Loading…
Protective effects of ethanolic extract of Delphinium denudatum in a rat model of Parkinson's disease
Parkinson's disease (PD) is one of the major neurodegenerative disorders, and oxidative stress has been implicated in playing an important role in the pathogenesis of the disease. In the present study, we investigated if Delphinium denudatum extract can slow down the neuronal injury in 6-hydrox...
Saved in:
Published in: | Human & experimental toxicology 2006-07, Vol.25 (7), p.361-368 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Request full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c438t-5db07b083316bb8eff0f048ed74cbc0a5379f06fb9ccb2d3ccc105c9daf0c3fb3 |
---|---|
cites | cdi_FETCH-LOGICAL-c438t-5db07b083316bb8eff0f048ed74cbc0a5379f06fb9ccb2d3ccc105c9daf0c3fb3 |
container_end_page | 368 |
container_issue | 7 |
container_start_page | 361 |
container_title | Human & experimental toxicology |
container_volume | 25 |
creator | Ahmad, Muzamil Yousuf, Seema Khan, M Badruzzaman Ahmad, Abdullah Shafique Saleem, Sofiyan Hoda, Md Nasrul Islam, Fakhrul |
description | Parkinson's disease (PD) is one of the major neurodegenerative disorders, and oxidative stress has been implicated in playing an important role in the pathogenesis of the disease. In the present study, we investigated if Delphinium denudatum extract can slow down the neuronal injury in 6-hydroxydopamine (6-OHDA) rat model of Parkinsonism. Rats were treated with 200, 400 and 600 mg/kg body weight (b.w.) of D. denudatum extract for 3 weeks. On day 22, 2 mL of 6-OHDA (10 mgin 0.1% ascorbic acid-saline) or vehicle was infused into the right striatum of the animals. Three weeks after the 6-OHDA injections, the rats were killed for estimation of lipid peroxidation (LPO), reduced glutathione (GSH) content, superoxide dismutase (SOD) and catalase (CAT) activities, catecholamines, dopaminergic D2 receptor binding and tyrosine hydroxylase (TH) expression. Increased LPO and significant depletion of reduced GSH content in the substantia nigra resulting from the lesion were appreciably prevented with Delphinium treatment. Delphinium extract also dose-dependently attenuated the activities of SOD and CAT in striatum, which had been reduced significantly by lesioning. A significant decrease in the level of dopamine (DA) and its metabolites and an increase in the number of dopaminergic D2 receptors in striatum were observed after 6-OHDA injection, both parameters were significantly recovered with treatment of the extract. Finally, all these results were confirmed by an increase in expression of TH in the ipsilateral striatum of the lesioned groups following treatment with Delphinium extract.
Thus, the study indicates that D. denudatum extract may be helpful in checking neuronal injury in Parkinsonism. |
doi_str_mv | 10.1191/0960327106ht635oa |
format | article |
fullrecord | <record><control><sourceid>proquest_AFRWT</sourceid><recordid>TN_cdi_proquest_journals_220814202</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1191_0960327106ht635oa</sage_id><sourcerecordid>1064902541</sourcerecordid><originalsourceid>FETCH-LOGICAL-c438t-5db07b083316bb8eff0f048ed74cbc0a5379f06fb9ccb2d3ccc105c9daf0c3fb3</originalsourceid><addsrcrecordid>eNp1kE9r3DAQxUVJaTZpP0AvQQRCTk5Gli1bx7Jpk0Cge2jPRn9GXW281laSQ_vtY7MLewg5zTDze_OGR8hXBjeMSXYLUgAvGwZinQWvg_pAFqxqmgIk8BOymPfFDJySs5Q2ACBkzT6RUyZa2TJRLQiuYshosn9Bis5NXaLBUcxrNYTeG4r_clQmz8M77HdrP_hxSy0Oo1V56vxAFY0q022w2M_YSsVnP6QwXCdqfUKV8DP56FSf8MuhnpPfP77_Wj4UTz_vH5ffngpT8TYXtdXQaGg5Z0LrdvoHHFQt2qYy2oCqeSMdCKelMbq03BjDoDbSKgeGO83PyeX-7i6GvyOm3G3CGIfJsitLaFlVQjlBbA-ZGFKK6Lpd9FsV_3cMujnX7k2uk-bicHjUW7RHxSHICbg6ACoZ1buoBuPTkWukqEveTtzNnkvqDx6_e9_5Fd6NkKU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>220814202</pqid></control><display><type>article</type><title>Protective effects of ethanolic extract of Delphinium denudatum in a rat model of Parkinson's disease</title><source>SAGE Open Access</source><creator>Ahmad, Muzamil ; Yousuf, Seema ; Khan, M Badruzzaman ; Ahmad, Abdullah Shafique ; Saleem, Sofiyan ; Hoda, Md Nasrul ; Islam, Fakhrul</creator><creatorcontrib>Ahmad, Muzamil ; Yousuf, Seema ; Khan, M Badruzzaman ; Ahmad, Abdullah Shafique ; Saleem, Sofiyan ; Hoda, Md Nasrul ; Islam, Fakhrul</creatorcontrib><description>Parkinson's disease (PD) is one of the major neurodegenerative disorders, and oxidative stress has been implicated in playing an important role in the pathogenesis of the disease. In the present study, we investigated if Delphinium denudatum extract can slow down the neuronal injury in 6-hydroxydopamine (6-OHDA) rat model of Parkinsonism. Rats were treated with 200, 400 and 600 mg/kg body weight (b.w.) of D. denudatum extract for 3 weeks. On day 22, 2 mL of 6-OHDA (10 mgin 0.1% ascorbic acid-saline) or vehicle was infused into the right striatum of the animals. Three weeks after the 6-OHDA injections, the rats were killed for estimation of lipid peroxidation (LPO), reduced glutathione (GSH) content, superoxide dismutase (SOD) and catalase (CAT) activities, catecholamines, dopaminergic D2 receptor binding and tyrosine hydroxylase (TH) expression. Increased LPO and significant depletion of reduced GSH content in the substantia nigra resulting from the lesion were appreciably prevented with Delphinium treatment. Delphinium extract also dose-dependently attenuated the activities of SOD and CAT in striatum, which had been reduced significantly by lesioning. A significant decrease in the level of dopamine (DA) and its metabolites and an increase in the number of dopaminergic D2 receptors in striatum were observed after 6-OHDA injection, both parameters were significantly recovered with treatment of the extract. Finally, all these results were confirmed by an increase in expression of TH in the ipsilateral striatum of the lesioned groups following treatment with Delphinium extract.
Thus, the study indicates that D. denudatum extract may be helpful in checking neuronal injury in Parkinsonism.</description><identifier>ISSN: 0960-3271</identifier><identifier>EISSN: 1477-0903</identifier><identifier>DOI: 10.1191/0960327106ht635oa</identifier><identifier>PMID: 16898164</identifier><language>eng</language><publisher>Thousand Oaks, CA: SAGE Publications</publisher><subject>Animals ; Biological and medical sciences ; Brain - drug effects ; Brain - enzymology ; Catalase - metabolism ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Delphinium ; Disease Models, Animal ; Dopamine - metabolism ; Dose-Response Relationship, Drug ; Glutathione - metabolism ; Lipid Peroxidation ; Medical sciences ; Nervous system (semeiology, syndromes) ; Nervous system as a whole ; Neurology ; Neuroprotective Agents - pharmacology ; Oxidative Stress ; Oxidopamine ; Parkinson Disease, Secondary - chemically induced ; Parkinson Disease, Secondary - enzymology ; Parkinson Disease, Secondary - prevention & control ; Plant Extracts - pharmacology ; Rats ; Rats, Wistar ; Receptors, Dopamine D2 - metabolism ; Superoxide Dismutase - metabolism ; Toxicology ; Tyrosine 3-Monooxygenase - metabolism</subject><ispartof>Human & experimental toxicology, 2006-07, Vol.25 (7), p.361-368</ispartof><rights>2006 INIST-CNRS</rights><rights>2006 Arnold</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-5db07b083316bb8eff0f048ed74cbc0a5379f06fb9ccb2d3ccc105c9daf0c3fb3</citedby><cites>FETCH-LOGICAL-c438t-5db07b083316bb8eff0f048ed74cbc0a5379f06fb9ccb2d3ccc105c9daf0c3fb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1191/0960327106ht635oa$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1191/0960327106ht635oa$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,776,780,21947,27832,27903,27904,44924,45312</link.rule.ids><linktorsrc>$$Uhttps://journals.sagepub.com/doi/full/10.1191/0960327106ht635oa?utm_source=summon&utm_medium=discovery-provider$$EView_record_in_SAGE_Publications$$FView_record_in_$$GSAGE_Publications</linktorsrc><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17965238$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16898164$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ahmad, Muzamil</creatorcontrib><creatorcontrib>Yousuf, Seema</creatorcontrib><creatorcontrib>Khan, M Badruzzaman</creatorcontrib><creatorcontrib>Ahmad, Abdullah Shafique</creatorcontrib><creatorcontrib>Saleem, Sofiyan</creatorcontrib><creatorcontrib>Hoda, Md Nasrul</creatorcontrib><creatorcontrib>Islam, Fakhrul</creatorcontrib><title>Protective effects of ethanolic extract of Delphinium denudatum in a rat model of Parkinson's disease</title><title>Human & experimental toxicology</title><addtitle>Hum Exp Toxicol</addtitle><description>Parkinson's disease (PD) is one of the major neurodegenerative disorders, and oxidative stress has been implicated in playing an important role in the pathogenesis of the disease. In the present study, we investigated if Delphinium denudatum extract can slow down the neuronal injury in 6-hydroxydopamine (6-OHDA) rat model of Parkinsonism. Rats were treated with 200, 400 and 600 mg/kg body weight (b.w.) of D. denudatum extract for 3 weeks. On day 22, 2 mL of 6-OHDA (10 mgin 0.1% ascorbic acid-saline) or vehicle was infused into the right striatum of the animals. Three weeks after the 6-OHDA injections, the rats were killed for estimation of lipid peroxidation (LPO), reduced glutathione (GSH) content, superoxide dismutase (SOD) and catalase (CAT) activities, catecholamines, dopaminergic D2 receptor binding and tyrosine hydroxylase (TH) expression. Increased LPO and significant depletion of reduced GSH content in the substantia nigra resulting from the lesion were appreciably prevented with Delphinium treatment. Delphinium extract also dose-dependently attenuated the activities of SOD and CAT in striatum, which had been reduced significantly by lesioning. A significant decrease in the level of dopamine (DA) and its metabolites and an increase in the number of dopaminergic D2 receptors in striatum were observed after 6-OHDA injection, both parameters were significantly recovered with treatment of the extract. Finally, all these results were confirmed by an increase in expression of TH in the ipsilateral striatum of the lesioned groups following treatment with Delphinium extract.
Thus, the study indicates that D. denudatum extract may be helpful in checking neuronal injury in Parkinsonism.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Brain - drug effects</subject><subject>Brain - enzymology</subject><subject>Catalase - metabolism</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Delphinium</subject><subject>Disease Models, Animal</subject><subject>Dopamine - metabolism</subject><subject>Dose-Response Relationship, Drug</subject><subject>Glutathione - metabolism</subject><subject>Lipid Peroxidation</subject><subject>Medical sciences</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Nervous system as a whole</subject><subject>Neurology</subject><subject>Neuroprotective Agents - pharmacology</subject><subject>Oxidative Stress</subject><subject>Oxidopamine</subject><subject>Parkinson Disease, Secondary - chemically induced</subject><subject>Parkinson Disease, Secondary - enzymology</subject><subject>Parkinson Disease, Secondary - prevention & control</subject><subject>Plant Extracts - pharmacology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, Dopamine D2 - metabolism</subject><subject>Superoxide Dismutase - metabolism</subject><subject>Toxicology</subject><subject>Tyrosine 3-Monooxygenase - metabolism</subject><issn>0960-3271</issn><issn>1477-0903</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNp1kE9r3DAQxUVJaTZpP0AvQQRCTk5Gli1bx7Jpk0Cge2jPRn9GXW281laSQ_vtY7MLewg5zTDze_OGR8hXBjeMSXYLUgAvGwZinQWvg_pAFqxqmgIk8BOymPfFDJySs5Q2ACBkzT6RUyZa2TJRLQiuYshosn9Bis5NXaLBUcxrNYTeG4r_clQmz8M77HdrP_hxSy0Oo1V56vxAFY0q022w2M_YSsVnP6QwXCdqfUKV8DP56FSf8MuhnpPfP77_Wj4UTz_vH5ffngpT8TYXtdXQaGg5Z0LrdvoHHFQt2qYy2oCqeSMdCKelMbq03BjDoDbSKgeGO83PyeX-7i6GvyOm3G3CGIfJsitLaFlVQjlBbA-ZGFKK6Lpd9FsV_3cMujnX7k2uk-bicHjUW7RHxSHICbg6ACoZ1buoBuPTkWukqEveTtzNnkvqDx6_e9_5Fd6NkKU</recordid><startdate>20060701</startdate><enddate>20060701</enddate><creator>Ahmad, Muzamil</creator><creator>Yousuf, Seema</creator><creator>Khan, M Badruzzaman</creator><creator>Ahmad, Abdullah Shafique</creator><creator>Saleem, Sofiyan</creator><creator>Hoda, Md Nasrul</creator><creator>Islam, Fakhrul</creator><general>SAGE Publications</general><general>Arnold</general><general>Sage Publications Ltd</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>3V.</scope><scope>7RV</scope><scope>7ST</scope><scope>7TK</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>SOI</scope></search><sort><creationdate>20060701</creationdate><title>Protective effects of ethanolic extract of Delphinium denudatum in a rat model of Parkinson's disease</title><author>Ahmad, Muzamil ; Yousuf, Seema ; Khan, M Badruzzaman ; Ahmad, Abdullah Shafique ; Saleem, Sofiyan ; Hoda, Md Nasrul ; Islam, Fakhrul</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-5db07b083316bb8eff0f048ed74cbc0a5379f06fb9ccb2d3ccc105c9daf0c3fb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Brain - drug effects</topic><topic>Brain - enzymology</topic><topic>Catalase - metabolism</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Delphinium</topic><topic>Disease Models, Animal</topic><topic>Dopamine - metabolism</topic><topic>Dose-Response Relationship, Drug</topic><topic>Glutathione - metabolism</topic><topic>Lipid Peroxidation</topic><topic>Medical sciences</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Nervous system as a whole</topic><topic>Neurology</topic><topic>Neuroprotective Agents - pharmacology</topic><topic>Oxidative Stress</topic><topic>Oxidopamine</topic><topic>Parkinson Disease, Secondary - chemically induced</topic><topic>Parkinson Disease, Secondary - enzymology</topic><topic>Parkinson Disease, Secondary - prevention & control</topic><topic>Plant Extracts - pharmacology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Receptors, Dopamine D2 - metabolism</topic><topic>Superoxide Dismutase - metabolism</topic><topic>Toxicology</topic><topic>Tyrosine 3-Monooxygenase - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ahmad, Muzamil</creatorcontrib><creatorcontrib>Yousuf, Seema</creatorcontrib><creatorcontrib>Khan, M Badruzzaman</creatorcontrib><creatorcontrib>Ahmad, Abdullah Shafique</creatorcontrib><creatorcontrib>Saleem, Sofiyan</creatorcontrib><creatorcontrib>Hoda, Md Nasrul</creatorcontrib><creatorcontrib>Islam, Fakhrul</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>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Environment Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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)</collection><collection>ProQuest Central</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</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>Environment Abstracts</collection><jtitle>Human & experimental toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Ahmad, Muzamil</au><au>Yousuf, Seema</au><au>Khan, M Badruzzaman</au><au>Ahmad, Abdullah Shafique</au><au>Saleem, Sofiyan</au><au>Hoda, Md Nasrul</au><au>Islam, Fakhrul</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protective effects of ethanolic extract of Delphinium denudatum in a rat model of Parkinson's disease</atitle><jtitle>Human & experimental toxicology</jtitle><addtitle>Hum Exp Toxicol</addtitle><date>2006-07-01</date><risdate>2006</risdate><volume>25</volume><issue>7</issue><spage>361</spage><epage>368</epage><pages>361-368</pages><issn>0960-3271</issn><eissn>1477-0903</eissn><abstract>Parkinson's disease (PD) is one of the major neurodegenerative disorders, and oxidative stress has been implicated in playing an important role in the pathogenesis of the disease. In the present study, we investigated if Delphinium denudatum extract can slow down the neuronal injury in 6-hydroxydopamine (6-OHDA) rat model of Parkinsonism. Rats were treated with 200, 400 and 600 mg/kg body weight (b.w.) of D. denudatum extract for 3 weeks. On day 22, 2 mL of 6-OHDA (10 mgin 0.1% ascorbic acid-saline) or vehicle was infused into the right striatum of the animals. Three weeks after the 6-OHDA injections, the rats were killed for estimation of lipid peroxidation (LPO), reduced glutathione (GSH) content, superoxide dismutase (SOD) and catalase (CAT) activities, catecholamines, dopaminergic D2 receptor binding and tyrosine hydroxylase (TH) expression. Increased LPO and significant depletion of reduced GSH content in the substantia nigra resulting from the lesion were appreciably prevented with Delphinium treatment. Delphinium extract also dose-dependently attenuated the activities of SOD and CAT in striatum, which had been reduced significantly by lesioning. A significant decrease in the level of dopamine (DA) and its metabolites and an increase in the number of dopaminergic D2 receptors in striatum were observed after 6-OHDA injection, both parameters were significantly recovered with treatment of the extract. Finally, all these results were confirmed by an increase in expression of TH in the ipsilateral striatum of the lesioned groups following treatment with Delphinium extract.
Thus, the study indicates that D. denudatum extract may be helpful in checking neuronal injury in Parkinsonism.</abstract><cop>Thousand Oaks, CA</cop><pub>SAGE Publications</pub><pmid>16898164</pmid><doi>10.1191/0960327106ht635oa</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | ISSN: 0960-3271 |
ispartof | Human & experimental toxicology, 2006-07, Vol.25 (7), p.361-368 |
issn | 0960-3271 1477-0903 |
language | eng |
recordid | cdi_proquest_journals_220814202 |
source | SAGE Open Access |
subjects | Animals Biological and medical sciences Brain - drug effects Brain - enzymology Catalase - metabolism Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Delphinium Disease Models, Animal Dopamine - metabolism Dose-Response Relationship, Drug Glutathione - metabolism Lipid Peroxidation Medical sciences Nervous system (semeiology, syndromes) Nervous system as a whole Neurology Neuroprotective Agents - pharmacology Oxidative Stress Oxidopamine Parkinson Disease, Secondary - chemically induced Parkinson Disease, Secondary - enzymology Parkinson Disease, Secondary - prevention & control Plant Extracts - pharmacology Rats Rats, Wistar Receptors, Dopamine D2 - metabolism Superoxide Dismutase - metabolism Toxicology Tyrosine 3-Monooxygenase - metabolism |
title | Protective effects of ethanolic extract of Delphinium denudatum in a rat model of Parkinson's disease |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T13%3A55%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_AFRWT&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Protective%20effects%20of%20ethanolic%20extract%20of%20Delphinium%20denudatum%20in%20a%20rat%20model%20of%20Parkinson's%20disease&rft.jtitle=Human%20&%20experimental%20toxicology&rft.au=Ahmad,%20Muzamil&rft.date=2006-07-01&rft.volume=25&rft.issue=7&rft.spage=361&rft.epage=368&rft.pages=361-368&rft.issn=0960-3271&rft.eissn=1477-0903&rft_id=info:doi/10.1191/0960327106ht635oa&rft_dat=%3Cproquest_AFRWT%3E1064902541%3C/proquest_AFRWT%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c438t-5db07b083316bb8eff0f048ed74cbc0a5379f06fb9ccb2d3ccc105c9daf0c3fb3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=220814202&rft_id=info:pmid/16898164&rft_sage_id=10.1191_0960327106ht635oa&rfr_iscdi=true |