Welcome! This blog contains research, information on lifestyle, nutrition, dietary supplements and health for those with MS, as well as continuing information on the understanding of CCSVI and cerebral hypoperfusion. This blog is informative only--all medical decisions should be discussed with your own physicians.

The posts are searchable---simply type in your topic of interest in the search box at the top left.

Almost all of MS research is initiated and funded by pharmaceutical companies. This maintains the EAE mouse model and the immune paradigm of MS, and continues the 15 billion dollar a year MS treatment industry. But as we learn more about slowed blood flow, gray matter atrophy, and environmental links to MS progression and disability--all things the current drugs do not address--we're discovering more about how to help those with MS.

To learn how this journey began, read my first post from August, 2009. Be well! Joan

Tuesday, December 4, 2012


Fibrinogen---found In ALL neurodegenerative diseases, not just MS

December 4, 2012 at 9:29am

The "news" this week was that fibrinogen, an essential clotting protein, crosses over the blood brain barrier in the mouse model of MS and initiates the disease process by destroying nerve cells.  

Fibrinogen-induced perivascular microglial clustering is required for the development of axonal damage in neuroinflammation

But this isn't news.  Researchers have been studying this process in neurodegenerative disease for a decade.  Because this process happens when the blood brain barrier breaks down.

The overall findings from study of Alzheimer's Disease brain tissue and in vivo in Abeta(1-42) and Abeta(1-42) plus fibrinogen stimulated rat hippocampus suggest microglial responses to promote increased extravasation of blood protein as a critical component in amplifying inflammatory reactivity and causing neuronal damage in inflamed AD brain.

Fibrinogen is a pleiotropic blood protein that regulates coagulation, inflammation and tissue repair. Fibrinogen extravasates in the nervous system after injury or disease associated with vascular damage or blood-brain barrier (BBB) disruption. Fibrinogen is not merely a marker of BBB disruption, but plays a causative role in neurologic disease as a potent inducer of inflammation and an inhibitor of neurite outgrowth. Fibrinogen mediates functions in the nervous system as a ligand for cell-specific receptors. In microglia, fibrinogen mediates activation of Akt and Rho via the CD11b/CD18 integrin receptor, while in neurons fibrinogen induces phosphorylation of epidermal growth factor (EGF) receptor via the alphavbeta3 integrin. Pharmacologic targeting of the interactions of fibrinogen with its nervous system receptors could provide novel strategies for therapeutic intervention in neuroinflammatory and neurodegenerative diseases.

Why the race for researchers to understand fibrinogen?
Because pharma wants to monetize a way to block it.
That's right....researchers are not studying WHY fibrinogen is breaking through the blood brain barrier.  No one is looking at causation.
Everyone is studying this to find a pharmacological means of stopping fibrinogen.

But, what if there is an underlying mechanism which begins fibrinogen activation in all neurodegenerative disease?
Wouldn't that be something to study?  Wouldn't that be causation, and lead to potential answers in disease aetiology?

Here's a paper I researched and wrote up for CCSVI Alliance on the discovery of CCSVI in other neurological disease.  It proposes the mechanism found in common with CCSVI in neurodegenerative disease.  Slowed cerebral bloodflow.

HYPOPERFUSION.   A mechanism found in all neurodegenerative disease, which starts fibrin deposition in the brain. This is being studied by stroke researchers.  A decline in cerebral bloodflow initiates fibrin deposition in the brain immediately.

One of the most surprising findings of the present study is that the decline of cerebral blood flow (CBF) in conjunction with hypoxia is sufficient to induce rapid microvascular thrombosis and fibrin deposition within the brain (Figure 9). By analyzing challenged fibrinogen-null mice we have established that fibrin(ogen) plays an important role the reperfusion deficits and brain infarction (Figure 10). These results suggest that if cerebral ischemia is accompanied with hypoxia, this combination can precipitate local coagulation and impede reperfusion after ischemia, similar to the previously described no-reflow phenomenon after cerebral ischemia5 and cardiac arrest.56 It seems likely that fibrin stabilization of platelet thrombi is a major determinant of brain tissue damage. If so, we would predict that a similar, if not more impressive, protection from tissue damage could be realized in mice with a profound defect in platelet function. It is also conceivable that fibrin-mediated inflammatory processes drive secondary tissue damage in the brain. Thus, the modified Levine/Vannucci model described here may be useful for testing new therapies to restore postischemic reperfusion in the face of thrombolytic agents and other approaches to reopened large vessels.
Regarding the mechanism of ischemia/hypoxia-induced thrombosis, it seems likely that hypoxia alters the balance between anti- and procoagulation properties of the endothelial cells in cerebral blood vessels. Although focal ischemia can trigger platelet accumulation and fibrin deposition, these events typically show a late-onset after a transient hyperemia phase.49,53 In contrast, the present study shows that the combination of ischemia and hypoxia precipitates these events almost immediately. 

Please encourage and support the researchers of the International Society for Neurovascular Disease.  
Please support CCSVI Alliance. http://www.ccsvi.org
There are only a few groups looking at disease aetiology, or what is causing the disease process.

Blocking fibrinogen won't cure MS.  
Understanding why there is fibrinogen in brain tissue may.
Joan

4 comments:

  1. il fibrinogeno, si riduce alla normalità, da 30-90 gg utilizzando,in sinergia, in primis, semi di Lino germogliati o ammollati, in insalata con pezzi di cladodi, max un anno di vita, per minor fibra, erba Portulaca e 1,5g circa di foglie gialle, giammai verdi !, di Ginkgo Biloba .

    Per miglioramento tissutale , utilizzare, 1,5 g di polvere micronizzata , da osso di Seppia, guscio e/o Perla di Ostriche di mare !! .

    ReplyDelete
    Replies
    1. Translated, from Italy, with GOOGLE:
      To regularize the FIBRINOGEN Triglycerides and Cholesterol-enough, in about 30-90 days, for the woman, also using the Pill Anti-Conceptional, use, per day, during the day, oil Linseed, better even if you used the seeds!, if realized cold, transported-sold in the refrigerator!, in total dose of 60 g, combined with 1.5 g of yellow powder and NO green, the leaves of the Ginkgo Biloba! and, even better if used with weed in salads, the Portulaca with bits of the inside of cladodes, commonly called blades of prickly pear of about a year, because less fibrosis, with plenty of olive oil, EVOO Yellow GOLD dense live to the mill, from ripe olives with endocarp inner pulp purple dense live up to the core and, NEVER NOT mATURE oLIVE GREEN OR WORSE iN TOTO! OIL AND GREEN EVOO! poisons centellinanti!, and ripe olives, fresh or used, all year, if dried in the oven at a maximum temperature of 35 ° C and stored, shriveled, for use throughout the year, in a vacuum! partaking least No. 50 a day!

      Delete
    2. Translated, from Italy, with GOOGLE:
      To regularize the FIBRINOGEN Triglycerides and Cholesterol-enough, in about 30-90 days, for the woman, also using the Pill Anti-Conceptional, use, per day, during the day, oil Linseed, better even if you used the seeds!, if realized cold, transported-sold in the refrigerator!, in total dose of 60 g, combined with 1.5 g of yellow powder and NO green, the leaves of the Ginkgo Biloba! and, even better if used with weed in salads, the Portulaca with bits of the inside of cladodes, commonly called blades of prickly pear of about a year, because less fibrosis, with plenty of olive oil, EVOO Yellow GOLD dense live to the mill, from ripe olives with endocarp inner pulp purple dense live up to the core and, NEVER NOT mATURE oLIVE GREEN OR WORSE iN TOTO! OIL AND GREEN EVOO! poisons centellinanti!, and ripe olives, fresh or used, all year, if dried in the oven at a maximum temperature of 35 ° C and stored, shriveled, for use throughout the year, in a vacuum! partaking least No. 50 a day!

      Delete
  2. I'll forward this to my neurologist, hoping he doesn't lol, although I don't have MS but something else.

    ReplyDelete