2012
DOI: 10.1016/j.domaniend.2012.02.005
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Energy metabolism in the newborn farm animal with emphasis on the calf: endocrine changes and responses to milk-born and systemic hormones

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Cited by 82 publications
(125 citation statements)
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References 162 publications
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“…Previous studies showed that the ether extract concentration varied from 4.6 to 6.7% (Kehoe et al, 2007;Morril et al, 2012;Contarini et al, 2014) and similar values were observed in the present study. High-fat colostrum is desirable when there is a high demand for energy for the newborn, since calves are born with reduced energy reserves (Okamota et al, 1986) and have high energy requirements to maintain thermogenesis (Hammon et al, 2012).…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Previous studies showed that the ether extract concentration varied from 4.6 to 6.7% (Kehoe et al, 2007;Morril et al, 2012;Contarini et al, 2014) and similar values were observed in the present study. High-fat colostrum is desirable when there is a high demand for energy for the newborn, since calves are born with reduced energy reserves (Okamota et al, 1986) and have high energy requirements to maintain thermogenesis (Hammon et al, 2012).…”
Section: Discussionmentioning
confidence: 99%
“…Fat, the main energy source for newborns, represents approximately 6.7% of colostrum (Foley and Otterby, 1978) and is important for heat production and maintenance, as well as for providing fatty acids for glucose homeostasis via gluconeogenesis (Hammon et al, 2012). In addition to the lipid content, lactose, despite its low colostrum concentration (2.7%), has also an important function in the energy supply of newborns (Davis and Drackely, 1998).…”
Section: Introductionmentioning
confidence: 99%
“…Possible critical points for these differences in favour of the CONTROL group may be a lower quantity or quality of milk in the sows that were exposed to nutritional challenges during their foetal development (because such characteristics are highly influenced by nutritional and metabolic cues in all mammals; Shingfield et al 2013), a lower capacity of the neonates for endogenous glucose production (which is critical for adequate early-postnatal development; Hammon et al 2012) and/or a lower ability of the offspring to absorb and utilize milk nutrients check these hypotheses under the conditions of this study, but our results pave the way for future studies focused on both animal production and biomedicine.…”
Section: Discussionmentioning
confidence: 99%
“…In neonatal calves, eGP, through gluconeogenesis and glycogenolysis, increases after birth to meet glucose demands, because lactose intake is not sufficient to meet postnatal glucose requirements (Girard, 1990;Steinhoff-Wagner et al, 2011b;Hammon et al, 2013). Due to fat intake by colostrum feeding, reflected by increasing plasma concentrations of triacylglycerides and several proteins related to lipid transport in colostrumfed calves (Hammon and Blum, 1998;Rauprich et al, 2000;Herosimczyk et al, 2013), fat sources become an additional fuel to meet energy requirements in the neonate that requires adaptation of neonatal energy metabolism (Girard, 1990;Hammon et al, 2012).…”
Section: Introductionmentioning
confidence: 99%
“…The dominant adrenergic receptor (AR) subtypes in the liver of neonatal calves are α 1 -and β 2 -AR, which are involved in postnatal maturation of energy metabolism (Carron et al, 2005a,b;Ontsouka et al, 2006), whereas hepatic glucocorticoid receptors (GR) have scarcely been investigated in neonatal calves. However, postnatal energy status, specifically glucose and lipid metabolism, depends on diet, as indicated by an improved energy status in colostrum-fed calves and an impaired energy status in calves fed milk with comparable nutrient density as colostrum, but without bioactive growth-promoting factors (Blum, 2006;Hammon et al, 2012Hammon et al, , 2013.…”
Section: Introductionmentioning
confidence: 99%