Further Observations on Use of D-penicillamine in Cystinuria.

نویسندگان

  • J C CRAWHALL
  • E F SCOWEN
  • R W WATTS
چکیده

It was shown in a previous communication (Crawhall et al., 1963) that the abnormally high level of cystine excretion found in homozygotes for cystinuria could be reduced for short periods by the administration of D-penicillamine. This paper reports the results of administering the drug continuously to a group of cystinuric patients for periods of five months to one year. We have used the D-isomer of penicillamine rather than the racemic (DL) mixture because L-penicillamine antagonizes pyridoxal phosphate and is known to be toxic in experimental animals (Aposhian and Aposhian, 1959). Continuous treatment with D-penicillamine hasbeen used in other diseases, and no serious toxic effects have been reported. Rash, fever, lymphadenopathy, and leucopenia sometimes occur soon after the beginning of treatment but can be overcome by the administration of anti-inflammatory steroids for short periods (Scheinberg and Sternlieb, 1960). Goldberg et al. (1963) reported proteinuria in a patient with chronic lead-poisoning who was treated with D-penicillamine, and Walshe (1960) observed that a patient who was allergic to penicillin was abnormally sensitive to penicillamine. Levine (1960) noted cutaneous cross-sensitivity reactions to penicillin, benzylpenicilloic acid, and penicillamine. We have previously reported chromatographic evidence for the presence of L-cysteine-D-penicillamine in the urine of cystinuric patients taking D-penicillamine (Crawhall et al., 1963). This substance has now been synthesized and purified. Its solubility properties have been studied, and it has been shown to be identical with the new disulphide which appears in the urine of cystinuric patients taking D-penicillamine.

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عنوان ژورنال:
  • British medical journal

دوره 1 5395  شماره 

صفحات  -

تاریخ انتشار 1964