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Journal of Pharmacology And Experimental Therapeutics Fast Forward
First published on May 7, 2008; DOI: 10.1124/jpet.108.139543


0022-3565/08/3262-363-368$20.00
JPET 326:363-368, 2008
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PERSPECTIVES IN PHARMACOLOGY

Mineral Arsenicals in Traditional Medicines: Orpiment, Realgar, and Arsenolite

Jie Liu, Yuanfu Lu, Qin Wu, Robert A. Goyer, and Michael P. Waalkes

Inorganic Carcinogenesis Section, Laboratory of Comparative Carcinogenesis, Centers for Cancer Research, National Cancer Institute at National Institute of Environmental Health Sciences (NIEHS), Research Triangle Park, North Carolina (J.L., R.A.G., M.P.W.); and Department of Pharmacology, Zunyi Medical College, China (Y.L., Q.W.)

Mineral arsenicals have long been used in traditional medicines for various diseases, yet arsenic can be highly toxic and carcinogenic. Arsenic in traditional medicines typically comes from deliberate addition for therapeutic purposes, mainly in the form of mineral arsenicals, including orpiment (As2S3), realgar (As4S4), and arsenolite (contains arsenic trioxide, As2O3). Inorganic arsenic is now accepted in Western medicine as a first line chemotherapeutic agent against certain hematopoietic cancers. This perspective analyzes the pharmacology and toxicology of these arsenicals used in traditional medicines. Orpiment and realgar are less soluble and poorly absorbed from the gastrointestinal tract, whereas the bioavailability of arsenic trioxide is similar to inorganic arsenic salts such as sodium arsenite. Pharmacological studies show that arsenic trioxide and realgar are effective against certain malignancies. Orpiment and realgar are used externally for various skin diseases. Realgar is frequently included as an ingredient in oral traditional remedies for its antipyretic, anti-inflammatory, antiulcer, anti-convulsive, and anti-schistosomiasis actions, but the pharmacological basis for this inclusion still remains to be fully justified. Toxicological studies show that cardiovascular toxicity is the major concern for arsenic trioxide and that the gastrointestinal and dermal adverse effects may occur after prolonged use of mineral arsenicals. Little is known regarding the possible secondary cancers resulting from the long-term use of any of these arsenicals. Similar to the safety evaluation of seafood arsenicals, total arsenic content alone appears to be insufficient for mineral arsenical safety evaluation. Arsenic speciation, bioavailability, and toxicity/benefit should be considered in evaluation of mineral arsenical-containing traditional medicines.


Address correspondence to: Dr. Jie Liu, Inorganic Carcinogenesis Section, NCI at NIEHS, Mail Drop F0-09, Research Triangle Park, NC 27709. E-mail: liu6{at}niehs.nih.gov







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