Literature DB >> 7584670

A synthetic inhibitor of interleukin-1 beta converting enzyme prevents endotoxin-induced interleukin-1 beta production in vitro and in vivo.

D S Fletcher1, L Agarwal, K T Chapman, J Chin, L A Egger, G Limjuco, S Luell, D E MacIntyre, E P Peterson, N A Thornberry.   

Abstract

A potent, reversible, tetrapeptide inhibitor of interleukin-1 beta converting enzyme (ICE), L-709,049, has been shown to suppress the in vitro production of mature IL-1 beta. We now report that this inhibitor also effectively suppresses the production of mature IL-1 beta in a murine model of endotoxic shock. Intraperitoneal administration of L-709,049 reduced the elevations of IL-1 beta in the plasma and peritoneal fluid of mice treated with LPS in a dose-related manner (ED50 = 2 +/- 0.9 mg/kg). LPS-induced elevations in IL-1 alpha and IL-6 in these mice were unaffected, indicating that the inhibitor specifically affected IL-1 beta production. Immunoblot analysis of plasma and peritoneal fluid indicated that L-709,049 suppressed the formation of mature IL-1 beta production in vivo. When mouse blood was incubated in vitro with LPS, IL-1 beta was released into the plasma. This assay was used to determine ex vivo the activity of an ICE inhibitor in the blood following its administration to mice. Blood obtained 15 minutes after ip administration of 10 mg/kg of L-709,049 to mice produced 80% less IL-1 beta than control blood, and IL-1 beta production returned to control levels in blood obtained 30 minutes after injection of this inhibitor. In addition, the capacity of the blood plasma obtained from these animals to prevent the cleavage of a synthetic substrate by ICE disappeared within 1 h of ip administration of 50 mg/kg of inhibitor.

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Year:  1995        PMID: 7584670     DOI: 10.1089/jir.1995.15.243

Source DB:  PubMed          Journal:  J Interferon Cytokine Res        ISSN: 1079-9907            Impact factor:   2.607


  10 in total

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2.  Peptidomimetic fluoromethylketone rescues mice from lethal endotoxic shock.

Authors:  S R Grobmyer; R C Armstrong; S C Nicholson; C Gabay; W P Arend; S H Potter; M Melchior; L C Fritz; C F Nathan
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3.  Targeting caspase-1 by inhalation-therapy: effects of Ac-YVAD-CHO on IL-1 beta, IL-18 and downstream proinflammatory parameters as detected in rat endotoxaemia.

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4.  Caspase-1-inhibitor ac-YVAD-cmk reduces LPS-lethality in rats without affecting haematology or cytokine responses.

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9.  Complementary regulation of caspase-1 and IL-1β reveals additional mechanisms of dampened inflammation in bats.

Authors:  Geraldine Goh; Matae Ahn; Feng Zhu; Lim Beng Lee; Dahai Luo; Aaron T Irving; Lin-Fa Wang
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Authors:  N J McCarthy; M K Whyte; C S Gilbert; G I Evan
Journal:  J Cell Biol       Date:  1997-01-13       Impact factor: 10.539

  10 in total

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