M. Masuda et al., INHIBITORY EFFECT OF CENTRAL DOPAMINE ON BASAL PANCREATIC-SECRETION IN CONSCIOUS RATS, American journal of physiology: Gastrointestinal and liver physiology, 37(1), 1998, pp. 29-34
We examined the role and the peripheral mechanism of action of central
dopamine on basal pancreatic exocrine secretion in conscious rats. Ra
ts were fitted with bile and pancreatic catheters to collect bile and
pancreatic juice separately and also with a left lateral brain ventric
le and external jugular vein catheters. After 90-min basal collection,
the D-1- and D-2-receptor antagonists (Sch-23390 and eticlopride, res
pectively) and dopamine were administered into the lateral brain ventr
icle. Sch-23390 (30, 100, and 300 nmol/rat), but not eticlopride (300
nmol/rat), stimulated pancreatic fluid and protein secretion. Dopamine
(30, 100, and 300 nmol/rat) inhibited pancreatic secretion dose depen
dently. Pretreatment with Sch-23390 prevented the inhibitory effect of
dopamine. Intravenously injected Sch-23390 or dopamine had no effect
on pancreatic secretion. The inhibitory effect of dopamine was blocked
by bretylium, an inhibitor of norepinephrine release, and phentolamin
e, an cu-blocker, but not by vagotomy. The beta-antagonist propranolol
alone significantly inhibited basal pancreatic secretion, and dopamin
e did not modify the inhibitory effect of propranolol. The proton pump
inhibitor omeprazole partially but not completely reduced the inhibit
ion by dopamine. These results suggest that central dopamine inhibits
pancreatic exocrine secretion via D-1-like receptors and that the inhi
bitory effect is mediated via sympathetic nerves, especially alpha-adr
enoceptors.