Superoxide and bone resorption

The reaction of superoxide with nitroblue tetrazolium produces an electron-dense diformazan precipitate which can be used to localize areas of superoxide production. Transmission electron microscopy was used to demonstrate that difomazan granules formed by the reaction of nitroblue tetrazolium with...

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Veröffentlicht in:Bone (New York, N.Y.) N.Y.), 1994-07, Vol.15 (4), p.431-436
Hauptverfasser: Key, L.L., Wolf, W.C., Gundberg, C.M., Ries, W.L.
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container_end_page 436
container_issue 4
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container_title Bone (New York, N.Y.)
container_volume 15
creator Key, L.L.
Wolf, W.C.
Gundberg, C.M.
Ries, W.L.
description The reaction of superoxide with nitroblue tetrazolium produces an electron-dense diformazan precipitate which can be used to localize areas of superoxide production. Transmission electron microscopy was used to demonstrate that difomazan granules formed by the reaction of nitroblue tetrazolium with excess superoxide are electron dense, whereas monoformazan granules generated by hydrogen peroxide were not. On the basis of these observations, superoxide formed along the osteoclast-bone interface was localized by demonstrating the electron-dense diformazan granules between the osteoclastic membrane and the bone surface. The formation of this reaction product was inhibited by a superoxide scavenger, the deferoxamine mesylate-manganese complex (the “green” complex), confirming the specificity of the reaction product. The scavenger also inhibited bone resorption. High concentrations of superoxide generated in vitro at a neutral pH degraded osteocalcin into numerous peptide fragments, demonstrating the ability of superoxide to break peptide bonds. These studies localize superoxide production to the ruffled border space and suggest that superoxide generated at the osteoclast-bone interface is involved in bone matrix degradation.
doi_str_mv 10.1016/8756-3282(94)90821-4
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These studies localize superoxide production to the ruffled border space and suggest that superoxide generated at the osteoclast-bone interface is involved in bone matrix degradation.</description><subject>Animals</subject><subject>Azo Compounds - metabolism</subject><subject>Biological and medical sciences</subject><subject>Bone resorption</subject><subject>Bone Resorption - etiology</subject><subject>Bone Resorption - physiopathology</subject><subject>Deferoxamine - analogs &amp; derivatives</subject><subject>Deferoxamine - pharmacology</subject><subject>Free Radical Scavengers - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Hydrogen Peroxide</subject><subject>Hydrogen-Ion Concentration</subject><subject>In Vitro Techniques</subject><subject>Manganese - pharmacology</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Microscopy, Electron</subject><subject>Nitroblue Tetrazolium - metabolism</subject><subject>Organometallic Compounds - pharmacology</subject><subject>Osteocalcin - metabolism</subject><subject>Osteoclast</subject><subject>Osteoclasts - metabolism</subject><subject>Parathyroid Hormone - pharmacology</subject><subject>Skeleton and joints</subject><subject>Superoxide</subject><subject>Superoxides - metabolism</subject><subject>Vertebrates: osteoarticular system, musculoskeletal system</subject><subject>X-Ray Diffraction</subject><issn>8756-3282</issn><issn>1873-2763</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtKw0AUhgdRaq2-gUoXIrqIzv2yEaR4g4ILdT1MJicwkiZxphF9exMbutTVOXC-_-fwIXRM8BXBRF5rJWTGqKYXhl8arCnJ-A6aEq1YRpVku2i6RfbRQUrvGGNmFJmgiTJECc2m6PSlayE2X6GAuauLed7UMI-QmtiuQ1Mfor3SVQmOxjlDb_d3r4vHbPn88LS4XWaec7nODBhfKtBCUpcTjPsl94XBQopCSMmo1znD1DFnALQD6gTvP3ECOyy5c2yGzje9bWw-OkhruwrJQ1W5GpouWSUV1ZiQf0EihcFKsR7kG9DHJqUIpW1jWLn4bQm2gz87yLGDHGu4_fVneR87Gfu7fAXFNjQK6-9n490l76oyutqHtMU4wZKSoeZmg0Ev7TNAtMkHqD0UIYJf26IJf__xA8y_iXg</recordid><startdate>19940701</startdate><enddate>19940701</enddate><creator>Key, L.L.</creator><creator>Wolf, W.C.</creator><creator>Gundberg, C.M.</creator><creator>Ries, W.L.</creator><general>Elsevier Inc</general><general>Elsevier Science</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>7QP</scope><scope>7X8</scope></search><sort><creationdate>19940701</creationdate><title>Superoxide and bone resorption</title><author>Key, L.L. ; Wolf, W.C. ; Gundberg, C.M. ; Ries, W.L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c446t-9e9cf7e8562ab100856bcd90565d56632c8b302a3a9ee8ae2a54397a50a064aa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Animals</topic><topic>Azo Compounds - metabolism</topic><topic>Biological and medical sciences</topic><topic>Bone resorption</topic><topic>Bone Resorption - etiology</topic><topic>Bone Resorption - physiopathology</topic><topic>Deferoxamine - analogs &amp; derivatives</topic><topic>Deferoxamine - pharmacology</topic><topic>Free Radical Scavengers - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Hydrogen Peroxide</topic><topic>Hydrogen-Ion Concentration</topic><topic>In Vitro Techniques</topic><topic>Manganese - pharmacology</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Microscopy, Electron</topic><topic>Nitroblue Tetrazolium - metabolism</topic><topic>Organometallic Compounds - pharmacology</topic><topic>Osteocalcin - metabolism</topic><topic>Osteoclast</topic><topic>Osteoclasts - metabolism</topic><topic>Parathyroid Hormone - pharmacology</topic><topic>Skeleton and joints</topic><topic>Superoxide</topic><topic>Superoxides - metabolism</topic><topic>Vertebrates: osteoarticular system, musculoskeletal system</topic><topic>X-Ray Diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Key, L.L.</creatorcontrib><creatorcontrib>Wolf, W.C.</creatorcontrib><creatorcontrib>Gundberg, C.M.</creatorcontrib><creatorcontrib>Ries, W.L.</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>Calcium &amp; Calcified Tissue Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Bone (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Key, L.L.</au><au>Wolf, W.C.</au><au>Gundberg, C.M.</au><au>Ries, W.L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Superoxide and bone resorption</atitle><jtitle>Bone (New York, N.Y.)</jtitle><addtitle>Bone</addtitle><date>1994-07-01</date><risdate>1994</risdate><volume>15</volume><issue>4</issue><spage>431</spage><epage>436</epage><pages>431-436</pages><issn>8756-3282</issn><eissn>1873-2763</eissn><abstract>The reaction of superoxide with nitroblue tetrazolium produces an electron-dense diformazan precipitate which can be used to localize areas of superoxide production. Transmission electron microscopy was used to demonstrate that difomazan granules formed by the reaction of nitroblue tetrazolium with excess superoxide are electron dense, whereas monoformazan granules generated by hydrogen peroxide were not. On the basis of these observations, superoxide formed along the osteoclast-bone interface was localized by demonstrating the electron-dense diformazan granules between the osteoclastic membrane and the bone surface. The formation of this reaction product was inhibited by a superoxide scavenger, the deferoxamine mesylate-manganese complex (the “green” complex), confirming the specificity of the reaction product. The scavenger also inhibited bone resorption. High concentrations of superoxide generated in vitro at a neutral pH degraded osteocalcin into numerous peptide fragments, demonstrating the ability of superoxide to break peptide bonds. 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subjects Animals
Azo Compounds - metabolism
Biological and medical sciences
Bone resorption
Bone Resorption - etiology
Bone Resorption - physiopathology
Deferoxamine - analogs & derivatives
Deferoxamine - pharmacology
Free Radical Scavengers - pharmacology
Fundamental and applied biological sciences. Psychology
Humans
Hydrogen Peroxide
Hydrogen-Ion Concentration
In Vitro Techniques
Manganese - pharmacology
Mice
Mice, Inbred C57BL
Microscopy, Electron
Nitroblue Tetrazolium - metabolism
Organometallic Compounds - pharmacology
Osteocalcin - metabolism
Osteoclast
Osteoclasts - metabolism
Parathyroid Hormone - pharmacology
Skeleton and joints
Superoxide
Superoxides - metabolism
Vertebrates: osteoarticular system, musculoskeletal system
X-Ray Diffraction
title Superoxide and bone resorption
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