Growth hormone and milking frequency act differently on goat mammary gland in late lactation.

In ruminants, milk yield can be affected by treatment with growth hormone (rbGH) and/or changes in frequency of milking. Frequent milkings encourage the maintenance of lactation, whereas infrequent milkings result in mammary involution. Our objective was to evaluate the influence of rbGH treatment and milking frequency on mammary gland morphology and milk composition. After adaptation to twice-daily milkings, six Saanen goats in late lactation were milked once daily from one udder-half and thrice-daily from the other udder-half. Concurrently, three of the six goats received daily injections of rbGH. After 23 d of treatment, milking frequency significantly affected milk yield (+8% vs. -26% for thrice- vs. once-daily milking). Additionally, treatments of rbGH increased milk yield from thrice-daily milked udder-halves (+19%), but failed to abate the reduction in milk yield from once-daily milked udder-halves (-31%). Mammary glands were heavier in the frequently milked udder-halves and in GH-treated goats. Based on histological and DNA analysis of mammary tissues, it was determined that milking frequency clearly affected epithelial cell numbers and alveolar diameter, whereas rbGH induced a potential cell hypertrophy and only a tendency to increase and/or maintain the mammary cell number. RNA concentration and kappa casein gene expression were not affected by treatments. In udder-halves milked once-daily, low casein:whey protein ratios, high Na+:K+ ratios, and high somatic cell counts (SCC) were indicative of changes in epithelial permeability, which rbGH treatment facilitated. The present data suggest that milking frequency and exogenous treatments of rbGH use different cellular mechanisms to influence mammary gland morphology and milk production.

[1]  A. Baldi,et al.  Bovine somatotropin administration to dairy goats in late lactation: effects on mammary gland function, composition and morphology. , 2002, Journal of dairy science.

[2]  D. Keisler,et al.  Use of somatic cells from goat milk for dynamic studies of gene expression in the mammary gland. , 2002, Journal of animal science.

[3]  M. Paape,et al.  Mammary cell number, proliferation, and apoptosis during a bovine lactation: relation to milk production and effect of bST. , 2001, Journal of dairy science.

[4]  K. Stelwagen Effect of Milking Frequency on Mammary Functioning and Shape of the Lactation Curve , 2001 .

[5]  V. Preedy,et al.  Differential expression of suppressors of cytokine signalling genes in response to nutrition and growth hormone in the septic rat. , 2001, The Journal of endocrinology.

[6]  G. Ooi,et al.  Role of the Suppressor of Cytokine Signaling-3 in Mediating the Inhibitory Effects of Interleukin-1β on the Growth Hormone-dependent Transcription of the Acid-labile Subunit Gene in Liver Cells* , 2000, The Journal of Biological Chemistry.

[7]  M. Paape,et al.  Modulation of the inflammatory reaction and neutrophil defense of the bovine lactating mammary gland by growth hormone. , 1999, Domestic animal endocrinology.

[8]  P. Rudland,et al.  Modulation of mammary development and programmed cell death by the frequency of milk removal in lactating goats , 1999, The Journal of physiology.

[9]  A. Kelly,et al.  Effect of decreased milking frequency of cows in late lactation on milk somatic cell count, polymorphonuclear leucocyte numbers, composition and proteolytic activity , 1998, Journal of Dairy Research.

[10]  C. Addey,et al.  Autocrine regulation of milk secretion. , 1998, Biochemical Society symposium.

[11]  S. Davis,et al.  Time course of milk accumulation-induced opening of mammary tight junctions, and blood clearance of milk components. , 1997, The American journal of physiology.

[12]  K. Stelwagen,et al.  Effect of milking frequency on milk somatic cell count characteristics and mammary secretory cell damage in cows. , 1996, American journal of veterinary research.

[13]  D. Flint,et al.  The role of prolactin and growth hormone in the regulation of casein gene expression and mammary cell survival: relationships to milk synthesis and secretion. , 1996, Endocrinology.

[14]  S. Davis,et al.  Continuous versus single drainage of milk from the bovine mammary gland during a 24 hour period , 1996, Experimental physiology.

[15]  A. Capuco,et al.  Comparison of growth hormone-releasing factor and somatotropin: thyroid status of lactating, primiparous cows. , 1995, Journal of dairy science.

[16]  S. Davis,et al.  EGTA-induced disruption of epithelial cell tight junctions in the lactating caprine mammary gland. , 1995, The American journal of physiology.

[17]  F. Ternois,et al.  Effects of recombinant bovine somatotropin on goat milk yield, composition and plasma metabolites , 1995 .

[18]  Davis,et al.  Effect of once daily milking (ODM) on enzyme activities in the bovine mammary gland , 1995 .

[19]  R. Dewhurst,et al.  Once daliy milking of dairy cows: relationship between yield loss and cisternal milk storage , 1994, Journal of Dairy Research.

[20]  S. Davis,et al.  Effect of once daily milking and concurrent somatotropin on mammary tight junction permeability and yield of cows. , 1994, Journal of dairy science.

[21]  S. Nickerson,et al.  The effects of a sustained-release recombinant bovine somatotropin (somidobove) on udder health for a full lactation. , 1994, Journal of dairy science.

[22]  C. J. Wilcox,et al.  Effects on production of milking three times daily on first lactation Holsteins and Jerseys in Florida. , 1994, Journal of dairy science.

[23]  R. Sherlock,et al.  Mammary epithelial cell tight junction integrity and mammary blood flow during an extended milking interval in goats. , 1994, Journal of dairy science.

[24]  C. Addey,et al.  Effect of unilateral changes in milking frequency on mammary mRNA concentrations in the lactating goat. , 1993, Biochemical Society transactions.

[25]  M. T. Travers,et al.  Isolation of a goat acetyl-CoA carboxylase complementary DNA and effect of milking frequency on the expression of the acetyl-CoA carboxylase and fatty acid synthase genes in goat mammary gland. , 1993, Comparative biochemistry and physiology. B, Comparative biochemistry.

[26]  C. Knight Milk yield responses to sequential treatments with recombinant bovine somatotrophin and frequent milking in lactating goats , 1992, Journal of Dairy Research.

[27]  C. Wilde,et al.  Milk yield and mammary function in goats during and after once-daily milking , 1990, Journal of Dairy Research.

[28]  C. Wilde,et al.  Galactopoietic and mammogenic effects of long-term treatment with bovine growth hormone and thrice daily milking in goats. , 1990, The Journal of endocrinology.

[29]  C. Knight,et al.  Milk yield and mammary function in dairy cows milked four times daily , 1990, Journal of Dairy Research.

[30]  L. Houdebine,et al.  An improvement of the single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. , 1990, BioTechniques.

[31]  A. Capuco,et al.  Somatotrophin increases thyroxine-5'-monodeiodinase activity in lactating mammary tissue of the cow. , 1989, The Journal of endocrinology.

[32]  I. Colditz Studies on the inflammatory response during involution of the ovine mammary gland. , 1988, Quarterly journal of experimental physiology.

[33]  Esther Seiden,et al.  Switch-back designs , 1988 .

[34]  M. O. Nielsen Effect of recombinantly derived bovine somatotropin on mammary gland synthetic capacity in lactating goats , 1988 .

[35]  C. Wilde,et al.  Effects of long-term thrice-daily milking on mammary enzyme activity, cell population and milk yield in the goat. , 1987, Journal of animal science.

[36]  M. Peaker,et al.  The effects of long-term thrice-daily milking on milk secretion in the goat: evidence for mammary growth. , 1985, Quarterly journal of experimental physiology.

[37]  T. Kiser,et al.  Influence of milking frequency on productive and reproductive efficiencies of dairy cows. , 1985, Journal of dairy science.

[38]  I. Hart,et al.  Effects of exogenous growth hormone on mammary function in lactating goats. , 1984, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

[39]  J. Bachellerie,et al.  Complete nucleotide sequence of mouse 18 S rRNA gene: comparison with other available homologs , 1984, FEBS letters.

[40]  W. E. Shainline,et al.  Sequential response of milk leukocytes, albumin, immunoglobulins, monovalent ions, citrate, and lactose in cows given infusions of Escherichia coli endotoxin into the mammary gland. , 1983, American journal of veterinary research.

[41]  M. Neville,et al.  Ionized calcium in milk and the integrity of the mammary epithelium in the goat. , 1981, The Journal of physiology.

[42]  K. Paigen,et al.  A simple, rapid, and sensitive DNA assay procedure. , 1980, Analytical biochemistry.

[43]  S. Pearl,et al.  Intramammary pressure and mammary blood flow in lactating goats. , 1973, Journal of dairy science.

[44]  H. Tucker,et al.  Relationships among mammary nucleic acids, milk yield, serum prolactin, and growth hormone in heifers from 3 months of age to lactation. , 1973, Journal of dairy science.

[45]  H. Tucker Regulation of mammary nucleic acid content by various suckling intensities. , 1966, The American journal of physiology.