Buspirone alleviates anxiety, depression, and colitis; and modulates gut microbiota in mice

Abstract Gut microbiota regulate the neurodevelopmental processes and brain functions through the regulation of the microbiota–gut interaction and gut–brain communication. Buspirone, an agonist for serotonin 5-HT1A receptors, is used for the treatment of anxiety/depression. Therefore, to understand...

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Main Authors: Jeon-Kyung Kim, Sang-Kap Han, Min-Kyung Joo, Dong-Hyun Kim
Format: Article
Language:English
Published: Nature Publishing Group 2021-03-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-85681-w
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spelling doaj-17456cd6195c4a41b191879db53c15452021-03-21T12:33:03ZengNature Publishing GroupScientific Reports2045-23222021-03-0111111210.1038/s41598-021-85681-wBuspirone alleviates anxiety, depression, and colitis; and modulates gut microbiota in miceJeon-Kyung Kim0Sang-Kap Han1Min-Kyung Joo2Dong-Hyun Kim3Neurobiota Research Center, College of Pharmacy, Kyung Hee UniversityNeurobiota Research Center, College of Pharmacy, Kyung Hee UniversityNeurobiota Research Center, College of Pharmacy, Kyung Hee UniversityNeurobiota Research Center, College of Pharmacy, Kyung Hee UniversityAbstract Gut microbiota regulate the neurodevelopmental processes and brain functions through the regulation of the microbiota–gut interaction and gut–brain communication. Buspirone, an agonist for serotonin 5-HT1A receptors, is used for the treatment of anxiety/depression. Therefore, to understand the gut microbiota-mediated mechanism of buspirone on anxiety/depression, we examined its effect on the immobilization stress (IS) or Escherichia coli K1 (EC)-induced anxiety/depression in mice. Oral or intraperitoneal administration of buspirone significantly suppressed stressor-induced anxiety/depression-like behaviors in the elevated plus maze, light/dark transition, tail suspension, and forced swimming tasks. Their treatments also reduced TNF-α expression and NF-κB+/Iba1+ cell population in the hippocampus and myeloperoxidase activity and NF-κB+/CD11c+ cell population in the colon. Buspirone treatments partially restored IS- or EC-induced gut microbiota perturbation such as β-diversity to those of normal control mice: they reduced the IS- or EC-induced gut Proteobacteria population. In particular, the anxiolytic activity of buspirone was positively correlated with the populations of Bacteroides and PAC001066_g in EC- or IS-exposed mice, while the populations of Lachnospiraceae, KE159660_g, LLKB_g, Helicobacter, and PAC001228_g were negatively correlated. The anti-depressant effect of buspirone was positively correlated with the Roseburia population. The fecal microbiota transplantations from buspirone-treated mice with IS-induced anxiety/depression or normal control mice suppressed IS-induced anxiety/depression-like behaviors and reduced hippocampal NF-κB+/Iba1+ and colonic NF-κB+/CD11c+ cell populations in the transplanted mice. Furthermore, they modified IS-induced perturbation of gut microbiota composition, particularly Proteobacteria, in the transplanted mice. In conclusion, buspirone alleviates IS as well as EC-induced anxiety/depression and colitis. It also suppresses associated neuroinflammation and modulates gut microbiota. Future studies can help to explain the relationship, if any, in the central and peripheral effects of buspirone.https://doi.org/10.1038/s41598-021-85681-w
collection DOAJ
language English
format Article
sources DOAJ
author Jeon-Kyung Kim
Sang-Kap Han
Min-Kyung Joo
Dong-Hyun Kim
spellingShingle Jeon-Kyung Kim
Sang-Kap Han
Min-Kyung Joo
Dong-Hyun Kim
Buspirone alleviates anxiety, depression, and colitis; and modulates gut microbiota in mice
Scientific Reports
author_facet Jeon-Kyung Kim
Sang-Kap Han
Min-Kyung Joo
Dong-Hyun Kim
author_sort Jeon-Kyung Kim
title Buspirone alleviates anxiety, depression, and colitis; and modulates gut microbiota in mice
title_short Buspirone alleviates anxiety, depression, and colitis; and modulates gut microbiota in mice
title_full Buspirone alleviates anxiety, depression, and colitis; and modulates gut microbiota in mice
title_fullStr Buspirone alleviates anxiety, depression, and colitis; and modulates gut microbiota in mice
title_full_unstemmed Buspirone alleviates anxiety, depression, and colitis; and modulates gut microbiota in mice
title_sort buspirone alleviates anxiety, depression, and colitis; and modulates gut microbiota in mice
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-03-01
description Abstract Gut microbiota regulate the neurodevelopmental processes and brain functions through the regulation of the microbiota–gut interaction and gut–brain communication. Buspirone, an agonist for serotonin 5-HT1A receptors, is used for the treatment of anxiety/depression. Therefore, to understand the gut microbiota-mediated mechanism of buspirone on anxiety/depression, we examined its effect on the immobilization stress (IS) or Escherichia coli K1 (EC)-induced anxiety/depression in mice. Oral or intraperitoneal administration of buspirone significantly suppressed stressor-induced anxiety/depression-like behaviors in the elevated plus maze, light/dark transition, tail suspension, and forced swimming tasks. Their treatments also reduced TNF-α expression and NF-κB+/Iba1+ cell population in the hippocampus and myeloperoxidase activity and NF-κB+/CD11c+ cell population in the colon. Buspirone treatments partially restored IS- or EC-induced gut microbiota perturbation such as β-diversity to those of normal control mice: they reduced the IS- or EC-induced gut Proteobacteria population. In particular, the anxiolytic activity of buspirone was positively correlated with the populations of Bacteroides and PAC001066_g in EC- or IS-exposed mice, while the populations of Lachnospiraceae, KE159660_g, LLKB_g, Helicobacter, and PAC001228_g were negatively correlated. The anti-depressant effect of buspirone was positively correlated with the Roseburia population. The fecal microbiota transplantations from buspirone-treated mice with IS-induced anxiety/depression or normal control mice suppressed IS-induced anxiety/depression-like behaviors and reduced hippocampal NF-κB+/Iba1+ and colonic NF-κB+/CD11c+ cell populations in the transplanted mice. Furthermore, they modified IS-induced perturbation of gut microbiota composition, particularly Proteobacteria, in the transplanted mice. In conclusion, buspirone alleviates IS as well as EC-induced anxiety/depression and colitis. It also suppresses associated neuroinflammation and modulates gut microbiota. Future studies can help to explain the relationship, if any, in the central and peripheral effects of buspirone.
url https://doi.org/10.1038/s41598-021-85681-w
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