BAK ameliorated cerebral infarction/ischemia–reperfusion injury by activating AMPK/Nrf2 to inhibit TXNIP/NLRP3/caspase-1 axis

•Active alkaloids of Psoralea corylifolia Linn. in alleviating MACO/R injury.•Clarifying Bakuchiol reduced neuronal apoptosis and pyroptosis to relieve MACO/R injury.•Bakuchiol was found to suppress inflammation and cell pyroptosis through regulating Nrf2/NLRP3/Caspase-1.•AMPK inhibitor CC could rev...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Neuroscience letters 2025-01, Vol.844, p.138037, Article 138037
Hauptverfasser: Xu, Yue-Wei, Yao, Chang-Heng, Gao, Xiao-Ming, Wang, Li, Zhang, Meng-Xiang, Yang, Xiao-Dan, Li, Jing, Dai, Wen-Ling, Yang, Man-Qin, Cai, Ming
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page 138037
container_title Neuroscience letters
container_volume 844
creator Xu, Yue-Wei
Yao, Chang-Heng
Gao, Xiao-Ming
Wang, Li
Zhang, Meng-Xiang
Yang, Xiao-Dan
Li, Jing
Dai, Wen-Ling
Yang, Man-Qin
Cai, Ming
description •Active alkaloids of Psoralea corylifolia Linn. in alleviating MACO/R injury.•Clarifying Bakuchiol reduced neuronal apoptosis and pyroptosis to relieve MACO/R injury.•Bakuchiol was found to suppress inflammation and cell pyroptosis through regulating Nrf2/NLRP3/Caspase-1.•AMPK inhibitor CC could reverse BAK induced upregulation of Nrf2. Cerebral ischemia/reperfusion (I/R) injury is a serious vascular disease with extremely high mortality and disability rate. Bakuchiol (BAK) was found in leaves and seeds of Psoralea corylifolia Linn and has been shown to decrease inflammation and reduce oxidative stress, while the mechanism of BAK in ameliorating cerebral I/R injury remains unclear. Middle cerebral artery occlusion reperfusion (MACO/R) was used to establish mouse model. The protective effect of BAK in MCAO/R mices was detected by performing neurological deficit testing, TTC staining, and H&E staining. Oxygen/glucose deprivation and reperfusion (OGD/R) was used to stimulate SH-SY5Y cells in vitro. Protein expression was detected by western blotting, gene expression was detected by quantitative real-time polymerase chain reaction and apoptosis was detected by immunofluorescence. Our study indicated that BAK protected ischemia–reperfusion injury in MACO/R mice, and upregulated superoxide dismutase (SOD) and the catalase (CAT) enzyme activity. BAK also inhibited the expression of TNF-α, IL-1β, IL-6, and IL-18 and suppressed apoptosis and pyroptosis both in MACO/R mice and in OGD/R SH-SY5Y cells. Further results showed that BAK could suppress TXNIP, ASC, NLRP3, and caspase-1 mRNA levels to reverse assembly of inflammasome. And BAK could also upregulate the expression of phosphorylated AMP-activated protein kinase (AMPK) and nuclear factor erythroid 2-related factor (Nrf2). In addition, Nrf2 inhibitor ML385 reversed the BAK induced reduction of TXNIP, ASC, NLRP3, and the AMPK inhibitor also abolished BAK’ the effect on the regulation of Nrf2, TXNIP, ASC, NLRP3, caspase-1, and pro-inflammatory cytokines. In conclusion, BAK, found in leaves and seeds of Psoralea corylifolia Linn, could ameliorated cerebral I/R injury through activating AMPK/Nrf2 to inhibit NLRP3 inflammasome, which might present new therapeutic strategy for cerebral I/R injury.
doi_str_mv 10.1016/j.neulet.2024.138037
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3128742012</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0304394024004166</els_id><sourcerecordid>3128742012</sourcerecordid><originalsourceid>FETCH-LOGICAL-c241t-41bada28b4a8e1f0af8809dea69c0a295866e410d3884629dfd240849451dabe3</originalsourceid><addsrcrecordid>eNp9kEuO1DAQhi0EYpqBGyDkJZt0_EribJCaEY_RNE0LDRI7q2JXGLfyaOxkRK_gDtyQk-BRBpasqlT6qkr_R8hzztac8TI_rAecO5zWggm15lIzWT0gK64rkVV1JR6SFZNMZbJW7Iw8ifHAGCt4oR6TM1mnpiyqFfnxenNFocfOjwEmdNRiwCZAR_3QQrCTH4fcR3uDvYffP38FPGJo55jGiTjM4USbE4XE3cLkh69082F_le9CK-g0JuLGN36i1192l_t8t_20l7mFeISIGafw3cen5FELXcRn9_WcfH775vrifbb9-O7yYrPNrFB8yhRvwIHQjQKNvGXQas1qh1DWloGoC12WqDhzUmtVitq1TiimVa0K7qBBeU5eLnePYfw2Y5xMn1Jh18GA4xyN5EJXSjAuEqoW1IYxxoCtOQbfQzgZzsydenMwi3pzp94s6tPai_sPc9Oj-7f013UCXi0Appy3HoOJ1uNg0fmAdjJu9P__8Ad_0pgC</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3128742012</pqid></control><display><type>article</type><title>BAK ameliorated cerebral infarction/ischemia–reperfusion injury by activating AMPK/Nrf2 to inhibit TXNIP/NLRP3/caspase-1 axis</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Xu, Yue-Wei ; Yao, Chang-Heng ; Gao, Xiao-Ming ; Wang, Li ; Zhang, Meng-Xiang ; Yang, Xiao-Dan ; Li, Jing ; Dai, Wen-Ling ; Yang, Man-Qin ; Cai, Ming</creator><creatorcontrib>Xu, Yue-Wei ; Yao, Chang-Heng ; Gao, Xiao-Ming ; Wang, Li ; Zhang, Meng-Xiang ; Yang, Xiao-Dan ; Li, Jing ; Dai, Wen-Ling ; Yang, Man-Qin ; Cai, Ming</creatorcontrib><description>•Active alkaloids of Psoralea corylifolia Linn. in alleviating MACO/R injury.•Clarifying Bakuchiol reduced neuronal apoptosis and pyroptosis to relieve MACO/R injury.•Bakuchiol was found to suppress inflammation and cell pyroptosis through regulating Nrf2/NLRP3/Caspase-1.•AMPK inhibitor CC could reverse BAK induced upregulation of Nrf2. Cerebral ischemia/reperfusion (I/R) injury is a serious vascular disease with extremely high mortality and disability rate. Bakuchiol (BAK) was found in leaves and seeds of Psoralea corylifolia Linn and has been shown to decrease inflammation and reduce oxidative stress, while the mechanism of BAK in ameliorating cerebral I/R injury remains unclear. Middle cerebral artery occlusion reperfusion (MACO/R) was used to establish mouse model. The protective effect of BAK in MCAO/R mices was detected by performing neurological deficit testing, TTC staining, and H&amp;E staining. Oxygen/glucose deprivation and reperfusion (OGD/R) was used to stimulate SH-SY5Y cells in vitro. Protein expression was detected by western blotting, gene expression was detected by quantitative real-time polymerase chain reaction and apoptosis was detected by immunofluorescence. Our study indicated that BAK protected ischemia–reperfusion injury in MACO/R mice, and upregulated superoxide dismutase (SOD) and the catalase (CAT) enzyme activity. BAK also inhibited the expression of TNF-α, IL-1β, IL-6, and IL-18 and suppressed apoptosis and pyroptosis both in MACO/R mice and in OGD/R SH-SY5Y cells. Further results showed that BAK could suppress TXNIP, ASC, NLRP3, and caspase-1 mRNA levels to reverse assembly of inflammasome. And BAK could also upregulate the expression of phosphorylated AMP-activated protein kinase (AMPK) and nuclear factor erythroid 2-related factor (Nrf2). In addition, Nrf2 inhibitor ML385 reversed the BAK induced reduction of TXNIP, ASC, NLRP3, and the AMPK inhibitor also abolished BAK’ the effect on the regulation of Nrf2, TXNIP, ASC, NLRP3, caspase-1, and pro-inflammatory cytokines. In conclusion, BAK, found in leaves and seeds of Psoralea corylifolia Linn, could ameliorated cerebral I/R injury through activating AMPK/Nrf2 to inhibit NLRP3 inflammasome, which might present new therapeutic strategy for cerebral I/R injury.</description><identifier>ISSN: 0304-3940</identifier><identifier>ISSN: 1872-7972</identifier><identifier>EISSN: 1872-7972</identifier><identifier>DOI: 10.1016/j.neulet.2024.138037</identifier><identifier>PMID: 39515657</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>AMP-Activated Protein Kinases - metabolism ; AMPK ; Animals ; Apoptosis - drug effects ; Bakuchiol ; Carrier Proteins - metabolism ; Caspase 1 - metabolism ; Cell Cycle Proteins - metabolism ; Humans ; Infarction, Middle Cerebral Artery - metabolism ; Ischemia–reperfusion injury ; Male ; Mice ; Mice, Inbred C57BL ; NF-E2-Related Factor 2 - metabolism ; NLR Family, Pyrin Domain-Containing 3 Protein - antagonists &amp; inhibitors ; NLR Family, Pyrin Domain-Containing 3 Protein - metabolism ; NLRP3 inflammasome ; Nrf2 ; Phenols - pharmacology ; Reperfusion Injury - drug therapy ; Reperfusion Injury - metabolism ; Signal Transduction - drug effects ; Thioredoxins</subject><ispartof>Neuroscience letters, 2025-01, Vol.844, p.138037, Article 138037</ispartof><rights>2024 Elsevier B.V.</rights><rights>Copyright © 2024 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c241t-41bada28b4a8e1f0af8809dea69c0a295866e410d3884629dfd240849451dabe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.neulet.2024.138037$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39515657$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xu, Yue-Wei</creatorcontrib><creatorcontrib>Yao, Chang-Heng</creatorcontrib><creatorcontrib>Gao, Xiao-Ming</creatorcontrib><creatorcontrib>Wang, Li</creatorcontrib><creatorcontrib>Zhang, Meng-Xiang</creatorcontrib><creatorcontrib>Yang, Xiao-Dan</creatorcontrib><creatorcontrib>Li, Jing</creatorcontrib><creatorcontrib>Dai, Wen-Ling</creatorcontrib><creatorcontrib>Yang, Man-Qin</creatorcontrib><creatorcontrib>Cai, Ming</creatorcontrib><title>BAK ameliorated cerebral infarction/ischemia–reperfusion injury by activating AMPK/Nrf2 to inhibit TXNIP/NLRP3/caspase-1 axis</title><title>Neuroscience letters</title><addtitle>Neurosci Lett</addtitle><description>•Active alkaloids of Psoralea corylifolia Linn. in alleviating MACO/R injury.•Clarifying Bakuchiol reduced neuronal apoptosis and pyroptosis to relieve MACO/R injury.•Bakuchiol was found to suppress inflammation and cell pyroptosis through regulating Nrf2/NLRP3/Caspase-1.•AMPK inhibitor CC could reverse BAK induced upregulation of Nrf2. Cerebral ischemia/reperfusion (I/R) injury is a serious vascular disease with extremely high mortality and disability rate. Bakuchiol (BAK) was found in leaves and seeds of Psoralea corylifolia Linn and has been shown to decrease inflammation and reduce oxidative stress, while the mechanism of BAK in ameliorating cerebral I/R injury remains unclear. Middle cerebral artery occlusion reperfusion (MACO/R) was used to establish mouse model. The protective effect of BAK in MCAO/R mices was detected by performing neurological deficit testing, TTC staining, and H&amp;E staining. Oxygen/glucose deprivation and reperfusion (OGD/R) was used to stimulate SH-SY5Y cells in vitro. Protein expression was detected by western blotting, gene expression was detected by quantitative real-time polymerase chain reaction and apoptosis was detected by immunofluorescence. Our study indicated that BAK protected ischemia–reperfusion injury in MACO/R mice, and upregulated superoxide dismutase (SOD) and the catalase (CAT) enzyme activity. BAK also inhibited the expression of TNF-α, IL-1β, IL-6, and IL-18 and suppressed apoptosis and pyroptosis both in MACO/R mice and in OGD/R SH-SY5Y cells. Further results showed that BAK could suppress TXNIP, ASC, NLRP3, and caspase-1 mRNA levels to reverse assembly of inflammasome. And BAK could also upregulate the expression of phosphorylated AMP-activated protein kinase (AMPK) and nuclear factor erythroid 2-related factor (Nrf2). In addition, Nrf2 inhibitor ML385 reversed the BAK induced reduction of TXNIP, ASC, NLRP3, and the AMPK inhibitor also abolished BAK’ the effect on the regulation of Nrf2, TXNIP, ASC, NLRP3, caspase-1, and pro-inflammatory cytokines. In conclusion, BAK, found in leaves and seeds of Psoralea corylifolia Linn, could ameliorated cerebral I/R injury through activating AMPK/Nrf2 to inhibit NLRP3 inflammasome, which might present new therapeutic strategy for cerebral I/R injury.</description><subject>AMP-Activated Protein Kinases - metabolism</subject><subject>AMPK</subject><subject>Animals</subject><subject>Apoptosis - drug effects</subject><subject>Bakuchiol</subject><subject>Carrier Proteins - metabolism</subject><subject>Caspase 1 - metabolism</subject><subject>Cell Cycle Proteins - metabolism</subject><subject>Humans</subject><subject>Infarction, Middle Cerebral Artery - metabolism</subject><subject>Ischemia–reperfusion injury</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>NF-E2-Related Factor 2 - metabolism</subject><subject>NLR Family, Pyrin Domain-Containing 3 Protein - antagonists &amp; inhibitors</subject><subject>NLR Family, Pyrin Domain-Containing 3 Protein - metabolism</subject><subject>NLRP3 inflammasome</subject><subject>Nrf2</subject><subject>Phenols - pharmacology</subject><subject>Reperfusion Injury - drug therapy</subject><subject>Reperfusion Injury - metabolism</subject><subject>Signal Transduction - drug effects</subject><subject>Thioredoxins</subject><issn>0304-3940</issn><issn>1872-7972</issn><issn>1872-7972</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEuO1DAQhi0EYpqBGyDkJZt0_EribJCaEY_RNE0LDRI7q2JXGLfyaOxkRK_gDtyQk-BRBpasqlT6qkr_R8hzztac8TI_rAecO5zWggm15lIzWT0gK64rkVV1JR6SFZNMZbJW7Iw8ifHAGCt4oR6TM1mnpiyqFfnxenNFocfOjwEmdNRiwCZAR_3QQrCTH4fcR3uDvYffP38FPGJo55jGiTjM4USbE4XE3cLkh69082F_le9CK-g0JuLGN36i1192l_t8t_20l7mFeISIGafw3cen5FELXcRn9_WcfH775vrifbb9-O7yYrPNrFB8yhRvwIHQjQKNvGXQas1qh1DWloGoC12WqDhzUmtVitq1TiimVa0K7qBBeU5eLnePYfw2Y5xMn1Jh18GA4xyN5EJXSjAuEqoW1IYxxoCtOQbfQzgZzsydenMwi3pzp94s6tPai_sPc9Oj-7f013UCXi0Appy3HoOJ1uNg0fmAdjJu9P__8Ad_0pgC</recordid><startdate>20250101</startdate><enddate>20250101</enddate><creator>Xu, Yue-Wei</creator><creator>Yao, Chang-Heng</creator><creator>Gao, Xiao-Ming</creator><creator>Wang, Li</creator><creator>Zhang, Meng-Xiang</creator><creator>Yang, Xiao-Dan</creator><creator>Li, Jing</creator><creator>Dai, Wen-Ling</creator><creator>Yang, Man-Qin</creator><creator>Cai, Ming</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>20250101</creationdate><title>BAK ameliorated cerebral infarction/ischemia–reperfusion injury by activating AMPK/Nrf2 to inhibit TXNIP/NLRP3/caspase-1 axis</title><author>Xu, Yue-Wei ; Yao, Chang-Heng ; Gao, Xiao-Ming ; Wang, Li ; Zhang, Meng-Xiang ; Yang, Xiao-Dan ; Li, Jing ; Dai, Wen-Ling ; Yang, Man-Qin ; Cai, Ming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c241t-41bada28b4a8e1f0af8809dea69c0a295866e410d3884629dfd240849451dabe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2025</creationdate><topic>AMP-Activated Protein Kinases - metabolism</topic><topic>AMPK</topic><topic>Animals</topic><topic>Apoptosis - drug effects</topic><topic>Bakuchiol</topic><topic>Carrier Proteins - metabolism</topic><topic>Caspase 1 - metabolism</topic><topic>Cell Cycle Proteins - metabolism</topic><topic>Humans</topic><topic>Infarction, Middle Cerebral Artery - metabolism</topic><topic>Ischemia–reperfusion injury</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>NF-E2-Related Factor 2 - metabolism</topic><topic>NLR Family, Pyrin Domain-Containing 3 Protein - antagonists &amp; inhibitors</topic><topic>NLR Family, Pyrin Domain-Containing 3 Protein - metabolism</topic><topic>NLRP3 inflammasome</topic><topic>Nrf2</topic><topic>Phenols - pharmacology</topic><topic>Reperfusion Injury - drug therapy</topic><topic>Reperfusion Injury - metabolism</topic><topic>Signal Transduction - drug effects</topic><topic>Thioredoxins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Yue-Wei</creatorcontrib><creatorcontrib>Yao, Chang-Heng</creatorcontrib><creatorcontrib>Gao, Xiao-Ming</creatorcontrib><creatorcontrib>Wang, Li</creatorcontrib><creatorcontrib>Zhang, Meng-Xiang</creatorcontrib><creatorcontrib>Yang, Xiao-Dan</creatorcontrib><creatorcontrib>Li, Jing</creatorcontrib><creatorcontrib>Dai, Wen-Ling</creatorcontrib><creatorcontrib>Yang, Man-Qin</creatorcontrib><creatorcontrib>Cai, Ming</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>Neuroscience letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Yue-Wei</au><au>Yao, Chang-Heng</au><au>Gao, Xiao-Ming</au><au>Wang, Li</au><au>Zhang, Meng-Xiang</au><au>Yang, Xiao-Dan</au><au>Li, Jing</au><au>Dai, Wen-Ling</au><au>Yang, Man-Qin</au><au>Cai, Ming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>BAK ameliorated cerebral infarction/ischemia–reperfusion injury by activating AMPK/Nrf2 to inhibit TXNIP/NLRP3/caspase-1 axis</atitle><jtitle>Neuroscience letters</jtitle><addtitle>Neurosci Lett</addtitle><date>2025-01-01</date><risdate>2025</risdate><volume>844</volume><spage>138037</spage><pages>138037-</pages><artnum>138037</artnum><issn>0304-3940</issn><issn>1872-7972</issn><eissn>1872-7972</eissn><abstract>•Active alkaloids of Psoralea corylifolia Linn. in alleviating MACO/R injury.•Clarifying Bakuchiol reduced neuronal apoptosis and pyroptosis to relieve MACO/R injury.•Bakuchiol was found to suppress inflammation and cell pyroptosis through regulating Nrf2/NLRP3/Caspase-1.•AMPK inhibitor CC could reverse BAK induced upregulation of Nrf2. Cerebral ischemia/reperfusion (I/R) injury is a serious vascular disease with extremely high mortality and disability rate. Bakuchiol (BAK) was found in leaves and seeds of Psoralea corylifolia Linn and has been shown to decrease inflammation and reduce oxidative stress, while the mechanism of BAK in ameliorating cerebral I/R injury remains unclear. Middle cerebral artery occlusion reperfusion (MACO/R) was used to establish mouse model. The protective effect of BAK in MCAO/R mices was detected by performing neurological deficit testing, TTC staining, and H&amp;E staining. Oxygen/glucose deprivation and reperfusion (OGD/R) was used to stimulate SH-SY5Y cells in vitro. Protein expression was detected by western blotting, gene expression was detected by quantitative real-time polymerase chain reaction and apoptosis was detected by immunofluorescence. Our study indicated that BAK protected ischemia–reperfusion injury in MACO/R mice, and upregulated superoxide dismutase (SOD) and the catalase (CAT) enzyme activity. BAK also inhibited the expression of TNF-α, IL-1β, IL-6, and IL-18 and suppressed apoptosis and pyroptosis both in MACO/R mice and in OGD/R SH-SY5Y cells. Further results showed that BAK could suppress TXNIP, ASC, NLRP3, and caspase-1 mRNA levels to reverse assembly of inflammasome. And BAK could also upregulate the expression of phosphorylated AMP-activated protein kinase (AMPK) and nuclear factor erythroid 2-related factor (Nrf2). In addition, Nrf2 inhibitor ML385 reversed the BAK induced reduction of TXNIP, ASC, NLRP3, and the AMPK inhibitor also abolished BAK’ the effect on the regulation of Nrf2, TXNIP, ASC, NLRP3, caspase-1, and pro-inflammatory cytokines. In conclusion, BAK, found in leaves and seeds of Psoralea corylifolia Linn, could ameliorated cerebral I/R injury through activating AMPK/Nrf2 to inhibit NLRP3 inflammasome, which might present new therapeutic strategy for cerebral I/R injury.</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>39515657</pmid><doi>10.1016/j.neulet.2024.138037</doi></addata></record>
fulltext fulltext
identifier ISSN: 0304-3940
ispartof Neuroscience letters, 2025-01, Vol.844, p.138037, Article 138037
issn 0304-3940
1872-7972
1872-7972
language eng
recordid cdi_proquest_miscellaneous_3128742012
source MEDLINE; Access via ScienceDirect (Elsevier)
subjects AMP-Activated Protein Kinases - metabolism
AMPK
Animals
Apoptosis - drug effects
Bakuchiol
Carrier Proteins - metabolism
Caspase 1 - metabolism
Cell Cycle Proteins - metabolism
Humans
Infarction, Middle Cerebral Artery - metabolism
Ischemia–reperfusion injury
Male
Mice
Mice, Inbred C57BL
NF-E2-Related Factor 2 - metabolism
NLR Family, Pyrin Domain-Containing 3 Protein - antagonists & inhibitors
NLR Family, Pyrin Domain-Containing 3 Protein - metabolism
NLRP3 inflammasome
Nrf2
Phenols - pharmacology
Reperfusion Injury - drug therapy
Reperfusion Injury - metabolism
Signal Transduction - drug effects
Thioredoxins
title BAK ameliorated cerebral infarction/ischemia–reperfusion injury by activating AMPK/Nrf2 to inhibit TXNIP/NLRP3/caspase-1 axis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-19T02%3A38%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=BAK%20ameliorated%20cerebral%20infarction/ischemia%E2%80%93reperfusion%20injury%20by%20activating%20AMPK/Nrf2%20to%20inhibit%20TXNIP/NLRP3/caspase-1%20axis&rft.jtitle=Neuroscience%20letters&rft.au=Xu,%20Yue-Wei&rft.date=2025-01-01&rft.volume=844&rft.spage=138037&rft.pages=138037-&rft.artnum=138037&rft.issn=0304-3940&rft.eissn=1872-7972&rft_id=info:doi/10.1016/j.neulet.2024.138037&rft_dat=%3Cproquest_cross%3E3128742012%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3128742012&rft_id=info:pmid/39515657&rft_els_id=S0304394024004166&rfr_iscdi=true