[1]薛慧芝,曾家莹,陈晓聪 姚楠,等.参骨颗粒治疗绝经后骨质疏松的作用机制[J].中国中医骨伤科杂志,2026,34(03):16-22.[doi:10.20085/j.cnki.issn1005-0205.260303]
 XUE Huizhi,ZENG Jiaying,CHEN Xiaocong,et al.Exploring the Mechanism of Shengu Granules in Treating Postmenopausal Osteoporosis[J].Chinese Journal of Traditional Medical Traumatology & Orthopedics,2026,34(03):16-22.[doi:10.20085/j.cnki.issn1005-0205.260303]
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参骨颗粒治疗绝经后骨质疏松的作用机制()

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

卷:
第34卷
期数:
2026年03期
页码:
16-22
栏目:
基础研究
出版日期:
2026-03-15

文章信息/Info

Title:
Exploring the Mechanism of Shengu Granules in Treating Postmenopausal Osteoporosis
文章编号:
1005-0205(2026)03-0016-07
作者:
薛慧芝1曾家莹1陈晓聪1 姚楠23李伟举12陈慧龙1章雨童1吕朝晖2△
1广州中医药大学第五临床医学院(广州,510095); 2广东省第二中医院; 3广东省中医药研究开发重点实验室
Author(s):
XUE Huizhi1ZENG Jiaying1CHEN Xiaocong1YAO Nan23LI Weiju12CHEN Huilong1ZHANG Yutong1LÜ Zhaohui2△
1The Fifth Clinical College of Guangzhou University of Chinese Medicine,Guangzhou 510095,China; 2Guangdong Provincial Second Hospital of Traditional Chinese Medicine,Guangzhou 510095,China; 3Guangdong Provincial Key Laboratory of Research and Development in Traditional Chinese Medicine,Guangzhou 510095,China.
关键词:
参骨颗粒 肠-骨轴 绝经后骨质疏松症 肠道菌群 炎症因子
Keywords:
Shengu granules gut-bone axis postmenopausal osteoporosis intestinal microbiota inflammatory factors
分类号:
R285.5
DOI:
10.20085/j.cnki.issn1005-0205.260303
文献标志码:
A
摘要:
目的:探讨参骨颗粒对去卵巢大鼠肠道菌群和炎症因子的影响,阐述其治疗绝经后骨质疏松症的作用机制。方法:将36只雌性大鼠随机均分为假手术组、模型组和参骨颗粒组。参骨颗粒溶液灌胃12周后,Micro-CT测量分析右侧股骨远端骨密度和骨微结构; ELISA法检测血清中骨转换标志物Ⅰ型胶原氨基端前肽(PINP)、β-胶原特殊序列(β-CTX)及炎症因子白细胞介素-10(IL-10)、白细胞介素-17(IL-17)、转化生长因子-β(TGF-β)、肿瘤坏死因子-α(TNF-α); Western Blot法检测胫骨组织中破骨细胞抑制因子和核因子κB受体活化因子配体(RANKL)的蛋白表达水平; 16S rRNA扩增及测序法检测肠道菌群。结果:与假手术组相比,参骨颗粒组大鼠的骨密度及BV/TV水平降低,Tb.Sp升高,结合骨微观结构,说明卵巢切除后大鼠骨结构呈骨质疏松样变。与模型组相比,参骨颗粒组大鼠PINP、IL-10、TGF-β及骨保护素(OPG)蛋白表达水平升高,β-CTX、IL-17、TNF-α及RANKL蛋白表达水平降低,差异均有统计学意义(P<0.05),说明参骨颗粒治疗可减少骨丢失,改善骨微结构。与模型组相比,参骨颗粒组大鼠肠道菌群的群落多样性提高、群落组成改善,差异有统计学意义(P<0.05),说明参骨颗粒可以减轻骨质疏松引起的肠道菌群失调。结论:参骨颗粒能够改善绝经后骨质疏松,其机制可能与肠道菌群和炎症因子介导的RANKL/OPG通路有关。
Abstract:
Objective:The effect of Shengu granules on intestinal microflora and inflammatory factors in ovariectomized rats was studied based on the gut-bone axis to reveal its mechanism in treating postmenopausal osteoporosis.Methods:Thirty-six female rats were randomly divided into three groups:Sham group,model group,and Shengu granules-treated group.After 12 weeks of oral gavage with Shengu granule solution,bone mineral density(BMD)and bone micros- tructures were measured by Micro-CT,and bone turnover markers(PINP,β-CTX)and inflammatory cytokines(IL-10,IL-17,TGF-β,TNF-α)were detected by ELISA.The protein expression levels of osteoprotegerin(OPG)and receptor activator of NF-κB ligand(RANKL)were detected by Western Blot,and the intestinal microbiota was analyzed by 16S rRNA amplification and sequencing.Results:Compared with the Sham group,the Shengu granules-treated group exhibited decreased BMD and BV/TV levels and increased Tb.Sp; combined with bone microstructure analysis,these findings indicate that ovariectomized rats developed osteoporotic-like bone changes.Compared with the model group,the Shengu granules-treated group showed significantly higher protein expression levels of PINP,IL-10,TGF-β,and OPG,as well as significantly lower expression levels of β-CTX,IL-17,TNF-α,and RANKL.All these differences were statistically significant(P<0.05),indicating that Shengu granules treatment reduces bone loss and improves bone microstructure in the Shengu granules-treated group.Furthermore,compared with the model group,the Shengu granules-treated group demonstrated increased gut microbiota community diversity and improved community composition(P<0.05),suggesting that Shengu granules can alleviate gut microbiota dysbiosis associated with osteoporosis.Conclusion:Shengu granules can improve postmenopausal osteoporosis,and the underlying mechanism may be related to the RANKL/OPG pathway mediated by gut microbiota and inflammatory factors.

参考文献/References:

[1] The North American Menopause Society.Management of osteoporosis in postmenopausal women:the 2021 position statement of The North American Menopause Society[J].Menopause,2021,28(9):973-997.
[2] 郑修竹,朱春雨,梁彦博,等.冬凌草甲素对绝经后骨质疏松小鼠肠道菌群的影响[J].中国骨质疏松杂志,2025,31(6):799-805.
[3] 陈晓聪,吕朝晖,曾家莹,等.参骨方对脾虚湿困型老年骨质疏松性骨折患者术后疗效影响研究[J].广州中医药大学学报,2024,41(2):348-353.
[4] 段小云,仲瑞雪,吴传红,等.基于数据挖掘和网络药理学探讨中医药治疗骨质疏松症的用药规律及机制[J].中国医院用药评价与分析,2023,23(2):162-168.
[5] 徐叔云.药理实验方法学[M].3版.北京:人民卫生出版社,2002:202-204.
[6] RAVESCHOT C,COUTTE F,FRÉMONT M,et al.Probiotic Lactobacillus strains from Mongolia improve calcium transport and uptake by intestinal cells in vitro[J].Food Research International,2020,133:109201.
[7] LI W,ZHANG L,XU Q B,et al.Taxifolin alleviates DSS-induced ulcerative colitis by acting on gut microbiome to produce butyric acid[J].Nutrients,2022,14(5):1069.
[8] MALESZA I J,MALESZA M,WALKOWIAK J,et al.High-fat,western-style diet,systemic inflammation,and gut microbiota:a narrative review[J].Cells,2021,10(11):3164.
[9] DENG L,YANG Y,XU G S.Empagliflozin ameliorates type 2 diabetes mellitus-related diabetic nephropathy via altering the gut microbiota[J].Biochimica et Biophysica Acta(BBA)-Molecular and Cell Biology of Lipids,2022,1867(12):159234.
[10] 曹盼举,张晓刚,王志鹏,等.中医古籍对骨质疏松症病因病机及治则的认识探析[J].中医药信息,2018,35(5):31-34.
[11] 安国俊,张起.中医药治疗骨质疏松症研究进展[J].光明中医,2023,38(18):3662-3666.
[12] 盛彤,谢培凤,王新祥,等.骨质疏松症中医脾虚病机认识的现代医学基础[J].中国骨质疏松杂志,2013,19(5):509-513.
[13] DE VOS W M,TILG H,VAN HUL M,et al.Gut microbiome and health:mechanistic insights[J].Gut,2022,71(5):1020-1032.
[14] FISCHER V,HAFFNER-LUNTZER M.Interaction between bone and immune cells:implications for postmenopausal osteoporosis[J].Seminars in Cell & Developmental Biology,2022,123:14-21.
[15] WU D,CLINE-SMITH A,SHASHKOVA E,et al.T-cell mediated inflammation in postmenopausal osteoporosis[J].Frontiers in Immunology,2021,12:687551.
[16] CLINE-SMITH A,AXELBAUM A,SHASHKOVA E,et al.Ovariectomy activates chronic low-grade inflammation mediated by memory T cells,which promotes osteoporosis in mice[J].Journal of Bone and Mineral Research,2020,35(6):1174-1187.
[17] ZHANG Z D,ZHANG X Z,ZHAO D W,et al.TGF-β1 promotes the osteoinduction of human osteoblasts via the PI3K/AKT/mTOR/S6K1 signalling pathway[J].Molecular Medicine Reports,2019,19(5):3505-3518.
[18] TAKAYANAGI H.RANKL as the master regulator of osteoclast differentiation[J].Journal of Bone and Mineral Metabolism,2021,39(1):13-18.
[19] UDAGAWA N,KOIDE M,NAKAMURA M,et al.Osteoclast differentiation by RANKL and OPG signaling pathways[J].Journal of Bone and Mineral Metabolism,2021,39(1):19-26.
[20] ONO T,HAYASHI M,SASAKI F,et al.RANKL biology:bone metabolism,the immune system,and beyond[J].Inflammation and Regeneration,2020,40(1):2.
[21] JANN J,GASCON S,ROUX S,et al.Influence of the TGF-β superfamily on osteoclasts/osteoblasts balance in physiological and pathological bone conditions[J].International Journal of Molecular Sciences,2020,21(20):7597.
[22] LI S H,HE Y C,ZHANG H O,et al.Formulation of traditional Chinese medicine and its application on intestinal flora of constipated rats[J].Microbial Cell Factories,2020,19(1):212.
[23] CHENG M,TAN B,WU X J,et al.Gut microbiota is involved in alcohol-induced osteoporosis in young and old rats through immune regulation[J].Frontiers in Cellular and Infection Microbiology,2021,11:636231.
[24] MCCABE L R,PARAMESWARAN N.Advances in probiotic regulation of bone and mineral metabolism[J].Calcified Tissue International,2018,102(4):480-488.
[25] 王欣,朱敏,董思晶,等.芍药苷对结肠炎小鼠肠道菌群及胆汁酸代谢的调节作用[J].药学学报,2021,56(7):1811-1819.
[26] MUKHERJEE A,LORDAN C,ROSS R P,et al.Gut microbes from the phylogenetically diverse genus Eubacterium and their various contributions to gut health[J].Gut Microbes,2020,12(1):1802866.
(收稿日期:2025-08-06)

备注/Memo

备注/Memo:
基金项目:广东省基础与应用基础研究基金项目(2025A1515010409)
广东省中医药局科研项目(20251020)
广东省第二中医院科研创新基金项目(SEZYY2023A08)
通信作者 E-mail:zhaohuilv@163.com
更新日期/Last Update: 2026-03-15