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Their Mechanism of Action and Application

C. THORPE RAY, M.D.

AMA Arch Intern Med. 1958;102(6):1016-1023.

	Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

The origins and development of mercurial diuretic therapy have been reviewed extensively in recent years.^1-5 The mercurial diuretics have been subjected to much clinical testing and investigation over the past 35 years and have been shown to be potent, dependable, and of relatively low intrinsic toxicity. The addition of theophylline resulted in reduced local reaction at the site of injection and an increase in the diuretic potency.⁶ Additional reduction of cardiovascular toxicity was achieved by substituting a thiol group to produce a mercaptomercurial.^7-9 A number of modifications in the molecule have resulted in new names, but there is no appreciable difference in the diuretic potency of the various injectable preparations of organomercurials currently available. Since the pharmacodynamics of the organomercurials is the same for all preparations, the following brief review of mechanism of action applies to all the mercurial diuretics, both oral and parenteral.

For any compound . . . [Full Text PDF of this Article]

Author Affiliations
Columbia, Mo.

Footnotes
Submitted for publication June 26, 1958.

Read in the Symposium on Recent Advances in the Knowledge of the Causes of Edema and in Diuretic Therapy before the Joint Meeting of the Section on Experimental Medicine and Therapeutics and the Section on Internal Medicine at the 107th Annual Meeting of the American Medical Association, San Francisco, June 26. 1958.

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