Suppr超能文献

软枣猕猴桃提取物可减轻炎症小体激活:可能涉及 NLRP3 泛素化。

Actinidia arguta extract attenuates inflammasome activation: Potential involvement in NLRP3 ubiquitination.

机构信息

Department of Applied Life Science, Graduate School, Konkuk University, Chungju, Republic of Korea.

Department of Food Science and Engineering, Seowon University, Cheongju, Republic of Korea.

出版信息

J Ethnopharmacol. 2018 Mar 1;213:159-165. doi: 10.1016/j.jep.2017.11.023. Epub 2017 Nov 21.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Actinidia arguta (A. arguta) has been widely used in Asian countries as a traditional medicinal herb to treat inflammation-related diseases, such as gastritis, bronchitis, and arthritis.

AIM OF THE STUDY

The inhibitory effect of A. arguta leaves' extract (AA) on inflammasome activation was investigated to verify its traditional use in treating inflammation-related diseases.

MATERIALS AND METHODS

Bone marrow-derived macrophages (BMDMs) primed by lipopolysaccharide (LPS) were activated by selective inflammasome stimulators, and the effect of AA on inflammasome activation was investigated. A monosodium urate crystal (MSU)-induced peritonitis mouse model was used to study the in vivo efficacy of AA on inflammasome activation.

RESULTS

In the in vitro study, AA regulated NLRP3 ubiquitination and apoptosis-associated speck-like protein containing a CARD (ASC) oligomerization, leading to the inhibition of NLRP3 inflammasome-mediated interleukin (IL)-1β secretion. The inhibitory effect of AA on inflammasome activation in vitro was further confirmed in vivo using an MSU-induced peritonitis mouse model.

CONCLUSION

AA provided scientific evidence, substantiating the traditional claims for its use in the treatment of inflammation and inflammation-mediated metabolic disorders, including gout.

摘要

民族药理学相关性

中华猕猴桃(A. arguta)在亚洲国家被广泛用作传统草药,用于治疗与炎症相关的疾病,如胃炎、支气管炎和关节炎。

研究目的

研究中华猕猴桃叶提取物(AA)对炎症小体激活的抑制作用,以验证其在治疗炎症相关疾病中的传统用途。

材料和方法

用脂多糖(LPS)预刺激的骨髓来源的巨噬细胞(BMDMs)被选择性炎症小体激动剂激活,并研究 AA 对炎症小体激活的影响。使用尿酸单钠晶体(MSU)诱导的腹膜炎小鼠模型研究 AA 对炎症小体激活的体内疗效。

结果

在体外研究中,AA 调节 NLRP3 泛素化和凋亡相关斑点样蛋白(ASC)寡聚化,从而抑制 NLRP3 炎症小体介导体细胞介素(IL)-1β的分泌。AA 对体外炎症小体激活的抑制作用在 MSU 诱导的腹膜炎小鼠模型中得到了进一步证实。

结论

AA 为其用于治疗炎症和炎症介导的代谢紊乱(包括痛风)的传统用途提供了科学证据。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验