Shi Xiao-Lin, Liang Bo-Cheng, Wu Peng, Wang Bo, Shi Zhen-Yu, Kong Ling-Cheng, Yao Jian-Liang, Huang Jun-Jun, Li Chun-Wen
College of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou 310053, Zhejiang, China;
Zhongguo Gu Shang. 2017 Aug 25;30(8):743-750. doi: 10.3969/j.issn.1003-0034.2017.08.013.
To explore the effects and related mechanisms of total flavone of epimedium treatment(TFE)on primary callus for mation in ovariectomized rats.
Forty male SD rats weighted from 209 to 246 g and aged 6 to 8 weeks were selected. Six weeks after ovariectomy a femur fracture model with middiaphyseal segment fracture was established, estimated and randomly divided into TFE group (150 mg·kg⁻¹·d⁻¹) and control group(received saline). HE staining was used to evaluate the morphologic difference of primary callus during the bone callus healing between these two groups. The relative expression of Runt-related transcription factor 2(Runx2) mRNA in the callus was identified by real-time polymerase chain reaction. Immunohistochemical technique was used to observe the Casein kinase 2-interacting protein 1(CKIP-1) protein level in the callus of the two groups. Maximum fracture load was tested by three point bend test.
The BMD, primary callus volume, trabecular member(Tb.N) and trabecular thickness(Tb.Th) were higher in TFE group than that in control group(<0.001). The Tb.N and Tb.Th of primary callus were higher in TFE group than control group (=0.001). The volume and bone volume/tissue volume of primary callus were in TFE group than control group(<0.01). The trabecular separation(Tb.Sp) of primary callus were in control group higher than TFE group(<0.01). The HE staining of the 6 week slices showed that the degree of cartilage ossification in callus of the TFE group was significantly higher than that in control group under high magnification. Real-time PCR revealed that the comparative expression of Runx2 mRNA in control group was higher than that in TFE group(<0.001); the positive number of CKIP-1 was less in TFE group than that in control group (<0.001). TFE could increase the maximum load of the primary callus (<0.001).
TFE can promote the cartiage ossification of callus in ovariectomized rats, enhancing the bone strength and bone quality in the process of fracture healing via the CKIP-1/Runx2 pathway.
探讨淫羊藿总黄酮(TFE)对去卵巢大鼠骨折初期骨痂形成的影响及相关机制。
选取40只体重209~246 g、6~8周龄的雄性SD大鼠。去卵巢6周后建立股骨中段骨折模型,评估后随机分为TFE组(150 mg·kg⁻¹·d⁻¹)和对照组(给予生理盐水)。采用苏木精-伊红(HE)染色评价两组在骨痂愈合过程中初期骨痂的形态学差异。通过实时聚合酶链反应鉴定骨痂中Runt相关转录因子2(Runx2)mRNA的相对表达。采用免疫组织化学技术观察两组骨痂中酪蛋白激酶2相互作用蛋白1(CKIP-1)蛋白水平。通过三点弯曲试验检测最大骨折负荷。
TFE组的骨密度、初期骨痂体积、骨小梁数量(Tb.N)和骨小梁厚度(Tb.Th)均高于对照组(<0.001)。TFE组初期骨痂的Tb.N和Tb.Th高于对照组(=0.001)。TFE组初期骨痂的体积和骨体积/组织体积高于对照组(<0.01)。对照组初期骨痂的骨小梁间距(Tb.Sp)高于TFE组(<0.01)。6周切片的HE染色显示,高倍镜下TFE组骨痂软骨骨化程度明显高于对照组。实时聚合酶链反应显示,对照组Runx2 mRNA的相对表达高于TFE组(<0.001);TFE组CKIP-1阳性数少于对照组(<0.001)。TFE可增加初期骨痂的最大负荷(<0.001)。
TFE可促进去卵巢大鼠骨痂的软骨骨化,通过CKIP-1/Runx2途径增强骨折愈合过程中的骨强度和骨质量。