-551.
[15] CHEN S,ZHANG S,WU H G,ZHANG D B,YOU G L,YOU J,et al.Protective effect of phillyrin against cerebral ischemia/reperfusion injury in rats and oxidative stress-induced cell apoptosis and autophagy in neurons[J].Bioengineered,2022,13(3):7940-7950.
[16] YU J W,ZHOU J J,XUE J J,ZHANG G L.Downregulation of circ-UBAP2 ameliorates oxidative stress and dysfunctions of human retinal microvascular endothelial cells (hRMECs) via miR-589-5p/EGR1 axis[J].Bioengineered,2021,12(1):7508-7518.
[17] 王化湘,刘光化,简唯求,彭辉灿,李姣.迷迭香酸对高糖诱导人视网膜血管内皮细胞迁移、凋亡的作用[J].中南医学科学杂志,2022,50(3):331-335.
WANG H X,LIU G H,JIANG W Q,PENG H C,LI J.The effect of rosmarinic acid on high glucose induced migration and apoptosis of human retinal endothelial cells[J].J Univ South China(Med Ed),2022,50(3):331-335.
[18] SONG Y,ZHANG Y,WAN Z,PAN J,GAO F,LI F, et al.CTRP3 alleviates cardiac ischemia/reperfusion injury via LAMP1/JIP2/JNK signaling pathway[J].Aging (Albany NY),2022,14(3):1321-1335.
[19] DING H,WANG Z,SONG W.CTRP3 protects hippocampal neurons from oxygen-glucose deprivation-induced injury through the AMPK/Nrf2/ARE pathway[J].Hum Exp Toxicol,2021,40(7):1153-1162.
[20] ZENG Y,XU Y,PAN Y,GUO H.KLF10 knockdown negatively regulates CTRP3 to improve OGD/R-induced brain microvascular endothelial cell injury and barrier dysfunction through Nrf2/HO-1 signaling pathway[J].Tissue Cell,2023,82(1):102106-102116.

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备注/Memo

备注/Memo:
河北省卫生健康委员会基金项目(编号:20191762)
更新日期/Last Update: 2024-05-05