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Ionophores Stimulate Prostaglandin and Thromboxane Biosynthesis
The role of calcium in triggering prostaglandin and thromboxane synthesis was studied in several systems with ionophores of different ion specificities. Divalent cationophore A23187 stimulates prostaglandin and thromboxane production by washed human platelets in a concentration-dependent manner (0.3...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 1977-10, Vol.74 (10), p.4251-4255 |
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creator | Knapp, Howard R. Oelz, Oswald Roberts, L. Jackson Sweetman, Brian J. Oates, John A. Reed, Peter W. |
description | The role of calcium in triggering prostaglandin and thromboxane synthesis was studied in several systems with ionophores of different ion specificities. Divalent cationophore A23187 stimulates prostaglandin and thromboxane production by washed human platelets in a concentration-dependent manner (0.3-9 μ M). A23187 also induces an antimycin A-insensitive burst in oxygen utilization which is partially blocked by 5 mM aspirin or 10 μ M indomethacin. Under our conditions, A23187 (up to 10 μ M does not appear to damage platelet membranes since it does not cause appreciable loss of lactate dehydrogenase or β -glucuronidase. Mono- and divalent cationophore X537A also stimulates platelet thromboxane B2production and oxygen utilization, but monovalent cationophores nigericin, monensin A, A204, and valinomycin have no effect. The synthesis of prostaglandins E2, D2, and F2αby rat renal medulla mince is stimulated by 1 and 5 μ M A23187 without changes in tissue ATP content, lactate output, or K+efflux. X537A, monensin A, and nigericin (all 5 μ M stimulate both prostaglandin output and K+efflux from renal medulla, while 5 μ M valinomycin or A204 has no effect on either. None of the ionophores stimulates renomedullary prostaglandin production if calcium is omitted from the incubation medium. A23187 also stimulates prostaglandin production by human lymphoma cells, rat stomach and trachea preparations, and guinea pig polymorphonuclear leukocytes. These observations suggest a major role for Ca2+in stimulating prostaglandin and thromboxane biosynthesis, and also indicate that prostaglandin and/or thromboxane release may partially mediate some of the previously described effects of ionophores on cells and tissues. |
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Jackson ; Sweetman, Brian J. ; Oates, John A. ; Reed, Peter W.</creator><creatorcontrib>Knapp, Howard R. ; Oelz, Oswald ; Roberts, L. Jackson ; Sweetman, Brian J. ; Oates, John A. ; Reed, Peter W.</creatorcontrib><description>The role of calcium in triggering prostaglandin and thromboxane synthesis was studied in several systems with ionophores of different ion specificities. Divalent cationophore A23187 stimulates prostaglandin and thromboxane production by washed human platelets in a concentration-dependent manner (0.3-9 μ M). A23187 also induces an antimycin A-insensitive burst in oxygen utilization which is partially blocked by 5 mM aspirin or 10 μ M indomethacin. Under our conditions, A23187 (up to 10 μ M does not appear to damage platelet membranes since it does not cause appreciable loss of lactate dehydrogenase or β -glucuronidase. Mono- and divalent cationophore X537A also stimulates platelet thromboxane B2production and oxygen utilization, but monovalent cationophores nigericin, monensin A, A204, and valinomycin have no effect. The synthesis of prostaglandins E2, D2, and F2αby rat renal medulla mince is stimulated by 1 and 5 μ M A23187 without changes in tissue ATP content, lactate output, or K+efflux. X537A, monensin A, and nigericin (all 5 μ M stimulate both prostaglandin output and K+efflux from renal medulla, while 5 μ M valinomycin or A204 has no effect on either. None of the ionophores stimulates renomedullary prostaglandin production if calcium is omitted from the incubation medium. A23187 also stimulates prostaglandin production by human lymphoma cells, rat stomach and trachea preparations, and guinea pig polymorphonuclear leukocytes. These observations suggest a major role for Ca2+in stimulating prostaglandin and thromboxane biosynthesis, and also indicate that prostaglandin and/or thromboxane release may partially mediate some of the previously described effects of ionophores on cells and tissues.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.74.10.4251</identifier><identifier>PMID: 270668</identifier><language>eng</language><publisher>United States: National Academy of Sciences of the United States of America</publisher><subject>Arachidonic Acids - metabolism ; Biological Sciences: Biochemistry ; Biosynthesis ; Blood Platelets - drug effects ; Blood Platelets - metabolism ; Calcium ; Ethanol ; Humans ; In Vitro Techniques ; Ionophores - pharmacology ; Kidney Medulla - drug effects ; Kidney Medulla - metabolism ; Lactates ; Male ; Monovalent cations ; Oxygen ; Platelets ; Potassium ; Prostaglandins ; Prostaglandins - biosynthesis ; Stimulation, Chemical ; Thromboxane B2 - biosynthesis ; Thromboxanes ; Thromboxanes - biosynthesis ; Time Factors</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1977-10, Vol.74 (10), p.4251-4255</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c460t-32e852fd5f702a6bcee7e31267cba12d49e360b4e0e776418aaae6dbc19c0963</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/74/10.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/67713$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/67713$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771,58216,58449</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/270668$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Knapp, Howard R.</creatorcontrib><creatorcontrib>Oelz, Oswald</creatorcontrib><creatorcontrib>Roberts, L. Jackson</creatorcontrib><creatorcontrib>Sweetman, Brian J.</creatorcontrib><creatorcontrib>Oates, John A.</creatorcontrib><creatorcontrib>Reed, Peter W.</creatorcontrib><title>Ionophores Stimulate Prostaglandin and Thromboxane Biosynthesis</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>The role of calcium in triggering prostaglandin and thromboxane synthesis was studied in several systems with ionophores of different ion specificities. Divalent cationophore A23187 stimulates prostaglandin and thromboxane production by washed human platelets in a concentration-dependent manner (0.3-9 μ M). A23187 also induces an antimycin A-insensitive burst in oxygen utilization which is partially blocked by 5 mM aspirin or 10 μ M indomethacin. Under our conditions, A23187 (up to 10 μ M does not appear to damage platelet membranes since it does not cause appreciable loss of lactate dehydrogenase or β -glucuronidase. Mono- and divalent cationophore X537A also stimulates platelet thromboxane B2production and oxygen utilization, but monovalent cationophores nigericin, monensin A, A204, and valinomycin have no effect. The synthesis of prostaglandins E2, D2, and F2αby rat renal medulla mince is stimulated by 1 and 5 μ M A23187 without changes in tissue ATP content, lactate output, or K+efflux. X537A, monensin A, and nigericin (all 5 μ M stimulate both prostaglandin output and K+efflux from renal medulla, while 5 μ M valinomycin or A204 has no effect on either. None of the ionophores stimulates renomedullary prostaglandin production if calcium is omitted from the incubation medium. A23187 also stimulates prostaglandin production by human lymphoma cells, rat stomach and trachea preparations, and guinea pig polymorphonuclear leukocytes. These observations suggest a major role for Ca2+in stimulating prostaglandin and thromboxane biosynthesis, and also indicate that prostaglandin and/or thromboxane release may partially mediate some of the previously described effects of ionophores on cells and tissues.</description><subject>Arachidonic Acids - metabolism</subject><subject>Biological Sciences: Biochemistry</subject><subject>Biosynthesis</subject><subject>Blood Platelets - drug effects</subject><subject>Blood Platelets - metabolism</subject><subject>Calcium</subject><subject>Ethanol</subject><subject>Humans</subject><subject>In Vitro Techniques</subject><subject>Ionophores - pharmacology</subject><subject>Kidney Medulla - drug effects</subject><subject>Kidney Medulla - metabolism</subject><subject>Lactates</subject><subject>Male</subject><subject>Monovalent cations</subject><subject>Oxygen</subject><subject>Platelets</subject><subject>Potassium</subject><subject>Prostaglandins</subject><subject>Prostaglandins - biosynthesis</subject><subject>Stimulation, Chemical</subject><subject>Thromboxane B2 - biosynthesis</subject><subject>Thromboxanes</subject><subject>Thromboxanes - biosynthesis</subject><subject>Time Factors</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1977</creationdate><recordtype>article</recordtype><recordid>eNp9kEtP4zAURq3RvEqHNRJCKCtYpVw_aieLEQLEoxISI033lpPc0KAk7tgOgn8_jtrpwIaNravvHD8-Qg4ozCgofrbujZ8pEYeZYHP6iUwo5DSVIofPZALAVJoJJr6TPe-fACCfZ_CNfGUKpMwm5Hxhe7teWYc--R2abmhNwOSXsz6Yx9b0VdMncU2WK2e7wr6YHpPLxvrXPqzQN_4H-VKb1uP-dp-S5c318uouvX-4XVxd3KelkBBSzjCbs7qa1wqYkUWJqJBTJlVZGMoqkSOXUAgEVEoKmhljUFZFSfMScsmn5Ofm2PVQdFiV2AdnWr12TWfcq7am0e-TvlnpR_usBac5VdE_2frO_hnQB901vsQ2_hDt4LXiSggBPIJnG7CMFXiH9e4OCnosXI-FayXGeSw8Gkdvn7bjNw3H-HQbj96_8L-v66FtA76ESB5_SEbgcAM8-WDdjpBKUc7_AqCIn3U</recordid><startdate>19771001</startdate><enddate>19771001</enddate><creator>Knapp, Howard R.</creator><creator>Oelz, Oswald</creator><creator>Roberts, L. Jackson</creator><creator>Sweetman, Brian J.</creator><creator>Oates, John A.</creator><creator>Reed, Peter W.</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><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>19771001</creationdate><title>Ionophores Stimulate Prostaglandin and Thromboxane Biosynthesis</title><author>Knapp, Howard R. ; Oelz, Oswald ; Roberts, L. Jackson ; Sweetman, Brian J. ; Oates, John A. ; Reed, Peter W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c460t-32e852fd5f702a6bcee7e31267cba12d49e360b4e0e776418aaae6dbc19c0963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1977</creationdate><topic>Arachidonic Acids - metabolism</topic><topic>Biological Sciences: Biochemistry</topic><topic>Biosynthesis</topic><topic>Blood Platelets - drug effects</topic><topic>Blood Platelets - metabolism</topic><topic>Calcium</topic><topic>Ethanol</topic><topic>Humans</topic><topic>In Vitro Techniques</topic><topic>Ionophores - pharmacology</topic><topic>Kidney Medulla - drug effects</topic><topic>Kidney Medulla - metabolism</topic><topic>Lactates</topic><topic>Male</topic><topic>Monovalent cations</topic><topic>Oxygen</topic><topic>Platelets</topic><topic>Potassium</topic><topic>Prostaglandins</topic><topic>Prostaglandins - biosynthesis</topic><topic>Stimulation, Chemical</topic><topic>Thromboxane B2 - biosynthesis</topic><topic>Thromboxanes</topic><topic>Thromboxanes - biosynthesis</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Knapp, Howard R.</creatorcontrib><creatorcontrib>Oelz, Oswald</creatorcontrib><creatorcontrib>Roberts, L. Jackson</creatorcontrib><creatorcontrib>Sweetman, Brian J.</creatorcontrib><creatorcontrib>Oates, John A.</creatorcontrib><creatorcontrib>Reed, Peter W.</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>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Knapp, Howard R.</au><au>Oelz, Oswald</au><au>Roberts, L. Jackson</au><au>Sweetman, Brian J.</au><au>Oates, John A.</au><au>Reed, Peter W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ionophores Stimulate Prostaglandin and Thromboxane Biosynthesis</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1977-10-01</date><risdate>1977</risdate><volume>74</volume><issue>10</issue><spage>4251</spage><epage>4255</epage><pages>4251-4255</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>The role of calcium in triggering prostaglandin and thromboxane synthesis was studied in several systems with ionophores of different ion specificities. Divalent cationophore A23187 stimulates prostaglandin and thromboxane production by washed human platelets in a concentration-dependent manner (0.3-9 μ M). A23187 also induces an antimycin A-insensitive burst in oxygen utilization which is partially blocked by 5 mM aspirin or 10 μ M indomethacin. Under our conditions, A23187 (up to 10 μ M does not appear to damage platelet membranes since it does not cause appreciable loss of lactate dehydrogenase or β -glucuronidase. Mono- and divalent cationophore X537A also stimulates platelet thromboxane B2production and oxygen utilization, but monovalent cationophores nigericin, monensin A, A204, and valinomycin have no effect. The synthesis of prostaglandins E2, D2, and F2αby rat renal medulla mince is stimulated by 1 and 5 μ M A23187 without changes in tissue ATP content, lactate output, or K+efflux. X537A, monensin A, and nigericin (all 5 μ M stimulate both prostaglandin output and K+efflux from renal medulla, while 5 μ M valinomycin or A204 has no effect on either. None of the ionophores stimulates renomedullary prostaglandin production if calcium is omitted from the incubation medium. A23187 also stimulates prostaglandin production by human lymphoma cells, rat stomach and trachea preparations, and guinea pig polymorphonuclear leukocytes. These observations suggest a major role for Ca2+in stimulating prostaglandin and thromboxane biosynthesis, and also indicate that prostaglandin and/or thromboxane release may partially mediate some of the previously described effects of ionophores on cells and tissues.</abstract><cop>United States</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>270668</pmid><doi>10.1073/pnas.74.10.4251</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Arachidonic Acids - metabolism Biological Sciences: Biochemistry Biosynthesis Blood Platelets - drug effects Blood Platelets - metabolism Calcium Ethanol Humans In Vitro Techniques Ionophores - pharmacology Kidney Medulla - drug effects Kidney Medulla - metabolism Lactates Male Monovalent cations Oxygen Platelets Potassium Prostaglandins Prostaglandins - biosynthesis Stimulation, Chemical Thromboxane B2 - biosynthesis Thromboxanes Thromboxanes - biosynthesis Time Factors |
title | Ionophores Stimulate Prostaglandin and Thromboxane Biosynthesis |
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