Polysaccharide accumulation in the central nervous system ofd-penicillamine-treated rats
Short Original Communications
Received:
Accepted:
- 16 Downloads
- 1 Citations
Summary
A complex polysaccharide accumulation was observed in the central nervous system (CNS) of rats treated withd-penicillamine similar to Lafora-like bodies. They have histochemical similarities comparable to bodies described in previous studies of Lafora disease. The clinical usefulness ofd-penicillamine has been limited by many side effects including renal damage. It is suggested that, in addition tod-penicillamine nephropathy, there are toxic effects of this drug on the CNS.
Key words
Polysaccharide d-penicillamine Lafora-like bodies NephropathyPreview
Unable to display preview. Download preview PDF.
References
- Collins GH, Cowden RR, Nevis AH (1968) Myoclonus epilepsy with Lafora bodies. An ultrastructural and cytochemical study. Arch Pathol 86:239–254Google Scholar
- harriman DCF, Miller JHD (1955) Progressive familial myoclonic epilepsy in three families; its clinical features and pathological basis. Brain 78:325–349Google Scholar
- Harris ED, Sojoerdsma A (1966) Effect of penicillamine in human collagen and its possible application to treatment of scleroderma. Lancet II:996–999Google Scholar
- Huskisson EC (1976b) Specific therapy for rheumatoid arthritis. Rheumatol Rehabil 15:133–135Google Scholar
- Jaffe IA, Treser G, Suzuki Y, Ehrenreich T (1968) Nephropathy induced byd-penicillamine. Ann Intern Med 69:549–556Google Scholar
- Jayaraj AP (1972) Collagenase and its inhibition, Thesis, LondonGoogle Scholar
- Multicentre Trial Group (1973) Control trial ofd-penicillamine in severe rheumatoid arthritis. Lancet I:275–280Google Scholar
- Nimni AE (1968) A defect in the intramolecular and intermolecular cross-linking of collagen caused by penicillamine. J Biol Chem 243:1457–1468Google Scholar
- Pinell SR, Martin GR, Miller EJ (1968) Desmosine biosynthesis. Nature of inhibition byd-penicillamine. Science 161:475–476Google Scholar
- Schwarz GA, Yanoff M (1965) Lafora's disease. Distinct clinicopathologic form of Unverricht's syndrome. Arch Neurol 12:172–188Google Scholar
- Stephan J, Scheur PJ, Somourian S, McGee J O'D, Sherlock S (1976) A control trial ofd-penicillamine therapy in the primary biliary cirrhosis. Gut 17:822Google Scholar
- Suski K, David E, Kutschman B (1970) Presenile dementia with Lafora-like intraneuronal inclusions. Arch Neurol 25:69–80Google Scholar
- Takahaski K, Agari M, Nakamura H (1975) Intaaxonal corpora amylacea in ventral and lateral horns of the spinal cord. Acta Neuropathol (Berl) 31:151–158Google Scholar
- Van Hoff F, Haeman-Bal M (1967) Progressive familial myoclonic epilepsy with Lafora bodies. Electron microscopic and histochemical study of a cerebral biopsy. Acta Neuropathol (Berl) 7:325–349Google Scholar
- Walshe JM (1956) Penicillamine, a new oral therapy for Wilson's disease. Am J Med 21:487–495Google Scholar
Copyright information
© Springer-Verlag 1980