Osteopractic total flavone promoting rat extra-articular tendon-bone healing through mTOR pathway.
- Author:
Xin-Tao ZHANG
1
,
2
;
Hua-Ji JIANG
;
Zu-Ru LIANG
;
Fei-Lin HE
;
Xiao-Qing LIAO
;
Yu-Xiang REN
;
Wen-Tao ZHANG
Author Information
- Publication Type:Journal Article
- Keywords: Achilles tendon; Drynaria fortunei; Flavone; Rats
- MeSH: Animals; Biomechanical Phenomena; Bone Transplantation; Cell Differentiation; Cells, Cultured; Flavones; pharmacology; Male; Osteogenesis; Rats; Stem Cells; cytology; TOR Serine-Threonine Kinases; metabolism; Tendons; cytology; transplantation; Wound Healing
- From: China Journal of Orthopaedics and Traumatology 2018;31(3):248-253
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo explore function and related molecular mechanism of osteopractic total flavone (OTF) on tendon healing in rats.
METHODSTen male rats aged for 8 weeks were collected and weighted from 180 to 220 g. Tendon stem cells were cultivated, the third tendon stem cells were used for experiment. OTP treated with 0, 0.1, 1, 10 ng/ml were added into tendon stem cells, and expression change of ALP, Runx2, OCN, VEGF, P-S6, P-4E/BP1 were detected after 14 days. Forty male rats aged for 8 weeks (weighted 180 to 220 g) were established extra-articular tendon-bone transplanting healing model, and divided into experimental group and control group. Experimental group were treated with OTF(100 mg·kg⁻¹·d⁻¹), while control group was treated by normal saline with the same volume. Tendon-bone healing degree were detected by biomechanical testing at 3 and 6 weeks after surgery, histological detection were applied to detect tendon-bone healing and number of new vessles.
RESULTSAfter treated by OTP, ALP staining and active index detection showed there were statistical differences among 0, 0.1, 1, 10 ng/ml group. After 14 days' cultivation, western blotting results showed mTOR downstream marker protein P-S6 protein expression were gradually increased with increase of density of OTP, expression of P-4E/BP1 was reduced, while expression of Runx2, OCN, VEGF were increased. Biological detection results showed that there was no significant difference in mechanical strength between experimental group(0.78±0.05) N/mm and control group (0.51±0.02) N/mm at 3 weeks after surgery, while mechanical strength in experimental group (1.36±0.09) N/mm was higher than control group (1.01±0.08) N/mm at 6 weeks after surgery. Histological results showed maturity of tendon-bone surface cell were higher at 3 and 6 weeks in experimental group, sharpey fiber growth more density, calcification extent of mesenchyme was high, and new bone, vessels were increased.
CONCLUSIONSOTF could promote osteogenic differentiation of tendon stem cells through mTOR signaling in vitro, and stimulate tendon-bone healing in bone tunnel and enhance connection quality between tendon and bone.
