Vitamin and Mineral Supplementation and Rate of Gain in Beef Heifers I: Effects on Dam Hormonal and Metabolic Status, Fetal Tissue and Organ Mass, and Concentration of Glucose and Fructose in Fetal Fluids at d 83 of Gestation

Simple Summary Cow-calf operations rely mostly in forage-based systems. Different supplementation strategies are used by beef producers in order to overcome nutrient deficiencies and achieve targeted growth or reproductive performances. This study provides information on the impacts of feeding pregnant replacement heifers with vitamin/mineral and protein/energy supplements on heifer performance and fetal outcomes. Our study shows that moderate rates of gain (achieved via protein/energy supplementation) resulted in fetuses with heavier femurs and reduced liver mass relative to fetal body weight. Moreover, vitamin and mineral supplementation increased fetal liver mass, and vitamin and mineral supplementation combined with moderate gain treatments resulted in greater fetal intestinal weights. These findings indicate that replacement heifer nutrition during early gestation can alter the development of organs in the fetus that are relevant for future offspring performance. Liver and intestines are key organs related to energy metabolism; therefore, this study shows that compensatory mechanisms are in place in the developing conceptus that can alter the growth rate of key metabolic organs possibly in an attempt to increase or decrease energy utilization. Abstract Thirty-five crossbred Angus heifers (initial BW = 359.5 ± 7.1 kg) were randomly assigned to a 2 × 2 factorial design to evaluate effects of vitamin and mineral supplementation [VMSUP; supplemented (VTM) vs. unsupplemented (NoVTM)] and different rates of gain [GAIN; low gain (LG), 0.28 kg/d, vs. moderate gain (MG), 0.79 kg/d] during the first 83 d of gestation on dam hormone and metabolic status, fetal tissue and organ mass, and concentration of glucose and fructose in fetal fluids. The VMSUP was initiated 71 to 148 d before artificial insemination (AI), allowing time for mineral status of heifers to be altered in advance of breeding. At AI heifers were assigned their GAIN treatment. Heifers received treatments until the time of ovariohysterectomy (d 83 ± 0.27 after AI). Throughout the experiment, serum samples were collected and analyzed for non-esterified fatty acids (NEFA), progesterone (P4), insulin, and insulin-like growth factor 1 (IGF-1). At ovariohysterectomy, gravid reproductive tracts were collected, measurements were taken, samples of allantoic (ALF) and amniotic (AMF) fluids were collected, and fetuses were dissected. By design, MG had greater ADG compared to LG (0.85 vs. 0.34 ± 0.04 kg/d, respectively; p < 0.01). Concentrations of NEFA were greater for LG than MG (p = 0.04) and were affected by a VMSUP × day interaction (p < 0.01), with greater concentrations for NoVTM on d 83. Insulin was greater for NoVTM than VTM (p = 0.01). A GAIN × day interaction (p < 0.01) was observed for IGF-1, with greater concentrations for MG on d 83. At d 83, P4 concentrations were greater for MG than LG (GAIN × day, p < 0.01), and MG had greater (p < 0.01) corpus luteum weights versus LG. Even though fetal BW was not affected (p ≥ 0.27), MG fetuses had heavier (p = 0.01) femurs than LG, and VTM fetuses had heavier (p = 0.05) livers than those from NoVTM. Additionally, fetal liver as a percentage of BW was greater in fetuses from VTM (P = 0.05; 3.96 ± 0.06% BW) than NoVTM (3.79 ± 0.06% BW), and from LG (p = 0.04; 3.96 ± 0.06% BW) than MG (3.78 ± 0.06% BW). A VMSUP × GAIN interaction was observed for fetal small intestinal weight (p = 0.03), with VTM-MG being heavier than VTM-LG. Therefore, replacement heifer nutrition during early gestation can alter the development of organs that are relevant for future offspring performance. These data imply that compensatory mechanisms are in place in the developing conceptus that can alter the growth rate of key metabolic organs possibly in an attempt to increase or decrease energy utilization.

[1]  M. Hall,et al.  Rumen volatile fatty acid molar proportions, rumen epithelial gene expression, and blood metabolite concentration responses to ruminally degradable starch and fiber supplies. , 2021, Journal of dairy science.

[2]  J. Caton,et al.  Maternal Vitamin and Mineral Supplementation and Rate of Maternal Weight Gain Affects Placental Expression of Energy Metabolism and Transport-Related Genes , 2021, Genes.

[3]  J. Caton,et al.  Vitamin and mineral supplementation and rate of gain during the first trimester of gestation affect concentrations of amino acids in maternal serum and allantoic fluid of beef heifers. , 2021, Journal of animal science.

[4]  J. Caton,et al.  The effects of maternal nutrition during the first 50 days of gestation on the location and abundance of hexose and cationic amino acid transporters in beef heifer utero-placental tissues. , 2020, Journal of animal science.

[5]  R. Cushman,et al.  Maternal periconceptual nutrition, early pregnancy, and developmental outcomes in beef cattle. , 2020, Journal of animal science.

[6]  Pallavi Dubey,et al.  Role of Minerals and Trace Elements in Diabetes and Insulin Resistance , 2020, Nutrients.

[7]  S. Hansen,et al.  Invited Review: Linking road transportation with oxidative stress in cattle and other species , 2020 .

[8]  C. Ferrell,et al.  Biochemical and metabolic profiles in in vivo- and in vitro-derived concepti in cattle , 2020 .

[9]  A. Noya,et al.  A negative energy balance during the peri-implantational period reduces dam IGF-1 but does not alter progesterone or pregnancy-specific protein B (PSPB) or fertility in suckled cows. , 2019, Domestic animal endocrinology.

[10]  J. Caton,et al.  Developmental Programming of Fetal Growth and Development. , 2019, The Veterinary clinics of North America. Food animal practice.

[11]  J. Caton,et al.  Maternal nutrition and programming of offspring energy requirements1 , 2019, Translational animal science.

[12]  R. Cushman,et al.  Moderate nutrient restriction of beef heifers alters expression of genes associated with tissue metabolism, accretion, and function in fetal liver, muscle, and cerebrum by day 50 of gestation , 2019, Translational animal science.

[13]  L. A. Silva,et al.  Ultrasonography-accessed luteal size endpoint that most closely associates with circulating progesterone during the estrous cycle and early pregnancy in beef cows. , 2019, Animal reproduction science.

[14]  M. D’Occhio,et al.  Influence of nutrition, body condition, and metabolic status on reproduction in female beef cattle: A review. , 2019, Theriogenology.

[15]  J. Caton,et al.  Maternal nutrition and stage of early pregnancy in beef heifers: impacts on hexose and AA concentrations in maternal and fetal fluids1. , 2019, Journal of animal science.

[16]  Matthew Shapero,et al.  Mineral status of California beef cattle1 , 2018, Translational animal science.

[17]  S. Hileman,et al.  Influences of maternal nutrient restriction and arginine supplementation on visceral metabolism and hypothalamic circuitry of offspring. , 2018, Domestic animal endocrinology.

[18]  I. Casasús,et al.  Influence of postweaning feeding management of beef heifers on performance and physiological profiles through rearing and first lactation. , 2018, Domestic animal endocrinology.

[19]  A. Hoeflich,et al.  Increased Concentrations of Insulin-Like Growth Factor Binding Protein (IGFBP)-2, IGFBP-3, and IGFBP-4 Are Associated With Fetal Mortality in Pregnant Cows , 2018, Front. Endocrinol..

[20]  N. Dilorenzo,et al.  Administration of recombinant bovine somatotropin prior to fixed-time artificial insemination and the effects on fertility, embryo, and fetal size in beef heifers. , 2018, Journal of animal science.

[21]  J. Caton,et al.  Maternal nutrition and stage of early pregnancy in beef heifers: Impacts on expression of glucose, fructose, and cationic amino acid transporters in utero-placental tissues. , 2017, Journal of animal science.

[22]  D. Bohnert,et al.  Physiologic, health, and performance responses of beef steers supplemented with an immunomodulatory feed ingredient during feedlot receiving. , 2017, Journal of animal science.

[23]  K. Vonnahme,et al.  Livestock as models for developmental programming , 2017 .

[24]  R. Cooke,et al.  Supplementing an immunomodulatory feed ingredient to modulate thermoregulation, physiologic, and production responses in lactating dairy cows under heat stress conditions. , 2017, Journal of dairy science.

[25]  J. Yelich,et al.  Effects of trace mineral supplement source during gestation and lactation in Angus and Brangus cows and subsequent calf immunoglobulin concentrations, growth, and development , 2017 .

[26]  J. Caton,et al.  Technical note: A new surgical technique for ovariohysterectomy during early pregnancy in beef heifers. , 2016, Journal of animal science.

[27]  J. Caton,et al.  Nutrient restriction and realimentation in beef cows during early and mid-gestation and maternal and fetal hepatic and small intestinal in vitro oxygen consumption. , 2016, Animal : an international journal of animal bioscience.

[28]  T. Spencer,et al.  Role of progesterone in embryo development in cattle. , 2016, Reproduction, fertility, and development.

[29]  Board on Agriculture Nutrient requirements of beef cattle: eighth revised edition (2016). , 2016 .

[30]  J. Caton,et al.  Role of the Small Intestine in Developmental Programming: Impact of Maternal Nutrition on the Dam and Offspring. , 2016, Advances in nutrition.

[31]  R. Arsenault,et al.  Models and Methods to Investigate Acute Stress Responses in Cattle , 2015, Animals : an open access journal from MDPI.

[32]  D. Keisler,et al.  Effects of oral meloxicam administration to beef cattle receiving lipopolysaccharide administration or vaccination against respiratory pathogens. , 2015, Journal of animal science.

[33]  K. Olson COW SUPPLEMENTATION:GETTING THE BEST BANGFOR YOUR BUCK , 2015 .

[34]  B. Awda,et al.  Effects of nutrient restriction and melatonin supplementation on maternal and foetal hepatic and small intestinal energy utilization. , 2014, Journal of animal physiology and animal nutrition.

[35]  D. Keisler,et al.  Supplementation based on protein or energy ingredients to beef cattle consuming low-quality cool-season forages: II. Performance, reproductive, and metabolic responses of replacement heifers. , 2014, Journal of animal science.

[36]  D. Bohnert,et al.  Supplementation based on protein or energy ingredients to beef cattle consuming low-quality cool-season forages: I. Forage disappearance parameters in rumen-fistulated steers and physiological responses in pregnant heifers. , 2014, Journal of animal science.

[37]  Guoyao Wu,et al.  Amino acid nutrition in animals: protein synthesis and beyond. , 2014, Annual review of animal biosciences.

[38]  G. Smith,et al.  Effects of maternal environment during gestation on ovarian folliculogenesis and consequences for fertility in bovine offspring. , 2012, Reproduction in domestic animals = Zuchthygiene.

[39]  J. Stevenson,et al.  Control of the estrous cycle to improve fertility for fixed-time artificial insemination in beef cattle: a review. , 2010, Journal of animal science.

[40]  J. Caton,et al.  Developmental programming: the concept, large animal models, and the key role of uteroplacental vascular development. , 2010, Journal of animal science.

[41]  K. Olson,et al.  DELIVERY OF SUPPLEMENTS ON RANGELANDS , 2007 .

[42]  G. Mann,et al.  Effects of time of progesterone supplementation on embryo development and interferon-tau production in the cow. , 2006, Veterinary journal.

[43]  W. Hay Placental-fetal glucose exchange and fetal glucose metabolism. , 2006, Transactions of the American Clinical and Climatological Association.

[44]  J. Luthman,et al.  Insulin Sensitivity of Heifers on Different Diets , 2002, Acta veterinaria Scandinavica.

[45]  P. V. Soest,et al.  Methods for dietary fiber, neutral detergent fiber, and nonstarch polysaccharides in relation to animal nutrition. , 1991, Journal of dairy science.

[46]  C. West,et al.  Effects of animal and supplement characteristics on average daily gain of grazing beef cattle. , 1991, Journal of animal science.