The effect and mechanism of naringin on callus angiogenesis of ovariectomized rats' fractures
10.3760/cma.j.issn.0253-2352.2016.03.008
- VernacularTitle:柚皮苷对去势大鼠骨折骨痂血管发生的影响及其机制
- Author:
Zhihu ZHAO
;
Xinmin MENG
;
Xiaolei SUN
;
Jianxiong MA
;
Fengbo LI
;
Yanjun LI
;
Jianwei LYU
;
Xinlong MA
- Publication Type:Journal Article
- Keywords:
Drynaria fortunei;
Fracture healing;
Neovascularization,physiologic;
Rats;
Ovariectomy
- From:
Chinese Journal of Orthopaedics
2016;(3):177-183
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the angiogenesis&neovascularization effects of naringin treatment in ovariectomized rats’fracture healing. Methods Upper 1/3 transverse tibial fracture model 4 weeks later after ovariectomized were estimated and randomly divided into the naringin group and control group. Microfil perfusion technique was used to analysis the angiogene?sis situation at two weeks after bone fracture. HE staining was used to evaluate the level of angiogenesis&neovascularization of tis?sue from histological point of view. The relative expression of VEGF in the callus was identified by real?time polymerase chain re?action. Immunohistochemical technique was used to observe the vessel endothelial growth factor?2 in the callus of the two groups. Maximum fracture load was tested by three?point bend test. Results The vascular volume and vascular density were more in nar?ingin group than control group. The HE staining of the 2 week group slices shows that the VA, VN2 of the unit of high magnifica?tion vision of the naringin group was significantly larger compared to the control group. Real?time PCR revealed that the compara?tive expression of VEGF is more in naringin group than in control group; the positive number of VEGFR?2 is more in naringin group than in control group. Naringin can promote the maximum load of the callus. Conclusion Naringin can promote ovariecto?mized rats’angiogenesis&neovascularization in the early process of fracture healing. It may be act on the signaling pathway of VEGF/VEGFR?2.
