Inhibitory effect of nafamostat mesilate (FUT-175) on O2- production in rat polymorphonuclear leucocytes
Effect of nafamostat mesilate (FUT-175), a serine protease inhibitor, having anti-inflammatory effects was studied on superoxide (O2-) production in rat polymorphonuclear leucocytes (PMN) and compared with those of other serine protease inhibitors and typical anti-inflammatory agents. 1) O2- product...
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Veröffentlicht in: | Folia Pharmacologica Japonica 1986, Vol.87(5), pp.521-526 |
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description | Effect of nafamostat mesilate (FUT-175), a serine protease inhibitor, having anti-inflammatory effects was studied on superoxide (O2-) production in rat polymorphonuclear leucocytes (PMN) and compared with those of other serine protease inhibitors and typical anti-inflammatory agents. 1) O2- productions in rat PMN stimulated with concanavalin A (Con A) and cytochalasin B (Cyt B) were too weak to observe. With NADH, however, strong O2- production was induced by Con A and Cyt B. 2) FUT-175 at 10-6 and 10-5 Minhibited O2- production in rat PMN induced by Con A and Cyt B with NADH in a concentration-dependent manner. 3) The serine protease inhibitor L-tosylamido-2-phenylethyl-chloromethyl ketone (TPCK) and soybean trypsin inhibitor (SBTI) inhibited O2- production at 10-5 M and 10-4 M, respectively, while aprotinin, chymostatin and leupeptin did not. 4) Neither indomethacin nor dexamethasone, typical anti-inflammatory agents, inhibited O2- production. Mepacrine, a phospholipase A2 inhibitor, strongly inhibited it. 5) O2- production in PMN prepared from the rat administered FUT-175, 200 mg/kg, p.o., was significantly decreased in comparison with that of the control rat. 6) FUT-175 had no effect on O2- production by hypoxanthine-xanthine oxidase. These results showed FUT-175 had a strong inhibitory effect on O2- production in rat PMN which other typical anti-inflammatory agents did not have. |
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With NADH, however, strong O2- production was induced by Con A and Cyt B. 2) FUT-175 at 10-6 and 10-5 Minhibited O2- production in rat PMN induced by Con A and Cyt B with NADH in a concentration-dependent manner. 3) The serine protease inhibitor L-tosylamido-2-phenylethyl-chloromethyl ketone (TPCK) and soybean trypsin inhibitor (SBTI) inhibited O2- production at 10-5 M and 10-4 M, respectively, while aprotinin, chymostatin and leupeptin did not. 4) Neither indomethacin nor dexamethasone, typical anti-inflammatory agents, inhibited O2- production. Mepacrine, a phospholipase A2 inhibitor, strongly inhibited it. 5) O2- production in PMN prepared from the rat administered FUT-175, 200 mg/kg, p.o., was significantly decreased in comparison with that of the control rat. 6) FUT-175 had no effect on O2- production by hypoxanthine-xanthine oxidase. These results showed FUT-175 had a strong inhibitory effect on O2- production in rat PMN which other typical anti-inflammatory agents did not have.</description><identifier>ISSN: 0015-5691</identifier><identifier>EISSN: 1347-8397</identifier><identifier>DOI: 10.1254/fpj.87.521</identifier><identifier>PMID: 3015753</identifier><language>jpn</language><publisher>Japan: The Japanese Pharmacological Society</publisher><subject>Animals ; Anti-Inflammatory Agents - pharmacology ; Concanavalin A - antagonists & inhibitors ; Cytochalasin B - antagonists & inhibitors ; Guanidines - pharmacology ; Guinea Pigs ; Hypoxanthine ; Hypoxanthines - pharmacology ; In Vitro Techniques ; Male ; NAD - antagonists & inhibitors ; Neutrophils - metabolism ; Protease Inhibitors - pharmacology ; Rats ; Rats, Inbred Strains ; Superoxides - metabolism ; Xanthine Oxidase - pharmacology</subject><ispartof>Folia Pharmacologica Japonica, 1986, Vol.87(5), pp.521-526</ispartof><rights>The Japanese PharmacologicalSociety</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3501-18a7f301c945b7cdc361db06a6d8a726d2cffb2746151f7f2fc3b5fd77bb9f1a3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3015753$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ODA, Minoru</creatorcontrib><creatorcontrib>OGIHARA, Madoka</creatorcontrib><creatorcontrib>SATO, Takuo</creatorcontrib><creatorcontrib>KURUMI, Masateru</creatorcontrib><creatorcontrib>IWAKI, Masahiro</creatorcontrib><title>Inhibitory effect of nafamostat mesilate (FUT-175) on O2- production in rat polymorphonuclear leucocytes</title><title>Folia Pharmacologica Japonica</title><addtitle>Nihon Yakurigaku Zasshi</addtitle><description>Effect of nafamostat mesilate (FUT-175), a serine protease inhibitor, having anti-inflammatory effects was studied on superoxide (O2-) production in rat polymorphonuclear leucocytes (PMN) and compared with those of other serine protease inhibitors and typical anti-inflammatory agents. 1) O2- productions in rat PMN stimulated with concanavalin A (Con A) and cytochalasin B (Cyt B) were too weak to observe. With NADH, however, strong O2- production was induced by Con A and Cyt B. 2) FUT-175 at 10-6 and 10-5 Minhibited O2- production in rat PMN induced by Con A and Cyt B with NADH in a concentration-dependent manner. 3) The serine protease inhibitor L-tosylamido-2-phenylethyl-chloromethyl ketone (TPCK) and soybean trypsin inhibitor (SBTI) inhibited O2- production at 10-5 M and 10-4 M, respectively, while aprotinin, chymostatin and leupeptin did not. 4) Neither indomethacin nor dexamethasone, typical anti-inflammatory agents, inhibited O2- production. Mepacrine, a phospholipase A2 inhibitor, strongly inhibited it. 5) O2- production in PMN prepared from the rat administered FUT-175, 200 mg/kg, p.o., was significantly decreased in comparison with that of the control rat. 6) FUT-175 had no effect on O2- production by hypoxanthine-xanthine oxidase. These results showed FUT-175 had a strong inhibitory effect on O2- production in rat PMN which other typical anti-inflammatory agents did not have.</description><subject>Animals</subject><subject>Anti-Inflammatory Agents - pharmacology</subject><subject>Concanavalin A - antagonists & inhibitors</subject><subject>Cytochalasin B - antagonists & inhibitors</subject><subject>Guanidines - pharmacology</subject><subject>Guinea Pigs</subject><subject>Hypoxanthine</subject><subject>Hypoxanthines - pharmacology</subject><subject>In Vitro Techniques</subject><subject>Male</subject><subject>NAD - antagonists & inhibitors</subject><subject>Neutrophils - metabolism</subject><subject>Protease Inhibitors - pharmacology</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Superoxides - metabolism</subject><subject>Xanthine Oxidase - pharmacology</subject><issn>0015-5691</issn><issn>1347-8397</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kMFLwzAUh4Moc6gX70JOokJn0jTJepThVBjssp1DkiYuo21qkh723xvd2OU9Ht-PH48PgHuMZrik1asd9rM5n9ESX4ApJhUv5qTml2CKEKYFZTW-BncxOoUQ5SVnBE_AhGTGKZmC3Ve_c8olHw7QWGt0gt7CXlrZ-Zhkgp2JrpXJwKfldlNgTp-h7-G6LOAQfDPq5PLpehhydvDtofNh2Pl-1K2RAbZm1F4fkom34MrKNpq7074B2-X7ZvFZrNYfX4u3VaEJRbjAc8lt_k7XFVVcN5ow3CjEJGsyKVlTamtVySuGKbbcllYTRW3DuVK1xZLcgMdjb37vZzQxic5FbdpW9saPUXBWU4YYy8GXY1AHH2MwVgzBdTIcBEbiz6zIZsWci2w2hx9OraPqTHOOnjxmvjjyfZb2bc5chuSyib8qXFfVf91x5NYz1TsZhOnJL_Q-jGM</recordid><startdate>1986</startdate><enddate>1986</enddate><creator>ODA, Minoru</creator><creator>OGIHARA, Madoka</creator><creator>SATO, Takuo</creator><creator>KURUMI, Masateru</creator><creator>IWAKI, Masahiro</creator><general>The Japanese Pharmacological Society</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></search><sort><creationdate>1986</creationdate><title>Inhibitory effect of nafamostat mesilate (FUT-175) on O2- production in rat polymorphonuclear leucocytes</title><author>ODA, Minoru ; OGIHARA, Madoka ; SATO, Takuo ; KURUMI, Masateru ; IWAKI, Masahiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3501-18a7f301c945b7cdc361db06a6d8a726d2cffb2746151f7f2fc3b5fd77bb9f1a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>jpn</language><creationdate>1986</creationdate><topic>Animals</topic><topic>Anti-Inflammatory Agents - pharmacology</topic><topic>Concanavalin A - antagonists & inhibitors</topic><topic>Cytochalasin B - antagonists & inhibitors</topic><topic>Guanidines - pharmacology</topic><topic>Guinea Pigs</topic><topic>Hypoxanthine</topic><topic>Hypoxanthines - pharmacology</topic><topic>In Vitro Techniques</topic><topic>Male</topic><topic>NAD - antagonists & inhibitors</topic><topic>Neutrophils - metabolism</topic><topic>Protease Inhibitors - pharmacology</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Superoxides - metabolism</topic><topic>Xanthine Oxidase - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ODA, Minoru</creatorcontrib><creatorcontrib>OGIHARA, Madoka</creatorcontrib><creatorcontrib>SATO, Takuo</creatorcontrib><creatorcontrib>KURUMI, Masateru</creatorcontrib><creatorcontrib>IWAKI, Masahiro</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>Folia Pharmacologica Japonica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ODA, Minoru</au><au>OGIHARA, Madoka</au><au>SATO, Takuo</au><au>KURUMI, Masateru</au><au>IWAKI, Masahiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibitory effect of nafamostat mesilate (FUT-175) on O2- production in rat polymorphonuclear leucocytes</atitle><jtitle>Folia Pharmacologica Japonica</jtitle><addtitle>Nihon Yakurigaku Zasshi</addtitle><date>1986</date><risdate>1986</risdate><volume>87</volume><issue>5</issue><spage>521</spage><epage>526</epage><pages>521-526</pages><issn>0015-5691</issn><eissn>1347-8397</eissn><abstract>Effect of nafamostat mesilate (FUT-175), a serine protease inhibitor, having anti-inflammatory effects was studied on superoxide (O2-) production in rat polymorphonuclear leucocytes (PMN) and compared with those of other serine protease inhibitors and typical anti-inflammatory agents. 1) O2- productions in rat PMN stimulated with concanavalin A (Con A) and cytochalasin B (Cyt B) were too weak to observe. With NADH, however, strong O2- production was induced by Con A and Cyt B. 2) FUT-175 at 10-6 and 10-5 Minhibited O2- production in rat PMN induced by Con A and Cyt B with NADH in a concentration-dependent manner. 3) The serine protease inhibitor L-tosylamido-2-phenylethyl-chloromethyl ketone (TPCK) and soybean trypsin inhibitor (SBTI) inhibited O2- production at 10-5 M and 10-4 M, respectively, while aprotinin, chymostatin and leupeptin did not. 4) Neither indomethacin nor dexamethasone, typical anti-inflammatory agents, inhibited O2- production. Mepacrine, a phospholipase A2 inhibitor, strongly inhibited it. 5) O2- production in PMN prepared from the rat administered FUT-175, 200 mg/kg, p.o., was significantly decreased in comparison with that of the control rat. 6) FUT-175 had no effect on O2- production by hypoxanthine-xanthine oxidase. These results showed FUT-175 had a strong inhibitory effect on O2- production in rat PMN which other typical anti-inflammatory agents did not have.</abstract><cop>Japan</cop><pub>The Japanese Pharmacological Society</pub><pmid>3015753</pmid><doi>10.1254/fpj.87.521</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Anti-Inflammatory Agents - pharmacology Concanavalin A - antagonists & inhibitors Cytochalasin B - antagonists & inhibitors Guanidines - pharmacology Guinea Pigs Hypoxanthine Hypoxanthines - pharmacology In Vitro Techniques Male NAD - antagonists & inhibitors Neutrophils - metabolism Protease Inhibitors - pharmacology Rats Rats, Inbred Strains Superoxides - metabolism Xanthine Oxidase - pharmacology |
title | Inhibitory effect of nafamostat mesilate (FUT-175) on O2- production in rat polymorphonuclear leucocytes |
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