Hostname: page-component-848d4c4894-v5vhk Total loading time: 0 Render date: 2024-06-15T23:45:28.752Z Has data issue: false hasContentIssue false

Effect of stage of lactation on transport of colloidal carbon or Staphylococcus aureus from the mammary gland lumen to lymph nodes in guinea pigs

Published online by Cambridge University Press:  01 June 2009

Daniel I. Schenkman
Affiliation:
Department of Veterinary Science
David T. Berman
Affiliation:
Department of Veterinary Science
Brian S. Yandell
Affiliation:
Departments of Statistics and Horticulture, University of Wisconsin-Madison, Madison, WI 53706, USA

Summary

Guinea pig mammary glands which were either lactating, involuting or dry were infused with colloidal carbon or killed staphylococci. At different time intervals following infusion, animals were killed and the superficial inguinal lymph nodes examined for the presence of carbon. Sides which had nodes with visible carbon were designated ‘positive’. The time intervals from infusion to positive for the three groups were compared using logistic regression. The times required for 50 % of the sides to be positive were estimated to be ˜4 h for lactating glands, 32 h for those in involution, and 13 min for dry glands. Histological differences in distribution of carbon in the mammary tissue suggest that differences in transit time may have been due to different mechanisms of transport through the glands in the three different physiological states. The distribution of bacteria was similar to that of the carbon in the corresponding tissues.

Type
Original Articles
Copyright
Copyright © Proprietors of Journal of Dairy Research 1985

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Allen, J. C., Neville, M. C., Seacat, J. M., Casey, C. E. & Neifert, M. R. 1984 Amino acids in milk in cystinuria. New England Journal of Medicine. 310 1332Google Scholar
Baker, R. J. & Nelder, J. A. 1978 The GLIM system, release. 3: generalized linear interactive modeling. Oxford: Numerical Algorithms GroupGoogle Scholar
Bookman, D. E., Boydston, W. R. & Beezhold, D. H. 1983 The role of epithelial cells in gut-associated immune reactivity. Annals of the New York Academy of Sciences 409 129143Google Scholar
Bourne, F. J., Newby, T. J. & Chidlow, J. W. 1975 The influence of route of administration of vaccination on the systemic and local immune response in the pig. Research in Veterinary Science 18 244248Google Scholar
Brandon, M. R., Watson, D. L. & Lascelles, A. K. 1971 The mechanism of transfer of immunoglobulin into the mammary secretion of cows. Australian Journal of Experimental Biology and Medical Science 49 613623CrossRefGoogle ScholarPubMed
Brooker, B. E. 1983 Pseudopod formation and phagocytosis of milk components by epithelial cells of the bovine mammary gland. Cell and Tissue Research 229 639650CrossRefGoogle ScholarPubMed
Brooker, B. E., Frost, A. J. & Hill, A. W. 1981 At least two toxins are involved in Escherichia coli mastitis. Experientia 37 290292Google Scholar
Chandler, R. L., Smith, K. & Turkey, B. A. 1980 Studies on the phagocytic potential of secretory epithelial cells in experimental mastitis. Journal of Comparative Pathology 90 385394CrossRefGoogle ScholarPubMed
Chang, C. C., Winter, A. J. & Norcross, N. L. 1981 Immune response in the bovine mammary gland after intestinal, local, and systemic immunization. Infection and Immunity 31 650659Google Scholar
De Cueninck, B. J. 1979 Immune-mediated inflammation in the lumen of the bovine mammary gland. International Archives of Allergy and Applied Immunology 59 394402CrossRefGoogle ScholarPubMed
Derbyshire, J. B. & Berman, D. T. 1968 Leukocytic responses of the bovine udder to infusion of certain irritants. American Journal of Veterinary Research 29 19711977Google ScholarPubMed
Desiderio, J. V. & Campbell, S. G. 1980 Bovine mammary gland macrophage: isolation, morphological features, and cytophilic immunoglobulins. American Journal of Veterinary Research 41 15951599Google Scholar
Fieller, E. C. 1940 The biological standardization of insulin. Journal of the Royal Statistical Society supp. 7 164Google Scholar
Jensen, D. L. & Eberhart, R. J. 1975 Macrophages in bovine milk. American Journal of Veterinary Research 36 619624Google Scholar
Lee, C. S. & Lasoelles, A. K. 1969 The histological changes in involuting mammary glands of ewes in relation to local allergic response. Australian Journal of Experimental Biology and Medical Science. 47 613623CrossRefGoogle ScholarPubMed
Lee, C. S., Mcdowell, G. H. & Lascelles, A. K. 1969 The importance of macrophages in the removal of fat from the involuting mammary gland. Research in Veterinary Science 10 3438CrossRefGoogle ScholarPubMed
Linzell, J. L. & Peaker, M. 1971 The permeability of mammary ducts. Journal of Physiology 216 701716CrossRefGoogle ScholarPubMed
Mcghee, J. R. & Mestecky, J. (Eds) 1983 The secretory immune system. Annals of the New York Academy of Sciences 409.Google Scholar
Naukarrinen, A. & Sorvari, T. E. 1980 Cellular transport of colloidal carbon in the follicle-associated epithelium of the chicken bursa of Fabricius. Journal of the Reticuloendothelial Society 28 473482Google Scholar
Pitelka, D. R. 1983 The mammary gland. In Histology: Cell and Tissue Biology (5th ed.) pp, 944965 (Ed. Weiss, L.). New York: Elsevier BiomedicalGoogle Scholar
Taroowski, S. P. & Berman, D. T. 1975 Leukocytic response of bovine mammary gland to injection of killed cells and cell walls of Staphylococcus aureus. American Journal of Veterinary Research 36 15611565Google Scholar
Watson, D. L. 1982 The influence of site of antigen deposition on the local immune response in the mammary gland of the ewe. Microbiology and Immunology 26 423430Google Scholar