Parallel efflux of Ca2+ and Pi in energized rat liver mitochondria
Addition of Ruthenium Red to energized rat liver mitochondria that have previously accumulated Ca2+ and phosphate from the external medium induces a parallel efflux of both these ions. Mersalyl or dithioerythritol, which decrease Ruthenium Red-insensitive Ca2+ efflux, also decrease phosphate efflux...
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Veröffentlicht in: | Biochemical journal 1981-12, Vol.200 (3), p.481-486 |
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creator | Rugolo, M Siliprandi, D Siliprandi, N Toninello, A |
description | Addition of Ruthenium Red to energized rat liver mitochondria that have previously accumulated Ca2+ and phosphate from the external medium induces a parallel efflux of both these ions. Mersalyl or dithioerythritol, which decrease Ruthenium Red-insensitive Ca2+ efflux, also decrease phosphate efflux to the same extent. Conversely diazenedicarboxylic acid bis(NN-dimethylamide) (DDBA), which increases the Ruthenium Red-induced Ca2+ efflux concurrently increases phosphate release. Dithioerythritol and DDBA, reducing and oxidizing agents of thiol groups respectively, modify Ca2+ and Pi efflux without penetrating the mitochondrial inner membrane. Under all the adopted conditions the membrane potential is preserved. The release of resting respiration and the parallel efflux of Mg2+ and adenine nucleotides, events closely correlated to Ca2+ cycling, are equally prevented either by mersalyl, which inhibits phosphate transport, or dithioerythritol; DDBA has the opposite effect. These findings and the observation that suggest that Ca2+ and phosphate transport in energized liver mitochondria are closely related and dependent on the redox state of membrane-bound thiol groups. |
doi_str_mv | 10.1042/bj2000481 |
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Mersalyl or dithioerythritol, which decrease Ruthenium Red-insensitive Ca2+ efflux, also decrease phosphate efflux to the same extent. Conversely diazenedicarboxylic acid bis(NN-dimethylamide) (DDBA), which increases the Ruthenium Red-induced Ca2+ efflux concurrently increases phosphate release. Dithioerythritol and DDBA, reducing and oxidizing agents of thiol groups respectively, modify Ca2+ and Pi efflux without penetrating the mitochondrial inner membrane. Under all the adopted conditions the membrane potential is preserved. The release of resting respiration and the parallel efflux of Mg2+ and adenine nucleotides, events closely correlated to Ca2+ cycling, are equally prevented either by mersalyl, which inhibits phosphate transport, or dithioerythritol; DDBA has the opposite effect. These findings and the observation that suggest that Ca2+ and phosphate transport in energized liver mitochondria are closely related and dependent on the redox state of membrane-bound thiol groups.</description><identifier>ISSN: 0264-6021</identifier><identifier>EISSN: 1470-8728</identifier><identifier>DOI: 10.1042/bj2000481</identifier><identifier>PMID: 6177312</identifier><language>eng</language><publisher>England</publisher><subject>Adenine Nucleotides - metabolism ; Animals ; Biological Transport - drug effects ; Calcium - metabolism ; In Vitro Techniques ; Magnesium - metabolism ; Mitochondria, Liver - drug effects ; Mitochondria, Liver - metabolism ; Models, Biological ; Oxygen Consumption - drug effects ; Phosphates - metabolism ; Rats ; Ruthenium Red - pharmacology</subject><ispartof>Biochemical journal, 1981-12, Vol.200 (3), p.481-486</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-570608f63bddee74d15cb0f7809c296061deb1dddb0a373f4bccf4a3c77a91bb3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1163567/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1163567/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6177312$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rugolo, M</creatorcontrib><creatorcontrib>Siliprandi, D</creatorcontrib><creatorcontrib>Siliprandi, N</creatorcontrib><creatorcontrib>Toninello, A</creatorcontrib><title>Parallel efflux of Ca2+ and Pi in energized rat liver mitochondria</title><title>Biochemical journal</title><addtitle>Biochem J</addtitle><description>Addition of Ruthenium Red to energized rat liver mitochondria that have previously accumulated Ca2+ and phosphate from the external medium induces a parallel efflux of both these ions. Mersalyl or dithioerythritol, which decrease Ruthenium Red-insensitive Ca2+ efflux, also decrease phosphate efflux to the same extent. Conversely diazenedicarboxylic acid bis(NN-dimethylamide) (DDBA), which increases the Ruthenium Red-induced Ca2+ efflux concurrently increases phosphate release. Dithioerythritol and DDBA, reducing and oxidizing agents of thiol groups respectively, modify Ca2+ and Pi efflux without penetrating the mitochondrial inner membrane. Under all the adopted conditions the membrane potential is preserved. The release of resting respiration and the parallel efflux of Mg2+ and adenine nucleotides, events closely correlated to Ca2+ cycling, are equally prevented either by mersalyl, which inhibits phosphate transport, or dithioerythritol; DDBA has the opposite effect. These findings and the observation that suggest that Ca2+ and phosphate transport in energized liver mitochondria are closely related and dependent on the redox state of membrane-bound thiol groups.</description><subject>Adenine Nucleotides - metabolism</subject><subject>Animals</subject><subject>Biological Transport - drug effects</subject><subject>Calcium - metabolism</subject><subject>In Vitro Techniques</subject><subject>Magnesium - metabolism</subject><subject>Mitochondria, Liver - drug effects</subject><subject>Mitochondria, Liver - metabolism</subject><subject>Models, Biological</subject><subject>Oxygen Consumption - drug effects</subject><subject>Phosphates - metabolism</subject><subject>Rats</subject><subject>Ruthenium Red - pharmacology</subject><issn>0264-6021</issn><issn>1470-8728</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1981</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkEtLAzEUhYMotVYX_gAhK0Fk9GaSSWY2ghZfULALXYc825R5aGamqL_ekZaiq7u4H985HIROCVwRYOm1XqUAwHKyh8aECUhykeb7aAwpZwmHlByio7ZdARAGDEZoxIkQlKRjdDdXUZWlK7Hzvuw_cePxVKWXWNUWzwMONXa1i4vw7SyOqsNlWLuIq9A1ZtnUNgZ1jA68Klt3sr0T9PZw_zp9SmYvj8_T21liqIAuyQRwyD2n2lrnBLMkMxq8yKEwacGBE-s0sdZqUFRQz7QxnilqhFAF0ZpO0M3G-97rylnj6m6oLt9jqFT8ko0K8v-nDku5aNaSEE4zLgbB-VYQm4_etZ2sQmtcWaraNX0rBS0yQXkxgBcb0MSmbaPzuxAC8ndwuRt8YM_-ttqR24XpD6nNe7g</recordid><startdate>19811215</startdate><enddate>19811215</enddate><creator>Rugolo, M</creator><creator>Siliprandi, D</creator><creator>Siliprandi, N</creator><creator>Toninello, A</creator><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>7X8</scope><scope>5PM</scope></search><sort><creationdate>19811215</creationdate><title>Parallel efflux of Ca2+ and Pi in energized rat liver mitochondria</title><author>Rugolo, M ; Siliprandi, D ; Siliprandi, N ; Toninello, A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-570608f63bddee74d15cb0f7809c296061deb1dddb0a373f4bccf4a3c77a91bb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1981</creationdate><topic>Adenine Nucleotides - metabolism</topic><topic>Animals</topic><topic>Biological Transport - drug effects</topic><topic>Calcium - metabolism</topic><topic>In Vitro Techniques</topic><topic>Magnesium - metabolism</topic><topic>Mitochondria, Liver - drug effects</topic><topic>Mitochondria, Liver - metabolism</topic><topic>Models, Biological</topic><topic>Oxygen Consumption - drug effects</topic><topic>Phosphates - metabolism</topic><topic>Rats</topic><topic>Ruthenium Red - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rugolo, M</creatorcontrib><creatorcontrib>Siliprandi, D</creatorcontrib><creatorcontrib>Siliprandi, N</creatorcontrib><creatorcontrib>Toninello, A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biochemical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rugolo, M</au><au>Siliprandi, D</au><au>Siliprandi, N</au><au>Toninello, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Parallel efflux of Ca2+ and Pi in energized rat liver mitochondria</atitle><jtitle>Biochemical journal</jtitle><addtitle>Biochem J</addtitle><date>1981-12-15</date><risdate>1981</risdate><volume>200</volume><issue>3</issue><spage>481</spage><epage>486</epage><pages>481-486</pages><issn>0264-6021</issn><eissn>1470-8728</eissn><abstract>Addition of Ruthenium Red to energized rat liver mitochondria that have previously accumulated Ca2+ and phosphate from the external medium induces a parallel efflux of both these ions. Mersalyl or dithioerythritol, which decrease Ruthenium Red-insensitive Ca2+ efflux, also decrease phosphate efflux to the same extent. Conversely diazenedicarboxylic acid bis(NN-dimethylamide) (DDBA), which increases the Ruthenium Red-induced Ca2+ efflux concurrently increases phosphate release. Dithioerythritol and DDBA, reducing and oxidizing agents of thiol groups respectively, modify Ca2+ and Pi efflux without penetrating the mitochondrial inner membrane. Under all the adopted conditions the membrane potential is preserved. The release of resting respiration and the parallel efflux of Mg2+ and adenine nucleotides, events closely correlated to Ca2+ cycling, are equally prevented either by mersalyl, which inhibits phosphate transport, or dithioerythritol; DDBA has the opposite effect. These findings and the observation that suggest that Ca2+ and phosphate transport in energized liver mitochondria are closely related and dependent on the redox state of membrane-bound thiol groups.</abstract><cop>England</cop><pmid>6177312</pmid><doi>10.1042/bj2000481</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenine Nucleotides - metabolism Animals Biological Transport - drug effects Calcium - metabolism In Vitro Techniques Magnesium - metabolism Mitochondria, Liver - drug effects Mitochondria, Liver - metabolism Models, Biological Oxygen Consumption - drug effects Phosphates - metabolism Rats Ruthenium Red - pharmacology |
title | Parallel efflux of Ca2+ and Pi in energized rat liver mitochondria |
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