Hostname: page-component-8448b6f56d-mp689 Total loading time: 0 Render date: 2024-04-19T10:52:44.468Z Has data issue: false hasContentIssue false

Rumen-protected choline supplementation in periparturient dairy goats: effects on liver and mammary gland

Published online by Cambridge University Press:  02 February 2011

A. BALDI
Affiliation:
Department of Veterinary Sciences and Technology for Food Safety, Veterinary Faculty, Università degli Studi di Milano, Via Celoria 10, 20133, Milano, Italy
R. BRUCKMAIER
Affiliation:
The Veterinary Medicine Faculty, University of Bern, Switzerland
F. D'AMBROSIO
Affiliation:
Department of Veterinary Sciences and Technology for Food Safety, Veterinary Faculty, Università degli Studi di Milano, Via Celoria 10, 20133, Milano, Italy
A. CAMPAGNOLI
Affiliation:
Department of Veterinary Sciences and Technology for Food Safety, Veterinary Faculty, Università degli Studi di Milano, Via Celoria 10, 20133, Milano, Italy
C. PECORINI
Affiliation:
Department of Veterinary Sciences and Technology for Food Safety, Veterinary Faculty, Università degli Studi di Milano, Via Celoria 10, 20133, Milano, Italy
R. REBUCCI
Affiliation:
Department of Veterinary Sciences and Technology for Food Safety, Veterinary Faculty, Università degli Studi di Milano, Via Celoria 10, 20133, Milano, Italy
L. PINOTTI*
Affiliation:
Department of Veterinary Sciences and Technology for Food Safety, Veterinary Faculty, Università degli Studi di Milano, Via Celoria 10, 20133, Milano, Italy
*
*To whom all correspondence should be addressed. Email: luciano.pinotti@unimi.it

Summary

The current study investigated the effects of supplementing rumen-protected choline (RPC) on metabolic profile, selected liver constituents and transcript levels of selected enzymes, transcription factors and nuclear receptors involved in mammary lipid metabolism in dairy goats. Eight healthy lactating goats were studied: four received no choline supplementation (CTR group) and four received 4 g RPC chloride/day (RPC group). The treatment was administered individually starting 4 weeks before expected kidding and continuing for 4 weeks after parturition. In the first month of lactation, milk yield and composition were measured weekly. On days 7, 14, 21 and 27 of lactation, blood samples were collected and analysed for glucose, β-hydroxybutyrate, non-esterified fatty acids and cholesterol. On day 28 of lactation, samples of liver and mammary gland tissue were obtained. Liver tissue was analysed for total lipid and DNA content; mammary tissue was analysed for transcripts of lipoprotein lipase (LPL), fatty acid synthase (FAS), sterol regulatory binding proteins 1 and 2, peroxisome proliferator-activated receptor γ and liver X receptor α. Milk yield was very similar in the two groups, but RPC goats had lower (P<0·05) plasma β-hydroxybutyrate. The total lipid content of liver was unaffected (P=0·890), but the total lipid/DNA ratio was lower (both P<0·05) in RPC than CTR animals. Choline had no effect on the expression of the mammary gland transcripts involved in lipid metabolism. The current plasma and liver data indicate that choline has a positive effect on liver lipid metabolism, whereas it appears to have little effect on transcript levels in mammary gland of various proteins involved in lipid metabolism. Nevertheless, the current results were obtained from a limited number of animals, and choline requirement and function in lactating dairy ruminants deserve further investigation.

Type
Animals
Copyright
Copyright © Cambridge University Press 2011

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

Baldi, A. & Pinotti, L. (2006). Choline metabolism in high-producing dairy cows; metabolic and nutritional basis. Canadian Journal of Animal Science 86, 207212.Google Scholar
Bauman, D. E., Perfield, J. W., Harvatine, K. J. & Baumgard, L. H. (2008). Regulation of fat synthesis by conjugated linoleic acid, lactation and the ruminant model. Journal of Nutrition 138, 403409.CrossRefGoogle ScholarPubMed
Bernard, L., Leroux, C. & Chilliard, Y. (2006). Characterisation and nutritional regulation of the main lipogenic genes in the ruminant lactating mammary gland. In Ruminant Physiology, Digestion, Metabolism and Impact of Nutrition on Gene Expression, Immunology and Stress (Eds Sejrsen, K., Hvelplund, T. & Nielsen, M. O.), pp. 295326. Wageningen, The Netherlands: Wageningen Academic Publishers.CrossRefGoogle Scholar
Brüsemeister, F. & Südekum, K. H. (2006). Rumen-protected choline for dairy cows, the in situ evaluation of a commercial source and literature evaluation of effects on performance and interactions between methionine and choline metabolism. Animal Research 55, 93104.CrossRefGoogle Scholar
Burton, K. (1956). A study of the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid. Biochemical Journal 62, 315323.CrossRefGoogle ScholarPubMed
Chung, Y. H., Cassidy, T. W., Girard, I. D., Cavassini, P. & Varga, G. A. (2005). Effects of rumen protected choline and dry propylene glycol on feed intake and blood metabolites of Holstein dairy cows. Journal of Dairy Science 88 (Suppl. 1), 61.Google Scholar
Cooke, R. F., Silva Del Río, N., Caraviello, D. Z., Bertics, S. J., Ramos, M. H. & Grummer, R. R. (2007). Supplemental choline for prevention and alleviation of fatty liver in dairy cattle. Journal of Dairy Science 90, 24132418.CrossRefGoogle ScholarPubMed
Emmanuel, B. & Kennelly, J. J. (1984). Kinetics of methionine and choline and their incorporation into plasma lipids and milk components in lactating goats. Journal of Dairy Science 67, 19121918.CrossRefGoogle ScholarPubMed
Folch, J., Lees, M. & Sloane-Stanley, G. H. (1957). A simple method for the isolation and purification of total lipids from animal tissues. Journal of Biological Chemistry 226, 497509.CrossRefGoogle ScholarPubMed
Grummer, R. R. (2006). Etiology, pathophysiology of fatty liver in dairy cows. In Production Diseases in Farm Animals (Eds Joshi, N. P. & Herdt, T. H.), pp. 141153. Wageningen, The Netherlands: Wageningen Academic Publishers.Google Scholar
Harvatine, K. J. & Bauman, D. E. (2006). SREBP1 and thyroid hormone responsive spot 14 (S14) are involved in the regulation of bovine mammary lipid synthesis during diet-induced milk fat depression and treatment with CLA. Journal of Nutrition 136, 24682474.CrossRefGoogle ScholarPubMed
Kinsella, J. E. (1973). Preferential labeling of phosphatidylcholine during phospholipid synthesis by bovine mammary tissue. Lipids 8, 393400.CrossRefGoogle ScholarPubMed
Lock, A. L., Rovai, M., Gipson, T. A., De Veth, M. J. & Bauman, D. E. (2008). A conjugated linoleic acid supplement containing trans-10, cis-12 conjugated linoleic acid reduces milk fat synthesis in lactating goats. Journal of Dairy Science 91, 32913299.CrossRefGoogle ScholarPubMed
Mcpherson, A. V. & Kitchen, B. J. (1983). Reviews of the progress of dairy science: the bovine milk fat globule membrane – its formation, composition, structure and behaviour in milk and dairy products. Journal of Dairy Research 50, 107133.Google Scholar
NRC (1981). Nutrient Requirements of Goats: Angora, Dairy, and Meat Goats in Temperate and Tropical Countries. Washington, DC: National Academy of Science.Google Scholar
Piepenbrink, M. S. & Overton, T. R. (2003). Liver metabolism and production of cows fed increasing amounts of rumen-protected choline during the periparturient period. Journal of Dairy Science 86, 17221733.CrossRefGoogle ScholarPubMed
Pinotti, L., Baldi, A. & Dell'Orto, V. (2002). Comparative mammalian choline metabolism with emphasis on role in ruminants, especially the high yielding dairy cow. Nutrition Research Reviews 15, 315331.CrossRefGoogle Scholar
Pinotti, L., Baldi, A., Politis, I., Rebucci, R., Sangalli, L. & Dell'Orto, V. (2003). Rumen protected choline administration to transition cows, effects on milk production and vitamin E status. Journal of Veterinary Medicine (Series A) 50, 1821.Google Scholar
Pinotti, L., Campagnoli, A., Sangalli, L., Rebucci, R., Dell'Orto, V. & Baldi, A. (2004). Metabolism in periparturient dairy cows fed rumen-protected choline. Journal of Animal and Feed Science 13 (Suppl. 1), 551554.CrossRefGoogle Scholar
Pinotti, L., Campagnoli, A., D'Ambrosio, F., Susca, F., Innocenti, M., Rebucci, R., Fusi, E., Cheli, F., Savoini, G., Dell'Orto, V. & Baldi, A. (2008). Rumen-protected choline and vitamin e supplementation in periparturient dairy goats, effects on milk production and folate, vitamin b12 and vitamin E status. Animal 2, 10191027.CrossRefGoogle ScholarPubMed
SAS (1999). SAS/STAT Software, Release 8.02. Cary, NC: SAS Institute Inc.Google Scholar
Zeisel, S. H. (1988). “Vitamin-like” molecules: A choline. In Modern Nutrition and Health and Disease (Eds Shils, M. E. & Young, V. R.), pp. 440452. Philadelphia, PA: Lea & Febiger.Google Scholar