Isoalantolactone relieves depression-like behaviors in mice after chronic social defeat stress via the gut-brain axis.
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| Title: | Isoalantolactone relieves depression-like behaviors in mice after chronic social defeat stress via the gut-brain axis. |
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| Authors: | Wang, Siming (AUTHOR), Cai, Qihan (AUTHOR), Xu, Lu (AUTHOR), Sun, Yanan (AUTHOR), Wang, Mengmeng (AUTHOR), Wang, Yu (AUTHOR), Zhang, Lili (AUTHOR), Li, Keqing (AUTHOR), Ni, Zhiyu (AUTHOR) |
| Source: | Psychopharmacology. Aug2023, Vol. 240 Issue 8, p1775-1787. 13p. 1 Diagram, 5 Graphs. |
| Subjects: | Social defeat, Brain-derived neurotrophic factor, Serotonin uptake inhibitors, Postsynaptic density protein, Animal social behavior, Butyric acid, Glutamate receptors |
| Abstract: | Rationale: The management of depression continues to be challenging despite the variety of available antidepressants. Herbal medicines are used in many cultures but lack stringent testing to understand their efficacy and mechanism of action. Isoalantolactone (LAT) from Elecampane (Inula helenium) improved the chronic social defeat stress (CSDS)-induced anhedonia-like phenotype in mice comparable to fluoxetine, a selective serotonin reuptake inhibitor (SSRI). Objectives: Compare the effects of LAT and fluoxetine on depression-like behaviors in mice exposed to CSDS. Result: The CSDS-induced decrease in protein expression of postsynaptic density (PSD95), brain derived neurotrophic factor (BDNF), and glutamate receptor subunit-1 (GluA1) in the prefrontal cortex was restored by LAT. LAT showed robust anti-inflammatory activity and can lessen the increase in IL-6 and TNF-α caused by CSDS. CSDS altered the gut microbiota at the taxonomic level, resulting in significant changes in α- and β-diversity. LAT treatment reestablished the bacterial abundance and diversity and increased the production of butyric acid in the gut that was inhibited by CSDS. The levels of butyric acid were negatively correlated with the abundance of Bacteroidetes, and positively correlated with those of Proteobacteria and Firmicutes across all treatment groups. Conclusions: The current data suggest that, similar to fluoxetine, LAT show antidepressant-like effects in mice exposed to CSDS through the modulation of the gut-brain axis. [ABSTRACT FROM AUTHOR] |
| Copyright of Psychopharmacology is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Psychology and Behavioral Sciences Collection |
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| Header | DbId: pbh DbLabel: Psychology and Behavioral Sciences Collection An: 164947282 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Isoalantolactone relieves depression-like behaviors in mice after chronic social defeat stress via the gut-brain axis. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Wang%2C+Siming%22">Wang, Siming</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Cai%2C+Qihan%22">Cai, Qihan</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Xu%2C+Lu%22">Xu, Lu</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Sun%2C+Yanan%22">Sun, Yanan</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wang%2C+Mengmeng%22">Wang, Mengmeng</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wang%2C+Yu%22">Wang, Yu</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhang%2C+Lili%22">Zhang, Lili</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Li%2C+Keqing%22">Li, Keqing</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ni%2C+Zhiyu%22">Ni, Zhiyu</searchLink> (AUTHOR) – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Psychopharmacology%22">Psychopharmacology</searchLink>. Aug2023, Vol. 240 Issue 8, p1775-1787. 13p. 1 Diagram, 5 Graphs. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Social+defeat%22">Social defeat</searchLink><br /><searchLink fieldCode="DE" term="%22Brain-derived+neurotrophic+factor%22">Brain-derived neurotrophic factor</searchLink><br /><searchLink fieldCode="DE" term="%22Serotonin+uptake+inhibitors%22">Serotonin uptake inhibitors</searchLink><br /><searchLink fieldCode="DE" term="%22Postsynaptic+density+protein%22">Postsynaptic density protein</searchLink><br /><searchLink fieldCode="DE" term="%22Animal+social+behavior%22">Animal social behavior</searchLink><br /><searchLink fieldCode="DE" term="%22Butyric+acid%22">Butyric acid</searchLink><br /><searchLink fieldCode="DE" term="%22Glutamate+receptors%22">Glutamate receptors</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Rationale: The management of depression continues to be challenging despite the variety of available antidepressants. Herbal medicines are used in many cultures but lack stringent testing to understand their efficacy and mechanism of action. Isoalantolactone (LAT) from Elecampane (Inula helenium) improved the chronic social defeat stress (CSDS)-induced anhedonia-like phenotype in mice comparable to fluoxetine, a selective serotonin reuptake inhibitor (SSRI). Objectives: Compare the effects of LAT and fluoxetine on depression-like behaviors in mice exposed to CSDS. Result: The CSDS-induced decrease in protein expression of postsynaptic density (PSD95), brain derived neurotrophic factor (BDNF), and glutamate receptor subunit-1 (GluA1) in the prefrontal cortex was restored by LAT. LAT showed robust anti-inflammatory activity and can lessen the increase in IL-6 and TNF-α caused by CSDS. CSDS altered the gut microbiota at the taxonomic level, resulting in significant changes in α- and β-diversity. LAT treatment reestablished the bacterial abundance and diversity and increased the production of butyric acid in the gut that was inhibited by CSDS. The levels of butyric acid were negatively correlated with the abundance of Bacteroidetes, and positively correlated with those of Proteobacteria and Firmicutes across all treatment groups. Conclusions: The current data suggest that, similar to fluoxetine, LAT show antidepressant-like effects in mice exposed to CSDS through the modulation of the gut-brain axis. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Psychopharmacology is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1007/s00213-023-06413-8 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 13 StartPage: 1775 Subjects: – SubjectFull: Social defeat Type: general – SubjectFull: Brain-derived neurotrophic factor Type: general – SubjectFull: Serotonin uptake inhibitors Type: general – SubjectFull: Postsynaptic density protein Type: general – SubjectFull: Animal social behavior Type: general – SubjectFull: Butyric acid Type: general – SubjectFull: Glutamate receptors Type: general Titles: – TitleFull: Isoalantolactone relieves depression-like behaviors in mice after chronic social defeat stress via the gut-brain axis. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Wang, Siming – PersonEntity: Name: NameFull: Cai, Qihan – PersonEntity: Name: NameFull: Xu, Lu – PersonEntity: Name: NameFull: Sun, Yanan – PersonEntity: Name: NameFull: Wang, Mengmeng – PersonEntity: Name: NameFull: Wang, Yu – PersonEntity: Name: NameFull: Zhang, Lili – PersonEntity: Name: NameFull: Li, Keqing – PersonEntity: Name: NameFull: Ni, Zhiyu IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 08 Text: Aug2023 Type: published Y: 2023 Identifiers: – Type: issn-print Value: 00333158 Numbering: – Type: volume Value: 240 – Type: issue Value: 8 Titles: – TitleFull: Psychopharmacology Type: main |
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