Article date: August 1999
By: S M Gardiner, J E March, P A Kemp, T Bennett, in Volume 127, Issue 7, pages 1611-1618
The functional involvement of the vasodilator peptides, adrenomedullin (ADM) and calcitonin gene‐related peptide (CGRP), in the haemodynamic sequelae of continuous infusion of lipopolysaccharide (LPS) was assessed in conscious, male, Long Evans rats, by the use of peptide antagonists.
It was demonstrated that ADM (22–52) at a dose of 500 nmol kg−1 h−1 caused significant inhibition of the effects of ADM (1 nmol kg−1), without affecting responses to CGRP (0.1 or 1 nmol kg−1).
Even when the regional vasodilator responses to LPS infusion were enhanced (by pre‐treatment with dexamethasone and the endothelin antagonist, SB 209670, or by pretreatment with SB 209670 and the AT1‐receptor antagonist, losartan), ADM (22–52) had no significant cardiovascular effects. In contrast, the CGRP1‐receptor antagonist, CGRP (8–37), caused small, but significant, inhibitions of the hypotensive and renal and mesenteric vasodilator effects of LPS, but only 6 h after onset of infusion in the presence of dexamethasone and SB 209670.
The results indicate that, in this model of endotoxaemia, the marked regional vasodilatations seen in the presence of dexamethasone and SB 209670 do not involve ADM, but do involve CGRP, albeit only to a small extent.
The functional involvement of the vasodilator peptides, adrenomedullin (ADM) and calcitonin gene‐related peptide (CGRP), in the haemodynamic sequelae of continuous infusion of lipopolysaccharide (LPS) was assessed in conscious, male, Long Evans rats, by the use of peptide antagonists.
It was demonstrated that ADM (22–52) at a dose of 500 nmol kg−1 h−1 caused significant inhibition of the effects of ADM (1 nmol kg−1), without affecting responses to CGRP (0.1 or 1 nmol kg−1).
Even when the regional vasodilator responses to LPS infusion were enhanced (by pre‐treatment with dexamethasone and the endothelin antagonist, SB 209670, or by pretreatment with SB 209670 and the AT1‐receptor antagonist, losartan), ADM (22–52) had no significant cardiovascular effects. In contrast, the CGRP1‐receptor antagonist, CGRP (8–37), caused small, but significant, inhibitions of the hypotensive and renal and mesenteric vasodilator effects of LPS, but only 6 h after onset of infusion in the presence of dexamethasone and SB 209670.
The results indicate that, in this model of endotoxaemia, the marked regional vasodilatations seen in the presence of dexamethasone and SB 209670 do not involve ADM, but do involve CGRP, albeit only to a small extent.
British Journal of Pharmacology (1999) 127, 1611–1618; doi:10.1038/sj.bjp.0702718
DOI: 10.1038/sj.bjp.0702718
View this article