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基于p38丝裂原活化蛋白激酶信号通路的山奈酚对椎间盘退变的作用机制

[Mechanism of kaempferol on intervertebral disc degeneration based on p38 MAPK signaling pathway].

作者信息

Wang Chen-Mo-Ji, Wu Ya-Dong, Liang Song-Lin, Gao Shang, Yue Ze-Lin, Kong Lu-Ming, Gao Kuan-Hui, Li Nian-Hu

机构信息

the First Clinical Medical College of Shandong University of Traditional Chinese Medicine Ji'nan 250014, China.

the First Clinical Medical College of Shandong University of Traditional Chinese Medicine Ji'nan 250014, China Rizhao City Hospital of Traditional Chinese Medicine Rizhao 276800, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2024 Nov;49(21):5721-5729. doi: 10.19540/j.cnki.cjcmm.20240625.401.

Abstract

This study investigated the mechanism by which kaempferol(KAE) affected intervertebral disc degeneration(IDD) through the p38 mitogen-activated protein kinase(p38 MAPK) signaling pathway. Rats were randomly divided into five groups: control group, model group, low-dose KAE group, medium-dose KAE group, and high-dose KAE group. An IDD model was established by needle puncture of the caudal intervertebral discs. Four weeks post-surgery, the rats were administered KAE via gavage for 8 consecutive weeks. Magnetic resonance imaging(MRI) was performed, and samples were collected. In vitro, an inflammation model of nucleus pulposus cells(NPCs) induced by tumor necrosis factor-alpha(TNF-α) was constructed. Anisomycin was used to activate the p38 MAPK signaling pathway. NPCs were divided into blank, model, KAE, agonist, and KAE + agonist groups. After 1 day of treatment, cell proliferation activity was assessed using the CCK-8. Protein expression levels were determined by Western blot, and mRNA expression was measured by real-time quantitative polymerase chain reaction. Cell apoptosis was detected by TUNEL staining, and immunofluorescence staining was used to detect type Ⅱ collagen and matrix metalloproteinase 3(MMP3). In vivo results indicated significant improvement in the degree of IDD in the treatment groups compared to the model group, with the medium-dose group showing more pronounced therapeutic effects than the low-and high-dose groups. In vitro results demonstrated that KAE treatment significantly enhanced NPC proliferation activity, down-regulated the expression levels of Bcl-2-associated X protein(Bax), interleukin-6(IL-6), interleukin-17A(IL-17A), MMP3, and a disintegrin and metalloproteinase with thrombospondin motifs 5, and inhibited the phosphorylation of p38 MAPK pathway-related proteins. Activation of the p38 MAPK signaling pathway by anisomycin reduced the therapeutic effects of KAE. The study concluded that KAE could improve the proliferation activity of degenerated NPCs, reduce inflammation levels, and slow the progression of IDD in rats, and the mechanism was likely related to the regulation of the p38 MAPK signaling pathway.

摘要

本研究探讨了山奈酚(KAE)通过p38丝裂原活化蛋白激酶(p38 MAPK)信号通路影响椎间盘退变(IDD)的机制。将大鼠随机分为五组:对照组、模型组、低剂量KAE组、中剂量KAE组和高剂量KAE组。通过针刺大鼠尾椎椎间盘建立IDD模型。术后4周,大鼠连续8周经口灌胃给予KAE。进行磁共振成像(MRI)检查并采集样本。在体外,构建肿瘤坏死因子-α(TNF-α)诱导的髓核细胞(NPCs)炎症模型。使用茴香霉素激活p38 MAPK信号通路。将NPCs分为空白组、模型组、KAE组、激动剂组和KAE +激动剂组。处理1天后,使用CCK-8评估细胞增殖活性。通过蛋白质免疫印迹法测定蛋白表达水平,通过实时定量聚合酶链反应测量mRNA表达。通过TUNEL染色检测细胞凋亡,使用免疫荧光染色检测Ⅱ型胶原蛋白和基质金属蛋白酶3(MMP3)。体内结果表明,与模型组相比,治疗组的IDD程度有显著改善,中剂量组的治疗效果比低剂量组和高剂量组更明显。体外结果表明,KAE处理显著增强了NPCs的增殖活性,下调了Bcl-2相关X蛋白(Bax)、白细胞介素-6(IL-6)、白细胞介素-17A(IL-17A)、MMP3以及含血小板反应蛋白基序的解聚素和金属蛋白酶5的表达水平,并抑制了p38 MAPK信号通路相关蛋白的磷酸化。茴香霉素激活p38 MAPK信号通路降低了KAE的治疗效果。该研究得出结论,KAE可以提高退变NPCs的增殖活性,降低炎症水平,并减缓大鼠IDD的进展,其机制可能与调节p38 MAPK信号通路有关。

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