Promethazine Downregulates Wnt/β-Catenin Signaling and Increases the Biomechanical Forces of the Injured Achilles Tendon in the Early Stage of Healing

医学 Wnt信号通路 肌腱 跟腱 WNT3A型 伤口愈合 解剖 外科 信号转导 细胞生物学 生物
作者
Takahiro Sakaguchi,Bisei Ohkawara,Yasuzumi Kishimoto,Kentaro Miyamoto,Shinya Ishizuka,Hideki Hiraiwa,Naoki Ishiguro,Shiro Imagama,Kinji Ohno
出处
期刊:American Journal of Sports Medicine [SAGE]
卷期号:50 (5): 1317-1327 被引量:3
标识
DOI:10.1177/03635465221077116
摘要

Wnt/β-catenin signaling suppresses the differentiation of cultured tenocytes, but its roles in tendon repair remain mostly elusive. No chemical compounds are currently available to treat tendon injury.We hypothesized that the inhibition of Wnt/β-catenin signaling would accelerate tendon healing.Controlled laboratory study.Tendon-derived cells (TDCs) were isolated from rat Achilles tendons. The right Achilles tendon was injured via a dermal punch, while the left tendon was sham operated. A Wnt/β-catenin inhibitor, IWR-1, and an antihistamine agent, promethazine (PH), were locally and intramuscularly injected, respectively, for 2 weeks after surgery. The healing tendons were histologically and biomechanically evaluated.The amount of β-catenin protein was increased in the injured tendons from postoperative weeks 0.5 to 2. Inhibition of Wnt/β-catenin signaling by IWR-1 in healing tendons improved the histological abnormalities and decreased β-catenin, but it compromised the biomechanical properties. As we previously reported that antihistamine agents suppressed Wnt/β-catenin signaling in human chondrosarcoma cells, we examined the effects of antihistamines on TDCs. We found that a first-generation antihistamine agent, PH, increased the expression of the tendon marker genes Mkx and Tnmd in TDCs. Intramuscular injection of PH did not improve histological abnormalities, but it decreased β-catenin in healing tendons and increased the peak force and stiffness of the healing tendons on postoperative week 2. On postoperative week 8, however, the biomechanical properties of vehicle-treated tendons became similar to those of PH-treated tendons.IWR-1 and PH suppressed Wnt/β-catenin signaling and improved the histological abnormalities of healing tendons. IWR-1, however, compromised the biomechanical properties of healing tendons, whereas PH improved them.PH is a candidate repositioned drug that potentially accelerates tendon repair.
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