M. Yoneda et al., CENTRAL NEUROPEPTIDE-Y ENHANCES BILE SECRETION THROUGH VAGAL AND MUSCARINIC BUT NOT NITRIC-OXIDE PATHWAYS IN RATS, Peptides, 16(4), 1995, pp. 727-732
Neuropeptide Y (NPY) acts in the central nervous system to regulate ga
strointestinal functions in rats and dogs. The effects of intracistern
al injection of NPY on bile secretion and biliary components were inve
stigated in urethane-anesthetized rats with bile duct cannula. Intraci
sternal NPY (0.02-0.12 nmol) dose-dependently increased bile secretion
by 9.2-19.5%. The secretory response occurred within the first 20-40
min and lasted for the 120-min observation period. Intravenous injecti
on of NPY (0.12 nmol) did not modify bile secretion under identical co
nditions. Biliary bile acid, phospholipid, and cholesterol secretion w
ere not modified by intracisternal injection of NPY (0.12 nmol), where
as bicarbonate was increased by 19.0 +/- 1.7% from 40 to 120 min after
NPY injection. Cervical cord transection at the C6 level, acute bilat
eral adrenalectomy (-120 min), or injection of NG-nitro-L-arginine met
hyl ester (10 mg/kg, IV, -15 min), an inhibitor of nitric oxide biosyn
thesis, did not alter intracisternal NPY (0.12 nmol)-induced stimulati
on of bile secretion. Atropine (2.0 mg/kg, IP, -30 min) and bilateral
cervical vagotomy (-120 min) completely abolished the stimulatory effe
ct of intracisternal NPY (0.12 nmol) on bile secretion. These findings
indicate that NPY acts in the brain to stimulate bicarbonate-dependen
t bile secretion through vagal and muscarinic pathways and suggest tha
t peptides in the central nervous system may be involved in the vagal
regulation of bile secretion.