Enhanced In Vitro Efficacy of Verbascoside in Suppressing Hepatic Stellate Cell Activation via ROS Scavenging with Reverse Microemulsion

Author:

Xiao Xiao12,Yang Feiyu13,Huang Yuling4,Liu Shaohui12,Hu Zhenhua25ORCID,Liao Shanggao13,Li Yuanyuan12467

Affiliation:

1. School of Pharmacy, Guizhou Medical University, Guiyang 550025, China

2. Zhongshan Institute for Drug Discovery, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Zhongshan 528400, China

3. University Engineering Research Center for the Prevention and Treatment of Chronic Diseases by Authentic Medicinal Materials in Guizhou Province & School of Pharmacy, Guiyang 550025, China

4. School of Pharmaceutical Sciences, Southern Medical University, Guangzhou 510515, China

5. Department of Health and Nursing, Nanfang College of Sun Yat-sen University, Guangzhou 510970, China

6. Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China

7. University of Chinese Academy of Sciences, Beijing 100049, China

Abstract

Numerous approaches targeting hepatic stellate cells (HSCs) have emerged as pivotal therapeutic strategies to mitigate liver fibrosis and are currently undergoing clinical trials. The investigation of herbal drugs or isolated natural active compounds is particularly valuable, due to their multifaceted functions and low risk of side effects. Recent studies have hinted at the potential efficacy of verbascoside (VB) in ameliorating renal and lung fibrosis, yet its impact on hepatic fibrosis remains to be elucidated. This study aims to evaluate the potential effects of VB on liver fibrosis by assessing its ability to inhibit HSC activation. VB demonstrated significant efficacy in suppressing the expression of fibrogenic genes in activated LX-2 cells. Additionally, VB inhibited the migration and proliferation of these activated HSCs by scavenging reactive oxygen species (ROS) and downregulating the AMPK pathway. Furthermore, a biosafe reverse microemulsion loaded with VB (VB-ME) was developed to improve VB’s instability and low bioavailability. The optimal formulation of VB-ME was meticulously characterized, revealing substantial enhancements in cellular uptake, ROS-scavenging capacity, and the suppression of HSC activation.

Funder

National Natural Science Foundation of China

Shanghai Pujiang Program

Guangdong Basic and Applied Basic Research Foundation

Zhongshan Municipal Bureau of Science and Technology

Zhongshan Institute for Drug Discovery

Shanghai Institute of Materia Medica

Chinese Academy of Sciences

Publisher

MDPI AG

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