Absence of age-related changes in nigral dopaminergic neurons of Asian Indians: Relevance to lower incidence of Parkinson's disease
Abstract Age-related loss of melanized nigral neurons reported in the British Caucasians is not observed in Asian Indian, American and French adults. In the Americans, loss of dopaminergic phenotype occurs from midlife, without frank neurodegeneration. Here, we investigated whether nigral dopaminerg...
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description | Abstract Age-related loss of melanized nigral neurons reported in the British Caucasians is not observed in Asian Indian, American and French adults. In the Americans, loss of dopaminergic phenotype occurs from midlife, without frank neurodegeneration. Here, we investigated whether nigral dopaminergic neurons in Asian Indians are lost with age or undergo morphological or biochemical dysfunction. Using unbiased stereology we estimated volume, number of melanized, borderline/non-melanized ( n =34, 28 gestational weeks to 80 years) and tyrosine hydroxylase (TH)–Nurr1 co-labeled neurons ( n =32, 28 gestational weeks to 80 years) in substantia nigra pars compacta. We quantified Nurr1 and TH proteins by immunoblotting ( n =18, 28 gestational weeks to 69 years) and apoptotic neurons by terminal deoxynucleotidyl transferase mediated dUTP nick end labeling (TUNEL) staining. Nuclear and soma size was estimated by morphometry. There was no age-related decline in volume, neuronal density, neuronal numbers and TH-Nurr1 co-labeled neurons. TH and Nurr1 protein expression remained stable. Lack of TUNEL-TH co-labeled cells confirmed absence of neuronal apoptosis. The neuronal size remained unaltered. Our findings of preserved nigral dopaminergic neurons suggest no age-related loss of nigral function in Asian Indians, unlike the Americans. This may explain the lower incidence of Parkinson's disease in Asian Indians. |
doi_str_mv | 10.1016/j.neuroscience.2008.11.051 |
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In the Americans, loss of dopaminergic phenotype occurs from midlife, without frank neurodegeneration. Here, we investigated whether nigral dopaminergic neurons in Asian Indians are lost with age or undergo morphological or biochemical dysfunction. Using unbiased stereology we estimated volume, number of melanized, borderline/non-melanized ( n =34, 28 gestational weeks to 80 years) and tyrosine hydroxylase (TH)–Nurr1 co-labeled neurons ( n =32, 28 gestational weeks to 80 years) in substantia nigra pars compacta. We quantified Nurr1 and TH proteins by immunoblotting ( n =18, 28 gestational weeks to 69 years) and apoptotic neurons by terminal deoxynucleotidyl transferase mediated dUTP nick end labeling (TUNEL) staining. Nuclear and soma size was estimated by morphometry. There was no age-related decline in volume, neuronal density, neuronal numbers and TH-Nurr1 co-labeled neurons. TH and Nurr1 protein expression remained stable. Lack of TUNEL-TH co-labeled cells confirmed absence of neuronal apoptosis. The neuronal size remained unaltered. Our findings of preserved nigral dopaminergic neurons suggest no age-related loss of nigral function in Asian Indians, unlike the Americans. This may explain the lower incidence of Parkinson's disease in Asian Indians.</description><identifier>ISSN: 0306-4522</identifier><identifier>EISSN: 1873-7544</identifier><identifier>DOI: 10.1016/j.neuroscience.2008.11.051</identifier><identifier>PMID: 19135503</identifier><identifier>CODEN: NRSCDN</identifier><language>eng</language><publisher>Amsterdam: Elsevier Ltd</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Aging ; aging human substantia nigra ; Apoptosis - physiology ; Asian Indians ; Biological and medical sciences ; Cell Size ; Child ; Child, Preschool ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; DNA-Binding Proteins - metabolism ; Dopamine - metabolism ; Female ; Fetus ; Fundamental and applied biological sciences. Psychology ; Humans ; In Situ Nick-End Labeling - methods ; India - ethnology ; Infant ; Infant, Newborn ; Male ; Medical sciences ; melanized and non-melanized neurons ; Middle Aged ; Neurology ; Neurons - metabolism ; Nuclear Receptor Subfamily 4, Group A, Member 2 ; Reference Values ; Staining and Labeling - methods ; stereology and morphometry ; Stereotaxic Techniques ; Substantia Nigra - cytology ; Substantia Nigra - metabolism ; TH and Nurr1 immunohistochemistry ; Transcription Factors - metabolism ; TUNEL staining ; Tyrosine 3-Monooxygenase - metabolism ; Vertebrates: nervous system and sense organs ; Young Adult</subject><ispartof>Neuroscience, 2009-03, Vol.159 (1), p.236-245</ispartof><rights>IBRO</rights><rights>2009 IBRO</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c494t-38c072756bf48601549e320437f3296e176c623fba2d8ea52dc05b53ebb64daf3</citedby><cites>FETCH-LOGICAL-c494t-38c072756bf48601549e320437f3296e176c623fba2d8ea52dc05b53ebb64daf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0306452208017211$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21218154$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19135503$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Alladi, P.A</creatorcontrib><creatorcontrib>Mahadevan, A</creatorcontrib><creatorcontrib>Yasha, T.C</creatorcontrib><creatorcontrib>Raju, T.R</creatorcontrib><creatorcontrib>Shankar, S.K</creatorcontrib><creatorcontrib>Muthane, U</creatorcontrib><title>Absence of age-related changes in nigral dopaminergic neurons of Asian Indians: Relevance to lower incidence of Parkinson's disease</title><title>Neuroscience</title><addtitle>Neuroscience</addtitle><description>Abstract Age-related loss of melanized nigral neurons reported in the British Caucasians is not observed in Asian Indian, American and French adults. In the Americans, loss of dopaminergic phenotype occurs from midlife, without frank neurodegeneration. Here, we investigated whether nigral dopaminergic neurons in Asian Indians are lost with age or undergo morphological or biochemical dysfunction. Using unbiased stereology we estimated volume, number of melanized, borderline/non-melanized ( n =34, 28 gestational weeks to 80 years) and tyrosine hydroxylase (TH)–Nurr1 co-labeled neurons ( n =32, 28 gestational weeks to 80 years) in substantia nigra pars compacta. We quantified Nurr1 and TH proteins by immunoblotting ( n =18, 28 gestational weeks to 69 years) and apoptotic neurons by terminal deoxynucleotidyl transferase mediated dUTP nick end labeling (TUNEL) staining. Nuclear and soma size was estimated by morphometry. There was no age-related decline in volume, neuronal density, neuronal numbers and TH-Nurr1 co-labeled neurons. TH and Nurr1 protein expression remained stable. Lack of TUNEL-TH co-labeled cells confirmed absence of neuronal apoptosis. The neuronal size remained unaltered. Our findings of preserved nigral dopaminergic neurons suggest no age-related loss of nigral function in Asian Indians, unlike the Americans. This may explain the lower incidence of Parkinson's disease in Asian Indians.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Aging</subject><subject>aging human substantia nigra</subject><subject>Apoptosis - physiology</subject><subject>Asian Indians</subject><subject>Biological and medical sciences</subject><subject>Cell Size</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Dopamine - metabolism</subject><subject>Female</subject><subject>Fetus</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>In Situ Nick-End Labeling - methods</subject><subject>India - ethnology</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Male</subject><subject>Medical sciences</subject><subject>melanized and non-melanized neurons</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Neurons - metabolism</subject><subject>Nuclear Receptor Subfamily 4, Group A, Member 2</subject><subject>Reference Values</subject><subject>Staining and Labeling - methods</subject><subject>stereology and morphometry</subject><subject>Stereotaxic Techniques</subject><subject>Substantia Nigra - cytology</subject><subject>Substantia Nigra - metabolism</subject><subject>TH and Nurr1 immunohistochemistry</subject><subject>Transcription Factors - metabolism</subject><subject>TUNEL staining</subject><subject>Tyrosine 3-Monooxygenase - metabolism</subject><subject>Vertebrates: nervous system and sense organs</subject><subject>Young Adult</subject><issn>0306-4522</issn><issn>1873-7544</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkkmPEzEQhVsIxISBv4AsJODUweWtO3NAioZtpJFALGfLbVcHZzru4EoGzZk_jpuERVygLnX56r1SvaqqR8DnwME8W88T7vNIPmLyOBect3OAOddwq5pB28i60UrdrmZcclMrLcRJdY9ozUtpJe9WJ7AAqTWXs-rbsqNJhY09cyusMw5uh4H5zy6tkFhMLMVVdgML49ZtYsK8ip79WCDRNLWk6BK7SKE0OmPvccBrNynuRjaMXzEXDR_DT5N3Ll_FRGN6SixEQkd4v7rTu4HwwbGfVp9evfx4_qa-fPv64nx5WXu1ULtatp43otGm61VrOGi1QCm4kk0vxcIgNMYbIfvOidCi0yJ4rjstseuMCq6Xp9WTg-42j1_2SDu7ieRxGFzCcU_WmIXhqtH_BItpYwzwAp4dQF_ioIy93ea4cfnGArdTVnZt_8zKTllZAFuyKsMPjy77boPh9-gxnAI8PgKOvBv6XM4a6RcnQEBbrlC4FwcOy_GuI2Z7tAsxo9_ZMMb_2-f5XzJ-iCkW5yu8QVqP-5xKPBYsCcvth-m7pufiLYdGAMjvdgTO1A</recordid><startdate>20090303</startdate><enddate>20090303</enddate><creator>Alladi, P.A</creator><creator>Mahadevan, A</creator><creator>Yasha, T.C</creator><creator>Raju, T.R</creator><creator>Shankar, S.K</creator><creator>Muthane, U</creator><general>Elsevier 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><scope>7X8</scope></search><sort><creationdate>20090303</creationdate><title>Absence of age-related changes in nigral dopaminergic neurons of Asian Indians: Relevance to lower incidence of Parkinson's disease</title><author>Alladi, P.A ; Mahadevan, A ; Yasha, T.C ; Raju, T.R ; Shankar, S.K ; Muthane, U</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c494t-38c072756bf48601549e320437f3296e176c623fba2d8ea52dc05b53ebb64daf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Aging</topic><topic>aging human substantia nigra</topic><topic>Apoptosis - physiology</topic><topic>Asian Indians</topic><topic>Biological and medical sciences</topic><topic>Cell Size</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Dopamine - metabolism</topic><topic>Female</topic><topic>Fetus</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>In Situ Nick-End Labeling - methods</topic><topic>India - ethnology</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Male</topic><topic>Medical sciences</topic><topic>melanized and non-melanized neurons</topic><topic>Middle Aged</topic><topic>Neurology</topic><topic>Neurons - metabolism</topic><topic>Nuclear Receptor Subfamily 4, Group A, Member 2</topic><topic>Reference Values</topic><topic>Staining and Labeling - methods</topic><topic>stereology and morphometry</topic><topic>Stereotaxic Techniques</topic><topic>Substantia Nigra - cytology</topic><topic>Substantia Nigra - metabolism</topic><topic>TH and Nurr1 immunohistochemistry</topic><topic>Transcription Factors - metabolism</topic><topic>TUNEL staining</topic><topic>Tyrosine 3-Monooxygenase - metabolism</topic><topic>Vertebrates: nervous system and sense organs</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alladi, P.A</creatorcontrib><creatorcontrib>Mahadevan, A</creatorcontrib><creatorcontrib>Yasha, T.C</creatorcontrib><creatorcontrib>Raju, T.R</creatorcontrib><creatorcontrib>Shankar, S.K</creatorcontrib><creatorcontrib>Muthane, U</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><collection>MEDLINE - Academic</collection><jtitle>Neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alladi, P.A</au><au>Mahadevan, A</au><au>Yasha, T.C</au><au>Raju, T.R</au><au>Shankar, S.K</au><au>Muthane, U</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Absence of age-related changes in nigral dopaminergic neurons of Asian Indians: Relevance to lower incidence of Parkinson's disease</atitle><jtitle>Neuroscience</jtitle><addtitle>Neuroscience</addtitle><date>2009-03-03</date><risdate>2009</risdate><volume>159</volume><issue>1</issue><spage>236</spage><epage>245</epage><pages>236-245</pages><issn>0306-4522</issn><eissn>1873-7544</eissn><coden>NRSCDN</coden><abstract>Abstract Age-related loss of melanized nigral neurons reported in the British Caucasians is not observed in Asian Indian, American and French adults. In the Americans, loss of dopaminergic phenotype occurs from midlife, without frank neurodegeneration. Here, we investigated whether nigral dopaminergic neurons in Asian Indians are lost with age or undergo morphological or biochemical dysfunction. Using unbiased stereology we estimated volume, number of melanized, borderline/non-melanized ( n =34, 28 gestational weeks to 80 years) and tyrosine hydroxylase (TH)–Nurr1 co-labeled neurons ( n =32, 28 gestational weeks to 80 years) in substantia nigra pars compacta. We quantified Nurr1 and TH proteins by immunoblotting ( n =18, 28 gestational weeks to 69 years) and apoptotic neurons by terminal deoxynucleotidyl transferase mediated dUTP nick end labeling (TUNEL) staining. Nuclear and soma size was estimated by morphometry. There was no age-related decline in volume, neuronal density, neuronal numbers and TH-Nurr1 co-labeled neurons. TH and Nurr1 protein expression remained stable. Lack of TUNEL-TH co-labeled cells confirmed absence of neuronal apoptosis. The neuronal size remained unaltered. Our findings of preserved nigral dopaminergic neurons suggest no age-related loss of nigral function in Asian Indians, unlike the Americans. This may explain the lower incidence of Parkinson's disease in Asian Indians.</abstract><cop>Amsterdam</cop><pub>Elsevier Ltd</pub><pmid>19135503</pmid><doi>10.1016/j.neuroscience.2008.11.051</doi><tpages>10</tpages></addata></record> |
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subjects | Adolescent Adult Aged Aged, 80 and over Aging aging human substantia nigra Apoptosis - physiology Asian Indians Biological and medical sciences Cell Size Child Child, Preschool Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases DNA-Binding Proteins - metabolism Dopamine - metabolism Female Fetus Fundamental and applied biological sciences. Psychology Humans In Situ Nick-End Labeling - methods India - ethnology Infant Infant, Newborn Male Medical sciences melanized and non-melanized neurons Middle Aged Neurology Neurons - metabolism Nuclear Receptor Subfamily 4, Group A, Member 2 Reference Values Staining and Labeling - methods stereology and morphometry Stereotaxic Techniques Substantia Nigra - cytology Substantia Nigra - metabolism TH and Nurr1 immunohistochemistry Transcription Factors - metabolism TUNEL staining Tyrosine 3-Monooxygenase - metabolism Vertebrates: nervous system and sense organs Young Adult |
title | Absence of age-related changes in nigral dopaminergic neurons of Asian Indians: Relevance to lower incidence of Parkinson's disease |
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