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Dose-dependent action of cordycepin on the microbiome-gut-brain-adipose axis in mice exposed to stress - 11/11/23

Doi : 10.1016/j.biopha.2023.115796 
Xiaoyuan Jing a, b, 1, Feng Hong b, 1, Yinfang Xie a, Yutong Xie a, Feng Shi e, Ruoxi Wang a, b, Liping Wang a, b, c, Zuxin Chen a, b, c, d, , Xin-an Liu a, b, c,
a Guangdong Provincial Key Laboratory of Brain Connectome and Behavior, CAS Key Laboratory of Brain Connectome and Manipulation, Brain Cognition and Brain Disease Institute (BCBDI), Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China 
b Shenzhen-Hong Kong Institute of Brain Science-Shenzhen Fundamental Research Institutions, Shenzhen, China 
c University of Chinese Academy of Sciences, Beijing, China 
d Shenzhen Key Laboratory of Drug Addiction, Shenzhen Neher Neural Plasticity Laboratory, The Brain Cognition and Brain Disease Institute, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China 
e Shenzhen Chenlu Biotechnology Co., Ltd, Shenzhen, China 

Corresponding authors at: Guangdong Provincial Key Laboratory of Brain Connectome and Behavior, CAS Key Laboratory of Brain Connectome and Manipulation, Brain Cognition and Brain Disease Institute (BCBDI), Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.Guangdong Provincial Key Laboratory of Brain Connectome and Behavior, CAS Key Laboratory of Brain Connectome and Manipulation, Brain Cognition and Brain Disease Institute (BCBDI), Shenzhen Institute of Advanced Technology, Chinese Academy of SciencesShenzhenChina.

Abstract

The high risk for anxiety and depression among individuals with stress has become a growing concern globally. Stress-related mental disorders are often accompanied by symptoms of metabolic dysfunction. Cordycepin is a Chinese herbal medicine commonly used for its metabolism-enhancing effects. We aimed to investigate the dose-dependent effects of cordycepin on psycho-metabolic disorders induced by stress. Our behavioral tests revealed that 12.5 mg/kg cordycepin by oral gavage significantly attenuated the anxiety- and depression-like behaviors induced by stress in mice. At 25 mg/kg, cordycepin restored the reduced weight and cell size of adipose tissues caused by stress. Besides ameliorating the metabolic dysbiosis of gut microbiota due to stress, cordycepin significantly reduced the elevated contents of 5-hydroxyindoleacetic acid in the serum and prefrontal cortex at 12.5 mg/kg and reversed the decrease in adipose induced by stress at 25 mg/kg. Correlation analyses further revealed that 12.5 mg/kg cordycepin reversed stress-induced changes in the intestinal microbiome of NK4A214_group and decreased serum Myristic acid and PC(15:0/18:1(11Z)) and cytokines, such as IFN-γ and IL-1β. 25 mg/kg cordycepin reversed stress-induced changes in the abundances of Prevoteaceae_UCG-001 and Desulfovibrio, increased serum L-alanine level, and decreased serum Inosine-5'-monophosphate level. Cordycepin thereby ameliorated the anxiety- and depression-like behaviors as well as disturbances in the adipose metabolism of mice exposed to stress. Overall, these findings offer evidence indicating that the prominent effects of cordycepin in the brain and adipose tissues are dose dependent, thus highlight the importance of evaluating the precise therapeutic effects of different cordycepin doses on psycho-metabolic diseases.

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Highlights

12.5 mg/kg cordycepin by gavage for four weeks attenuates the anxiety/depression-like behaviors induced by stress in mice.
25 mg/kg cordycepin restores the reduced weights and cell size of adipose tissues caused by stress.
Body weight gain and center time in the OFT are positively correlated.
Adipose tissue-to-body weight ratio and the center time in the OFT are negatively correlated.
Correlations of microbiome-gut-brain-adipose suggests dose-dependent effects of cordycepin on emotion and adipose metabolism under stress.

Le texte complet de cet article est disponible en PDF.

Keywords : Cordycepin, Anxiety, Depression, Adipose metabolism, Gut microbiota


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