Purification engineering technology research center of Sichuan Province Natural Medicine
四川省天然药物分离纯化工程技术研究中心

文献

Chang Ke, et al."β-Eudesmol in Rhizoma Atractylodis targets AVPR2 to inhibit the cAMP-AQP2 pathway and promote fluid metabolism.."Phytomedicine : international journal of phytotherapy and phytopharmacology 145.(2025):157035.

本文来自:    发布时间:2025-12-22

发表期刊:Phytomedicine

发表时间:2025

Abstract:

Background

Rhizoma Atractylodis, a classic dryness traditional Chinese medicine (TCM), demonstrates potent fluid metabolism–promoting properties. Previous studies have identified volatile oils as the primary active fraction of Rhizoma Atractylodis in regulating fluid metabolism, and β-eudesmol was predicted as the key component; however, the bioactivity of β-eudesmol has not been experimentally verified and the mechanism promotes fluid metabolism and causes dryness remains unclear.

Purpose

This study seeks to validate the dryness effect of β-eudesmol and elucidate its key mechanisms in regulating fluid metabolism to produce dryness effect.

Methods

This study used normal mice to compare the effects of Rhizoma Atractylodis volatile oil and β-eudesmol on fluid metabolism regulation. Transcriptomic analysis was used to predict the potential mechanisms by which β-eudesmol modulates fluid metabolism. Through molecular docking and cellular thermal shift assay (CETSA), preliminary identification of potential target mediating β-eudesmol's dryness effect was achieved. In vitro target validation was performed using TCMK-1 cells with plasmid transfection or siRNA interference. In vivo target validation was conducted in mice transfected with adeno-associated virus (AAV)

Results

β-Eudesmol significantly altered water intake, urine output, aquaporin 2 (AQP2) expression. Transcriptomic analysis revealed the cAMP-AQP2 pathway as the core component of the renal transcriptional regulatory network of β-eudesmol. Therefore, the inhibitory effect of β-eudesmol on the cAMP-AQP2 pathway was validated in mouse kidneys and TCMK-1 cells, and its targeted binding to the arginine vasopressin receptor 2 (AVPR2) was demonstrated via molecular docking and CETSA. However, after AVPR2 overexpression, the fluid metabolism–promoting effect of β-eudesmol decreased, and the dryness manifestations in mice were alleviated.

Conclusion

This study determined that β-udesmol is the key component for the dryness of Atractylodes macrocephalaelucidates the mechanism of moisture removal and diuresis by Rhizoma Atractylodis, providing a scientific basis for its clinical use to treat dampness-related conditions experimental evidence for reducing dryness and increasing. Moreover, it provides a new reference for theoretical research on the properties of TCM.

https://doi.org/10.1016/j.phymed.2025.157035

 


上一篇:没有了

下一篇:Yingying Ke, et al."High-energy fluidic microfluidization: Enhancing

联系我们

4000-369-963  028-85370565

3004654993@qq.com

四川省 成都市 武侯区 武科西二路8号

关于普思

 新闻资讯

研发机构

 服务平台

产品

中药化学对照品

化合物库

热销原料

技术服务

高分辨质谱分析

药物单体纯化

中药创新药

普思生物为您提供中药化学对照品、高纯化学试剂、天然产物化合物库等优质产品,
仅用于科学研究、工业应用等非医疗用途范畴,不可用于人的临床治疗或试验,非药用,非食用。

友情链接:全球化学品供应商搜索   盖德化工网    成都普思生物科技股份有限公司版权所有   蜀ICP备08100078号

在线
咨询

在线咨询服务时间:8:30-17:30

选择客服在线沟通:

咨询
热线

4000-369-963  
7*24小时客服服务热线


028-85370565 / 18080489829 (何女士)

关注
微信

关注官方微信
顶部