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ThisIsMS.com :: View topic - They could be on to something
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They could be on to something
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rainer
Family Elder


Joined: Jan 18, 2008
Posts: 223

PostPosted: Tue Apr 08, 2008 4:46 pm    Post subject: Reply with quote

good to see another possible avenue for treatment but frustrating to see you were posting this in 2005 Confused
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dignan
Family Elder


Joined: Aug 12, 2004
Posts: 1192

PostPosted: Tue Apr 08, 2008 8:36 pm    Post subject: Reply with quote

I agree, it is a bit frustrating, and the UC Irvine group isn't even at the IND stage, they're still doing pre-clinical work. One company that is working on the same target is Bionomics. They still haven't even selected their drug candidate yet, although if you believe their material, they are due to pick their candidate any day now.
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gibbledygook
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Joined: Feb 15, 2005
Posts: 723
Location: London

PostPosted: Fri Apr 11, 2008 10:33 am    Post subject: Reply with quote

Genistein inhibits kv1.3 (give up milk and eat soy!).
<shortened url>
Red wine
<shortened url>
Zinc
<shortened url>

looks like green tea and curcumin inhibit potassium channels with different numbers...
_________________
1st traceable symptoms Jan 01, last edss by doctor 6.5. Feeling better on ginkgo, salvia, capsaicin, curcumin, scutellaria. Interested in other vascular strengthening herbs; pycnogenol, butcher's broom, horsechestnut, centenella, hersperidin
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dignan
Family Elder


Joined: Aug 12, 2004
Posts: 1192

PostPosted: Mon Apr 21, 2008 10:20 pm    Post subject: Reply with quote

Gibbledygook, thanks for the info. I'm always interested in excuses for drinking more red wine, and I already use soy milk...now to go read some of jimmylegs' rantings about zinc...

I also found this on Kv1.3


Minocycline decreases in vitro microglial motility, beta1-integrin, and Kv1.3 channel expression.

J Neurochem. 2007 Dec;103(5):2035-46. Epub 2007 Sep 14.
Nutile-McMenemy N, Elfenbein A, Deleo JA.
Department of Anesthesiology, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA.

Minocycline is a semisynthetic, tetracycline derivative that exerts anti-inflammatory and neuroprotective effects unrelated to its anti-microbial action. We have previously shown that minocycline prevented peripheral nerve injury-induced mechanical allodynia. Minocycline's mechanisms of action as a neuroprotective and anti-allodynic agent are unknown.

In response to injury, microglia become activated, proliferate, and migrate. Resting microglia express voltage-dependent inward K(+) currents and blocking Kv1.3 channels has been shown to inhibit microglial-mediated neuronal death. We investigated the effect of minocycline on the expression of Kv channels, cell motility, and beta-integrin expression using primary rat cortical microglia, transwell assays, and by flow cytometry.

Minocycline significantly reduced microglial migration to cellular debris, astrocyte-conditioned medium, ADP, and algesic mediators and significantly reduced the expression of CD29 (beta(1)-integrin) but not CD18 (beta(2)-integrin). Minocycline reduced the effect of extracellular potassium and later decreased microglial Kv1.3 expression. In summary, we uncovered a novel effect of minocycline that demonstrates this agent decreases microglial beta(1)-integrin expression, which leads to inhibition of motility. We propose an in vivo model whereby reduced microglial trafficking to injured neurons following nerve injury decreases the release of proinflammatory mediators into the synaptic milieu, preventing neuronal sensitization, the pathological correlate to chronic pain.

Pubmed link
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