Two experiments were conducted to investigate the effect of i.v. administra
tion of L-carnitine on selected metabolites in sheep and to determine the f
easibility of using L-carnitine to ameliorate the deleterious effects of hy
perammonemia in sheep. In Exp. 1, i.v. L-carnitine solutions were administe
red at three levels in a replicated Latin square: 0 (CONT), 6.36 (CAR 1), a
nd 12.72 (CAR 2) mmol L-carnitine/kg(.75) BW using Suffolk ewes (n = 6; ave
rage BW 75 +/- 3 kg). Plasma L-carnitine concentration was increased (P <.0
5) by treatment (51.9 vs 102.3, and 96.4 mu mol/L in CONT, CAR 1, and CAR 2
, respectively). Plasma glucose concentration was elevated (P <.05) in CAR
2 and CAR 1. Plasma NEFA concentration was highest (P <.05) in CAR 2. Area
under the response curve for glucose was greater (P <.02) in CAR 2. In Exp.
2, Suffolk ewes (n = 16; average BW 48 +/- 2 kg) were used in a randomized
complete block design with a 2 x 2 factorial treatment arrangement to dete
rmine the effects of i.v. L-carnitine administration during an oral urea lo
ad test (OULT). L-Carnitine (0 and 6.36 mmol/kg(.75) BW) was administered i
.v. at; 30 min, and an oral urea drench (50% wt/vol; 0 and 300 mg/kg BW) wa
s administered at 60 min. Plasma L-carnitine was increased (P < .0001) by i
.v. L-carnitine. Plasma ammonia N was highest (P <.0001) in the UREA treatm
ent compared with the CONT, CARN, and CARN + UREA treatments (148 vs 95, 10
1, and 108 mu mol/L, respectively). Intravenous L-carnitine administration
influenced plasma glucose and NEFA concentrations in sheep and, when admini
stered 30 min preceding an OULT, prevented the development of subclinical h
yperammonemia in sheep.