Supplementation with methyl donors during lactation to high-fat-sucrose-fed dams protects offspring against liver fat accumulation when consuming an obesogenic diet
Abstract
Methyl donor supplementation has been reported to prevent obesity-induced liver fat accumulation in adult rats. We hypothesized that this protection could be mediated by perinatal nutrition. For this purpose, we assessed the response to an obesogenic diet (high-fat-sucrose, HFS) during adulthood depending on maternal diet during lactation. Female Wistar rats fed control diet during pregnancy were assigned to four postpartum dietary groups: control, control supplemented with methyl donors (choline, betaine, folic acid, vitamin B 12), HFS and HFS supplemented with methyl donors. At weaning, the male offspring was transferred to a chow diet and at week 12th assigned to a control or a HFS diet during 8 weeks. The offspring whose mothers were fed HFS during lactation showed increased adiposity (19%,P<0.001). When fed the HFS diet as adults, offspring whose mothers were HFS supplemented had more body fat (23%,P<0.001) than those from HFS non-supplemented. However, they showed lower liver fat accumulation (−18%,P<0.001). Srebf1, Dnmt1 and Lepr liver mRNA levels increased after adulthood HFS feeding. In those animals HFS fed during adulthood, previous maternal HFS decreased Lepr and Dnmt1 expression levels when compared with c-HFS offspring, while the supplementation of control and HFS-fed dams, respectively, induced higher hepatic Mme and Lepr mRNA levels after adult HFS intake compared with hfs-HFS offspring. In conclusion, maternal HFS diet during lactation influenced the response to an obesogenic diet in the adult progeny. Interestingly, dietary methyl donor supplementation in lactating mothers fed an obesogenic diet reduced liver fat accumulation, but increased adipose tissue storage in adult HFS-fed offspring.
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Maternal dietary supplementation with methyl donors during gestation or lactation partially prevented the development of an obese phenotype in the offspring from high sucrose diet-fed mothers.
“There have already been interesting studies in this area, including data showing that maternal dietary supplementation with methyl donors during gestation or lactation partially prevented the development of an obese phenotype in the offspring from high sucrose diet-fed mothers [155].”
From Developmental programming of offspring adipose tissue biology and obesity risk (2021) · cites this paper as [155]
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References 57 · Cited by 45
- Authors
- Cordero, P., Milagro, F. I., Campion, J., & Martinez, J. A.
- Affiliations
- Universidad de Navarra (ES)
- Instituto de Salud Carlos III (ES)
- Venue
- Journal of Developmental Origins of Health and Disease
- Publisher
- Cambridge University Press (CUP)
- Published
- 2014-08-01
- Volume
- 5
- Issue
- 5
- Pages
- 385-395
- ISSN
- 2040-1744 (ISSN-L)
- 2040-1752
- OpenAlex
- W2172008160
- Cited by
- 45
- References
- 57
- Citations by year
- 2026: 1 · 2024: 1 · 2023: 3 · 2022: 4 · 2021: 4 · 2020: 5 · 2019: 2 · 2018: 4 · 2017: 5 · 2016: 7 · 2015: 8 · 2014: 1
- FWCI
- 6.58
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Developmental Origins of Health and Disease (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Centro de Investigación Biomédica en Red-Fisiopatología de la Obesidad y Nutrición
- Topics
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Birth, Development, and Health
- Health Sciences › Medicine › Rheumatology › Folate and B Vitamins Research
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diet, Metabolism, and Disease
- Keywords
- methyl donor supplementation, lactation, maternal diet, high-fat sucrose diet, obesogenic diet, hepatic lipid accumulation, hepatic steatosis, offspring adiposity, perinatal nutrition, choline, betaine, folic acid, vitamin B12, SREBF1, DNMT1, leptin receptor, MME, epigenetic programming, developmental origins of health and disease
- MeSH terms
- DNA (Cytosine-5-)-Methyltransferase 1, Adipose Tissue, Animals, Betaine, Body Composition, Choline, Diet, Female, Folic Acid, Lactation, Liver, Male, Obesity, Pregnancy, RNA, Messenger, Vitamin B 12, Gene Expression, Rats, Wistar, DNA Methylation, Dietary Sucrose, Dietary Supplements, Maternal Nutritional Physiological Phenomena, Rats, Receptors, Leptin, Diet, High-Fat
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