The hepatic clearance of recombinant tissue-type plasminogen activator decreases after an inflammatory stimulus

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dc.contributor.authorNagaoka, Márcia Regina [UNIFESP]
dc.contributor.authorKouyoumdjian, Maria [UNIFESP]
dc.contributor.authorBorges, Durval Rosa [UNIFESP]
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.date.accessioned2015-06-14T13:24:59Z
dc.date.available2015-06-14T13:24:59Z
dc.date.issued2000-01-01
dc.description.abstractWe have shown that tissue-type plasminogen activator (tPA) and plasma kallikrein share a common pathway for liver clearance and that the hepatic clearance rate of plasma kallikrein increases during the acute-phase (AP) response. We now report the clearance of tPA from the circulation and by the isolated, exsanguinated and in situ perfused rat liver during the AP response (48-h ex-turpentine treatment). For the sake of comparison, the hepatic clearance of a tissue kallikrein and thrombin was also studied. We verified that, in vivo, the clearance of 125I-tPA from the circulation of turpentine-treated rats (2.2 ± 0.2 ml/min, N = 7) decreases significantly (P = 0.016) when compared to normal rats (3.2 ± 0.3 ml/min, N = 6). The AP response does not modify the tissue distribution of administered 125I-tPA and the liver accounts for most of the 125I-tPA (>80%) cleared from the circulation. The clearance rate of tPA by the isolated and perfused liver of turpentine-treated rats (15.5 ± 1.3 µg/min, N = 4) was slower (P = 0.003) than the clearance rate by the liver of normal rats (22.5 ± 0.7 µg/min, N = 10). After the inflammatory stimulus and additional Kupffer cell ablation (GdCl3 treatment), tPA was cleared by the perfused liver at 16.2 ± 2.4 µg/min (N = 5), suggesting that Kupffer cells have a minor influence on the hepatic tPA clearance during the AP response. In contrast, hepatic clearance rates of thrombin and pancreatic kallikrein were not altered during the AP response. These results contribute to explaining why the thrombolytic efficacy of tPA does not correlate with the dose administered.en
dc.description.affiliationUniversidade Federal de São Paulo (UNIFESP)
dc.description.affiliationUnifespUNIFESP
dc.description.sourceSciELO
dc.format.extent119-125
dc.identifierhttp://dx.doi.org/10.1590/S0100-879X2000000100016
dc.identifier.citationBrazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 33, n. 1, p. 119-125, 2000.
dc.identifier.doi10.1590/S0100-879X2000000100016
dc.identifier.fileS0100-879X2000000100016.pdf
dc.identifier.issn0100-879X
dc.identifier.scieloS0100-879X2000000100016
dc.identifier.urihttp://repositorio.unifesp.br/handle/11600/892
dc.identifier.wosWOS:000085031800016
dc.language.isoeng
dc.publisherAssociação Brasileira de Divulgação Científica
dc.relation.ispartofBrazilian Journal of Medical and Biological Research
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectliver clearanceen
dc.subjectinflammationen
dc.subjectkallikreinen
dc.subjectthrombinen
dc.subjecttissue-type plasminogen activatoren
dc.titleThe hepatic clearance of recombinant tissue-type plasminogen activator decreases after an inflammatory stimulusen
dc.typeinfo:eu-repo/semantics/article
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