Modulating effects of Astragalus polysaccharide on immune disorders via gut microbiota and the TLR4/NF-κB pathway in rats with syndrome of dampness stagnancy due to spleen deficiency
The syndrome of dampness stagnancy due to spleen deficiency (DSSD) is relatively common globally. Although the pathogenesis of DSSD remains unclear, evidence has suggested that the gut microbiota might play a significant role. Radix Astragali , used as both medicine and food, exerts the effects of t...
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Published in | Journal of Zhejiang University. B. Science Vol. 24; no. 7; pp. 650 - 662 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hangzhou
Zhejiang University Press
01.07.2023
Springer Nature B.V School of Nursing,Shandong University of Traditional Chinese Medicine,Jinan 250355,China%College of Traditional Chinese Medicine,Shandong Co-Innovation Center of Classic Traditional Chinese Medicine Formula,Shandong University of Traditional Chinese Medicine,Jinan 250355,China%School of Pharmaceutical Sciences,Cheeloo College of Medicine,Shandong University,Jinan 250012,China |
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Abstract | The syndrome of dampness stagnancy due to spleen deficiency (DSSD) is relatively common globally. Although the pathogenesis of DSSD remains unclear, evidence has suggested that the gut microbiota might play a significant role.
Radix Astragali
, used as both medicine and food, exerts the effects of tonifying spleen and qi.
Astragalus
polysaccharide (APS) comprises a macromolecule substance extracted from the dried root of
Radix Astragali
, which has many pharmacological functions. However, whether APS mitigates the immune disorders underlying the DSSD syndrome via regulating gut microbiota and the relevant mechanism remains unknown. Here, we used DSSD rats induced by high-fat and low-protein (HFLP) diet plus exhaustive swimming, and found that APS of moderate molecular weight increased the body weight gain and immune organ indexes, decreased the levels of interleukin-1β (IL-1β), IL-6, and endotoxin, and suppressed the Toll-like receptor 4/nuclear factor-κB (TLR4/NF-κB) pathway. Moreover, a total of 27 critical genera were significantly enriched according to the linear discriminant analysis effect size (LEfSe). APS increased the diversity of the gut microbiota and changed its composition, such as reducing the relative abundance of
Pseudoflavonifractor
and
Paraprevotella
, and increasing that of
Parasutterella
,
Parabacteroides
,
Clostridium XIVb
,
Oscillibacter
,
Butyricicoccus
, and
Dorea
. APS also elevated the contents of short-chain fatty acids (SCFAs). Furthermore, the correlation analysis indicated that 12 critical bacteria were related to the body weight gain and immune organ indexes. In general, our study demonstrated that APS ameliorated the immune disorders in DSSD rats via modulating their gut microbiota, especially for some bacteria involving immune and inflammatory response and SCFA production, as well as the TLR4/NF-κB pathway. This study provides an insight into the function of APS as a unique potential prebiotic through exerting systemic activities in treating DSSD. |
---|---|
AbstractList | The syndrome of dampness stagnancy due to spleen deficiency (DSSD) is relatively common globally. Although the pathogenesis of DSSD remains unclear, evidence has suggested that the gut microbiota might play a significant role.
Radix Astragali
, used as both medicine and food, exerts the effects of tonifying spleen and qi.
Astragalus
polysaccharide (APS) comprises a macromolecule substance extracted from the dried root of
Radix Astragali
, which has many pharmacological functions. However, whether APS mitigates the immune disorders underlying the DSSD syndrome via regulating gut microbiota and the relevant mechanism remains unknown. Here, we used DSSD rats induced by high-fat and low-protein (HFLP) diet plus exhaustive swimming, and found that APS of moderate molecular weight increased the body weight gain and immune organ indexes, decreased the levels of interleukin-1β (IL-1β), IL-6, and endotoxin, and suppressed the Toll-like receptor 4/nuclear factor-κB (TLR4/NF-κB) pathway. Moreover, a total of 27 critical genera were significantly enriched according to the linear discriminant analysis effect size (LEfSe). APS increased the diversity of the gut microbiota and changed its composition, such as reducing the relative abundance of
Pseudoflavonifractor
and
Paraprevotella
, and increasing that of
Parasutterella
,
Parabacteroides
,
Clostridium XIVb
,
Oscillibacter
,
Butyricicoccus
, and
Dorea
. APS also elevated the contents of short-chain fatty acids (SCFAs). Furthermore, the correlation analysis indicated that 12 critical bacteria were related to the body weight gain and immune organ indexes. In general, our study demonstrated that APS ameliorated the immune disorders in DSSD rats via modulating their gut microbiota, especially for some bacteria involving immune and inflammatory response and SCFA production, as well as the TLR4/NF-κB pathway. This study provides an insight into the function of APS as a unique potential prebiotic through exerting systemic activities in treating DSSD. The syndrome of dampness stagnancy due to spleen deficiency (DSSD) is relatively common globally. Although the pathogenesis of DSSD remains unclear, evidence has suggested that the gut microbiota might play a significant role. Radix Astragali, used as both medicine and food, exerts the effects of tonifying spleen and qi. Astragalus polysaccharide (APS) comprises a macromolecule substance extracted from the dried root of Radix Astragali, which has many pharmacological functions. However, whether APS mitigates the immune disorders underlying the DSSD syndrome via regulating gut microbiota and the relevant mechanism remains unknown. Here, we used DSSD rats induced by high-fat and low-protein (HFLP) diet plus exhaustive swimming, and found that APS of moderate molecular weight increased the body weight gain and immune organ indexes, decreased the levels of interleukin-1β (IL-1β), IL-6, and endotoxin, and suppressed the Toll-like receptor 4/nuclear factor-κB (TLR4/NF-κB) pathway. Moreover, a total of 27 critical genera were significantly enriched according to the linear discriminant analysis effect size (LEfSe). APS increased the diversity of the gut microbiota and changed its composition, such as reducing the relative abundance of Pseudoflavonifractor and Paraprevotella, and increasing that of Parasutterella, Parabacteroides, Clostridium XIVb, Oscillibacter, Butyricicoccus, and Dorea. APS also elevated the contents of short-chain fatty acids (SCFAs). Furthermore, the correlation analysis indicated that 12 critical bacteria were related to the body weight gain and immune organ indexes. In general, our study demonstrated that APS ameliorated the immune disorders in DSSD rats via modulating their gut microbiota, especially for some bacteria involving immune and inflammatory response and SCFA production, as well as the TLR4/NF-κB pathway. This study provides an insight into the function of APS as a unique potential prebiotic through exerting systemic activities in treating DSSD. The syndrome of dampness stagnancy due to spleen deficiency (DSSD) is relatively common globally. Although the pathogenesis of DSSD remains unclear, evidence has suggested that the gut microbiota might play a significant role. , used as both medicine and food, exerts the effects of tonifying spleen and qi. polysaccharide (APS) comprises a macromolecule substance extracted from the dried root of , which has many pharmacological functions. However, whether APS mitigates the immune disorders underlying the DSSD syndrome via regulating gut microbiota and the relevant mechanism remains unknown. Here, we used DSSD rats induced by high-fat and low-protein (HFLP) diet plus exhaustive swimming, and found that APS of moderate molecular weight increased the body weight gain and immune organ indexes, decreased the levels of interleukin-1β (IL-1β), IL-6, and endotoxin, and suppressed the Toll-like receptor 4/nuclear factor-κB (TLR4/NF-κB) pathway. Moreover, a total of 27 critical genera were significantly enriched according to the linear discriminant analysis effect size (LEfSe). APS increased the diversity of the gut microbiota and changed its composition, such as reducing the relative abundance of and , and increasing that of , , , , , and . APS also elevated the contents of short-chain fatty acids (SCFAs). Furthermore, the correlation analysis indicated that 12 critical bacteria were related to the body weight gain and immune organ indexes. In general, our study demonstrated that APS ameliorated the immune disorders in DSSD rats via modulating their gut microbiota, especially for some bacteria involving immune and inflammatory response and SCFA production, as well as the TLR4/NF-κB pathway. This study provides an insight into the function of APS as a unique potential prebiotic through exerting systemic activities in treating DSSD. |
Author | Wang, Shijun Zhao, Xuelian Duan, Chenchen Lyu, Qin Lu, Guangying Liu, Xiumei Zhao, Wenxiao Liu, Yanli Zheng, Jun Zhao, Haijun |
AuthorAffiliation | School of Nursing,Shandong University of Traditional Chinese Medicine,Jinan 250355,China%College of Traditional Chinese Medicine,Shandong Co-Innovation Center of Classic Traditional Chinese Medicine Formula,Shandong University of Traditional Chinese Medicine,Jinan 250355,China%School of Pharmaceutical Sciences,Cheeloo College of Medicine,Shandong University,Jinan 250012,China |
AuthorAffiliation_xml | – name: School of Nursing,Shandong University of Traditional Chinese Medicine,Jinan 250355,China%College of Traditional Chinese Medicine,Shandong Co-Innovation Center of Classic Traditional Chinese Medicine Formula,Shandong University of Traditional Chinese Medicine,Jinan 250355,China%School of Pharmaceutical Sciences,Cheeloo College of Medicine,Shandong University,Jinan 250012,China |
Author_xml | – sequence: 1 givenname: Wenxiao orcidid: 0000-0001-7165-5870 surname: Zhao fullname: Zhao, Wenxiao email: zhaowx@sdutcm.edu.cn organization: School of Nursing, Shandong University of Traditional Chinese Medicine – sequence: 2 givenname: Chenchen surname: Duan fullname: Duan, Chenchen organization: School of Nursing, Shandong University of Traditional Chinese Medicine – sequence: 3 givenname: Yanli surname: Liu fullname: Liu, Yanli organization: School of Nursing, Shandong University of Traditional Chinese Medicine – sequence: 4 givenname: Guangying surname: Lu fullname: Lu, Guangying organization: College of Traditional Chinese Medicine, Shandong Co-Innovation Center of Classic Traditional Chinese Medicine Formula, Shandong University of Traditional Chinese Medicine – sequence: 5 givenname: Qin surname: Lyu fullname: Lyu, Qin organization: College of Traditional Chinese Medicine, Shandong Co-Innovation Center of Classic Traditional Chinese Medicine Formula, Shandong University of Traditional Chinese Medicine – sequence: 6 givenname: Xiumei surname: Liu fullname: Liu, Xiumei organization: School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University – sequence: 7 givenname: Jun surname: Zheng fullname: Zheng, Jun organization: School of Nursing, Shandong University of Traditional Chinese Medicine – sequence: 8 givenname: Xuelian surname: Zhao fullname: Zhao, Xuelian organization: School of Nursing, Shandong University of Traditional Chinese Medicine – sequence: 9 givenname: Shijun surname: Wang fullname: Wang, Shijun organization: College of Traditional Chinese Medicine, Shandong Co-Innovation Center of Classic Traditional Chinese Medicine Formula, Shandong University of Traditional Chinese Medicine – sequence: 10 givenname: Haijun orcidid: 0000-0003-0858-7486 surname: Zhao fullname: Zhao, Haijun email: haijunzhao@sdutcm.edu.cn organization: College of Traditional Chinese Medicine, Shandong Co-Innovation Center of Classic Traditional Chinese Medicine Formula, Shandong University of Traditional Chinese Medicine |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37455140$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1007_s12272_024_01489_y crossref_primary_10_1016_j_biopha_2024_116350 crossref_primary_10_1631_jzus_B2310001 crossref_primary_10_3390_encyclopedia4010014 crossref_primary_10_3389_fphar_2024_1356324 crossref_primary_10_1007_s00018_024_05332_x crossref_primary_10_1039_D3FO02110F crossref_primary_10_3389_fimmu_2024_1369110 crossref_primary_10_3389_fphar_2024_1336122 |
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DocumentTitleAlternate | 黄芪多糖通过肠道菌群和TLR4/NF-κB途径对脾虚水湿不化大鼠免疫功能紊乱的调节作用 |
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Keywords | Gut microbiota Toll-like receptor 4/nuclear factor-κB (TLR4/NF-κB) pathway 黄芪多糖 polysaccharide Immune disorder TLR4/NF-κB通路 短链脂肪酸 Short-chain fatty acid Dampness stagnancy due to spleen deficiency 免疫功能紊乱 肠道菌群 脾虚水湿不化 Astragalus polysaccharide Toll-like receptor 4/nuclear factor-κB(TLR4/NF-κB)pathway |
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Notes | Haijun ZHAO, https://orcid.org/0000-0003-0858-7486 Wenxiao ZHAO, https://orcid.org/0000-0001-7165-5870 |
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Publisher | Zhejiang University Press Springer Nature B.V School of Nursing,Shandong University of Traditional Chinese Medicine,Jinan 250355,China%College of Traditional Chinese Medicine,Shandong Co-Innovation Center of Classic Traditional Chinese Medicine Formula,Shandong University of Traditional Chinese Medicine,Jinan 250355,China%School of Pharmaceutical Sciences,Cheeloo College of Medicine,Shandong University,Jinan 250012,China |
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Snippet | The syndrome of dampness stagnancy due to spleen deficiency (DSSD) is relatively common globally. Although the pathogenesis of DSSD remains unclear, evidence... The syndrome of dampness stagnancy due to spleen deficiency(DSSD)is relatively common globally.Although the pathogenesis of DSSD remains unclear,evidence has... |
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SubjectTerms | Animals Astragalus Plant - metabolism Bacteria Biomedical and Life Sciences Biomedicine Body Weight Body weight gain Correlation analysis Discriminant analysis Disorders Endotoxins Fatty acids Gastrointestinal Microbiome High fat diet High protein diet Immune System Diseases - drug therapy Inflammation Inflammatory response Interleukin 6 Intestinal microflora Low fat diet Low protein diet Microbiota Microorganisms Moisture content Molecular weight NF-kappa B - metabolism NF-κB protein Nutrient deficiency Pathogenesis Polysaccharides Polysaccharides - pharmacology Rats Relative abundance Research Article Spleen Swimming TLR4 protein Toll-Like Receptor 4 Toll-like receptors Traditional Chinese medicine |
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Title | Modulating effects of Astragalus polysaccharide on immune disorders via gut microbiota and the TLR4/NF-κB pathway in rats with syndrome of dampness stagnancy due to spleen deficiency |
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