Catalpol prevents the loss of CA1 hippocampal neurons and reduces working errors in gerbils after ischemia-reperfusion injury
Catalpol, an iridoid glycoside, contained richly in the roots of Rehmannia glutinosa, was found for the first time to be of neuroprotection in gerbils subjected to transient global cerebral ischemia. Catalpol (1 mg/kg ip) used immediately after reperfusion and repeatedly at 12, 24, 48 and 72 h signi...
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Veröffentlicht in: | Toxicon (Oxford) 2005-12, Vol.46 (8), p.845-851 |
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creator | Li, Dan-Qing Li, Yang Liu, Yuxin Bao, Yong-Ming Hu, Bo An, Li-Jia |
description | Catalpol, an iridoid glycoside, contained richly in the roots of
Rehmannia glutinosa, was found for the first time to be of neuroprotection in gerbils subjected to transient global cerebral ischemia. Catalpol (1
mg/kg ip) used immediately after reperfusion and repeatedly at 12, 24, 48 and 72
h significantly rescued neurons in hippocampal CA1 subfield and reduced working errors during behavioral testing. The neuroprotective efficacy of catalpol became more evident when the doses of catalpol were increased to 5 and 10
mg/kg. In addition, it was exciting that the significant neuroprotection by catalpol was also evident when catalpol was applied up to 3
h after ischemia. But the neuroprotective efficacy of catalpol became weak when catalpol was given at 6
h after ischemia. Of great encouragement was the finding that the neuroprotection of catalpol could be seen not only in a short post-ischemic period (12 days) but also in a long period (35 days). All these indicated that catalpol was truly neuroprotective rather than simply delayed the onset of neuronal damage and might be of therapeutic value for the treatment of global cerebral ischemia. |
doi_str_mv | 10.1016/j.toxicon.2004.09.007 |
format | Article |
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Rehmannia glutinosa, was found for the first time to be of neuroprotection in gerbils subjected to transient global cerebral ischemia. Catalpol (1
mg/kg ip) used immediately after reperfusion and repeatedly at 12, 24, 48 and 72
h significantly rescued neurons in hippocampal CA1 subfield and reduced working errors during behavioral testing. The neuroprotective efficacy of catalpol became more evident when the doses of catalpol were increased to 5 and 10
mg/kg. In addition, it was exciting that the significant neuroprotection by catalpol was also evident when catalpol was applied up to 3
h after ischemia. But the neuroprotective efficacy of catalpol became weak when catalpol was given at 6
h after ischemia. Of great encouragement was the finding that the neuroprotection of catalpol could be seen not only in a short post-ischemic period (12 days) but also in a long period (35 days). All these indicated that catalpol was truly neuroprotective rather than simply delayed the onset of neuronal damage and might be of therapeutic value for the treatment of global cerebral ischemia.</description><identifier>ISSN: 0041-0101</identifier><identifier>EISSN: 1879-3150</identifier><identifier>DOI: 10.1016/j.toxicon.2004.09.007</identifier><identifier>PMID: 16269165</identifier><identifier>CODEN: TOXIA6</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Analysis of Variance ; Animals ; Behavioral Symptoms - drug therapy ; Behavioral Symptoms - physiopathology ; Biological and medical sciences ; Catalpol ; Cognition ; Dose-Response Relationship, Drug ; General pharmacology ; Gerbillinae ; Gerbils ; Glucosides - chemistry ; Glucosides - pharmacology ; Glucosides - therapeutic use ; Hippocampus ; Hippocampus - cytology ; Hippocampus - drug effects ; Iridoid Glucosides ; Iridoids - chemistry ; Iridoids - pharmacology ; Iridoids - therapeutic use ; Ischemia ; Medical sciences ; Neurons - drug effects ; Neuroprotection ; Neuroprotective Agents - chemistry ; Neuroprotective Agents - pharmacology ; Neuroprotective Agents - therapeutic use ; Pharmacognosy. Homeopathy. Health food ; Pharmacology. Drug treatments ; Reperfusion Injury - drug therapy ; Reperfusion Injury - physiopathology ; Time Factors</subject><ispartof>Toxicon (Oxford), 2005-12, Vol.46 (8), p.845-851</ispartof><rights>2004 Elsevier Ltd</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-5ef422d3eb33d7db973394f84c570ae99e85748d73b19954f2196e64c7c41beb3</citedby><cites>FETCH-LOGICAL-c405t-5ef422d3eb33d7db973394f84c570ae99e85748d73b19954f2196e64c7c41beb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.toxicon.2004.09.007$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17345952$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16269165$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Dan-Qing</creatorcontrib><creatorcontrib>Li, Yang</creatorcontrib><creatorcontrib>Liu, Yuxin</creatorcontrib><creatorcontrib>Bao, Yong-Ming</creatorcontrib><creatorcontrib>Hu, Bo</creatorcontrib><creatorcontrib>An, Li-Jia</creatorcontrib><title>Catalpol prevents the loss of CA1 hippocampal neurons and reduces working errors in gerbils after ischemia-reperfusion injury</title><title>Toxicon (Oxford)</title><addtitle>Toxicon</addtitle><description>Catalpol, an iridoid glycoside, contained richly in the roots of
Rehmannia glutinosa, was found for the first time to be of neuroprotection in gerbils subjected to transient global cerebral ischemia. Catalpol (1
mg/kg ip) used immediately after reperfusion and repeatedly at 12, 24, 48 and 72
h significantly rescued neurons in hippocampal CA1 subfield and reduced working errors during behavioral testing. The neuroprotective efficacy of catalpol became more evident when the doses of catalpol were increased to 5 and 10
mg/kg. In addition, it was exciting that the significant neuroprotection by catalpol was also evident when catalpol was applied up to 3
h after ischemia. But the neuroprotective efficacy of catalpol became weak when catalpol was given at 6
h after ischemia. Of great encouragement was the finding that the neuroprotection of catalpol could be seen not only in a short post-ischemic period (12 days) but also in a long period (35 days). All these indicated that catalpol was truly neuroprotective rather than simply delayed the onset of neuronal damage and might be of therapeutic value for the treatment of global cerebral ischemia.</description><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Behavioral Symptoms - drug therapy</subject><subject>Behavioral Symptoms - physiopathology</subject><subject>Biological and medical sciences</subject><subject>Catalpol</subject><subject>Cognition</subject><subject>Dose-Response Relationship, Drug</subject><subject>General pharmacology</subject><subject>Gerbillinae</subject><subject>Gerbils</subject><subject>Glucosides - chemistry</subject><subject>Glucosides - pharmacology</subject><subject>Glucosides - therapeutic use</subject><subject>Hippocampus</subject><subject>Hippocampus - cytology</subject><subject>Hippocampus - drug effects</subject><subject>Iridoid Glucosides</subject><subject>Iridoids - chemistry</subject><subject>Iridoids - pharmacology</subject><subject>Iridoids - therapeutic use</subject><subject>Ischemia</subject><subject>Medical sciences</subject><subject>Neurons - drug effects</subject><subject>Neuroprotection</subject><subject>Neuroprotective Agents - chemistry</subject><subject>Neuroprotective Agents - pharmacology</subject><subject>Neuroprotective Agents - therapeutic use</subject><subject>Pharmacognosy. Homeopathy. Health food</subject><subject>Pharmacology. Drug treatments</subject><subject>Reperfusion Injury - drug therapy</subject><subject>Reperfusion Injury - physiopathology</subject><subject>Time Factors</subject><issn>0041-0101</issn><issn>1879-3150</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0c1u1DAUBWALgehQeASQN7DLYMd2HK9QNeJPqsQG1pbj3HQ8JHa4Tlq64N1xNZG67MoLf8e-uoeQt5ztOePNx9N-SX-DT3FfMyb3zOwZ08_IjrfaVIIr9pzsygWvWOEX5FXOJ8aYaE3zklzwpm4Mb9SO_Du4xY1zGumMcAtxyXQ5Ah1TzjQN9HDF6THMc_Jumt1II6yYYqYu9hShXz1kepfwd4g3FBATZhoivQHswljUsADSkP0RpuAqhBlwWHNIsajTivevyYvBjRnebOcl-fXl88_Dt-r6x9fvh6vrykumlkrBIOu6F9AJ0eu-M1oII4dWeqWZA2OgVVq2vRYdN0bJoeamgUZ67SXvSuqSfDi_O2P6s0Je7FSmgnF0EdKabdO2qmTkk5DrmtdMiALVGXosq0IY7IxhcnhvObMPBdmT3QqyDwVZZmwpqOTebR-s3QT9Y2prpID3G3DZu3FAF33Ij04LqYyqi_t0dlD2dhsAbfYBooc-IPjF9ik8Mcp_ws6zbw</recordid><startdate>20051215</startdate><enddate>20051215</enddate><creator>Li, Dan-Qing</creator><creator>Li, Yang</creator><creator>Liu, Yuxin</creator><creator>Bao, Yong-Ming</creator><creator>Hu, Bo</creator><creator>An, Li-Jia</creator><general>Elsevier Ltd</general><general>Elsevier Science</general><scope>IQODW</scope><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>7U7</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>20051215</creationdate><title>Catalpol prevents the loss of CA1 hippocampal neurons and reduces working errors in gerbils after ischemia-reperfusion injury</title><author>Li, Dan-Qing ; Li, Yang ; Liu, Yuxin ; Bao, Yong-Ming ; Hu, Bo ; An, Li-Jia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-5ef422d3eb33d7db973394f84c570ae99e85748d73b19954f2196e64c7c41beb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Behavioral Symptoms - drug therapy</topic><topic>Behavioral Symptoms - physiopathology</topic><topic>Biological and medical sciences</topic><topic>Catalpol</topic><topic>Cognition</topic><topic>Dose-Response Relationship, Drug</topic><topic>General pharmacology</topic><topic>Gerbillinae</topic><topic>Gerbils</topic><topic>Glucosides - chemistry</topic><topic>Glucosides - pharmacology</topic><topic>Glucosides - therapeutic use</topic><topic>Hippocampus</topic><topic>Hippocampus - cytology</topic><topic>Hippocampus - drug effects</topic><topic>Iridoid Glucosides</topic><topic>Iridoids - chemistry</topic><topic>Iridoids - pharmacology</topic><topic>Iridoids - therapeutic use</topic><topic>Ischemia</topic><topic>Medical sciences</topic><topic>Neurons - drug effects</topic><topic>Neuroprotection</topic><topic>Neuroprotective Agents - chemistry</topic><topic>Neuroprotective Agents - pharmacology</topic><topic>Neuroprotective Agents - therapeutic use</topic><topic>Pharmacognosy. Homeopathy. Health food</topic><topic>Pharmacology. Drug treatments</topic><topic>Reperfusion Injury - drug therapy</topic><topic>Reperfusion Injury - physiopathology</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Dan-Qing</creatorcontrib><creatorcontrib>Li, Yang</creatorcontrib><creatorcontrib>Liu, Yuxin</creatorcontrib><creatorcontrib>Bao, Yong-Ming</creatorcontrib><creatorcontrib>Hu, Bo</creatorcontrib><creatorcontrib>An, Li-Jia</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Toxicon (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Dan-Qing</au><au>Li, Yang</au><au>Liu, Yuxin</au><au>Bao, Yong-Ming</au><au>Hu, Bo</au><au>An, Li-Jia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Catalpol prevents the loss of CA1 hippocampal neurons and reduces working errors in gerbils after ischemia-reperfusion injury</atitle><jtitle>Toxicon (Oxford)</jtitle><addtitle>Toxicon</addtitle><date>2005-12-15</date><risdate>2005</risdate><volume>46</volume><issue>8</issue><spage>845</spage><epage>851</epage><pages>845-851</pages><issn>0041-0101</issn><eissn>1879-3150</eissn><coden>TOXIA6</coden><abstract>Catalpol, an iridoid glycoside, contained richly in the roots of
Rehmannia glutinosa, was found for the first time to be of neuroprotection in gerbils subjected to transient global cerebral ischemia. Catalpol (1
mg/kg ip) used immediately after reperfusion and repeatedly at 12, 24, 48 and 72
h significantly rescued neurons in hippocampal CA1 subfield and reduced working errors during behavioral testing. The neuroprotective efficacy of catalpol became more evident when the doses of catalpol were increased to 5 and 10
mg/kg. In addition, it was exciting that the significant neuroprotection by catalpol was also evident when catalpol was applied up to 3
h after ischemia. But the neuroprotective efficacy of catalpol became weak when catalpol was given at 6
h after ischemia. Of great encouragement was the finding that the neuroprotection of catalpol could be seen not only in a short post-ischemic period (12 days) but also in a long period (35 days). All these indicated that catalpol was truly neuroprotective rather than simply delayed the onset of neuronal damage and might be of therapeutic value for the treatment of global cerebral ischemia.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>16269165</pmid><doi>10.1016/j.toxicon.2004.09.007</doi><tpages>7</tpages></addata></record> |
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subjects | Analysis of Variance Animals Behavioral Symptoms - drug therapy Behavioral Symptoms - physiopathology Biological and medical sciences Catalpol Cognition Dose-Response Relationship, Drug General pharmacology Gerbillinae Gerbils Glucosides - chemistry Glucosides - pharmacology Glucosides - therapeutic use Hippocampus Hippocampus - cytology Hippocampus - drug effects Iridoid Glucosides Iridoids - chemistry Iridoids - pharmacology Iridoids - therapeutic use Ischemia Medical sciences Neurons - drug effects Neuroprotection Neuroprotective Agents - chemistry Neuroprotective Agents - pharmacology Neuroprotective Agents - therapeutic use Pharmacognosy. Homeopathy. Health food Pharmacology. Drug treatments Reperfusion Injury - drug therapy Reperfusion Injury - physiopathology Time Factors |
title | Catalpol prevents the loss of CA1 hippocampal neurons and reduces working errors in gerbils after ischemia-reperfusion injury |
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