FASEB J. Pierce now sold as Thermo Scientific
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


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 reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Aposhian, H. V.
Right arrow Articles by Aposhian, M. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Aposhian, H. V.
Right arrow Articles by Aposhian, M. M.

The FASEB Journal, Vol 6, 2472-2476, Copyright © 1992 by The Federation of American Societies for Experimental Biology


RESEARCH COMMUNICATIONS

Urinary mercury after administration of 2,3-dimercaptopropane-1- sulfonic acid: correlation with dental amalgam score

HV Aposhian, DC Bruce, W Alter, RC Dart, KM Hurlbut and MM Aposhian
University Department of Molecular and Cellular Biology, University of Arizona, Tucson 85721.

There is considerable controversy as to whether dental amalgams may cause systemic health effects in humans because they liberate elemental mercury. Most such amalgams contain as much as 50% metallic mercury. To determine the influence of dental amalgams on the mercury body burden of humans, we have given volunteers, with and without amalgams in their mouth, the sodium salt of 2,3-dimercaptopropane-1-sulfonic acid (DMPS), a chelating agent safely used in the Soviet Union and West Germany for a number of years. The diameters of dental amalgams of the subjects were determined to obtain the amalgam score. Administration of 300 mg DMPS by mouth increased the mean urinary mercury excretion of the amalgam group from 0.70 to 17.2 micrograms and that of the nonamalgam group from 0.27 to 5.1 micrograms over a 9-h period. Two-thirds of the mercury excreted in the urine of those with dental amalgams appears to be derived originally from the mercury vapor released from their amalgams. Linear regression analysis indicated a highly significant positive correlation between the mercury excreted in the urine 2 h after DMPS administration and the dental amalgam scores. DMPS can be used to increase the urinary excretion of mercury and thus increase the significance and reliability of this measure of mercury exposure or burden, especially in cases of micromercurialism.


This article has been cited by other articles:


Home page
Toxicol SciHome page
S. D. Pingree, P. L. Simmonds, and J. S. Woods
Effects of 2,3-Dimercapto-1-propanesulfonic Acid (DMPS) on Tissue and Urine Mercury Levels following Prolonged Methylmercury Exposure in Rats
Toxicol. Sci., June 1, 2001; 61(2): 224 - 233.
[Abstract] [Full Text] [PDF]


Home page
J Am Coll CardiolHome page
F. Lorscheider and M. Vimy
Mercury and idiopathic dilated cardiomyopathy
J. Am. Coll. Cardiol., March 1, 2000; 35(3): 819 - 819.
[Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
D. Gonzalez-Ramirez, M. Zuniga-Charles, A. Narro-Juarez, Y. Molina-Recio, K. M. Hurlbut, R. C. Dart, and H. V. Aposhian
DMPS (2,3-Dimercaptopropane-1-sulfonate, Dimaval) Decreases the Body Burden of Mercury in Humans Exposed to Mercurous Chloride
J. Pharmacol. Exp. Ther., October 1, 1998; 287(1): 8 - 12.
[Abstract] [Full Text]


Home page
J. Pharmacol. Exp. Ther.Home page
H. V. Aposhian, A. Arroyo, M. E. Cebrian, L. M. Del Razo, K. M. Hurlbut, R. C. Dart, D. Gonzalez-Ramirez, H. Kreppel, H. Speisky, A. Smith, et al.
DMPS-Arsenic Challenge Test. I: Increased Urinary Excretion of Monomethylarsonic Acid in Humans Given Dimercaptopropane Sulfonate
J. Pharmacol. Exp. Ther., July 1, 1997; 282(1): 192 - 200.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1992 by The Federation of American Societies for Experimental Biology.