Xueshuantong injection (lyophilized) combined with salvianolate lyophilized injection protects against focal cerebral ischemia/reperfusion injury in rats through attenuation of oxidative stress
Salvianolate lyophilized injection (SLI) and Xueshuantong injection (lyophilized) (XST) are two herbal standardized preparations that have been widely used in China for the treatment of acute cerebral infarction. In this study, we investigated the neuroprotective effects of SLI combined with XST in...
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description | Salvianolate lyophilized injection (SLI) and Xueshuantong injection (lyophilized) (XST) are two herbal standardized preparations that have been widely used in China for the treatment of acute cerebral infarction. In this study, we investigated the neuroprotective effects of SLI combined with XST in a rat model of middle cerebral artery occlusion-reperfusion (MCAO/R). Wistar rats were subjected to 1.5 h of MCAO followed by reperfusion for 3 h, then were treated with SLI or XST alone, or with their combinations via tail vein injection daily for 3 d. Edaravone (EDI, 6 mg·kg
−1
·d
−1
) was used as a positive control drug, We showed that administration of a combination of 1X1S (XST 100 mg·kg
−1
·d
−1
plus SLI 21 mg·kg
−1
·d
−1
) more effectively protected the ischemic brains than SLI or XST used alone. Administration of 1X1S not only significantly decreased neurological deficit scores and infarct volumes and increased regional cerebral blood flow, but also inhibited the activation of both microglia and astrocytes in the hippocampus. Furthermore, administration of 1X1S significantly decreased the levels of MDA and ROS with concomitant increases in the levels of antioxidant activity (SOD, CAT and GSH) in the brain tissues as compared with SLI and XST used alone. Moreover, administration of 1X1S remarkably upregulated the expression of Nrf-2, HO-1 and NQO-1, and downregulated the expression of Keap1 and facilitated the nuclear translocation of Nrf-2 in the brain tissues as compared with XST used alone. Our study demonstrates that a combination of 1X1S effectively protects MCAO/R injury via suppressing oxidative stress and the Nrf-2/Keap1 pathway. |
doi_str_mv | 10.1038/aps.2017.128 |
format | Article |
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−1
·d
−1
) was used as a positive control drug, We showed that administration of a combination of 1X1S (XST 100 mg·kg
−1
·d
−1
plus SLI 21 mg·kg
−1
·d
−1
) more effectively protected the ischemic brains than SLI or XST used alone. Administration of 1X1S not only significantly decreased neurological deficit scores and infarct volumes and increased regional cerebral blood flow, but also inhibited the activation of both microglia and astrocytes in the hippocampus. Furthermore, administration of 1X1S significantly decreased the levels of MDA and ROS with concomitant increases in the levels of antioxidant activity (SOD, CAT and GSH) in the brain tissues as compared with SLI and XST used alone. Moreover, administration of 1X1S remarkably upregulated the expression of Nrf-2, HO-1 and NQO-1, and downregulated the expression of Keap1 and facilitated the nuclear translocation of Nrf-2 in the brain tissues as compared with XST used alone. Our study demonstrates that a combination of 1X1S effectively protects MCAO/R injury via suppressing oxidative stress and the Nrf-2/Keap1 pathway.</description><identifier>ISSN: 1671-4083</identifier><identifier>EISSN: 1745-7254</identifier><identifier>DOI: 10.1038/aps.2017.128</identifier><identifier>PMID: 29022576</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Animals ; Antioxidants ; Antioxidants - administration & dosage ; Astrocytes ; Astrocytes - drug effects ; Astrocytes - metabolism ; Astrocytes - pathology ; Behavior, Animal - drug effects ; Biomarkers - metabolism ; Biomedical and Life Sciences ; Biomedicine ; Blood flow ; Brain ; Cerebral blood flow ; Cerebral infarction ; Cerebrovascular Circulation - drug effects ; Disease Models, Animal ; Drugs, Chinese Herbal - administration & dosage ; Freeze Drying ; GA-binding protein ; Hippocampus - drug effects ; Hippocampus - metabolism ; Hippocampus - pathology ; Hippocampus - physiopathology ; Immunology ; Infarction ; Infarction, Middle Cerebral Artery - complications ; Infarction, Middle Cerebral Artery - drug therapy ; Infarction, Middle Cerebral Artery - metabolism ; Infarction, Middle Cerebral Artery - pathology ; Injection ; Injections, Intravenous ; Internal Medicine ; Ischemia ; Kelch-Like ECH-Associated Protein 1 - genetics ; Kelch-Like ECH-Associated Protein 1 - metabolism ; Male ; Malondialdehyde - metabolism ; Medical Microbiology ; Medicine, Chinese Traditional ; Microglia ; Microglia - drug effects ; Microglia - metabolism ; Microglia - pathology ; Neuroprotection ; Neuroprotective Agents - administration & dosage ; NF-E2-Related Factor 2 - genetics ; NF-E2-Related Factor 2 - metabolism ; Nuclear transport ; Occlusion ; Oxidative stress ; Oxidative Stress - drug effects ; Pharmacology/Toxicology ; Plant Extracts - administration & dosage ; Rats ; Rats, Wistar ; Reactive oxygen species ; Reactive Oxygen Species - metabolism ; Reperfusion ; Reperfusion Injury - etiology ; Reperfusion Injury - metabolism ; Reperfusion Injury - pathology ; Reperfusion Injury - prevention & control ; Rodents ; Signal Transduction - drug effects ; Time Factors ; Tissues ; Translocation ; Vaccine</subject><ispartof>Acta pharmacologica Sinica, 2018-06, Vol.39 (6), p.998-1011</ispartof><rights>CPS and SIMM 2018</rights><rights>Copyright Nature Publishing Group Jun 2018</rights><rights>Copyright © 2018 CPS and SIMM 2018 CPS and SIMM</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-abb9c3689b922b55f9eb8deb38eb5b7cb6ec1e41f6fa18e3ee4e847467a304033</citedby><cites>FETCH-LOGICAL-c478t-abb9c3689b922b55f9eb8deb38eb5b7cb6ec1e41f6fa18e3ee4e847467a304033</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/PMC6256270/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6256270/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,315,729,782,786,887,27931,27932,53798,53800</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29022576$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Fu-jiang</creatorcontrib><creatorcontrib>Wang, Shao-xia</creatorcontrib><creatorcontrib>Chai, Li-juan</creatorcontrib><creatorcontrib>Zhang, Yue</creatorcontrib><creatorcontrib>Guo, Hong</creatorcontrib><creatorcontrib>Hu, Li-min</creatorcontrib><title>Xueshuantong injection (lyophilized) combined with salvianolate lyophilized injection protects against focal cerebral ischemia/reperfusion injury in rats through attenuation of oxidative stress</title><title>Acta pharmacologica Sinica</title><addtitle>Acta Pharmacol Sin</addtitle><addtitle>Acta Pharmacol Sin</addtitle><description>Salvianolate lyophilized injection (SLI) and Xueshuantong injection (lyophilized) (XST) are two herbal standardized preparations that have been widely used in China for the treatment of acute cerebral infarction. In this study, we investigated the neuroprotective effects of SLI combined with XST in a rat model of middle cerebral artery occlusion-reperfusion (MCAO/R). Wistar rats were subjected to 1.5 h of MCAO followed by reperfusion for 3 h, then were treated with SLI or XST alone, or with their combinations via tail vein injection daily for 3 d. Edaravone (EDI, 6 mg·kg
−1
·d
−1
) was used as a positive control drug, We showed that administration of a combination of 1X1S (XST 100 mg·kg
−1
·d
−1
plus SLI 21 mg·kg
−1
·d
−1
) more effectively protected the ischemic brains than SLI or XST used alone. Administration of 1X1S not only significantly decreased neurological deficit scores and infarct volumes and increased regional cerebral blood flow, but also inhibited the activation of both microglia and astrocytes in the hippocampus. Furthermore, administration of 1X1S significantly decreased the levels of MDA and ROS with concomitant increases in the levels of antioxidant activity (SOD, CAT and GSH) in the brain tissues as compared with SLI and XST used alone. Moreover, administration of 1X1S remarkably upregulated the expression of Nrf-2, HO-1 and NQO-1, and downregulated the expression of Keap1 and facilitated the nuclear translocation of Nrf-2 in the brain tissues as compared with XST used alone. Our study demonstrates that a combination of 1X1S effectively protects MCAO/R injury via suppressing oxidative stress and the Nrf-2/Keap1 pathway.</description><subject>Animals</subject><subject>Antioxidants</subject><subject>Antioxidants - administration & dosage</subject><subject>Astrocytes</subject><subject>Astrocytes - drug effects</subject><subject>Astrocytes - metabolism</subject><subject>Astrocytes - pathology</subject><subject>Behavior, Animal - drug effects</subject><subject>Biomarkers - metabolism</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Blood flow</subject><subject>Brain</subject><subject>Cerebral blood flow</subject><subject>Cerebral infarction</subject><subject>Cerebrovascular Circulation - drug effects</subject><subject>Disease Models, Animal</subject><subject>Drugs, Chinese Herbal - administration & dosage</subject><subject>Freeze Drying</subject><subject>GA-binding protein</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - metabolism</subject><subject>Hippocampus - pathology</subject><subject>Hippocampus - physiopathology</subject><subject>Immunology</subject><subject>Infarction</subject><subject>Infarction, Middle Cerebral Artery - complications</subject><subject>Infarction, Middle Cerebral Artery - drug therapy</subject><subject>Infarction, Middle Cerebral Artery - metabolism</subject><subject>Infarction, Middle Cerebral Artery - pathology</subject><subject>Injection</subject><subject>Injections, Intravenous</subject><subject>Internal Medicine</subject><subject>Ischemia</subject><subject>Kelch-Like ECH-Associated Protein 1 - genetics</subject><subject>Kelch-Like ECH-Associated Protein 1 - metabolism</subject><subject>Male</subject><subject>Malondialdehyde - metabolism</subject><subject>Medical Microbiology</subject><subject>Medicine, Chinese Traditional</subject><subject>Microglia</subject><subject>Microglia - drug effects</subject><subject>Microglia - metabolism</subject><subject>Microglia - pathology</subject><subject>Neuroprotection</subject><subject>Neuroprotective Agents - administration & dosage</subject><subject>NF-E2-Related Factor 2 - genetics</subject><subject>NF-E2-Related Factor 2 - metabolism</subject><subject>Nuclear transport</subject><subject>Occlusion</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Pharmacology/Toxicology</subject><subject>Plant Extracts - administration & dosage</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Reactive oxygen species</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Reperfusion</subject><subject>Reperfusion Injury - etiology</subject><subject>Reperfusion Injury - metabolism</subject><subject>Reperfusion Injury - pathology</subject><subject>Reperfusion Injury - prevention & control</subject><subject>Rodents</subject><subject>Signal Transduction - drug effects</subject><subject>Time Factors</subject><subject>Tissues</subject><subject>Translocation</subject><subject>Vaccine</subject><issn>1671-4083</issn><issn>1745-7254</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kk2LFDEQhhtR3HX15lkCXlawZ_PZHxdBFr9gwYuCt5Ckq7sz9CRtkh6d_Xf7z8w46zqKeEqFeuqtVOUtiqcErwhmzYWa44piUq8Ibe4Vp6Tmoqyp4PdzXNWk5LhhJ8WjGNcYM8pI-7A4oS2mVNTVaXHzZYE4Lsol7wZk3RpMst6h82nn59FO9hq6F8j4jbYOOvTNphFFNW2tcn5SCdARd1Q-B59yGJEalHUxod4bNSEDAXTIgY1mhI1VFwFmCP0S90W5fAm7fKCgcmkag1-GEamUwC3qp67vkf9uu3zZAoopQIyPiwe9miI8uT3Pis9v33y6fF9efXz34fL1VWl43aRSad0aVjWtbinVQvQt6KYDzRrQQtdGV2AIcNJXvSINMAAODa95VSuGOWbsrHh10J0XvYHOgEt5EjkHu1FhJ72y8s-Ms6Mc_FZWVFS0xlng_FYg-K9560lu8hpgmpQDv0RJWoE5EflrMvr8L3Ttl-DyeJIyhrFoOCf_pTBvBcMt37d9eaBM8DEG6O-eTLDcO0hmB8m9g2R2UMafHY95B_-yTAbKAxBzyg0Qfnf9p-APEibYSQ</recordid><startdate>20180601</startdate><enddate>20180601</enddate><creator>Wang, Fu-jiang</creator><creator>Wang, Shao-xia</creator><creator>Chai, Li-juan</creator><creator>Zhang, Yue</creator><creator>Guo, Hong</creator><creator>Hu, Li-min</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</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>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TK</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20180601</creationdate><title>Xueshuantong injection (lyophilized) combined with salvianolate lyophilized injection protects against focal cerebral ischemia/reperfusion injury in rats through attenuation of oxidative stress</title><author>Wang, Fu-jiang ; Wang, Shao-xia ; Chai, Li-juan ; Zhang, Yue ; Guo, Hong ; Hu, Li-min</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c478t-abb9c3689b922b55f9eb8deb38eb5b7cb6ec1e41f6fa18e3ee4e847467a304033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Antioxidants</topic><topic>Antioxidants - administration & dosage</topic><topic>Astrocytes</topic><topic>Astrocytes - drug effects</topic><topic>Astrocytes - metabolism</topic><topic>Astrocytes - pathology</topic><topic>Behavior, Animal - drug effects</topic><topic>Biomarkers - metabolism</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Blood flow</topic><topic>Brain</topic><topic>Cerebral blood flow</topic><topic>Cerebral infarction</topic><topic>Cerebrovascular Circulation - drug effects</topic><topic>Disease Models, Animal</topic><topic>Drugs, Chinese Herbal - administration & dosage</topic><topic>Freeze Drying</topic><topic>GA-binding protein</topic><topic>Hippocampus - drug effects</topic><topic>Hippocampus - metabolism</topic><topic>Hippocampus - pathology</topic><topic>Hippocampus - physiopathology</topic><topic>Immunology</topic><topic>Infarction</topic><topic>Infarction, Middle Cerebral Artery - complications</topic><topic>Infarction, Middle Cerebral Artery - drug therapy</topic><topic>Infarction, Middle Cerebral Artery - metabolism</topic><topic>Infarction, Middle Cerebral Artery - pathology</topic><topic>Injection</topic><topic>Injections, Intravenous</topic><topic>Internal Medicine</topic><topic>Ischemia</topic><topic>Kelch-Like ECH-Associated Protein 1 - genetics</topic><topic>Kelch-Like ECH-Associated Protein 1 - metabolism</topic><topic>Male</topic><topic>Malondialdehyde - metabolism</topic><topic>Medical Microbiology</topic><topic>Medicine, Chinese Traditional</topic><topic>Microglia</topic><topic>Microglia - drug effects</topic><topic>Microglia - metabolism</topic><topic>Microglia - pathology</topic><topic>Neuroprotection</topic><topic>Neuroprotective Agents - administration & dosage</topic><topic>NF-E2-Related Factor 2 - genetics</topic><topic>NF-E2-Related Factor 2 - metabolism</topic><topic>Nuclear transport</topic><topic>Occlusion</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>Pharmacology/Toxicology</topic><topic>Plant Extracts - administration & dosage</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Reactive oxygen species</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Reperfusion</topic><topic>Reperfusion Injury - etiology</topic><topic>Reperfusion Injury - metabolism</topic><topic>Reperfusion Injury - pathology</topic><topic>Reperfusion Injury - prevention & control</topic><topic>Rodents</topic><topic>Signal Transduction - drug effects</topic><topic>Time Factors</topic><topic>Tissues</topic><topic>Translocation</topic><topic>Vaccine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Fu-jiang</creatorcontrib><creatorcontrib>Wang, Shao-xia</creatorcontrib><creatorcontrib>Chai, Li-juan</creatorcontrib><creatorcontrib>Zhang, Yue</creatorcontrib><creatorcontrib>Guo, Hong</creatorcontrib><creatorcontrib>Hu, Li-min</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Acta pharmacologica Sinica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Fu-jiang</au><au>Wang, Shao-xia</au><au>Chai, Li-juan</au><au>Zhang, Yue</au><au>Guo, Hong</au><au>Hu, Li-min</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Xueshuantong injection (lyophilized) combined with salvianolate lyophilized injection protects against focal cerebral ischemia/reperfusion injury in rats through attenuation of oxidative stress</atitle><jtitle>Acta pharmacologica Sinica</jtitle><stitle>Acta Pharmacol Sin</stitle><addtitle>Acta Pharmacol Sin</addtitle><date>2018-06-01</date><risdate>2018</risdate><volume>39</volume><issue>6</issue><spage>998</spage><epage>1011</epage><pages>998-1011</pages><issn>1671-4083</issn><eissn>1745-7254</eissn><abstract>Salvianolate lyophilized injection (SLI) and Xueshuantong injection (lyophilized) (XST) are two herbal standardized preparations that have been widely used in China for the treatment of acute cerebral infarction. In this study, we investigated the neuroprotective effects of SLI combined with XST in a rat model of middle cerebral artery occlusion-reperfusion (MCAO/R). Wistar rats were subjected to 1.5 h of MCAO followed by reperfusion for 3 h, then were treated with SLI or XST alone, or with their combinations via tail vein injection daily for 3 d. Edaravone (EDI, 6 mg·kg
−1
·d
−1
) was used as a positive control drug, We showed that administration of a combination of 1X1S (XST 100 mg·kg
−1
·d
−1
plus SLI 21 mg·kg
−1
·d
−1
) more effectively protected the ischemic brains than SLI or XST used alone. Administration of 1X1S not only significantly decreased neurological deficit scores and infarct volumes and increased regional cerebral blood flow, but also inhibited the activation of both microglia and astrocytes in the hippocampus. Furthermore, administration of 1X1S significantly decreased the levels of MDA and ROS with concomitant increases in the levels of antioxidant activity (SOD, CAT and GSH) in the brain tissues as compared with SLI and XST used alone. Moreover, administration of 1X1S remarkably upregulated the expression of Nrf-2, HO-1 and NQO-1, and downregulated the expression of Keap1 and facilitated the nuclear translocation of Nrf-2 in the brain tissues as compared with XST used alone. Our study demonstrates that a combination of 1X1S effectively protects MCAO/R injury via suppressing oxidative stress and the Nrf-2/Keap1 pathway.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>29022576</pmid><doi>10.1038/aps.2017.128</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; PubMed Central; Alma/SFX Local Collection |
subjects | Animals Antioxidants Antioxidants - administration & dosage Astrocytes Astrocytes - drug effects Astrocytes - metabolism Astrocytes - pathology Behavior, Animal - drug effects Biomarkers - metabolism Biomedical and Life Sciences Biomedicine Blood flow Brain Cerebral blood flow Cerebral infarction Cerebrovascular Circulation - drug effects Disease Models, Animal Drugs, Chinese Herbal - administration & dosage Freeze Drying GA-binding protein Hippocampus - drug effects Hippocampus - metabolism Hippocampus - pathology Hippocampus - physiopathology Immunology Infarction Infarction, Middle Cerebral Artery - complications Infarction, Middle Cerebral Artery - drug therapy Infarction, Middle Cerebral Artery - metabolism Infarction, Middle Cerebral Artery - pathology Injection Injections, Intravenous Internal Medicine Ischemia Kelch-Like ECH-Associated Protein 1 - genetics Kelch-Like ECH-Associated Protein 1 - metabolism Male Malondialdehyde - metabolism Medical Microbiology Medicine, Chinese Traditional Microglia Microglia - drug effects Microglia - metabolism Microglia - pathology Neuroprotection Neuroprotective Agents - administration & dosage NF-E2-Related Factor 2 - genetics NF-E2-Related Factor 2 - metabolism Nuclear transport Occlusion Oxidative stress Oxidative Stress - drug effects Pharmacology/Toxicology Plant Extracts - administration & dosage Rats Rats, Wistar Reactive oxygen species Reactive Oxygen Species - metabolism Reperfusion Reperfusion Injury - etiology Reperfusion Injury - metabolism Reperfusion Injury - pathology Reperfusion Injury - prevention & control Rodents Signal Transduction - drug effects Time Factors Tissues Translocation Vaccine |
title | Xueshuantong injection (lyophilized) combined with salvianolate lyophilized injection protects against focal cerebral ischemia/reperfusion injury in rats through attenuation of oxidative stress |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-04T03%3A03%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Xueshuantong%20injection%20(lyophilized)%20combined%20with%20salvianolate%20lyophilized%20injection%20protects%20against%20focal%20cerebral%20ischemia/reperfusion%20injury%20in%20rats%20through%20attenuation%20of%20oxidative%20stress&rft.jtitle=Acta%20pharmacologica%20Sinica&rft.au=Wang,%20Fu-jiang&rft.date=2018-06-01&rft.volume=39&rft.issue=6&rft.spage=998&rft.epage=1011&rft.pages=998-1011&rft.issn=1671-4083&rft.eissn=1745-7254&rft_id=info:doi/10.1038/aps.2017.128&rft_dat=%3Cproquest_pubme%3E2049530940%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2049530940&rft_id=info:pmid/29022576&rfr_iscdi=true |