A Nuclear Microscopic Study of Elemental Changes in the Rat Hippocampus After Kainate‐Induced Neuronal Injury

: The effect of intracerebroventricular kainate injection on the elemental composition of the hippocampus was studied in adult Wistar rats, at 1 day and 1, 2, 3, and 4 weeks postinjection, using a nuclear microscope. An increase in calcium concentration was observed on the injected side from 1 day p...

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Veröffentlicht in:Journal of neurochemistry 1999-04, Vol.72 (4), p.1574-1579
Hauptverfasser: Ong, Wei‐Yi, Ren, Min‐Qin, Makjanić, Jagoda, Lim, Tit‐Meng, Watt, Frank
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container_issue 4
container_start_page 1574
container_title Journal of neurochemistry
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creator Ong, Wei‐Yi
Ren, Min‐Qin
Makjanić, Jagoda
Lim, Tit‐Meng
Watt, Frank
description : The effect of intracerebroventricular kainate injection on the elemental composition of the hippocampus was studied in adult Wistar rats, at 1 day and 1, 2, 3, and 4 weeks postinjection, using a nuclear microscope. An increase in calcium concentration was observed on the injected side from 1 day postinjection. The increase peaked at 3 weeks postinjection, reaching a concentration of 18 times normal. Large numbers of glial cells but no neurons were observed in the lesioned CA fields at this time, suggesting that an increased calcium level was present in glial cells. This was confirmed by high‐resolution elemental maps of the lesioned areas, which showed very high intracellular calcium concentrations in almost all glial cells. It is possible that the high intracellular calcium level could activate calcium‐dependent enzymes, including calpain II and cytosolic phospholipase A2, shown to be expressed in reactive glial cells after kainate injections. In addition to calcium, an increase in iron content was also observed at the periphery of the glial scar at 4 weeks postinjection. Because free iron could catalyze the formation of free radicals, the late increase in iron content may be related to oxygen radical formation during neurodegeneration.
doi_str_mv 10.1046/j.1471-4159.1999.721574.x
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An increase in calcium concentration was observed on the injected side from 1 day postinjection. The increase peaked at 3 weeks postinjection, reaching a concentration of 18 times normal. Large numbers of glial cells but no neurons were observed in the lesioned CA fields at this time, suggesting that an increased calcium level was present in glial cells. This was confirmed by high‐resolution elemental maps of the lesioned areas, which showed very high intracellular calcium concentrations in almost all glial cells. It is possible that the high intracellular calcium level could activate calcium‐dependent enzymes, including calpain II and cytosolic phospholipase A2, shown to be expressed in reactive glial cells after kainate injections. In addition to calcium, an increase in iron content was also observed at the periphery of the glial scar at 4 weeks postinjection. 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Because free iron could catalyze the formation of free radicals, the late increase in iron content may be related to oxygen radical formation during neurodegeneration.</description><subject>Alzheimer’s disease</subject><subject>Animals</subject><subject>Astrocytes</subject><subject>Astrocytes - chemistry</subject><subject>Astrocytes - cytology</subject><subject>Astrocytes - ultrastructure</subject><subject>Biological and medical sciences</subject><subject>Calcium</subject><subject>Calcium - analysis</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Excitatory Amino Acid Agonists</subject><subject>Excitotoxicity</subject><subject>Hippocampus - chemistry</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - pathology</subject><subject>Injections, Intraventricular</subject><subject>Kainic Acid</subject><subject>Macrophages</subject><subject>Macrophages - chemistry</subject><subject>Macrophages - cytology</subject><subject>Macrophages - ultrastructure</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microscopy, Electron, Scanning Transmission</subject><subject>Nerve Degeneration - chemically induced</subject><subject>Nerve Degeneration - pathology</subject><subject>Neurology</subject><subject>Neurotoxins</subject><subject>Nissl Bodies - pathology</subject><subject>Nuclear microscope</subject><subject>Pyramidal Cells - chemistry</subject><subject>Pyramidal Cells - pathology</subject><subject>Pyramidal Cells - ultrastructure</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Spectrometry, X-Ray Emission</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEuO1DAQhi0EYpqBKyAjIXYJfuXhZas1wzQMjcRjbTl2hXErcYIdi-kdR-CMnIREaQFLVpZd3--q-hB6QUlOiShfH3MqKpoJWsicSinzitGiEvn9A7T5U3mINoQwlnEi2AV6EuOREFqKkj5GF5QQWdcl36Bhiw_JdKADfu9MGKIZRmfwpynZEx5afNVBD37SHd7daf8VInYeT3eAP-oJ37hxHIzuxxTxtp0g4HfaeT3Brx8_994mAxYfIIXBz_m9P6ZweooetbqL8Ox8XqIv11efdzfZ7Yc3-932NjOiZiKzmla2aTmvKwHUlLVoSwuEW1lzCwU3ZVvIxpha2rlesJo3fH5q2oZJLrTml-jV-u8Yhm8J4qR6Fw10nfYwpKhoxWRBqnoG5Qouy8cArRqD63U4KUrUYlsd1eJULU7VYlutttX9nH1-bpKaHuw_yVXvDLw8Azoa3bVBe-PiX66SlFE2Y9sV--46OP3_AOrtYUfWC_8Ndhqddw</recordid><startdate>199904</startdate><enddate>199904</enddate><creator>Ong, Wei‐Yi</creator><creator>Ren, Min‐Qin</creator><creator>Makjanić, Jagoda</creator><creator>Lim, Tit‐Meng</creator><creator>Watt, Frank</creator><general>Blackwell Science Ltd</general><general>Blackwell</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></search><sort><creationdate>199904</creationdate><title>A Nuclear Microscopic Study of Elemental Changes in the Rat Hippocampus After Kainate‐Induced Neuronal Injury</title><author>Ong, Wei‐Yi ; Ren, Min‐Qin ; Makjanić, Jagoda ; Lim, Tit‐Meng ; Watt, Frank</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4824-da17dbf33874e1c684f6de03d983de53c6f59bcc89d4e15283b36f5bfb2934aa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Alzheimer’s disease</topic><topic>Animals</topic><topic>Astrocytes</topic><topic>Astrocytes - chemistry</topic><topic>Astrocytes - cytology</topic><topic>Astrocytes - ultrastructure</topic><topic>Biological and medical sciences</topic><topic>Calcium</topic><topic>Calcium - analysis</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Excitatory Amino Acid Agonists</topic><topic>Excitotoxicity</topic><topic>Hippocampus - chemistry</topic><topic>Hippocampus - drug effects</topic><topic>Hippocampus - pathology</topic><topic>Injections, Intraventricular</topic><topic>Kainic Acid</topic><topic>Macrophages</topic><topic>Macrophages - chemistry</topic><topic>Macrophages - cytology</topic><topic>Macrophages - ultrastructure</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microscopy, Electron, Scanning Transmission</topic><topic>Nerve Degeneration - chemically induced</topic><topic>Nerve Degeneration - pathology</topic><topic>Neurology</topic><topic>Neurotoxins</topic><topic>Nissl Bodies - pathology</topic><topic>Nuclear microscope</topic><topic>Pyramidal Cells - chemistry</topic><topic>Pyramidal Cells - pathology</topic><topic>Pyramidal Cells - ultrastructure</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Spectrometry, X-Ray Emission</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ong, Wei‐Yi</creatorcontrib><creatorcontrib>Ren, Min‐Qin</creatorcontrib><creatorcontrib>Makjanić, Jagoda</creatorcontrib><creatorcontrib>Lim, Tit‐Meng</creatorcontrib><creatorcontrib>Watt, Frank</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><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ong, Wei‐Yi</au><au>Ren, Min‐Qin</au><au>Makjanić, Jagoda</au><au>Lim, Tit‐Meng</au><au>Watt, Frank</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Nuclear Microscopic Study of Elemental Changes in the Rat Hippocampus After Kainate‐Induced Neuronal Injury</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>1999-04</date><risdate>1999</risdate><volume>72</volume><issue>4</issue><spage>1574</spage><epage>1579</epage><pages>1574-1579</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>: The effect of intracerebroventricular kainate injection on the elemental composition of the hippocampus was studied in adult Wistar rats, at 1 day and 1, 2, 3, and 4 weeks postinjection, using a nuclear microscope. An increase in calcium concentration was observed on the injected side from 1 day postinjection. The increase peaked at 3 weeks postinjection, reaching a concentration of 18 times normal. Large numbers of glial cells but no neurons were observed in the lesioned CA fields at this time, suggesting that an increased calcium level was present in glial cells. This was confirmed by high‐resolution elemental maps of the lesioned areas, which showed very high intracellular calcium concentrations in almost all glial cells. It is possible that the high intracellular calcium level could activate calcium‐dependent enzymes, including calpain II and cytosolic phospholipase A2, shown to be expressed in reactive glial cells after kainate injections. In addition to calcium, an increase in iron content was also observed at the periphery of the glial scar at 4 weeks postinjection. Because free iron could catalyze the formation of free radicals, the late increase in iron content may be related to oxygen radical formation during neurodegeneration.</abstract><cop>Oxford UK</cop><pub>Blackwell Science Ltd</pub><pmid>10098863</pmid><doi>10.1046/j.1471-4159.1999.721574.x</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Alzheimer’s disease
Animals
Astrocytes
Astrocytes - chemistry
Astrocytes - cytology
Astrocytes - ultrastructure
Biological and medical sciences
Calcium
Calcium - analysis
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
Excitatory Amino Acid Agonists
Excitotoxicity
Hippocampus - chemistry
Hippocampus - drug effects
Hippocampus - pathology
Injections, Intraventricular
Kainic Acid
Macrophages
Macrophages - chemistry
Macrophages - cytology
Macrophages - ultrastructure
Male
Medical sciences
Microscopy, Electron, Scanning Transmission
Nerve Degeneration - chemically induced
Nerve Degeneration - pathology
Neurology
Neurotoxins
Nissl Bodies - pathology
Nuclear microscope
Pyramidal Cells - chemistry
Pyramidal Cells - pathology
Pyramidal Cells - ultrastructure
Rats
Rats, Wistar
Spectrometry, X-Ray Emission
title A Nuclear Microscopic Study of Elemental Changes in the Rat Hippocampus After Kainate‐Induced Neuronal Injury
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