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Kansas State University, Manhattan 66506
Abstract
Thirty-six steers (148 to 500 kg) divided into six equal groups were used in a toxic syndrome study of lasalocid and monensin given as a single oral dose. One group was given a placebo, a second group received monensin (25 mg/kg body weight) and the other four groups received lasalocid at 1, 10, 50 or 100 mg/kg body weight (bw). No toxic signs developed in cattle given placebo or lasalocid at 1 or 10 mg/kg bw dose. The earliest toxic signs were muscle tremors, tachycardia and rumen atony. After 24 h, the cattle were dehydrated, anorectic and had diarrhea. Deaths occurred between d 1 and 22.5 in the groups receiving lasalocid at 50 and 100 mg/kg bw and monensin. Altered values in blood leucocytes, erythrocytes, hemoglobin, hematocrit, total protein, albumin, creatinine, urea nitrogen, total bilirubin, creatine kinase, lactic dehydrogenase, calcium, chloride and inorganic phosphate occurred 1 d after dosing; urine pH and specific gravity also changed 1 d after dosing. Maximum changes occurred at d 3. Most of the changes were indicative of dehydration rather than specific organ damage.
1 Contribution No. 84-518-J, Dept. of Anim. Sci. & Industry, Surgery & Medicine and Statistics, Kansas Agr. Exp. Sta. This research was supported in part by a grant from Hoffmann-LaRoche, Inc., Nutley, NJ.
2 The authors are grateful to Mr. Lloyd Manthe for his invaluable assistance.
3 This study was one of the last projects Dr. Bartley completed before his death.
4 Present address: Pfizer, Inc., Anim. Health Res., P.O. Box 88, Terre Haute, IN 47808.
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