Print

Print


Schneider, J. et al: Neur 1995; 45:1149-1154
The glycolipid monosialoganglioside GM1 is normally abundant in neuron
membranes of the brain, and is thought to modulate the self-repair by
damaged neurons, particularly the dopaminergic ones of the substantia
nigra, in ways poorly understood. In continuing studies evidently
sponsored by Sygen, who have extracted GM1 from cattle, it has been tried
in animals, including MPTP monkeys, and recently in human volunteers. Ten
subjects with uncomplicated PD got 1000mg iv, followed by 200mg subcut-
aneous daily for 18 weeks. GM1 proved generally safe and well-tolerated
(despite some earlier reports of association with Guillain-Barre syndrome)
and produced small but significant improvement in cognitive and motor
function. A double-blind follow-up study is now underway, and subjects
are still being recruited by Hahnemann University, (215) 782-3066. The
trial requires frequent presence for testing in Philadelphia. The group
is also working on LIGA 20, a more potent semi-synthetic derivative of
GM1 that may be taken orally.
 
J. R. Bruman (818) 789-3694
3527 Cody Road
Sherman Oaks CA 91403