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Isolation of various forms of sterol beta-D-glucoside from the seed of Cycas circinalis: neurotoxicity and implications for ALS-parkinsonism dementia complex.

Authors
Khabazian, I; Bains, JS; Williams, DE; Cheung, J; Wilson, JM; Pasqualotto, BA; Pelech, SL; Andersen, RJ; Wang, YT; Liu, L; Nagai, A; Kim, SU; Craig, UK; Shaw, CA
Citation
Journal of neurochemistry, 82(3):516-528, 2002
Journal Title
Journal of neurochemistry
ISSN
0022-30421471-4159
Abstract
The factors responsible for ALS-parkinsonism dementia complex (ALS-PDC), the unique neurological disorder of Guam, remain unresolved, but identification of causal factors could lead to clues for related neurodegenerative disorders elsewhere. Earlier studies focused on the consumption and toxicity of the seed of Cycas circinalis, a traditional staple of the indigenous diet, but found no convincing evidence for toxin-linked neurodegeneration. We have reassessed the issue in a series of in vitro bioassays designed to isolate non-water soluble compounds from washed cycad flour and have identified three sterol beta-d-glucosides as potential neurotoxins. These compounds give depolarizing field potentials in cortical slices, induce alterations in the activity of specific protein kinases, and cause release of glutamate. They are also highly toxic, leading to release of lactate dehydrogenase (LDH). Theaglycone form, however, is non-toxic. NMDA receptor antagonists block the actions of the sterol glucosides, but do not compete for binding to the NMDA receptor. The most probable mechanism leading to cell death may involve glutamate neuro/excitotoxicity. Mice fed cycad seed flour containing the isolated sterol glucosides show behavioral and neuropathological outcomes, including increased TdT-mediated biotin-dUTP nick-end labelling (TUNEL) positivity in various CNS regions. Astrocytes in culture showed increased caspase-3 labeling after exposure to sterol glucosides. The present results support the hypothesis that cycad consumption may be an important factor in the etiology of ALS-PDC and further suggest that some sterol glucosides may be involved in other neurodegenerative disorders.
MeSH terms
Amyotrophic Lateral Sclerosis/complications/*etiologyAnimalsAstrocytes/cytology/drug effectsBiological AssayCells, CulturedCerebral Cortex/cytology/drug effects/physiologyCholesterol/*analogs & derivatives/chemistryCycasDementia/complications/etiologyGlucose/analogs & derivatives/chemistryGlucosides/isolation & purification/toxicityGuamHumansMaleMiceNeurons/cytology/*drug effects/physiologyNeurotoxins/isolation & purification/toxicityParkinsonian Disorders/complications/etiologyPatch-Clamp TechniquesPhytosterols/chemistry/*isolation & purification/*toxicityPlant Extracts/chemistry/toxicityRatsRats, Sprague-DawleyReceptors, N-Methyl-D-Aspartate/drug effects/metabolismSeeds/*chemistrySitosterols/isolation & purification/toxicityStigmasterol/analogs & derivatives/chemistry/isolation & purification/toxicity
PMID
12153476
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Neurology
AJOU Authors
김, 승업
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