4.7 Article

Indole Acetic Acid Exerts Anti-Depressive Effects on an Animal Model of Chronic Mild Stress

期刊

NUTRIENTS
卷 14, 期 23, 页码 -

出版社

MDPI
DOI: 10.3390/nu14235019

关键词

indole acetic acid; depression; HPA axis; serotonin; gut microbiota; indole derivative

资金

  1. National Natural Science Foundation of China
  2. Fundamental Research Funds for the Central Universities
  3. China National Postdoctoral Program for Innovative Talents
  4. China Postdoctoral Science Foundation
  5. Postdoctoral Science Foundation of Jiangsu Province
  6. Natural Science Foundation of Jiangsu Province
  7. Program of Collaborative Innovation Centre of Food Safety and Quality Control in Jiangsu Province
  8. [32201988]
  9. [31972052]
  10. [32021005]
  11. [31820103010]
  12. [JUSRP22006]
  13. [JUSRP51501]
  14. [BX2021114]
  15. [2021M691290]
  16. [2021K127B]
  17. [BK20210456]

向作者/读者索取更多资源

This study found that IAA treatment can alleviate depression and anxiety, improve brain-gut axis function. IAA can also enhance the serotonin pathway in the brain and gut. UCMS causes imbalance of microbial indole metabolites in the colon, which can be reversed by IAA treatment.
Indole acetic acid (IAA), an intestinal bacteria-derived tryptophan metabolite, has been detected at abnormal concentrations in the cerebrospinal fluid and urine of depressed individuals. The effects of such altered IAA concentrations on mood regulation are not known. A mouse model of unpredictable chronic mild stress (UCMS) was used to assess the effects of IAA administration (50 mg/kg). Treatment with IAA for 5 weeks attenuated depression and anxiety-like behaviours, improved hypothalamus-pituitary-adrenal axis dysfunction and increased brain-derived neurotrophic factor expression. IAA supplementation also enhanced the serotonin pathway in the brain and gut. UCMS caused an imbalance of microbial indole metabolites in the colon, whereas IAA treatment reversed this. However, IAA intake did not affect the concentrations of indoles in the brain. Intestinal bacteria in different sections of the gut were altered by IAA treatment, with the colon showing more changes than other segments. The gut microbiome in the colon had increased proportions of Ruminococcaceae UCG013, Ruminiclostridium 6, Prevotella, Alloprevotella and Bacteroides species, which can produce short-chain fatty acids and indole derivatives. Cumulatively, our study highlights the potential of IAA treatment to alleviate mood disorders and offers a theoretical basis for understanding the antidepressant effects of IAA.

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