Astaxanthin reduces ischemic brain injury in adult rats
Astaxanthin (ATX) is a dietary carotenoid of crustaceans and fish that contributes to their coloration. Dietary ATX is important for development and survival of salmonids and crustaceans and has been shown to reduce cardiac ischemic injury in rodents. The purpose of this study was to examine whether...
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Veröffentlicht in: | The FASEB journal 2009-06, Vol.23 (6), p.1958-1968 |
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container_end_page | 1968 |
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container_issue | 6 |
container_start_page | 1958 |
container_title | The FASEB journal |
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creator | Shen, Hui Kuo, Chi-Chung Chou, Jenny Delvolve, Alice Jackson, Shelley N Post, Jeremy Woods, Amina S Hoffer, Barry J Wang, Yun Harvey, Brandon K |
description | Astaxanthin (ATX) is a dietary carotenoid of crustaceans and fish that contributes to their coloration. Dietary ATX is important for development and survival of salmonids and crustaceans and has been shown to reduce cardiac ischemic injury in rodents. The purpose of this study was to examine whether ATX can protect against ischemic injury in the mammalian brain. Adult rats were injected intracerebroventricularly with ATX or vehicle prior to a 60-min middle cerebral artery occlusion (MCAo). ATX was present in the infarction area at 70-75 min after onset of MCAo. Treatment with ATX, compared to vehicle, increased locomotor activity in stroke rats and reduced cerebral infarction at 2 d after MCAo. To evaluate the protective mechanisms of ATX against stroke, brain tissues were assayed for free radical damage, apoptosis, and excitoxicity. ATX antagonized ischemia-mediated loss of aconitase activity and reduced glutamate release, lipid peroxidation, translocation of cytochrome c, and TUNEL labeling in the ischemic cortex. ATX did not alter physiological parameters, such as body temperature, brain temperature, cerebral blood flow, blood gases, blood pressure, and pH. Collectively, our data suggest that ATX can reduce ischemia-related injury in brain tissue through the inhibition of oxidative stress, reduction of glutamate release, and antiapoptosis. ATX may be clinically useful for patients vulnerable or prone to ischemic events.--Shen, H., Kuo, C.-C., Chou, J., Delvolve, A., Jackson, S. N., Post, J., Woods, A. S., Hoffer, B. J., Wang, Y., Harvey, B. K. Astaxanthin reduces ischemic brain injury in adult rats. |
doi_str_mv | 10.1096/fj.08-123281 |
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Dietary ATX is important for development and survival of salmonids and crustaceans and has been shown to reduce cardiac ischemic injury in rodents. The purpose of this study was to examine whether ATX can protect against ischemic injury in the mammalian brain. Adult rats were injected intracerebroventricularly with ATX or vehicle prior to a 60-min middle cerebral artery occlusion (MCAo). ATX was present in the infarction area at 70-75 min after onset of MCAo. Treatment with ATX, compared to vehicle, increased locomotor activity in stroke rats and reduced cerebral infarction at 2 d after MCAo. To evaluate the protective mechanisms of ATX against stroke, brain tissues were assayed for free radical damage, apoptosis, and excitoxicity. ATX antagonized ischemia-mediated loss of aconitase activity and reduced glutamate release, lipid peroxidation, translocation of cytochrome c, and TUNEL labeling in the ischemic cortex. ATX did not alter physiological parameters, such as body temperature, brain temperature, cerebral blood flow, blood gases, blood pressure, and pH. Collectively, our data suggest that ATX can reduce ischemia-related injury in brain tissue through the inhibition of oxidative stress, reduction of glutamate release, and antiapoptosis. ATX may be clinically useful for patients vulnerable or prone to ischemic events.--Shen, H., Kuo, C.-C., Chou, J., Delvolve, A., Jackson, S. N., Post, J., Woods, A. S., Hoffer, B. J., Wang, Y., Harvey, B. K. Astaxanthin reduces ischemic brain injury in adult rats.</description><identifier>ISSN: 0892-6638</identifier><identifier>EISSN: 1530-6860</identifier><identifier>DOI: 10.1096/fj.08-123281</identifier><identifier>PMID: 19218497</identifier><language>eng</language><publisher>United States: The Federation of American Societies for Experimental Biology</publisher><subject>Aconitate Hydratase - metabolism ; Animals ; antioxidant ; apoptosis ; Behavior, Animal - drug effects ; Brain Injuries - drug therapy ; Brain Injuries - pathology ; Brain Ischemia - drug therapy ; Brain Ischemia - pathology ; Brain Ischemia - prevention & control ; Cerebrovascular Circulation ; Crustacea ; Cytochromes c - metabolism ; Diet ; glutamate ; Glutamic Acid - metabolism ; Humans ; In Situ Nick-End Labeling ; Lipid Peroxidation ; Male ; Molecular Structure ; Motor Activity - drug effects ; neuroprotection ; Neuroprotective Agents - chemistry ; Neuroprotective Agents - pharmacology ; Neuroprotective Agents - therapeutic use ; Rats ; Rats, Sprague-Dawley ; Regional Blood Flow ; Research Communications ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ; stroke ; Xanthophylls - chemistry ; Xanthophylls - pharmacology ; Xanthophylls - therapeutic use</subject><ispartof>The FASEB journal, 2009-06, Vol.23 (6), p.1958-1968</ispartof><rights>FASEB</rights><rights>2009 FASEB 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5521-3ff1a6549f8724f1310a4ea695aee92aaab052c51ec4496e3572237c369428b03</citedby><cites>FETCH-LOGICAL-c5521-3ff1a6549f8724f1310a4ea695aee92aaab052c51ec4496e3572237c369428b03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1096%2Ffj.08-123281$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1096%2Ffj.08-123281$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19218497$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shen, Hui</creatorcontrib><creatorcontrib>Kuo, Chi-Chung</creatorcontrib><creatorcontrib>Chou, Jenny</creatorcontrib><creatorcontrib>Delvolve, Alice</creatorcontrib><creatorcontrib>Jackson, Shelley N</creatorcontrib><creatorcontrib>Post, Jeremy</creatorcontrib><creatorcontrib>Woods, Amina S</creatorcontrib><creatorcontrib>Hoffer, Barry J</creatorcontrib><creatorcontrib>Wang, Yun</creatorcontrib><creatorcontrib>Harvey, Brandon K</creatorcontrib><title>Astaxanthin reduces ischemic brain injury in adult rats</title><title>The FASEB journal</title><addtitle>FASEB J</addtitle><description>Astaxanthin (ATX) is a dietary carotenoid of crustaceans and fish that contributes to their coloration. Dietary ATX is important for development and survival of salmonids and crustaceans and has been shown to reduce cardiac ischemic injury in rodents. The purpose of this study was to examine whether ATX can protect against ischemic injury in the mammalian brain. Adult rats were injected intracerebroventricularly with ATX or vehicle prior to a 60-min middle cerebral artery occlusion (MCAo). ATX was present in the infarction area at 70-75 min after onset of MCAo. Treatment with ATX, compared to vehicle, increased locomotor activity in stroke rats and reduced cerebral infarction at 2 d after MCAo. To evaluate the protective mechanisms of ATX against stroke, brain tissues were assayed for free radical damage, apoptosis, and excitoxicity. ATX antagonized ischemia-mediated loss of aconitase activity and reduced glutamate release, lipid peroxidation, translocation of cytochrome c, and TUNEL labeling in the ischemic cortex. ATX did not alter physiological parameters, such as body temperature, brain temperature, cerebral blood flow, blood gases, blood pressure, and pH. Collectively, our data suggest that ATX can reduce ischemia-related injury in brain tissue through the inhibition of oxidative stress, reduction of glutamate release, and antiapoptosis. ATX may be clinically useful for patients vulnerable or prone to ischemic events.--Shen, H., Kuo, C.-C., Chou, J., Delvolve, A., Jackson, S. N., Post, J., Woods, A. S., Hoffer, B. J., Wang, Y., Harvey, B. K. Astaxanthin reduces ischemic brain injury in adult rats.</description><subject>Aconitate Hydratase - metabolism</subject><subject>Animals</subject><subject>antioxidant</subject><subject>apoptosis</subject><subject>Behavior, Animal - drug effects</subject><subject>Brain Injuries - drug therapy</subject><subject>Brain Injuries - pathology</subject><subject>Brain Ischemia - drug therapy</subject><subject>Brain Ischemia - pathology</subject><subject>Brain Ischemia - prevention & control</subject><subject>Cerebrovascular Circulation</subject><subject>Crustacea</subject><subject>Cytochromes c - metabolism</subject><subject>Diet</subject><subject>glutamate</subject><subject>Glutamic Acid - metabolism</subject><subject>Humans</subject><subject>In Situ Nick-End Labeling</subject><subject>Lipid Peroxidation</subject><subject>Male</subject><subject>Molecular Structure</subject><subject>Motor Activity - drug effects</subject><subject>neuroprotection</subject><subject>Neuroprotective Agents - chemistry</subject><subject>Neuroprotective Agents - pharmacology</subject><subject>Neuroprotective Agents - therapeutic use</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Regional Blood Flow</subject><subject>Research Communications</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><subject>stroke</subject><subject>Xanthophylls - chemistry</subject><subject>Xanthophylls - pharmacology</subject><subject>Xanthophylls - therapeutic use</subject><issn>0892-6638</issn><issn>1530-6860</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUFP3DAQRi1UBAvtjXObEydCZ2zHsS-VKGJbKqQeKGdr1muzXmUTaieF_fekygrKpaeRxs9vxp8ZO0E4RzDqc1ifgy6RC65xj82wElAqreAdm4E2vFRK6EN2lPMaABBQHbBDNBy1NPWM1Re5pydq-1Vsi-SXg_O5iNmt_Ca6YpFobMd2PaTtWApaDk1fJOrze7YfqMn-w64es7v51a_L7-XNz2_Xlxc3pasqjqUIAUlV0gRdcxlQIJD0pExF3htORAuouKvQOymN8qKqORe1E8pIrhcgjtmXyfswLDZ-6XzbJ2rsQ4obSlvbUbRvT9q4svfdH8uV0UrhKDjdCVL3e_C5t5vxeb5pqPXdkK2qBaKQcgTPJtClLufkw8sQBPs3aRvWFrSdkh7xj_8u9grvoh0BPQGPsfHb_8rs_PYrn_8A_eL-NF0N1Fm6TzHbu1sOKMbfEwZrI54BSNyTBw</recordid><startdate>200906</startdate><enddate>200906</enddate><creator>Shen, Hui</creator><creator>Kuo, Chi-Chung</creator><creator>Chou, Jenny</creator><creator>Delvolve, Alice</creator><creator>Jackson, Shelley N</creator><creator>Post, Jeremy</creator><creator>Woods, Amina S</creator><creator>Hoffer, Barry J</creator><creator>Wang, Yun</creator><creator>Harvey, Brandon K</creator><general>The Federation of American Societies for Experimental Biology</general><general>Federation of American Societies for Experimental Biology</general><scope>FBQ</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>200906</creationdate><title>Astaxanthin reduces ischemic brain injury in adult rats</title><author>Shen, Hui ; Kuo, Chi-Chung ; Chou, Jenny ; Delvolve, Alice ; Jackson, Shelley N ; Post, Jeremy ; Woods, Amina S ; Hoffer, Barry J ; Wang, Yun ; Harvey, Brandon K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5521-3ff1a6549f8724f1310a4ea695aee92aaab052c51ec4496e3572237c369428b03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Aconitate Hydratase - metabolism</topic><topic>Animals</topic><topic>antioxidant</topic><topic>apoptosis</topic><topic>Behavior, Animal - drug effects</topic><topic>Brain Injuries - drug therapy</topic><topic>Brain Injuries - pathology</topic><topic>Brain Ischemia - drug therapy</topic><topic>Brain Ischemia - pathology</topic><topic>Brain Ischemia - prevention & control</topic><topic>Cerebrovascular Circulation</topic><topic>Crustacea</topic><topic>Cytochromes c - metabolism</topic><topic>Diet</topic><topic>glutamate</topic><topic>Glutamic Acid - metabolism</topic><topic>Humans</topic><topic>In Situ Nick-End Labeling</topic><topic>Lipid Peroxidation</topic><topic>Male</topic><topic>Molecular Structure</topic><topic>Motor Activity - drug effects</topic><topic>neuroprotection</topic><topic>Neuroprotective Agents - chemistry</topic><topic>Neuroprotective Agents - pharmacology</topic><topic>Neuroprotective Agents - therapeutic use</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Regional Blood Flow</topic><topic>Research Communications</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</topic><topic>stroke</topic><topic>Xanthophylls - chemistry</topic><topic>Xanthophylls - pharmacology</topic><topic>Xanthophylls - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shen, Hui</creatorcontrib><creatorcontrib>Kuo, Chi-Chung</creatorcontrib><creatorcontrib>Chou, Jenny</creatorcontrib><creatorcontrib>Delvolve, Alice</creatorcontrib><creatorcontrib>Jackson, Shelley N</creatorcontrib><creatorcontrib>Post, Jeremy</creatorcontrib><creatorcontrib>Woods, Amina S</creatorcontrib><creatorcontrib>Hoffer, Barry J</creatorcontrib><creatorcontrib>Wang, Yun</creatorcontrib><creatorcontrib>Harvey, Brandon K</creatorcontrib><collection>AGRIS</collection><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>The FASEB journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shen, Hui</au><au>Kuo, Chi-Chung</au><au>Chou, Jenny</au><au>Delvolve, Alice</au><au>Jackson, Shelley N</au><au>Post, Jeremy</au><au>Woods, Amina S</au><au>Hoffer, Barry J</au><au>Wang, Yun</au><au>Harvey, Brandon K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Astaxanthin reduces ischemic brain injury in adult rats</atitle><jtitle>The FASEB journal</jtitle><addtitle>FASEB J</addtitle><date>2009-06</date><risdate>2009</risdate><volume>23</volume><issue>6</issue><spage>1958</spage><epage>1968</epage><pages>1958-1968</pages><issn>0892-6638</issn><eissn>1530-6860</eissn><abstract>Astaxanthin (ATX) is a dietary carotenoid of crustaceans and fish that contributes to their coloration. Dietary ATX is important for development and survival of salmonids and crustaceans and has been shown to reduce cardiac ischemic injury in rodents. The purpose of this study was to examine whether ATX can protect against ischemic injury in the mammalian brain. Adult rats were injected intracerebroventricularly with ATX or vehicle prior to a 60-min middle cerebral artery occlusion (MCAo). ATX was present in the infarction area at 70-75 min after onset of MCAo. Treatment with ATX, compared to vehicle, increased locomotor activity in stroke rats and reduced cerebral infarction at 2 d after MCAo. To evaluate the protective mechanisms of ATX against stroke, brain tissues were assayed for free radical damage, apoptosis, and excitoxicity. ATX antagonized ischemia-mediated loss of aconitase activity and reduced glutamate release, lipid peroxidation, translocation of cytochrome c, and TUNEL labeling in the ischemic cortex. ATX did not alter physiological parameters, such as body temperature, brain temperature, cerebral blood flow, blood gases, blood pressure, and pH. Collectively, our data suggest that ATX can reduce ischemia-related injury in brain tissue through the inhibition of oxidative stress, reduction of glutamate release, and antiapoptosis. ATX may be clinically useful for patients vulnerable or prone to ischemic events.--Shen, H., Kuo, C.-C., Chou, J., Delvolve, A., Jackson, S. N., Post, J., Woods, A. S., Hoffer, B. J., Wang, Y., Harvey, B. K. Astaxanthin reduces ischemic brain injury in adult rats.</abstract><cop>United States</cop><pub>The Federation of American Societies for Experimental Biology</pub><pmid>19218497</pmid><doi>10.1096/fj.08-123281</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aconitate Hydratase - metabolism Animals antioxidant apoptosis Behavior, Animal - drug effects Brain Injuries - drug therapy Brain Injuries - pathology Brain Ischemia - drug therapy Brain Ischemia - pathology Brain Ischemia - prevention & control Cerebrovascular Circulation Crustacea Cytochromes c - metabolism Diet glutamate Glutamic Acid - metabolism Humans In Situ Nick-End Labeling Lipid Peroxidation Male Molecular Structure Motor Activity - drug effects neuroprotection Neuroprotective Agents - chemistry Neuroprotective Agents - pharmacology Neuroprotective Agents - therapeutic use Rats Rats, Sprague-Dawley Regional Blood Flow Research Communications Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization stroke Xanthophylls - chemistry Xanthophylls - pharmacology Xanthophylls - therapeutic use |
title | Astaxanthin reduces ischemic brain injury in adult rats |
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