Abstract.
Objective and design: Investigation of the role of a novel inflammatory mediator 31-amino acid endothelin-1 [ET-1(1-31)], a major ET derivative in granulocytes, in eosinophil recruitment after its subcutaneous administration to mice.¶Methods: Various ET-1 derivatives (100 pmol), with or without ET receptor antagonists (200 pmol), were administered subcutaneously to mice, and then the eosinophil migration into and chemokine levels in the injected loci were analyzed.¶Results: ET-1(1-31) and a 21-amino acid endothelin-1 (ET-1), but not big ET-1, induced eosinophil migration into the injected loci with a peak after administration for 12 h, and increased the levels of eotaxin and interleukin-5 with peaks at 6 and 24 h, respectively. These effects of ET-1(1-31) and ET-1 were significantly inhibited by an ETA receptor antagonist, BQ-123, but not by an ETB receptor antagonist, BQ-788.¶Conclusion: Novel bioactive ET-1(1-31) induces local eosinophil migration, and increases in eotaxin and interleukin-5 through an ETA or ETA-like receptor.
Similar content being viewed by others
Author information
Authors and Affiliations
Additional information
Received 18 October 2001; returned for revision 8 December 2001; accepted by M. Katori 24 December 2001
Rights and permissions
About this article
Cite this article
Sharmin, S., Shiota, M., Murata, E. et al. A novel bioactive 31-amino acid ET-1 peptide stimulates eosinophil recruitment and increases the levels of eotaxin and IL-5. Inflamm. res. 51, 195–200 (2002). https://doi.org/10.1007/PL00000292
Issue Date:
DOI: https://doi.org/10.1007/PL00000292