Sc. Langley et al., THE ACUTE-PHASE RESPONSE OF ADULT-RATS IS ALTERED BY IN-UTERO EXPOSURE TO MATERNAL LOW-PROTEIN DIETS, The Journal of nutrition, 124(9), 1994, pp. 1588-1596
The immune system has been previously demonstrated to be under the inf
luence of maternal nutrition in pregnancy. Assessment was made of the
effects of low protein diets (12, 9 and 6 g casein/100 g diet) fed bef
ore conception and during pregnancy on the immune system of the result
ing offspring in early adulthood. Control animals were fed a diet cont
aining 18 g casein/100 g. At the end of pregnancy all dams were fed a
nonpurified diet containing 18.3 g protein/100 g. Male pups were weane
d onto this diet, which they consumed until the age of 7 wk. Rats expo
sed to 18 g casein/100 g diet in utero mounted a typical acute phase r
esponse following E. coil endotoxin challenge at age 7 wk. Food intake
was 75% lower, hepatic zinc concentrations 25% greater, and serum alb
umin 15% lower than in saline-injected controls. Pulmonary glutathione
levels were 35% greater in endotoxin-treated rats than in saline-trea
ted controls. In rats exposed to low protein diets in utero the trend
was for the acute phase response to be blunted. This was most noticeab
le with respect to the anorectic response, hepatic zinc uptake and pul
monary glutathione uptake. In rats not challenged with endotoxin, mate
rnal diet had pronounced effects on tissue zinc status at the age of 7
wk. Liver zinc concentrations were 21% and 16% lower in the groups ex
posed to 9 and 6 g casein/100 g diets relative to the control group ex
posed to 18 g casein/100 g diet. Glutathione status was altered in all
groups exposed to low dietary protein in utero. Glutathione reductase
and glutathione peroxidase activities were inversely proportional to
maternal protein intake. Glutamyl transpeptidase activities were signi
ficantly lower in groups exposed to 12 and 6 g casein/100 g diets rela
tive to controls. Nutritional deficit in pregnancy has effects upon gl
utathione status and significantly blunts the acute phase response to
endotoxin challenge.