Cholesterol for Synthesis of Myelin Is Made Locally, Not Imported into Brain

: We examined whether cholesterol needed for myelin formation is locally synthesized or whether it comes from the circulation. The experimental design was to inject [3H]water and to use incorporation of label into brain cholesterol as a measure of the rate of accumulation of newly synthesized choles...

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Veröffentlicht in:Journal of neurochemistry 1995-02, Vol.64 (2), p.895-901
Hauptverfasser: Jurevics, Helga, Morell, Pierre
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description : We examined whether cholesterol needed for myelin formation is locally synthesized or whether it comes from the circulation. The experimental design was to inject [3H]water and to use incorporation of label into brain cholesterol as a measure of the rate of accumulation of newly synthesized cholesterol in brain. The contribution of the circulation to this labeled cholesterol pool was minimized by repressing liver synthesis of cholesterol with a high cholesterol diet. The rate of accumulation of total cholesterol was calculated from the increasing amounts of sterol in brain regions at successive time intervals during development. Thus, accumulating cholesterol not explained as being newly synthesized (radioactive) could be assumed to have come from the circulation. Long‐Evans rats, ranging in age from birth to 35 days, were injected intraperitoneally with [3H]water (0.3–1.0 mCi/g of body weight) and killed 2 h later. The brain was dissected into brainstem, cerebellum, and cerebral hemispheres, and total lipids were extracted. Cholesterol and its precursors were quantified by HPLC. The radioactivity associated with the sterol fractions and the specific activity of body water determined from serum were used to calculate the absolute amount of newly synthesized sterol. The rates of cholesterol synthesis were compared with the rates of accumulation of total cholesterol in each brain region. The rate of accumulation of total sterol (cholesterol and desmosterol) closely followed that of newly synthesized total sterol in all brain regions from the second through the fifth postnatal weeks. Thus, all sterol accumulation in brain during the period of rapid myelination can be explained by local synthesis; neither diet nor production of cholesterol by other organs plays a direct role in supplying cholesterol for myelination in brain.
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The experimental design was to inject [3H]water and to use incorporation of label into brain cholesterol as a measure of the rate of accumulation of newly synthesized cholesterol in brain. The contribution of the circulation to this labeled cholesterol pool was minimized by repressing liver synthesis of cholesterol with a high cholesterol diet. The rate of accumulation of total cholesterol was calculated from the increasing amounts of sterol in brain regions at successive time intervals during development. Thus, accumulating cholesterol not explained as being newly synthesized (radioactive) could be assumed to have come from the circulation. Long‐Evans rats, ranging in age from birth to 35 days, were injected intraperitoneally with [3H]water (0.3–1.0 mCi/g of body weight) and killed 2 h later. The brain was dissected into brainstem, cerebellum, and cerebral hemispheres, and total lipids were extracted. Cholesterol and its precursors were quantified by HPLC. The radioactivity associated with the sterol fractions and the specific activity of body water determined from serum were used to calculate the absolute amount of newly synthesized sterol. The rates of cholesterol synthesis were compared with the rates of accumulation of total cholesterol in each brain region. The rate of accumulation of total sterol (cholesterol and desmosterol) closely followed that of newly synthesized total sterol in all brain regions from the second through the fifth postnatal weeks. Thus, all sterol accumulation in brain during the period of rapid myelination can be explained by local synthesis; neither diet nor production of cholesterol by other organs plays a direct role in supplying cholesterol for myelination in brain.</description><identifier>ISSN: 0022-3042</identifier><identifier>EISSN: 1471-4159</identifier><identifier>DOI: 10.1046/j.1471-4159.1995.64020895.x</identifier><identifier>PMID: 7830084</identifier><identifier>CODEN: JONRA9</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Aging - metabolism ; Animals ; Animals, Newborn ; Biochemistry and metabolism ; Biological and medical sciences ; Blood - metabolism ; Brain ; Brain - growth &amp; development ; Brain - physiology ; Central nervous system ; Cholesterol ; Cholesterol - physiology ; Desmosterol ; Desmosterol - metabolism ; Development ; Fundamental and applied biological sciences. 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The experimental design was to inject [3H]water and to use incorporation of label into brain cholesterol as a measure of the rate of accumulation of newly synthesized cholesterol in brain. The contribution of the circulation to this labeled cholesterol pool was minimized by repressing liver synthesis of cholesterol with a high cholesterol diet. The rate of accumulation of total cholesterol was calculated from the increasing amounts of sterol in brain regions at successive time intervals during development. Thus, accumulating cholesterol not explained as being newly synthesized (radioactive) could be assumed to have come from the circulation. Long‐Evans rats, ranging in age from birth to 35 days, were injected intraperitoneally with [3H]water (0.3–1.0 mCi/g of body weight) and killed 2 h later. The brain was dissected into brainstem, cerebellum, and cerebral hemispheres, and total lipids were extracted. Cholesterol and its precursors were quantified by HPLC. The radioactivity associated with the sterol fractions and the specific activity of body water determined from serum were used to calculate the absolute amount of newly synthesized sterol. The rates of cholesterol synthesis were compared with the rates of accumulation of total cholesterol in each brain region. The rate of accumulation of total sterol (cholesterol and desmosterol) closely followed that of newly synthesized total sterol in all brain regions from the second through the fifth postnatal weeks. Thus, all sterol accumulation in brain during the period of rapid myelination can be explained by local synthesis; neither diet nor production of cholesterol by other organs plays a direct role in supplying cholesterol for myelination in brain.</description><subject>Aging - metabolism</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Biochemistry and metabolism</subject><subject>Biological and medical sciences</subject><subject>Blood - metabolism</subject><subject>Brain</subject><subject>Brain - growth &amp; development</subject><subject>Brain - physiology</subject><subject>Central nervous system</subject><subject>Cholesterol</subject><subject>Cholesterol - physiology</subject><subject>Desmosterol</subject><subject>Desmosterol - metabolism</subject><subject>Development</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Myelin</subject><subject>Myelin Sheath - physiology</subject><subject>Nutrition</subject><subject>Rats</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkEtP4zAURi3ECArMT0CyBJoVKdePJLZYQXkVFWYxw9pyHVukcuNipxry7ydRS7eIla_1nfvQQeiMwJgALy4XY8JLknGSyzGRMh8XHCiIvvjYQ6Ndto9GAJRmDDg9REcpLQBIwQtygA5KwQAEH6HZ5C14m1obg8cuRPyna9o3m-qEg8PPnfV1g6cJP-vK4lkw2vvuAr-EFk-XqxBbW-G6aQO-ibpuTtAPp32yP7fvMXq9v_s7ecxmvx-mk-tZZjgr88yAnAsmDDVM6rksaS7c3BZOmko6xiW1llZ5ZSTjRnBCKw5SgACnpeZlSdgx-rWZu4rhfd1fr5Z1MtZ73diwTmpgGAH2JUiKEmTJ8x682oAmhpSidWoV66WOnSKgBulqoQaxahCrBunqU7r66LtPt2vW86Wtdr1by31-vs116g26qBtTpx3GeiuU0x673WD_am-771ygnl4mnz_2H6UpnP8</recordid><startdate>199502</startdate><enddate>199502</enddate><creator>Jurevics, Helga</creator><creator>Morell, Pierre</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><scope>7X8</scope></search><sort><creationdate>199502</creationdate><title>Cholesterol for Synthesis of Myelin Is Made Locally, Not Imported into Brain</title><author>Jurevics, Helga ; Morell, Pierre</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4375-c09b838c2c39ab97258fbe6f9cd9f3492ee2d5dc934c8412d4098080fa9a47713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Aging - metabolism</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Biochemistry and metabolism</topic><topic>Biological and medical sciences</topic><topic>Blood - metabolism</topic><topic>Brain</topic><topic>Brain - growth &amp; development</topic><topic>Brain - physiology</topic><topic>Central nervous system</topic><topic>Cholesterol</topic><topic>Cholesterol - physiology</topic><topic>Desmosterol</topic><topic>Desmosterol - metabolism</topic><topic>Development</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Myelin</topic><topic>Myelin Sheath - physiology</topic><topic>Nutrition</topic><topic>Rats</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jurevics, Helga</creatorcontrib><creatorcontrib>Morell, Pierre</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>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jurevics, Helga</au><au>Morell, Pierre</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cholesterol for Synthesis of Myelin Is Made Locally, Not Imported into Brain</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>1995-02</date><risdate>1995</risdate><volume>64</volume><issue>2</issue><spage>895</spage><epage>901</epage><pages>895-901</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>: We examined whether cholesterol needed for myelin formation is locally synthesized or whether it comes from the circulation. The experimental design was to inject [3H]water and to use incorporation of label into brain cholesterol as a measure of the rate of accumulation of newly synthesized cholesterol in brain. The contribution of the circulation to this labeled cholesterol pool was minimized by repressing liver synthesis of cholesterol with a high cholesterol diet. The rate of accumulation of total cholesterol was calculated from the increasing amounts of sterol in brain regions at successive time intervals during development. Thus, accumulating cholesterol not explained as being newly synthesized (radioactive) could be assumed to have come from the circulation. Long‐Evans rats, ranging in age from birth to 35 days, were injected intraperitoneally with [3H]water (0.3–1.0 mCi/g of body weight) and killed 2 h later. The brain was dissected into brainstem, cerebellum, and cerebral hemispheres, and total lipids were extracted. Cholesterol and its precursors were quantified by HPLC. The radioactivity associated with the sterol fractions and the specific activity of body water determined from serum were used to calculate the absolute amount of newly synthesized sterol. The rates of cholesterol synthesis were compared with the rates of accumulation of total cholesterol in each brain region. The rate of accumulation of total sterol (cholesterol and desmosterol) closely followed that of newly synthesized total sterol in all brain regions from the second through the fifth postnatal weeks. Thus, all sterol accumulation in brain during the period of rapid myelination can be explained by local synthesis; neither diet nor production of cholesterol by other organs plays a direct role in supplying cholesterol for myelination in brain.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>7830084</pmid><doi>10.1046/j.1471-4159.1995.64020895.x</doi><tpages>7</tpages></addata></record>
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subjects Aging - metabolism
Animals
Animals, Newborn
Biochemistry and metabolism
Biological and medical sciences
Blood - metabolism
Brain
Brain - growth & development
Brain - physiology
Central nervous system
Cholesterol
Cholesterol - physiology
Desmosterol
Desmosterol - metabolism
Development
Fundamental and applied biological sciences. Psychology
Myelin
Myelin Sheath - physiology
Nutrition
Rats
Vertebrates: nervous system and sense organs
title Cholesterol for Synthesis of Myelin Is Made Locally, Not Imported into Brain
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