补肾强毒方对DBA/1小鼠组织形态学及Wnt通路的影响

中国中西医结合杂志 Pub Date : 2017-01-01
Wen-Xue Yang, Xiao-Ping Yan, Yue Jin, Tong-Liang Zhou, Lan Zhang, Qing-Wen Tao, Wei-Ping Kong
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Celecoxib Capsule (0. 2 mL/0. 8 mg for each mouse, once per day) was administered to mice in the positive drug group by gastrogavage. Equal volume of normal saline was administered to mice in the model group and the blank control group by gastrogavage. All mice were fed and intragastically adminis- tered for 12 successive weeks. Body weight, diet, stools, and hair were routinely observed. Signs of ar- thritis were evaluated once per two weeks. Mice were sacrifice, and then general observation of achilles tendon was performed. The achilles tendon tissue was HE stained. Protein expressions of alkaline phos- phatase (ALP) , bone gamma-carboxyglutamic-acid-containing proteins (BGP) , Dickkopfl (DKK1) , and Wnt5a in the achilles tendon were detected using immunohistochemical method. Results Compared with the blank control group, the scoring of arthritis obviously increased in the model group (P <0. 05). 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引用次数: 0

摘要

目的观察补肾强都方(BQR)对自发性强直性脊柱炎(AS)小鼠关节韧带骨化组织形态学的影响,探讨其防治AS的机制。方法将30只12周龄雄性DBA/1小鼠随机分为模型组、阳性给药组和BQR低、中、高剂量组,每组6只。另取6只同龄C57BLE小鼠作为空白对照组。BQR包含11。25日,22。BQR低、中、高剂量组小鼠分别灌胃50、45.00 g/kg生药;每只小鼠2毫升,每天1次。塞来昔布胶囊(0。2 mL / 0。阳性给药组小鼠灌胃,每只小鼠8 mg,每天1次。模型组和空白对照组小鼠分别灌胃等量生理盐水。所有小鼠均连续喂养和灌胃12周。常规观察体重、饮食、大便和毛发。每两周评估一次关节炎的症状。处死小鼠,进行跟腱一般观察。跟腱组织HE染色。免疫组化法检测跟腱组织碱性磷相酶(ALP)、骨γ -羧谷氨酸含蛋白(BGP)、Dickkopfl (DKK1)、Wnt5a蛋白的表达。结果与空白对照组比较,模型组大鼠关节炎评分明显升高(P
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Effect of Bushen Qiangdu Recipe on Histomorphology and Wnt Pathway of DBA/1 Mice].

Objective To observe the effect of Bushen Qiangdu Recipe (BQR) on the entheses ossification histomorphology of articular ligament of DBA/1 mice with spontaneous ankylosing spondylitis (AS) , and to study its mechanism for prevention and treatment of AS. Methods Thirty 12-week old male DBA/1 mice were randomly divided into the model group, the positive drug group, low, medium, high dose BQR groups, 6 in each group. Another 6 C57BLE mice of the same age were recruited as a blank control group. BQR containing 11. 25, 22. 50, 45.00 g/kg crude drugs was respectively adminis- tered to mice in low, medium, high dose BQR groups by gastrogavage, 0. 2 mL for each mouse, once per day. Celecoxib Capsule (0. 2 mL/0. 8 mg for each mouse, once per day) was administered to mice in the positive drug group by gastrogavage. Equal volume of normal saline was administered to mice in the model group and the blank control group by gastrogavage. All mice were fed and intragastically adminis- tered for 12 successive weeks. Body weight, diet, stools, and hair were routinely observed. Signs of ar- thritis were evaluated once per two weeks. Mice were sacrifice, and then general observation of achilles tendon was performed. The achilles tendon tissue was HE stained. Protein expressions of alkaline phos- phatase (ALP) , bone gamma-carboxyglutamic-acid-containing proteins (BGP) , Dickkopfl (DKK1) , and Wnt5a in the achilles tendon were detected using immunohistochemical method. Results Compared with the blank control group, the scoring of arthritis obviously increased in the model group (P <0. 05). But the scoring of arthritis was obviously lower in the 3 BQR groups and the positive drug group than in the model group (P <0. 05). Histopathological results of achilles tendon tissue showed that no infiltration of inflammatory cells or fibroblasts occurred in the normal group. Their histomorphological structures were normal. Cartilage formation and bone formation at various degrees occurred in the model group. Filtration of fibroblast-like cells occurred in inflammatory cells and attachment points. Scattered lymphocyte infiltra- tion was often seen in the achilles tendon tissue of each medicated group. Cartilage formation and bone formation were rarely seen. Compared with the blank control group, the scoring of arthritis increased in the model group (P <0. 05). Compared with the model group, the scoring of arthritis was decreased in the 3 BQR groups and the positive drug group (P <0. 05). Compared with the blank control group, protein expression of DKK1 decreased and protein expression of Wnt5a increased in the model group (P <0. 05). Compared with the model group, protein expression of DKK1 increased and protein expression of Wnt5a decreased in middle and high dose BQR groups (P <0. 05). Conclusion BQR could delay the occur- rence and development of arthritis and ossification in DBA/1 mice of spontaneous AS model possibly by inhibiting classical Wnt pathway.

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