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研究(Thunb.)Makino 对骨关节炎的抗炎、镇痛和软骨保护作用:一项体外和体内研究。

Investigating the Anti-Inflammatory, Analgesic, and Chondroprotective Effects of (Thunb.) Makino in Osteoarthritis: An In Vitro and In Vivo Study.

机构信息

Department of Herbal Pharmacology, College of Korean Medicine, Gachon University, 1342 Seongnamdae-ro, Sujeong-gu, Seongnam-si 13120, Republic of Korea.

Naturalis Inc., 6 Daewangpangyo-ro, Bundang-gu, Seongnam-si 13549, Republic of Korea.

出版信息

Int J Mol Sci. 2024 Sep 4;25(17):9594. doi: 10.3390/ijms25179594.

Abstract

Osteoarthritis (OA) is an age-related disease characterized by inflammation, pain, articular cartilage damage, synovitis, and irreversible disability. (Thunb.) Makino (GP), a herbal medicine traditionally used in East Asia for its anti-inflammatory properties, was investigated for its potential to modulate OA pathology and symptoms. This study evaluated GP's efficacy in inhibiting pain, functional decline, and cartilage destruction in monosodium iodoacetate-induced OA and acetic acid-induced writhing models. Additionally, the effects of GP on OA-related inflammatory targets were assessed via mRNA and protein expression in rat knee cartilage and lipopolysaccharide-induced RAW 264.7 cells. The GP group demonstrated significant pain relief, functional improvement, and cartilage protection. Notably, GP inhibited key inflammatory mediators, including interleukin (IL)-1β, IL-6, matrix metalloproteinases (MMP)-3 and MMP-13, cyclooxygenase-2, and prostaglandin E receptor 2, surpassing the effects of active controls. These findings suggest that GP is a promising candidate for disease-modifying OA drugs and warrants further comprehensive studies.

摘要

骨关节炎(OA)是一种与年龄相关的疾病,其特征为炎症、疼痛、关节软骨损伤、滑膜炎和不可逆转的残疾。(Thunb.)Makino(GP)是一种传统上用于东亚的草药,具有抗炎特性,被研究用于调节 OA 病理和症状的潜力。本研究评估了 GP 在抑制疼痛、功能下降和软骨破坏方面的功效,使用单碘乙酸盐诱导的 OA 和乙酸诱导的扭体模型进行了评估。此外,通过大鼠膝关节软骨和脂多糖诱导的 RAW 264.7 细胞中的 mRNA 和蛋白质表达,评估了 GP 对 OA 相关炎症靶点的影响。GP 组表现出显著的疼痛缓解、功能改善和软骨保护。值得注意的是,GP 抑制了关键的炎症介质,包括白细胞介素(IL)-1β、IL-6、基质金属蛋白酶(MMP)-3 和 MMP-13、环氧化酶-2 和前列腺素 E 受体 2,超过了阳性对照的效果。这些发现表明,GP 是一种有前途的治疗 OA 的药物候选物,值得进一步进行全面研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17c7/11395165/9f606d1f9bd2/ijms-25-09594-g001.jpg

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