Hostname: page-component-586b7cd67f-g8jcs Total loading time: 0 Render date: 2024-11-26T20:26:27.507Z Has data issue: false hasContentIssue false

The effects of dietary selenium on growth and selected reproductive parameters in young boars

Published online by Cambridge University Press:  02 September 2010

M. C. Henson
Affiliation:
The University of Tennessee, Department of Animal Sciences, Knoxville, Tennessee 37996, USA
H. G. Kattesh
Affiliation:
The University of Tennessee, Department of Animal Sciences, Knoxville, Tennessee 37996, USA
J. P. Hitchcock
Affiliation:
The University of Tennessee, Department of Animal Sciences, Knoxville, Tennessee 37996, USA
S. A. Kincaid
Affiliation:
The University of Tennessee, Department of Animal Sciences, Knoxville, Tennessee 37996, USA
Get access

Abstract

Thirty-three crossbred boars, 47 to 58 days of age, were randomly allocated to receive maize-soya bean meal diets containing 0·05, 0·15 or 0·30 mg selenium per kg. Body weights, testicular widths, and blood samples from vena cava puncture were taken at regular intervals. Libido was subjectively scored upon exposure to ovariectomized-oestrogenized gilts. Seven animals from each group were slaughtered at 9 months of age and selected reproductive structures were retrieved. Analysis of the relationships among body weight, libido and plasma testosterone levels indicated that differences (P < 0·01) existed between treatments, as analyzed over time, but that the overall treatment effect was not significant. Testicular widths were also found to be different (P < 0·05) over time. Values for all four criteria as measured over time were greater for boars fed 0·05 mg selenium per kg than for those fed 0·15 which were in turn greater than those fed 0·30. Post-mortem examination showed no treatment differences (1) in testis weights; (2) spermatozoan concentrations within the capita, corporea or caudae segments of the epididymis and (3) spermatozoan morphology examined within the caudae epididymis. Also testis lengths, weights, circumferences and spermatozoan concentrations were not significantly different between treatments. These results suggest that boars fed selenium at 0·15 or 0·30 mg/kg may exhibit some signs of retarded sexual development for a short period preceding the onset of sexual maturity

Type
Research Article
Copyright
Copyright © British Society of Animal Science 1983

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

Amann, R. P. and Lambaise, J. T. Jr 1969. The male rabbit. III. Determination of daily sperm production by means of testicular homogenates. J. Anim. Sci. 28: 369374.Google Scholar
Anderson, L. L. 1974. Pigs. In Reproduction in Farm Animals. 3rd ed. (ed. Hafez, E. S. E.), pp. 275287. Lea and Febiger. Philadelphia.Google Scholar
Gould, T. C. 1970. Incorporation of minerals in spermatogenic pathway. J. Andrology 1: 5658.Google Scholar
Gray, R. C., Day, B. N., Lasley, J. F. and Tribble, L. F. 1971. Testosterone levels of boars at various ages. J. Anim. Sci. 33: 124126.CrossRefGoogle ScholarPubMed
Gunn, S. A. and Gould, T. C. 1970. Cadmium and other mineral elements. In The Testis. Vol. III (ed. Johnson, A. D., Gomes, W. R. and Vandemark, N. L.), pp. 377481. Academic Press. New York.Google Scholar
Gunn, S. A., Gould, T. C. and Anderson, W. A. D. 1967. Incorporation of selenium into spermatogenic pathway in mice. Proc. Soc. exp. Biol. Med. 124: 1260–1236.Google Scholar
Kattesh, H. G., Kornegay, E. T., Gwazdauskas, F. C., Knight, J. W. and Thomas, H. R. 1979. Periphera plasma testosterone concentration and sexual behavior in young prenatally stressed boars. Theriogenology 12: 289305.Google Scholar
Luna, L. C. 1968. Manual of Hisrologic Staining Methods of Armed Forces Institute of Pathology. 6th ed. McGraw-Hill, New York.Google Scholar
Mahone, J. P., Berger, T., Clegg, E. D. and Singleton, W. L. 1979. Photoinduction of puberty in boars during naturally occurring short day lengths. J. Anim. Sci. 48: 11591164.CrossRefGoogle ScholarPubMed
Nelssen, J. L., Davis, D. L., Hines, R. H., Craig, J. V. and Robl, J. M. 1980. Effects of exposure to mature females on boar reproductive development. J. Anim. Sci. 51: Suppl. 1, p. 309 (Abstr.).Google Scholar
Pond, W. G. and Houpt, K. A. 1978. The Biology of the Pig. Comstock, Ithaca. New York.Google Scholar
Rosenfield, I. 1964. Metabolic effects and metabolism of selenium in animals. Bull. Univ. Wyoming Agric. Exp. Stn No. 414, pp. 3552.Google Scholar
L, Senger. P. 1980. Influence of selenium supplementation on sperm and seminal quality. Adv. Anim. Breeder, May 15. p. 4.Google Scholar
Smith, D. G., Senger, P. L., McCutchan, J. F. and Landa, C. F. 1978. Selenium and glutathione peroxidase distribution in bovine semen. J. Anim. Sci. 47: Suppl. 1, p. 389 (Abstr).Google Scholar
Statistical Analysis System. 1979. SAS User's Guide, pp. 121130. Statistical Analysis Systems Institute, Cary, NC.Google Scholar
Wettemann, R. P., Wells, M. E., Omtvedt, I. T., Pope, C. E. and Turman, E. J. 1976. Influence of elevated ambient temperature on reproductive performance of boars. J. Anim. Sci. 42: 664669.CrossRefGoogle ScholarPubMed
Wu, A. S. H., Oldfield, J. E.Shull, L. R. and Cheeke, P. R. 1979. Specific effect of selenium deficiency on rat sperm. Biol. Reprod. 20: 793798.CrossRefGoogle ScholarPubMed
Wu, A. S. H., Oldfield, J. E., Whanger, P. D. and Weswig, P. H. 1973. Effect of selenium, vitamin E, and antioxidants on testicular function in rats. Biol. Reprod. 8: 625629.Google Scholar