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Thermogenesis, low-protein diets, and decreased development of AFB1-induced preneoplastic foci in rat liver

Horio, F.; Youngman, L. D.; Bell, R. C.; Campbell, T. C.

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1991

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10.1080/01635589109514138

PMID: 1681520

Abstract:

The development of hepatocellular, putatively preneoplastic, gamma-glutamyl transpeptidase positive (GGT+) foci and tumors induced by aflatoxin B1 (AFB1) has been shown to be reduced in male F344 rats fed a diet containing 6% protein (as casein). This reduction occurs despite increased energy intake, when compared with animals fed a diet containing 22% protein. Among its many effects, low protein intake is known to increase the proportion of energy intake expended in the form of heat (thermogenesis); thus, this investigation examined the association between the development of GGT+ foci and alterations in indices of thermogenesis induced by feeding varying levels of dietary protein. Five days following the completion of AFB1 dosing, animals were assigned to groups fed 4%, 8%, 12%, 16%, or 22% dietary protein for 6 weeks. Foci development (% liver volume occupied) was markedly reduced in animals fed the low-protein diet (4%, 8%), yet calorie consumption per 100 g body wt was greater. A modest negative linear trend was observed in oxygen consumption with increasing levels of dietary protein intake. Urinary norepinephrine levels were elevated in the groups fed 4% and 8% protein; urinary dopamine and norepinephrine turnover rates in brown adipose tissue were highest in animals fed 4% protein. These results suggest that GGT+ foci development occurs when a "critical level" (approx 12%) of dietary protein intake is reached. Inhibition of foci development at lower levels of protein intake is associated with several indicators of increased thermogenesis.

Automatic Tags

Animals; Male; Organ Size; Liver; Body Weight; Rats; Eating; Oxygen Consumption; Dietary Proteins; Dopamine; Body Temperature Regulation; gamma-Glutamyltransferase; Rats, Inbred F344; Norepinephrine; Caseins; Precancerous Conditions; Liver Neoplasms, Experimental; Aflatoxin B1

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