![]() |
|
|
Vol. 287, Issue 1, 8-12, October 1998
Department of Pharmacology, (D.G-R, M.Z-C, A.N-J, Y.M-R), Centro de
Investigacion Biomedica del Noreste, Instituto Mexicano del Seguro
Social, Monterrey, Mexico;
Rocky Mountain Poison Center (K.M.H.,
R.C.D.), Denver, Colorado and
Department of Molecular and Cellular
Biology (H.V.A.), University of Arizona, Tucson, Arizona
DMPS (2,3-dimercaptopropane-1-sulfonate, Na salt), when used as a
challenge test for mercury in workers involved in the production of a
calomel skin-bleaching lotion and in direct contact with mercurous
chloride, elevated urine levels of mercury. A DMPS treatment regimen
was devised and initiated. Three days after the challenge test, DMPS
was administered p.o. (400 mg per day) for 8 days, followed by a
no-treatment period of five days. A new cycle of DMPS treatment for 7 days was initiated and followed by 5 days without treatment. A third
period of treatment was begun for 6 days, followed by a 5-day
no-treatment period. The urinary mercury greatly increased during those
periods when DMPS was administered (1754, 314, and 173 µg/24 h for
the periods 1, 2 and 3, compared with 106, 48 and 53 µg/24 h on the
corresponding no-treatment periods). One of the workers presented signs
of drug intolerance and was discharged after receiving the first cycle
of treatment. DMPS treatment was effective in lowering the body burden
of mercury and in decreasing the urinary mercury concentration to
normal levels.
This article has been cited by other articles:
![]() |
B. C. Burckhardt, B. Drinkuth, C. Menzel, A. Konig, J. Steffgen, S. H. Wright, and G. Burckhardt The Renal Na+-Dependent Dicarboxylate Transporter, NaDC-3, Translocates Dimethyl- and Disulfhydryl-Compounds and Contributes to Renal Heavy Metal Detoxification J. Am. Soc. Nephrol., November 1, 2002; 13(11): 2628 - 2638. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Islinger, M. Gekle, and S. H. Wright Interaction of 2,3-Dimercapto-1-propane Sulfonate with the Human Organic Anion Transporter hOAT1 J. Pharmacol. Exp. Ther., November 1, 2001; 299(2): 741 - 747. [Abstract] [Full Text] [PDF] |
||||