Nitric oxide synthase activity is inducible in rat, but not rabbit alveolar macrophages, with a concomitant reduction in arginase activity
Alveolar macrophages were obtained by broncho-alveolar lavage of isolated rat and rabbit lungs and cultured (2.5 x 10(6) cells/dish) for 18 h in the absence or presence of bacterial lipopolysaccharides (LPS) alone or in combination with cytokines. Thereafter, accumulation of 3H-citrulline (NO syntha...
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Veröffentlicht in: | Naunyn-Schmiedeberg's archives of pharmacology 1995-06, Vol.351 (6), p.651-659 |
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description | Alveolar macrophages were obtained by broncho-alveolar lavage of isolated rat and rabbit lungs and cultured (2.5 x 10(6) cells/dish) for 18 h in the absence or presence of bacterial lipopolysaccharides (LPS) alone or in combination with cytokines. Thereafter, accumulation of 3H-citrulline (NO synthase activity) and 3H-ornithine (arginase activity) were determined. During incubation of rat alveolar macrophages with 3H-arginine clear amounts of 3H-citrulline and 3H-ornithine (3.8 and 4.6% of the added 3H-arginine, respectively) were formed and most of these metabolites appeared in the incubation medium (ratios extra-/intracellular of 17 and 70 for 3H-citrulline and 3H-ornithine, respectively). When rat alveolar macrophages had been cultured with LPS the formation of 3H-citrulline was increased about 30-fold and this was accompanied by a reduction in 3H-ornithine formation of about 60%. The effects of LPS were largely attenuated by dexamethasone (10 mumol/l). Inhibition of NO synthase by NG-monomethyl-L-arginine (L-NMMA, 100 mumol/l) in LPS treated alveolar macrophages reduced the formation 3H-citrulline by more than 90% and restored the 3H-ornithine formation. After culturing in the presence of LPS the ratios extra/intracellular of 3H-citrulline and 3H-ornithine were markedly enhanced and this effect was not dexamethasone sensitive. |
doi_str_mv | 10.1007/BF00170166 |
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Thereafter, accumulation of 3H-citrulline (NO synthase activity) and 3H-ornithine (arginase activity) were determined. During incubation of rat alveolar macrophages with 3H-arginine clear amounts of 3H-citrulline and 3H-ornithine (3.8 and 4.6% of the added 3H-arginine, respectively) were formed and most of these metabolites appeared in the incubation medium (ratios extra-/intracellular of 17 and 70 for 3H-citrulline and 3H-ornithine, respectively). When rat alveolar macrophages had been cultured with LPS the formation of 3H-citrulline was increased about 30-fold and this was accompanied by a reduction in 3H-ornithine formation of about 60%. The effects of LPS were largely attenuated by dexamethasone (10 mumol/l). Inhibition of NO synthase by NG-monomethyl-L-arginine (L-NMMA, 100 mumol/l) in LPS treated alveolar macrophages reduced the formation 3H-citrulline by more than 90% and restored the 3H-ornithine formation. 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Thereafter, accumulation of 3H-citrulline (NO synthase activity) and 3H-ornithine (arginase activity) were determined. During incubation of rat alveolar macrophages with 3H-arginine clear amounts of 3H-citrulline and 3H-ornithine (3.8 and 4.6% of the added 3H-arginine, respectively) were formed and most of these metabolites appeared in the incubation medium (ratios extra-/intracellular of 17 and 70 for 3H-citrulline and 3H-ornithine, respectively). When rat alveolar macrophages had been cultured with LPS the formation of 3H-citrulline was increased about 30-fold and this was accompanied by a reduction in 3H-ornithine formation of about 60%. The effects of LPS were largely attenuated by dexamethasone (10 mumol/l). Inhibition of NO synthase by NG-monomethyl-L-arginine (L-NMMA, 100 mumol/l) in LPS treated alveolar macrophages reduced the formation 3H-citrulline by more than 90% and restored the 3H-ornithine formation. After culturing in the presence of LPS the ratios extra/intracellular of 3H-citrulline and 3H-ornithine were markedly enhanced and this effect was not dexamethasone sensitive.</description><subject>Amino Acid Oxidoreductases - biosynthesis</subject><subject>Amino Acid Oxidoreductases - drug effects</subject><subject>Animals</subject><subject>Arginase - metabolism</subject><subject>Arginine - analogs & derivatives</subject><subject>Arginine - pharmacology</subject><subject>Citrulline - metabolism</subject><subject>Cytokines - pharmacology</subject><subject>Dexamethasone - pharmacology</subject><subject>Enzyme Induction</subject><subject>Female</subject><subject>In Vitro Techniques</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Macrophages, Alveolar - drug effects</subject><subject>Macrophages, Alveolar - enzymology</subject><subject>Male</subject><subject>Nitric Oxide - antagonists & inhibitors</subject><subject>Nitric Oxide Synthase</subject><subject>Nitrites - metabolism</subject><subject>omega-N-Methylarginine</subject><subject>Ornithine - metabolism</subject><subject>Rabbits</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><issn>0028-1298</issn><issn>1432-1912</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkE9PwyAYh4nRzDm9eDfh5MGsCnS0cNTFqcmiFz03QOmGaWECne4r-Kll2aKe3j958nvzPgCcY3SNESpv7mYI4RLhojgAQzzJSYY5JodgiBBhGSacHYOTEN4RQgWmdAAGJZ3QkvEh-H420RsF3ZepNQwbG5ciaChUNGsTN9AEaGzdKyNbnTroRRxD2UdoXUyDlCZC0a61a4WHnVDerZZiocMYfpq4hAIqZ5XrTBQ28TolRePsNkn4hbH_b52Co0a0QZ_t6wi8ze5fp4_Z_OXhaXo7zxRhJGZKcYJkzQqqG1HUmGDFRcO0SgK2m1whzAivGWekRpgqKWROCc05UTKXMh-By13uyruPXodYdSYo3bbCateHqiwpLieMJfBqB6avQvC6qVbedMJvKoyqrfjqT3yCL_apvex0_YvuTec_Bz2AbQ</recordid><startdate>199506</startdate><enddate>199506</enddate><creator>Hey, C</creator><creator>Wessler, I</creator><creator>Racké, K</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></search><sort><creationdate>199506</creationdate><title>Nitric oxide synthase activity is inducible in rat, but not rabbit alveolar macrophages, with a concomitant reduction in arginase activity</title><author>Hey, C ; Wessler, I ; Racké, K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c282t-cc920bd865efa6d121c9af8ec701efa63c01829d8982d015cbab3525392cb3bb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Amino Acid Oxidoreductases - biosynthesis</topic><topic>Amino Acid Oxidoreductases - drug effects</topic><topic>Animals</topic><topic>Arginase - metabolism</topic><topic>Arginine - analogs & derivatives</topic><topic>Arginine - pharmacology</topic><topic>Citrulline - metabolism</topic><topic>Cytokines - pharmacology</topic><topic>Dexamethasone - pharmacology</topic><topic>Enzyme Induction</topic><topic>Female</topic><topic>In Vitro Techniques</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Macrophages, Alveolar - drug effects</topic><topic>Macrophages, Alveolar - enzymology</topic><topic>Male</topic><topic>Nitric Oxide - antagonists & inhibitors</topic><topic>Nitric Oxide Synthase</topic><topic>Nitrites - metabolism</topic><topic>omega-N-Methylarginine</topic><topic>Ornithine - metabolism</topic><topic>Rabbits</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hey, C</creatorcontrib><creatorcontrib>Wessler, I</creatorcontrib><creatorcontrib>Racké, K</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><jtitle>Naunyn-Schmiedeberg's archives of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hey, C</au><au>Wessler, I</au><au>Racké, K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nitric oxide synthase activity is inducible in rat, but not rabbit alveolar macrophages, with a concomitant reduction in arginase activity</atitle><jtitle>Naunyn-Schmiedeberg's archives of pharmacology</jtitle><addtitle>Naunyn Schmiedebergs Arch Pharmacol</addtitle><date>1995-06</date><risdate>1995</risdate><volume>351</volume><issue>6</issue><spage>651</spage><epage>659</epage><pages>651-659</pages><issn>0028-1298</issn><eissn>1432-1912</eissn><abstract>Alveolar macrophages were obtained by broncho-alveolar lavage of isolated rat and rabbit lungs and cultured (2.5 x 10(6) cells/dish) for 18 h in the absence or presence of bacterial lipopolysaccharides (LPS) alone or in combination with cytokines. Thereafter, accumulation of 3H-citrulline (NO synthase activity) and 3H-ornithine (arginase activity) were determined. During incubation of rat alveolar macrophages with 3H-arginine clear amounts of 3H-citrulline and 3H-ornithine (3.8 and 4.6% of the added 3H-arginine, respectively) were formed and most of these metabolites appeared in the incubation medium (ratios extra-/intracellular of 17 and 70 for 3H-citrulline and 3H-ornithine, respectively). When rat alveolar macrophages had been cultured with LPS the formation of 3H-citrulline was increased about 30-fold and this was accompanied by a reduction in 3H-ornithine formation of about 60%. The effects of LPS were largely attenuated by dexamethasone (10 mumol/l). Inhibition of NO synthase by NG-monomethyl-L-arginine (L-NMMA, 100 mumol/l) in LPS treated alveolar macrophages reduced the formation 3H-citrulline by more than 90% and restored the 3H-ornithine formation. After culturing in the presence of LPS the ratios extra/intracellular of 3H-citrulline and 3H-ornithine were markedly enhanced and this effect was not dexamethasone sensitive.</abstract><cop>Germany</cop><pmid>7545789</pmid><doi>10.1007/BF00170166</doi><tpages>9</tpages></addata></record> |
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subjects | Amino Acid Oxidoreductases - biosynthesis Amino Acid Oxidoreductases - drug effects Animals Arginase - metabolism Arginine - analogs & derivatives Arginine - pharmacology Citrulline - metabolism Cytokines - pharmacology Dexamethasone - pharmacology Enzyme Induction Female In Vitro Techniques Lipopolysaccharides - pharmacology Macrophages, Alveolar - drug effects Macrophages, Alveolar - enzymology Male Nitric Oxide - antagonists & inhibitors Nitric Oxide Synthase Nitrites - metabolism omega-N-Methylarginine Ornithine - metabolism Rabbits Rats Rats, Sprague-Dawley |
title | Nitric oxide synthase activity is inducible in rat, but not rabbit alveolar macrophages, with a concomitant reduction in arginase activity |
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