Ultrastructure of Purkinje cell perikarya and their dendritic processes in the rat cerebellar cortex in experimental encephalopathy induced by chronic application of valproate
- 1 December 2001
- journal article
- research article
- Published by Wiley in International Journal of Experimental Pathology
- Vol. 82 (6) , 337-348
- https://doi.org/10.1046/j.1365-2613.2001.00206.x
Abstract
Long-term intragastric administration of the antiepileptic drug sodium valproate (Vuprol ‘Polfa’) to rats for 1, 3, 6, 9 and 12 months, once daily at the effective dose of 200 mg/kg body weight showed morphological evidence of encephalopathy, manifested by numerous nonspecific changes within Purkinje cell perikarya and their dendritic processes. The first ultrastructural abnormalities appeared after 3 months. They became more severe in animals with longer survival and were most pronounced after 12 months. The changes were maintained both 1 and 3 months after drug withdrawal. Mitochondria of Purkinje cell perikarya were most severely affected. Damage to mitochondria was accompanied by disintegration and fragmentation of granular endoplasmic reticulum, dilation of channels and cisterns of Golgi apparatus, enlargement of smooth endoplasmic reticulum elements including submembranous cisterns, and accumulation of profuse lipofuscin deposits. Frequently, Purkinje cells appeared as ‘dark’ ischemic neurones, with focally damaged cellular membrane and features of disintegration. Swollen Bergmann's astrocytes were seen among damaged Purkinje cells or at the site of their loss. The general pattern of submicroscopic alterations of Purkinje cell perikarya suggested severe disorders in several intercellular biochemical extents, including inhibition of oxidative phosphorylation and abnormal protein synthesis, both of which could lead to lethal damage. Ultrastructural abnormalities within dendrites were characterized by damage to elements of smooth endoplasmic reticulum, which was considerably enlarged, with formation of large vacuolar structures situated deep in the dendroplasm. Mitochondrial lesions and alterations in cytoskeletal elements – disintegration of microtubules or even their complete loss –were also observed. The general pattern of abnormalities within the organelles and cytoskeletal elements of dendritic processes in Purkinje cells in the VPA chronic experimental model imply that there are disturbances in detoxication processes. Furthermore these changes were irreversible, as they were maintained after drug withdrawal.Keywords
This publication has 70 references indexed in Scilit:
- Enzephalopathien durch ValproatFortschritte der Neurologie · Psychiatrie, 1999
- Valproate-induced limb malformations in mice associated with reduction of intracellular pHReproductive Toxicology, 1997
- Omphalocele in a newborn baby exposed to sodium valproate in uteroEuropean Journal of Pediatrics, 1995
- Omphalocele in a newborn baby exposed to sodium valproate in uteroEuropean Journal of Pediatrics, 1995
- Valproic acid inhibits the depolarizing rectification in neurons of rat amygdalaNeuropharmacology, 1994
- Neurologic Factors Predict a Favorable ValproateJournal of Clinical Psychopharmacology, 1994
- In vivo administration of valproate reduces the nerve terminal (synaptosomal) activity of GABA aminotransferase in discrete brain areas of ratsNeuroscience Letters, 1993
- Effects of the antiepileptic drug valproate on metabolism and function of inhibitory and excitatory amino acids in the brainNeurochemical Research, 1993
- Lipofuscin Granules in Purkinje Cells after Long‐Term Alcohol Consumption in RatsAlcohol, Clinical and Experimental Research, 1983
- The Number of Purkinje Cells after Diphenylhydantoin Intoxication in MonkeysEpilepsia, 1970