PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 14662737-21 2004 These results suggest that VIP and PACAP relax the pig ureter through smooth muscle receptors, probably of the VPAC(2) subtype, linked to a cAMP-PKA pathway. Cyclic AMP 140-144 vasoactive intestinal peptide Sus scrofa 27-30 16847435-9 2006 CONCLUSIONS AND IMPLICATIONS: PACAP 38 and VIP relax the pig urinary bladder neck through muscle VPAC(2) receptors linked to the cAMP-PKA pathway and involve activation of voltage-gated K(+) channels. Cyclic AMP 129-133 vasoactive intestinal peptide Sus scrofa 43-46 11212317-1 1999 A C-terminally elongated form of peptide histidine isoleucine amide (PHI) was isolated from porcine intestine based on its effect on cAMP production in IMR-32 cells. Cyclic AMP 133-137 vasoactive intestinal peptide Sus scrofa 69-72 1284568-11 1992 Vasoactive intestinal polypeptide (VIP) and isoprenaline, known to induce cell relaxation through an increase in intracellular cAMP level, inhibited CCK-induced cell contraction at concentrations ranging from 1 pM to 1 microM but failed to inhibit cell contraction induced by galanin. Cyclic AMP 127-131 vasoactive intestinal peptide Sus scrofa 0-33 1284568-11 1992 Vasoactive intestinal polypeptide (VIP) and isoprenaline, known to induce cell relaxation through an increase in intracellular cAMP level, inhibited CCK-induced cell contraction at concentrations ranging from 1 pM to 1 microM but failed to inhibit cell contraction induced by galanin. Cyclic AMP 127-131 vasoactive intestinal peptide Sus scrofa 35-38 11755723-2 2002 Additionally, the aim of this research was to examine the involvement of cyclic nucleotides (cAMP and cGMP) in transduction of signals induced by GnRH, OT and VIP in porcine pituitary cells. Cyclic AMP 93-97 vasoactive intestinal peptide Sus scrofa 159-162 11755723-14 2002 VIP stimulated cAMP release from pituitary cells derived from OVX, OVX+EB I and OVX+EB II animals. Cyclic AMP 15-19 vasoactive intestinal peptide Sus scrofa 0-3 11755723-16 2002 In conclusion, our results suggest that GnRH, OT and VIP can modulate beta-endorphin release from porcine pituitary cells and imply the involvement of cAMP and cGMP in transduction of signals induced by studied peptides in the cells. Cyclic AMP 151-155 vasoactive intestinal peptide Sus scrofa 53-56