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Hi Genene, Charles and All,
The studies are on the Internet...

In vivo evaluation in mice and metabolism in blood of human
volunteers of [123I]iodo-PK11195: a possible single-photon
emission tomography tracer for visualization of inflammation
Eur J Nucl Med 26 (1999) 3, 194-200
http://link.springer.de/link/service/journals/00259/bibs/9026003/90260194.htm



On 9 Oct 2000, at 22:03, Charles Williams wrote:

> Genene
>
> I am early stage PD or MSA and therefore I took part in a research scan that
> is apparently based on suggestions arising out of recent research that the
> loss of brain cells seen in Parkinsonian disorders is accompanied by
> inflammation and that this may contribute to the progression of the disease.
> As I said before, the literature describing the scans states that if this is
> the case, anti-inflammatory drugs such as aspirin might help in the future
> to protect patients with Parkinson's diseases and related disorders.
>
> At the MRC Cyclotron Unit of a London hospital, using PET scanning with a
> radiotracer called PK11195, researchers detect the presence of brain
> inflammation. They have learned what patterns of inflammation are typical
> for PD and MSA, and on this basis they can say what appears more or less
> likely; also PD gives a weaker signal, MSA a stronger one. The researchers
> might be annoyed at me putting it in these terms, as it's all couched in
> statistical-speak and is very complex, but that's how I understand it. The
> extent of inflammation is likely to have major prognostic implications as it
> will reflect disease severity, and in future will act as a guide as to
> whether anti-inflammatory and other protective treatments are effective. It
> must be borne in mind that the scans are experimental, and the objective of
> the project is to determine how useful the tool is. Also, not enough brains
> have been scanned yet - especially healthy ones - to give a sound
> statistical basis for comparison. So don't rush off and overdose on
> aspirin/ibuprofen just yet.
>
>
>
> -----Original Message-----
> From: Genene Hill <[log in to unmask]>
> To: [log in to unmask] <[log in to unmask]>
> Date: 08 October 2000 19:38
> Subject: Re: Ibuprofen v Parkinson's
>
>
> Charles,
>
> Can you tell us what specifically was studied and the results of the study?
>
>
>
> on 10/8/00 8:33 AM,  Charles Williams at [log in to unmask]
> wrote:
>
> > I have heard this theory too, in UK. In fact I took part in research on
> > scans that is based on the idea that MSA and PD are associated with
> > inflammation, which may contribute to progression. Documentation mentioned
> > the possibility of anti-inflammatory drugs like aspirin being used for
> > treatment.
> >
> > -----Original Message-----
> > From: William P. Taggart <[log in to unmask]>
> > To: [log in to unmask] <[log in to unmask]>
> > Date: 08 October 2000 11:36
> > Subject: Ibuprofen v Parkinson's
> >
> >
> > Ibuprofen may reduce the risk of Parkinson's and Alzheimer's     <<...>>
> >
> >
> > Although non-steroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen
> > have been found to reduce the risk of Alzheimer's disease (AD), the
> > underlying mechanisms of action are unknown. However, Casper and
> colleagues
> > have recently found that NSAIDs protect neurones from glutamate toxicity
> in
> > vitro - glutamate toxicity has been implicated in AD, Parkinson's disease
> > (PD), and other diseases.
> > Aspirin, acetaminophen, and ibuprofen were all found to attenuate the
> > reduction in dopamine uptake caused by glutamate on cultured primary rat
> > embryonic neurones taken from the mesencephalon area of the brain,
> > indicating preservation of neuronal integrity. Furthermore, ibuprofen
> 100µm
> > protected both dopaminergic neurones and neurones generally, against
> > glutamate toxicity. In addition, of the drugs tested, only ibuprofen
> > increased the relative number of dopaminergic neurons - by 47%.
> > The authors concluded that NSAIDs deserve further consideration as
> > neuroprotective agents in PD.
> > Source: Casper D et al. Neuroscience Letters 2000;289(3):201-204. Updated
> > September 2000.
> >


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