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离子导入脂质体雷奈酸锶联合低强度脉冲超声对大鼠创伤后骨关节炎的改善作用

Amelioration of Post-traumatic Osteoarthritis by Iontophoretic Liposomal Strontium Ranelate Collaborated with Low-Intensity Pulsed Ultrasound in Rats.

作者信息

Chen Chung-Hwan, Lin Syu-Lun, Kuo Shyh Ming, Lai Jyh-Mirn, Shih Wen-Ling, Shen Po-Chih, Kuo Yi-Wen, Huang Han Hsiang

机构信息

Orthopedic Research Center, Kaohsiung Medical University, Kaohsiung City 80708, Taiwan.

Regenerative Medicine and Cell Therapy Research Center, Kaohsiung Medical University, Kaohsiung City 80708, Taiwan.

出版信息

Int J Mol Sci. 2025 Sep 10;26(18):8815. doi: 10.3390/ijms26188815.

Abstract

Osteoarthritis (OA), the most common form of arthritis, affects the whole synovial joint. Post-traumatic osteoarthritis (PTOA) is an important subtype of OA which develops after joint injury. The anti-PTOA effects of iontophoretic liposome-encapsulated strontium ranelate (L-SR) combined with low-intensity pulsed ultrasound (LIPUS) were examined by a culture of human OA chondrocytes (HOACs) in alginate beads and verified on an anterior cruciate ligament transection PTOA rat model. The aim of this study is to evaluate and establish an anti-PTOA therapy combined with L-SR, transdermal iontophoresis, and LIPUS. Treatment with 10 M L-SR with LIPUS-enhanced type II collagen and glycosaminoglycans (GAGs) as L-SR with LIPUS reduced the MMP-13, IL-1β, and TNF-α in HOACs. Iontophoretic L-SR at 15 mg with LIPUS increased the weight bearing, exercise endurance, GAG density, and type II collagen intensity, while L-SR with or without LIPUS further decreased MMP13 and proinflammatory cytokines in vivo. The RBC, WBC, and serum biochemistry values were not significantly affected by the treatments. Liposome encapsulation and iontophoresis reinforce the anti-PTOA effects of SR and the addictive LIPUS further improves weight-bearing and endurance performance in the rats with PTOA. Thus, iontophoretic L-SR with LIPUS could be a potential therapy for PTOA.

摘要

骨关节炎(OA)是最常见的关节炎形式,会影响整个滑膜关节。创伤后骨关节炎(PTOA)是OA的一种重要亚型,在关节损伤后发展而来。通过在藻酸盐珠中培养人OA软骨细胞(HOACs)来研究离子导入脂质体包裹的雷奈酸锶(L-SR)联合低强度脉冲超声(LIPUS)的抗PTOA作用,并在前交叉韧带横断PTOA大鼠模型上进行验证。本研究的目的是评估并建立一种联合L-SR、经皮离子导入和LIPUS的抗PTOA疗法。用10 M L-SR联合LIPUS处理可增加HOACs中II型胶原蛋白和糖胺聚糖(GAGs),因为L-SR联合LIPUS可降低HOACs中的MMP-13、IL-1β和TNF-α。15 mg离子导入L-SR联合LIPUS可增加负重、运动耐力、GAG密度和II型胶原蛋白强度,而无论有无LIPUS,L-SR均可在体内进一步降低MMP13和促炎细胞因子。治疗对红细胞、白细胞和血清生化值无显著影响。脂质体包裹和离子导入增强了SR的抗PTOA作用,而附加的LIPUS进一步改善了PTOA大鼠的负重和耐力表现。因此,离子导入L-SR联合LIPUS可能是一种治疗PTOA的潜在疗法。

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