Lucigenin-derived chemiluminescence in intact isolated mitochondria
There are many data both in favor and against the use of lucigenin as a probe for superoxide anion (SA) in mitochondria, cells, and simple enzymatic systems. In the present work high concentrations (50-400 micro M) of lucigenin were used for continuous recording of rapid and reversible changes in th...
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Veröffentlicht in: | Biochemistry (Moscow) 2002-11, Vol.67 (11), p.1262-1270 |
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creator | Kruglov, A G Yurkov, I S Teplova, V V Evtodienko, Yu V |
description | There are many data both in favor and against the use of lucigenin as a probe for superoxide anion (SA) in mitochondria, cells, and simple enzymatic systems. In the present work high concentrations (50-400 micro M) of lucigenin were used for continuous recording of rapid and reversible changes in the SA level in intact isolated mitochondria. The SA level in the presence of lucigenin rapidly and reversibly changed during the transition of the mitochondria from one functional state to another: under conditions of ATP synthesis from ADP and Pi, of Ca2+ accumulation, and of reverse electron transfer. Induction of a Ca2+,cyclosporin A-sensitive pore in mitochondria completely suppressed the lucigenin-derived chemiluminescence (LDC). The electron transfer in the Q-cycle of the respiratory chain complex III and high electric potential difference across the inner membrane of mitochondria were obligatory conditions for generation of a SA-dependent chemiluminescent signal. Based on our own and literature data, a scheme of LDC generation is suggested. The origin of superoxide anion detected in intact mitochondria with lucigenin is discussed. |
doi_str_mv | 10.1023/A:1021305522632 |
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In the present work high concentrations (50-400 micro M) of lucigenin were used for continuous recording of rapid and reversible changes in the SA level in intact isolated mitochondria. The SA level in the presence of lucigenin rapidly and reversibly changed during the transition of the mitochondria from one functional state to another: under conditions of ATP synthesis from ADP and Pi, of Ca2+ accumulation, and of reverse electron transfer. Induction of a Ca2+,cyclosporin A-sensitive pore in mitochondria completely suppressed the lucigenin-derived chemiluminescence (LDC). The electron transfer in the Q-cycle of the respiratory chain complex III and high electric potential difference across the inner membrane of mitochondria were obligatory conditions for generation of a SA-dependent chemiluminescent signal. Based on our own and literature data, a scheme of LDC generation is suggested. The origin of superoxide anion detected in intact mitochondria with lucigenin is discussed.</description><identifier>ISSN: 0006-2979</identifier><identifier>EISSN: 1608-3040</identifier><identifier>DOI: 10.1023/A:1021305522632</identifier><identifier>PMID: 12495424</identifier><language>eng</language><publisher>United States: Springer Nature B.V</publisher><subject>Acridines - chemistry ; Adenosine diphosphate ; Adenosine Diphosphate - metabolism ; Adenosine Diphosphate - pharmacology ; Adenosine Triphosphate - chemistry ; Adenosine Triphosphate - metabolism ; Animals ; Calcium - chemistry ; Calcium - metabolism ; Calcium - pharmacology ; Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone - pharmacology ; Chemiluminescence ; Electric potential ; Electron Transport ; Electron Transport Complex III - antagonists & inhibitors ; Electron Transport Complex III - metabolism ; Enzyme Inhibitors - pharmacology ; Intracellular Membranes - drug effects ; Intracellular Membranes - metabolism ; Intracellular Membranes - physiology ; Luminescent Measurements ; Magnesium - chemistry ; Magnesium - metabolism ; Membrane Potentials - drug effects ; Membrane Potentials - physiology ; Mitochondria ; Mitochondria, Liver - metabolism ; Oxidation ; Pyruvic Acid - metabolism ; Rats ; Rats, Wistar ; Succinic Acid - metabolism ; Superoxides - metabolism</subject><ispartof>Biochemistry (Moscow), 2002-11, Vol.67 (11), p.1262-1270</ispartof><rights>MAIK "Nauka/Interperiodica" 2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c312t-58798f36ef79b6bfe8ccd6ca50d04457af388918acd9f155bbd10e284d50d3363</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12495424$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kruglov, A G</creatorcontrib><creatorcontrib>Yurkov, I S</creatorcontrib><creatorcontrib>Teplova, V V</creatorcontrib><creatorcontrib>Evtodienko, Yu V</creatorcontrib><title>Lucigenin-derived chemiluminescence in intact isolated mitochondria</title><title>Biochemistry (Moscow)</title><addtitle>Biochemistry (Mosc)</addtitle><description>There are many data both in favor and against the use of lucigenin as a probe for superoxide anion (SA) in mitochondria, cells, and simple enzymatic systems. In the present work high concentrations (50-400 micro M) of lucigenin were used for continuous recording of rapid and reversible changes in the SA level in intact isolated mitochondria. The SA level in the presence of lucigenin rapidly and reversibly changed during the transition of the mitochondria from one functional state to another: under conditions of ATP synthesis from ADP and Pi, of Ca2+ accumulation, and of reverse electron transfer. Induction of a Ca2+,cyclosporin A-sensitive pore in mitochondria completely suppressed the lucigenin-derived chemiluminescence (LDC). The electron transfer in the Q-cycle of the respiratory chain complex III and high electric potential difference across the inner membrane of mitochondria were obligatory conditions for generation of a SA-dependent chemiluminescent signal. Based on our own and literature data, a scheme of LDC generation is suggested. The origin of superoxide anion detected in intact mitochondria with lucigenin is discussed.</description><subject>Acridines - chemistry</subject><subject>Adenosine diphosphate</subject><subject>Adenosine Diphosphate - metabolism</subject><subject>Adenosine Diphosphate - pharmacology</subject><subject>Adenosine Triphosphate - chemistry</subject><subject>Adenosine Triphosphate - metabolism</subject><subject>Animals</subject><subject>Calcium - chemistry</subject><subject>Calcium - metabolism</subject><subject>Calcium - pharmacology</subject><subject>Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone - pharmacology</subject><subject>Chemiluminescence</subject><subject>Electric potential</subject><subject>Electron Transport</subject><subject>Electron Transport Complex III - antagonists & inhibitors</subject><subject>Electron Transport Complex III - metabolism</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Intracellular Membranes - drug effects</subject><subject>Intracellular Membranes - metabolism</subject><subject>Intracellular Membranes - physiology</subject><subject>Luminescent Measurements</subject><subject>Magnesium - chemistry</subject><subject>Magnesium - metabolism</subject><subject>Membrane Potentials - drug effects</subject><subject>Membrane Potentials - physiology</subject><subject>Mitochondria</subject><subject>Mitochondria, Liver - metabolism</subject><subject>Oxidation</subject><subject>Pyruvic Acid - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Succinic Acid - metabolism</subject><subject>Superoxides - metabolism</subject><issn>0006-2979</issn><issn>1608-3040</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp90E1LAzEQBuAgiq3VszcpHvS0mmSS3cRbKX5BwYuel2wya1N2s3WzK_TfG2i9eBAGXgYehpkh5JLRO0Y53C8eUjCgUnKeAz8iU5ZTlQEV9JhMKaV5xnWhJ-Qsxk1qOdVwSiaMCy0FF1OyXI3Wf2LwIXPY-290c7vG1jdj6wNGi8Hi3IdUg7HD3MeuMUNCrR86u-6C6705Jye1aSJeHHJGPp4e35cv2ert-XW5WGUWGB8yqQqtasixLnSVVzUqa11ujaSOCiELU4NSmiljna6ZlFXlGEWuhEsCIIcZud3P3fbd14hxKFufNmwaE7AbY1lIoRQvFE_y5n-ZlNqPvP4DN93Yh3RFMlwCMFAJXR3QWLXoym3vW9Pvyt8vwg8ebnM3</recordid><startdate>20021101</startdate><enddate>20021101</enddate><creator>Kruglov, A G</creator><creator>Yurkov, I S</creator><creator>Teplova, V V</creator><creator>Evtodienko, Yu V</creator><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7QL</scope><scope>7TM</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>7QP</scope></search><sort><creationdate>20021101</creationdate><title>Lucigenin-derived chemiluminescence in intact isolated mitochondria</title><author>Kruglov, A G ; Yurkov, I S ; Teplova, V V ; Evtodienko, Yu V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c312t-58798f36ef79b6bfe8ccd6ca50d04457af388918acd9f155bbd10e284d50d3363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Acridines - chemistry</topic><topic>Adenosine diphosphate</topic><topic>Adenosine Diphosphate - metabolism</topic><topic>Adenosine Diphosphate - pharmacology</topic><topic>Adenosine Triphosphate - chemistry</topic><topic>Adenosine Triphosphate - metabolism</topic><topic>Animals</topic><topic>Calcium - chemistry</topic><topic>Calcium - metabolism</topic><topic>Calcium - pharmacology</topic><topic>Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone - pharmacology</topic><topic>Chemiluminescence</topic><topic>Electric potential</topic><topic>Electron Transport</topic><topic>Electron Transport Complex III - antagonists & inhibitors</topic><topic>Electron Transport Complex III - metabolism</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Intracellular Membranes - drug effects</topic><topic>Intracellular Membranes - metabolism</topic><topic>Intracellular Membranes - physiology</topic><topic>Luminescent Measurements</topic><topic>Magnesium - chemistry</topic><topic>Magnesium - metabolism</topic><topic>Membrane Potentials - drug effects</topic><topic>Membrane Potentials - physiology</topic><topic>Mitochondria</topic><topic>Mitochondria, Liver - metabolism</topic><topic>Oxidation</topic><topic>Pyruvic Acid - metabolism</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Succinic Acid - metabolism</topic><topic>Superoxides - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kruglov, A G</creatorcontrib><creatorcontrib>Yurkov, I S</creatorcontrib><creatorcontrib>Teplova, V V</creatorcontrib><creatorcontrib>Evtodienko, Yu V</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Science Journals</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Calcium & Calcified Tissue Abstracts</collection><jtitle>Biochemistry (Moscow)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kruglov, A G</au><au>Yurkov, I S</au><au>Teplova, V V</au><au>Evtodienko, Yu V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lucigenin-derived chemiluminescence in intact isolated mitochondria</atitle><jtitle>Biochemistry (Moscow)</jtitle><addtitle>Biochemistry (Mosc)</addtitle><date>2002-11-01</date><risdate>2002</risdate><volume>67</volume><issue>11</issue><spage>1262</spage><epage>1270</epage><pages>1262-1270</pages><issn>0006-2979</issn><eissn>1608-3040</eissn><abstract>There are many data both in favor and against the use of lucigenin as a probe for superoxide anion (SA) in mitochondria, cells, and simple enzymatic systems. In the present work high concentrations (50-400 micro M) of lucigenin were used for continuous recording of rapid and reversible changes in the SA level in intact isolated mitochondria. The SA level in the presence of lucigenin rapidly and reversibly changed during the transition of the mitochondria from one functional state to another: under conditions of ATP synthesis from ADP and Pi, of Ca2+ accumulation, and of reverse electron transfer. Induction of a Ca2+,cyclosporin A-sensitive pore in mitochondria completely suppressed the lucigenin-derived chemiluminescence (LDC). The electron transfer in the Q-cycle of the respiratory chain complex III and high electric potential difference across the inner membrane of mitochondria were obligatory conditions for generation of a SA-dependent chemiluminescent signal. Based on our own and literature data, a scheme of LDC generation is suggested. The origin of superoxide anion detected in intact mitochondria with lucigenin is discussed.</abstract><cop>United States</cop><pub>Springer Nature B.V</pub><pmid>12495424</pmid><doi>10.1023/A:1021305522632</doi><tpages>9</tpages></addata></record> |
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subjects | Acridines - chemistry Adenosine diphosphate Adenosine Diphosphate - metabolism Adenosine Diphosphate - pharmacology Adenosine Triphosphate - chemistry Adenosine Triphosphate - metabolism Animals Calcium - chemistry Calcium - metabolism Calcium - pharmacology Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone - pharmacology Chemiluminescence Electric potential Electron Transport Electron Transport Complex III - antagonists & inhibitors Electron Transport Complex III - metabolism Enzyme Inhibitors - pharmacology Intracellular Membranes - drug effects Intracellular Membranes - metabolism Intracellular Membranes - physiology Luminescent Measurements Magnesium - chemistry Magnesium - metabolism Membrane Potentials - drug effects Membrane Potentials - physiology Mitochondria Mitochondria, Liver - metabolism Oxidation Pyruvic Acid - metabolism Rats Rats, Wistar Succinic Acid - metabolism Superoxides - metabolism |
title | Lucigenin-derived chemiluminescence in intact isolated mitochondria |
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