Optimization of Pulsation Rate of the Milking System for the Mammary Gland Remodeling during Involution in Thai Crossbred Holstein Cows

A. Tiantong, K. Sasiwimonrit, S. Saengwong, W. Inyawilert, A. Chaokaur, S. E. Chen

Abstract

This study aimed to investigate the effects of pulsation rate of the milking machine on the proteinous components and gelatinase activity in the mammary secretion for optimal tissue remodeling during the dry period in tropical dairy cows. Nine healthy primiparous Thai crossbred Holstein cows (75%HF) were milked with various pulsation rates (50, 60, and 70 cycles/min) one week after calving. The total protein contents of the secretions increased along the time course in 50 and 60 cycles/min groups but not in 70 cycles/min group and were not different among the 3 groups along the time course. Lactoferrin and BSA abundance of the 3 groups as well as γ-globulin in 50 and 70 cycles/min groups also increased in a time-dependent manner, in which only γ-globulin abundance in 60 cycles/min group 14 days before drying off and lactoferrin in 50 cycles/min group 14 days after drying off were significantly higher than those of the other 2 groups. In tissue remodeling by gelatinase activity analysis, 50 cycles/min group showed dramatic increases of Matrix metalloproteinase-9 (MMP-9) and MMP-2 activities after drying off, whereas 60 and 70 cycles/min groups had a significant but a smaller change (p<0.05) along the time course. Cows with 60 cycles/min exhibited dramatic increases of MMP-9 and MMP-2 activities than the other groups before drying off (p<0.05). The findings suggested that milking pulsation rate at 60 cycles/min resulted in higher activity of remodeling during mammary involution and thus may benefit the renewal and health of the udder in the long run.

References

Atigui, M., P.G. Marnet, A. Barmat, T. Khorchani, & M. Hammadi. 2015. Effects of vacuum level and pulsation rate on milk ejection and milk flow traits in Tunisian dairy camels (Camelus dromedarius). Trop. Anim. Health Prod. 47: 201-206. https://doi.org/10.1007/s11250-014-0708-0
Besier, J., & R.M. Bruckmaier. 2016. Vacuum levels and milk-flow-dependent vacuum drops affect machine milking performance and teat condition in dairy cows. J. Dairy Sci. 99: 3096-3102. https://doi.org/10.3168/jds.2015-10340
Besier, J., O. Lind, & R.M. Bruckmaier. 2016. Dynamics of teat-end vacuum during machine milking: types, causes and impacts on teat condition and udder health - a literature review. J. Appl. Anim. Res. 44: 263-272. https://doi.org/10.1080/09712119.2015.1031780
Boutinaud, M., C. Rousseau, D.H. Keisler, & H. Jammes. 2003. Growth hor-mone and milking frequency act differently on goat mammary gland in late lactation. J. Dairy Sci. 86: 509-510. https://doi.org/10.3168/jds.S0022-0302(03)73629-7
Chen, W.Y., M.H. Weng, S.E. Chen, H.C. Peh, W.B. Liu, T.C. Yu, M.T. Chen, H. Naganata, & C.J. Chang. 2007. Profile of gelatinolytic capacity in raw goat milk and the implication for milk quality. J. Dairy Sci. 90: 4954-4965. https://doi.org/10.3168/jds.2007-0366
De Vries, L.D., H. Dover, T. Casey, M.J. VandeHaar, & K. Plaut. 2010. Characterization of mammary stromal remodeling during the dry period. J. Dairy Sci. 93: 2433-2443. https://doi.org/10.3168/jds.2009-2764
Ferneborg, S., & K. Svennersten-Sjaunja. 2015. The effct of pulsation ratio on teat condition, milk somatic cell count and productivity in dairy cows in automatic milking. J. Dairy Res. 82: 453-459. https://doi.org/10.1017/S0022029915000515
Ferranti, P., M.V. Traisci, G. Picariello, A. Nasi, V. Boschi, M. Siervo, C. Falconi, L. Chianese, & F. Addeo. 2004. Casein proteolysis in human milk : tracing the pattern of casein breakdown and the formation of potential abioactive peptides. J. Dairy Res. 71: 74-87. https://doi.org/10.1017/S0022029903006599
Gifre-Renom, L., J.V. Carratalá, S. Parés, L. Sánchez-García, N. Ferrer-Miralles, A. Villaverde, A. Bach, Elena Garcia-Fruitós, & Anna Arís. 2020. Potential of MMP-9 based nanoparticles at optimizing the cow dry period: pulling apart the effects of MMP-9 and nanoparticles. Sci. Rep. 10: 11299. https://doi.org/10.1038/s41598-020-67176-2
Ho, C.H., C.J. Chang, W.B. Liu, H.C. Peh, S.E. Chen, H.Y. Chen, T.H. Ho, M.T. Chen, & H. Nagahata. 2010. In situ generation of milk protein derived peptides in drying-off cows. J. Dairy Res. 77: 487-497. https://doi.org/10.1017/S0022029910000634
Hurley, W.L. & P.K. Theil. 2011. Perspectives on immunoglobulins in colostrum and milk. Nutrients. 3: 442-474. https://doi.org/10.3390/nu3040442
Hynes, R.O. 2009. The extracellular matrix: Not just pretty fibrils. Science. 326: 1216-1219. https://doi.org/10.1126/science.1176009
Khokha, R., & Z. Werb. 2011. Mammary gland reprogramming:metalloproteinases couple form with function. Cold Spring Harb. Perspect. Biol. 3: a004333. https://doi.org/10.1101/cshperspect.a004333
Laemmli, U.K. 1970. Cleavage of structural proteins during assembly of the head bacteriophage T4. Nature 227:680-685. https://doi.org/10.1038/227680a0
Li, H., H. Zheng, L. Li, X. Shen, W. Zang, & Y. Sun. 2016. The effects of matrix metalloproteinase-9 on dairy goat mastitis and cell survival of goat mammary epithelial cells. Plos one. 11: e0160989. https://doi.org/10.1371/journal.pone.0160989
Maldonado, M., & J. Nam. 2013. The role of changes in extracellular matrix of cartilage in the presence of inflammation on the pathology of osteoarthritis. BioMed Res. Int. 2013: 284873. https://doi.org/10.1155/2013/284873
Mein, G.A. 2012. The role of the milking machine in mastitis control. Vet. Clin. N. Am. Food Anim. Pract. 28: 307-320. https://doi.org/10.1016/j.cvfa.2012.03.004
Miller, N., L. Delbecchi, D. Petitclerc, G.F. Wagner, B.G. Talbot, & P. Lacasse. 2006. Effect of stage of lactation and parity on mammary gland cell renewal. J. Dairy Sci. 89: 4669-4677. https://doi.org/10.3168/jds.S0022-0302(06)72517-6
Nielsen, S.S. 2002. Plasmin system and microbial proteases in milk: characteristics, roles, and relationship. J. Agric. Food Chem. 50: 6628-6634. https://doi.org/10.1021/jf0201881
Osteras, O., O. Ronningen, L. Sandvik, & S. Waage. 1995. Field studies show associations between pulsator characteristics and udder health. J. Dairy Res. 62:1-13. https://doi.org/10.1017/S0022029900033628
Penry, J.F., J. Upton, S. Leonardi, P.D. Thompson, & D.J. Reinemann. 2018. A method for assessing teatcup liner performance during the peak milk flow period. J. Dairy Sci. 101: 649-660. https://doi.org/10.3168/jds.2017-12942
Pezeshki, A., A.V. Capuco, B. De Spiegeleer, L. Peelman, M. Stevens, R.J. Collier, & C. Burvenich. 2010. An integrated view on how the management of the dry period length of lactating cows could affect mammary biology and defense. J. Anim. Physiol. Anim. Nutr. 94: e7-e30. https://doi.org/10.1111/j.1439-0396.2010.00991.x
Piamya, P., A. Tiantong, S.E. Chen, W.B. Liu, C. Yu, H. Nagahata, & C.J. Chang. 2015. Fingerprinting of gelatinase subtypes for different topographic regions on non-retaining placenta of Holstein cows. Animal. 9: 490-499. https://doi.org/10.1017/S1751731114002420
Raimondo, R.F.S., F.B. Brandespim, A.P. M. Prina, S.I. Miyashiro, J.P.E. Saut, C.S. Mori, F.C. Ponliani, & E.H. Birgel Junior. 2013. Dynamic in the concentration of whey proteins in the mammary secretion of goats during the dry period. Small Ruminant Res. 113: 239-246. https://doi.org/10.1016/j.smallrumres.2013.03.006
R Core Team. 2018. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. http://www.R-project.org/.
Romero, G., C. Peris, G. C. Fthenakis, & J. R. Diaz. 2020. Effects of machine milking on udder health in dairy ewes. Small Ruminant Res. 188: 106096. https://doi.org/10.1016/j.smallrumres.2020.106096
Sorensen, M.T., J.V. Norgaard, P.K. Theil, M. Vestergaard, & K. Sejrsen. 2006. Cell turnover and activity in mammary tissue during lactation and the dry period in dairy cows. J. Dairy Sci. 89: 4632-4639. https://doi.org/10.3168/jds.S0022-0302(06)72513-9
Stelwagen, K., & K. Singh. 2014. The role of tight junctions in mammary gland function. J. Mammary Gland Biol. Neoplasia. 19: 131-138. https://doi.org/10.1007/s10911-013-9309-1
Tiantong, A., & D.A. Mwabena. 2019. The effects of parity on protective protein components and MMP proteolytic activity of mammary secretion during involution in tropical dairy cows. Adv. Anim. Vet. Sci. 7: 914-920. https://doi.org/10.17582/journal.aavs/2019/7.10.914.920
Tiantong, A, H.Y. Peng, S.E. Chen, P. Piamya, W.B. Liu, M.T. Chen, C. Yu, H. Nagahata, & C.J. Chang. 2015a. Intramammary infusion of an Enterococcus faecium SF68 preparation promoted the involution of drying off Holstein cows partly related to neutrophil-associated matrix metalloproteinase 9. Anim. Sci. J. 86: 111-119. https://doi.org/10.1111/asj.12243
Tiantong, A, P. Piamya, S.E. Chen, W.B. Liu, F.Y. Chang, P.C. Lin, H. Nagahata, & C.J. Chang. 2015b. Systemic and local bactericidal potentiality in late lactation Holstein-Friesian cows following a combined antibiotics and Enterococcus faecium SF68 dry-cow treatment. Jpn. J. Vet. Res. 63: 139-150.
Tromas, C.V., D.K. Force, D.H. Bremel, & S. Strasser. 1991. Effects of pulsation ratio, pulsation rate, and teatcup liner design on milking rate and milk production. J. Dairy Sci. 74: 1234-1249. https://doi.org/10.3168/jds.S0022-0302(91)78280-5
Upton, J, J.F. Penry, M.D. Rasmussen, P.D. Thompson, & D.J. Reinemann. 2016. Effect of pulsation rest phase duration on teat end congestion. J. Dairy Sci. 99: 3958-3965. https://doi.org/10.3168/jds.2015-10466
Weng, M.H., T.C. Yu, S.E. Chen, H.C. Peh, W.B. Liu, M.T. Chen, H. Nagahata, & C.J. Chang. 2008. Regional accretion of gelatinase B in mammary gland during gradual and acute involution of dairy animals. J. Dairy Res. 75: 202-210. https://doi.org/10.1017/S0022029908003130
Wenz, J.R, L.K. Fox, F.J. Muller, M. Rinaldi, R. Zeng, & D.D. Bannerman. 2010. Factors associated with concentrations of select cytokine and acute phase proteins in dairy cows with naturally occurring clinical mastitis. J. Dairy Sci. 93: 2458-2470. https://doi.org/10.3168/jds.2009-2819
Yu, T.C., C.J. Chang, C.H. Ho, H.C. Peh, S.E. Chen, W.B. Liu, H.Y. Peng, P. Piamya, M.T. Chen, & H. Nagahata. 2011. Modifications of the defense and remodeling functionalities of bovine neutrophils inside the mammary gland of milk stasis cows received a commercial dry-cow treatment. Vet. Immunol. Immunopathol. 144: 210-219. https://doi.org/10.1016/j.vetimm.2011.09.006
Yu, T.C, S.E. Chen, T.H. Ho, H.C. Peh, W.B. Liu, A. Tiantong, H. Nagahata, & C. J. Chang. 2012 Involvement of TNF-α and MAPK pathway in the intramammary MMP-9 release via degranulation of cow neutrophils during acute mammary gland involution. Vet. Immunol. Immunopathol. 147: 161:169. https://doi.org/doi:10.1016/j.vetimm.2012.04.011

Authors

A. Tiantong
tiantong_a@su.ac.th (Primary Contact)
K. Sasiwimonrit
S. Saengwong
W. Inyawilert
A. Chaokaur
S. E. Chen
TiantongA., SasiwimonritK., SaengwongS., InyawilertW., ChaokaurA., & Chen S. E. (2021). Optimization of Pulsation Rate of the Milking System for the Mammary Gland Remodeling during Involution in Thai Crossbred Holstein Cows. Tropical Animal Science Journal, 44(1), 32-38. https://doi.org/10.5398/tasj.2021.44.1.32

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