Jd. Obourn et al., EVIDENCE THAT A8947 ENHANCES PANCREAS GROWTH VIA A TRYPSIN-INHIBITOR MECHANISM, Toxicology and applied pharmacology, 146(1), 1997, pp. 116-126
A8947 is a member of the sulfonyl urea class of compounds and is the a
ctive ingredient in a commercial broad leaf herbicide. This compound h
as been shown to produce pancreatic hypertrophy in rats, mice, and dog
s. The objectives of this study were to investigate the mechanism(s) f
or the A8947 induction of pancreatic acinar cell hypertrophy and proli
feration and to evaluate whether these pancreatic changes are reversib
le. A8947 was fed to male Crl:CD BR rats for up to 28 days (0, 300, 10
,000, 30,000 ppm) or 56 days (0, 30,000 ppm). Rats were terminated on
Test Days 7, 14, and 28 to assess the time course and dose response fo
r the A8947-induced pancreatic changes, while rats terminated on Test
Day 56 were used to assesss the reversibility of the pancreas effects
at 30,000 ppm A8947. A8947 produced significant increases in pancreati
c weight and acinar cell proliferation and diffuse acinar cell hypertr
ophy in 7 days at 10,000 and 30,000 ppm dose levels. By Day 14, absolu
te pancreas weights in the 10,000 and 30,000 ppm groups were maximally
increased and remained at these levels throughout the study. In contr
ast, acinar cell proliferation in the 30,000 ppm group was still eleva
ted at Test Day 14, but attenuated relative to the 7-day response, and
returned to control levels by Test Day 28. No effects were observed a
t 300 ppm after a 28-day exposure period, while complete reversibility
of A8947-induced pancreatic effects was demonstrated at 30,000 ppm fo
llowing a 1-month recovery period (Test Day 56). Cholecystokinin (CCK)
levels were increased by A8947 and closely followed the time course f
or pancreatic changes. MK-329, a specific CCKA receptor antagonist, co
mpletely ablated the ability of 30,000 ppm A8947 to increase pancreas
weight following 7 days of exposure. A8947 did not bind the CCKA recep
tor in a receptor competition assay, negating any potential agonist me
chanism. A8947 did, however, inhibit trypsin in vitro, suggesting a me
chanism of action similar to that of raw soy protein, in which trypsin
inhibition in vivo results in increased CCK levels followed by pancre
atic acinar cell hypertrophy and proliferation. (C) 1997 Academic Pres
s.