This study investigates the interaction between histamine and the aden
ylate cyclase systems involved in the secretion of amylase from the gu
inea-pig pancreatic lobules. Histamine increased amylase release, reac
hing a maximum response at 10(-5) M. Similarly, vasoactive intestinal
peptide (VIP) evoked significant increase in amylase release, though n
ot in a dose-dependent fashion. When the pancreatic lobules were incub
ated with histamine in combination with VIP, forskolin or 3-isobutyl-1
-methylxanthine (IBMX), amylase secretion was increased as compared to
histamine alone. The stimulatory effect of VIP was also increased by
the presence of forskolin or IBMX. These findings suggest that in guin
ea-pig pancreatic lobules, VIP, forskolin and IBMX, agents involved in
the cyclic adenosine monophosphate (cAMP) pathway, potentiate histami
ne stimulated amylase release.