UHPLC-MS-based metabolomics and chemoinformatics study reveals the neuroprotective effect and chemical characteristic in Parkinson's disease mice after oral administration of Wen-Shen-Yang-Gan decoction
Parkinson's disease (PD), the typical neurodegenerative disease, is characterized by the progressive loss of dopaminergic neurons in the substantia nigra (SN). However, no therapeutic agent used currently could slow down neuronal cell loss so as to decelerate or halt the progression of PD. Trad...
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Veröffentlicht in: | Aging (Albany, NY.) NY.), 2021-08, Vol.13 (15), p.19510-19528 |
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description | Parkinson's disease (PD), the typical neurodegenerative disease, is characterized by the progressive loss of dopaminergic neurons in the substantia nigra (SN). However, no therapeutic agent used currently could slow down neuronal cell loss so as to decelerate or halt the progression of PD. Traditional Chinese medicine (TCM) has been utilized to treat the dysfunction of the autonomic nervous system. Wen-Shen-Yang-Gan decoction (WSYGD) has a good effect on the clinical treatment of PD with constipation. However, it is not clear which ingredients and what mechanism are responsible for the therapeutic effect. In this study, the pharmacodynamic study of WSYGD in PD mice was applied. Concurrently, a novel method for the identification of metabolic profiles of WSYGD has been developed. Finally, we found that WSYGD could protect the PD mice induced by rotenone. The underlying mechanism of the protective effect may be related to the reduction of the DA neurons apoptosis via reducing inflammatory reaction. By virtue of UPLC-MS and chemoinformatics method, 35 prototype compounds and 27 metabolites were filtered out and tentatively characterized. In conclusion, this study provides an insight into the metabolism of WSYGD
to enable understanding of the metabolic process and therapeutic mechanism of PD. |
doi_str_mv | 10.18632/aging.203361 |
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to enable understanding of the metabolic process and therapeutic mechanism of PD.</description><identifier>ISSN: 1945-4589</identifier><identifier>EISSN: 1945-4589</identifier><identifier>DOI: 10.18632/aging.203361</identifier><identifier>PMID: 34339394</identifier><language>eng</language><publisher>United States: Impact Journals</publisher><subject>Administration, Oral ; Animals ; Antiparkinson Agents - isolation & purification ; Antiparkinson Agents - pharmacology ; Cheminformatics - methods ; Chromatography, High Pressure Liquid ; Disease Models, Animal ; Dopaminergic Neurons - drug effects ; Dopaminergic Neurons - pathology ; Male ; Metabolomics ; Mice ; Mice, Inbred C57BL ; Multivariate Analysis ; Neuroprotective Agents - isolation & purification ; Neuroprotective Agents - pharmacology ; Parkinson Disease - drug therapy ; Parkinson Disease - pathology ; Plant Extracts - isolation & purification ; Plant Extracts - pharmacology ; Research Paper ; Rotenone ; Substantia Nigra - drug effects ; Substantia Nigra - pathology ; Tandem Mass Spectrometry</subject><ispartof>Aging (Albany, NY.), 2021-08, Vol.13 (15), p.19510-19528</ispartof><rights>Copyright: © 2021 Zhu et al.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-652ac32d1465cbe3aa04ea3634f7f4b4a3318b2aeb4a5f2d1a6fb64d11f7f9353</citedby><cites>FETCH-LOGICAL-c387t-652ac32d1465cbe3aa04ea3634f7f4b4a3318b2aeb4a5f2d1a6fb64d11f7f9353</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8386550/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8386550/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34339394$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhu, Guoxue</creatorcontrib><creatorcontrib>Wang, Wang</creatorcontrib><creatorcontrib>Chen, Chang</creatorcontrib><creatorcontrib>Tang, Lili</creatorcontrib><creatorcontrib>Liang, Yan</creatorcontrib><creatorcontrib>Zhang, Zhennian</creatorcontrib><creatorcontrib>Lu, Yan</creatorcontrib><creatorcontrib>Zhao, Yang</creatorcontrib><title>UHPLC-MS-based metabolomics and chemoinformatics study reveals the neuroprotective effect and chemical characteristic in Parkinson's disease mice after oral administration of Wen-Shen-Yang-Gan decoction</title><title>Aging (Albany, NY.)</title><addtitle>Aging (Albany NY)</addtitle><description>Parkinson's disease (PD), the typical neurodegenerative disease, is characterized by the progressive loss of dopaminergic neurons in the substantia nigra (SN). However, no therapeutic agent used currently could slow down neuronal cell loss so as to decelerate or halt the progression of PD. Traditional Chinese medicine (TCM) has been utilized to treat the dysfunction of the autonomic nervous system. Wen-Shen-Yang-Gan decoction (WSYGD) has a good effect on the clinical treatment of PD with constipation. However, it is not clear which ingredients and what mechanism are responsible for the therapeutic effect. In this study, the pharmacodynamic study of WSYGD in PD mice was applied. Concurrently, a novel method for the identification of metabolic profiles of WSYGD has been developed. Finally, we found that WSYGD could protect the PD mice induced by rotenone. The underlying mechanism of the protective effect may be related to the reduction of the DA neurons apoptosis via reducing inflammatory reaction. By virtue of UPLC-MS and chemoinformatics method, 35 prototype compounds and 27 metabolites were filtered out and tentatively characterized. In conclusion, this study provides an insight into the metabolism of WSYGD
to enable understanding of the metabolic process and therapeutic mechanism of PD.</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>Antiparkinson Agents - isolation & purification</subject><subject>Antiparkinson Agents - pharmacology</subject><subject>Cheminformatics - methods</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Disease Models, Animal</subject><subject>Dopaminergic Neurons - drug effects</subject><subject>Dopaminergic Neurons - pathology</subject><subject>Male</subject><subject>Metabolomics</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Multivariate Analysis</subject><subject>Neuroprotective Agents - isolation & purification</subject><subject>Neuroprotective Agents - pharmacology</subject><subject>Parkinson Disease - drug therapy</subject><subject>Parkinson Disease - pathology</subject><subject>Plant Extracts - isolation & purification</subject><subject>Plant Extracts - pharmacology</subject><subject>Research Paper</subject><subject>Rotenone</subject><subject>Substantia Nigra - drug effects</subject><subject>Substantia Nigra - pathology</subject><subject>Tandem Mass Spectrometry</subject><issn>1945-4589</issn><issn>1945-4589</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkU9v1DAQxSMEoqVw5Ip8g0tKEv_Z5IKEVtAiLaJSqRAna2KPdw2JvbWTlfoV-VTMdsuqXOynmd-8GekVxeu6Oq9bxZv3sPZhfd5UnKv6SXFad0KWQrbd00f6pHiR86-qUlIK9bw44YLzjnfitPhzc3m1WpZfr8seMlo24gR9HOLoTWYQLDMbHKMPLqYRpn0xT7O9Ywl3CENm0wZZwDnFbYoTmsnvkKFzpI7T3sBAAhKYCZPP5MJ8YFeQfvuQY3ibmfUZaT0jFhk4wlhMNAV29IEmEq2OgUXHfmAorzf0_ISwLi8gMIsmmn37ZfHM0Un46uE_K24-f_q-vCxX3y6-LD-uSsPbxVQq2YDhja2FkqZHDlAJBK64cAsnegGc123fAJKUjjhQrlfC1jX1Oy75WfHh4Lud-xGtwUD3DXqb_AjpTkfw-v9O8Bu9jjvd8pYCqMjg3YNBircz5kmPPhscBggY56wbKRfEVWKPlgfUpJhzQndcU1f6Pn99n78-5E_8m8e3Hel_gfO_7mWzZw</recordid><startdate>20210802</startdate><enddate>20210802</enddate><creator>Zhu, Guoxue</creator><creator>Wang, Wang</creator><creator>Chen, Chang</creator><creator>Tang, Lili</creator><creator>Liang, Yan</creator><creator>Zhang, Zhennian</creator><creator>Lu, Yan</creator><creator>Zhao, Yang</creator><general>Impact Journals</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><scope>5PM</scope></search><sort><creationdate>20210802</creationdate><title>UHPLC-MS-based metabolomics and chemoinformatics study reveals the neuroprotective effect and chemical characteristic in Parkinson's disease mice after oral administration of Wen-Shen-Yang-Gan decoction</title><author>Zhu, Guoxue ; Wang, Wang ; Chen, Chang ; Tang, Lili ; Liang, Yan ; Zhang, Zhennian ; Lu, Yan ; Zhao, Yang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c387t-652ac32d1465cbe3aa04ea3634f7f4b4a3318b2aeb4a5f2d1a6fb64d11f7f9353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Administration, Oral</topic><topic>Animals</topic><topic>Antiparkinson Agents - isolation & purification</topic><topic>Antiparkinson Agents - pharmacology</topic><topic>Cheminformatics - methods</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Disease Models, Animal</topic><topic>Dopaminergic Neurons - drug effects</topic><topic>Dopaminergic Neurons - pathology</topic><topic>Male</topic><topic>Metabolomics</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Multivariate Analysis</topic><topic>Neuroprotective Agents - isolation & purification</topic><topic>Neuroprotective Agents - pharmacology</topic><topic>Parkinson Disease - drug therapy</topic><topic>Parkinson Disease - pathology</topic><topic>Plant Extracts - isolation & purification</topic><topic>Plant Extracts - pharmacology</topic><topic>Research Paper</topic><topic>Rotenone</topic><topic>Substantia Nigra - drug effects</topic><topic>Substantia Nigra - pathology</topic><topic>Tandem Mass Spectrometry</topic><toplevel>online_resources</toplevel><creatorcontrib>Zhu, Guoxue</creatorcontrib><creatorcontrib>Wang, Wang</creatorcontrib><creatorcontrib>Chen, Chang</creatorcontrib><creatorcontrib>Tang, Lili</creatorcontrib><creatorcontrib>Liang, Yan</creatorcontrib><creatorcontrib>Zhang, Zhennian</creatorcontrib><creatorcontrib>Lu, Yan</creatorcontrib><creatorcontrib>Zhao, Yang</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Aging (Albany, NY.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhu, Guoxue</au><au>Wang, Wang</au><au>Chen, Chang</au><au>Tang, Lili</au><au>Liang, Yan</au><au>Zhang, Zhennian</au><au>Lu, Yan</au><au>Zhao, Yang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>UHPLC-MS-based metabolomics and chemoinformatics study reveals the neuroprotective effect and chemical characteristic in Parkinson's disease mice after oral administration of Wen-Shen-Yang-Gan decoction</atitle><jtitle>Aging (Albany, NY.)</jtitle><addtitle>Aging (Albany NY)</addtitle><date>2021-08-02</date><risdate>2021</risdate><volume>13</volume><issue>15</issue><spage>19510</spage><epage>19528</epage><pages>19510-19528</pages><issn>1945-4589</issn><eissn>1945-4589</eissn><abstract>Parkinson's disease (PD), the typical neurodegenerative disease, is characterized by the progressive loss of dopaminergic neurons in the substantia nigra (SN). However, no therapeutic agent used currently could slow down neuronal cell loss so as to decelerate or halt the progression of PD. Traditional Chinese medicine (TCM) has been utilized to treat the dysfunction of the autonomic nervous system. Wen-Shen-Yang-Gan decoction (WSYGD) has a good effect on the clinical treatment of PD with constipation. However, it is not clear which ingredients and what mechanism are responsible for the therapeutic effect. In this study, the pharmacodynamic study of WSYGD in PD mice was applied. Concurrently, a novel method for the identification of metabolic profiles of WSYGD has been developed. Finally, we found that WSYGD could protect the PD mice induced by rotenone. The underlying mechanism of the protective effect may be related to the reduction of the DA neurons apoptosis via reducing inflammatory reaction. By virtue of UPLC-MS and chemoinformatics method, 35 prototype compounds and 27 metabolites were filtered out and tentatively characterized. In conclusion, this study provides an insight into the metabolism of WSYGD
to enable understanding of the metabolic process and therapeutic mechanism of PD.</abstract><cop>United States</cop><pub>Impact Journals</pub><pmid>34339394</pmid><doi>10.18632/aging.203361</doi><tpages>19</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Oral Animals Antiparkinson Agents - isolation & purification Antiparkinson Agents - pharmacology Cheminformatics - methods Chromatography, High Pressure Liquid Disease Models, Animal Dopaminergic Neurons - drug effects Dopaminergic Neurons - pathology Male Metabolomics Mice Mice, Inbred C57BL Multivariate Analysis Neuroprotective Agents - isolation & purification Neuroprotective Agents - pharmacology Parkinson Disease - drug therapy Parkinson Disease - pathology Plant Extracts - isolation & purification Plant Extracts - pharmacology Research Paper Rotenone Substantia Nigra - drug effects Substantia Nigra - pathology Tandem Mass Spectrometry |
title | UHPLC-MS-based metabolomics and chemoinformatics study reveals the neuroprotective effect and chemical characteristic in Parkinson's disease mice after oral administration of Wen-Shen-Yang-Gan decoction |
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