Cows exposed to short day photoperiod during the dry period produce significantly more milk in their subsequent lactation than cows exposed to long days. The mechanism(s) underlying this effect are unknown. Because concentrations of prolactin (PRL) in circulation are consistently affected by changes in photoperiod, we hypothesized that alterations in the prolactin axis and sensitivity of the mammary gland to prolactin signaling may mediate photoperiodic effects in dry cows. The objective of this study was to determine the effects of exposure to different lengths of daylight during the dry period on circulating PRL and PRL receptor (PRL-R) mRNA expression in lymphocytes and mammary tissue during the transition to lactation. Multiparous Holstein cows were dried off 62 d before calving and assigned to long day (16 h light: 8 h dark) or short day photoperiod (8 h light: 16 h dark). During the dry period, PRL and PRL-R mRNA were analyzed biweekly in plasma and lymphocytes, respectively. Expression of PRL-R mRNA was assessed in mammary biopsies during the dry and periparturient periods. Dry matter intake (DMI) was recorded through 21 d of lactation, and milk yield was recorded until 120 d in milk. Short day photoperiod was associated with reduced PRL, whereas milk yield and expression of PRL-R mRNA in lymphocytes and mammary tissue were increased. Cows on short days had higher DMI during the dry period but did not differ in DMI after parturition. These data support the concept that greater responsiveness and sensitivity to PRL during transition to lactation may be associated with an increase in subsequent milk yield.

Recent evidence suggests that photoperiod influences immune function. Interestingly, photoperiod has profound effects on concentrations of prolactin (PRL), a hormone also known to be involved in fluctuations of the immune system. However, the impact of photoperiod on PRL receptor (PRL-R) expression is poorly understood, particularly in tissues of the immune system. Two experiments were performed to increase the general understanding of how photoperiod interacts with the immune system. Our first objective was to determine the effects of photoperiod on PRL-R mRNA expression and cellular immune function. Lymphocytes were isolated from blood collected from calves (n=10) and PRL-R mRNA expression of both long and short forms was quantified using real-time PCR. Lymphocytes expressed PRL-R mRNA, suggesting that PRL could act directly on these cells. To determine the relationship between photoperiod and PRL-R mRNA expression in other tissues, hepatic and mammary biopsies were collected after calves were exposed to long days (LDPP; 16 h light:8 h darkness) or short days (SDPP; 8 h light:16 h darkness). Relative to LDPP, SDPP decreased circulating PRL, but increased expression of both forms of PRL-R mRNA in liver, mammary gland and lymphocytes. Short days also increased lymphocyte proliferation compared with long days. Reversal of photoperiodic treatments reversed the effects on circulating PRL, PRL-R mRNA expression and lymphocyte proliferation. Our second objective was to manipulate PRL concentration in photoperiod-treated animals, using bromocriptine. Concentrations of PRL in LDPP animals injected daily with bromocriptine for 1 week were decreased compared with LDPP controls, to a level similar to SDPP animals. Receptor expression was increased in LDPP+bromocriptine-treated animals relative to LDPP controls, as was lymphocyte proliferation. Overall, our results indicate that photoperiodic effects on PRL-R mRNA expression were inverse to those on circulating PRL, with short days stimulating expression of both forms of PRL-R mRNA. Expression of PRL-R mRNA changed in the same direction as lymphocyte proliferation with regard to photoperiod treatment, suggesting a link between photoperiodic effects on PRL sensitivity and immune function. Thus, PRL signaling may mediate photoperiodic effects on immune function.

Previous research has demonstrated that extended photoperiod accelerates pubescence in dairy heifers thereby limiting time for mammary development, which could be detrimental to future milk yield. We hypothesized that the potential negative effects of rapid growth and puberty through long-day photoperiod (LDPP) exposure could be overcome with a greater supply of metabolizable protein in dairy heifers fed rumen-undegradable protein (RUP). In an initial slaughter study, we compared deuterium oxide (D2O) and direct chemical analysis to assess body composition at 5 and 7 mo of age in heifers (n = 20) exposed to LDPP or short-day photoperiod (SDPP). Before slaughter, D2O dilution was used to estimate body composition and results were compared with actual values determined by direct chemical analysis of body tissue. In 5-mo-old heifers, the correlations between estimates of body protein, water, and mineral contents as determined by D2O dilution and direct chemical analysis of body tissue were 0.86, 0.85, and 0.76, respectively; however, fat content values were not correlated (r = -0.068). In 7-mo-old heifers, we were unable to accurately estimate body composition using the D2O dilution method. A second study was conducted to determine if LDPP, which has previously been shown to hasten puberty, could be combined with RUP to promote lean growth without limiting body stature in prepubertal heifers. Thirty-two weaned heifers (86 +/- 2 d old; 106.2 +/- 17.3 kg of body weight) were assigned to LDPP or SDPP and RUP or control diet in a 2 x 2 factorial arrangement until the onset of puberty. Relative to SDPP, LDPP increased prolactin secretion and promoted lean growth. Exposure to LDPP also enhanced body weight, withers height, and heart girth. Furthermore, RUP supplementation increased withers height and heart girth. There was a significant interaction between LDPP and RUP for hip height. Moreover, LDPP hastened the onset of puberty. In summary, D2O was a feasible method to estimate lean composition in heifers at younger ages; however, it failed to accurately estimate body composition in heifers around puberty. Long-day photoperiod hastened puberty and accelerated lean growth without limiting skeletal growth in dairy heifers.