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染料木黄酮通过下调 MAPK 和 NF-κB 通路延缓骨关节炎在大鼠模型中的发展。

Ononin delays the development of osteoarthritis by down-regulating MAPK and NF-κB pathways in rat models.

机构信息

Department of Orthopaedics Trauma and Hand Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.

Guangxi Colleges and Universities Key Laboratory of Prevention and Control of Highly Prevalent Diseases, Guangxi Medical University, Nanning, China.

出版信息

PLoS One. 2024 Oct 31;19(10):e0310293. doi: 10.1371/journal.pone.0310293. eCollection 2024.

Abstract

BACKGROUND

Osteoarthritis (OA) is featured as cartilage loss, joint pain and loss of labor, which the inflammatory reaction may play critical roles. Ononin is an isoflavone isolating from medicinal plants and has anti-inflammatory effects. Our study investigated the anti-inflammation response of ononin on OA.

METHODS

Anterior cruciate ligament transection (ACLT)-induced OA operation was used to establish research model, then treated with ononin for 8 weeks. The condition of joint injury was assessed using pathological staining. The concentration of tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β) and interleukin-6 (IL-6) in serum were measured by Elisa kit. The expression of collagen II and matrix metalloproteinase 13 (MMP-13) proteins to assess cartilage metabolism level by immunohistochemistry and Western blot. We detected the expression of proteins involved in the MAPK and NF-κB signaling pathways. Finally, we used molecular docking to assess the affinity of ononin for the target proteins ERK1/2, JNK1/2, p38 and p65.

RESULTS

Our results confirmed that ononin ameliorated cartilage impairment through histopathological analysis by improving the morphological structures and cartilage tidal lines and decreasing Osteoarthritis Research Society International (OARSI) scores in OA rats. Moreover, ononin inhibited the secretion of above factors in OA rats. Furthermore, ononin has been shown to improve cartilage content levels in OA rats. In addition, ononin inhibited the reactivity of MAPK and NF-κB pathways in OA rats. And molecular docking indicated the ligand molecules could stably bind to the proteins of above receptors.

CONCLUSION

Our results demonstrated that ononin may ameliorate cartilage damage and inflammatory response in OA rats by downgrading MAPK and NF-κB pathways, thus identifying ononin as a potential novel drug to treat OA.

摘要

背景

骨关节炎(OA)的特征是软骨损失、关节疼痛和劳动力丧失,其中炎症反应可能起着关键作用。染料木黄酮是从药用植物中分离出来的一种异黄酮,具有抗炎作用。我们的研究调查了染料木黄酮对 OA 的抗炎反应。

方法

采用前交叉韧带切断(ACLT)诱导的 OA 手术建立研究模型,然后用染料木黄酮治疗 8 周。通过病理染色评估关节损伤情况。采用 Elisa 试剂盒检测血清中肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6)的浓度。采用免疫组化和 Western blot 检测胶原 II 和基质金属蛋白酶 13(MMP-13)蛋白的表达,评估软骨代谢水平。检测丝裂原活化蛋白激酶(MAPK)和核因子-κB(NF-κB)信号通路相关蛋白的表达。最后,采用分子对接评估染料木黄酮与 ERK1/2、JNK1/2、p38 和 p65 靶蛋白的亲和力。

结果

我们的结果证实,通过改善 OA 大鼠的形态结构和软骨潮汐线,减少骨关节炎研究协会国际(OARSI)评分,染料木黄酮通过组织病理学分析改善了软骨损伤。此外,染料木黄酮抑制了 OA 大鼠上述因子的分泌。此外,染料木黄酮改善了 OA 大鼠的软骨含量水平。此外,染料木黄酮抑制了 OA 大鼠 MAPK 和 NF-κB 通路的反应性。分子对接表明配体分子可以稳定地结合到上述受体的蛋白质上。

结论

我们的结果表明,染料木黄酮可能通过下调 MAPK 和 NF-κB 通路改善 OA 大鼠的软骨损伤和炎症反应,从而鉴定染料木黄酮为治疗 OA 的潜在新型药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0589/11527302/4f17f47bb2d8/pone.0310293.g001.jpg

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