Distribution of lead in the cerebellum of suckling rats following low and high dose lead exposure: a micro-PIXE analysis
The distribution of lead in the cerebellum of suckling Sprague-Dawley rats was examined using a nuclear microprobe for elemental mapping of tissue sections (particle-induced X-ray emission, 3-microns beam of 2.5 MeV protons; micro-PIXE). The rats were injected intraperitoneally with a lead-containin...
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Veröffentlicht in: | Acta neuropathologica 1989-01, Vol.79 (2), p.149-153 |
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description | The distribution of lead in the cerebellum of suckling Sprague-Dawley rats was examined using a nuclear microprobe for elemental mapping of tissue sections (particle-induced X-ray emission, 3-microns beam of 2.5 MeV protons; micro-PIXE). The rats were injected intraperitoneally with a lead-containing vehicle or vehicle only from ages 1 to 14 days. The calculated doses were 7.8 (low-dose) and 15.6 (high-dose) micrograms lead/g body weight. The rats were killed at 20 days of age. The vascular system was rinsed quickly with 0.15 M ammonium acetate to obtain determinations of intra-parenchymal lead with minimal influence of lead bound to erythrocytes and plasma proteins. Brains were frozen in propane/propylene in liquid nitrogen. Cryostat sections, 15 microns thick, were air dried on formvar coats that covered a hole, 15 mm in diameter, in a plastic disc, and were used for lead analysis by micro-PIXE. Very low concentrations of lead were found in the brain of controls. Lead levels in homogenates from cerebrum and cerebellum measured by atomic absorption spectrometry (AAS) were: low-dose 1.2-2.2 micrograms/g wet weight and high-dose 1.4-2.4 micrograms/g wet weight. The lead levels measured with the micro-PIXE method were in good agreement with the levels found with AAS. Lead was present in the cerebellar white matter in two to three times higher amounts than in the cortical grey (low-dose white matter 11-18 micrograms/g dry weight, grey matter 2.0-5.5 micrograms/g dry weight). This was true for both low and high dose exposed rats. |
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G ; SOURANDER, P</creator><creatorcontrib>LINDH, U ; CONRADI, N. G ; SOURANDER, P</creatorcontrib><description>The distribution of lead in the cerebellum of suckling Sprague-Dawley rats was examined using a nuclear microprobe for elemental mapping of tissue sections (particle-induced X-ray emission, 3-microns beam of 2.5 MeV protons; micro-PIXE). The rats were injected intraperitoneally with a lead-containing vehicle or vehicle only from ages 1 to 14 days. The calculated doses were 7.8 (low-dose) and 15.6 (high-dose) micrograms lead/g body weight. The rats were killed at 20 days of age. The vascular system was rinsed quickly with 0.15 M ammonium acetate to obtain determinations of intra-parenchymal lead with minimal influence of lead bound to erythrocytes and plasma proteins. Brains were frozen in propane/propylene in liquid nitrogen. Cryostat sections, 15 microns thick, were air dried on formvar coats that covered a hole, 15 mm in diameter, in a plastic disc, and were used for lead analysis by micro-PIXE. Very low concentrations of lead were found in the brain of controls. Lead levels in homogenates from cerebrum and cerebellum measured by atomic absorption spectrometry (AAS) were: low-dose 1.2-2.2 micrograms/g wet weight and high-dose 1.4-2.4 micrograms/g wet weight. The lead levels measured with the micro-PIXE method were in good agreement with the levels found with AAS. Lead was present in the cerebellar white matter in two to three times higher amounts than in the cortical grey (low-dose white matter 11-18 micrograms/g dry weight, grey matter 2.0-5.5 micrograms/g dry weight). This was true for both low and high dose exposed rats.</description><identifier>ISSN: 0001-6322</identifier><identifier>EISSN: 1432-0533</identifier><identifier>DOI: 10.1007/BF00294372</identifier><identifier>PMID: 2596264</identifier><identifier>CODEN: ANPTAL</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Animals ; Biological and medical sciences ; Body Weight - drug effects ; Cerebellum - drug effects ; Cerebellum - metabolism ; Chemical and industrial products toxicology. Toxic occupational diseases ; Dose-Response Relationship, Drug ; Lead - pharmacokinetics ; Medical sciences ; Metals and various inorganic compounds ; Organ Size - drug effects ; Rats ; Rats, Inbred Strains ; Spectrometry, X-Ray Emission ; Toxicology</subject><ispartof>Acta neuropathologica, 1989-01, Vol.79 (2), p.149-153</ispartof><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c301t-fd550823a98aa77987e416e54f29bad0f0a61915c5a2095e0d4decfb0eedb3163</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6924378$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2596264$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LINDH, U</creatorcontrib><creatorcontrib>CONRADI, N. G</creatorcontrib><creatorcontrib>SOURANDER, P</creatorcontrib><title>Distribution of lead in the cerebellum of suckling rats following low and high dose lead exposure: a micro-PIXE analysis</title><title>Acta neuropathologica</title><addtitle>Acta Neuropathol</addtitle><description>The distribution of lead in the cerebellum of suckling Sprague-Dawley rats was examined using a nuclear microprobe for elemental mapping of tissue sections (particle-induced X-ray emission, 3-microns beam of 2.5 MeV protons; micro-PIXE). The rats were injected intraperitoneally with a lead-containing vehicle or vehicle only from ages 1 to 14 days. The calculated doses were 7.8 (low-dose) and 15.6 (high-dose) micrograms lead/g body weight. The rats were killed at 20 days of age. The vascular system was rinsed quickly with 0.15 M ammonium acetate to obtain determinations of intra-parenchymal lead with minimal influence of lead bound to erythrocytes and plasma proteins. Brains were frozen in propane/propylene in liquid nitrogen. Cryostat sections, 15 microns thick, were air dried on formvar coats that covered a hole, 15 mm in diameter, in a plastic disc, and were used for lead analysis by micro-PIXE. Very low concentrations of lead were found in the brain of controls. Lead levels in homogenates from cerebrum and cerebellum measured by atomic absorption spectrometry (AAS) were: low-dose 1.2-2.2 micrograms/g wet weight and high-dose 1.4-2.4 micrograms/g wet weight. The lead levels measured with the micro-PIXE method were in good agreement with the levels found with AAS. Lead was present in the cerebellar white matter in two to three times higher amounts than in the cortical grey (low-dose white matter 11-18 micrograms/g dry weight, grey matter 2.0-5.5 micrograms/g dry weight). This was true for both low and high dose exposed rats.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Body Weight - drug effects</subject><subject>Cerebellum - drug effects</subject><subject>Cerebellum - metabolism</subject><subject>Chemical and industrial products toxicology. Toxic occupational diseases</subject><subject>Dose-Response Relationship, Drug</subject><subject>Lead - pharmacokinetics</subject><subject>Medical sciences</subject><subject>Metals and various inorganic compounds</subject><subject>Organ Size - drug effects</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Spectrometry, X-Ray Emission</subject><subject>Toxicology</subject><issn>0001-6322</issn><issn>1432-0533</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9rFTEUhUNR6mvrpnshC3FRGL1JJpOJO-0PWyjYhYK7IZPc9EUzk2cyQ9v_3nm8R112dTmcjw8uh5BTBh8ZgPr09QqA61oofkBWrBa8AinEK7ICAFY1gvM35KiU30viqpaH5JBL3fCmXpHHi1CmHPp5CmmkydOIxtEw0mmN1GLGHmOch21TZvsnhvGeZjMV6lOM6WEbl0PN6Og63K-pSwV3DnzcpDJn_EwNHYLNqbq7-XW5kCY-lVBOyGtvYsG3-3tMfl5d_ji_rm6_f7s5_3JbWQFsqryTEloujG6NUUq3CmvWoKw9171x4ME0TDNppeGgJYKrHVrfA6LrBWvEMfmw825y-jtjmbohFLs8ZUZMc-mUFkq1wF4EmZRKN7A1nu3A5adSMvpuk8Ng8lPHoNvu0f3fY4Hf7a1zP6B7RvcDLP37fW-KNdFnM9pQnrFG80XTin-Nu5Iu</recordid><startdate>19890101</startdate><enddate>19890101</enddate><creator>LINDH, U</creator><creator>CONRADI, N. 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G ; SOURANDER, P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c301t-fd550823a98aa77987e416e54f29bad0f0a61915c5a2095e0d4decfb0eedb3163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Body Weight - drug effects</topic><topic>Cerebellum - drug effects</topic><topic>Cerebellum - metabolism</topic><topic>Chemical and industrial products toxicology. Toxic occupational diseases</topic><topic>Dose-Response Relationship, Drug</topic><topic>Lead - pharmacokinetics</topic><topic>Medical sciences</topic><topic>Metals and various inorganic compounds</topic><topic>Organ Size - drug effects</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Spectrometry, X-Ray Emission</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LINDH, U</creatorcontrib><creatorcontrib>CONRADI, N. G</creatorcontrib><creatorcontrib>SOURANDER, P</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>Acta neuropathologica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LINDH, U</au><au>CONRADI, N. G</au><au>SOURANDER, P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distribution of lead in the cerebellum of suckling rats following low and high dose lead exposure: a micro-PIXE analysis</atitle><jtitle>Acta neuropathologica</jtitle><addtitle>Acta Neuropathol</addtitle><date>1989-01-01</date><risdate>1989</risdate><volume>79</volume><issue>2</issue><spage>149</spage><epage>153</epage><pages>149-153</pages><issn>0001-6322</issn><eissn>1432-0533</eissn><coden>ANPTAL</coden><abstract>The distribution of lead in the cerebellum of suckling Sprague-Dawley rats was examined using a nuclear microprobe for elemental mapping of tissue sections (particle-induced X-ray emission, 3-microns beam of 2.5 MeV protons; micro-PIXE). The rats were injected intraperitoneally with a lead-containing vehicle or vehicle only from ages 1 to 14 days. The calculated doses were 7.8 (low-dose) and 15.6 (high-dose) micrograms lead/g body weight. The rats were killed at 20 days of age. The vascular system was rinsed quickly with 0.15 M ammonium acetate to obtain determinations of intra-parenchymal lead with minimal influence of lead bound to erythrocytes and plasma proteins. Brains were frozen in propane/propylene in liquid nitrogen. Cryostat sections, 15 microns thick, were air dried on formvar coats that covered a hole, 15 mm in diameter, in a plastic disc, and were used for lead analysis by micro-PIXE. Very low concentrations of lead were found in the brain of controls. Lead levels in homogenates from cerebrum and cerebellum measured by atomic absorption spectrometry (AAS) were: low-dose 1.2-2.2 micrograms/g wet weight and high-dose 1.4-2.4 micrograms/g wet weight. The lead levels measured with the micro-PIXE method were in good agreement with the levels found with AAS. Lead was present in the cerebellar white matter in two to three times higher amounts than in the cortical grey (low-dose white matter 11-18 micrograms/g dry weight, grey matter 2.0-5.5 micrograms/g dry weight). This was true for both low and high dose exposed rats.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>2596264</pmid><doi>10.1007/BF00294372</doi><tpages>5</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Body Weight - drug effects Cerebellum - drug effects Cerebellum - metabolism Chemical and industrial products toxicology. Toxic occupational diseases Dose-Response Relationship, Drug Lead - pharmacokinetics Medical sciences Metals and various inorganic compounds Organ Size - drug effects Rats Rats, Inbred Strains Spectrometry, X-Ray Emission Toxicology |
title | Distribution of lead in the cerebellum of suckling rats following low and high dose lead exposure: a micro-PIXE analysis |
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