C. Rodriguez-burford et al., Effect of reduced body weight gain on the evaluation of chemopreventive agents in the methylnitrosourea-induced mammary cancer model, CARCINOGENE, 20(1), 1999, pp. 71-76
These studies examined whether the small to moderate reductions in body wei
ght gain (less than or equal to 15%) affect mammary carcinogenesis. Beginni
ng 1 week prior to methylnitrosourea (MNU) administration (experiment 1), r
ats received diets supplemented with 4-hydroxyphenylretinamide (4-HPR) (782
mg/kg of diet) and retinyl acetate (328 mg/kg of diet) or underwent food r
estrictions. Rats were administered an i.v. dose of MNU (50 mg/kg body wt)
at 50 days of age. Although the final body weights were similarly depressed
by 4-HPR (8%) and by retinyl acetate (11%) from rats fed ad libitum, the k
inetics of inhibition were quite different. Whereas 4-HPR caused an acute d
ecrease in body weight at the time it was administered, the effect of retin
yl acetate was more chronic. At 110 days after the administration of MNU, t
he average number of mammary cancers per rat was 4.9 for rats fed ad libitu
m, 1.3 for rats fed 4-HPR, 3.1 when body weights were matched to 4-HPR-trea
ted rats, 1.9 for retinyl acetate and 3.2 when body weights were matched to
retinyl acetate, Experiment II was performed to determine the minimal degr
ee of acute body weight gain reduction that would alter MNU-induced mammary
carcinogenesis. Body weight gain depressions of 3, 6, 9, 12 and 15% were i
nitiated at 43 days of age by dietary restrictions and MNU was administered
at 50 days of age. At 120 days after MNU, the percentage decreases in mamm
ary cancer multiplicity in the various groups were 14, 15, 41, 44 and 55%,
respectively. These data demonstrate that moderate reductions (9-15%) in bo
dy weight gain, in particular when occurring during the initiation and earl
y promotion stages can greatly affect cancer multiplicity.