Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation
Search: search_blue_button Advanced Search
Circulation. 1965;31:228-233

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
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
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by LOWENSTEIN, J. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by LOWENSTEIN, J. M.

(Circulation. 1965;31:228.)
© 1965 American Heart Association, Inc.


A Method for Measuring Plasma Levels of Digitalis Glycosides

JEROLD M. LOWENSTEIN M.D.1

1 From the Isotope Laboratory, Presbyterian Medical Center and Children's Hospital, San Francisco, California.

A method is described for measuring plasma levels of cardiac glycosides, utilizing their inhibitory effect on the rubidium-86 uptake of human red cells. As little as 0.05 mµg. of digoxin/ml. of plasma produces detectable inhibition, but due to the variable effect of other substances in human plasma the practical limit of the method is 1.0 mµg./ml., about 20 times as sensitive as the duck embryo heart or the C14-labeled technics.

Patients on digitalis leaf were found to have much higher circulating levels than patients on digoxin (average value 7.5 mµg./ ml. of digoxin equivalent for digitalis leaf, 0.05 mµg./ml. for digoxin). Patients toxic on digoxin averaged 6 mµg./ml.

Of patients not taking digitalis, 7 per cent had significant levels of digitalis-like substances in their plasma; these were mostly individuals with metastatic carcinoma, severe fluid and electrolyte disturbances, or heart failure. No drug (other than cardiac glycosides) gave consistent high levels by this test.




This article has been cited by other articles:


Home page
J. Am. Soc. Nephrol.Home page
D. Kennedy, S Vetteth, S. Periyasamy, M Kanj, L Fedorova, S Khouri, M. Kahaleh, Z Xie, D Malhotra, N. Kolodkin, et al.
Uremic Cardiomyopathy--An Endogenous Digitalis Intoxication?: Central Role for the Cardiotonic Steroid Marinobufagenin in the Pathogenesis of Experimental Uremic Cardiomyopathy. Hypertension 47: 488-495, 2006
J. Am. Soc. Nephrol., June 1, 2006; 17(6): 1493 - 1497.
[Full Text] [PDF]


Home page
Clin. Chem.Home page
R. Valdes Jr., S. A. Jortani, and M. Gheorghiade
Standards of laboratory practice: cardiac drug monitoring
Clin. Chem., May 1, 1998; 44(5): 1096 - 1109.
[Abstract] [Full Text] [PDF]


Home page
J CARDIOVASC PHARMACOL THERHome page
J. T. Sullebarger, P. M. D'Ambra, L. C. Clark, L. Thanikarry, and H. L. Fontanet
Effect of Digoxin on Ventricular Remodeling and Responsiveness of {beta}-Adrenoceptors in Chronic Volume Overload
Journal of Cardiovascular Pharmacology and Therapeutics, January 1, 1998; 3(4): 281 - 290.
[Abstract] [PDF]


Home page
Cardiovasc ResHome page
W. E. Glover, M. J. D. Hanna, and R. N. Speden
Actions of Cardiac Glycosides on the Vessels of the Forearm and Hand
Cardiovasc Res, October 1, 1967; 1(4): 341 - 348.
[Abstract] [PDF]