Abstract
Lifetime milk production is maximized when dairycows are pregnant during approximately 70% of eachlactation. Between lactations, a nonlactating period isnecessary for optimal milk production in the succeeding lactation. With cessation of milking, alveolarstructure is largely maintained and little or no loss ofcells occurs. However, increased apoptosis and cellproliferation, relative to that in lactating glands during the same stage of gestation, suggestthat a nonlactating period serves to promote cellturnover prior to the next lactation. Even in theabsence of pregnancy, mammary involution in dairyanimals occurs at a slower rate than in rodents;alveolar structure is maintained for several weeks andlactation can be reinitiated after four weeks or more ofinvolution. Although apoptosis appears to be initiated within a similar time frame to that in rodents,the maximum proportion of apoptotic epithelial cellsappears to be lower than in rodents, and apoptosis maybe accompanied by an initial increase in cell proliferation. The ability to manipulateapoptosis and cell proliferation during the nonlactatingperiod and during lactation is expected to provideenormous benefits to the dairy industry.
Similar content being viewed by others
REFERENCES
H. G. Sanders (1928). The variation in milk yields caused by season of the year service age and dry period and their elimination. J. Agr. Sci. 18:209–251.
E. W. Swanson (1965). Comparing continuous milking with sixty-day dry periods in successive lactations. J. Dairy Sci. 48:1205–1209.
J. T. Sorensen and C. Enevoldsen (1991). Effect of dry period length on milk production in subsequent lactation. J. Dairy Sci. 74:1277–1283.
C. E. Coppock, R. W. Everett, R. P. Natzke, and H. R. Ainslie (1974). Effect of dry period length on Holstein milk production and selected disorders at parturition. J. Dairy Sci. 57:712–718.
A. Smith, J. V. Wheelock, and F. H. Dodd (1966). Effect of milking throughout pregnancy on milk yield in the succeeding lactation. J. Dairy Sci. 49:895–896.
A. Smith, J. V. Wheelock, and F. H. Dodd (1967). The effect of milking throughout pregnancy on milk secretion in the succeeding lactation. J. Dairy Res. 34:145–150.
M. J. Paape and H. A. Tucker (1969). Influence of length of dry period on subsequent lactation in the rat. J. Dairy Sci. 52:518–522.
C. H. Knight and C. J. Wilde (1988). Milk production in concurrently pregnant and lactating goats mated out of season. J. Dairy Res. 55:487–493.
P. A. Fowler, C. H. Knight, and M. A. Foster (1991). Omitting the dry period between lactations does not reduce subsequent milk production in goats. J. Dairy Res. 58:13–19.
J. Hamann and J. Reichmuth (1990). Compensatory milk production within the bovine udder: effects of short-term non-milking of single quarters. J. Dairy Res. 57:17–22.
A. J. Henderson and M. Peaker (1983). Compensatory increases in milk secretion in response to unilateral inhibition by colchicine during lactation in the goat. J. Physiol. (Lond.) 334: 433–440.
A. V. Capuco and R. M. Akers (1990). Thymidine incorporation by lactating mammary epithelium during compensatory mammary growth in beef cattle. J. Dairy Sci. 73:3094–3103.
C. W. Turner and E. P. Reineke (1936). A study of the involution of the mammary gland of the goat. In Agric. Sta. Res. Bull. No. 235. University of Missouri, Columbia, pp. 1–23.
R. M. Akers and J. E. Keys (1985). Effect of suckling intensity on human growth hormone binding, biochemical composition and histological characteristics of ovine mammary glands. Dom. Anim. Endocrinol. 2:159–172.
R. M. Akers and C. W. Heald (1978). Stimulatory effect of prepartum milk removal on secretory cell differentiation in the bovine mammary gland. J. Ultrastructural Res. 63:316–322.
A. V. Capuco, R. M. Akers, and J. J. Smith (1997). Mammary growth in Holstein cows during the dry period: Quantification of nucleic acids and histology. J. Dairy Sci. 80:477–487.
B. D. Holst, W. L. Hurley, and D. R. Nelson (1987). Involution of the bovine mammary gland: Histological and ultrastructural changes. J. Dairy Sci. 70:935–944.
L. M. Sordillo and S. C. Nickerson (1988). Morphologic changes in the bovine mammary gland during involution and lactogenesis. Am. J. Vet. Res. 49:1112–1120.
W. L. Hurley (1989). Mammary gland function during involution. J. Dairy Sci. 72:1637–1646.
R. E. Goodman and F. L. Schanbacher (1991). Bovine lactoferrin mRNA: Sequence, analysis, and expression in the mammary gland. Biochem. Biophys. Res. Commun. 180:75–84.
A. K. Lascelles and C. S. Lee (1978). Involution of the Mammary Gland. In B. L. Larson (ed.), Lactation: A Comprehensive Treatise, Vol. IV, Academic Press, Inc., New York, pp. 115–177.
R. Strange, F. Li, S. Saurer, A. Burkhardt, and R. R. Friis (1992). Apoptotic cell death and tissue remodeling during mouse mammary gland involution. Development 115:49–58.
M. L. Li, J. D. Hu, K. Heermeier, L. Hennighausen, and P. A. Furth (1996). Apoptosis and remodeling of mammary gland tissue during involution proceeds through p53–independent pathways. Cell Growth Differ. 7:13–20.
N. I. Walker, R. E. Bennett, and J. F. Kerr (1989). Cell death by apoptosis during involution of the lactating breast in mice and rats. Am. J. Anat. 185:19–32.
C. J. Wilde, C. V. P. Addey, P. Li, and D. G. Fernig (1997). Programmed cell death in bovine mammary tissue during lactation and involution. Exp. Physiol. 82:943–953.
L. H. Quarrie, C. V. P. Addey, and C. J. Wilde (1996). Programmed cell death during mammary tissue involution induced by weaning, litter removal, and milk stasis. J. Cell. Physiol. 168:559–569.
L. Tatarczuch, C. Philip, and C. S. Lee (1997). Involution of the sheep mammary gland. J. Anat. 190:405–416.
K. Heermeier, M. Benedict, M. L. Li, P. Furth, G. Nunez, and L. Henninghausen (1996). Bax and Bcl-xs are induced at the onset of apoptosis in involuting mammary epithelial cells. Mech. Dev. 56:197–207.
H. Augsburger (1985). Electron microscopic study of mammary gland involution in goats. Zentralbl. Veterinarmed. [A] 32: 337–355.
R. M. Akers, W. E. Beal, T. B. McFadden, and A. V. Capuco (1990). Morphometric analysis of involuting bovine mammary tissue after 21 or 42 days on non-suckling. J. Anim. Sci. 68:3604–3613.
H. S. Pitkow, R. P. Reece, and G. L. Waszilycsak (1972). The integrity of mammary alveolar cells in two consecutive lactations. Proc. Soc. Exp. Biol. Med. 139:845–850.
C. J. Wilde and C. H. Knight (1989). Metabolic adaptations in mammary gland during the declining phase of lactation. J. Dairy Sci. 72:1679–1692.
G. Chepko and G. H. Smith (1997). Three division-competent, structurally-distinct cell populations contribute to murine mammary epithelial renewal. Tissue Cell 29:239–253.
E. C. Kordon and G. H. Smith (1998). An entire functional mammary gland may comprise the progeny from a single cell. Development 125:1921–1930.
G. H. Smith (1996). Experimental mammary epithelial morphogenesis in an in vivo model: Evidence for distinct cellular progenitors of the ductal and lobular phenotype. Breast Cancer Res. Treat. 39:21–31.
L. H. Quarrie, C. V. P. Addey, and C. J. Wilde (1994). Local regulation of mammary apoptosis in the lactating goat. Biochem. Soc. Trans. 22:178S.
L. R. Lund, J. Romer, N. Thomasset, H. Solberg, C. Pyke, M. J. Bissell, K. Dano, and Z. Werb (1996). Two distinct phases of apoptosis in mammary gland involution: Proteinase-independent and-dependent pathways. Development 122:181–193.
C. J. Wilde, C. H. Knight, and D. J. Flint (1999). Control of milk secretion and apoptosis during mammary involution. J. Mam. Gland Biol. Neoplasia 4:129–136.
Rights and permissions
About this article
Cite this article
Capuco, A.V., Akers, R.M. Mammary Involution in Dairy Animals. J Mammary Gland Biol Neoplasia 4, 137–144 (1999). https://doi.org/10.1023/A:1018769022990
Issue Date:
DOI: https://doi.org/10.1023/A:1018769022990