The Effects of Maternal Nutrient Restriction during Mid to Late Gestation with Realimentation on Fetal Metabolic Profiles in the Liver, Skeletal Muscle, and Blood in Sheep

Author:

Smith Brandon I.1,Vásquez-Hidalgo Manuel A.2ORCID,Li Xiaomeng3,Vonnahme Kimberly A.2,Grazul-Bilska Anna T.2,Swanson Kendall C.2ORCID,Moore Timothy E.3ORCID,Reed Sarah A.1ORCID,Govoni Kristen E.1

Affiliation:

1. Department of Animal Science, University of Connecticut, Storrs, CT 06269, USA

2. Department of Animal Sciences, North Dakota State University, Fargo, ND 58102, USA

3. Department of Statistics, University of Connecticut, Storrs, CT 06269, USA

Abstract

Poor maternal nutrition during gestation negatively affects offspring growth and metabolism. To evaluate the impact of maternal nutrient restriction and realimentation on metabolism in the fetal liver, skeletal muscle, and circulation, on day 50 of gestation, ewes (n = 48) pregnant with singletons were fed 100% (CON) or 60% (RES) of requirements until day 90 of gestation, when a subset of ewes (n = 7/treatment) were euthanized, and fetal samples were collected. The remaining ewes were maintained on a current diet (CON-CON, n = 6; RES-RES, n = 7) or switched to an alternative diet (CON-RES, RES-CON; n = 7/treatment). On day 130 of gestation, the remaining ewes were euthanized, and fetal samples were collected. Fetal liver, longissimus dorsi (LD), and blood metabolites were analyzed using LC-MS/MS, and pathway enrichment analysis was conducted using MetaboAnalyst. Then, 600, 518, and 524 metabolites were identified in the liver, LD, and blood, respectively, including 345 metabolites that were present in all three. Nutrient restriction was associated with changes in amino acid, carbohydrate, lipid, and transulfuration/methionine metabolic pathways, some of which were alleviated by realimentation. Fetal age also affected metabolite abundance. The differential abundance of metabolites involved in amino acid, methionine, betaine, and bile acid metabolism could impact fetal epigenetic regulation, protein synthesis, lipid metabolism, and signaling associated with glucose and lipid metabolism.

Funder

USDA-AFRI

Publisher

MDPI AG

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