In the neonatal calf, insulin-like growth factor I (IGF-I) concentrations are markedly influenced by the amount of colostrum intake after birth, although colostral IGF-I is barely absorbed. In this study we have investigated effects of delayed colostrum intake in neonatal calves on metabolic traits and on IGF-I, IGF binding proteins (IGFBP), growth hormone (GH), and insulin concentrations in plasma. Calves received colostrum of first milking starting at 2 (GrA), 6 (GrB), 12 (GrC), and 24 h (GrD) after birth. Before third colostrum intake plasma total protein concentrations were higher in GrA than in GrD and plasma glucose concentrations were higher in GrC than GrD. Plasma IGF-I concentrations at first and third colostrum intake were higher in GrA than in GrD. Plasma IGFBP-2 concentrations before first colostrum intake were higher in GrD than in GrA and GrC, and were higher before third colostrum intake in GrD than in GrA. Plasma IGFBP-3 concentrations before first colostrum intake were lower in GrD than in GrA, and before third colostrum intake were lower in GrD than in GrA and GrB. Postprandial plasma insulin concentrations after first colostrum intake were higher in GrA than in GrC and GrD. In conclusion, the plasma IGF-I and insulin status are markedly, albeit transiently, decreased in calves fed colostrum with a delay of 12 to 24 h, and the decreased concentrations of plasma IGF-I were associated with decreased IGFBP-3/IGFBP-2 ratios.

Effects on beta-carotene, retinol and alpha-tocopherol status of feeding 1st colostrum at 0-2, 6-7, 12-13 and 24-25 h after birth were studied in calves. beta-carotene, retinol and alpha-tocopherol concentrations decreased in colostrum during the first 2.5 d of lactation. Plasma beta-carotene, retinol and alpha-tocopherol concentrations in newborn calves were very low. Plasma beta-carotene concentrations increased up to d 3 after the 1st meal and during the 1st month were higher in calves fed 1st colostrum at < 6-7 h than at > 12-13 h after birth. Plasma retinol concentrations increased up to d 5 after the 1st meal and were higher during the 1st month in calves fed 1st colostrum at < 12-13 h than at > 24-25 h after birth, whereas hepatic concentrations increased up to d 5 independent of time of 1st colostrum feeding. Plasma alpha-tocopherol concentrations increased after the 1st meal except in calves fed 1st colostrum at 24-25 h after birth and were higher during the 1st month in calves fed the 1st colostrum at 6-7 h than at 24-25 h after birth. In conclusion, delaying 1st colostrum intake by more than 12-13 h after birth impaired the plasma beta-carotene, retinol and alpha-tocopherol status during the 1st month of life, but did not negatively influence hepatic retinol concentrations.

Enzyme activities of gamma-glutamyltransferase (gamma-GT), alkaline phosphatase (AP) and aspartate-aminotransferase (AST) were measured from birth to the age of 28 days in calves which were fed colostrum at 0-2, 6-7, 12-13, or 24-25 h after birth. Enzyme activities were also measured in colostrum (first to fifth milking) and in mature milk. Activities were highest in the first colostrum milking and decreased to the lowest activities in mature milk. Plasma gamma-GT activity transiently increased after first colostrum intake and was greater in calves fed first colostrum within less than 6-7 h than in those fed first colostrum later than 12 h after birth. Activity of gamma-GT reflected the absorption of colostral gamma-GT, which decreased with time after birth. The AP activity transiently increased after colostrum intake and was higher in calves fed colostrum within the first 12 h of life than in those fed later after birth. The transient rise of plasma AP activity also indicated absorption of colostral AP, although endogenous sources of AP could not be excluded. The activity of AST also transiently increased after colostrum intake but there was no association with time of first colostrum feeding, indicating that the rise of plasma AST activity was the consequence of enhanced endogenous production and was independent of colostrum intake. In conclusion, there are different causes leading to postnatal changes in enzyme activities.

Calves are born with a mostly inadequate essential amino acid (EAA) status. Studies were designed to test the hypothesis that delaying the intake of the first colostrum for 24 h, besides its early effects, also has late effects on plasma free amino acid levels and on the protein status. There were marked and rapid elevations (within 2 h) of plasma levels of various amino acids, and especially of EAA, after the intake of the first colostrum, whereas changes after the intake of mature milk on day 28 of life were mostly absent or concentrations even decreased. The EAA and non-essential amino acid (NEAA) status was rapidly normalized after intake of the first colostrum, but normal plasma levels of some amino acids were also reached during the first 24 h of life even when the first meal was withheld. Delaying colostrum intake had only transient effects on EAA and NEAA (except hydroxyproline), in contrast to its effects on plasma immunoglobulin G and total protein levels.

To test the hypothesis that delaying first colostrum feeding of calves after birth exerts long-lasting effects on haematological, metabolic and endocrine traits and on growth performance, neonatal calves were fed first colostrum at 0-2 and 24-25 h after birth. Delayed feeding of first colostrum for 24-25 h after birth caused reduced plasma levels of total protein and globulin for up to 30 days and of insulin-like growth factor-I for up to 7 days, whereas concentrations of nonesterified fatty acids were elevated during the first day of life. There were no significant effects of delaying feeding for 24-25 h on leucocyte and erythrocyte number, packed cell volume and on haemoglobin levels and on plasma concentrations of albumin, urea, glucose, triglycerides, phospholipids, cholesterol, insulin, growth hormone, 3.5.3'-triiodothyronine and thyroxine and on growth performance. Thus, calves fed first colostrum with a delay of 24-25 h after birth were able to compensate rapidly for nutritional deficiencies on day 1 of life, i.e. there was no evidence for permanent imprinting of haematological, metabolic and of endocrine traits by starvation on the first day of life.