Intervention effects of medicated serum of Liuwei Dihuang Decoction on Runx2 and OPG/RANKL of oxidative damaged MC3T3⁃E1 cells induced by H<sub>2</sub>O<sub>2</sub> and investigating its mechanism

Lewei TAO; Xu HAN; Qingguang CHEN; Juanfei XU; Hao LU

doi:10.16305/j.1007-1334.2022.2111083

您当前的位置：

首页 >

文章列表页 >

Intervention effects of medicated serum of Liuwei Dihuang Decoction on Runx2 and OPG/RANKL of oxidative damaged MC3T3⁃E1 cells induced by H₂O₂ and investigating its mechanism

更新时间：2022-08-12

- Intervention effects of medicated serum of Liuwei Dihuang Decoction on Runx2 and OPG/RANKL of oxidative damaged MC3T3⁃E1 cells induced by H₂O₂ and investigating its mechanism
- Shanghai Journal of Traditional Chinese Medicine Vol. 56, Issue 8, Pages: 102-106(2022)
- 作者机构：
  
  1.上海中医药大学附属曙光医院内分泌科（上海 201203）
- 作者简介：
- 基金信息：
- DOI：10.16305/j.1007-1334.2022.2111083
  CLC：
扫描看全文
陶乐维,韩煦,陈清光等.六味地黄方含药血清对H₂O₂诱导的氧化损伤MC3T3⁃E1细胞Runx2、OPG/RANKL的干预作用及其机制探讨[J].上海中医药杂志,2022,56(08):102-106.

TAO Lewei,HAN Xu,CHEN Qingguang,et al.Intervention effects of medicated serum of Liuwei Dihuang Decoction on Runx2 and OPG/RANKL of oxidative damaged MC3T3⁃E1 cells induced by H₂O₂ and investigating its mechanism[J].Shanghai Journal of Traditional Chinese Medicine,2022,56(08):102-106.
陶乐维,韩煦,陈清光等.六味地黄方含药血清对H₂O₂诱导的氧化损伤MC3T3⁃E1细胞Runx2、OPG/RANKL的干预作用及其机制探讨[J].上海中医药杂志,2022,56(08):102-106. DOI： 10.16305/j.1007-1334.2022.2111083.

TAO Lewei,HAN Xu,CHEN Qingguang,et al.Intervention effects of medicated serum of Liuwei Dihuang Decoction on Runx2 and OPG/RANKL of oxidative damaged MC3T3⁃E1 cells induced by H₂O₂ and investigating its mechanism[J].Shanghai Journal of Traditional Chinese Medicine,2022,56(08):102-106. DOI： 10.16305/j.1007-1334.2022.2111083.

摘要

目的,2,观察六味地黄方含药血清对过氧化氢（H,2,O,2,）诱导的氧化损伤小鼠胚胎成骨细胞前体细胞（MC3T3-E1）Runt相关转录因子2（Runx2）及护骨素/核因子-κB受体活化因子配体（OPG/RANKL）的干预作用，并从抗氧化角度初步探讨其作用机制。,方法,2,制作六味地黄方汤剂，对成年Wistar大鼠进行灌胃，获取六味地黄方含药血清。除正常组外，其余各组先用1.0 mmol/L H,2,O,2, 预处理MC3T3-E1细胞6 h，随后模型组更换正常培养基，N-乙酰半胱氨酸（NAC）组更换含有2.5 mmol/L NAC的培养基，六味地黄方含药血清组更换含有10%药物血清的培养基，各组均处理24 h。采用DCFH-DA荧光探针检测MC3T3-E1细胞内活性氧（ROS）水平。根据试剂盒说明书检测过氧化氢酶（CAT）、超氧化物歧化酶（SOD）、谷胱甘肽过氧化物酶（GSH-PX）、还原型谷胱甘肽（GSH）。采用Western blot法检测Runx2、OPG、RANKL、肿瘤抑制蛋白P53及磷酸化状态的P53蛋白（p-P53）表达。,结果,2,与正常组比较，模型组ROS明显升高（,P,<,0.05），同时CAT、SOD、GSH-PX、GSH均明显降低（,P,<,0.05）；在蛋白表达方面，与正常组相比，模型组Runx2、OPG蛋白表达均明显降低（,P,<,0.05），RANKL蛋白表达明显升高（,P,<,0.05），同时p-P53/P53也有明显升高（,P,<,0.05）。与模型组相比，六味地黄方含药血清组GSH明显升高（,P,<,0.05），ROS水平明显下降（,P,<,0.05）。在蛋白表达方面，与模型组比较，六味地黄方含药血清组Runx2、OPG蛋白表达均明显升高（,P,<,0.05），RANKL蛋白表达明显降低（,P,<,0.05），同时p-P53/P53明显降低（,P,<,0.05）。,结论,2,六味地黄方含药血清能促进H,2,O,2,致氧化损伤MC3T3-E1细胞内Runx2蛋白表达，升高OPG蛋白表达，降低RANKL蛋白表达，这可能与其升高GSH的含量、抑制P53蛋白的磷酸化，进而降低细胞内ROS水平有关。

Abstract

Objective,2,To observe the intervention effects of medicated serum of Liuwei Dihuang Decoction on Runt-related transcription factor 2 （Runx2） and osteoprotegerin / nuclear factor-κB receptor activator ligand （OPG/RANKL） in preparietal osteoblasts （MC3T3-E1） of mice with oxidative injury induced by hydrogen peroxide （H,2,O,2,）， and to explore its mechanism from the point of view of antioxidation.,Methods,2,The Liuwei Dihuang Decoction was prepared and given to the adult Wistar rats by intragastric administration，and then the medicated serum of Liuwei Dihuang Decoction was collected. Except for the normal group， the other groups of MC3T3-E1 cells were first pretreated with 1.0 mmol/L H,2,O,2, for 6 h， and then the culture medium of the model group was replaced with normal culture medium， the N-acetylcysteine （NAC） group replaced with 2.5 mmol/L NAC and the medicated serum groups with 10% medicated serum. Each group was treated for 24 hours. The level of reactive oxygen species （ROS） in MC3T3-E1 cells was detected by DCFH-DA fluorescence probe. Catalase （CAT）， superoxide dismutase （SOD）， glutathione peroxidase （GSH-PX） and reduced glutathione （GSH） were detected according to the kit instructions. The expressions of Runx2， OPG， RANKL， tumor suppressor protein p53 and phosphorylated p53 protein （p-P53） were detected by Western blot.,Results,2,Compared with the normal group， ROS in the model group was significantly increased （,P,<,0.05）， while CAT， SOD， GSH-PX， and GSH were significantly decreased （all ,P,<,0.05）. In terms of protein expression， compared with the normal group， the protein expressions of Runx2 and OPG in the model group were significantly decreased （all ,P,<,0.05）， while the RANKL was significantly increased （,P,<,0.05）， and p-P53/P53 was also significantly increased （,P,<,0.05）. Compared with the model group， the GSH in the medicated serum group of Liuwei Dihuang Decoction was significantly increased （,P,<,0.05） and the level of ROS was significantly decreased （,P,<,0.05）. In terms of protein expression， compared with the model group， the protein expressions of Runx2 and OPG in the medicated serum group of Liuwei Dihuang Decoction were significantly increased （,P,<,0.05）， while the expression of RANKL was significantly decreased （,P,<,0.05）， and p-P53/P53 was also significantly decreased （,P,<,0.05）.,Conclusions,2,In H,2,O,2,-induced oxidatively damaged MC3T3-E1 cells， the medicated serum of Liuwei Dihuang Decoction could promote the protein expression of Runx2， and it could increase the protein expression of OPG and decrease the protein expression of RANKL. This may be related to the fact that it could increase the content of GSH， inhibit the phosphorylation of P53 protein， and reduce the level of ROS in MC3T3-E1 cells.

关键词

骨质疏松六味地黄方Runt相关转录因子2护骨素/核因子-κB受体活化因子配体成骨细胞中药研究

Keywords

osteoporosisLiuwei Dihuang DecoctionRunx2OPG/RANKLosteoblast cellstraditional Chinese herbal medicine research

references

陶乐维，韩煦，陈清光，等. 六味地黄汤含药血清对H2O2诱导的氧化损伤MC3T3-E1细胞的干预作用［J］. 上海中医药杂志，2022，56（6）：92-99.

FU C， XU D， WANG C Y， et al. Alpha-lipoic acid promotes osteoblastic formation in H2O2 -treated MC3T3-E1 cells and prevents bone loss in ovariectomized rats［J］. J Cell Physiol， 2015， 230（9）： 2184-2201.

KOMORI T. Molecular mechanism of Runx2-dependent bone development［J］. Mol Cells， 2020， 43（2）： 168-175.

CHEN X， WANG Z， DUAN N， et al. Osteoblast-osteoclast interactions［J］. Connect Tissue Res， 2018， 59（2）： 99-107.

QUARLES L D， YOHAY D A， LEVER L W， et al. Distinct proliferative and differentiated stages of murine MC3T3-E1 cells in culture： an in vitro model of osteoblast development［J］. J Bone Miner Res， 1992， 7（6）： 683-692.

HENDRICKX G， BOUDIN E， VAN HUL W. A look behind the scenes： the risk and pathogenesis of primary osteoporosis［J］. Nat Rev Rheumatol， 2015， 11（8）： 462-474.

MANOLAGAS S C. From estrogen-centric to aging and oxidative stress： a revised perspective of the pathogenesis of osteoporosis［J］. Endocr Rev， 2010， 31（3）： 266-300.

DOMAZETOVIC V， MARCUCCI G， IANTOMASI T， et al. Oxidative stress in bone remodeling： role of antioxidants［J］. Clin Cases Miner Bone Metab， 2017， 14（2）： 209-216.

梁华，王燕，朱明雪，等.金匮肾气丸及六味地黄丸对自然衰老小鼠血浆代谢物的影响［J］.中国中医药信息杂志，2020，27（6）：50-55.

刘继平. 六味地黄汤有效部位/成分防治糖尿病脑病作用及机制研究［D］. 南京：中国药科大学，2013.

李亚丽，楚伟，周利霞，等. 中药六味地黄汤对衰老大鼠卵巢组织抗氧化能力的研究［J］.河北医药，2012，34（24）：3703-3704.

QIN D， ZHANG H， ZHANG H， et al. Anti-osteoporosis effects of osteoking via reducing reactive oxygen species［J/OL］. J Ethnopharmacol， 2019［2021-11-10］. https：//www.sciencedirect.com/science/article/abs/pii/S0378874119305835？via%3Dihubhttps://www.sciencedirect.com/science/article/abs/pii/S0378874119305835?via%3Dihub.

LIU J， YANG J. Uncarboxylated osteocalcin inhibits high glucose-induced ROS production and stimulates osteoblastic differentiation by preventing the activation of PI3K/Akt in MC3T3-E1 cells［J］. Int J Mol Med， 2016， 37（1）： 173-181.

CAI W W， ZHANG M H， YU Y S， et al. Treatment with hydrogen molecule alleviates TNFα-induced cell injury in osteoblast［J］. Mol Cell Biochem， 2013， 373（1-2）： 1-9.

JING Z， WANG C， WEN S， et al. Phosphocreatine promotes osteoblastic activities in H2O2-Induced MC3T3-E1 cells by regulating SIRT1/FOXO1/PGC-1α signaling pathway［J］. Curr Pharm Biotechnol， 2021， 22（5）： 609-621.

VIGNERON A， VOUSDEN K H. p53， ROS and senescence in the control of aging［J］. Aging， 2010， 2（8）： 471-474.

DU Y， YOU L， NI B， et al. Phillyrin mitigates apoptosis and oxidative stress in hydrogen peroxide-treated RPE cells through activation of the Nrf2 signaling pathway［J/OL］. Oxid Med Cell Longev， 2020［2021-11-10］. https：//www.ncbi.nlm.nih.gov/pmc/articles/PMC7576358/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576358/.

LIU B， CHEN Y， ST CLAIR D K. ROS and p53： a versatile partnership［J］. Free Radic Biol Med， 2008， 44（8）： 1529-1535.

LIU H， LI B. p53 control of bone remodeling［J］. J Cell Biochem， 2010， 111（3）： 529-534.

ARTIGAS N， GÁMEZ B， CUBILLOS-ROJAS M， et al. p53 inhibits SP7/Osterix activity in the transcriptional program of osteoblast differentiation［J］. Cell Death Differ， 2017， 24（12）： 2022-2031.

LENGNER C J， STEINMAN H A， GAGNON J， et al. Osteoblast differentiation and skeletal development are regulated by Mdm2-p53 signaling［J］. J Cell Biol， 2006， 172（6）： 909-921.

RACHED M T， KODE A， XU L， et al. FoxO1 is a positive regulator of bone formation by favoring protein synthesis and resistance to oxidative stress in osteoblasts［J］. Cell Metab， 2010， 11（2）： 147-160.

SASA K， YOSHIMURA K， YAMADA A， et al. Monocarboxylate transporter-1 promotes osteoblast differentiation via suppression of p53， a negative regulator of osteoblast differentiation［J］. Sci Rep， 2018， 8（1）： 10579.

NAKAMURA H， NAKAMURA K， YODOI J. Redox regulation of cellular activation［J］. Annu Rev Immunol， 1997， 15： 351-369.

NOGUEIRA V， PARK Y， CHEN C C， et al. Akt determines replicative senescence and oxidative or oncogenic premature senescence and sensitizes cells to oxidative apoptosis［J］. Cancer Cell， 2008， 14（6）： 458-470.

Views

325

下载量

CSCD

CNKI被引量

Alert me when the article has been cited

提交

Tools

Publicity Resources

Intervention effect of Liuwei Dihuang Decoction on ovariectomized rats and H₂O₂⁃induced oxidative damaged MC3T3⁃E1 cells based on antioxidant effect of FOXO1

Intervention effect of medicated serum of Liuwei Dihuang Decoction on oxidative damaged MC3T3⁃E1 cells induced by H₂O₂

Effects of Xinqian Ganjie Decoction on lncRNA SNHG16， EGFR and MUC5AC mRNA expression in chronic rhinosinusitis mice

Mechanism of Yucan Granules improving podocyte damage and treating diabetic nephropathy

Mechanism of Huangqi Decoction against liver fibrosis by network pharmacological analysis combined with related cell experiment

Related Author

No data

Related Institution

Department of Otolaryngology， Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine

Department of Vascular Surgery， Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine

Department of Nephrology， Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine

Institute of Interdisciplinary Integrative Medicine Research， Shanghai University of Traditional Chinese Medicine

School of Traditional Chinese Medicine， Shanghai University of Traditional Chinese Medicine

⁰

Intervention effects of medicated serum of Liuwei Dihuang Decoction on Runx2 and OPG/RANKL of oxidative damaged MC3T3⁃E1 cells induced by H2O2 and investigating its mechanism

DOI：10.16305/j.1007-1334.2022.2111083

摘要

Abstract

关键词

Keywords

references

Intervention effects of medicated serum of Liuwei Dihuang Decoction on Runx2 and OPG/RANKL of oxidative damaged MC3T3⁃E1 cells induced by H₂O₂ and investigating its mechanism