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Xenobiotica
the fate of foreign compounds in biological systems
Volume 6, 1976 - Issue 9
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Original Article

Disposition and Metabolism of [3HCocaine in Acutely and Chronically treated Dogs

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Pages 537-552 | Received 29 Jan 1976, Published online: 30 Sep 2009
 

Abstract

1. Beagle dogs were chronically treated with cocaine, 5 mg/kg subcutaneously twice daily for 6 weeks, followed by same dose of [3H]cocaine given intravenously.

2. The thalf values of cocaine in plasma, liver, spleen and heart, in acutely and chronically treated dogs, were: 1·2, 1·1; 2·2, 1·8; 1·8, 1·3; 2·0, 1·2 h, respectively. In both groups, cocaine disappeared from all areas of the central nervous system 12–24 h after injection but significant amounts of radioactivity due to benzoyl-norecgonine and benzoylecgonine persisted in the CNS even 1 week after administration of cocaine. Brain-to-plasma ratios of cocaine were lower in chronically-treated than in acutely-treated dogs 2 and 4 h after injection.

3. Norcocaine, benzoylnorecgonine, benzoylecgonine and ecgonine were metabolites of cocaine in dog brain in both groups. Norcocaine and benzoylnorecgonine were present in higher amounts in brains of chronically treated dogs. Rate of disappearance of norcocaine was similar to cocaine in both groups.

4. The amounts of cocaine excreted in urine and faeces as percentage of dose were 0-9-5-0, 1-1-6 in the acute and 2-2-3-3 and 0-2-0-3 in the chronically treated dogs. Major excretion of radioactivity occurred in urine within 24 h in both groups. Total radioactivity (65% of dose) in urine plus faeces was similar in both groups.

5. Norcocaine, benzoylnorecgonine, benzoylecgonine, ecgonine, norecgonine, ecgonine methyl ester and unidentified compounds were urinary metabolites of cocaine in both groups. Benzoylnorecgonine and ecgonine were excreted in higher amounts and benzoylecgonine and norecgonine in lower amounts in the acute than in the chronically treated dogs.

6. The possible role of persistence of benzoylnorecgonine and benzoylecgonine (which possessed potent stimulant activity intracisternally) in the CNS is discussed.

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