The gut microbiome in patients with Cushing's disease affects depression- and anxiety-like behavior in mice.


Journal

Microbiome
ISSN: 2049-2618
Titre abrégé: Microbiome
Pays: England
ID NLM: 101615147

Informations de publication

Date de publication:
01 Nov 2024
Historique:
received: 28 03 2024
accepted: 23 09 2024
medline: 1 11 2024
pubmed: 1 11 2024
entrez: 1 11 2024
Statut: epublish

Résumé

Depression and anxiety significantly impact the quality of life in individuals with Cushing's disease (CD), which originates from pituitary neuroendocrine tumors (PitNETs), yet our understanding of the underlying mechanisms is limited. There is substantial evidence linking gut microbes to depression, anxiety, and endocrinology. The gut bacterial phenotype of patients with Cushing's disease was significantly different from that of the control group, and when the mice were treated with fecal bacteria from these patients, both anxiety- and depression-like behavior were significantly increased. However, this effect can be alleviated by supplementing with 2-(14, 15-epoxyeicosatrienoyl) glycerol (2-14,15-EG) which was found at reduced levels in the peripheral blood of mice treated with coprofecal bacteria from Cushing's disease. In this process, the effects of hormone levels and immune factors were not significant. In addition, in an animal model, corticosterone has been observed to affect behavioral changes in mice through gut microbiota composition, clarifying the cause-and-effect relationship between hormones, microbiota, and behavior. Finally, there was no significant difference in gut microbiome composition and its effects on mouse behavior in patients with Cushing's disease with different levels of depression and anxiety. In summary, this research enhances our current understanding of how gut microbes in patients with Cushing's disease contribute to depression and anxiety, offering novel insights for clinical treatment approaches. Video Abstract.

Sections du résumé

BACKGROUND BACKGROUND
Depression and anxiety significantly impact the quality of life in individuals with Cushing's disease (CD), which originates from pituitary neuroendocrine tumors (PitNETs), yet our understanding of the underlying mechanisms is limited. There is substantial evidence linking gut microbes to depression, anxiety, and endocrinology.
RESULTS RESULTS
The gut bacterial phenotype of patients with Cushing's disease was significantly different from that of the control group, and when the mice were treated with fecal bacteria from these patients, both anxiety- and depression-like behavior were significantly increased. However, this effect can be alleviated by supplementing with 2-(14, 15-epoxyeicosatrienoyl) glycerol (2-14,15-EG) which was found at reduced levels in the peripheral blood of mice treated with coprofecal bacteria from Cushing's disease. In this process, the effects of hormone levels and immune factors were not significant. In addition, in an animal model, corticosterone has been observed to affect behavioral changes in mice through gut microbiota composition, clarifying the cause-and-effect relationship between hormones, microbiota, and behavior. Finally, there was no significant difference in gut microbiome composition and its effects on mouse behavior in patients with Cushing's disease with different levels of depression and anxiety.
CONCLUSIONS CONCLUSIONS
In summary, this research enhances our current understanding of how gut microbes in patients with Cushing's disease contribute to depression and anxiety, offering novel insights for clinical treatment approaches. Video Abstract.

Identifiants

pubmed: 39482760
doi: 10.1186/s40168-024-01939-1
pii: 10.1186/s40168-024-01939-1
doi:

Substances chimiques

Corticosterone W980KJ009P

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

225

Informations de copyright

© 2024. The Author(s).

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Auteurs

Ding Nie (D)

Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.

Dawei Wang (D)

Department of Neurosurgery, Air Force Medical University Tangdu Hospital, Xi'an, China.

Zhenhua Wang (Z)

Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.

Qiuyue Fang (Q)

Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.

Hongyun Wang (H)

Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.

Weiyan Xie (W)

Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.

Chuzhong Li (C)

Beijing Neurosurgical Institute, Capital Medical University, Beijing, China. lichuzhong@163.com.

Yazhuo Zhang (Y)

Beijing Neurosurgical Institute, Capital Medical University, Beijing, China. zyztxzz@126.com.

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