[Mechanism of Syngnathus extract in treating knee osteoarthritis of rats via regulating PI3K/Akt/mTOR signaling pathway].

Q3 Pharmacology, Toxicology and Pharmaceutics
Quan-Wei Zheng, Guo-Wei Wang, Si-Xian Wu, Tao Zhuo, Yi He, Jian-Hang Liu
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引用次数: 0

Abstract

To investigate the mechanism of action of Syngnathus extract in treating knee osteoarthritis of rats, forty-eight male SD rats were randomly divided into the blank group, model group, positive drug group, as well as low-dose, medium-dose, and high-dose groups of Syngnathus extract. The rat model of knee osteoarthritis was constructed by intra-articular injection of sodium iodoacetate. After successful modeling, celecoxib(18 mg·kg~(-1)·d~(-1)) and Syngnathus extract(0.4, 0.8, and 1.6 g·kg~(-1)·d~(-1)) were given in different groups by gavage intervention for two weeks. Hematoxylin-eosin(HE) staining was used to observe the histopathological changes of cartilage in knee joints, and enzyme-linked immunosorbent assay(ELISA) was used to detect the expression level of inflammatory factors in serum. Real-time fluorescence quantitative PCR, Western blot, and immunohistochemistry were used to detect the levels of phosphatidylinositol 3-kinase(PI3K)/protein kinase B(Akt)/mammalian target protein of rapamycin(mTOR) pathway-related mRNA and protein expression. The results showed that, comparied with the blank group, the cartilage surface of the knee joints of rats in the model group was uneven, with disorganized levels and defective cartilage tissue. The serum levels of interleukin-1β(IL-1β), interleukin-6(IL-6), and tumor necrosis factor-α(TNF-α) and the mRNA levels of PI3K, Akt, and mTOR in cartilage tissue, as well as the protein expression levels of phosphorylated PI3K(p-PI3K)/PI3K, phosphorylated Akt(p-Akt)/Akt, phosphorylated mTOR(p-mTOR)/mTOR, and P62 were significantly increased. Beclin1 protein expression was decreased. Comparied with the model group, the number of chondrocytes in the knee joint of rats in each group of Syngnathus extract increased, and the arrangement of chondrocytes was relatively neat. The cartilage layer was restored, and the serum levels of IL-1β, IL-6, and TNF-α, as well as the mRNA expression levels of PI3K, Akt, and mTOR in cartilage tissue were significantly reduced. The protein expression levels of p-PI3K/PI3K, p-Akt/Akt, p-mTOR/mTOR, and P62 were significantly reduced in the rats in the middle-dose and high-dose groups of Syngnathus extract, and the Beclin1 protein expression was significantly increased. The protein expression levels of p-PI3K/PI3K, p-Akt/Akt, and P62 in rats in the low-dose group of Syngnathus extract were significantly reduced. In summary, Syngnathus extract may be used to treat knee osteoarthritis by inhibiting the expression of PI3K/Akt/mTOR signaling pathway, so as to alleviate the inflammatory response in the organism, enhance the autophagy activity of chondrocytes, and reduce the apoptosis of chondrocytes.

[syngnath提取物通过调节PI3K/Akt/mTOR信号通路治疗大鼠膝骨性关节炎的机制]。
为探讨syngnatha提取物治疗大鼠膝关节骨性关节炎的作用机制,将48只雄性SD大鼠随机分为空白组、模型组、阳性药物组以及syngnatha提取物低、中、高剂量组。采用碘乙酸钠关节内注射法建立大鼠膝关节骨性关节炎模型。造模成功后,各组分别给予塞来昔布(18 mg·kg~(-1)·d~(-1))和Syngnathus提取物(0.4、0.8、1.6 g·kg~(-1)·d~(-1))灌胃干预2周。采用苏木精-伊红(HE)染色观察膝关节软骨组织病理学变化,采用酶联免疫吸附试验(ELISA)检测血清炎症因子表达水平。采用实时荧光定量PCR、Western blot、免疫组化检测各组小鼠磷脂酰肌醇3-激酶(PI3K)/蛋白激酶B(Akt)/哺乳动物雷帕霉素靶蛋白(mTOR)通路相关mRNA及蛋白表达水平。结果显示,与空白组比较,模型组大鼠膝关节软骨表面凹凸不平,软骨组织层次紊乱,软骨组织缺损。血清白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、肿瘤坏死因子-α(TNF-α)水平及软骨组织中PI3K、Akt、mTOR mRNA水平,磷酸化PI3K(p-PI3K)/PI3K、磷酸化Akt(p-Akt)/Akt、磷酸化mTOR(p-mTOR)/mTOR、P62蛋白表达水平均显著升高。Beclin1蛋白表达降低。与模型组比较,各给药组大鼠膝关节内软骨细胞数量增加,软骨细胞排列较为整齐。软骨层恢复后,血清IL-1β、IL-6、TNF-α水平及软骨组织中PI3K、Akt、mTOR mRNA表达水平均显著降低。中、高剂量组大鼠p-PI3K/PI3K、p-Akt/Akt、p-mTOR/mTOR、P62蛋白表达水平均显著降低,Beclin1蛋白表达水平显著升高。低剂量组大鼠p-PI3K/PI3K、p-Akt/Akt、P62蛋白表达水平均显著降低。综上所述,syngnaththus提取物可能通过抑制PI3K/Akt/mTOR信号通路的表达来治疗膝关节骨性关节炎,从而减轻机体内的炎症反应,增强软骨细胞的自噬活性,减少软骨细胞的凋亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
自引率
0.00%
发文量
581
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