[1]徐西林 赵军 杨福彪 于长岁 张晓峰△ 申意伟 吕航.活骨灌注液不同给药途径对激素性股骨头坏死相关炎性因子表达的影响[J].中国中医骨伤科杂志,2019,27(10):10-13.
 XU Xilin ZHAO Jun YANG Fubiao YU Changsui ZHANG Xiaofeng SHEN Yiwei LYU Hang.Effects of Different Routes of Administration on the Expression of Steroid-induced Osteonecrosis of the Femoral Head-associated Inflammatory Factors by Huogu Perfusion Fluid[J].Chinese Journal of Traditional Medical Traumatology & Orthopedics,2019,27(10):10-13.
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活骨灌注液不同给药途径对激素性股骨头坏死相关炎性因子表达的影响()
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《中国中医骨伤科杂志》[ISSN:1005-0205/CN:42-1340/R]

卷:
第27卷
期数:
2019年10期
页码:
10-13
栏目:
实验研究
出版日期:
2019-10-10

文章信息/Info

Title:
Effects of Different Routes of Administration on the Expression of Steroid-induced Osteonecrosis of the Femoral Head-associated Inflammatory Factors by Huogu Perfusion Fluid
文章编号:
1005-0205(2019)10-0010-04
作者:
徐西林1 赵军1 杨福彪1 于长岁1 张晓峰1△ 申意伟1 吕航1
1黑龙江中医药大学附属第二医院(哈尔滨,150001)
Author(s):
XU Xilin1 ZHAO Jun1 YANG Fubiao1 YU Changsui1 ZHANG Xiaofeng1△ SHEN Yiwei1 LYU Hang1
1The Second Affiliated Hospital of Heilongjiang University of Traditional Chinese Medicine,Harbin 150001,China.
关键词:
活骨灌注液 激素性股骨头坏死 补肾活血法 给药途径
Keywords:
Huogu perfusion solution steroid-induced osteonecrosis of the femoral head tonifying kidney and activating blood circulation method administration route
分类号:
R-33
文献标志码:
A
摘要:
目的:观察活骨灌注液不同给药途径对兔激素性股骨头坏死(SONFH)的治疗作用,为临床治疗股骨坏死提供新的治疗方案。方法:雄性新西兰大白兔随机分为空白组(15 只)和造模组(60 只)。造模组行兔股骨头坏死动物造模后(采用 Matsui造模方法,末次腹腔注射用甲泼尼龙琥珀酸钠4周后开始治疗)再随机分为 4组:耳缘静脉组(E)、灌胃组(W)、外敷组(F)、模型组(M)各15只。空白组(K)正常饲养,不给予任何药物治疗。耳缘静脉组给予活骨灌注液10 mg/kg,1周2次; 灌胃组给予活骨灌注液 7.8 mg/kg,每日 1 次; 外敷组给予双后肢上部内侧外敷透皮贴剂,每次7.5 g/贴,每3日1次。治疗12周后,采用苏木精-伊红染色观察股骨头病理学变化及MRI检查证明造模成功,采用ELISA法检测血清IL-1β,IL-6及IL-8水平。 结果:ELISA 法检测结果:模型组中的IL-1β,IL-6及IL-8 含量测定相对正常组有明显增高,差异有统计学意义(P<0.01); 与模型组相比,不同给药途径中,IL-1β,IL-6及IL-8蛋白含量均有不同程度的降低,差异有统计学意义(P<0.01)。 苏木精-伊红染色观察显示:模型组股骨头软骨膜脱失,骨髓腔内脂肪细胞明显增多,关节腔内水肿,骨内压增高。活骨灌注液组方的不同给药途径均可以不同程度改变股骨头的病理变化,包括软骨层增生、骨小梁结构规整、软骨陷窝数量减少、骨髓腔内脂肪细胞明显减少、水肿及骨内压明显减轻。结论:活骨灌注液不同给药途径均能够对SONFH的病理变化起到治疗作用,活骨灌注液耳缘静脉给药方法对兔SONFH的治疗作用效果显著。
Abstract:
Objective:To observe the therapeutic effect of four different administration routes of living bone perfusion solution on steroid-induced necrosis of femoral head(SONFH)in rabbits,and to provide a new therapeutic scheme for clinical treatment of femoral necrosis.Methods:Male New Zealand white rabbits were randomly divided into two groups:blank group(n=15)and model group(n=60).The rabbits in the model group were randomly divided into 5 groups:auricular vein group(E),gastric perfusion group(W),external application group(F)and model group(M)with 15 animals each.The model of steroid-induced osteonecrosis of femoral head was established by Matsui,and the treatment began 4 weeks after the last intraperitoneal injection of methylprednisolone succinate sodium.The blank group(K)was raised normally and no drug treatment was given.The auricular vein was given live bone perfusion solution 10 mg/kg,twice a week,gastric perfusion group was given live bone perfusion fluid 7.8 mg/kg,once a day.The external application group was given transdermal patch on the upper and medial side of the upper hindlimb,Every 7.5 g/post,once every 3 d.After 12 weeks of treatment,the pathological and imaging changes of femoral head were observed by HE staining and electron microscope.The levels of serum IL-1 β,IL-6,IL-8 were detected by ELISA.Results:The contents of IL-1β,IL-6,IL-8,in the model group were significantly higher than those in the normal group(P<0.01),and those in the model group were significantly higher than those in the normal group(P<0.01).HE staining observation showed that in the model group,perichondrium of femoral head was lost,adipocytes in bone marrow cavity increased significantly,intra-articular edema and intra-osseous pressure increased.The pathological changes of femoral head could be changed by different administration routes of Huogu perfusion solution,including cartilage layer hyperplasia,regular trabecular structure,reduction of cartilage lacunae,decrease of adipocytes in bone marrow cavity,and decrease of edema and intraosseous pressure.Conclusion:The results showed that different routes of administration of bone-activating perfusate could treat the pathological changes of SONFH,and the therapeutic effect of auricular vein administration of bone-activating perfusate on SONFH in rabbits was significant.

参考文献/References:

[1] KURODA Y,MATSUDA S AND AKIYAMA H.Joint-preserving regenerative therapy for patients with early-stage osteonecrosis of the femoral head[J].Inflamm Regen,2016,36:4. [2] LI J K,CHENG L,ZHAO Y P,et al.ADAMTS-7 exhibits elevated expression in cartilage of osteonecrosis of femoral head and has a positive correlation with TNF-alpha and NF-kappa B P65[J].Mediators Inflamm,2015:196702. [3] 刘泽霖,徐西林,张晓峰.活骨注射液治疗股骨头缺血性坏死组织形态学实验研究[J].中医药学报,2013,41(2):30-32. [4] 张翔,董晓俊,吴泱,等.早期激素性股骨头缺血性坏死动物模型的建立研究[J].中国中医骨伤科杂志,2018,26(2):67-71. [5] ZHAO D,WANG B,GUO L,et al.Will a vascularized greater trochanter graft preserve the necrotic femoral head?[J].Clin Orthop Relat Res,2010,468(5):1316-1324. [6] SAMARA S,KOLLIA P,DAILIANA Z,et al.Predictive role of cytokine gene polymorphisms for the development of femoral head osteonecrosis[J].Dis Markers,2012,33(4):215-221. [7] CHEN B,LIU Y,CHENG L.IL-21 enhances the degradation of cartilage through the JAK-STAT signaling pathway during osteonecrosis of femoral head cartilage[J].Inflammation,2018,41(2):595-605. [8] TANG W,LU Y,TIAN Q Y,et al.The growth factor progranulin binds to tnf receptors and is therapeutic against inflammatory arthritis in mice[J].Science,2011,332(6028):478-484. [9] KNUDSEN J G,GUDIKSEN A,BERTHOLDT L,et al.Skeletal muscle IL-6 regulates muscle substrate utilization and adipose tissue metabolism during recovery from an acute bout of exercise[J].PLoS One,2017,12(12):e0189301. [10] CAREY A L,STEINBERG G R,MACAULAY S L,et al.Interleukin-6 increases insulin stimulated glucose disposal in humans and glucose uptake and fatty acid oxidation in vitro via AMP-activated protein kinase[J].Diabetes,2006,55(10):2688-2697. [11] WOLSK E,MYGIND H,GRONDAHL T S,et al.IL-6 selectively stimulates fat metabolism in human skeletal muscle[J].AJP-Endocrinology and Metabolism,2010,299(5):208-216. [12] WAN Z,RITCHIE I,BEAUDOIN M S,et al.IL-6 indirectly modulates the induction of glyceroneogenic enzymes in adipose tissue during exercise[J].PloS One,2012,7(7):e41719. [13] CARLOS ALFARO,MIGUEL F,SANMAMED,et al.Interleukin-8 in cancer pathogenesis,treatment and follow-up[J].Cancer Treat Rev,2017,60:24-31. [14] MARTIN D,GALISTEO R,GUTKIND J S.CXCL8/IL8 stimulates vascular endothelial growth factor(VEGF)expression and the autocrine activation of VEGFR2 in endothelial cells by activating NF-kappa B through the CBM(Carma3/Bcl10/Malt1)complex[J].J Biol Chem,2009,284(10):6038-6042. [15] PALOMO J,DIETRICH D,MARTIN P,et al.The interleukin(IL)-1 cytokine family-Balance between agonists and antagonists in inflammatory diseases[J].Cytokine,2015,76(1):25-37. [16] 张文进,张晓峰,孙志华,等.中西医结合治疗早期股骨头缺血性坏死的临床观察[J].中医药信息,2016,33(2):89-91.

备注/Memo

备注/Memo:
基金项目:哈尔滨市科学技术局创新人才项目(2017RAXXJ047)通信作者 E-mail:hlj542833@sina.com
更新日期/Last Update: 2019-10-10