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1.三峡大学基础医学院,湖北 宜昌;443002
2.三峡大学国家中医药管理局中药药理(肿瘤)科研三级实验室,湖北 宜昌 443002
Published:15 May 2023,
Received:28 October 2022,
Revised:23 February 2023,
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邓颖,金璨,段志豪等.资木瓜总苷对RA模型小鼠的骨保护作用及机制 Δ[J].中国药房,2023,34(09):1042-1047.
DENG Ying,JIN Can,DUAN Zhihao,et al.The osteoprotective effects and mechanisms of RA model mice by total saponins of Chaenomeles speciosa[J].ZHONGGUO YAOFANG,2023,34(09):1042-1047.
邓颖,金璨,段志豪等.资木瓜总苷对RA模型小鼠的骨保护作用及机制 Δ[J].中国药房,2023,34(09):1042-1047. DOI: 10.6039/j.issn.1001-0408.2023.09.04.
DENG Ying,JIN Can,DUAN Zhihao,et al.The osteoprotective effects and mechanisms of RA model mice by total saponins of Chaenomeles speciosa[J].ZHONGGUO YAOFANG,2023,34(09):1042-1047. DOI: 10.6039/j.issn.1001-0408.2023.09.04.
目的
2
研究资木瓜总苷对类风湿关节炎(RA)模型小鼠的骨保护作用及可能机制,为进一步将其开发为抗RA药物提供参考。
方法
2
将70只雄性DBA/1小鼠按随机数字表法分为正常组、模型组、资木瓜总苷低剂量组(60 mg/kg)、资木瓜总苷高剂量组(240 mg/kg)和雷公藤多苷片组(阳性对照,30 mg/kg),每组14只。除正常组外,其余各组小鼠均采用葡萄糖-6-磷酸异构酶混合多肽诱导制备RA小鼠模型。观察并记录各组小鼠的体质量、后足趾厚度、关节炎评分;采用苏木精-伊红染色法、抗酒石酸酸性磷酸酶染色法及番红固绿染色法观察小鼠踝关节组织的滑膜炎症及骨、软骨破坏情况;采用酶联免疫吸附测定法检测小鼠血清中白细胞介素6(IL-6)和踝关节组织中肿瘤坏死因子α(TNF-α)、IL-4、IL-10的含量;采用Western blot法检测小鼠踝关节组织中核因子κB受体活化因子配体(RANKL)、核因子κB受体活化因子(RANK)、骨保护素(OPG)、肿瘤坏死因子受体相关蛋白6(TRAF6)、活化T细胞核因子1(NFATC1)的蛋白表达水平。
结果
2
在给药结束时,与正常组比较,模型组小鼠的体质量显著降低(
P
<0.05),关节炎评分和左、右后足趾厚度均显著增加(
P
<0.05);踝关节组织出现明显滑膜增生和炎症细胞浸润,破骨细胞数目明显增多,软骨组织破坏明显;血清中IL-6含量及踝关节组织中TNF-α含量和RANKL、RANK、TRAF6、NFATC1蛋白表达水平均显著升高(
P
<0.05),而踝关节组织中IL-4、IL-10含量和OPG蛋白表达水平均显著降低(
P
<0.05)。与模型组比较,各给药组小鼠的上述病理形态学变化和指标含量/水平均得到显著改善(
P
<0.05)。
结论
2
资木瓜总苷对RA模型小鼠具有一定的骨保护作用;其机制可能与降低IL-6、TNF-α含量,升高IL-4、IL-10含量,抑制RANKL/RANK/OPG信号通路活化,从而抑制破骨细胞增殖和促进软骨及骨组织修复有关。
OBJECTIVE
2
To study the osteoprotective effects and possible mechanism of total saponins of
Chaenomeles speciosa
on rheumatoid arthritis (RA) model mice, and to provide reference for further development of anti-RA drugs.
METHODS
2
Seventy male DBA/1 mice were randomly divided into normal group, model group, low-dose and high-dose groups of
C. speciose
total saponins (60, 240 mg/kg),
Tripterygium wilfordii
polyglycoside tablets group (positive control, 30 mg/kg), with 14 mice in each group. In addition to the normal group, the other groups of mice were induced by glucose-6-phosphate isomerase mixed polypeptide to prepare RA model. The body weight, rear toes thickness and arthritis scores of each group were recorded; the synovial inflammation, bone and cartilage destruction of ankle joint tissues were observed by hematoxylin-eosin staining, tartrate-resistant acid phosphatase staining and safranin O-fast green staining; the contents of interleukin-6 (IL-6) in serum and tumor necrosis factor α (TNF-α), IL-4 and IL-10 in ankle joint tissues were detected by ELISA; the expression levels of receptor activator of nuclear factor-κB ligand (RANKL), receptor activator of nuclear factor-κB (RANK), osteoprotegerin (OPG), tumor necrosis factor receptor-associated protein 6 (TRAF6) and nuclear factor of activated T cells 1 (NFATC1) protein in ankle joint tissues were detected by Western blot assay.
RESULTS
2
At the end of administration, compared with normal group, the body mass of mice in the model group was significantly reduced (
P
<0.05), and the arthritis score and the thickness of the left and right rear toes were significantly increased (
P
<0.05); the ankle joint tissues of mice in the model group showed significant synovial proliferation and inflammatory infiltration, the number of osteoclasts increased significantly and significant destruction of cartilage tissue. The content of IL-6 in serum, the content of TNF-α, the protein expression levels of RANKL, RANK, TRAF6 and NFATC1 in the ankle joint tissues were increased significantly (
P
<0.05), while the contents of IL-4 and IL-10, the protein expression level of OPG in the ankle joint tissues were decreased significantly (
P
<0.05). Compared with model group, above pathomorphological changes and the content/level of indicators of mice in each administration group were significantly improved (
P
<0.05).
CONCLUSIONS
2
Total saponins of
C. speciosa
may exert osteoprotective effects on RA model mice, the mechanism of which may be associated with reducing the contents of IL-6 and TNF-α, increasing the contents of IL-4 and IL-10, inhibiting the activation of RANKL/RANK/OPG signal pathway, thus inhibiting the proliferation of osteoclasts and promoting the repair of cartilage and bone tissue.
资木瓜总苷类风湿关节炎核因子κB受体活化因子配体核因子κB受体活化因子骨保护素
rheumatoid arthritisreceptor activator of nuclear factor-κB ligandreceptor activator of nuclear factor-κBosteoprotegerin
WU C Y,YANG H Y,LUO S F,et al. From rheumatoid factor to anti-citrullinated protein antibodies and anti-carbamylated protein antibodies for diagnosis and prognosis prediction in patients with rheumatoid arthritis[J]. Int J Mol Sci,2021,22(2):686.
XIN P L,JIE L F,CHENG Q,et al. Pathogenesis and function of interleukin-35 in rheumatoid arthritis[J]. Front Pharmacol,2021,12:655114.
LI Y Q,YANG C,JIA K X,et al. Fengshi Qutong capsule ameliorates bone destruction of experimental rheumatoid arthritis by inhibiting osteoclastogenesis[J]. J Ethnopharmacol,2022,282:114602.
FRAENKEL L,BATHON J M,ENGLAND B R, et al. 2021 American college of rheumatology guideline for the treatment of rheumatoid arthritis[J]. Arthritis Care Res (Hoboken),2021,73(7) :924-939.
闫梦真,余婕,董甜甜,等. 由肠道菌群变化研究资木瓜总苷对K/B×N小鼠血清转移性关节炎的治疗作用[J].现代免疫学,2020,40(4):265-271.
陈桂婷,郑倩倩,余婕,等.资木瓜中莽草酸通过减少RBL-2H3细胞脱颗粒抑制大鼠软骨细胞分化[J]. 细胞与分子免疫学杂志,2020,36(10):890-896.
TAKAYANAGI H. RANKL as the master regulator of osteoclast differentiation[J]. J Bone Miner Metab,2021,39(1):13-18.
李丽. 血清及关节液ANGPTL4、IL-17及RANKL与类风湿关节炎活动度的关系分析[J]. 中国医学创新,2022,19(18):149-152.
BRUNS L,FREY O,MORAWIETZ L,et al. Immunization with an immunodominant self-peptide derived from glucose-6-phosphate isomerase induces arthritis in DBA/1 mice[J]. Arthritis Res Ther,2009,11(4):R117.
MENG M,CHEN S D,GAO X,et al. Adoptive immunotherapy of iNKT cells in glucose-6-phosphate isomerase (G6PI)-induced RA mice[J/OL]. J Vis Exp,2020,31(155)[2023-03-13]. https://pubmed.ncbi.nlm.nih.gov/32065164/.DOI:10.3791/60048https://pubmed.ncbi.nlm.nih.gov/32065164/.DOI:10.3791/60048.
张瑞.电针对CIA模型大鼠TNF-α、IL-1β和ICAM-1影响的实验研究[D].北京:北京中医药大学,2016.
周婷婷,陈先勇,陈桂婷,等.通过MC-Tryptase-PAR-2-FLS途径探讨资木瓜总苷对K/B×N小鼠血清转移性关节炎的治疗作用[J]. 中国免疫学杂志,2021,37(4):395-399,409.
冯群,孙蓉.雷公藤多苷片抗炎作用及伴随肝毒性研究[J].中药新药与临床药理,2014,25(6):713-716.
WANG Q,QIN X Y,FANG J Y,et al. Nanomedicines for the treatment of rheumatoid arthritis:state of art and potential therapeutic strategies[J]. Acta Pharm Sin B,2021,11(5):1158-1174.
马阮昕,詹晓婷,谢静文,等.木瓜水提液抗炎、镇痛及免疫调节作用的实验研究[J].中国中医药科技,2017,24(5):581-583.
ZHENG W H,MEI Y F,CHEN C H,et al. The effectiveness and safety of Tripterygium wilfordii glycosides combined with disease-modifying anti-rheumatic drugs in the treatment of rheumatoid arthritis:a systematic review and meta-analysis of 40 randomized controlled trials[J]. Phytother Res,2021,35(6) :2902-2924.
HUANG Z Y,LUO R,YANG L,et al. CPT1A-mediated fatty acid oxidation promotes precursor osteoclast fusion in rheumatoid arthritis[J]. Front Immunol,2022,13:838664.
AMARASEKARA D S,YUN H,KIM S,et al. Regulation of osteoclast differentiation by cytokine networks[J]. Immune Netw,2018,18(1):e8.
HONMA M,IKEBUCHI Y,SUZUKI H. Mechanisms of RANKL delivery to the osteoclast precursor cell surface[J]. J Bone Miner Metab,2021,39(1):27-33.
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