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牛磺酸可预防实验性大鼠模型中的膝骨关节炎发展。

Taurine protects against knee osteoarthritis development in experimental rat models.

作者信息

Bian Yiqun, Zhang Meng, Wang Kai

机构信息

Liaocheng People's Hospital, Liaocheng, Shandong, China.

Liaocheng People's Hospital, Liaocheng, Shandong, China.

出版信息

Knee. 2018 Jun;25(3):374-380. doi: 10.1016/j.knee.2018.03.004. Epub 2018 Apr 9.

Abstract

BACKGROUND

Osteoarthritis (OA) is one of the complex diseases that affect a large population of the world. The aim of the current study was to explore the roles of taurine in OA rat models, and discover the related mechanisms.

METHODS

OA rat models were established by anterior cruciate ligament transection (ACLT) plus medial meniscus resection (MMx) surgery on the right knees. Secondary mechanical allodynia, weight-bearing alterations and knee joint width were evaluated before surgery and every two weeks after surgery. At 14weeks, histopathological analysis was conducted on the knee joint cartilage. Protein amount of MMP-3 and CHOP was evaluated by western blot.

RESULTS

Taurine injection after surgery significantly relieved the symptoms of OA in rat models in a dose-dependent and time-dependent manner, as shown by alleviation of secondary mechanical allodynia, decrease in hind limb weight-bearing alterations, and inhibited knee swelling. Moreover, histopathological analysis showed that taurine inhibited matrix loss and cartilage degeneration in a dose-dependent manner. Taurine administration strikingly suppressed the expression of matrix metalloproteinase-3 (MMP-3) and CHOP.

CONCLUSION

These results indicated that taurine administration exhibited protective effects by inhibiting MMP-3 and CHOP expression, and subsequently alleviated the OA symptoms in experimental rat models.

摘要

背景

骨关节炎(OA)是影响全球大量人群的复杂疾病之一。本研究的目的是探讨牛磺酸在OA大鼠模型中的作用,并发现相关机制。

方法

通过对右膝进行前交叉韧带横断术(ACLT)加内侧半月板切除术(MMx)建立OA大鼠模型。在手术前以及手术后每两周评估继发性机械性痛觉过敏、负重改变和膝关节宽度。在第14周时,对膝关节软骨进行组织病理学分析。通过蛋白质印迹法评估基质金属蛋白酶-3(MMP-3)和C/EBP同源蛋白(CHOP)的蛋白量。

结果

手术后注射牛磺酸以剂量和时间依赖性方式显著缓解了大鼠模型中的OA症状,表现为继发性机械性痛觉过敏减轻、后肢负重改变减少以及膝关节肿胀受到抑制。此外,组织病理学分析表明牛磺酸以剂量依赖性方式抑制基质丢失和软骨退变。给予牛磺酸显著抑制了基质金属蛋白酶-3(MMP-3)和CHOP的表达。

结论

这些结果表明,给予牛磺酸通过抑制MMP-3和CHOP表达发挥保护作用,随后减轻了实验大鼠模型中的OA症状。

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