Evidence that kinin B2 receptor expression is upregulated by endothelial overexpression of B1 receptors

Eliete S. Rodrigues, Rafael F. Silva, Renan P. Martin, Suzana M. Oliveira, Clovis R. Nakaie, Regiane A. Sabatini, Vanessa F. Merino, João B. Pesquero, Michael Bader, Suma I. Shimuta

Research output: Contribution to journalArticlepeer-review

12 Scopus citations


Bradykinin (BK) and des-Arg9-bradykinin (DBK) of kallikrein-kinin system exert its effects mediated by the B2 (B 2R) and B1 (B1R) receptors, respectively. It was already shown that the deletion of kinin B1R or of B2R induces upregulation of the remaining receptor subtype [10,12,16,28,36]. However studies on overexpression of B1R or B2R in transgenic animals have supported the importance of the overexpressed receptor but the expression of another receptor subtype has not been determined [17,19,33]. Previous study described a marked vasodilatation and increased susceptibility to endotoxic shock which was associated with increased mortality in response to DBK in thoracic aorta from transgenic rat overexpressing the kinin B1R (TGR(Tie2B1)) exclusively in the endothelium. In another study, mice overexpressing B1R in multiple tissues were shown to present high susceptibility to inflammation and to lipopolysaccharide-induced endotoxic shock. Therefore the role of B2R was investigated in the thoracic aorta isolated from TGR(Tie2B 1) rats overexpressing the B1R exclusively in the vascular endothelium. Our findings provided evidence for highly increased expression level of the B2R in the transgenic rats. It was reported that under endotoxic shock, these rats exhibited exaggerated hypotension, bradycardia and mortality. It can be suggested that the high mortality during the pathogenesis of endotoxic shock provoked in the transgenic TGR(Tie2B1) rats could be due to the enhanced expression of B2R associated with the overexpression of the B1R.

Original languageEnglish (US)
Pages (from-to)1-7
Number of pages7
StatePublished - Apr 2013


  • ACE
  • AngiotensinII
  • Bradykinin
  • Kinin receptors
  • des-Arg-bradykinin

ASJC Scopus subject areas

  • Biochemistry
  • Physiology
  • Endocrinology
  • Cellular and Molecular Neuroscience


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