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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Veröffentlicht in:Acta pharmacologica Sinica 2018-06, Vol.39 (6), p.998-1011
Hauptverfasser: Wang, Fu-jiang, Wang, Shao-xia, Chai, Li-juan, Zhang, Yue, Guo, Hong, Hu, Li-min
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Wang, Shao-xia
Chai, Li-juan
Zhang, Yue
Guo, Hong
Hu, Li-min
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
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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. 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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 &amp; 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 &amp; 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 &amp; 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 &amp; 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 &amp; 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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
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