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Old 10-08-2012, 03:07 PM #1
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Default Hyperactive neuro immune response and neuronal destruction

Study identifies biological mechanism that plays key role in early-onset dementia October 8, 2012 in Neuroscience

Using animal models, scientists at the Gladstone Institutes have discovered how a protein deficiency may be linked to frontotemporal dementia (FTD)—a form of early-onset dementia that is similar to Alzheimer's disease...

As its name implies, FTD is a fatal disease that destroys cells, or neurons, that comprise the frontal and temporal lobes of the brain..
A new study ...show(s) how a protein called progranulin prevents a class of cells called microglia from becoming "hyperactive." Without adequate progranulin to keep microglia in check, this hyperactivity becomes toxic, causing abnormally prolonged inflammation that destroys neurons over time—and leads to debilitating symptoms... "Understanding the inflammatory process in the brain is critical if we are to develop better treatments not only for FTD, but for other forms of brain injury such as Parkinson's disease, Huntington's disease and multiple sclerosis (MS)—which are likely also linked to abnormal microglial activity." ...

Microglia—which are a type of immune cells that reside in the CNS—normally secrete progranulin. Early studies on traumatic CNS injury found that progranulin accumulates at the injury site alongside microglia, suggesting that both play a role in injury response. So, Dr. Farese and his team designed a series of experiments to decipher the nature of the relationship between progranulin and microglia. First, the team generated genetically modified mice that lack progranulin. They then monitored how the brains of these mice responded to toxins, comparing this reaction to a control group. "As expected, the toxin destroys neurons in both sets of mice—but the progranulin-deficient mice lost twice as many neurons as the control group," said Lauren Herl Martens, a Gladstone and UCSF graduate student and the study's lead author. "This showed us that progranulin is crucial for neuron survival. We then wanted to see whether a lack of progranulin itself would injure these cells—even in the absence of toxins." In a petri dish, the researchers artificially prevented microglia from secreting progranulin and monitored how these modified microglia interacted with neurons. They observed that a significantly greater number of neurons died in the presence of the progranulin-deficient microglia when compared to unmodified microglia...

Microglia are the CNS's first line of defense. When the microglia sense toxins or injury, they trigger protective inflammation—which can become toxic to neurons if left unchecked. Dr. Farese's team discovered that progranulin works by tempering the microglia's response, thereby minimizing inflammation. Without progranulin, the microglia are unrestricted—and induce prolonged and excessive inflammation that leads to neuron damage—and can contribute to the vast array of symptoms that afflict sufferers FTD and other fatal forms of brain disease. "However, we found that boosting progranulin levels in microglia reduced inflammation—keeping neurons alive and healthy in cell culture," explained Dr. Farese. "Our next step is to determine if this method could also work in live animals. We believe this to be a therapeutic strategy that could... halt the progression of FTD... our findings about progranulin and inflammation could have therapeutic implications for... diseases such as Alzheimer's, Parkinson's and MS." Journal reference: Journal of Clinical Investigation search and more info website

Read more at: http://medicalxpress.com/news/2012-1...onset.html#jCp
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Old 10-08-2012, 03:47 PM #2
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If they send my Nobel by UPS they can leave it behind my neighbor's doghouse. :-)
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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 10-08-2012, 04:22 PM #3
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Default While we are waiting

In the meantime there is the herb Andrographis paniculata http://www.ncbi.nlm.nih.gov/pubmed/14718612

Dextromethorphan http://www.ncbi.nlm.nih.gov/pubmed/12649371

Curcumin (longvida kind) http://www.ncbi.nlm.nih.gov/pubmed/18214347

Green tea (ECGC) http://www.ncbi.nlm.nih.gov/pubmed/15478178

DHA from fish oil http://www.fasebj.org/cgi/content/me...ct/21/6/A736-b

I take everything but the dextromethorphan.
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Old 10-10-2012, 08:40 AM #4
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Rick, I thought they mistakenly left your name off the authors' list.
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