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Effects of berberine on 6-hydroxydopamine-induced neurotoxicity in PC12 cells and a rat model of Parkinson's disease
[Display omitted] ▶ Berberine is one of protoberberine isoquinoline alkaloids. ▶ Aggravation of 6-hydroxydopamine (6-OHDA)-induced cytotoxicity in PC12 cells. ▶ Enhancement of the degeneration of dopaminergic neuronal cells in the substantia nigra of 6-OHDA-lesioned rats. ▶ It is suggested that the...
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Published in: | Neuroscience letters 2010-12, Vol.486 (1), p.29-33 |
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▶ Berberine is one of protoberberine isoquinoline alkaloids. ▶ Aggravation of 6-hydroxydopamine (6-OHDA)-induced cytotoxicity in PC12 cells. ▶ Enhancement of the degeneration of dopaminergic neuronal cells in the substantia nigra of 6-OHDA-lesioned rats. ▶ It is suggested that the use of long-term
l-DOPA therapy with isoquinoline derivatives including berberine may need to be examined for the presence of adverse symptoms.
Protoberberine isoquinoline alkaloids including berberine inhibit dopamine biosynthesis and aggravate
l-DOPA-induced cytotoxicity in PC12 cells. In this study, the effects of berberine on 6-hydroxydopamine (6-OHDA)-induced cytotoxicity in PC12 cells and on unilateral 6-OHDA-lesioned rats were investigated. In PC12 cells, berberine at 10 and 30
μM associated with 6-OHDA (10, 20, and 50
μM) enhanced cytotoxicity at 48
h compared to 6-OHDA alone, indicated by an increase in apoptotic cell death. In addition, treatment with berberine (5 and 30
mg/kg, i.p.) for 21 days in 6-OHDA-lesioned rats markedly depleted tyrosine hydroxylase-immunopositive cells in the substantia nigra as compared to berberine-untreated rats. Further, the levels of dopamine and norepinephrine were also significantly decreased by berberine administration (5 and 30
mg/kg) in the striatal regions of 6-OHDA-lesioned rats. These results suggested that berberine aggravated 6-OHDA-induced cytotoxicity in PC12 cells, and led to the degeneration of dopaminergic neuronal cells in the substantia nigra of 6-OHDA-lesioned rats. It is, therefore, suggested that the use of long-term
l-DOPA therapy with isoquinoline derivatives including berberine may need to be examined for the presence of adverse symptoms. |
doi_str_mv | 10.1016/j.neulet.2010.09.038 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_867739881</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0304394010012553</els_id><sourcerecordid>867739881</sourcerecordid><originalsourceid>FETCH-LOGICAL-c455t-69a51df23b66f053a92ad2f677d858df843533d3075008faf4468a29076b9c2b3</originalsourceid><addsrcrecordid>eNqFkU2LFDEQhoMo7rj6D0RykT31WOl0vi6CDOsHLLgHPYd0PjBjTzIm3bLz700zo94UAoHiqbeKehB6SWBLgPA3-23yy-TnbQ-tBGoLVD5CGyJF3wkl-sdoAxSGjqoBrtCzWvcAwAgbnqKrHiQjhIsNmm9D8HauOAc8-tJeTB7nhHn37eRKfji5fDSHVuxicov1DrexJc_5Ido4n3BM-H5Hemz9NFVsksMGFzPjQ3Z-WlPvTfkeU83ppmIXqzfVP0dPgpmqf3H5r9HX97dfdh-7u88fPu3e3XV2YGzuuDKMuNDTkfMAjBrVG9cHLoSTTLogB8oodRQEA5DBhGHg0vQKBB-V7Ud6jW7OuceSfyy-zvoQ67qoST4vVcsWRZWU5P8ka6jksJLDmbQl11p80McSD6acNAG9itF7fRajVzEalG5iWtury4BlPHj3p-m3iQa8vgCmWjOFYpKN9S9HqRCKrUFvz5xvh_sZfdHVRp-amFiaSO1y_PcmvwCNL61O</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>856778601</pqid></control><display><type>article</type><title>Effects of berberine on 6-hydroxydopamine-induced neurotoxicity in PC12 cells and a rat model of Parkinson's disease</title><source>ScienceDirect Journals</source><creator>Kwon, Ik Hyun ; Choi, Hyun Sook ; Shin, Kun Seong ; Lee, Byung Koo ; Lee, Chong Kil ; Hwang, Bang Yeon ; Lim, Sung Cil ; Lee, Myung Koo</creator><creatorcontrib>Kwon, Ik Hyun ; Choi, Hyun Sook ; Shin, Kun Seong ; Lee, Byung Koo ; Lee, Chong Kil ; Hwang, Bang Yeon ; Lim, Sung Cil ; Lee, Myung Koo</creatorcontrib><description>[Display omitted]
▶ Berberine is one of protoberberine isoquinoline alkaloids. ▶ Aggravation of 6-hydroxydopamine (6-OHDA)-induced cytotoxicity in PC12 cells. ▶ Enhancement of the degeneration of dopaminergic neuronal cells in the substantia nigra of 6-OHDA-lesioned rats. ▶ It is suggested that the use of long-term
l-DOPA therapy with isoquinoline derivatives including berberine may need to be examined for the presence of adverse symptoms.
Protoberberine isoquinoline alkaloids including berberine inhibit dopamine biosynthesis and aggravate
l-DOPA-induced cytotoxicity in PC12 cells. In this study, the effects of berberine on 6-hydroxydopamine (6-OHDA)-induced cytotoxicity in PC12 cells and on unilateral 6-OHDA-lesioned rats were investigated. In PC12 cells, berberine at 10 and 30
μM associated with 6-OHDA (10, 20, and 50
μM) enhanced cytotoxicity at 48
h compared to 6-OHDA alone, indicated by an increase in apoptotic cell death. In addition, treatment with berberine (5 and 30
mg/kg, i.p.) for 21 days in 6-OHDA-lesioned rats markedly depleted tyrosine hydroxylase-immunopositive cells in the substantia nigra as compared to berberine-untreated rats. Further, the levels of dopamine and norepinephrine were also significantly decreased by berberine administration (5 and 30
mg/kg) in the striatal regions of 6-OHDA-lesioned rats. These results suggested that berberine aggravated 6-OHDA-induced cytotoxicity in PC12 cells, and led to the degeneration of dopaminergic neuronal cells in the substantia nigra of 6-OHDA-lesioned rats. It is, therefore, suggested that the use of long-term
l-DOPA therapy with isoquinoline derivatives including berberine may need to be examined for the presence of adverse symptoms.</description><identifier>ISSN: 0304-3940</identifier><identifier>EISSN: 1872-7972</identifier><identifier>DOI: 10.1016/j.neulet.2010.09.038</identifier><identifier>PMID: 20851167</identifier><identifier>CODEN: NELED5</identifier><language>eng</language><publisher>Shannon: Elsevier Ireland Ltd</publisher><subject>6-Hydroxydopamine-induced cytotoxicity ; 6-Hydroxydopamine-lesioned rats ; Animals ; Berberine ; Berberine - pharmacology ; Biological and medical sciences ; Cell Death - drug effects ; Corpus Striatum - drug effects ; Corpus Striatum - metabolism ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Disease Models, Animal ; Dopamine - metabolism ; Dopaminergic neuronal cells ; Dose-Response Relationship, Drug ; Drug Synergism ; Fundamental and applied biological sciences. Psychology ; Male ; Medical sciences ; Neurology ; Neurotoxicity Syndromes - metabolism ; Neurotoxicity Syndromes - pathology ; Norepinephrine - metabolism ; Oxidopamine - toxicity ; Parkinsonian Disorders - chemically induced ; Parkinsonian Disorders - metabolism ; Parkinsonian Disorders - pathology ; PC12 Cells ; Rats ; Rats, Sprague-Dawley ; Substantia Nigra - drug effects ; Substantia Nigra - metabolism ; Tyrosine 3-Monooxygenase - metabolism ; Vertebrates: nervous system and sense organs</subject><ispartof>Neuroscience letters, 2010-12, Vol.486 (1), p.29-33</ispartof><rights>2010 Elsevier Ireland Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-69a51df23b66f053a92ad2f677d858df843533d3075008faf4468a29076b9c2b3</citedby><cites>FETCH-LOGICAL-c455t-69a51df23b66f053a92ad2f677d858df843533d3075008faf4468a29076b9c2b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23377958$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20851167$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kwon, Ik Hyun</creatorcontrib><creatorcontrib>Choi, Hyun Sook</creatorcontrib><creatorcontrib>Shin, Kun Seong</creatorcontrib><creatorcontrib>Lee, Byung Koo</creatorcontrib><creatorcontrib>Lee, Chong Kil</creatorcontrib><creatorcontrib>Hwang, Bang Yeon</creatorcontrib><creatorcontrib>Lim, Sung Cil</creatorcontrib><creatorcontrib>Lee, Myung Koo</creatorcontrib><title>Effects of berberine on 6-hydroxydopamine-induced neurotoxicity in PC12 cells and a rat model of Parkinson's disease</title><title>Neuroscience letters</title><addtitle>Neurosci Lett</addtitle><description>[Display omitted]
▶ Berberine is one of protoberberine isoquinoline alkaloids. ▶ Aggravation of 6-hydroxydopamine (6-OHDA)-induced cytotoxicity in PC12 cells. ▶ Enhancement of the degeneration of dopaminergic neuronal cells in the substantia nigra of 6-OHDA-lesioned rats. ▶ It is suggested that the use of long-term
l-DOPA therapy with isoquinoline derivatives including berberine may need to be examined for the presence of adverse symptoms.
Protoberberine isoquinoline alkaloids including berberine inhibit dopamine biosynthesis and aggravate
l-DOPA-induced cytotoxicity in PC12 cells. In this study, the effects of berberine on 6-hydroxydopamine (6-OHDA)-induced cytotoxicity in PC12 cells and on unilateral 6-OHDA-lesioned rats were investigated. In PC12 cells, berberine at 10 and 30
μM associated with 6-OHDA (10, 20, and 50
μM) enhanced cytotoxicity at 48
h compared to 6-OHDA alone, indicated by an increase in apoptotic cell death. In addition, treatment with berberine (5 and 30
mg/kg, i.p.) for 21 days in 6-OHDA-lesioned rats markedly depleted tyrosine hydroxylase-immunopositive cells in the substantia nigra as compared to berberine-untreated rats. Further, the levels of dopamine and norepinephrine were also significantly decreased by berberine administration (5 and 30
mg/kg) in the striatal regions of 6-OHDA-lesioned rats. These results suggested that berberine aggravated 6-OHDA-induced cytotoxicity in PC12 cells, and led to the degeneration of dopaminergic neuronal cells in the substantia nigra of 6-OHDA-lesioned rats. It is, therefore, suggested that the use of long-term
l-DOPA therapy with isoquinoline derivatives including berberine may need to be examined for the presence of adverse symptoms.</description><subject>6-Hydroxydopamine-induced cytotoxicity</subject><subject>6-Hydroxydopamine-lesioned rats</subject><subject>Animals</subject><subject>Berberine</subject><subject>Berberine - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Cell Death - drug effects</subject><subject>Corpus Striatum - drug effects</subject><subject>Corpus Striatum - metabolism</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Disease Models, Animal</subject><subject>Dopamine - metabolism</subject><subject>Dopaminergic neuronal cells</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Synergism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Neurology</subject><subject>Neurotoxicity Syndromes - metabolism</subject><subject>Neurotoxicity Syndromes - pathology</subject><subject>Norepinephrine - metabolism</subject><subject>Oxidopamine - toxicity</subject><subject>Parkinsonian Disorders - chemically induced</subject><subject>Parkinsonian Disorders - metabolism</subject><subject>Parkinsonian Disorders - pathology</subject><subject>PC12 Cells</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Substantia Nigra - drug effects</subject><subject>Substantia Nigra - metabolism</subject><subject>Tyrosine 3-Monooxygenase - metabolism</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0304-3940</issn><issn>1872-7972</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqFkU2LFDEQhoMo7rj6D0RykT31WOl0vi6CDOsHLLgHPYd0PjBjTzIm3bLz700zo94UAoHiqbeKehB6SWBLgPA3-23yy-TnbQ-tBGoLVD5CGyJF3wkl-sdoAxSGjqoBrtCzWvcAwAgbnqKrHiQjhIsNmm9D8HauOAc8-tJeTB7nhHn37eRKfji5fDSHVuxicov1DrexJc_5Ido4n3BM-H5Hemz9NFVsksMGFzPjQ3Z-WlPvTfkeU83ppmIXqzfVP0dPgpmqf3H5r9HX97dfdh-7u88fPu3e3XV2YGzuuDKMuNDTkfMAjBrVG9cHLoSTTLogB8oodRQEA5DBhGHg0vQKBB-V7Ud6jW7OuceSfyy-zvoQ67qoST4vVcsWRZWU5P8ka6jksJLDmbQl11p80McSD6acNAG9itF7fRajVzEalG5iWtury4BlPHj3p-m3iQa8vgCmWjOFYpKN9S9HqRCKrUFvz5xvh_sZfdHVRp-amFiaSO1y_PcmvwCNL61O</recordid><startdate>20101203</startdate><enddate>20101203</enddate><creator>Kwon, Ik Hyun</creator><creator>Choi, Hyun Sook</creator><creator>Shin, Kun Seong</creator><creator>Lee, Byung Koo</creator><creator>Lee, Chong Kil</creator><creator>Hwang, Bang Yeon</creator><creator>Lim, Sung Cil</creator><creator>Lee, Myung Koo</creator><general>Elsevier Ireland Ltd</general><general>Elsevier</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>7TK</scope></search><sort><creationdate>20101203</creationdate><title>Effects of berberine on 6-hydroxydopamine-induced neurotoxicity in PC12 cells and a rat model of Parkinson's disease</title><author>Kwon, Ik Hyun ; Choi, Hyun Sook ; Shin, Kun Seong ; Lee, Byung Koo ; Lee, Chong Kil ; Hwang, Bang Yeon ; Lim, Sung Cil ; Lee, Myung Koo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-69a51df23b66f053a92ad2f677d858df843533d3075008faf4468a29076b9c2b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>6-Hydroxydopamine-induced cytotoxicity</topic><topic>6-Hydroxydopamine-lesioned rats</topic><topic>Animals</topic><topic>Berberine</topic><topic>Berberine - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Cell Death - drug effects</topic><topic>Corpus Striatum - drug effects</topic><topic>Corpus Striatum - metabolism</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Disease Models, Animal</topic><topic>Dopamine - metabolism</topic><topic>Dopaminergic neuronal cells</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Synergism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Neurology</topic><topic>Neurotoxicity Syndromes - metabolism</topic><topic>Neurotoxicity Syndromes - pathology</topic><topic>Norepinephrine - metabolism</topic><topic>Oxidopamine - toxicity</topic><topic>Parkinsonian Disorders - chemically induced</topic><topic>Parkinsonian Disorders - metabolism</topic><topic>Parkinsonian Disorders - pathology</topic><topic>PC12 Cells</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Substantia Nigra - drug effects</topic><topic>Substantia Nigra - metabolism</topic><topic>Tyrosine 3-Monooxygenase - metabolism</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kwon, Ik Hyun</creatorcontrib><creatorcontrib>Choi, Hyun Sook</creatorcontrib><creatorcontrib>Shin, Kun Seong</creatorcontrib><creatorcontrib>Lee, Byung Koo</creatorcontrib><creatorcontrib>Lee, Chong Kil</creatorcontrib><creatorcontrib>Hwang, Bang Yeon</creatorcontrib><creatorcontrib>Lim, Sung Cil</creatorcontrib><creatorcontrib>Lee, Myung Koo</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>Neurosciences Abstracts</collection><jtitle>Neuroscience letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kwon, Ik Hyun</au><au>Choi, Hyun Sook</au><au>Shin, Kun Seong</au><au>Lee, Byung Koo</au><au>Lee, Chong Kil</au><au>Hwang, Bang Yeon</au><au>Lim, Sung Cil</au><au>Lee, Myung Koo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of berberine on 6-hydroxydopamine-induced neurotoxicity in PC12 cells and a rat model of Parkinson's disease</atitle><jtitle>Neuroscience letters</jtitle><addtitle>Neurosci Lett</addtitle><date>2010-12-03</date><risdate>2010</risdate><volume>486</volume><issue>1</issue><spage>29</spage><epage>33</epage><pages>29-33</pages><issn>0304-3940</issn><eissn>1872-7972</eissn><coden>NELED5</coden><abstract>[Display omitted]
▶ Berberine is one of protoberberine isoquinoline alkaloids. ▶ Aggravation of 6-hydroxydopamine (6-OHDA)-induced cytotoxicity in PC12 cells. ▶ Enhancement of the degeneration of dopaminergic neuronal cells in the substantia nigra of 6-OHDA-lesioned rats. ▶ It is suggested that the use of long-term
l-DOPA therapy with isoquinoline derivatives including berberine may need to be examined for the presence of adverse symptoms.
Protoberberine isoquinoline alkaloids including berberine inhibit dopamine biosynthesis and aggravate
l-DOPA-induced cytotoxicity in PC12 cells. In this study, the effects of berberine on 6-hydroxydopamine (6-OHDA)-induced cytotoxicity in PC12 cells and on unilateral 6-OHDA-lesioned rats were investigated. In PC12 cells, berberine at 10 and 30
μM associated with 6-OHDA (10, 20, and 50
μM) enhanced cytotoxicity at 48
h compared to 6-OHDA alone, indicated by an increase in apoptotic cell death. In addition, treatment with berberine (5 and 30
mg/kg, i.p.) for 21 days in 6-OHDA-lesioned rats markedly depleted tyrosine hydroxylase-immunopositive cells in the substantia nigra as compared to berberine-untreated rats. Further, the levels of dopamine and norepinephrine were also significantly decreased by berberine administration (5 and 30
mg/kg) in the striatal regions of 6-OHDA-lesioned rats. These results suggested that berberine aggravated 6-OHDA-induced cytotoxicity in PC12 cells, and led to the degeneration of dopaminergic neuronal cells in the substantia nigra of 6-OHDA-lesioned rats. It is, therefore, suggested that the use of long-term
l-DOPA therapy with isoquinoline derivatives including berberine may need to be examined for the presence of adverse symptoms.</abstract><cop>Shannon</cop><pub>Elsevier Ireland Ltd</pub><pmid>20851167</pmid><doi>10.1016/j.neulet.2010.09.038</doi><tpages>5</tpages></addata></record> |
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subjects | 6-Hydroxydopamine-induced cytotoxicity 6-Hydroxydopamine-lesioned rats Animals Berberine Berberine - pharmacology Biological and medical sciences Cell Death - drug effects Corpus Striatum - drug effects Corpus Striatum - metabolism Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Disease Models, Animal Dopamine - metabolism Dopaminergic neuronal cells Dose-Response Relationship, Drug Drug Synergism Fundamental and applied biological sciences. Psychology Male Medical sciences Neurology Neurotoxicity Syndromes - metabolism Neurotoxicity Syndromes - pathology Norepinephrine - metabolism Oxidopamine - toxicity Parkinsonian Disorders - chemically induced Parkinsonian Disorders - metabolism Parkinsonian Disorders - pathology PC12 Cells Rats Rats, Sprague-Dawley Substantia Nigra - drug effects Substantia Nigra - metabolism Tyrosine 3-Monooxygenase - metabolism Vertebrates: nervous system and sense organs |
title | Effects of berberine on 6-hydroxydopamine-induced neurotoxicity in PC12 cells and a rat model of Parkinson's disease |
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