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Pathological Changes in Pregnant Mice Infected with Coxsackievirus B3 and Given Dietary Casein Hydrolysate Supplement

Overview
Journal Br J Exp Pathol
Specialty Pathology
Date 1975 Aug 1
PMID 1174463
Citations 1
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Abstract

Coxsackievirus B3 infection in pregnant mice leads to a severe pancreatic exocrine insufficiency in the mothers and retarded foetal growth. As a consequence of the pancreatic damage, the animals are rendered incapable of digesting sufficient amounts of dietary proteins to allow maternal liver development to proceed as normal for the pregnant rodent. Faecal nitrogen was increased and the maternal livers were small for the weights of the animals and exhibited a lower than normal nitrogen content. Feeding of additional amino acids and simple peptides in the diet in the form of casein hydrolysate either from before or after virus injection appeared to compensate for the inability of these animals to digest dietary protein nitrogen and allowed maternal liver development and foetal growth to proceed at a rate not significantly different from normal. Although these results apply to infections with Coxsackievirus B3 in pregnancy, they may be relevant to other infections which adversely affect foetal growth by their pathological effects on maternal organs necessary for maintaining optimal foetal growth.

Citing Articles

Immunization of mice against Coxsackievirus B3 and prevention of foetal growth retardation.

Lansdown A, Brown J Br J Exp Pathol. 1976; 57(5):521-4.

PMID: 999788 PMC: 2041221.

References
1.
Coid C, Ramsden D . Retardation of foetal growth and plasma protein development in foetuses from mice injected with Coxsackie B3 virus. Nature. 1973; 241(5390):460-1. DOI: 10.1038/241460a0. View

2.
Coid C, Ramsden D, Healy M . Fetal mouse weights and albumin-alpha 1-fetoprotein ratios after maternal infection with Coxsackievirus B3. Med Microbiol Immunol. 1974; 159(4):285-8. DOI: 10.1007/BF02123738. View

3.
Lansdown A, Coid C . Pathological changes in pregnant mice infected with Coxsackie B3 virus as a possible cause of retarded foetal development. Br J Exp Pathol. 1974; 55(2):101-9. PMC: 2072521. View

4.
Lansdown A, Coid C, Ramsden D . Mitigation of virus-induced foetal growth retardation in mice by dietary casein hydrolysate. Nature. 1975; 254(5501):599-600. DOI: 10.1038/254599a0. View

5.
KIBRICK S, Benirschke K . Severe generalized disease (encephalohepatomyocarditis) occurring in the newborn period and due to infection with Coxsackie virus, group B; evidence of intrauterine infection with this agent. Pediatrics. 1958; 22(5):857-75. View