Print

Print


>    Subject: Sinemet
>    From: ervinmccarthy <[log in to unmask]>
>    Date: Tue, 10 Jul 2001 21:39:16 -0400

Subject: Chronic LD not toxic, may promote neural recovery
Date: 1/19/99

Chronic levodopa is not toxic for remaining dopamine neurons, but instead
promotes their recovery, in rats with moderate nigrostriatal lesions

MG Murer, G Dziewczapolski, LB Menalled, MC Garcia, Y Agid, O Gershanik, R
Raisman-Vozari

Annals of Neurology, 1998, Vol 43, Iss 5, pp 561-575

Six months of oral l-dopa caused no excess loss of dopaminergic neurons
versus untreated controls, and may have promoted recovery of surviving
neurons, according to this study on OHDA-lesioned rats. Rats were
unilaterally injected with either saline or one of two quantities of OHDA
(to produce moderate vs. severe lesions). Members of each group were
randomly assigned to receive either vehicle or oral l-dopa. Neuronal
survival was quantified by immunoautoradiography of tyrosine hydroxylase,
vesicular monoamine transporter, and dopamine transporter.

Results showed:
a) L-dopa treatment caused no loss of dopaminergic neurons in either
sham-lesioned or OHDA-lesioned rats compared to sham-lesioned,
non-treated controls
b) L-dopa treatment caused no reduction in terminal axonal arborization
c) In the moderately lesioned group, treated rats showed, "in the
denervated regions of the striatum, significantly higher levels of the
three dopaminergic markers than their corresponding vehicle-treated
control group, and also an increased density of TH-immunoreactive
fibers."

The authors suggest the recovery is likely to be due to axonal sprouting of
surviving dopaminergic neurons. They also note that their study provided no
evidence of accompanying functional recovery in this subgroup. In discussing
the relevance of these findings to human PD
patients, they state "our results cannot be considered as definitive
evidence of an absence of toxicity of chronic levodopa in PD patients" but
note that other recent findings support the absence of l-dopa toxicity as
well.

An editorial by Stanley Fahn accompanies the article.


----------------------------------------------------------------------------
----
Copyright 2000 WE MOVE
Editor: Richard Robinson ([log in to unmask])
This service is provided free of charge to the Internet community, courtesy
of WEMOVE.org. This document may be freely redistributed by email only in
its unedited form. We encourage you to share it with your colleagues.

E-MOVE archives, plus information on subscribing, are available at
http://www.wemove.org/em_intro.html. To unsubscribe, send an e-mail to
[log in to unmask], with "unsubscribe e-move" in the message body.

E-MOVE is a service of WE MOVE (Worldwide Education and Awareness for
Movement Disorders)
204 West 84th Street
New York, NY 10024


TEL 800-437-MOV2
TEL 212-241-8567
FAX 212-987-7363
http://www.wemove.org

[log in to unmask]

----------------------------------------------------------------------
To sign-off Parkinsn send a message to: mailto:[log in to unmask]
In the body of the message put: signoff parkinsn