Protective effect of Pai-Nong-San against AOM/DSS-induced CAC in mice through inhibiting the Wnt signaling pathway

Pai-Nong-San (PNS), a prescription of traditional Chinese medicine, has been used for years to treat abscessation-induced diseases including colitis and colorectal cancer. This study was aimed to investigate the preventive effects and possible protective mechanism of PNS on a colitis-associated colo...

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Veröffentlicht in:Chinese journal of natural medicines 2021-12, Vol.19 (12), p.912-920
Hauptverfasser: ZHANG, Meng-Meng, YIN, Deng-Ke, RUI, Xue-Lin, SHAO, Fu-Ping, LI, Jia-Cheng, XU, Li, YANG, Ye
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container_issue 12
container_start_page 912
container_title Chinese journal of natural medicines
container_volume 19
creator ZHANG, Meng-Meng
YIN, Deng-Ke
RUI, Xue-Lin
SHAO, Fu-Ping
LI, Jia-Cheng
XU, Li
YANG, Ye
description Pai-Nong-San (PNS), a prescription of traditional Chinese medicine, has been used for years to treat abscessation-induced diseases including colitis and colorectal cancer. This study was aimed to investigate the preventive effects and possible protective mechanism of PNS on a colitis-associated colorectal cancer (CAC) mouse model induced by azoxymethane (AOM)/dextran sodium sulfate (DSS). The macroscopic and histopathologic examinations of colon injury and DAI score were observed. The inflammatory indicators of intestinal immunity were determined by immunohistochemistry and immunofluorescence. The high throughput 16S rRNA sequence of gut microbiota in the feces of mice was performed. Western blot was used to investigate the protein expression of the Wnt signaling pathway in colon tissues. PNS improved colon injury, as manifested by the alleviation of hematochezia, decreased DAI score, increased colon length, and reversal of pathological changes. PNS treatment protected against AOM/DSS-induced colon inflammation by regulating the expression of CD4+ and CD8+ T cells, inhibiting the production of HIF-α, IL-6, and TNF-α, and promoting the expression of IL-4 and IFN-γ in colon tissues. Meanwhile, PNS improved the components of gut microbiota, as measured by the adjusted levels of Firmicutes, Bacteroidetes, Proteobacteria, and Lactobacillus. PNS down-regulated the protein expression of p-GSK-3β, β-catenin, and c-Myc, while up-regulating the GSK-3β and p-β-catenin in colon tissues of CAC mice. In conclusion, our results suggested that PNS exhibits protective effect on AOM/DSS-induced colon injury and alleviates the development of CAC through suppressing inflammation, improving gut microbiota, and inhibiting the Wnt signaling pathway.
doi_str_mv 10.1016/S1875-5364(22)60143-2
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This study was aimed to investigate the preventive effects and possible protective mechanism of PNS on a colitis-associated colorectal cancer (CAC) mouse model induced by azoxymethane (AOM)/dextran sodium sulfate (DSS). The macroscopic and histopathologic examinations of colon injury and DAI score were observed. The inflammatory indicators of intestinal immunity were determined by immunohistochemistry and immunofluorescence. The high throughput 16S rRNA sequence of gut microbiota in the feces of mice was performed. Western blot was used to investigate the protein expression of the Wnt signaling pathway in colon tissues. PNS improved colon injury, as manifested by the alleviation of hematochezia, decreased DAI score, increased colon length, and reversal of pathological changes. PNS treatment protected against AOM/DSS-induced colon inflammation by regulating the expression of CD4+ and CD8+ T cells, inhibiting the production of HIF-α, IL-6, and TNF-α, and promoting the expression of IL-4 and IFN-γ in colon tissues. Meanwhile, PNS improved the components of gut microbiota, as measured by the adjusted levels of Firmicutes, Bacteroidetes, Proteobacteria, and Lactobacillus. PNS down-regulated the protein expression of p-GSK-3β, β-catenin, and c-Myc, while up-regulating the GSK-3β and p-β-catenin in colon tissues of CAC mice. In conclusion, our results suggested that PNS exhibits protective effect on AOM/DSS-induced colon injury and alleviates the development of CAC through suppressing inflammation, improving gut microbiota, and inhibiting the Wnt signaling pathway.</description><identifier>ISSN: 1875-5364</identifier><identifier>EISSN: 1875-5364</identifier><identifier>DOI: 10.1016/S1875-5364(22)60143-2</identifier><identifier>PMID: 34961589</identifier><language>eng</language><publisher>China: Elsevier B.V</publisher><subject>Animals ; AOM-DSS ; Azoxymethane - toxicity ; CAC ; CD8-Positive T-Lymphocytes ; Colitis - chemically induced ; Colitis - drug therapy ; Colitis - genetics ; Dextran Sulfate - toxicity ; Disease Models, Animal ; Drugs, Chinese Herbal - pharmacology ; Glycogen Synthase Kinase 3 beta ; Gut microbiota ; Mice ; Mice, Inbred C57BL ; Pai-Nong-San ; RNA, Ribosomal, 16S ; Wnt signaling pathway ; Wnt Signaling Pathway - drug effects</subject><ispartof>Chinese journal of natural medicines, 2021-12, Vol.19 (12), p.912-920</ispartof><rights>2021 China Pharmaceutical University</rights><rights>Copyright © 2021 China Pharmaceutical University. 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This study was aimed to investigate the preventive effects and possible protective mechanism of PNS on a colitis-associated colorectal cancer (CAC) mouse model induced by azoxymethane (AOM)/dextran sodium sulfate (DSS). The macroscopic and histopathologic examinations of colon injury and DAI score were observed. The inflammatory indicators of intestinal immunity were determined by immunohistochemistry and immunofluorescence. The high throughput 16S rRNA sequence of gut microbiota in the feces of mice was performed. Western blot was used to investigate the protein expression of the Wnt signaling pathway in colon tissues. PNS improved colon injury, as manifested by the alleviation of hematochezia, decreased DAI score, increased colon length, and reversal of pathological changes. PNS treatment protected against AOM/DSS-induced colon inflammation by regulating the expression of CD4+ and CD8+ T cells, inhibiting the production of HIF-α, IL-6, and TNF-α, and promoting the expression of IL-4 and IFN-γ in colon tissues. Meanwhile, PNS improved the components of gut microbiota, as measured by the adjusted levels of Firmicutes, Bacteroidetes, Proteobacteria, and Lactobacillus. PNS down-regulated the protein expression of p-GSK-3β, β-catenin, and c-Myc, while up-regulating the GSK-3β and p-β-catenin in colon tissues of CAC mice. In conclusion, our results suggested that PNS exhibits protective effect on AOM/DSS-induced colon injury and alleviates the development of CAC through suppressing inflammation, improving gut microbiota, and inhibiting the Wnt signaling pathway.</description><subject>Animals</subject><subject>AOM-DSS</subject><subject>Azoxymethane - toxicity</subject><subject>CAC</subject><subject>CD8-Positive T-Lymphocytes</subject><subject>Colitis - chemically induced</subject><subject>Colitis - drug therapy</subject><subject>Colitis - genetics</subject><subject>Dextran Sulfate - toxicity</subject><subject>Disease Models, Animal</subject><subject>Drugs, Chinese Herbal - pharmacology</subject><subject>Glycogen Synthase Kinase 3 beta</subject><subject>Gut microbiota</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Pai-Nong-San</subject><subject>RNA, Ribosomal, 16S</subject><subject>Wnt signaling pathway</subject><subject>Wnt Signaling Pathway - drug effects</subject><issn>1875-5364</issn><issn>1875-5364</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1rGzEQhkVJaUyan9CiY3LYZkeytOtTMc5HA24ScEuPQtLOrlVsrStpE_LvI8eO6S1iQKOXd2Y0DyFfoPwGJciLBdSVKASX4zPGzmUJY16wD2R0kI_-y4_JaYx_y3ykAA7yEznm44kEUU9GJDyEPqFN7hEptm3OaN_SB-2Ku953xUJ7qjvtfEx0ev_z4nKxKJxvBosNnU1n1Hm6dhZpWoZ-6Jb5vXTGJee7LCH94xONrvN6tVU2Oi2f9PNn8rHVq4in-_uE_L6--jX7Uczvb25n03lhuRSpqFDUDCrT2opxy8DqCqw0ORgTDa-MRuT5w40YCyOMhFqWpmmATywalCU_IWe7vpvQ_xswJrV20eJqpT32Q1QsIwAoZQ3ZKnZWG_oYA7ZqE9xah2cFpdoSV6_E1RanYky9Elcs133djxjMGptD1RvfbPi-M2Be9NFhUNE69BmfC5m1anr3zogXvCGQUA</recordid><startdate>202112</startdate><enddate>202112</enddate><creator>ZHANG, Meng-Meng</creator><creator>YIN, Deng-Ke</creator><creator>RUI, Xue-Lin</creator><creator>SHAO, Fu-Ping</creator><creator>LI, Jia-Cheng</creator><creator>XU, Li</creator><creator>YANG, Ye</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202112</creationdate><title>Protective effect of Pai-Nong-San against AOM/DSS-induced CAC in mice through inhibiting the Wnt signaling pathway</title><author>ZHANG, Meng-Meng ; YIN, Deng-Ke ; RUI, Xue-Lin ; SHAO, Fu-Ping ; LI, Jia-Cheng ; XU, Li ; YANG, Ye</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-7e58217bfc723c21ca71c6bc6b225d37baee3fecd545b5b61860bdd139cebe603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>AOM-DSS</topic><topic>Azoxymethane - toxicity</topic><topic>CAC</topic><topic>CD8-Positive T-Lymphocytes</topic><topic>Colitis - chemically induced</topic><topic>Colitis - drug therapy</topic><topic>Colitis - genetics</topic><topic>Dextran Sulfate - toxicity</topic><topic>Disease Models, Animal</topic><topic>Drugs, Chinese Herbal - pharmacology</topic><topic>Glycogen Synthase Kinase 3 beta</topic><topic>Gut microbiota</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Pai-Nong-San</topic><topic>RNA, Ribosomal, 16S</topic><topic>Wnt signaling pathway</topic><topic>Wnt Signaling Pathway - drug effects</topic><toplevel>online_resources</toplevel><creatorcontrib>ZHANG, Meng-Meng</creatorcontrib><creatorcontrib>YIN, Deng-Ke</creatorcontrib><creatorcontrib>RUI, Xue-Lin</creatorcontrib><creatorcontrib>SHAO, Fu-Ping</creatorcontrib><creatorcontrib>LI, Jia-Cheng</creatorcontrib><creatorcontrib>XU, Li</creatorcontrib><creatorcontrib>YANG, Ye</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Chinese journal of natural medicines</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ZHANG, Meng-Meng</au><au>YIN, Deng-Ke</au><au>RUI, Xue-Lin</au><au>SHAO, Fu-Ping</au><au>LI, Jia-Cheng</au><au>XU, Li</au><au>YANG, Ye</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protective effect of Pai-Nong-San against AOM/DSS-induced CAC in mice through inhibiting the Wnt signaling pathway</atitle><jtitle>Chinese journal of natural medicines</jtitle><addtitle>Chin J Nat Med</addtitle><date>2021-12</date><risdate>2021</risdate><volume>19</volume><issue>12</issue><spage>912</spage><epage>920</epage><pages>912-920</pages><issn>1875-5364</issn><eissn>1875-5364</eissn><abstract>Pai-Nong-San (PNS), a prescription of traditional Chinese medicine, has been used for years to treat abscessation-induced diseases including colitis and colorectal cancer. This study was aimed to investigate the preventive effects and possible protective mechanism of PNS on a colitis-associated colorectal cancer (CAC) mouse model induced by azoxymethane (AOM)/dextran sodium sulfate (DSS). The macroscopic and histopathologic examinations of colon injury and DAI score were observed. The inflammatory indicators of intestinal immunity were determined by immunohistochemistry and immunofluorescence. The high throughput 16S rRNA sequence of gut microbiota in the feces of mice was performed. Western blot was used to investigate the protein expression of the Wnt signaling pathway in colon tissues. PNS improved colon injury, as manifested by the alleviation of hematochezia, decreased DAI score, increased colon length, and reversal of pathological changes. PNS treatment protected against AOM/DSS-induced colon inflammation by regulating the expression of CD4+ and CD8+ T cells, inhibiting the production of HIF-α, IL-6, and TNF-α, and promoting the expression of IL-4 and IFN-γ in colon tissues. Meanwhile, PNS improved the components of gut microbiota, as measured by the adjusted levels of Firmicutes, Bacteroidetes, Proteobacteria, and Lactobacillus. PNS down-regulated the protein expression of p-GSK-3β, β-catenin, and c-Myc, while up-regulating the GSK-3β and p-β-catenin in colon tissues of CAC mice. In conclusion, our results suggested that PNS exhibits protective effect on AOM/DSS-induced colon injury and alleviates the development of CAC through suppressing inflammation, improving gut microbiota, and inhibiting the Wnt signaling pathway.</abstract><cop>China</cop><pub>Elsevier B.V</pub><pmid>34961589</pmid><doi>10.1016/S1875-5364(22)60143-2</doi><tpages>9</tpages></addata></record>
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source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Animals
AOM-DSS
Azoxymethane - toxicity
CAC
CD8-Positive T-Lymphocytes
Colitis - chemically induced
Colitis - drug therapy
Colitis - genetics
Dextran Sulfate - toxicity
Disease Models, Animal
Drugs, Chinese Herbal - pharmacology
Glycogen Synthase Kinase 3 beta
Gut microbiota
Mice
Mice, Inbred C57BL
Pai-Nong-San
RNA, Ribosomal, 16S
Wnt signaling pathway
Wnt Signaling Pathway - drug effects
title Protective effect of Pai-Nong-San against AOM/DSS-induced CAC in mice through inhibiting the Wnt signaling pathway
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