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Pituitary adenylate cyclase activating polypeptide is a potent vasodilator and oedema potentiator in rabbit skin in vivo

1992; Wiley; Volume: 106; Issue: 2 Linguagem: Inglês

10.1111/j.1476-5381.1992.tb14336.x

1476-5381

Jamie B. Warren, S Larkin, M.L. Coughlan, Radhika Kajekar, T.J. Williams,

Receptor Mechanisms and Signaling

The effects of pituitary adenylate cyclase activating polypeptide (PACAP) on microvascular blood flow and plasma protein leakage were investigated in rabbit skin in vivo . Intradermal injection of PACAP38, the 38 amino acid form of the peptide, caused a dose‐dependent increase in blood flow measured by a 133 Xe clearance technique. An equivalent increase in blood flow was induced by 10 −12 mol per site of PACAP38, 10 −12 mol per site of human α‐calcitonin gene‐related peptide (CGRP) and 10 −10 mol per site of vasoactive intestinal polypeptide (VIP). The vasodilator activity of PACAP38 was not significantly different from that of the 27 amino acid form of the peptide, PACAP27, when measured with a laser Doppler flow meter, causing a 104 ± 14% compared with 110 ± 18% increase above basal blood flow at 10 −12 mol per site respectively. At 10 −12 mol per site the effect of PACAP38 was longer lasting than that of CGRP. Blood flow remained significantly increased above control at 2 h with PACAP38 ( P < 0.05) whereas blood flow after intradermal CGRP had returned to control values by this time. PACAP38 injected alone had no significant effect on microvascular leakage of 125 I‐labelled albumin. However, PACAP38 significantly potentiated bradykinin‐induced oedema where it was approximately 100 fold more potent than VIP. Oedema potentiation induced by PACAP38 was not inhibited by indomethacin at a dose which did inhibit potentiation of bradykinin‐induced oedema by arachidonic acid. PACAP38 is at least as potent as other peptides which have been postulated to be involved in the inflammatory response when tested in rabbit skin in vivo . PACAP may contribute to both the hyperaemia and oedema components of inflammation.