Abstract
The adminstration of GM1 ganglioside, 30 mg/kg per day i.p., begun 3 days prior to an intrastriatal injection of the excitotoxic tryptophan metabolite quinolinic acid (QUIN) and continued for 8-16 days thereafter, significantly decreased QUIN-induced striatal damage, as evaluated by measuring the activity of the marker enzymes, choline acetyltransferase and L-glutamic acid decarboxylase. Since an increased production of QUIN has been demonstrated in Huntington's chorea patients it is possible that repeated GM1 administration could reduce the occurence of progressive striatal neuronal loss in this neurological disorder.
| Original language | English |
|---|---|
| Pages (from-to) | 123-125 |
| Number of pages | 3 |
| Journal | European Journal of Pharmacology |
| Volume | 174 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 12 Dec 1989 |
| Externally published | Yes |
Keywords
- Choline acetyltransferase
- Excitotoxicity
- Gangliosides
- Huntington's chorea
- L-Glutamic acid decarboxylase
- Quinolinic acid
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