Effects of parenteral administration of vitamin E on health of periparturient dairy cows

Ronald J. Erskine From the Department of Large Animal Clinical Sciences, College of Veterinary Medicine, Michigan State University, East Lansing, MI 48824.

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 DVM, PhD
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Paul C. Bartlett From the Department of Large Animal Clinical Sciences, College of Veterinary Medicine, Michigan State University, East Lansing, MI 48824.

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Thomas Herdt From the Department of Large Animal Clinical Sciences, College of Veterinary Medicine, Michigan State University, East Lansing, MI 48824.

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Patrick Gaston From the Department of Large Animal Clinical Sciences, College of Veterinary Medicine, Michigan State University, East Lansing, MI 48824.

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Objective—

To determine the effect of administration of vitamin E (D-α-tocopherol) on the incidence of retained placenta, metritis, and clinical mastitis during early lactation and on tocopherol concentrations.

Design—

Prospective randomized controlled study.

Animals—

420 Holstein cows

Procedure—

Vitamin E (3,000 mg, IM, once) was administered to 204 cows 8 to 14 days before expected parturition, and 216 control cows were not treated. The number of cows that had retained placenta, metritis, clinical mastitis, displaced abomasum, and clinically apparent acetonemia or hypocalcemia were recorded. Serum concentrations of tocopherol, the tocopherol:cholesterol ratio, and glutathione-peroxidase activity were determined from samples obtained before administration of vitamin E, 7 and 14 days after administration, and at 30 days after parturition from 36 treated and 36 control cows.

Results—

Administration of vitamin E significantly decreased the incidence of retained placenta and metritis (13/204 [6.4%] and 8/204 [3.9%], respectively, for the vitamin E-treated group; 27/216 [12.5%] and 19/216 [8.8%], respectively, for the untreated group) but did not affect the incidence of clinical mastitis. Serum vitamin E concentration was significantly higher in treated than in control cattle at 7 and 14 days after administration, but serum tocopherohcholesterol ratio was significantly higher only at 7 days after administration.

Clinical Implications—

Parenteral administration of a single injection of vitamin E before parturition may decrease the incidence of retained placenta and metritis in dairy cows but will increase serum concentrations for 7 to 14 days after administration. (J Am Vet Med Assoc 1997;211:466–469)

Objective—

To determine the effect of administration of vitamin E (D-α-tocopherol) on the incidence of retained placenta, metritis, and clinical mastitis during early lactation and on tocopherol concentrations.

Design—

Prospective randomized controlled study.

Animals—

420 Holstein cows

Procedure—

Vitamin E (3,000 mg, IM, once) was administered to 204 cows 8 to 14 days before expected parturition, and 216 control cows were not treated. The number of cows that had retained placenta, metritis, clinical mastitis, displaced abomasum, and clinically apparent acetonemia or hypocalcemia were recorded. Serum concentrations of tocopherol, the tocopherol:cholesterol ratio, and glutathione-peroxidase activity were determined from samples obtained before administration of vitamin E, 7 and 14 days after administration, and at 30 days after parturition from 36 treated and 36 control cows.

Results—

Administration of vitamin E significantly decreased the incidence of retained placenta and metritis (13/204 [6.4%] and 8/204 [3.9%], respectively, for the vitamin E-treated group; 27/216 [12.5%] and 19/216 [8.8%], respectively, for the untreated group) but did not affect the incidence of clinical mastitis. Serum vitamin E concentration was significantly higher in treated than in control cattle at 7 and 14 days after administration, but serum tocopherohcholesterol ratio was significantly higher only at 7 days after administration.

Clinical Implications—

Parenteral administration of a single injection of vitamin E before parturition may decrease the incidence of retained placenta and metritis in dairy cows but will increase serum concentrations for 7 to 14 days after administration. (J Am Vet Med Assoc 1997;211:466–469)

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