Chuanxiong Renshen Decoction Inhibits Alzheimer's Disease Neuroinflammation by Regulating PPAR[gamma]/NF-[kappa]B Pathway
Background and Aim: Previous studies of our research group have shown that Chuanxiong Renshen Decoction (CRD) has the effect of treating AD, but the exact mechanism of its effect is still not clarified. The aim of this study was to investigate the effect and mechanism of CRD on AD neuroinflammation....
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Veröffentlicht in: | Drug design, development and therapy development and therapy, 2024-07, Vol.18, p.3209 |
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description | Background and Aim: Previous studies of our research group have shown that Chuanxiong Renshen Decoction (CRD) has the effect of treating AD, but the exact mechanism of its effect is still not clarified. The aim of this study was to investigate the effect and mechanism of CRD on AD neuroinflammation. Materials and Methods: Morris Water Maze (MWM) tests were employed to assess the memory and learning capacity of AD mice. HE and Nissl staining were used to observe the neural cells of mice. The expression of Iba-1 and CD86 were detected by immunohistochemical staining. Utilize UHPLC-MS/MS metabolomics techniques and the KEGG to analyze the metabolic pathways of CRD against AD. Lipopolysaccharide (LPS) induced BV2 microglia cells to construct a neuroinflammatory model. The expression of Iba-1 and CD86 were detected by immunofluorescence and flow cytometry. The contents of TNF-[alpha] and IL-1[beta] were detected by ELISA. Western blot assay was used to detect the expression of PPAR[gamma], p-NF-[kappa]B p65, NF-[kappa]B p65 proteins and inflammatory cytokines iNOS and COX-2 in PPAR[gamma]/NF-[kappa]B pathway with and without PPAR[gamma] inhibitor GW9662. Results: CRD ameliorated the learning and memory ability of 3xTg-AD mice, repaired the damaged nerve cells in the hippocampus, reduced the area of Iba-1 and CD86 positive areas in both the hippocampus and cortex regions, as well as attenuated serum levels of IL-1[beta] and TNF-[alpha] in mice. CRD-containing serum significantly decreased the expression level of Iba-1, significantly reduced the levels of TNF--[alpha] and IL-1[beta], significantly increased the protein expression of PPAR[gamma], and significantly decreased the proteins expression of iNOS, COX-2 and p-NF-[kappa]B p65 in BV2 microglia cells. After addition of PPAR[gamma] inhibitor GW9662, the inhibitory effect of CRD-containing serum on NF-[kappa]B activation was significantly weakened. Conclusion: CRD can activate PPAR[gamma], regulating PPAR[gamma]/NF-[kappa]B signaling pathway, inhibiting microglia over-activation and reducing AD neuroinflammation. Keywords: Alzheimer'disease, Chuanxiong Renshen Decoction, UHPLC-MS/MS, neuroinflammation, PPAR[gamma] |
doi_str_mv | 10.2147/DDDT.S462266 |
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fullrecord | <record><control><sourceid>gale</sourceid><recordid>TN_cdi_gale_infotracmisc_A809282540</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A809282540</galeid><sourcerecordid>A809282540</sourcerecordid><originalsourceid>FETCH-LOGICAL-g980-e63ca12c80c265745dced1a1fcfbbbd7f50b0e240f7553964212b2e4f90532df3</originalsourceid><addsrcrecordid>eNptkF1LwzAUhoMoOKd3_oCCoFfdkrRN28u6Oh2MOebuxhhpetJE-zGWFp2_3ky9mCDn4nw978vhIHRN8IASPxymabocvPiMUsZOUI-QMHSjKCKnR_U5ujDmFWPmMYp7aD9SHa8_dFMXzgJqo6B2UhCNaO3ImdRKZ7o1TlJ-KtAV7O6Mk2oD3IAzg27X6FqWvKr4N57trUfRlbazdvN5slgVh-V6OBu7qze-3fL1vTPnrXrn-0t0Jnlp4Oo399Fy_LAcPbnT58fJKJm6RRxhF5gnOKEiwoKyIPSDXEBOOJFCZlmWhzLAGQbqYxkGgRcznxKaUfBljAOP5tLro5sf24KXsLHnNu2Oi0obsUkiHNOIBj621OAfykYOlRZNDVLb-R_B7ZFAAS9bZZqyO_zBHINfoFx7wg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Chuanxiong Renshen Decoction Inhibits Alzheimer's Disease Neuroinflammation by Regulating PPAR[gamma]/NF-[kappa]B Pathway</title><source>DOAJ Directory of Open Access Journals</source><source>Dove Press Free</source><source>PubMed Central Open Access</source><source>Access via Taylor & Francis (Open Access Collection)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Hou, Jinling ; Wang, Xiaoyan ; Zhang, Jian ; Shen, Zhuojun ; Li, Xiang ; Yang, Yuanxiao</creator><creatorcontrib>Hou, Jinling ; Wang, Xiaoyan ; Zhang, Jian ; Shen, Zhuojun ; Li, Xiang ; Yang, Yuanxiao</creatorcontrib><description>Background and Aim: Previous studies of our research group have shown that Chuanxiong Renshen Decoction (CRD) has the effect of treating AD, but the exact mechanism of its effect is still not clarified. The aim of this study was to investigate the effect and mechanism of CRD on AD neuroinflammation. Materials and Methods: Morris Water Maze (MWM) tests were employed to assess the memory and learning capacity of AD mice. HE and Nissl staining were used to observe the neural cells of mice. The expression of Iba-1 and CD86 were detected by immunohistochemical staining. Utilize UHPLC-MS/MS metabolomics techniques and the KEGG to analyze the metabolic pathways of CRD against AD. Lipopolysaccharide (LPS) induced BV2 microglia cells to construct a neuroinflammatory model. The expression of Iba-1 and CD86 were detected by immunofluorescence and flow cytometry. The contents of TNF-[alpha] and IL-1[beta] were detected by ELISA. Western blot assay was used to detect the expression of PPAR[gamma], p-NF-[kappa]B p65, NF-[kappa]B p65 proteins and inflammatory cytokines iNOS and COX-2 in PPAR[gamma]/NF-[kappa]B pathway with and without PPAR[gamma] inhibitor GW9662. Results: CRD ameliorated the learning and memory ability of 3xTg-AD mice, repaired the damaged nerve cells in the hippocampus, reduced the area of Iba-1 and CD86 positive areas in both the hippocampus and cortex regions, as well as attenuated serum levels of IL-1[beta] and TNF-[alpha] in mice. CRD-containing serum significantly decreased the expression level of Iba-1, significantly reduced the levels of TNF--[alpha] and IL-1[beta], significantly increased the protein expression of PPAR[gamma], and significantly decreased the proteins expression of iNOS, COX-2 and p-NF-[kappa]B p65 in BV2 microglia cells. After addition of PPAR[gamma] inhibitor GW9662, the inhibitory effect of CRD-containing serum on NF-[kappa]B activation was significantly weakened. Conclusion: CRD can activate PPAR[gamma], regulating PPAR[gamma]/NF-[kappa]B signaling pathway, inhibiting microglia over-activation and reducing AD neuroinflammation. Keywords: Alzheimer'disease, Chuanxiong Renshen Decoction, UHPLC-MS/MS, neuroinflammation, PPAR[gamma]</description><identifier>ISSN: 1177-8881</identifier><identifier>EISSN: 1177-8881</identifier><identifier>DOI: 10.2147/DDDT.S462266</identifier><language>eng</language><publisher>Dove Medical Press Limited</publisher><subject>Advertising executives ; Alzheimer's disease ; Canada ; China ; Diseases ; Enzyme-linked immunosorbent assay ; Neurons ; Proteins</subject><ispartof>Drug design, development and therapy, 2024-07, Vol.18, p.3209</ispartof><rights>COPYRIGHT 2024 Dove Medical Press Limited</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,865,27926,27927</link.rule.ids></links><search><creatorcontrib>Hou, Jinling</creatorcontrib><creatorcontrib>Wang, Xiaoyan</creatorcontrib><creatorcontrib>Zhang, Jian</creatorcontrib><creatorcontrib>Shen, Zhuojun</creatorcontrib><creatorcontrib>Li, Xiang</creatorcontrib><creatorcontrib>Yang, Yuanxiao</creatorcontrib><title>Chuanxiong Renshen Decoction Inhibits Alzheimer's Disease Neuroinflammation by Regulating PPAR[gamma]/NF-[kappa]B Pathway</title><title>Drug design, development and therapy</title><description>Background and Aim: Previous studies of our research group have shown that Chuanxiong Renshen Decoction (CRD) has the effect of treating AD, but the exact mechanism of its effect is still not clarified. The aim of this study was to investigate the effect and mechanism of CRD on AD neuroinflammation. Materials and Methods: Morris Water Maze (MWM) tests were employed to assess the memory and learning capacity of AD mice. HE and Nissl staining were used to observe the neural cells of mice. The expression of Iba-1 and CD86 were detected by immunohistochemical staining. Utilize UHPLC-MS/MS metabolomics techniques and the KEGG to analyze the metabolic pathways of CRD against AD. Lipopolysaccharide (LPS) induced BV2 microglia cells to construct a neuroinflammatory model. The expression of Iba-1 and CD86 were detected by immunofluorescence and flow cytometry. The contents of TNF-[alpha] and IL-1[beta] were detected by ELISA. Western blot assay was used to detect the expression of PPAR[gamma], p-NF-[kappa]B p65, NF-[kappa]B p65 proteins and inflammatory cytokines iNOS and COX-2 in PPAR[gamma]/NF-[kappa]B pathway with and without PPAR[gamma] inhibitor GW9662. Results: CRD ameliorated the learning and memory ability of 3xTg-AD mice, repaired the damaged nerve cells in the hippocampus, reduced the area of Iba-1 and CD86 positive areas in both the hippocampus and cortex regions, as well as attenuated serum levels of IL-1[beta] and TNF-[alpha] in mice. CRD-containing serum significantly decreased the expression level of Iba-1, significantly reduced the levels of TNF--[alpha] and IL-1[beta], significantly increased the protein expression of PPAR[gamma], and significantly decreased the proteins expression of iNOS, COX-2 and p-NF-[kappa]B p65 in BV2 microglia cells. After addition of PPAR[gamma] inhibitor GW9662, the inhibitory effect of CRD-containing serum on NF-[kappa]B activation was significantly weakened. Conclusion: CRD can activate PPAR[gamma], regulating PPAR[gamma]/NF-[kappa]B signaling pathway, inhibiting microglia over-activation and reducing AD neuroinflammation. Keywords: Alzheimer'disease, Chuanxiong Renshen Decoction, UHPLC-MS/MS, neuroinflammation, PPAR[gamma]</description><subject>Advertising executives</subject><subject>Alzheimer's disease</subject><subject>Canada</subject><subject>China</subject><subject>Diseases</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Neurons</subject><subject>Proteins</subject><issn>1177-8881</issn><issn>1177-8881</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNptkF1LwzAUhoMoOKd3_oCCoFfdkrRN28u6Oh2MOebuxhhpetJE-zGWFp2_3ky9mCDn4nw978vhIHRN8IASPxymabocvPiMUsZOUI-QMHSjKCKnR_U5ujDmFWPmMYp7aD9SHa8_dFMXzgJqo6B2UhCNaO3ImdRKZ7o1TlJ-KtAV7O6Mk2oD3IAzg27X6FqWvKr4N57trUfRlbazdvN5slgVh-V6OBu7qze-3fL1vTPnrXrn-0t0Jnlp4Oo399Fy_LAcPbnT58fJKJm6RRxhF5gnOKEiwoKyIPSDXEBOOJFCZlmWhzLAGQbqYxkGgRcznxKaUfBljAOP5tLro5sf24KXsLHnNu2Oi0obsUkiHNOIBj621OAfykYOlRZNDVLb-R_B7ZFAAS9bZZqyO_zBHINfoFx7wg</recordid><startdate>20240730</startdate><enddate>20240730</enddate><creator>Hou, Jinling</creator><creator>Wang, Xiaoyan</creator><creator>Zhang, Jian</creator><creator>Shen, Zhuojun</creator><creator>Li, Xiang</creator><creator>Yang, Yuanxiao</creator><general>Dove Medical Press Limited</general><scope/></search><sort><creationdate>20240730</creationdate><title>Chuanxiong Renshen Decoction Inhibits Alzheimer's Disease Neuroinflammation by Regulating PPAR[gamma]/NF-[kappa]B Pathway</title><author>Hou, Jinling ; Wang, Xiaoyan ; Zhang, Jian ; Shen, Zhuojun ; Li, Xiang ; Yang, Yuanxiao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g980-e63ca12c80c265745dced1a1fcfbbbd7f50b0e240f7553964212b2e4f90532df3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Advertising executives</topic><topic>Alzheimer's disease</topic><topic>Canada</topic><topic>China</topic><topic>Diseases</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Neurons</topic><topic>Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hou, Jinling</creatorcontrib><creatorcontrib>Wang, Xiaoyan</creatorcontrib><creatorcontrib>Zhang, Jian</creatorcontrib><creatorcontrib>Shen, Zhuojun</creatorcontrib><creatorcontrib>Li, Xiang</creatorcontrib><creatorcontrib>Yang, Yuanxiao</creatorcontrib><jtitle>Drug design, development and therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hou, Jinling</au><au>Wang, Xiaoyan</au><au>Zhang, Jian</au><au>Shen, Zhuojun</au><au>Li, Xiang</au><au>Yang, Yuanxiao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chuanxiong Renshen Decoction Inhibits Alzheimer's Disease Neuroinflammation by Regulating PPAR[gamma]/NF-[kappa]B Pathway</atitle><jtitle>Drug design, development and therapy</jtitle><date>2024-07-30</date><risdate>2024</risdate><volume>18</volume><spage>3209</spage><pages>3209-</pages><issn>1177-8881</issn><eissn>1177-8881</eissn><abstract>Background and Aim: Previous studies of our research group have shown that Chuanxiong Renshen Decoction (CRD) has the effect of treating AD, but the exact mechanism of its effect is still not clarified. The aim of this study was to investigate the effect and mechanism of CRD on AD neuroinflammation. Materials and Methods: Morris Water Maze (MWM) tests were employed to assess the memory and learning capacity of AD mice. HE and Nissl staining were used to observe the neural cells of mice. The expression of Iba-1 and CD86 were detected by immunohistochemical staining. Utilize UHPLC-MS/MS metabolomics techniques and the KEGG to analyze the metabolic pathways of CRD against AD. Lipopolysaccharide (LPS) induced BV2 microglia cells to construct a neuroinflammatory model. The expression of Iba-1 and CD86 were detected by immunofluorescence and flow cytometry. The contents of TNF-[alpha] and IL-1[beta] were detected by ELISA. Western blot assay was used to detect the expression of PPAR[gamma], p-NF-[kappa]B p65, NF-[kappa]B p65 proteins and inflammatory cytokines iNOS and COX-2 in PPAR[gamma]/NF-[kappa]B pathway with and without PPAR[gamma] inhibitor GW9662. Results: CRD ameliorated the learning and memory ability of 3xTg-AD mice, repaired the damaged nerve cells in the hippocampus, reduced the area of Iba-1 and CD86 positive areas in both the hippocampus and cortex regions, as well as attenuated serum levels of IL-1[beta] and TNF-[alpha] in mice. CRD-containing serum significantly decreased the expression level of Iba-1, significantly reduced the levels of TNF--[alpha] and IL-1[beta], significantly increased the protein expression of PPAR[gamma], and significantly decreased the proteins expression of iNOS, COX-2 and p-NF-[kappa]B p65 in BV2 microglia cells. After addition of PPAR[gamma] inhibitor GW9662, the inhibitory effect of CRD-containing serum on NF-[kappa]B activation was significantly weakened. Conclusion: CRD can activate PPAR[gamma], regulating PPAR[gamma]/NF-[kappa]B signaling pathway, inhibiting microglia over-activation and reducing AD neuroinflammation. Keywords: Alzheimer'disease, Chuanxiong Renshen Decoction, UHPLC-MS/MS, neuroinflammation, PPAR[gamma]</abstract><pub>Dove Medical Press Limited</pub><doi>10.2147/DDDT.S462266</doi></addata></record> |
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subjects | Advertising executives Alzheimer's disease Canada China Diseases Enzyme-linked immunosorbent assay Neurons Proteins |
title | Chuanxiong Renshen Decoction Inhibits Alzheimer's Disease Neuroinflammation by Regulating PPAR[gamma]/NF-[kappa]B Pathway |
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