A study using 20 Holstein Friesian cows was conducted to investigate the
influence of calf gender on metabolism during the transition period in dairy
cattle. Blood samples were collected at three time points: 2–4 days
prepartum (time 1), and 1 week and 2 weeks postpartum (time 2 and time
3 respectively). Serum samples obtained were analysed for total proteins,
albumin, urea, glucose, non-esterified fatty acids (NEFA) and
The ability of an individual to adapt to the natural change of energy balance during early lactation is an important aspect of the transition period for dairy cows. During this period, the cow undergoes physiological, metabolic and nutritional changes. As this period presents a huge metabolic challenge to high-yielding dairy cows, any changes in haematochemical profiles are important (Piccione et al., 2012; Tóthová et al., 2014). Cows that are unable to adapt adequately to these changes often develop hyperketonemia, which can also cause other health complications.
In dairy cows, key metabolic parameters used as indicators of negative
energy balance (NEB) and subclinical ketosis are non-esterified fatty acids
(NEFA) and
Fetal sex can also affect different aspects of dairy cows, such as “days open” as well as milk production. In one study, cows with bull calves had fewer days open than cows with heifer calves (Cordova-Izquierdo et al., 2008). The number of days between calving and conception affects profitability in terms of breeding cost, increased risk of culling and replacement costs; hence, long days open reduce profitability (De Vries, 2004). Other studies have shown that a positive relationship between age at first calving and milk production (Müller et al., 2005), and a significant biological effect of sex-biased milk production in favour of daughters (Hinde et al., 2014) exists in Holstein dairy cows.
While many studies have focused on how mammalian females could influence the sex of the offspring both before and after conception (Hardy, 1997; Grant et al., 2008; Grant and Chamley, 2010), there is little understanding of how offspring sex can affect metabolism in dairy cows during the transition period. Fetal hormones may provide a means for understanding the influence of offspring sex on maternal metabolism during the early transition period, especially since they can readily diffuse into maternal circulation. Ruminants may be especially valuable for understanding mammary gland development during pregnancy as a function of fetal sex because of their cotyledonary placenta. As a by-product of the greater placental surface area, fetal hormones can readily diffuse into maternal circulation (Klisch and Mess, 2007).
Currently, it is known that the amount of hormone insulin-like peptide 3 (INSL3), a major secretory product of the Leydig cells from both fetal and adult testes, declines during mid-pregnancy and is undetectable in cows carrying a female fetus. In contrast, circulating maternal INSL3 increases in cows carrying a male fetus. This increase in INSL3 levels may be a result of the transplacental transfer of fetal INSL3 into maternal circulation. While this gender-specific fetal hormone may influence both placental and maternal physiology (Anand-Ivell et al., 2011), the extent to which fetal-origin INSL3 influences mammary gland development is unknown.
In general, cows undergo significant metabolic changes during the early transition period; however, these changes are greater in Holstein Friesian cows than in other breeds (Adamski et al., 2011; Kupczyński et al., 2011). A greater understanding of how the sex of the offspring influences these changes could provide insight to clinicians and producers on ways of reducing risk of hyperketonemia and other diseases in dairy cows. Therefore, the aim of this study was to evaluate differences in metabolic parameters during the early transition period in dairy cows calving bulls or heifers.
Twenty multiparous Holstein Friesian cows belonging to an intensive dairy herd
located in northern Italy (45
Blood samples were collected by jugular venipuncture into 10 mL
Vacutainer tubes (Terumo Corporation, Tokyo, Japan) at three different time
points between 08:00 and 09:00 (central european standard time
Chemical composition of diets used during steaming-up and subsequent early lactation.
NDF (neutral detergent fiber), ADF (acid detergent fiber), NFC (non-fiber carbohydrates).
A two-way repeated measures analysis of variance (two-way ANOVA) was used to
evaluate the influence of time and offspring sex effects on the metabolic
parameters of blood samples. Unpaired data were analysed using the Student's
Pattern of total proteins, albumin, globulins,
Pattern of glucose, BHB, and NEFA in Group 1 and Group 2 dairy cows monitored at 1 week before the expected partum (T1), and at 1 week (T2) and 2 weeks (T3) after.
The results of the statistical analysis on the nitrogen parameter data in
the early transition period are illustrated in Fig. 1. For Group 1, total
proteins were significantly higher during T3 than during T1 (
Figure 2 shows the results of the analysis on energy parameters. A
significant effect of time was found on the NEFA pattern for both groups of
cows. For Group 1, levels were significantly increased at T2 and T3 when
compared to T1 (
The results of this study indicate that the sex of the offspring can affect nitrogen and energy metabolism during the transition period in Holstein Friesian dairy cows. The increase in total proteins, albumin, and globulins in dams of heifers could suggest a greater dehydration than what was observed for dams of bulls. These differences could be a result of offspring gender differences in physiological dehydration which is generally linked with increased milk production. Serum protein patterns can provide information about dehydration in dairy cows during the peripartum period (Piccione et al., 2011). Although Hinde et al. (2014) reported that gestation of a daughter on the first parity increased milk production over the first two lactations, we have no data for cows in their third to fifth lactation in this study. Since dams of heifers showed a greater plasma dehydration than dams of bulls, it is possible that they also have greater milk production; however, further studies are necessary to validate this hypothesis. While there were increases in serum protein parameters, these concentrations remained within the normal range reported for dairy cows (Alberghina et al., 2011). The different percentage changes in albumin and globulins also suggest that mechanisms other than dehydration may be involved in these differences. Low albumin levels associated with low urea levels are due to reduced protein catabolism – quite normal in this condition of protein anabolism.
Cows calving bulls had significantly higher levels of albumin at T1 and
significantly lower levels of total proteins at T3. These results could be
due to a different long-term effect of sex hormones on liver metabolism. It
is possible that the significant decrease in
The decrease of urea postpartum could be due to a decrease in nitrogen catabolism for milk protein synthesis. Values found at T2 in Group 2 cows are significantly lower than values in Group 1. Furthermore, this pattern difference could be explained by a long-term effect of fetal sex hormones on nitrogen metabolism. It is possible that male hormones divert proteins from catabolism to tissue formation in dams rather than in protein milk since lower milk yield for bulls is not compensated by higher protein and fat production (Hinde et al., 2014).
Serum glucose in dairy cows is derived mostly from gluconeogenesis. The findings that there were lower glucose concentrations in Group 2 cows pre- and postpartum than Group 1 cows suggest that gluconeogenesis in cows calving bulls is less effective in increasing blood glucose than those calving heifers. One regulator of glucose in ruminants is cortisol, which acts to increase gluconeogenesis from amino acids (Trenkle, 1981). It is possible that fetal sex could also affect cortisol levels during pregnancy as differences in cortisol have been reported in humans. For instance,women carrying male fetuses had lower levels of salivary cortisol during the second half of pregnancy compared with those carrying female fetuses (Di Pietro et al., 2011). For dairy cows, however, it is unknown as to whether there are differences in maternal cortisol levels related to differences in fetus gender. On the other hand, INSL3, a fetal hormone that is present only in cows carrying bull calves, has been reported to affect placental and maternal physiology (Anand-Ivell et al., 2011). It is possible that this hormone also affects postpartum glucose levels in cows with bull calves. In dairying, calves are removed on the day of birth and standardized mechanical procedures are used for milking, therefore results of sex differences on postpartum maternal serum are difficult to explain. Further studies are necessary to clarify these results.
Increased NEFA postpartum increases lipolysis of adipose tissue reserve in response to the energy deficit (Roche et al., 2009). In this study, the significantly higher levels of NEFA in Group 1 cows at T2 indicates a greater mobilization of energetically important tissue than in Group 2 cows, which could also explain the findings that total production of milk energy was greater in cows with a heifer calf (Hinde et al., 2014).
Taken together, the results of this study show that there are differences in hepatic metabolism in cows after partus of a bull or heifer. While BHB was not significantly affected by time or gender, there were significantly lower postpartum levels of total protein, albumin, urea, and glucose in cows with a bull than those with a heifer calf. Dairy cows undergo many metabolic adaptations as they transition from late pregnancy to early lactation. While these changes are normally coordinated by maternal hormones, the present findings suggest that fetal hormones also play a significant role in altering the physiological state of the cow during the transition period.
This work has been supported by the research funds of PRA 2013 code 60A08-0083/13 of the University of Padua. We would like to thank Francesca Arfuso for her valuable help in manuscript preparation and Winnie Y. Chan for her comments and help in English correction. Edited by: A.-E. Freifrau von Tiele-Winckler Reviewed by: two anonymous referees