Literature DB >> 33196782

Effects of birth weight and dietary fat on intake, body composition, and plasma thyroxine in neonatal lambs.

Jose M Ramos-Nieves1, Sarah L Giesy1, Molly M McGuckin1, Yves R Boisclair1.   

Abstract

Intrauterine growth restriction (IUGR) is often observed in one of the fetuses carried by well-fed prolific ewes. This condition is the result of an insufficient placental size to cover the nutritional needs of the fetus during the near exponential growth phase of the last trimester. After birth, these IUGR offspring have an elevated appetite and lower maintenance energy requirements, suggesting dysregulation of homeostatic systems governing energy metabolism. It is also unknown whether the consequent increase in fatness occurs similarly in both visceral and carcass fractions. To address these questions, lambs differing in birth size (BS, IUGR vs. Normal, 2.6 ± 0.05 vs. 4.2 ± 0.07 kg, P < 0.001) were offered unlimited amounts of a low fat [LF; 22% of dry matter (DM)] or a high fat (HF; 38% of DM) milk replacer and slaughtered on day 14 of postnatal age (n = 7 to 8 for each BS × Diet); a second group of IUGR lambs (n = 3 for each diet) was slaughtered when they reached 8.5 kg, corresponding to the weight of Normal lambs on day 14. When normalized to body weight (BW), the DM and energy intake of IUGR lambs were higher than those of Normal lambs over the first 14 d of life (BS, P < 0.01), but contrary to expectations, the HF diet did not exacerbate these effects of the IUGR condition. Intrauterine growth restricted lambs had increased viscera fat with both diets (BS and Diet, P < 0.05) but increased carcass fat only with the LF diet (BS × Diet, P = 0.08); the fatness promoting effect of the IUGR condition was increased in both body fractions when lamb groups were compared at the fixed BW of 8.5 kg. A subset of metabolic hormones was analyzed, including the metabolic rate-setting hormone thyroxine (T4) and its possible positive regulator leptin. Plasma T4 was lower in IUGR than in Normal lambs at birth (P < 0.05) but then disappeared by day 7 of postnatal life (BS × Day, P < 0.01). On the other hand, the HF diet had no effect on plasma T4 over the first 3 d but caused an increase, irrespective of BS by day 11 (Diet × Day, P < 0.001). Plasma leptin increased with dietary fat and time (P < 0.06) but bore no relation to the effects of BS or Diet on plasma T4. These data show that IUGR and Normal lambs are similarly unable to adjust caloric intake in early life and that the fatness promoting effects of the IUGR condition are more pronounced in the viscera than in the carcass. These data also reveal dynamic regulation of plasma T4 by BS and Diet in neonatal lambs.
© The Author(s) 2020. Published by Oxford University Press on behalf of the American Society of Animal Science. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  fatness; fetal programming; leptin; visceral fat

Mesh:

Substances:

Year:  2020        PMID: 33196782      PMCID: PMC7718858          DOI: 10.1093/jas/skaa364

Source DB:  PubMed          Journal:  J Anim Sci        ISSN: 0021-8812            Impact factor:   3.159


  37 in total

1.  Influences on fetal and placental weights during mid to late gestation in prolific ewes well nourished throughout pregnancy.

Authors:  P L Greenwood; R M Slepetis; A W Bell
Journal:  Reprod Fertil Dev       Date:  2000       Impact factor: 2.311

2.  Placental restriction of fetal growth reduces size at birth and alters postnatal growth, feeding activity, and adiposity in the young lamb.

Authors:  Miles J De Blasio; Kathryn L Gatford; Jeffrey S Robinson; Julie A Owens
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2006-10-05       Impact factor: 3.619

3.  Role of the thyroid gland in seasonal reproduction: thyroidectomy blocks seasonal suppression of reproductive neuroendocrine activity in ewes.

Authors:  S M Moenter; C J Woodfill; F J Karsch
Journal:  Endocrinology       Date:  1991-03       Impact factor: 4.736

Review 4.  Early developmental conditioning of later health and disease: physiology or pathophysiology?

Authors:  M A Hanson; P D Gluckman
Journal:  Physiol Rev       Date:  2014-10       Impact factor: 37.312

5.  The effects of poor maternal nutrition during gestation on postnatal growth and development of lambs.

Authors:  M L Hoffman; K N Peck; M E Forella; A R Fox; K E Govoni; S A Zinn
Journal:  J Anim Sci       Date:  2016-02       Impact factor: 3.159

6.  Maternal obesity eliminates the neonatal lamb plasma leptin peak.

Authors:  Nathan M Long; Stephen P Ford; Peter W Nathanielsz
Journal:  J Physiol       Date:  2011-01-24       Impact factor: 5.182

7.  Development of a specific radioimmunoassay to measure physiological changes of circulating leptin in cattle and sheep.

Authors:  R A Ehrhardt; R M Slepetis; J Siegal-Willott; M E Van Amburgh; A W Bell; Y R Boisclair
Journal:  J Endocrinol       Date:  2000-09       Impact factor: 4.286

8.  Increased plasma leptin attenuates adaptive metabolism in early lactating dairy cows.

Authors:  Richard A Ehrhardt; Andreas Foskolos; Sarah L Giesy; Stephanie R Wesolowski; Christopher S Krumm; W Ronald Butler; Susan M Quirk; Matthew R Waldron; Yves R Boisclair
Journal:  J Endocrinol       Date:  2016-03-08       Impact factor: 4.286

9.  Maternal perinatal undernutrition drastically reduces postnatal leptin surge and affects the development of arcuate nucleus proopiomelanocortin neurons in neonatal male rat pups.

Authors:  Fabien Delahaye; Christophe Breton; Pierre-Yves Risold; Mihaela Enache; Isabelle Dutriez-Casteloot; Christine Laborie; Jean Lesage; Didier Vieau
Journal:  Endocrinology       Date:  2007-11-15       Impact factor: 4.736

10.  Effects of birth weight and postnatal nutrition on neonatal sheep: I. Body growth and composition, and some aspects of energetic efficiency.

Authors:  P L Greenwood; A S Hunt; J W Hermanson; A W Bell
Journal:  J Anim Sci       Date:  1998-09       Impact factor: 3.159

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