JPET xPharm- The Comprehensive Pharmacology Reference

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hansson, E.
Right arrow Articles by Schmiterlöw, C. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hansson, E.
Right arrow Articles by Schmiterlöw, C. C.
Journal of Pharmacology And Experimental Therapeutics, Vol. 137, Issue 1, 91-102, 1962
Copyright © 1962 by American Society for Pharmacology and Experimental Therapeutics


PHYSIOLOGICAL DISPOSITION AND FATE OF C14-LABELLED NICOTINE IN MICE AND RATS

Eskil Hansson 1 and Carl C. Schmiterlöw 1

1 Department of Pharmacology, Royal Veterinary College, Stockholm, Sweden

Mice of 20 g body weight were injected intramuscularly or intravenously with (-)-nicotine-methyl-C14. The distribution was studied with an autoradiographic technique. Within 5 minutes after the injection, high concentration of nicotine was found in brain, adrenal medulla, stomach wall and kidney. Lower concentrations were found in, e.g., blood, liver and skeletal muscles. All tissue concentrations were higher than the blood concentration. The distribution following i.v. and i.m. injections was approximately the same, indicating fast absorption from the intramuscular depot. The same distribution of radioactivity remained in the animals sacrificed at 15 and 30 minutes after the injection. Thereafter the distribution picture changed apparently due to the rapid metabolism of nicotine.

The metabolic studies indicated that nicotine is very rapidly metabolized to a compound which presumably is cotinine.

A large amount of nicotine is excreted into the stomach via the fundus mucosa and 2 to 3% excreted via the bile of rat during a 6-hour period. Sixty to 80 % of the radioactivity was found in the urine of mice and rats and 8 to 15% in the exhaled carbon dioxide of mice after 24 hours. Chromatographic separation of the urine radioactivity revealed at least 8 nicotine metabolites. Two of these compounds had the same Rf-values on paper chromatograms as cotinine and hydroxycotinine.

The significance of the tissue distribution in relation to the pharmacological effects of nicotine and the elucidation of the biological fate of nicotine is discussed.

Submitted on February 12, 1962







Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
All ASPET Journals Molecular Pharmacology Pharmacological Reviews
 Molecular Interventions Drug Metabolism and Disposition

Copyright © 1962 by the American Society for Pharmacology and Experimental Therapeutics.