This document discusses heavy metals and their chelators. It describes the chemical and clinical effects of lead, arsenic, mercury, cadmium, and the chelator dimercaprol (BAL). Lead poisoning can cause CNS deficits and kidney damage, and is treated with chelation therapy. Arsenic affects the cardiovascular and nervous systems and treatment involves terminating exposure. Mercury primarily impacts the kidneys and CNS, while cadmium accumulates in the kidneys and has been linked to cancer and high blood pressure. Dimercaprol was developed to treat arsenic and mercury poisoning and protects against their lethal effects if given soon after exposure.
This document discusses heavy metals and their chelators. It describes the chemical and clinical effects of lead, arsenic, mercury, cadmium, and the chelator dimercaprol (BAL). Lead poisoning can cause CNS deficits and kidney damage, and is treated with chelation therapy. Arsenic affects the cardiovascular and nervous systems and treatment involves terminating exposure. Mercury primarily impacts the kidneys and CNS, while cadmium accumulates in the kidneys and has been linked to cancer and high blood pressure. Dimercaprol was developed to treat arsenic and mercury poisoning and protects against their lethal effects if given soon after exposure.
This document discusses heavy metals and their chelators. It describes the chemical and clinical effects of lead, arsenic, mercury, cadmium, and the chelator dimercaprol (BAL). Lead poisoning can cause CNS deficits and kidney damage, and is treated with chelation therapy. Arsenic affects the cardiovascular and nervous systems and treatment involves terminating exposure. Mercury primarily impacts the kidneys and CNS, while cadmium accumulates in the kidneys and has been linked to cancer and high blood pressure. Dimercaprol was developed to treat arsenic and mercury poisoning and protects against their lethal effects if given soon after exposure.
CHEMICAL DESCRIPTION MECHANISM OF ACTION CLINICAL EFFECTS TREATMENT have widespread commercial application, including production of storage batteries CNS deficits; peripheral • Chelation therapy with DMSA Inhibits enzymes; interferes LEAD ammunition, metal alloys, with essential cations; alters neuropathy; anemia; (succimer) solder, glass, plastics, pigments, nephropathy; hypertension; • BAL, D-penicillamine, and EDTA membrane structure and ceramics reproductive toxicity • Whole bowel irrigation
a naturally occurring element in
the earth’s crust with a long Cardiovascular -shock- • termination of exposure and Inhibits enzymes; interferes history of use as a constituent arrhythmias nonspecific supportive care. with oxidative ARSENIC of commercial and industrial phosphorylation; CNS-encephalopathy -peripheral • oral chelation with unithiol or products, as a component in neuropathy succimer for symptomatic alters cell signaling, gene pharmaceuticals, and as an OTHER-Gastroenteritis - individuals expression agent of deliberate poisoning pancytopenia-cancer • dietary supplementation of folate
“quicksilver”—the only metal
Inhibits enzymes; alters that is liquid under ordinary membranes CNS: tremor, behavioral • oral or intravenous unithiol, Conditions—has attracted After absorption, mercury is (erethism); gingivastomatitis, intramuscular dimercaprol, or oral MERCURY scholarly and scientific interest distributed to the tissues peripheral neuropathy; succimer from antiquity. The mining of within a few hours, with the acrodynia; pneumonitis (high- • Unithiol and succimer increase urine mercury was early recognized highest concentration dose) mercury excretion as being hazardous to health. occurring in the kidney.
there is no effective treatment for
Long-term exposure may cause Cadmium is a natural element accumulates especially in the cadmium intoxication, and patients kidney stones and lung damage, in the earth's crust. It is usually kidneys leading to dysfunction are given supportive treatment CADMIUM found as a mineral combined of the and have been linked to lung according to their symptoms. some cancer and high blood pressure. with other elements such as kidney with increased of new chelating agents may be Short-term exposure may irritate oxygen, chlorine, or sulfur. secretion of proteins in urine effective the lungs. an oily, colorless liquid with a strong mercaptan-like odor, prevents and reverses arsenic was developed in Great Britain single-agent treatment of acute dimercaprol is associated with a high DIMERCAPROL induced during World War II as a poisoning by arsenic and incidence of adverse effects, inhibition of sulfhydryl- (2,3-DIMERCA- therapeutic antidote against inorganic mercury and for the including hypertension, tachycardia, containing enzymes and, if PTOPROPANOL, poisoning by the arsenic- given soon after exposure, may treatment of severe lead nausea, vomiting, lacrimation, BAL) containing warfare agent poisoning when used in salivation, fever protect against the lethal lewisite. It thus became known conjunction with edetate (particularly in children), and pain at effects of inorganic and as British anti-lewisite, or BAL. calcium disodium (EDTA) the injection site. organic arsenicals.