Parkinson's Disease Tulip


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Old 02-09-2009, 06:47 AM #1
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Default Adding to the BBB list

I have over the years made a list of substances or events which make PD symptoms worse, and those whichreduce symptoms.
Typical on the "worsen" list are
Stress
Ageing
Pesticides etc
Typical of the improve list are
Curcumin
Alpha lipoic acid,
CDP Choline
GDNF
antihypertension drugs
So far, everything on the worsen list increases BBB permeability.
Everything on the improve list decreases BBB permeability.
I am still adding to each list, and recently caffeine is shown to decrease the incidence of PD.
http://www.medicine.ox.ac.uk/bandoli...d78/b78-6.html

We can add caffeine to the "improve" list since, of course, it reduces the BBB permeability. See
http://content.karger.com/ProdukteDB...ame=136581.pdf

In another post, aluminium, implicated in causing AD, increases BBB permeability, so can be added to the worsen list.

So not a [U][single exception/U] has been found.
Can this be a coincidence??? Surely not, but it is an area much neglected by research.
Ron
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Old 02-11-2009, 02:59 AM #2
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Default Yet another additiion, magnesium

Have a look at another PD forum thread, on the benefits of magnesium.
http://pduk.org/forum/index.php/topic,1955.0.html
Magnesium can also be added to the list of beneficial substances which reduce BBB permeability.
http://ep.physoc.org/cgi/content/abs....2007.039966v1
"Magnesium sulphate treatment decreases blood-brain barrier permeability"

How many more do we need to find before the medical profession takes some notice.
Ron
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Old 02-11-2009, 06:54 AM #3
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Lightbulb I think you should have

Essential fatty acids on your "improve" list.

These fats actually make up the BBB as well as other membranes. A diet low in them, leads to poor vascular tone.

http://www3.interscience.wiley.com/j...TRY=1&SRETRY=0

http://cat.inist.fr/?aModele=afficheN&cpsidt=17416789

There are channels in the BBB called Zonulin channels. They are similar to the ones in the GI mucosa.
http://findarticles.com/p/articles/m...ne/ai_75178698

The Celiac community is researching this, and I believe their findings will help PD and other CNS Neuro disorders. A drug is in trials to "close the Zonulin channels".
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Old 02-11-2009, 02:49 PM #4
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Default tight BBB

Does a tight BBB mean the meds don't get in as quick or as much?
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Old 02-11-2009, 03:10 PM #5
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Lightbulb yes...

a tight BBB only allows certain drugs thru..mostly a function of
lipid solubility. For example, alcohol and anesthetics pass the
easiest.

In the case of the Zonulin channels, these would allow bacteria thru, and large water soluble substances and peptides. This would be the CNS version of "leaky gut syndrome". Leaky gut was always pooh poohed by doctors and now with the new information, that is no longer that controversial.

Some drugs like H2 antagonists, Zantac and Pepcid, pass the BBB more often in the elderly. They cause a delirium when that happens. That is one example of how the BBB changes with age.
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Old 02-11-2009, 05:12 PM #6
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Default MrsD

Do you have any info on things that might simultaneously increase permeability of both BBB and gut? Given our slow GI motility that would seem to dump toxins into the bloodstream at the worst possible time.
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Born in 1953, 1st symptoms and misdiagnosed as essential tremor in 1992. Dx with PD in 2000.
Currently (2011) taking 200/50 Sinemet CR 8 times a day + 10/100 Sinemet 3 times a day. Functional 90% of waking day but fragile. Failure at exercise but still trying. Constantly experimenting. Beta blocker and ACE inhibitor at present. Currently (01/2013) taking ldopa/carbadopa 200/50 CR six times a day + 10/100 form 3 times daily. Functional 90% of day. Update 04/2013: L/C 200/50 8x; Beta Blocker; ACE Inhib; Ginger; Turmeric; Creatine; Magnesium; Potassium. Doing well.
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Old 02-11-2009, 05:18 PM #7
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Default Sorry, I should have looked first

We already know that stress opens the BBB. It works both ends of the street, it seems,


1: Curr Mol Med. 2008 Jun;8(4):299-312.

The effects of physical and psychological stress on the gastro-intestinal tract:
lessons from animal models.

Caso JR, Leza JC, Menchén L.

Sección de Gastroenterología, Servicio de Aparato Digestivo, Hospital General
Universitario "Gregorio Marañón", C/ Dr Esquerdo 46. 28007 Madrid, Spain.

Physical and psychological stresses are widely accepted as triggers and / or
modifiers of the clinical course of diverse gastrointestinal disorders such as
peptic ulcer, irritable bowel syndrome or inflammatory bowel disease. Growing
experimental evidence from a variety of models such as immobilization, thermal
injury or early maternal deprivation in laboratory animals uniformly supports the
ability of stress to induce the development of gastric ulcers, altered
gastrointestinal motility and ion secretion, and increased intestinal
permeability leading to the passage of antigens to the lamina propria and
bacterial translocation. Stress can also synergize with other pathogenic factors
such as Helicobacter pylori, non-steroidal anti-inflammatory drugs or
colitis-inducing chemicals to produce gastrointestinal disease. The brain-gut
axis provides the anatomical basis through emotions and environmental influences
modulate the gastrointestinal function through the regulation of gastrointestinal
immune system and mucosal inflammation; in this sense, mucosal mast cells - at
cellular level - and corticotropin releasing factor (CRF) - at molecular level -
seem to play a crucial role. On the other hand, an array of adaptive responses
have been evolved in order to maintain the homeostasis and to ensure the survival
of the individual. In the gut mucosa anti-inflammatory pathways counteract the
deleterious effect of the stressful stimuli on the gastrointestinal homeostasis.
In the present review we discuss the several experimental approaches used to
mimic human stressful events or chronic stress in laboratory animals, the
evidence of stress-induced gastrointestinal inflammation and dysfunction derived
from them, and the involved cellular and molecular mechanisms that are being
discovered during the last years.


PMID: 18537637 [PubMed - indexed for MEDLINE]
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Born in 1953, 1st symptoms and misdiagnosed as essential tremor in 1992. Dx with PD in 2000.
Currently (2011) taking 200/50 Sinemet CR 8 times a day + 10/100 Sinemet 3 times a day. Functional 90% of waking day but fragile. Failure at exercise but still trying. Constantly experimenting. Beta blocker and ACE inhibitor at present. Currently (01/2013) taking ldopa/carbadopa 200/50 CR six times a day + 10/100 form 3 times daily. Functional 90% of day. Update 04/2013: L/C 200/50 8x; Beta Blocker; ACE Inhib; Ginger; Turmeric; Creatine; Magnesium; Potassium. Doing well.
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Old 02-12-2009, 06:51 AM #8
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Lightbulb I've been watching Zonulin for

a long time now, and have read the Celiac boards for years.

I can't recall finding out the "why" it is higher in some people than others.
It just "is".

If you Google it there are many hits, including the drug company who has a compound in trials.

Here is an interesting Wiki, with illustrations:
http://en.wikipedia.org/wiki/Tight_junction

I think PD along with other CNS neuro problems, may have a connection to gluten intolerance.
Here is the Gluten file:
http://jccglutenfree.googlepages.com/

It is a huge collection of data, including neuro issues and very helpful.
Going gluten free may be very helpful for some people here.
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