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The Lignan-Rich Fraction from Sambucus williamsii Hance Exerts Bone Protective Effects via Altering Circulating Serotonin and Gut Microbiota in Rats
Our previous study revealed that the bone anabolic effects of the lignan-rich fraction (SWCA) from Sambucus williamsii Hance was involved in modulating the metabolism of tryptophan in vivo and inhibiting serotonin (5-HT) synthesis in vitro. This study aimed to determine how SWCA modulates bone metab...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9692752/ https://www.ncbi.nlm.nih.gov/pubmed/36432403 http://dx.doi.org/10.3390/nu14224718 |
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author | Xiao, Hui-Hui Zhu, Yu-Xin Lu, Lu Zhou, Li-Ping Poon, Christina Chui-Wa Chan, Chi-On Wang, Li-Jing Cao, Sisi Yu, Wen-Xuan Wong, Ka-Ying Mok, Daniel Kam-Wah Wong, Man-Sau |
author_facet | Xiao, Hui-Hui Zhu, Yu-Xin Lu, Lu Zhou, Li-Ping Poon, Christina Chui-Wa Chan, Chi-On Wang, Li-Jing Cao, Sisi Yu, Wen-Xuan Wong, Ka-Ying Mok, Daniel Kam-Wah Wong, Man-Sau |
author_sort | Xiao, Hui-Hui |
collection | PubMed |
description | Our previous study revealed that the bone anabolic effects of the lignan-rich fraction (SWCA) from Sambucus williamsii Hance was involved in modulating the metabolism of tryptophan in vivo and inhibiting serotonin (5-HT) synthesis in vitro. This study aimed to determine how SWCA modulates bone metabolism via serotonin in vivo. The effects of SWCA were evaluated by using 4-month-old Sprague-Dawley (SD) ovariectomized rats. The serum levels of 5-HT and kynurenine, the protein expressions of tryptophan hydroxylase 1 (TPH-1) and TPH-2, the genes and proteins related to the 5-HT signaling pathway as well as gut microbiota composition were determined. SWCA treatment alleviated bone loss and decreased serum levels of serotonin, which was negatively related to bone mineral density (BMD) in rats. It suppressed the protein expression of TPH-1 in the colon, and reversed the gene and protein expressions of FOXO1 and ATF4 in the femur in OVX rats, while it did not affect the TPH-2 protein expression in the cortex. SWCA treatment escalated the relative abundance of Antinobacteria and modulated several genera relating to BMD. These findings verified that the bone protective effects of lignans were mediated by serotonin, and provided evidence that lignans might be a good source of TPH-1 inhibitors. |
format | Online Article Text |
id | pubmed-9692752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96927522022-11-26 The Lignan-Rich Fraction from Sambucus williamsii Hance Exerts Bone Protective Effects via Altering Circulating Serotonin and Gut Microbiota in Rats Xiao, Hui-Hui Zhu, Yu-Xin Lu, Lu Zhou, Li-Ping Poon, Christina Chui-Wa Chan, Chi-On Wang, Li-Jing Cao, Sisi Yu, Wen-Xuan Wong, Ka-Ying Mok, Daniel Kam-Wah Wong, Man-Sau Nutrients Article Our previous study revealed that the bone anabolic effects of the lignan-rich fraction (SWCA) from Sambucus williamsii Hance was involved in modulating the metabolism of tryptophan in vivo and inhibiting serotonin (5-HT) synthesis in vitro. This study aimed to determine how SWCA modulates bone metabolism via serotonin in vivo. The effects of SWCA were evaluated by using 4-month-old Sprague-Dawley (SD) ovariectomized rats. The serum levels of 5-HT and kynurenine, the protein expressions of tryptophan hydroxylase 1 (TPH-1) and TPH-2, the genes and proteins related to the 5-HT signaling pathway as well as gut microbiota composition were determined. SWCA treatment alleviated bone loss and decreased serum levels of serotonin, which was negatively related to bone mineral density (BMD) in rats. It suppressed the protein expression of TPH-1 in the colon, and reversed the gene and protein expressions of FOXO1 and ATF4 in the femur in OVX rats, while it did not affect the TPH-2 protein expression in the cortex. SWCA treatment escalated the relative abundance of Antinobacteria and modulated several genera relating to BMD. These findings verified that the bone protective effects of lignans were mediated by serotonin, and provided evidence that lignans might be a good source of TPH-1 inhibitors. MDPI 2022-11-08 /pmc/articles/PMC9692752/ /pubmed/36432403 http://dx.doi.org/10.3390/nu14224718 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Xiao, Hui-Hui Zhu, Yu-Xin Lu, Lu Zhou, Li-Ping Poon, Christina Chui-Wa Chan, Chi-On Wang, Li-Jing Cao, Sisi Yu, Wen-Xuan Wong, Ka-Ying Mok, Daniel Kam-Wah Wong, Man-Sau The Lignan-Rich Fraction from Sambucus williamsii Hance Exerts Bone Protective Effects via Altering Circulating Serotonin and Gut Microbiota in Rats |
title | The Lignan-Rich Fraction from Sambucus williamsii Hance Exerts Bone Protective Effects via Altering Circulating Serotonin and Gut Microbiota in Rats |
title_full | The Lignan-Rich Fraction from Sambucus williamsii Hance Exerts Bone Protective Effects via Altering Circulating Serotonin and Gut Microbiota in Rats |
title_fullStr | The Lignan-Rich Fraction from Sambucus williamsii Hance Exerts Bone Protective Effects via Altering Circulating Serotonin and Gut Microbiota in Rats |
title_full_unstemmed | The Lignan-Rich Fraction from Sambucus williamsii Hance Exerts Bone Protective Effects via Altering Circulating Serotonin and Gut Microbiota in Rats |
title_short | The Lignan-Rich Fraction from Sambucus williamsii Hance Exerts Bone Protective Effects via Altering Circulating Serotonin and Gut Microbiota in Rats |
title_sort | lignan-rich fraction from sambucus williamsii hance exerts bone protective effects via altering circulating serotonin and gut microbiota in rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9692752/ https://www.ncbi.nlm.nih.gov/pubmed/36432403 http://dx.doi.org/10.3390/nu14224718 |
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