Z. Benzvi et al., LIDOCAINE ELIMINATION AND MONOETHYLGLYCINEXYLIDIDE FORMATION IN THE DEHYDRATED CAMEL, Journal of veterinary pharmacology and therapeutics, 18(6), 1995, pp. 442-445
The elimination kinetics and the formation of the monoethylglycinexyli
dide (MEGX), a major metabolite of lidocaine, were studied in camels d
eprived of water for 14 days. The study was conducted on four camels i
n a crossover design. Lidocaine was administered intravenously at a do
se of 1 mg/kg to adult female camels when water was given ad libitum (
stage 1) and to the same camels after 14 days of dehydration. Blood sa
mples were taken up to 6 h after dosing. Serum lidocaine and MEGX leve
ls were analysed by polarization fluorescence immunoassay, The elimina
tion profiles of lidocaine and the formation of the metabolite MEGX in
the two phases of the study were essentially identical, No difference
in any pharmacokinetic parameter was noticed between normally hydrate
d and water-deprived camels. It is thus concluded that dehydration doe
s not affect the cytochrome P450 isozymes involved in degradation of l
idocaine to MEGX nor does it affect the hepatic blood flow, which is a
major determinant in the clearance of lidocaine. The very low clearan
ce of lidocaine in the camel in comparison with other ruminant or mono
gastric mammals may be associated with the camel's ability to survive
drought in the desert.