Objectives were to determine effects of continuous milking (CM) and bovine somatotropin (bST) administration on 1) mammary epithelial cell (MEC) proliferation, apoptosis, and ultrastructure during late gestation and early lactation, 2) expression of genes associated with proliferation, and apoptosis in mammary epithelial cells, and 3) milk yield and composition. Second-gestation, first dry-period cows were randomly assigned to either continuous bST throughout late gestation and early lactation (+bST; n = 4) or no bST (-bST; n = 4) administration. Within each animal, udder halves were randomly assigned to CM or a 60-d dry period (control) treatment. Daily milk yield and weekly milk composition were measured during the last 60 d of gestation in CM halves and from 1 to 30 d postpartum for both halves. Mammary biopsies were obtained at -20 +/- 7, -8 +/- 3, +1 +/- 0, +7 +/- 0, and +20 +/- 0 d (mean +/- standard error) relative to parturition. Prepartum half-udder milk yield was greater in +bST cows than in -bST cows (9.9 vs. 8.2 kg/d) and postpartum half-udder milk yields were dramatically reduced in CM halves compared with control halves (10.6 vs. 22.2 kg/d), regardless of bST treatment. Proliferation of MEC was reduced in CM halves at -8 d (2.7 vs. 5.4%). Apoptosis of MEC was elevated during early lactation for d +1 and +7 in control halves, but was only increased at d +1 in CM halves. Turnover of MEC was not affected by bST. Ultrastructure data indicated complete involution of the control half and lactation maintenance in CM glands (d -20). By d -8, control tissue contained alveoli in an immature secretory state, but CM tissue contained both lactating and immature alveoli. Postpartum ultrastructure parameters were similar between halves until d 20 when control tissue was composed of a homogeneous population of lactating alveoli, but CM tissue contained lactating, engorged, and resting alveoli. Expression of CCAAT/enhancer binding protein-beta (CEBP-beta), cyclin D1, and bcl(2) were up-regulated during late gestation, but did not differ between control and CM halves. Expression of alpha-lactalbumin was increased in CM halves during late gestation, but was not different in CM and control tissue after parturition. Other genes evaluated (bax, insulin-like growth factor binding protein 5, ATP-binding cassette 1, and p27) were not differentially expressed at any timepoints evaluated. Results indicate that CM reduced subsequent half-udder milk yield in primiparous cows through altered MEC turnover and secretory capacity. Negative effects of CM on the subsequent lactation were not alleviated by bST supplementation.
A dry period, typically 40 to 60 d, between lactations is believed to be required to maximize milk yield in the subsequent lactation. Several hypotheses have been proposed to explain the requirement for the dry period, including (1) replenishment of body reserves, (2) regeneration of mammary tissue, and (3) optimization of benefits from endocrine events near the time of parturition. Continuously milked cows or glands have depressed milk yields but no differences in mammary DNA content or cell number. Nutritional status and endocrine hormones are not factors in reduced milk yield in continuously milked glands. Data from continuous lactation studies suggest that depressed milk yields are due to reduced functionality of mammary parenchyma. There is a need to reevaluate effects of continuous lactation on milk yield in today's high-producing dairy cow because studies on this topic were done using cows achieving peak milk production of 18 to 30 kg/d compared with 45 to 50 kg/d in today's dairy cows. Another factor that has not been considered in conjunction with current milk production levels is the use of bovine somatotropin (bST). Supplementation with bST increases milk yield, improves lactation persistency, and may improve milk yield in continuously milked cows. Future research goals are to examine the effects of continuous lactation in high-producing cows and to determine the effects of bST on milk yield and mammary functionality in continuously milked cows.
As an important source of nutrients, milk provides high-quality protein, energy, calcium and a variety of vitamins and minerals. Recent research has focused on altering the fat and protein content of milk and other dairy products in order to improve the nutrient content of these foods so that they more aptly reflect current dietary recommendations and trends. For example, diet is a contributing factor to the onset or progression of some cancers, with epidemiological studies indicating diet composition may be related to 35 percent of human cancer deaths.11 A few substances in our diet have been identified as anti-carcinogens, but most are of plant origin and are only present in trace concentrations. However, conjugated linoleic acid (CLA), a component of milk fat, introduces an exciting twist to what we know about diet and cancer. Unlike most naturally occurring anticarcinogens, CLA is potent at extremely low levels and present in foods from ruminant animals.
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