Maternal Diet High in Linoleic Acid Alters Offspring Lipids and Hepatic Regulators of Lipid Metabolism in an Adolescent Rat Model

Author:

Shrestha Nirajan1ORCID,Sleep Simone L.1ORCID,Holland Olivia J.12ORCID,Vidimce Josif1,Bulmer Andrew C.1,Cuffe James S. M.3ORCID,Perkins Anthony V.14ORCID,McAinch Andrew J.56ORCID,Hryciw Deanne H.578ORCID

Affiliation:

1. School of Pharmacy and Medical Science, Griffith University, Southport, QLD 4222, Australia

2. Women’s, Newborn and Childrens Services, Gold Coast Health, Southport, QLD 4222, Australia

3. School of Biomedical Sciences, The University of Queensland, St Lucia, QLD 4072, Australia

4. School of Health, University of Sunshine Coast, Sunshine Coast, Sippy Downs, QLD 4556, Australia

5. Institute for Health and Sport, Victoria University, Melbourne, VIC 3001, Australia

6. Australian Institute for Musculoskeletal Science (AIMSS), Victoria University, St. Albans, VIC 3021, Australia

7. School of Environment and Science, Griffith University, Nathan, QLD 4111, Australia

8. Griffith Institute of Drug Discovery, Griffith University, Nathan, QLD 4111, Australia

Abstract

Linoleic acid (LA), an n-6 polyunsaturated fatty acid (PUFA), is essential for fetal growth and development. A maternal high LA (HLA) diet alters cardiovascular development in adolescent rats and hepatic function in adult rats in a sex-specific manner. We investigated the effects of an HLA diet on adolescent offspring hepatic lipids and hepatic lipid metabolism gene expression, and the ability of the postnatal diet to alter these effects. Female Wistar Kyoto rats were fed low LA (LLA; 1.44% energy from LA) or high LA (HLA; 6.21% energy from LA) diets during pregnancy and gestation/lactation. Offspring, weaned at postnatal day (PN) 25, were fed LLA or HLA and euthanised at PN40 (n = 6–8). Maternal HLA increased circulating uric acid, decreased hepatic cholesterol and increased hepatic Pparg in males, whereas only hepatic Srebf1 and Hmgcr increased in females. Postnatal (post-weaning) HLA decreased liver weight (% body weight) and increased hepatic Hmgcr in males, and decreased hepatic triglycerides in females. Maternal and postnatal HLA had an interaction effect on Lpl, Cpt1a and Pparg in females. These findings suggest that an HLA diet both during and after pregnancy should be avoided to improve offspring disease risk.

Funder

Allen Foundation, Inc.

Australian Government’s Collaborative Research Networks (CRN) program

Publisher

MDPI AG

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