Compartmental organization and chemical profile of dopaminergic and GABAergic neurons in the substantia nigra of the rat
The substantia nigra (SN) is a midbrain center composed of dopaminergic (DA‐) and gamma aminobutyric acid (GABA)ergic (GABA‐) neurons. In this study, we investigated the topographical relationship between both cell populations and their chemical profile by using single and double immunostaining for...
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Published in | Journal of comparative neurology (1911) Vol. 421; no. 1; pp. 107 - 135 |
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Main Authors | , |
Format | Journal Article |
Language | English |
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New York
John Wiley & Sons, Inc
22.05.2000
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ISSN | 0021-9967 1096-9861 |
DOI | 10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F |
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Abstract | The substantia nigra (SN) is a midbrain center composed of dopaminergic (DA‐) and gamma aminobutyric acid (GABA)ergic (GABA‐) neurons. In this study, we investigated the topographical relationship between both cell populations and their chemical profile by using single and double immunostaining for tyrosine hydroxylase (TH), glutamic acid decarboxylase (GAD), cholecystokinin (CCK), calretinin (CR), calbindin (CB), parvalbumin (PV), and nitric oxide synthase (NOS). Our results showed that DA‐cells are arranged in two bands, one rostrodorsal that corresponds to the SN pars compacta (SNC), and another caudoventral that corresponds to the SN pars reticulata (SNR) and emits cell bridges that make contact with the rostrodorsal one. In the SNR, GABA‐cells are arranged in dorsoventrally elongated clusters that occupy DA‐cell free regions. According to cytoarchitectural, topographical, and chemical criteria, we identified ten different cell groups: five dopaminergic ones, and five GABAergic ones. Within DA‐cells, we found a cell group in the dorsomedial portion of the SNC which contains CCK, CR, and CB (dmSNC); DA‐cells in the SN pars lateralis (SNL) which also contain CCK, CR and CB; DA‐cells in the rostral half of the SNC containing CCK and CR (rSNC); DA‐cells in the SNR and the caudal half of the SNC which only express CR (cSNC‐SNR), and a DA‐cell group in the lateral part of the SNC that contains none of the markers studied (lSNC). Within GABA‐cells, we distinguished: large GABA‐cells in the SNL that contain PV; large GABA‐cells in the rostrolateral part of the SNR containing PV and NOS (rlSNR), small GABA‐cells in the caudomedial part of the SNR containing PV (cmSNR), and two groups of small GABA‐cells in the rostromedial portion of the SNR, one of them containing CR (rmcSNR), and the other containing NOS (rmnSNR). These data suggest that over a compartmental and complementary organization, DA‐ and GABA‐nigral cells form a mosaic of neurochemically different subnuclei which probably differ in their physiological and pharmacological properties and vulnerability to aggression. J. Comp. Neurol. 421:107–135, 2000. © 2000 Wiley‐Liss, Inc. |
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AbstractList | The substantia nigra (SN) is a midbrain center composed of dopaminergic (DA-) and gamma aminobutyric acid (GABA)ergic (GABA-) neurons. In this study, we investigated the topographical relationship between both cell populations and their chemical profile by using single and double immunostaining for tyrosine hydroxylase (TH), glutamic acid decarboxylase (GAD), cholecystokinin (CCK), calretinin (CR), calbindin (CB), parvalbumin (PV), and nitric oxide synthase (NOS). Our results showed that DA-cells are arranged in two bands, one rostrodorsal that corresponds to the SN pars compacta (SNC), and another caudoventral that corresponds to the SN pars reticulata (SNR) and emits cell bridges that make contact with the rostrodorsal one. In the SNR, GABA-cells are arranged in dorsoventrally elongated clusters that occupy DA-cell free regions. According to cytoarchitectural, topographical, and chemical criteria, we identified ten different cell groups: five dopaminergic ones, and five GABAergic ones. Within DA-cells, we found a cell group in the dorsomedial portion of the SNC which contains CCK, CR, and CB (dmSNC); DA-cells in the SN pars lateralis (SNL) which also contain CCK, CR and CB; DA-cells in the rostral half of the SNC containing CCK and CR (rSNC); DA-cells in the SNR and the caudal half of the SNC which only express CR (cSNC-SNR), and a DA-cell group in the lateral part of the SNC that contains none of the markers studied (lSNC). Within GABA-cells, we distinguished: large GABA-cells in the SNL that contain PV; large GABA-cells in the rostrolateral part of the SNR containing PV and NOS (rlSNR), small GABA-cells in the caudomedial part of the SNR containing PV (cmSNR), and two groups of small GABA-cells in the rostromedial portion of the SNR, one of them containing CR (rmcSNR), and the other containing NOS (rmnSNR). These data suggest that over a compartmental and complementary organization, DA- and GABA-nigral cells form a mosaic of neurochemically different subnuclei which probably differ in their physiological and pharmacological properties and vulnerability to aggression. The substantia nigra (SN) is a midbrain center composed of dopaminergic (DA‐) and gamma aminobutyric acid (GABA)ergic (GABA‐) neurons. In this study, we investigated the topographical relationship between both cell populations and their chemical profile by using single and double immunostaining for tyrosine hydroxylase (TH), glutamic acid decarboxylase (GAD), cholecystokinin (CCK), calretinin (CR), calbindin (CB), parvalbumin (PV), and nitric oxide synthase (NOS). Our results showed that DA‐cells are arranged in two bands, one rostrodorsal that corresponds to the SN pars compacta (SNC), and another caudoventral that corresponds to the SN pars reticulata (SNR) and emits cell bridges that make contact with the rostrodorsal one. In the SNR, GABA‐cells are arranged in dorsoventrally elongated clusters that occupy DA‐cell free regions. According to cytoarchitectural, topographical, and chemical criteria, we identified ten different cell groups: five dopaminergic ones, and five GABAergic ones. Within DA‐cells, we found a cell group in the dorsomedial portion of the SNC which contains CCK, CR, and CB (dmSNC); DA‐cells in the SN pars lateralis (SNL) which also contain CCK, CR and CB; DA‐cells in the rostral half of the SNC containing CCK and CR (rSNC); DA‐cells in the SNR and the caudal half of the SNC which only express CR (cSNC‐SNR), and a DA‐cell group in the lateral part of the SNC that contains none of the markers studied (lSNC). Within GABA‐cells, we distinguished: large GABA‐cells in the SNL that contain PV; large GABA‐cells in the rostrolateral part of the SNR containing PV and NOS (rlSNR), small GABA‐cells in the caudomedial part of the SNR containing PV (cmSNR), and two groups of small GABA‐cells in the rostromedial portion of the SNR, one of them containing CR (rmcSNR), and the other containing NOS (rmnSNR). These data suggest that over a compartmental and complementary organization, DA‐ and GABA‐nigral cells form a mosaic of neurochemically different subnuclei which probably differ in their physiological and pharmacological properties and vulnerability to aggression. J. Comp. Neurol. 421:107–135, 2000. © 2000 Wiley‐Liss, Inc. |
Author | Rodríguez, Manuel González-Hernández, Tomás |
Author_xml | – sequence: 1 givenname: Tomás surname: González-Hernández fullname: González-Hernández, Tomás email: tgonhern@ull.es organization: Department of Anatomy Faculty of Medicine, University of La Laguna, La Laguna, Tenerife, Spain – sequence: 2 givenname: Manuel surname: Rodríguez fullname: Rodríguez, Manuel organization: Department of Physiology. Faculty of Medicine, University of La Laguna, La Laguna, Tenerife, Spain |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/10813775$$D View this record in MEDLINE/PubMed |
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A subpopulation of mesencephalic dopamine neurons projecting to limbic areas contains a cholecystokinin-like peptide: evidence fro 1994; 134 1991; 14 1991; 12 1995; 38 1996; 72 1996; 74 1996; 73 1992; 526 1987a; 7 1998; 276 1998; 154 1994; 63 1997; 9 1996; 75 1992; 50 1992; 51 1998; 394 1997; 146 1995; 20 1992; 8 1989; 33 1984; 311 1991; 88 1994; 263 1994; 78 1985; 333 1979; 4 1985 1993; 250 1992; 46 1983 1992; 43 1993; 133 1984; 40 1993; 624 1989; 498 1982; 208 1995; 57 1997a; 378 1998 1964; 232 1997 1970; 11 1996; 93 1997; 27 1984; 229 1995 1996; 364 1980; 192 1985; 82 1970; 17 1996; 10 1980; 199 1996; 369 1982; 46 1984; 4 1992; 137 1994; 99 1994; 14 1989a; 279 1994; 17 1998; 784 1990; 6 1974; 16 1993; 605 1990; 301 1990; 302 1987; 265 1991; 56 1994; 170 1993; 60 1989; 279 1994; 173 1992; 13 1992; 15 1991; 558 1992; 12 1982; 23 1995; 64 1997; 103 1989; 74 1990; 87 1994; 103 1994; 345 1991; 43 1999; 19 1991; 40 1995; 65 1982; 9 1997; 17 1999; 10 1987b; 7 1996; 730 1991; 304 1996; 2 1980; 189 1993; 331 1996; 7 1982; 78 1985; 1 1991; 254 1991; 37 1994; 350 1992; 587 1978; 19 1983; 37 1998; 21 1989; 28 1983; 218 1989; 29 1987; 23 1989; 12 1979; 175 1989b; 74 1987; 259 1987; 411 1997b; 9 1995; 109 1987; 416 1980; 5 1992; 216 1985; 236 1989; 290 1999; 72 1980; 283 1994; 5 Heizmann (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB53) 1984; 40 Seroogy (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB119) 1989; 279 Albin (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB1) 1989; 12 Schmidt (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB111) 1994; 78 Baimbridge (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB6) 1992; 15 Kemp (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB68) 1970; 17 Mugnaini (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB89) 1985 Ottersen (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB93) 1984; 229 O'Dell (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB92) 1991; 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331 Yelnik (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB130) 1987; 265 Cortes (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB14) 1990; 6 Moncada (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB84) 1991; 43 Liang (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB72) 1996; 75 Parent (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB95) 1995; 20 Shi (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB122) 1997; 17 Montague (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB85) 1994; 263 Nagai (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB90) 1983; 218 Gartwaite (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB37) 1995; 57 Reiner (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB102) 1993; 624 Bredt (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB10) 1994; 63 Redgrave (10.1002/(SICI)1096-9861(20000522)421:1<107::AID-CNE7>3.0.CO;2-F-BIB101) 1992; 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Snippet | The substantia nigra (SN) is a midbrain center composed of dopaminergic (DA‐) and gamma aminobutyric acid (GABA)ergic (GABA‐) neurons. In this study, we... The substantia nigra (SN) is a midbrain center composed of dopaminergic (DA-) and gamma aminobutyric acid (GABA)ergic (GABA-) neurons. In this study, we... |
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SubjectTerms | Animals calcium-binding proteins cholecystokinin coexpression Dopamine - physiology Fluorescent Antibody Technique, Indirect gamma-Aminobutyric Acid - physiology Glutamate Decarboxylase - metabolism Immunohistochemistry Male midbrain Neurons - physiology NOS Rats Rats, Sprague-Dawley Substantia Nigra - anatomy & histology Substantia Nigra - cytology Substantia Nigra - metabolism topographical distribution Tyrosine 3-Monooxygenase - metabolism |
Title | Compartmental organization and chemical profile of dopaminergic and GABAergic neurons in the substantia nigra of the rat |
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