Integrated Network Pharmacology and Proteomic Analyses of Targets and Mechanisms of Jianpi Tianjing Decoction in Treating Vascular Dementia
Background. Vascular dementia (VD), associated with cerebrovascular injury, is characterized by severe cognitive impairment. Jianpi Tianjing Decoction (JTD) has been widely used to treat VD. However, its molecular targets and mechanisms of action in this treatment remain unclear. This study integrat...
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Veröffentlicht in: | Evidence-based complementary and alternative medicine 2023, Vol.2023 (1), p.9021546-9021546 |
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description | Background. Vascular dementia (VD), associated with cerebrovascular injury, is characterized by severe cognitive impairment. Jianpi Tianjing Decoction (JTD) has been widely used to treat VD. However, its molecular targets and mechanisms of action in this treatment remain unclear. This study integrated network pharmacology and proteomics to identify targets and mechanisms of JTD in the treatment of VD and to provide new insights and goals for clinical treatments. Methods. Systematic network pharmacology was used to identify active chemical compositions, potential targets, and mechanisms of JTD in VD treatment. Then, a mouse model of VD was induced via transient bilateral common carotid artery occlusion to verify the identified targets and mechanisms of JTD against VD using 4D label-free quantitative proteomics. Results. By screening active chemical compositions and potential targets in relevant databases, 187 active chemical compositions and 416 disease-related compound targets were identified. In vivo experiments showed that JTD improved learning and memory in mice. Proteomics also identified 112 differentially expressed proteins in the model and sham groups and the JTD and model groups. Integrating the network pharmacology and proteomics results revealed that JTD may regulate expressions of cytochrome c oxidase subunit 7C, metabotropic glutamate receptor 2, Slc30a1 zinc transporter 1, and apolipoprotein A-IV in VD mice and that their mechanisms involve biological processes like oxidative phosphorylation, regulation of neuron death, glutamate secretion, cellular ion homeostasis, and lipoprotein metabolism. Conclusions. JTD may suppress VD development via multiple components, targets, and pathways. It may thus serve as a complementary treatment option for patients with VD. |
doi_str_mv | 10.1155/2023/9021546 |
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Vascular dementia (VD), associated with cerebrovascular injury, is characterized by severe cognitive impairment. Jianpi Tianjing Decoction (JTD) has been widely used to treat VD. However, its molecular targets and mechanisms of action in this treatment remain unclear. This study integrated network pharmacology and proteomics to identify targets and mechanisms of JTD in the treatment of VD and to provide new insights and goals for clinical treatments. Methods. Systematic network pharmacology was used to identify active chemical compositions, potential targets, and mechanisms of JTD in VD treatment. Then, a mouse model of VD was induced via transient bilateral common carotid artery occlusion to verify the identified targets and mechanisms of JTD against VD using 4D label-free quantitative proteomics. Results. By screening active chemical compositions and potential targets in relevant databases, 187 active chemical compositions and 416 disease-related compound targets were identified. In vivo experiments showed that JTD improved learning and memory in mice. Proteomics also identified 112 differentially expressed proteins in the model and sham groups and the JTD and model groups. Integrating the network pharmacology and proteomics results revealed that JTD may regulate expressions of cytochrome c oxidase subunit 7C, metabotropic glutamate receptor 2, Slc30a1 zinc transporter 1, and apolipoprotein A-IV in VD mice and that their mechanisms involve biological processes like oxidative phosphorylation, regulation of neuron death, glutamate secretion, cellular ion homeostasis, and lipoprotein metabolism. Conclusions. JTD may suppress VD development via multiple components, targets, and pathways. It may thus serve as a complementary treatment option for patients with VD.</description><identifier>ISSN: 1741-427X</identifier><identifier>EISSN: 1741-4288</identifier><identifier>DOI: 10.1155/2023/9021546</identifier><identifier>PMID: 36714532</identifier><language>eng</language><publisher>United States: Hindawi</publisher><subject>Animal cognition ; Apolipoprotein A ; Apoptosis ; Atherosclerosis ; Carotid artery ; Cell death ; Cerebral blood flow ; Chinese medicine ; Cognitive ability ; Cytochrome-c oxidase ; Dementia ; Dementia disorders ; Disease ; Drug dosages ; Genes ; Glutamic acid receptors (metabotropic) ; Homeostasis ; Ischemia ; Laboratory animals ; Lipid metabolism ; Medical research ; Oxidative phosphorylation ; Oxidative stress ; Pharmacology ; Phosphorylation ; Proteins ; Proteomics ; Sexually transmitted diseases ; STD ; Vascular dementia ; Zinc transporter</subject><ispartof>Evidence-based complementary and alternative medicine, 2023, Vol.2023 (1), p.9021546-9021546</ispartof><rights>Copyright © 2023 Jidan Liu et al.</rights><rights>Copyright © 2023 Jidan Liu et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2023 Jidan Liu et al. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-2161279be6327fa4260955ca503268664c3b286af2557208afbfd8782c14897d3</citedby><cites>FETCH-LOGICAL-c448t-2161279be6327fa4260955ca503268664c3b286af2557208afbfd8782c14897d3</cites><orcidid>0000-0002-8736-1735 ; 0000-0001-7202-5790 ; 0000-0003-4548-7935 ; 0000-0003-3440-4567 ; 0000-0001-5357-7418</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9876684/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9876684/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,4010,27900,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36714532$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Emran, Talha Bin</contributor><creatorcontrib>Liu, Jidan</creatorcontrib><creatorcontrib>Gong, Juanfen</creatorcontrib><creatorcontrib>Xu, Jinchao</creatorcontrib><creatorcontrib>Fang, Mengyuan</creatorcontrib><creatorcontrib>Su, Meng</creatorcontrib><creatorcontrib>Li, Weiguang</creatorcontrib><creatorcontrib>Wu, Yiyi</creatorcontrib><creatorcontrib>Hui, Yang</creatorcontrib><creatorcontrib>He, Yingchun</creatorcontrib><title>Integrated Network Pharmacology and Proteomic Analyses of Targets and Mechanisms of Jianpi Tianjing Decoction in Treating Vascular Dementia</title><title>Evidence-based complementary and alternative medicine</title><addtitle>Evid Based Complement Alternat Med</addtitle><description>Background. Vascular dementia (VD), associated with cerebrovascular injury, is characterized by severe cognitive impairment. Jianpi Tianjing Decoction (JTD) has been widely used to treat VD. However, its molecular targets and mechanisms of action in this treatment remain unclear. This study integrated network pharmacology and proteomics to identify targets and mechanisms of JTD in the treatment of VD and to provide new insights and goals for clinical treatments. Methods. Systematic network pharmacology was used to identify active chemical compositions, potential targets, and mechanisms of JTD in VD treatment. Then, a mouse model of VD was induced via transient bilateral common carotid artery occlusion to verify the identified targets and mechanisms of JTD against VD using 4D label-free quantitative proteomics. Results. By screening active chemical compositions and potential targets in relevant databases, 187 active chemical compositions and 416 disease-related compound targets were identified. In vivo experiments showed that JTD improved learning and memory in mice. Proteomics also identified 112 differentially expressed proteins in the model and sham groups and the JTD and model groups. Integrating the network pharmacology and proteomics results revealed that JTD may regulate expressions of cytochrome c oxidase subunit 7C, metabotropic glutamate receptor 2, Slc30a1 zinc transporter 1, and apolipoprotein A-IV in VD mice and that their mechanisms involve biological processes like oxidative phosphorylation, regulation of neuron death, glutamate secretion, cellular ion homeostasis, and lipoprotein metabolism. Conclusions. JTD may suppress VD development via multiple components, targets, and pathways. It may thus serve as a complementary treatment option for patients with VD.</description><subject>Animal cognition</subject><subject>Apolipoprotein A</subject><subject>Apoptosis</subject><subject>Atherosclerosis</subject><subject>Carotid artery</subject><subject>Cell death</subject><subject>Cerebral blood flow</subject><subject>Chinese medicine</subject><subject>Cognitive ability</subject><subject>Cytochrome-c oxidase</subject><subject>Dementia</subject><subject>Dementia disorders</subject><subject>Disease</subject><subject>Drug dosages</subject><subject>Genes</subject><subject>Glutamic acid receptors (metabotropic)</subject><subject>Homeostasis</subject><subject>Ischemia</subject><subject>Laboratory animals</subject><subject>Lipid metabolism</subject><subject>Medical research</subject><subject>Oxidative phosphorylation</subject><subject>Oxidative stress</subject><subject>Pharmacology</subject><subject>Phosphorylation</subject><subject>Proteins</subject><subject>Proteomics</subject><subject>Sexually transmitted diseases</subject><subject>STD</subject><subject>Vascular dementia</subject><subject>Zinc 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Network Pharmacology and Proteomic Analyses of Targets and Mechanisms of Jianpi Tianjing Decoction in Treating Vascular Dementia</title><author>Liu, Jidan ; Gong, Juanfen ; Xu, Jinchao ; Fang, Mengyuan ; Su, Meng ; Li, Weiguang ; Wu, Yiyi ; Hui, Yang ; He, Yingchun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-2161279be6327fa4260955ca503268664c3b286af2557208afbfd8782c14897d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animal cognition</topic><topic>Apolipoprotein A</topic><topic>Apoptosis</topic><topic>Atherosclerosis</topic><topic>Carotid artery</topic><topic>Cell death</topic><topic>Cerebral blood flow</topic><topic>Chinese medicine</topic><topic>Cognitive ability</topic><topic>Cytochrome-c oxidase</topic><topic>Dementia</topic><topic>Dementia disorders</topic><topic>Disease</topic><topic>Drug dosages</topic><topic>Genes</topic><topic>Glutamic acid receptors (metabotropic)</topic><topic>Homeostasis</topic><topic>Ischemia</topic><topic>Laboratory animals</topic><topic>Lipid metabolism</topic><topic>Medical research</topic><topic>Oxidative phosphorylation</topic><topic>Oxidative stress</topic><topic>Pharmacology</topic><topic>Phosphorylation</topic><topic>Proteins</topic><topic>Proteomics</topic><topic>Sexually transmitted diseases</topic><topic>STD</topic><topic>Vascular dementia</topic><topic>Zinc transporter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Jidan</creatorcontrib><creatorcontrib>Gong, Juanfen</creatorcontrib><creatorcontrib>Xu, Jinchao</creatorcontrib><creatorcontrib>Fang, Mengyuan</creatorcontrib><creatorcontrib>Su, Meng</creatorcontrib><creatorcontrib>Li, Weiguang</creatorcontrib><creatorcontrib>Wu, Yiyi</creatorcontrib><creatorcontrib>Hui, Yang</creatorcontrib><creatorcontrib>He, Yingchun</creatorcontrib><collection>Hindawi Publishing 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Talha Bin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Integrated Network Pharmacology and Proteomic Analyses of Targets and Mechanisms of Jianpi Tianjing Decoction in Treating Vascular Dementia</atitle><jtitle>Evidence-based complementary and alternative medicine</jtitle><addtitle>Evid Based Complement Alternat Med</addtitle><date>2023</date><risdate>2023</risdate><volume>2023</volume><issue>1</issue><spage>9021546</spage><epage>9021546</epage><pages>9021546-9021546</pages><issn>1741-427X</issn><eissn>1741-4288</eissn><abstract>Background. Vascular dementia (VD), associated with cerebrovascular injury, is characterized by severe cognitive impairment. Jianpi Tianjing Decoction (JTD) has been widely used to treat VD. However, its molecular targets and mechanisms of action in this treatment remain unclear. This study integrated network pharmacology and proteomics to identify targets and mechanisms of JTD in the treatment of VD and to provide new insights and goals for clinical treatments. Methods. Systematic network pharmacology was used to identify active chemical compositions, potential targets, and mechanisms of JTD in VD treatment. Then, a mouse model of VD was induced via transient bilateral common carotid artery occlusion to verify the identified targets and mechanisms of JTD against VD using 4D label-free quantitative proteomics. Results. By screening active chemical compositions and potential targets in relevant databases, 187 active chemical compositions and 416 disease-related compound targets were identified. In vivo experiments showed that JTD improved learning and memory in mice. Proteomics also identified 112 differentially expressed proteins in the model and sham groups and the JTD and model groups. Integrating the network pharmacology and proteomics results revealed that JTD may regulate expressions of cytochrome c oxidase subunit 7C, metabotropic glutamate receptor 2, Slc30a1 zinc transporter 1, and apolipoprotein A-IV in VD mice and that their mechanisms involve biological processes like oxidative phosphorylation, regulation of neuron death, glutamate secretion, cellular ion homeostasis, and lipoprotein metabolism. Conclusions. JTD may suppress VD development via multiple components, targets, and pathways. It may thus serve as a complementary treatment option for patients with VD.</abstract><cop>United States</cop><pub>Hindawi</pub><pmid>36714532</pmid><doi>10.1155/2023/9021546</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-8736-1735</orcidid><orcidid>https://orcid.org/0000-0001-7202-5790</orcidid><orcidid>https://orcid.org/0000-0003-4548-7935</orcidid><orcidid>https://orcid.org/0000-0003-3440-4567</orcidid><orcidid>https://orcid.org/0000-0001-5357-7418</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animal cognition Apolipoprotein A Apoptosis Atherosclerosis Carotid artery Cell death Cerebral blood flow Chinese medicine Cognitive ability Cytochrome-c oxidase Dementia Dementia disorders Disease Drug dosages Genes Glutamic acid receptors (metabotropic) Homeostasis Ischemia Laboratory animals Lipid metabolism Medical research Oxidative phosphorylation Oxidative stress Pharmacology Phosphorylation Proteins Proteomics Sexually transmitted diseases STD Vascular dementia Zinc transporter |
title | Integrated Network Pharmacology and Proteomic Analyses of Targets and Mechanisms of Jianpi Tianjing Decoction in Treating Vascular Dementia |
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