Decreased liver triglyceride content in adult rats exposed to protein restriction during gestation and lactation: Role of hepatic triglyceride utilization

Summary We have previously demonstrated that protein restriction throughout gestation and lactation reduces liver triglyceride content in adult rat offspring. However, the mechanisms mediating the decrease in liver triglyceride content are not understood. The aim of the current study was to use a ne...

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Published inClinical and experimental pharmacology & physiology Vol. 42; no. 4; pp. 380 - 388
Main Authors Qasem, Rani J, Li, Jing, Tang, Hee Man, Browne, Veron, Mendez-Garcia, Claudia, Yablonski, Elizabeth, Pontiggia, Laura, D'Mello, Anil P
Format Journal Article
LanguageEnglish
Published Australia Blackwell Publishing Ltd 01.04.2015
Wiley Subscription Services, Inc
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Summary:Summary We have previously demonstrated that protein restriction throughout gestation and lactation reduces liver triglyceride content in adult rat offspring. However, the mechanisms mediating the decrease in liver triglyceride content are not understood. The aim of the current study was to use a new group of pregnant animals and their offspring and determine the contribution of increased triglyceride utilization via the hepatic fatty‐acid oxidation and triglyceride secretory pathways to the reduction in liver triglyceride content. Pregnant Sprague–Dawley rats received either a control or a low protein diet throughout pregnancy and lactation. Pups were weaned onto laboratory chow on day 28 and killed on day 65. Liver triglyceride content was reduced in male, but not female, low‐protein offspring, both in the fed and fasted states. The reduction was accompanied by a trend towards higher liver carnitine palmitoyltransferase‐1a activity, suggesting increased fatty‐acid transport into the mitochondrial matrix. However, medium‐chain acyl coenzyme A dehydrogenase activity within the mitochondrial matrix, expression of nuclear peroxisome proliferator activated receptor‐α, and plasma levels of β‐hydroxybutyrate were similar between low protein and control offspring, indicating a lack of change in fatty‐acid oxidation. Hepatic triglyceride secretion, assessed by blocking peripheral triglyceride utilization and measuring serum triglyceride accumulation rate, and the activity of microsomal transfer protein, were similar between low protein and control offspring. Because enhanced triglyceride utilization is not a significant contributor, the decrease in liver triglyceride content in male low‐protein offspring is likely due to alterations in liver fatty‐acid transport or triglyceride biosynthesis.
Bibliography:istex:29F34B4E2E36AC308819595085ADC55C055FCB75
ark:/67375/WNG-0NT8TB28-B
Jenrin Discovery
ArticleID:CEP12359
National Institutes of Child Health and Human Development - No. R15-HD-066267
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
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Jing Li, Regeneron Pharmaceuticals, 777 Old Saw Mill River Road, Tarrytown, NY 10591
Present Address
Rani J Qasem, Department of Pharmaceutical Sciences, School of Pharmacy, King Saud Bin Abdul Aziz University for Health Sciences, Riyadh, Kingdom Saudi Arabia (KSA)
ISSN:0305-1870
1440-1681
DOI:10.1111/1440-1681.12359