Absorption of Codonopsis pilosula Saponins by Coexisting Polysaccharides Alleviates Gut Microbial Dysbiosis with Dextran Sulfate Sodium-Induced Colitis in Model Mice

Objectives. Inflammatory Bowel Disease (IBD) is an autoimmune disease, and the gut microbiota has become a new therapeutic target. Herbal medicine (HM) has shown good efficacy in the clinical treatment of IBD; however, the synergistic actions of the dominant chemicals in HM decoctions are unclear. M...

Full description

Bibliographic Details
Main Authors: Yaping Jing, Anping Li, Zhirong Liu, Pingrong Yang, Junshu Wei, Xinjun Chen, Tang Zhao, Yanrui Bai, Lajia Zha, Chunjiang Zhang
Format: Article
Language:English
Published: Hindawi Limited 2018-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2018/1781036
id doaj-2ae883b69a714dad866f0c11f599477c
record_format Article
spelling doaj-2ae883b69a714dad866f0c11f599477c2020-11-25T00:46:35ZengHindawi LimitedBioMed Research International2314-61332314-61412018-01-01201810.1155/2018/17810361781036Absorption of Codonopsis pilosula Saponins by Coexisting Polysaccharides Alleviates Gut Microbial Dysbiosis with Dextran Sulfate Sodium-Induced Colitis in Model MiceYaping Jing0Anping Li1Zhirong Liu2Pingrong Yang3Junshu Wei4Xinjun Chen5Tang Zhao6Yanrui Bai7Lajia Zha8Chunjiang Zhang9School of Life Sciences, Lanzhou University, Lanzhou 730000, ChinaGansu Institute of Drug Control, Lanzhou 730030, ChinaGansu Institute of Drug Control, Lanzhou 730030, ChinaGansu Institute of Drug Control, Lanzhou 730030, ChinaSchool of Life Sciences, Lanzhou University, Lanzhou 730000, ChinaSchool of Life Sciences, Lanzhou University, Lanzhou 730000, ChinaSchool of Life Sciences, Lanzhou University, Lanzhou 730000, ChinaSchool of Life Sciences, Lanzhou University, Lanzhou 730000, ChinaSchool of Life Sciences, Lanzhou University, Lanzhou 730000, ChinaSchool of Life Sciences, Lanzhou University, Lanzhou 730000, ChinaObjectives. Inflammatory Bowel Disease (IBD) is an autoimmune disease, and the gut microbiota has become a new therapeutic target. Herbal medicine (HM) has shown good efficacy in the clinical treatment of IBD; however, the synergistic actions of the dominant chemicals in HM decoctions are unclear. Methods. In this study, we explored whether the complicated interconnections between HM and the gut microbiota could allow crosstalk between HM ingredients. Saponins and polysaccharides, i.e., the dominant chemicals in the Codonopsis pilosula Nannf (CPN) decoction, were investigated in a dextran sulfate sodium- (DSS-) induced mouse model. Bacterial 16S rRNA sequencing analyzed the change of gut microbiota structure and diversity. Gas chromatography (GC) determined the content of short-chain fatty acids (SCFAs) in feces. ELISA detected the expression of proinflammatory and anti-inflammatory cytokines associated with TH17/Treg balance. UPLC-QTOF-MS technology combined with PKsolver software analyzed the absorption of the highest exposure for monomeric compounds of CPN saponins in serum. The results indicated that CPN polysaccharides showed prebiotic-like effects in mice with DSS-induced colitis by simultaneously stimulating the growth of three important probiotics, i.e., Bifidobacterium spp., Lactobacillus spp., and Akkermansia spp., and inhibiting the growth of pathogenic bacteria, including Desulfovibrio spp., Alistipes spp., and Helicobacter spp. Moreover, CPN polysaccharides improved intestinal metabolism, enhanced the production of short-chain fatty acids, upregulated the expression of anti-inflammatory cytokines and downregulated the secretion of proinflammatory cytokines correlated with Th17/Treg balance, promoted the absorption of certain CPN saponins in the serum, and stimulated recovery of the holistic gut microbiota. Conclusion. CPN polysaccharides have the good prebiotic properties and shown good application prospects in the prevention and treatment of acute colitis. These findings provide insights into the specific bacteria responsible for active, inactive biotransformation of HM ingredients and those that are altered by HM administration.http://dx.doi.org/10.1155/2018/1781036
collection DOAJ
language English
format Article
sources DOAJ
author Yaping Jing
Anping Li
Zhirong Liu
Pingrong Yang
Junshu Wei
Xinjun Chen
Tang Zhao
Yanrui Bai
Lajia Zha
Chunjiang Zhang
spellingShingle Yaping Jing
Anping Li
Zhirong Liu
Pingrong Yang
Junshu Wei
Xinjun Chen
Tang Zhao
Yanrui Bai
Lajia Zha
Chunjiang Zhang
Absorption of Codonopsis pilosula Saponins by Coexisting Polysaccharides Alleviates Gut Microbial Dysbiosis with Dextran Sulfate Sodium-Induced Colitis in Model Mice
BioMed Research International
author_facet Yaping Jing
Anping Li
Zhirong Liu
Pingrong Yang
Junshu Wei
Xinjun Chen
Tang Zhao
Yanrui Bai
Lajia Zha
Chunjiang Zhang
author_sort Yaping Jing
title Absorption of Codonopsis pilosula Saponins by Coexisting Polysaccharides Alleviates Gut Microbial Dysbiosis with Dextran Sulfate Sodium-Induced Colitis in Model Mice
title_short Absorption of Codonopsis pilosula Saponins by Coexisting Polysaccharides Alleviates Gut Microbial Dysbiosis with Dextran Sulfate Sodium-Induced Colitis in Model Mice
title_full Absorption of Codonopsis pilosula Saponins by Coexisting Polysaccharides Alleviates Gut Microbial Dysbiosis with Dextran Sulfate Sodium-Induced Colitis in Model Mice
title_fullStr Absorption of Codonopsis pilosula Saponins by Coexisting Polysaccharides Alleviates Gut Microbial Dysbiosis with Dextran Sulfate Sodium-Induced Colitis in Model Mice
title_full_unstemmed Absorption of Codonopsis pilosula Saponins by Coexisting Polysaccharides Alleviates Gut Microbial Dysbiosis with Dextran Sulfate Sodium-Induced Colitis in Model Mice
title_sort absorption of codonopsis pilosula saponins by coexisting polysaccharides alleviates gut microbial dysbiosis with dextran sulfate sodium-induced colitis in model mice
publisher Hindawi Limited
series BioMed Research International
issn 2314-6133
2314-6141
publishDate 2018-01-01
description Objectives. Inflammatory Bowel Disease (IBD) is an autoimmune disease, and the gut microbiota has become a new therapeutic target. Herbal medicine (HM) has shown good efficacy in the clinical treatment of IBD; however, the synergistic actions of the dominant chemicals in HM decoctions are unclear. Methods. In this study, we explored whether the complicated interconnections between HM and the gut microbiota could allow crosstalk between HM ingredients. Saponins and polysaccharides, i.e., the dominant chemicals in the Codonopsis pilosula Nannf (CPN) decoction, were investigated in a dextran sulfate sodium- (DSS-) induced mouse model. Bacterial 16S rRNA sequencing analyzed the change of gut microbiota structure and diversity. Gas chromatography (GC) determined the content of short-chain fatty acids (SCFAs) in feces. ELISA detected the expression of proinflammatory and anti-inflammatory cytokines associated with TH17/Treg balance. UPLC-QTOF-MS technology combined with PKsolver software analyzed the absorption of the highest exposure for monomeric compounds of CPN saponins in serum. The results indicated that CPN polysaccharides showed prebiotic-like effects in mice with DSS-induced colitis by simultaneously stimulating the growth of three important probiotics, i.e., Bifidobacterium spp., Lactobacillus spp., and Akkermansia spp., and inhibiting the growth of pathogenic bacteria, including Desulfovibrio spp., Alistipes spp., and Helicobacter spp. Moreover, CPN polysaccharides improved intestinal metabolism, enhanced the production of short-chain fatty acids, upregulated the expression of anti-inflammatory cytokines and downregulated the secretion of proinflammatory cytokines correlated with Th17/Treg balance, promoted the absorption of certain CPN saponins in the serum, and stimulated recovery of the holistic gut microbiota. Conclusion. CPN polysaccharides have the good prebiotic properties and shown good application prospects in the prevention and treatment of acute colitis. These findings provide insights into the specific bacteria responsible for active, inactive biotransformation of HM ingredients and those that are altered by HM administration.
url http://dx.doi.org/10.1155/2018/1781036
work_keys_str_mv AT yapingjing absorptionofcodonopsispilosulasaponinsbycoexistingpolysaccharidesalleviatesgutmicrobialdysbiosiswithdextransulfatesodiuminducedcolitisinmodelmice
AT anpingli absorptionofcodonopsispilosulasaponinsbycoexistingpolysaccharidesalleviatesgutmicrobialdysbiosiswithdextransulfatesodiuminducedcolitisinmodelmice
AT zhirongliu absorptionofcodonopsispilosulasaponinsbycoexistingpolysaccharidesalleviatesgutmicrobialdysbiosiswithdextransulfatesodiuminducedcolitisinmodelmice
AT pingrongyang absorptionofcodonopsispilosulasaponinsbycoexistingpolysaccharidesalleviatesgutmicrobialdysbiosiswithdextransulfatesodiuminducedcolitisinmodelmice
AT junshuwei absorptionofcodonopsispilosulasaponinsbycoexistingpolysaccharidesalleviatesgutmicrobialdysbiosiswithdextransulfatesodiuminducedcolitisinmodelmice
AT xinjunchen absorptionofcodonopsispilosulasaponinsbycoexistingpolysaccharidesalleviatesgutmicrobialdysbiosiswithdextransulfatesodiuminducedcolitisinmodelmice
AT tangzhao absorptionofcodonopsispilosulasaponinsbycoexistingpolysaccharidesalleviatesgutmicrobialdysbiosiswithdextransulfatesodiuminducedcolitisinmodelmice
AT yanruibai absorptionofcodonopsispilosulasaponinsbycoexistingpolysaccharidesalleviatesgutmicrobialdysbiosiswithdextransulfatesodiuminducedcolitisinmodelmice
AT lajiazha absorptionofcodonopsispilosulasaponinsbycoexistingpolysaccharidesalleviatesgutmicrobialdysbiosiswithdextransulfatesodiuminducedcolitisinmodelmice
AT chunjiangzhang absorptionofcodonopsispilosulasaponinsbycoexistingpolysaccharidesalleviatesgutmicrobialdysbiosiswithdextransulfatesodiuminducedcolitisinmodelmice
_version_ 1725264355622125568