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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Veröffentlicht in:Neuroscience 2009-03, Vol.159 (1), p.236-245
Hauptverfasser: Alladi, P.A, Mahadevan, A, Yasha, T.C, Raju, T.R, Shankar, S.K, Muthane, U
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container_title Neuroscience
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creator Alladi, P.A
Mahadevan, A
Yasha, T.C
Raju, T.R
Shankar, S.K
Muthane, U
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. 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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>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=21218154$$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. 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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.</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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