| Literature DB >> 14201250 |
A C GREINER, G A NICOLSON, R A BAKER.
Abstract
Melanosis observed in association with prolonged chlorpromazine therapy has become a serious problem in mental institutions. Skin pigmentation has produced an appearance which is cosmetically undesirable. Ocular deposits have caused visual impairment. Diffuse visceral involvement has been accompanied by functional disturbances of the involved organs.Withholding chlorpromazine did not diminish the pigment deposits already present in eight patients with chlorpromazine-induced melanosis. Therefore therapy for existing cases and means of preventing this side effect were investigated. A method of blocking melanin synthesis by depressing tyrosinase activity was devised. A copperchelating agent, D-penicillamine, was administered for a period of four weeks (300 mg. three times daily for six days each week, with mineral supplement substituted on the seventh day). Four of six days patients thus treated improved markedly as evidenced by diminution of skin pigmentation. Urinary copper excretion was substantially increased during the trial period. An alternative method of treatment designed to stimulate melatonin production by the pineal gland was employed. Two patients were kept in darkness for a period of four weeks. One improved markedly, the other only slightly.Entities:
Keywords: CHLORPROMAZINE TOXICOLOGY; COPPER; DARKNESS; DRUG THERAPY; EYE DISEASES; HISTOCYTOCHEMISTRY; HOSPITALS, PSYCHIATRIC; KIDNEY; LIVER; LUNG; MACROPHAGES; MELANOSIS; METABOLISM; PENICILLAMINE; PIGMENTATION; SCHIZOPHRENIA; TOXICOLOGIC REPORT; TYROSINE DECARBOXYLASE; URINE
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Year: 1964 PMID: 14201250 PMCID: PMC1927525
Source DB: PubMed Journal: Can Med Assoc J ISSN: 0008-4409 Impact factor: 8.262