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Angiotensin II receptor type 1 blockade improves hyporesponsiveness to vasopressors in septic shock.
Fernandes, Daniel; Pacheco, Letícia Kramer; Sordi, Regina; Scheschowitsch, Karin; Ramos, Gustavo Campos; Assreuy, Jamil.
Afiliação
  • Fernandes D; Department of Pharmacology, Universidade Federal de Santa Catarina, Florianópolis, Brazil.
  • Pacheco LK; Department of Pharmacology, Universidade Federal de Santa Catarina, Florianópolis, Brazil.
  • Sordi R; Department of Pharmacology, Universidade Federal de Santa Catarina, Florianópolis, Brazil.
  • Scheschowitsch K; Department of Pharmacology, Universidade Federal de Santa Catarina, Florianópolis, Brazil.
  • Ramos GC; Department of Pharmacology, Universidade Federal de Santa Catarina, Florianópolis, Brazil.
  • Assreuy J; Department of Pharmacology, Universidade Federal de Santa Catarina, Florianópolis, Brazil. Electronic address: jamil.assreuy@ufsc.br.
Eur J Pharmacol ; 897: 173953, 2021 Apr 15.
Article em En | MEDLINE | ID: mdl-33617825
Sepsis activates the renin-angiotensin system and the production of angiotensin II, which has a key role in the regulation of blood pressure through AT1 receptors. However, excessive activation of AT1 receptor is associated with deleterious effects. We investigated the consequences of a differential blockade of AT1 receptor caused by two doses of losartan (0.25 mg/kg or 15 mg/kg, s.c), a selective AT1 receptor antagonist on sepsis outcome. These doses reduced the effect of angiotensin II in normal rats by 30% and >90% 8 h after administration, respectively, but only the higher dose maintained its inhibitory effect (~70%) 24 h after injection. Sepsis was induced by cecal ligation and puncture (CLP). Losartan was injected 2 h after CLP and parameters were evaluated 6 and 24 h after CLP. Septic rats developed hypotension and hyporesponsiveness to vasoconstrictors, an intense inflammatory process and increase in plasma markers of organ dysfunction. The lower dose of losartan improved the vasoconstrictive response to phenylephrine and angiotensin II, reduced lung myeloperoxidase and prevented leukopenia 24 h after CLP, but it did not reduce NOS-2 expression, plasma IL-6 levels or organ injury parameters of septic rats. On the other hand, the higher dose of losartan worsened the response to vasoconstrictors, potentiated the hypotension and increased further levels of creatine, urea and lactate in septic rats. Therefore, an early and partial blockade of AT1 receptor with a low dose of losartan may counteract sepsis-induced refractoriness to vasoconstrictors thus providing an opportunity to improve the outcome of this condition.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sistema Renina-Angiotensina / Choque Séptico / Vasoconstrição / Vasoconstritores / Losartan / Bloqueadores do Receptor Tipo 1 de Angiotensina II / Pressão Arterial / Hipotensão Limite: Animals Idioma: En Revista: Eur J Pharmacol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Brasil País de publicação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sistema Renina-Angiotensina / Choque Séptico / Vasoconstrição / Vasoconstritores / Losartan / Bloqueadores do Receptor Tipo 1 de Angiotensina II / Pressão Arterial / Hipotensão Limite: Animals Idioma: En Revista: Eur J Pharmacol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Brasil País de publicação: Holanda