» Articles » PMID: 38642668

Gastrodin Alleviates the Deterioration of Depressive-like Behavior and Glucolipid Metabolism Promoted by Chronic Stress in Type 2 Diabetic Mice

Overview
Journal Eur J Pharmacol
Specialty Pharmacology
Date 2024 Apr 20
PMID 38642668
Authors
Affiliations
Soon will be listed here.
Abstract

The growing burden of psychological stress among diabetes patients has contributed to a rising incidence of depression within this population. It is of significant importance to conduct research on the impact of stress on diabetes patients and to explore potential pharmacological interventions to counteract the stress-induced exacerbation of their condition. Gastrodin is a low molecular weight bioactive compound extracted from the rhizome of Gastrodiae elata Blume, and it may be a preventive strategy for diabetes and a novel treatment for depression symptoms. However, its relevant pharmacological mechanisms for protecting against the impacts of psychological stress in diabetic patients are unclear. In this study, we performed 5 weeks CUMS intervention and simultaneously administered gastrodin (140 mg/kg, once daily) on T2DM mice, to investigate the potential protective effects of gastrodin. The protective effect of gastrodin was evaluated by behavioral tests, biochemical analysis, histopathological examination, RT-qPCR and gut microbiota analysis. We found that the depressive-like behavior and glucolipid metabolism could be deteriorated by chronic stress in type 2 diabetic mice, while gastrodin showed a protective effect against these exacerbations by regulating HPA hormones, activating FXR and Cyp7a1, reducing inflammatory and oxidative stress responses, and regulating ileal gut microbiota abundance. Gastrodin might be a potential therapeutic agent for mitigating the deterioration of diabetes conditions due to chronic stress.

Citing Articles

Investigation of the Pharmacodynamic Components of Blume for Treatment of Type 2 Diabetes Mellitus through HPLC, Bioactivity, Network Pharmacology and Molecular Docking.

Yang X, Li L, Yan Y, Hu X, Li Q, Li L Int J Mol Sci. 2024; 25(19).

PMID: 39408825 PMC: 11476761. DOI: 10.3390/ijms251910498.