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Impact of aging on the 6-OHDA-induced rat model of Parkinson’s disease
Parkinson’s disease (PD) is the second most common age-related neurodegenerative disorder. The neurodegeneration leading to incapacitating motor abnormalities mainly occurs in the nigrostriatal pathway due to the loss of dopaminergic neurons in the substantia nigra pars compacta (SNpc). Several anim...
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Published in: | International journal of molecular sciences 2020-05, Vol.21 (10), p.3459 |
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description | Parkinson’s disease (PD) is the second most common age-related neurodegenerative disorder. The neurodegeneration leading to incapacitating motor abnormalities mainly occurs in the nigrostriatal pathway due to the loss of dopaminergic neurons in the substantia nigra pars compacta (SNpc). Several animal models have been developed not only to better understand the mechanisms underlying neurodegeneration but also to test the potential of emerging disease-modifying therapies. However, despite aging being the main risk factor for developing idiopathic PD, most of the studies do not use aged animals. Therefore, this study aimed at assessing the effect of aging in the unilateral 6-hydroxydopamine (6-OHDA)-induced animal model of PD. For this, female young adult and aged rats received a unilateral injection of 6-OHDA into the medial forebrain bundle. Subsequently, the impact of aging on 6-OHDA-induced effects on animal welfare, motor performance, and nigrostriatal integrity were assessed. The results showed that aging had a negative impact on animal welfare after surgery. Furthermore, 6-OHDA-induced impairments on skilled motor function were significantly higher in aged rats when compared with their younger counterparts. Nigrostriatal histological analysis further revealed an increased 6-OHDA-induced dopaminergic cell loss in the SNpc of aged animals when compared to young animals. Overall, our results demonstrate a higher susceptibility of aged animals to 6-OHDA toxic insult.
This research was funded by Prémios Santa Casa Neurociências—Prize Mantero Belard for Neurodegenerative Diseases Research (MB-28-2019); Portuguese Foundation for Science and Technology [Ph.D. fellowship to S.B.-A. (PD/BDE/135568/2018), B.M.-P. (SFRH/BD/120124/2016), A.M. (PDE/BDE/113598/2015), and D.S. (PD/BDE/135567/2018)]. This work was also funded by FEDER, through the Competitiveness Internationalization Operational Programme (POCI), and by National funds, through the Foundation for Science and Technology (FCT), under the scope of the projects POCI-01-0145-FEDER-007038; POCI-01-0145-FEDER-029751 and POCI-01-0145-FEDER-032619. This article has also been developed under the scope of the project NORTE-01-0145-FEDER-000023, supported by the Northern Portugal Regional Operational Programme (NORTE 2020), under the Portugal 2020 Partnership Agreement, through the European Regional Development Fund (FEDER). |
doi_str_mv | 10.3390/ijms21103459 |
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This research was funded by Prémios Santa Casa Neurociências—Prize Mantero Belard for Neurodegenerative Diseases Research (MB-28-2019); Portuguese Foundation for Science and Technology [Ph.D. fellowship to S.B.-A. (PD/BDE/135568/2018), B.M.-P. (SFRH/BD/120124/2016), A.M. (PDE/BDE/113598/2015), and D.S. (PD/BDE/135567/2018)]. This work was also funded by FEDER, through the Competitiveness Internationalization Operational Programme (POCI), and by National funds, through the Foundation for Science and Technology (FCT), under the scope of the projects POCI-01-0145-FEDER-007038; POCI-01-0145-FEDER-029751 and POCI-01-0145-FEDER-032619. This article has also been developed under the scope of the project NORTE-01-0145-FEDER-000023, supported by the Northern Portugal Regional Operational Programme (NORTE 2020), under the Portugal 2020 Partnership Agreement, through the European Regional Development Fund (FEDER).</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms21103459</identifier><identifier>PMID: 32422916</identifier><language>eng</language><publisher>Switzerland: Multidisciplinary Digital Publishing Institute</publisher><subject>6-Hydroxydopamine ; Abnormalities ; Age ; Aging ; Aging (artificial) ; Aging - metabolism ; Aging - pathology ; Animal model ; Animal models ; Animal welfare ; Animals ; Asymmetry ; Ciências da Saúde ; Ciências Médicas ; Corpus Striatum - drug effects ; Corpus Striatum - metabolism ; Corpus Striatum - pathology ; Disease Models, Animal ; Dopamine ; Dopamine - metabolism ; Dopamine receptors ; Dopaminergic Neurons - drug effects ; Dopaminergic Neurons - metabolism ; Dopaminergic Neurons - pathology ; Experiments ; Female ; Forebrain ; Humans ; Male ; Medial forebrain bundle ; Motor Disorders - chemically induced ; Motor Disorders - metabolism ; Motor Disorders - pathology ; Motor skill ; Motor task performance ; Neurodegeneration ; Oxidative stress ; Oxidopamine - toxicity ; Parkinson Disease - metabolism ; Parkinson Disease - physiopathology ; Parkinson Disease, Secondary - chemically induced ; Parkinson Disease, Secondary - metabolism ; Parkinson Disease, Secondary - physiopathology ; Parkinson's disease ; Rats ; Risk analysis ; Risk factors ; Rodents ; Science & Technology ; Substantia nigra ; Substantia Nigra - drug effects ; Substantia Nigra - metabolism ; Substantia Nigra - pathology ; Surgery ; Symmetry ; Young adults</subject><ispartof>International journal of molecular sciences, 2020-05, Vol.21 (10), p.3459</ispartof><rights>2020. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 by the authors. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c503t-1137e976f0e3b947b1d39f495560617d1747e8c494ef8c04f37bb82ae32f565c3</citedby><cites>FETCH-LOGICAL-c503t-1137e976f0e3b947b1d39f495560617d1747e8c494ef8c04f37bb82ae32f565c3</cites><orcidid>0000-0003-1858-4318 ; 0000-0003-1461-9077</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2404483196/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2404483196?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,25734,27905,27906,36993,44571,53772,53774,74875</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32422916$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Barata-Antunes, Sandra</creatorcontrib><creatorcontrib>Teixeira, Fábio G.</creatorcontrib><creatorcontrib>Mendes-Pinheiro, Bárbara</creatorcontrib><creatorcontrib>Domingues, Ana V.</creatorcontrib><creatorcontrib>Vilaça-Faria, Helena</creatorcontrib><creatorcontrib>Marote, Ana</creatorcontrib><creatorcontrib>Silva, Deolinda</creatorcontrib><creatorcontrib>Sousa, R. A.</creatorcontrib><creatorcontrib>Salgado, A. J.</creatorcontrib><title>Impact of aging on the 6-OHDA-induced rat model of Parkinson’s disease</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Parkinson’s disease (PD) is the second most common age-related neurodegenerative disorder. The neurodegeneration leading to incapacitating motor abnormalities mainly occurs in the nigrostriatal pathway due to the loss of dopaminergic neurons in the substantia nigra pars compacta (SNpc). Several animal models have been developed not only to better understand the mechanisms underlying neurodegeneration but also to test the potential of emerging disease-modifying therapies. However, despite aging being the main risk factor for developing idiopathic PD, most of the studies do not use aged animals. Therefore, this study aimed at assessing the effect of aging in the unilateral 6-hydroxydopamine (6-OHDA)-induced animal model of PD. For this, female young adult and aged rats received a unilateral injection of 6-OHDA into the medial forebrain bundle. Subsequently, the impact of aging on 6-OHDA-induced effects on animal welfare, motor performance, and nigrostriatal integrity were assessed. The results showed that aging had a negative impact on animal welfare after surgery. Furthermore, 6-OHDA-induced impairments on skilled motor function were significantly higher in aged rats when compared with their younger counterparts. Nigrostriatal histological analysis further revealed an increased 6-OHDA-induced dopaminergic cell loss in the SNpc of aged animals when compared to young animals. Overall, our results demonstrate a higher susceptibility of aged animals to 6-OHDA toxic insult.
This research was funded by Prémios Santa Casa Neurociências—Prize Mantero Belard for Neurodegenerative Diseases Research (MB-28-2019); Portuguese Foundation for Science and Technology [Ph.D. fellowship to S.B.-A. (PD/BDE/135568/2018), B.M.-P. (SFRH/BD/120124/2016), A.M. (PDE/BDE/113598/2015), and D.S. (PD/BDE/135567/2018)]. This work was also funded by FEDER, through the Competitiveness Internationalization Operational Programme (POCI), and by National funds, through the Foundation for Science and Technology (FCT), under the scope of the projects POCI-01-0145-FEDER-007038; POCI-01-0145-FEDER-029751 and POCI-01-0145-FEDER-032619. This article has also been developed under the scope of the project NORTE-01-0145-FEDER-000023, supported by the Northern Portugal Regional Operational Programme (NORTE 2020), under the Portugal 2020 Partnership Agreement, through the European Regional Development Fund (FEDER).</description><subject>6-Hydroxydopamine</subject><subject>Abnormalities</subject><subject>Age</subject><subject>Aging</subject><subject>Aging (artificial)</subject><subject>Aging - metabolism</subject><subject>Aging - pathology</subject><subject>Animal model</subject><subject>Animal models</subject><subject>Animal welfare</subject><subject>Animals</subject><subject>Asymmetry</subject><subject>Ciências da Saúde</subject><subject>Ciências Médicas</subject><subject>Corpus Striatum - drug effects</subject><subject>Corpus Striatum - metabolism</subject><subject>Corpus Striatum - pathology</subject><subject>Disease Models, Animal</subject><subject>Dopamine</subject><subject>Dopamine - metabolism</subject><subject>Dopamine receptors</subject><subject>Dopaminergic Neurons - drug effects</subject><subject>Dopaminergic Neurons - metabolism</subject><subject>Dopaminergic Neurons - pathology</subject><subject>Experiments</subject><subject>Female</subject><subject>Forebrain</subject><subject>Humans</subject><subject>Male</subject><subject>Medial forebrain bundle</subject><subject>Motor Disorders - chemically induced</subject><subject>Motor Disorders - metabolism</subject><subject>Motor Disorders - pathology</subject><subject>Motor skill</subject><subject>Motor task performance</subject><subject>Neurodegeneration</subject><subject>Oxidative stress</subject><subject>Oxidopamine - toxicity</subject><subject>Parkinson Disease - metabolism</subject><subject>Parkinson Disease - physiopathology</subject><subject>Parkinson Disease, Secondary - chemically induced</subject><subject>Parkinson Disease, Secondary - metabolism</subject><subject>Parkinson Disease, Secondary - physiopathology</subject><subject>Parkinson's disease</subject><subject>Rats</subject><subject>Risk analysis</subject><subject>Risk factors</subject><subject>Rodents</subject><subject>Science & Technology</subject><subject>Substantia nigra</subject><subject>Substantia Nigra - drug effects</subject><subject>Substantia Nigra - metabolism</subject><subject>Substantia Nigra - pathology</subject><subject>Surgery</subject><subject>Symmetry</subject><subject>Young adults</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpVkMtKxDAYhYMoXkZ3riXg1mruaTaCjJcZEMaFrkOapmPGaVOTVnDna_h6PokdRmVc_QfOx_kPB4BjjM4pVejCL-pEMEaUcbUF9jEjJENIyO0NvQcOUlogRCjhahfsUTI4Cot9MJnWrbEdDBU0c9_MYWhg9-ygyGaT66vMN2VvXQmj6WAdSrdcgQ8mvvgmhebr4zPB0idnkjsEO5VZJnf0c0fg6fbmcTzJ7md30_HVfWY5ol2GMZVOSVEhRwvFZIFLqiqmOBdIYFliyaTLLVPMVblFrKKyKHJiHCUVF9zSEbhc57Z9UbvSuqaLZqnb6GsT33UwXv93Gv-s5-FNSyIVonQIOP0JiOG1d6nTi9DHZuisCUOM5RQrMVBna8rGkFJ01d8HjPRqd725-4CfbLb6g3-HHgC4BqI1ptXRvfnUmaRxTogWnCNGvwGYLIg1</recordid><startdate>20200514</startdate><enddate>20200514</enddate><creator>Barata-Antunes, Sandra</creator><creator>Teixeira, Fábio G.</creator><creator>Mendes-Pinheiro, Bárbara</creator><creator>Domingues, Ana V.</creator><creator>Vilaça-Faria, Helena</creator><creator>Marote, Ana</creator><creator>Silva, Deolinda</creator><creator>Sousa, R. 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J.</creator><general>Multidisciplinary Digital Publishing Institute</general><general>MDPI AG</general><general>MDPI</general><scope>RCLKO</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>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1858-4318</orcidid><orcidid>https://orcid.org/0000-0003-1461-9077</orcidid></search><sort><creationdate>20200514</creationdate><title>Impact of aging on the 6-OHDA-induced rat model of Parkinson’s disease</title><author>Barata-Antunes, Sandra ; Teixeira, Fábio G. ; Mendes-Pinheiro, Bárbara ; Domingues, Ana V. ; Vilaça-Faria, Helena ; Marote, Ana ; Silva, Deolinda ; Sousa, R. A. ; Salgado, A. J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c503t-1137e976f0e3b947b1d39f495560617d1747e8c494ef8c04f37bb82ae32f565c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>6-Hydroxydopamine</topic><topic>Abnormalities</topic><topic>Age</topic><topic>Aging</topic><topic>Aging (artificial)</topic><topic>Aging - metabolism</topic><topic>Aging - pathology</topic><topic>Animal model</topic><topic>Animal models</topic><topic>Animal welfare</topic><topic>Animals</topic><topic>Asymmetry</topic><topic>Ciências da Saúde</topic><topic>Ciências Médicas</topic><topic>Corpus Striatum - drug effects</topic><topic>Corpus Striatum - metabolism</topic><topic>Corpus Striatum - pathology</topic><topic>Disease Models, Animal</topic><topic>Dopamine</topic><topic>Dopamine - metabolism</topic><topic>Dopamine receptors</topic><topic>Dopaminergic Neurons - drug effects</topic><topic>Dopaminergic Neurons - metabolism</topic><topic>Dopaminergic Neurons - pathology</topic><topic>Experiments</topic><topic>Female</topic><topic>Forebrain</topic><topic>Humans</topic><topic>Male</topic><topic>Medial forebrain bundle</topic><topic>Motor Disorders - chemically induced</topic><topic>Motor Disorders - metabolism</topic><topic>Motor Disorders - pathology</topic><topic>Motor skill</topic><topic>Motor task performance</topic><topic>Neurodegeneration</topic><topic>Oxidative stress</topic><topic>Oxidopamine - toxicity</topic><topic>Parkinson Disease - metabolism</topic><topic>Parkinson Disease - physiopathology</topic><topic>Parkinson Disease, Secondary - chemically induced</topic><topic>Parkinson Disease, Secondary - metabolism</topic><topic>Parkinson Disease, Secondary - physiopathology</topic><topic>Parkinson's disease</topic><topic>Rats</topic><topic>Risk analysis</topic><topic>Risk factors</topic><topic>Rodents</topic><topic>Science & Technology</topic><topic>Substantia nigra</topic><topic>Substantia Nigra - drug effects</topic><topic>Substantia Nigra - metabolism</topic><topic>Substantia Nigra - pathology</topic><topic>Surgery</topic><topic>Symmetry</topic><topic>Young adults</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Barata-Antunes, Sandra</creatorcontrib><creatorcontrib>Teixeira, Fábio G.</creatorcontrib><creatorcontrib>Mendes-Pinheiro, Bárbara</creatorcontrib><creatorcontrib>Domingues, Ana V.</creatorcontrib><creatorcontrib>Vilaça-Faria, Helena</creatorcontrib><creatorcontrib>Marote, Ana</creatorcontrib><creatorcontrib>Silva, Deolinda</creatorcontrib><creatorcontrib>Sousa, R. 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A.</au><au>Salgado, A. J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of aging on the 6-OHDA-induced rat model of Parkinson’s disease</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2020-05-14</date><risdate>2020</risdate><volume>21</volume><issue>10</issue><spage>3459</spage><pages>3459-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Parkinson’s disease (PD) is the second most common age-related neurodegenerative disorder. The neurodegeneration leading to incapacitating motor abnormalities mainly occurs in the nigrostriatal pathway due to the loss of dopaminergic neurons in the substantia nigra pars compacta (SNpc). Several animal models have been developed not only to better understand the mechanisms underlying neurodegeneration but also to test the potential of emerging disease-modifying therapies. However, despite aging being the main risk factor for developing idiopathic PD, most of the studies do not use aged animals. Therefore, this study aimed at assessing the effect of aging in the unilateral 6-hydroxydopamine (6-OHDA)-induced animal model of PD. For this, female young adult and aged rats received a unilateral injection of 6-OHDA into the medial forebrain bundle. Subsequently, the impact of aging on 6-OHDA-induced effects on animal welfare, motor performance, and nigrostriatal integrity were assessed. The results showed that aging had a negative impact on animal welfare after surgery. Furthermore, 6-OHDA-induced impairments on skilled motor function were significantly higher in aged rats when compared with their younger counterparts. Nigrostriatal histological analysis further revealed an increased 6-OHDA-induced dopaminergic cell loss in the SNpc of aged animals when compared to young animals. Overall, our results demonstrate a higher susceptibility of aged animals to 6-OHDA toxic insult.
This research was funded by Prémios Santa Casa Neurociências—Prize Mantero Belard for Neurodegenerative Diseases Research (MB-28-2019); Portuguese Foundation for Science and Technology [Ph.D. fellowship to S.B.-A. (PD/BDE/135568/2018), B.M.-P. (SFRH/BD/120124/2016), A.M. (PDE/BDE/113598/2015), and D.S. (PD/BDE/135567/2018)]. This work was also funded by FEDER, through the Competitiveness Internationalization Operational Programme (POCI), and by National funds, through the Foundation for Science and Technology (FCT), under the scope of the projects POCI-01-0145-FEDER-007038; POCI-01-0145-FEDER-029751 and POCI-01-0145-FEDER-032619. This article has also been developed under the scope of the project NORTE-01-0145-FEDER-000023, supported by the Northern Portugal Regional Operational Programme (NORTE 2020), under the Portugal 2020 Partnership Agreement, through the European Regional Development Fund (FEDER).</abstract><cop>Switzerland</cop><pub>Multidisciplinary Digital Publishing Institute</pub><pmid>32422916</pmid><doi>10.3390/ijms21103459</doi><orcidid>https://orcid.org/0000-0003-1858-4318</orcidid><orcidid>https://orcid.org/0000-0003-1461-9077</orcidid><oa>free_for_read</oa></addata></record> |
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recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7279033 |
source | Publicly Available Content Database; PubMed Central |
subjects | 6-Hydroxydopamine Abnormalities Age Aging Aging (artificial) Aging - metabolism Aging - pathology Animal model Animal models Animal welfare Animals Asymmetry Ciências da Saúde Ciências Médicas Corpus Striatum - drug effects Corpus Striatum - metabolism Corpus Striatum - pathology Disease Models, Animal Dopamine Dopamine - metabolism Dopamine receptors Dopaminergic Neurons - drug effects Dopaminergic Neurons - metabolism Dopaminergic Neurons - pathology Experiments Female Forebrain Humans Male Medial forebrain bundle Motor Disorders - chemically induced Motor Disorders - metabolism Motor Disorders - pathology Motor skill Motor task performance Neurodegeneration Oxidative stress Oxidopamine - toxicity Parkinson Disease - metabolism Parkinson Disease - physiopathology Parkinson Disease, Secondary - chemically induced Parkinson Disease, Secondary - metabolism Parkinson Disease, Secondary - physiopathology Parkinson's disease Rats Risk analysis Risk factors Rodents Science & Technology Substantia nigra Substantia Nigra - drug effects Substantia Nigra - metabolism Substantia Nigra - pathology Surgery Symmetry Young adults |
title | Impact of aging on the 6-OHDA-induced 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=2025-01-19T01%3A07%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Impact%20of%20aging%20on%20the%206-OHDA-induced%20rat%20model%20of%20Parkinson%E2%80%99s%20disease&rft.jtitle=International%20journal%20of%20molecular%20sciences&rft.au=Barata-Antunes,%20Sandra&rft.date=2020-05-14&rft.volume=21&rft.issue=10&rft.spage=3459&rft.pages=3459-&rft.issn=1422-0067&rft.eissn=1422-0067&rft_id=info:doi/10.3390/ijms21103459&rft_dat=%3Cproquest_pubme%3E2404483196%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c503t-1137e976f0e3b947b1d39f495560617d1747e8c494ef8c04f37bb82ae32f565c3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2404483196&rft_id=info:pmid/32422916&rfr_iscdi=true |