Dopaminergic mesencephalic systems and behavioral performance in very old rats
Abstract Morphologic and functional studies describing the impact of aging on mesencephalic dopaminergic (DA) neurons in laboratory animals are rather scanty and inconclusive. In rats, stereological studies characterizing age changes in the mesencephalic DA neurons have not been documented. In order...
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description | Abstract Morphologic and functional studies describing the impact of aging on mesencephalic dopaminergic (DA) neurons in laboratory animals are rather scanty and inconclusive. In rats, stereological studies characterizing age changes in the mesencephalic DA neurons have not been documented. In order to fill this information gap and to determine whether the very old rat may serve as a suitable animal model of Parkinson's disease, we performed a stereological assessment of the mesencephalic tyrosine hydroxylase immunoreactive (TH-ir) neurons in young-adult (4–6 months), old (22–24 months) and senile (30–32 months) Sprague–Dawley female rats. Morphometric analysis of the TH-ir neurons of the substantia nigra (SN) and ventral tegmental area (VTA) was performed using an appropriate image analysis system. Age changes in motor performance were assessed measuring the endurance of rats to hang from a wire mesh pole or to remain on a ramp set at different angles to the floor. Age changes in locomotion and exploratory activity were evaluated by the open field test. We observed a significant age-related reduction in TH-ir neuron numbers in the SN (17 and 33% reduction in old and senile rats, respectively compared with young counterparts) but not in the VTA. The size of the TH-ir cells increased significantly in both the SN and VTA of the senescent animals but TH labeling intensity fell. Motor, locomotor and exploratory performance deteriorated markedly in the old and senile rats as compared with young animals. These findings reveal the existence of a moderate but significant vulnerability of mesencephalic DA neurons to aging in rats. This phenomenon, which is particularly marked in the SN of very old rats, may contribute to the age-related decline in motor and exploratory performance recorded in this species. |
doi_str_mv | 10.1016/j.neuroscience.2008.04.016 |
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In rats, stereological studies characterizing age changes in the mesencephalic DA neurons have not been documented. In order to fill this information gap and to determine whether the very old rat may serve as a suitable animal model of Parkinson's disease, we performed a stereological assessment of the mesencephalic tyrosine hydroxylase immunoreactive (TH-ir) neurons in young-adult (4–6 months), old (22–24 months) and senile (30–32 months) Sprague–Dawley female rats. Morphometric analysis of the TH-ir neurons of the substantia nigra (SN) and ventral tegmental area (VTA) was performed using an appropriate image analysis system. Age changes in motor performance were assessed measuring the endurance of rats to hang from a wire mesh pole or to remain on a ramp set at different angles to the floor. Age changes in locomotion and exploratory activity were evaluated by the open field test. We observed a significant age-related reduction in TH-ir neuron numbers in the SN (17 and 33% reduction in old and senile rats, respectively compared with young counterparts) but not in the VTA. The size of the TH-ir cells increased significantly in both the SN and VTA of the senescent animals but TH labeling intensity fell. Motor, locomotor and exploratory performance deteriorated markedly in the old and senile rats as compared with young animals. These findings reveal the existence of a moderate but significant vulnerability of mesencephalic DA neurons to aging in rats. This phenomenon, which is particularly marked in the SN of very old rats, may contribute to the age-related decline in motor and exploratory performance recorded in this species.</description><identifier>ISSN: 0306-4522</identifier><identifier>EISSN: 1873-7544</identifier><identifier>DOI: 10.1016/j.neuroscience.2008.04.016</identifier><identifier>PMID: 18554807</identifier><identifier>CODEN: NRSCDN</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>aging ; Aging - pathology ; Aging - physiology ; Animals ; Behavior, Animal - physiology ; Biological and medical sciences ; Dopamine - metabolism ; Female ; Fundamental and applied biological sciences. Psychology ; Immunohistochemistry ; mesencephalic ; Mesencephalon - pathology ; Mesencephalon - physiology ; morphometry ; Motor Activity - physiology ; motor tests ; Neurology ; Neurons - pathology ; Neurons - physiology ; open field ; Rats ; Rats, Sprague-Dawley ; Tyrosine 3-Monooxygenase - metabolism ; tyrosine hydroxylase ; Vertebrates: nervous system and sense organs</subject><ispartof>Neuroscience, 2008-07, Vol.154 (4), p.1598-1606</ispartof><rights>2008</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c494t-99d8051bb35b7cc1adccdc3bdfd24077125c87ead957a50997c87e52fe763c053</citedby><cites>FETCH-LOGICAL-c494t-99d8051bb35b7cc1adccdc3bdfd24077125c87ead957a50997c87e52fe763c053</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.neuroscience.2008.04.016$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,778,782,3539,27911,27912,45982</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20522575$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18554807$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sanchez, H.L</creatorcontrib><creatorcontrib>Silva, L.B</creatorcontrib><creatorcontrib>Portiansky, E.L</creatorcontrib><creatorcontrib>Herenu, C.B</creatorcontrib><creatorcontrib>Goya, R.G</creatorcontrib><creatorcontrib>Zuccolilli, G.O</creatorcontrib><title>Dopaminergic mesencephalic systems and behavioral performance in very old rats</title><title>Neuroscience</title><addtitle>Neuroscience</addtitle><description>Abstract Morphologic and functional studies describing the impact of aging on mesencephalic dopaminergic (DA) neurons in laboratory animals are rather scanty and inconclusive. In rats, stereological studies characterizing age changes in the mesencephalic DA neurons have not been documented. In order to fill this information gap and to determine whether the very old rat may serve as a suitable animal model of Parkinson's disease, we performed a stereological assessment of the mesencephalic tyrosine hydroxylase immunoreactive (TH-ir) neurons in young-adult (4–6 months), old (22–24 months) and senile (30–32 months) Sprague–Dawley female rats. Morphometric analysis of the TH-ir neurons of the substantia nigra (SN) and ventral tegmental area (VTA) was performed using an appropriate image analysis system. Age changes in motor performance were assessed measuring the endurance of rats to hang from a wire mesh pole or to remain on a ramp set at different angles to the floor. Age changes in locomotion and exploratory activity were evaluated by the open field test. We observed a significant age-related reduction in TH-ir neuron numbers in the SN (17 and 33% reduction in old and senile rats, respectively compared with young counterparts) but not in the VTA. The size of the TH-ir cells increased significantly in both the SN and VTA of the senescent animals but TH labeling intensity fell. Motor, locomotor and exploratory performance deteriorated markedly in the old and senile rats as compared with young animals. These findings reveal the existence of a moderate but significant vulnerability of mesencephalic DA neurons to aging in rats. This phenomenon, which is particularly marked in the SN of very old rats, may contribute to the age-related decline in motor and exploratory performance recorded in this species.</description><subject>aging</subject><subject>Aging - pathology</subject><subject>Aging - physiology</subject><subject>Animals</subject><subject>Behavior, Animal - physiology</subject><subject>Biological and medical sciences</subject><subject>Dopamine - metabolism</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Immunohistochemistry</subject><subject>mesencephalic</subject><subject>Mesencephalon - pathology</subject><subject>Mesencephalon - physiology</subject><subject>morphometry</subject><subject>Motor Activity - physiology</subject><subject>motor tests</subject><subject>Neurology</subject><subject>Neurons - pathology</subject><subject>Neurons - physiology</subject><subject>open field</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Tyrosine 3-Monooxygenase - metabolism</subject><subject>tyrosine hydroxylase</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0306-4522</issn><issn>1873-7544</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkk2LFDEQhoMo7rj6F6QR9NZt5WvS8SAsu37Bogf1HNJJtZuxv0y6B-bfm2YaFS-aSyjqqXqTt4qQZxQqCnT_8lANuMQxuYCDw4oB1BWIKqfukR2tFS-VFOI-2QGHfSkkYxfkUUoHyEcK_pBc0FpKUYPakY8342T7MGD8FlzRY1pbTne2y1E6pRn7VNjBFw3e2WMYo-2KCWM7xt5msAhDccR4KsbOF9HO6TF50Nou4ZPtviRf3775cv2-vP307sP11W3phBZzqbWvQdKm4bJRzlHrnfOON771TIBSlElXK7ReS2UlaK3WULIW1Z47kPySvDj3neL4Y8E0mz4kh11nBxyXZPaaaSmZ_ifIoOZcUJHBV2fQZWdTxNZMMfQ2ngwFs9puDuZP281quwFhcioXP91UlqZH_7t08zkDzzfAJme7Nmb3QvrFMchDkmr9182Zw2zeMWA0m5wPEd1s_Bj-7z2v_2rjujCErPwdT5gO4xKHPB5DTWIGzOd1UdY9gTpviNKC_wSwLL1m</recordid><startdate>20080717</startdate><enddate>20080717</enddate><creator>Sanchez, H.L</creator><creator>Silva, L.B</creator><creator>Portiansky, E.L</creator><creator>Herenu, C.B</creator><creator>Goya, R.G</creator><creator>Zuccolilli, G.O</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>7QG</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>20080717</creationdate><title>Dopaminergic mesencephalic systems and behavioral performance in very old rats</title><author>Sanchez, H.L ; Silva, L.B ; Portiansky, E.L ; Herenu, C.B ; Goya, R.G ; Zuccolilli, G.O</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c494t-99d8051bb35b7cc1adccdc3bdfd24077125c87ead957a50997c87e52fe763c053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>aging</topic><topic>Aging - pathology</topic><topic>Aging - physiology</topic><topic>Animals</topic><topic>Behavior, Animal - physiology</topic><topic>Biological and medical sciences</topic><topic>Dopamine - metabolism</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Immunohistochemistry</topic><topic>mesencephalic</topic><topic>Mesencephalon - pathology</topic><topic>Mesencephalon - physiology</topic><topic>morphometry</topic><topic>Motor Activity - physiology</topic><topic>motor tests</topic><topic>Neurology</topic><topic>Neurons - pathology</topic><topic>Neurons - physiology</topic><topic>open field</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Tyrosine 3-Monooxygenase - metabolism</topic><topic>tyrosine hydroxylase</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sanchez, H.L</creatorcontrib><creatorcontrib>Silva, L.B</creatorcontrib><creatorcontrib>Portiansky, E.L</creatorcontrib><creatorcontrib>Herenu, C.B</creatorcontrib><creatorcontrib>Goya, R.G</creatorcontrib><creatorcontrib>Zuccolilli, G.O</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>Animal Behavior Abstracts</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>Sanchez, H.L</au><au>Silva, L.B</au><au>Portiansky, E.L</au><au>Herenu, C.B</au><au>Goya, R.G</au><au>Zuccolilli, G.O</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dopaminergic mesencephalic systems and behavioral performance in very old rats</atitle><jtitle>Neuroscience</jtitle><addtitle>Neuroscience</addtitle><date>2008-07-17</date><risdate>2008</risdate><volume>154</volume><issue>4</issue><spage>1598</spage><epage>1606</epage><pages>1598-1606</pages><issn>0306-4522</issn><eissn>1873-7544</eissn><coden>NRSCDN</coden><abstract>Abstract Morphologic and functional studies describing the impact of aging on mesencephalic dopaminergic (DA) neurons in laboratory animals are rather scanty and inconclusive. In rats, stereological studies characterizing age changes in the mesencephalic DA neurons have not been documented. In order to fill this information gap and to determine whether the very old rat may serve as a suitable animal model of Parkinson's disease, we performed a stereological assessment of the mesencephalic tyrosine hydroxylase immunoreactive (TH-ir) neurons in young-adult (4–6 months), old (22–24 months) and senile (30–32 months) Sprague–Dawley female rats. Morphometric analysis of the TH-ir neurons of the substantia nigra (SN) and ventral tegmental area (VTA) was performed using an appropriate image analysis system. Age changes in motor performance were assessed measuring the endurance of rats to hang from a wire mesh pole or to remain on a ramp set at different angles to the floor. Age changes in locomotion and exploratory activity were evaluated by the open field test. We observed a significant age-related reduction in TH-ir neuron numbers in the SN (17 and 33% reduction in old and senile rats, respectively compared with young counterparts) but not in the VTA. The size of the TH-ir cells increased significantly in both the SN and VTA of the senescent animals but TH labeling intensity fell. Motor, locomotor and exploratory performance deteriorated markedly in the old and senile rats as compared with young animals. These findings reveal the existence of a moderate but significant vulnerability of mesencephalic DA neurons to aging in rats. This phenomenon, which is particularly marked in the SN of very old rats, may contribute to the age-related decline in motor and exploratory performance recorded in this species.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>18554807</pmid><doi>10.1016/j.neuroscience.2008.04.016</doi><tpages>9</tpages></addata></record> |
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subjects | aging Aging - pathology Aging - physiology Animals Behavior, Animal - physiology Biological and medical sciences Dopamine - metabolism Female Fundamental and applied biological sciences. Psychology Immunohistochemistry mesencephalic Mesencephalon - pathology Mesencephalon - physiology morphometry Motor Activity - physiology motor tests Neurology Neurons - pathology Neurons - physiology open field Rats Rats, Sprague-Dawley Tyrosine 3-Monooxygenase - metabolism tyrosine hydroxylase Vertebrates: nervous system and sense organs |
title | Dopaminergic mesencephalic systems and behavioral performance in very old rats |
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