[1]周鹃,李艳丽,杜世阳,等.独活寄生汤对白介素1β诱导髓核细胞凋亡和内质网应激的影响[J].中国中医骨伤科杂志,2024,32(04):1-7.[doi:10.20085/j.cnki.issn1005-0205.240401]
 ZHOU Juan,LI Yanli,DU Shiyang,et al.Effects of Duhuo Jisheng Decoction on Interleukin-1β-Induced Human Nucleus Pulposus Cell Apoptosis and Endoplasmic Reticulum Stress[J].Chinese Journal of Traditional Medical Traumatology & Orthopedics,2024,32(04):1-7.[doi:10.20085/j.cnki.issn1005-0205.240401]
点击复制

独活寄生汤对白介素1β诱导髓核细胞凋亡和内质网应激的影响()
分享到:

《中国中医骨伤科杂志》[ISSN:1005-0205/CN:42-1340/R]

卷:
第32卷
期数:
2024年04期
页码:
1-7
栏目:
实验研究
出版日期:
2024-04-01

文章信息/Info

Title:
Effects of Duhuo Jisheng Decoction on Interleukin-1β-Induced Human Nucleus Pulposus Cell Apoptosis and Endoplasmic Reticulum Stress
文章编号:
1005-0205(2024)04-0001-07
作者:
周鹃1李艳丽1杜世阳1杨若鹏1夏平2刘伟1△冯晶1△
1武汉市第一医院(武汉,430022)
2武汉市第四医院
Author(s):
ZHOU Juan1LI Yanli1DU Shiyang1YANG Ruopeng1XIA Ping2LIU Wei1△FENG Jing1△
1Wuhan No.1 Hospital,Wuhan 430022,China; 2Wuhan No.4 Hospital,Wuhan 430033,China.
关键词:
独活寄生汤 含药血清 椎间盘退变 内质网应激
Keywords:
Duhuo Jisheng decoction drug-contained serum intervertebral disc degeneration endoplasmic reticulum stress
分类号:
R-33
DOI:
10.20085/j.cnki.issn1005-0205.240401
文献标志码:
A
摘要:
目的:探讨独活寄生汤含药血清对白介素1β诱导髓核细胞凋亡和内质网应激及其关键途径PERK/elF2α通路的影响,探究独活寄生汤对椎间盘退变的作用和分子机制。方法:将40只10周龄的SD大鼠以独活寄生汤灌胃,连续灌胃2周后经腹主动脉取血,获取含药血清。采用不同浓度独活寄生汤对髓核细胞进行不同时间的处理,细胞活力检测试剂盒(CCK-8)检测髓核细胞的活性。将髓核细胞随机分成3组:对照组(未经IL-1β和独活寄生汤含药血清处理)、IL-1β组(加入10 ng/mL IL-1β溶液干预24 h)和独活寄生汤组(加入10 ng/mL IL-1β溶液和独活寄生汤含药血清干预24 h)。TUNEL法检测分析髓核细胞凋亡率; 免疫荧光法检测各组CHOP、GRP78的表达水平; qRT-PCR法检测各组CHOP、GRP78、Cleaved-caspase3、Bax、BCL-2和PERK、elF2α、ATF4通路mRNA的表达; Western Blot法检测CHOP、GRP78、Cleaved-caspase3、Bax、BCL-2、PERK、elF2α、p-PERK、p-elF2α、ATF4通路蛋白的表达。结果:独活寄生汤能够显著提高髓核细胞的活力,改善髓核细胞凋亡。与对照组相比,IL-1β组CHOP、GRP78、Cleaved-caspase3、Bax和PERK、elF2α、ATF4基因表达显著上升,BCL-2基因表达显著下降,差异有统计学意义(P<0.05); 与IL-1β组相比,独活寄生汤组CHOP、GRP78、Cleaved-caspase3、Bax和PERK、elF2α、ATF4基因表达显著下降,BCL-2基因表达显著上升,差异有统计学意义(P<0.05)。与对照组相比,IL-1β组CHOP、GRP78、Cleaved-caspase3、Bax和PERK、elF2α、ATF4、p-PERK、p-elF2α蛋白表达显著上升,BCL-2蛋白显著下降,差异有统计学意义(P<0.05); 与IL-1β组相比,独活寄生汤组CHOP、GRP78、Cleaved-caspase3、Bax和PERK、elF2α、ATF4、p-PERK、p-elF2α蛋白表达显著下降,BCL-2蛋白显著上升,差异有统计学意义(P<0.05)。结论:独活寄生汤含药血清能够抑制退变髓核细胞的内质网应激和凋亡,进而延缓椎间盘退变,作用途径可能与抑制PERK/elF2α通路有关。
Abstract:
Objective:To study the effect of Duhuo Jisheng decoction drug-contained serum on interleukin 1β-induced human nucleus pulposus cell apoptosis and endoplasmic reticulum stress,and to explore the mechanism of Duhuo Jisheng decoction in intervening intervertebral disc degeneration.Methods:The 40 ten-week-old SD rats were gavaged with Duhuo Jisheng decoction,and the abdominal aorta blood after 2 weeks continuous gavage was collected to obtain drug-contained serum.The nucleus pulposus cells were treated by different concentrations of Duhuo Jisheng decoction for different times.The cell viability test kit(CCK-8)was used to detect the activity of nucleus pulposus cells.The nucleus pulposus cells were randomly divide into three groups:control group(without the treatment of IL-1β and Duhuo Jisheng decoction drug-contained serum),IL-1β group(adding 10 ng/mL IL-1β solution for 24 h),Duhuo Jisheng decoction group(adding 10 ng/mL IL-1β solution and Duhuo Jisheng decoction drug-contained serum for 24 h).The TUNEL method was used to analyze the apoptosis rate of nucleus pulposus cells.Immunofluorescence assay was used to detect the expressions of CHOP and GRP78 in each group; qRT-PCR was used to detect the mRNA expressions of CHOP,GRP78,Cleaved-caspase3,Bax,BCL-2,PERK,elF2α and ATF4 in each group; Western Blot was used to detect CHOP,GRP78,Cleaved-caspase3,Bax,BCL-2,PERK,elF2α,p-elF2α,p-PERK and ATF4 protein expressions.Results:Duhuo Jisheng decoction can significantly enhance the vitality and improve the apoptosis of nucleus pulposus cells.Compared with the control group,the mRNA expression of CHOP,GRP78,Cleaved-caspase3,Bax,PERK,elF2α and ATF4 in IL-1β group was significantly decreased; the mRNA expression of BCL-2 was increased,and the difference was statistically significant(P<0.05).Compared with the IL-1β group,the mRNA expression of CHOP,GRP78,Cleaved-caspase3,Bax,PERK,elF2α and ATF4 in Duhuo Jisheng decoction group was significantly increased; the mRNA expression of BCL-2 was decreased,and the difference was statistically significant(P<0.05).Compared with the control group,CHOP,GRP78,Cleaved-caspase3,Bax,PERK,elF2α,ATF4,p-PERK,p-elF2α protein expression in IL-1β group was significantly decreased; the protein expression of BCL-2 was increased,and the difference was statistically significant(P<0.05).Compared with the IL-1β group,the CHOP,GRP78,Cleaved-caspase3,Bax,PERK,elF2 α,ATF4,p-PERK and p-elF2α protein expression in Juhuo Jisheng decoction group was significantly increased; the protein expression of BCL-2 was decreased,and the difference was statistically significant(P<0.05).Conclusion:The Duhuo Jisheng decoction drug-contained serum can inhibit endoplasmic reticulum stress and apoptosis in degenerated nucleus pulposus cells,thereby delaying intervertebral disc degeneration,which may be related to PERK/elF2α pathway.

参考文献/References:

[1] KHAN A N,JACOBSEN H E,KHAN J,et al.Inflammatory biomarkers of low back pain and disc degeneration:a review[J].Ann N Y Acad Sci,2017,1410(1):68-84.
[2] HOY D,BROOKS P,BLYTH F,et al.The epidemiology of low back pain[J].Best Pract Res Clin Rheumatol,2010,24(6):769-781.
[3] 张云辉,于栋,时宗庭,等.椎间盘退变程度与脊柱内镜手术治疗腰椎间盘突出症临床疗效的相关性研究[J].中国中医骨伤科杂志,2023,31(6):36-40.
[4] LIU W,JIN S,HUANG M,et al.Duhuo Jisheng decoction suppresses matrix degradation and apoptosis in human nucleus pulposus cells and ameliorates disc degeneration in a rat model[J].J Ethnopharmacol,2020,250:112494.
[5] 俞臻,诸磊,朱正桓,等.内质网应激在椎间盘退变过程中的作用[J].江苏医药,2022,48(10):1064-1069.
[6] 卢磊,刘晓丹,张培影.中药血清药理学及血清药物化学研究进展[J].中国中医急症,2018,27(1):178-181.
[7] PFIRRMANN C W,METZDORF A,ZANETTI M,et al.Magnetic resonance classification of lumbar intervertebral disc degeneration[J].Spine(Phila Pa 1976),2001,26(17):1873-1878.
[8] LIVAK K J,SCHMITTGEN T D.Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCt method[J].Methods,2001,25(4):402-408.
[9] CHENG X,ZHANG L,ZHANG K,et al.Circular RNA VMA21 protects against intervertebral disc degeneration through targeting miR-200c and X linked inhibitor-of-apoptosis protein[J].Ann Rheum Dis,2018,77(5):770-779.
[10] HE R,WANG Z,CUI M,et al.HIF1A alleviates compression-induced apoptosis of nucleus pulposus derived stem cells via upregulating autophagy[J].Autophagy,2021,17(11):3338-3360.
[11] URRA H,DUFEY E,LISBONA F,et al.When ER stress reaches a dead end[J].Biochim Biophys Acta,2013,1833(12):3507-3517.
[12] 廖太阳,杨楠,张力,等.白杨素对离体培养致炎大鼠软骨细胞凋亡及内质网应激GRP78/PERK/CHOP通路的影响[J].中国病理生理杂志,2022,38(12):2197-2204.
[13] 常斌,马斌祥,关永林,等.独活寄生汤治疗腰椎间盘突出症的研究进展[J].中医药临床杂志,2022,34(10):1976-1979.
[14] 吴广文,褚剑锋,许惠凤,等.独活寄生汤的药理作用及其在治疗骨性关节炎中的应用[J].中医正骨,2012,24(1):37-39.
[15] 唐智强,韩雪花,李敏,等.独活寄生汤治疗骨科疾病的临床应用研究进展[J].现代医药卫生,2023,39(22):3903-3906.
[16] 翟天宇,张灿,赵琳.内质网应激的调节方式及其在脊髓损伤中的靶向作用[J].中国生物化学与分子生物学报,2023,39(11):1534-1542.
[17] WANG W,QING X,WANG B,et al.Tauroursodeoxycholic acid protects nucleus pulposus cells from compression-induced apoptosis and necroptosis via inhibiting endoplasmic reticulum stress[J].Evid Based Complement Alternat Med,2018:6719460.
[18] NOVAIS E J,CHOI H,MADHU V,et al.Hypoxia and hypoxia-inducible factor-1α regulate endoplasmic reticulum stress in nucleus pulposus cells:implications of endoplasmic reticulum stress for extracellular matrix secretion[J].Am J Pathol,2021,191(3):487-502.
[19] WEN T,XUE P,YING J,et al.The role of unfolded protein response in human intervertebral disc degeneration:perk and IRE1-α as two potential therapeutic targets[J].Oxid Med Cell Longev,2021:6492879.
[20] CHEN L,HUANG Q,BAI Q,et al.Chlamydia psittaci induces autophagy in human bronchial epithelial cells via PERK and IRE1α,but not ATF6 pathway[J].Infect Immun,2022,90(5):e0007922.

备注/Memo

备注/Memo:
基金项目:国家自然科学基金项目(82104899)
武汉市知识创新专项项目(2022020801020531)
武汉市卫计委项目(WX21M02,WZ21C04,WZ21C18)
通信作者 E-mail:fjboys80@qq.com(冯晶) 845030601@qq.com(刘伟)
更新日期/Last Update: 2024-04-15