Changes of coagulation and fibrinolytic factors observed during heparin-urokinase-pulse combined therapy for nephritis resistant to conventional treatment in children
Coagulation and fibrinolytic factors in the blood were measured during heparinurokinase (UK)-pulse combined therapy in order to investigate the background for the availability of the therapy. Five patients with nephritis resistant to conventional treatment were treated with this combined therapy (he...
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Veröffentlicht in: | Nihon Jinzo Gakkai shi 1993/10/25, Vol.35(10), pp.1155-1161 |
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creator | KOITABASHI, YASUSHI IKOMA, MASAAKI SHIBAWAKA, TSUGUO YAMAGUCHI, YOSHIYA MIO, HITOSHI DOI, KEIJI MEGURO, TAKASHI YAMADA, KANEO |
description | Coagulation and fibrinolytic factors in the blood were measured during heparinurokinase (UK)-pulse combined therapy in order to investigate the background for the availability of the therapy. Five patients with nephritis resistant to conventional treatment were treated with this combined therapy (heparin:350-450 U/kg day, continuously i.v.during the therapy;UK:5000 IU/kg/2hrs, i.v., two times a day, for 3 days=l Kur; methyl-prednisolone 20mg/kg/2hrs, d.i.v., for 3 days=l Kur; 3 Kurs of UK and 3 Kurs of pulse were alternately administered).1) Blood levels of α2-plasmin inhibitor (α2PT) antigen were decreased and those of α2-plasmin inhibitor· plasmin complex (α2-PI. PmC) were elevated during 3 Kurs of UK administration.Accordingly, activation of the fibrinolytic system was confirmed during the combined therapy, suggesting that both α2-PI and α2-PI·PmC were relevant in monitoring the fibrinolytic state in blood.2) Both tissue-plasminogen activator (t-PA) and plasminogen activator inhibitor-1 (PAT-1) levels were sustained continuosly in the elevated levels in the blood during both UK administration and pulse therapy. This movement of t-PA and PAI-1 was independent of that of the other fibrinolytic factors, such as α2-PI, α2-PI·PmC and plasminogen.3) Inflammatory reactants such as fibrinogen, α2-PI, α2macroglobulin and α1-antitrypsin decreased more significantly during this heparinurokinase-pulse combined therapy than during our previous combined therapy consisting of only heparin and urokinase. Therefore, we conclude that the anti-inflammatory effect was reinforced by adding the pulse therapy and that the combined therapy had some effect on the release of t-PA from vascular endotherial cells |
doi_str_mv | 10.14842/jpnjnephrol1959.35.1155 |
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Five patients with nephritis resistant to conventional treatment were treated with this combined therapy (heparin:350-450 U/kg day, continuously i.v.during the therapy;UK:5000 IU/kg/2hrs, i.v., two times a day, for 3 days=l Kur; methyl-prednisolone 20mg/kg/2hrs, d.i.v., for 3 days=l Kur; 3 Kurs of UK and 3 Kurs of pulse were alternately administered).1) Blood levels of α2-plasmin inhibitor (α2PT) antigen were decreased and those of α2-plasmin inhibitor· plasmin complex (α2-PI. PmC) were elevated during 3 Kurs of UK administration.Accordingly, activation of the fibrinolytic system was confirmed during the combined therapy, suggesting that both α2-PI and α2-PI·PmC were relevant in monitoring the fibrinolytic state in blood.2) Both tissue-plasminogen activator (t-PA) and plasminogen activator inhibitor-1 (PAT-1) levels were sustained continuosly in the elevated levels in the blood during both UK administration and pulse therapy. This movement of t-PA and PAI-1 was independent of that of the other fibrinolytic factors, such as α2-PI, α2-PI·PmC and plasminogen.3) Inflammatory reactants such as fibrinogen, α2-PI, α2macroglobulin and α1-antitrypsin decreased more significantly during this heparinurokinase-pulse combined therapy than during our previous combined therapy consisting of only heparin and urokinase. Therefore, we conclude that the anti-inflammatory effect was reinforced by adding the pulse therapy and that the combined therapy had some effect on the release of t-PA from vascular endotherial cells</description><identifier>ISSN: 0385-2385</identifier><identifier>EISSN: 1884-0728</identifier><identifier>DOI: 10.14842/jpnjnephrol1959.35.1155</identifier><identifier>PMID: 7505345</identifier><language>jpn</language><publisher>Japan: Japanese Society of Nephrology</publisher><subject>Adolescent ; alpha-2-Antiplasmin - metabolism ; Antifibrinolytic Agents ; Blood Coagulation Factors - metabolism ; Child ; Child, Preschool ; Drug Administration Schedule ; Drug Therapy, Combination ; Female ; Fibrinolysin - metabolism ; Fibrinolysis ; Heparin - administration & dosage ; heparin-urokinase-pulse combined therapy, α2-plasmin inhibitor · plasmin complex (α2-PI · PmC), tissue-plasminogen activator (t-PA), coagulation factors, fibrinolytic factors ; Humans ; Male ; Nephritis - blood ; Nephritis - drug therapy ; Tissue Plasminogen Activator - metabolism ; Urokinase-Type Plasminogen Activator - administration & dosage</subject><ispartof>The Japanese Journal of Nephrology, 1993/10/25, Vol.35(10), pp.1155-1161</ispartof><rights>Japanese Society of Nephrology</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,1884,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7505345$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KOITABASHI, YASUSHI</creatorcontrib><creatorcontrib>IKOMA, MASAAKI</creatorcontrib><creatorcontrib>SHIBAWAKA, TSUGUO</creatorcontrib><creatorcontrib>YAMAGUCHI, YOSHIYA</creatorcontrib><creatorcontrib>MIO, HITOSHI</creatorcontrib><creatorcontrib>DOI, KEIJI</creatorcontrib><creatorcontrib>MEGURO, TAKASHI</creatorcontrib><creatorcontrib>YAMADA, KANEO</creatorcontrib><title>Changes of coagulation and fibrinolytic factors observed during heparin-urokinase-pulse combined therapy for nephritis resistant to conventional treatment in children</title><title>Nihon Jinzo Gakkai shi</title><addtitle>Jpn J Nephrol</addtitle><description>Coagulation and fibrinolytic factors in the blood were measured during heparinurokinase (UK)-pulse combined therapy in order to investigate the background for the availability of the therapy. Five patients with nephritis resistant to conventional treatment were treated with this combined therapy (heparin:350-450 U/kg day, continuously i.v.during the therapy;UK:5000 IU/kg/2hrs, i.v., two times a day, for 3 days=l Kur; methyl-prednisolone 20mg/kg/2hrs, d.i.v., for 3 days=l Kur; 3 Kurs of UK and 3 Kurs of pulse were alternately administered).1) Blood levels of α2-plasmin inhibitor (α2PT) antigen were decreased and those of α2-plasmin inhibitor· plasmin complex (α2-PI. PmC) were elevated during 3 Kurs of UK administration.Accordingly, activation of the fibrinolytic system was confirmed during the combined therapy, suggesting that both α2-PI and α2-PI·PmC were relevant in monitoring the fibrinolytic state in blood.2) Both tissue-plasminogen activator (t-PA) and plasminogen activator inhibitor-1 (PAT-1) levels were sustained continuosly in the elevated levels in the blood during both UK administration and pulse therapy. This movement of t-PA and PAI-1 was independent of that of the other fibrinolytic factors, such as α2-PI, α2-PI·PmC and plasminogen.3) Inflammatory reactants such as fibrinogen, α2-PI, α2macroglobulin and α1-antitrypsin decreased more significantly during this heparinurokinase-pulse combined therapy than during our previous combined therapy consisting of only heparin and urokinase. Therefore, we conclude that the anti-inflammatory effect was reinforced by adding the pulse therapy and that the combined therapy had some effect on the release of t-PA from vascular endotherial cells</description><subject>Adolescent</subject><subject>alpha-2-Antiplasmin - metabolism</subject><subject>Antifibrinolytic Agents</subject><subject>Blood Coagulation Factors - metabolism</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Drug Administration Schedule</subject><subject>Drug Therapy, Combination</subject><subject>Female</subject><subject>Fibrinolysin - metabolism</subject><subject>Fibrinolysis</subject><subject>Heparin - administration & dosage</subject><subject>heparin-urokinase-pulse combined therapy, α2-plasmin inhibitor · plasmin complex (α2-PI · PmC), tissue-plasminogen activator (t-PA), coagulation factors, fibrinolytic factors</subject><subject>Humans</subject><subject>Male</subject><subject>Nephritis - blood</subject><subject>Nephritis - drug therapy</subject><subject>Tissue Plasminogen Activator - metabolism</subject><subject>Urokinase-Type Plasminogen Activator - administration & dosage</subject><issn>0385-2385</issn><issn>1884-0728</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkc1u3CAUhVHVKh1N8wiVWHXnKRhj42U16p8UtZtkbfFzGTPF4AKONC_U5yxpRll0c-9F59MBzkUIU3Kgnejaj-c1nAOsc4qejnw8MH6glPNXaEeF6BoytOI12hEmeNPW8hbd5uwUoWIgjA_dDboZOOGs4zv05zjLcIKMo8U6ytPmZXExYBkMtk4lF6K_FKexlbrEVDmVIT2CwWar4gnPsMo6NFuKv1yQGZp18xmq2aJcqFyZIcn1gm1M-N-jXXEZJ8guFxkKLrGy4RHC073S45JAlqUesQtYz86bBOEdemNltb299j16-PL5_vitufv59fvx011zbruxNIPWPRn0KEk3tlwIBUZ240gG0yojKNC-CtaCIYYQ3jNCe2ss41apdhCkZXv04dl3TfH3BrlMi8savJcB4panoadd39cY9-j9FdzUAmZak1tkukzXYKv-41k_11-e4EWXqYbpYfpvhRPjEyXX-rTLF1DPMk0Q2F8vfqCV</recordid><startdate>199310</startdate><enddate>199310</enddate><creator>KOITABASHI, YASUSHI</creator><creator>IKOMA, MASAAKI</creator><creator>SHIBAWAKA, TSUGUO</creator><creator>YAMAGUCHI, YOSHIYA</creator><creator>MIO, HITOSHI</creator><creator>DOI, KEIJI</creator><creator>MEGURO, TAKASHI</creator><creator>YAMADA, KANEO</creator><general>Japanese Society of Nephrology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>199310</creationdate><title>Changes of coagulation and fibrinolytic factors observed during heparin-urokinase-pulse combined therapy for nephritis resistant to conventional treatment in children</title><author>KOITABASHI, YASUSHI ; IKOMA, MASAAKI ; SHIBAWAKA, TSUGUO ; YAMAGUCHI, YOSHIYA ; MIO, HITOSHI ; DOI, KEIJI ; MEGURO, TAKASHI ; YAMADA, KANEO</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-j249t-7cc607c9a0492588beda49907d2bd81e16049ffed0d00563016fdf35fbb278023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>jpn</language><creationdate>1993</creationdate><topic>Adolescent</topic><topic>alpha-2-Antiplasmin - metabolism</topic><topic>Antifibrinolytic Agents</topic><topic>Blood Coagulation Factors - metabolism</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Drug Administration Schedule</topic><topic>Drug Therapy, Combination</topic><topic>Female</topic><topic>Fibrinolysin - metabolism</topic><topic>Fibrinolysis</topic><topic>Heparin - administration & dosage</topic><topic>heparin-urokinase-pulse combined therapy, α2-plasmin inhibitor · plasmin complex (α2-PI · PmC), tissue-plasminogen activator (t-PA), coagulation factors, fibrinolytic factors</topic><topic>Humans</topic><topic>Male</topic><topic>Nephritis - blood</topic><topic>Nephritis - drug therapy</topic><topic>Tissue Plasminogen Activator - metabolism</topic><topic>Urokinase-Type Plasminogen Activator - administration & dosage</topic><toplevel>online_resources</toplevel><creatorcontrib>KOITABASHI, YASUSHI</creatorcontrib><creatorcontrib>IKOMA, MASAAKI</creatorcontrib><creatorcontrib>SHIBAWAKA, TSUGUO</creatorcontrib><creatorcontrib>YAMAGUCHI, YOSHIYA</creatorcontrib><creatorcontrib>MIO, HITOSHI</creatorcontrib><creatorcontrib>DOI, KEIJI</creatorcontrib><creatorcontrib>MEGURO, TAKASHI</creatorcontrib><creatorcontrib>YAMADA, KANEO</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Nihon Jinzo Gakkai shi</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KOITABASHI, YASUSHI</au><au>IKOMA, MASAAKI</au><au>SHIBAWAKA, TSUGUO</au><au>YAMAGUCHI, YOSHIYA</au><au>MIO, HITOSHI</au><au>DOI, KEIJI</au><au>MEGURO, TAKASHI</au><au>YAMADA, KANEO</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changes of coagulation and fibrinolytic factors observed during heparin-urokinase-pulse combined therapy for nephritis resistant to conventional treatment in children</atitle><jtitle>Nihon Jinzo Gakkai shi</jtitle><addtitle>Jpn J Nephrol</addtitle><date>1993-10</date><risdate>1993</risdate><volume>35</volume><issue>10</issue><spage>1155</spage><epage>1161</epage><pages>1155-1161</pages><issn>0385-2385</issn><eissn>1884-0728</eissn><abstract>Coagulation and fibrinolytic factors in the blood were measured during heparinurokinase (UK)-pulse combined therapy in order to investigate the background for the availability of the therapy. Five patients with nephritis resistant to conventional treatment were treated with this combined therapy (heparin:350-450 U/kg day, continuously i.v.during the therapy;UK:5000 IU/kg/2hrs, i.v., two times a day, for 3 days=l Kur; methyl-prednisolone 20mg/kg/2hrs, d.i.v., for 3 days=l Kur; 3 Kurs of UK and 3 Kurs of pulse were alternately administered).1) Blood levels of α2-plasmin inhibitor (α2PT) antigen were decreased and those of α2-plasmin inhibitor· plasmin complex (α2-PI. PmC) were elevated during 3 Kurs of UK administration.Accordingly, activation of the fibrinolytic system was confirmed during the combined therapy, suggesting that both α2-PI and α2-PI·PmC were relevant in monitoring the fibrinolytic state in blood.2) Both tissue-plasminogen activator (t-PA) and plasminogen activator inhibitor-1 (PAT-1) levels were sustained continuosly in the elevated levels in the blood during both UK administration and pulse therapy. This movement of t-PA and PAI-1 was independent of that of the other fibrinolytic factors, such as α2-PI, α2-PI·PmC and plasminogen.3) Inflammatory reactants such as fibrinogen, α2-PI, α2macroglobulin and α1-antitrypsin decreased more significantly during this heparinurokinase-pulse combined therapy than during our previous combined therapy consisting of only heparin and urokinase. Therefore, we conclude that the anti-inflammatory effect was reinforced by adding the pulse therapy and that the combined therapy had some effect on the release of t-PA from vascular endotherial cells</abstract><cop>Japan</cop><pub>Japanese Society of Nephrology</pub><pmid>7505345</pmid><doi>10.14842/jpnjnephrol1959.35.1155</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent alpha-2-Antiplasmin - metabolism Antifibrinolytic Agents Blood Coagulation Factors - metabolism Child Child, Preschool Drug Administration Schedule Drug Therapy, Combination Female Fibrinolysin - metabolism Fibrinolysis Heparin - administration & dosage heparin-urokinase-pulse combined therapy, α2-plasmin inhibitor · plasmin complex (α2-PI · PmC), tissue-plasminogen activator (t-PA), coagulation factors, fibrinolytic factors Humans Male Nephritis - blood Nephritis - drug therapy Tissue Plasminogen Activator - metabolism Urokinase-Type Plasminogen Activator - administration & dosage |
title | Changes of coagulation and fibrinolytic factors observed during heparin-urokinase-pulse combined therapy for nephritis resistant to conventional treatment in children |
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