Adverse Metabolic Phenotypes in Parenterally Fed Neonatal Pigs Do Not Persist into Adolescence

Research output: Contribution to journalJournal articleResearchpeer-review

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Adverse Metabolic Phenotypes in Parenterally Fed Neonatal Pigs Do Not Persist into Adolescence. / Elefson, Sarah K.; Stoll, Barbara; Davis, Teresa A.; Fiorotto, Marta L.; El-Kadi, Samer W.; Genovese, Kenneth; Thymann, Thomas; Sangild, Per T.; Burrin, Douglas G.

In: Journal of Nutrition, Vol. 154, No. 2, 2024, p. 638-647.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Elefson, SK, Stoll, B, Davis, TA, Fiorotto, ML, El-Kadi, SW, Genovese, K, Thymann, T, Sangild, PT & Burrin, DG 2024, 'Adverse Metabolic Phenotypes in Parenterally Fed Neonatal Pigs Do Not Persist into Adolescence', Journal of Nutrition, vol. 154, no. 2, pp. 638-647. https://doi.org/10.1016/j.tjnut.2023.12.048

APA

Elefson, S. K., Stoll, B., Davis, T. A., Fiorotto, M. L., El-Kadi, S. W., Genovese, K., Thymann, T., Sangild, P. T., & Burrin, D. G. (2024). Adverse Metabolic Phenotypes in Parenterally Fed Neonatal Pigs Do Not Persist into Adolescence. Journal of Nutrition, 154(2), 638-647. https://doi.org/10.1016/j.tjnut.2023.12.048

Vancouver

Elefson SK, Stoll B, Davis TA, Fiorotto ML, El-Kadi SW, Genovese K et al. Adverse Metabolic Phenotypes in Parenterally Fed Neonatal Pigs Do Not Persist into Adolescence. Journal of Nutrition. 2024;154(2):638-647. https://doi.org/10.1016/j.tjnut.2023.12.048

Author

Elefson, Sarah K. ; Stoll, Barbara ; Davis, Teresa A. ; Fiorotto, Marta L. ; El-Kadi, Samer W. ; Genovese, Kenneth ; Thymann, Thomas ; Sangild, Per T. ; Burrin, Douglas G. / Adverse Metabolic Phenotypes in Parenterally Fed Neonatal Pigs Do Not Persist into Adolescence. In: Journal of Nutrition. 2024 ; Vol. 154, No. 2. pp. 638-647.

Bibtex

@article{d636a4901b1f4e739faf18b80289c718,
title = "Adverse Metabolic Phenotypes in Parenterally Fed Neonatal Pigs Do Not Persist into Adolescence",
abstract = "Background: Nutrition during fetal and neonatal life is an important determinant for the risk of adult-onset diseases, especially type 2 diabetes and obesity. Objectives: We aimed to determine whether total parenteral nutrition (TPN) compared with enteral formula feeding [enteral nutrition (EN)] in term piglets during the first 2 wk after birth would increase the long-term (5-mo) development of metabolic syndrome phenotypes with adverse glucose homeostasis, fatty liver disease, and obesity. Methods: Neonatal female pigs were administered TPN (n = 12) or fed enterally with a liquid enteral milk-replacer formula (EN, n = 12) for 14 d. After transitioning TPN pigs to enteral feeding of liquid formula (days 15–26), both groups were adapted to a solid high-fat diet (30% of the total diet) and sucrose (20% of the total diet) diet (days 27–33), which was fed until the end of the study (140 d). Body composition was measured by dual-energy X-ray absorptiometry at 14, 45, and 140 d. Serum biochemistry and glucose-insulin values (after a fasting intravenous glucose tolerance test) were obtained at 140 d. Liver and muscle were analyzed for insulin receptor signaling and triglycerides. Results: Body weight was similar, but percent fat was higher, whereas percent lean and bone mineral density were lower in TPN than in EN pigs (P < 0.01) at 45 d of age but not at 140 d. At 140 d, there were no differences in serum markers of liver injury or lipidemia. Intravenous glucose tolerance test at 140 d showed a lower (P < 0.05) AUC for both glucose and insulin in TPN than in EN pigs, but the ratio of AUCs of insulin and glucose was not different between groups. Conclusions: Administration of TPN during the neonatal period increased adipose deposition that transiently persisted in early adolescence when challenged with a high-fat diet but was not sustained or manifested as glucose intolerance.",
keywords = "insulin resistance, neonatal programming, obesity, pig, total parenteral nutrition",
author = "Elefson, {Sarah K.} and Barbara Stoll and Davis, {Teresa A.} and Fiorotto, {Marta L.} and El-Kadi, {Samer W.} and Kenneth Genovese and Thomas Thymann and Sangild, {Per T.} and Burrin, {Douglas G.}",
note = "Publisher Copyright: {\textcopyright} 2024",
year = "2024",
doi = "10.1016/j.tjnut.2023.12.048",
language = "English",
volume = "154",
pages = "638--647",
journal = "Journal of Nutrition",
issn = "0022-3166",
publisher = "American Society for Nutrition",
number = "2",

}

RIS

TY - JOUR

T1 - Adverse Metabolic Phenotypes in Parenterally Fed Neonatal Pigs Do Not Persist into Adolescence

AU - Elefson, Sarah K.

AU - Stoll, Barbara

AU - Davis, Teresa A.

AU - Fiorotto, Marta L.

AU - El-Kadi, Samer W.

AU - Genovese, Kenneth

AU - Thymann, Thomas

AU - Sangild, Per T.

AU - Burrin, Douglas G.

N1 - Publisher Copyright: © 2024

PY - 2024

Y1 - 2024

N2 - Background: Nutrition during fetal and neonatal life is an important determinant for the risk of adult-onset diseases, especially type 2 diabetes and obesity. Objectives: We aimed to determine whether total parenteral nutrition (TPN) compared with enteral formula feeding [enteral nutrition (EN)] in term piglets during the first 2 wk after birth would increase the long-term (5-mo) development of metabolic syndrome phenotypes with adverse glucose homeostasis, fatty liver disease, and obesity. Methods: Neonatal female pigs were administered TPN (n = 12) or fed enterally with a liquid enteral milk-replacer formula (EN, n = 12) for 14 d. After transitioning TPN pigs to enteral feeding of liquid formula (days 15–26), both groups were adapted to a solid high-fat diet (30% of the total diet) and sucrose (20% of the total diet) diet (days 27–33), which was fed until the end of the study (140 d). Body composition was measured by dual-energy X-ray absorptiometry at 14, 45, and 140 d. Serum biochemistry and glucose-insulin values (after a fasting intravenous glucose tolerance test) were obtained at 140 d. Liver and muscle were analyzed for insulin receptor signaling and triglycerides. Results: Body weight was similar, but percent fat was higher, whereas percent lean and bone mineral density were lower in TPN than in EN pigs (P < 0.01) at 45 d of age but not at 140 d. At 140 d, there were no differences in serum markers of liver injury or lipidemia. Intravenous glucose tolerance test at 140 d showed a lower (P < 0.05) AUC for both glucose and insulin in TPN than in EN pigs, but the ratio of AUCs of insulin and glucose was not different between groups. Conclusions: Administration of TPN during the neonatal period increased adipose deposition that transiently persisted in early adolescence when challenged with a high-fat diet but was not sustained or manifested as glucose intolerance.

AB - Background: Nutrition during fetal and neonatal life is an important determinant for the risk of adult-onset diseases, especially type 2 diabetes and obesity. Objectives: We aimed to determine whether total parenteral nutrition (TPN) compared with enteral formula feeding [enteral nutrition (EN)] in term piglets during the first 2 wk after birth would increase the long-term (5-mo) development of metabolic syndrome phenotypes with adverse glucose homeostasis, fatty liver disease, and obesity. Methods: Neonatal female pigs were administered TPN (n = 12) or fed enterally with a liquid enteral milk-replacer formula (EN, n = 12) for 14 d. After transitioning TPN pigs to enteral feeding of liquid formula (days 15–26), both groups were adapted to a solid high-fat diet (30% of the total diet) and sucrose (20% of the total diet) diet (days 27–33), which was fed until the end of the study (140 d). Body composition was measured by dual-energy X-ray absorptiometry at 14, 45, and 140 d. Serum biochemistry and glucose-insulin values (after a fasting intravenous glucose tolerance test) were obtained at 140 d. Liver and muscle were analyzed for insulin receptor signaling and triglycerides. Results: Body weight was similar, but percent fat was higher, whereas percent lean and bone mineral density were lower in TPN than in EN pigs (P < 0.01) at 45 d of age but not at 140 d. At 140 d, there were no differences in serum markers of liver injury or lipidemia. Intravenous glucose tolerance test at 140 d showed a lower (P < 0.05) AUC for both glucose and insulin in TPN than in EN pigs, but the ratio of AUCs of insulin and glucose was not different between groups. Conclusions: Administration of TPN during the neonatal period increased adipose deposition that transiently persisted in early adolescence when challenged with a high-fat diet but was not sustained or manifested as glucose intolerance.

KW - insulin resistance

KW - neonatal programming

KW - obesity

KW - pig

KW - total parenteral nutrition

U2 - 10.1016/j.tjnut.2023.12.048

DO - 10.1016/j.tjnut.2023.12.048

M3 - Journal article

C2 - 38181968

AN - SCOPUS:85183615830

VL - 154

SP - 638

EP - 647

JO - Journal of Nutrition

JF - Journal of Nutrition

SN - 0022-3166

IS - 2

ER -

ID: 390191877