Related Experiment Video
Updated: Jan 14, 2026

Exploring the Two Herb Combination Strategy to Treat Injured PC12 Cells
Published on: November 18, 2022
Protective effects of 2,3,5,4'-tetrahydroxystilbene-2-O-β-D-glucoside against cadmium toxicity involve BDNF/TrkB and
Run-Ze Gu1, Abduwares Tursun1, Si-Jia Zhong2
1Key Laboratory of Ecology and Environment in Minority Areas National Ethnic Affairs Commission, Center on Translational Neuroscience, College of Life and Environmental Sciences, Minzu University of China, Beijing, China.
Abstract:
Polygonum multiflorum is a traditional Chinese medicinal herb used to nourish the blood, promote hair growth, and support neurological health. Its key bioactive component, 2,3,5,4'-tetrahydroxystilbene-2-O-β-D-glucoside (THSG), has shown potent antioxidant and anti-aging properties, making it a representative marker compound in modern pharmacological studies. We aimed to investigate the neuroprotective effects of THSG against cadmium (Cd)-induced neurotoxicity and to elucidate its underlying molecular mechanisms using both in vitro cellular models and an in vivo murine model. Male mice, 8 weeks of age, were randomly assigned to four groups: control, Cd-exposed, THSG-treated, and Cd+THSG co-treated. After 30 days of Cd exposure with or without THSG, behavioral tests, histological analysis, and assays for oxidative stress and inflammatory markers were conducted. In vitro, SH-SY5Y, BV2, and GL261 cells were used to investigate the cytoprotective and mechanistic effects of THSG against Cd-induced neurotoxicity via WST-1, RT-qPCR, Western blotting, LDH release, and immunofluorescence assays. THSG treatment significantly improved spatial learning and memory performance in Cd-exposed mice, while also effectively suppressing microglial and astrocyte activation and alleviating neuronal damage. In vitro, THSG alleviated Cd-induced cytotoxicity and morphological damage in neurons and glial cells. Western blot and immunofluorescence analyses revealed that THSG activated the BDNF/TrkB and PI3K/Akt signaling pathways, contributing to its neuroprotective effects. THSG confers robust neuroprotection against Cd-induced toxicity through multi-target mechanisms involving BDNF/TrkB and PI3K/Akt pathway activation, supporting its potential as a promising therapeutic agent for heavy metal-induced neurodegeneration.
More Related Videos
11:44Cellular Membrane Affinity Chromatography Columns to Identify Specialized Plant Metabolites Interacting with Immobilized Tropomyosin Kinase Receptor B
Published on: January 19, 2022
11:13Author Spotlight: Exploring Salidroside's Molecular Mechanisms in Breast Cancer Treatment
Published on: June 9, 2023