. . . Peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1alpha) is a protein that in humans is encoded by the PPARGC1A gene.[1]. . .
Berberine-containing herbs have been safely used for thousands of years. Can't elaborate on that now in this context. Although, herbs containing it are not the exact thing as that just that single part of it removed - or synthetically manufactured (?) depending upon source.
You might want to ask a LL ND (naturopathic doctor) about this, too.
Always more to learn. -
[ 07-21-2012, 04:31 PM: Message edited by: Keebler ]
Posts: 48021 | From Tree House | Registered: Jul 2007
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Keebler
Honored Contributor (25K+ posts)
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posted
- I tried to find the author at that examine.com site but could not so was unable to see their background and education. They may very well have an important point but would want to see more than just this one source to learn more.
The footnote for that point cites this single study on mice:
35. Wang H, et al.
Atrogin-1 affects muscle protein synthesis and degradation when energy metabolism is impaired by the antidiabetes drug berberine. Diabetes. (2010)
THE REQUIREMENTS OF PROTEIN & AMINO ACID DURING ACUTE & CHRONIC INFECTIONS
Indian J Med Res 124, August 2006, pp 129-148
- by Anura V. Kurpad
Fifteen pages of text.
Excerpt from abstract on page one:
. . . In general, the amount of extra protein that would appear to be needed is of the order of 20-25 per cent of the recommended intake, for most infections. . . . -
Posts: 48021 | From Tree House | Registered: Jul 2007
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posted
"None of this is to encroach upon Marnie's thread here, but just to offer some more detail until she comes along."
No, not at all! I didn't mean to insinuate that only she could post.
You posted lots of good stuff! And for that, I thank you.
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Razzle
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posted
Is ALA contra-indicated in those with amalgam fillings (and no, I cannot remove them; I'm allergic to the alternative filling materials).
-------------------- -Razzle Lyme IgM IGeneX Pos. 18+++, 23-25+, 30++, 31+, 34++, 39 IND, 83-93 IND; IgG IGeneX Neg. 30+, 39 IND; Mayo/CDC Pos. IgM 23+, 39+; IgG Mayo/CDC Neg. band 41+; Bart. (clinical dx; Fry Labs neg. for all coinfections), sx >30 yrs. Posts: 4167 | From WA | Registered: Feb 2011
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Lymeorsomething
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I just put myself on Berberine. I hope it does something...
-------------------- "Whatever can go wrong will go wrong." Posts: 2062 | From CT | Registered: Jul 2008
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Keebler
Honored Contributor (25K+ posts)
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- Razzle,
Don't know why ALA would be contra-indicated for those with amalgam fillings. I would think it would be of help.
But, that is not my area of expertise (actually, I have no such area). So, if you have some experts (more than one) who suggests otherwise, take their words into account.
Do you recall where you read or heard that?
Now, it may be that ALA is best used with binders, etc. if it is a mobilizer. But many folks have mercury in their bodies, not just those with amalgam fillings.
2/3 of the way down, Dr. Sahelian answers that question. (though the spacing here is so very hard on the eyes.
Poster question re: alpha lipoic acid mercury
Dr. S Answer:
We seriously doubt that the alpha lipoic acid and B12 side effects you report are due to mercury poisoning.
Most people have similar alpha lipoic acid side effects when they take high dosages and we don't think it is related to mercury poisoning. . . . -
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Razzle
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posted
Thanks for your reply, Keebler.
I was asking because I often see ALA mentioned as one thing to use during mercury detox.
Since many other things used during mercury detox are not safe to use when one has amalgam fillings still in the mouth, I wondered if the same would be true of ALA.
Also, I took ALA for a while before I knew I had Lyme, and was curious if it could have caused any problems from the amalgam fillings...
Thanks,
-------------------- -Razzle Lyme IgM IGeneX Pos. 18+++, 23-25+, 30++, 31+, 34++, 39 IND, 83-93 IND; IgG IGeneX Neg. 30+, 39 IND; Mayo/CDC Pos. IgM 23+, 39+; IgG Mayo/CDC Neg. band 41+; Bart. (clinical dx; Fry Labs neg. for all coinfections), sx >30 yrs. Posts: 4167 | From WA | Registered: Feb 2011
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NF-κB plays a key role in regulating the immune response to infection (kappa light chains are critical components of immunoglobulins).
Incorrect regulation of NF-κB has been linked to cancer, inflammatory and autoimmune diseases, septic shock, viral infection, and improper immune development. NF-κB has also been implicated in processes of synaptic plasticity and memory.
(Talk about "light chains"...yea, in response to Bb's OspB, we needed IgG1 KAPPA. But our antibody to Bb's OspB was damaged...so the "original" from which we make copies (!) -> ongoing wrong response...antibody wise.)
"Furthermore, berberine ***attenuated*** high glucose-induced generation of reactive oxygen species, cellular apoptosis, ***nuclear factor-kB activation***, and expression of adhesion molecules, thus suppressing monocyte attachment to endothelial cells."
What we have is something (berberine) that can impact ***infected macrophages*** to destroy a pathogen and is capable of knocking off cancer cells too. Amazing.
WHICH berberine? Are they talking about berberine chloride or berberine sulfate?
Do they have different effects? One activates PPARy and the other inhibits?
The only thing I see to PERHAPS add to Berberine chloride (to fight Bb ONLY...not babesia) MAYBE a MDR inhibitor.
Some pathogens export drugs/chemicals they don't want. MDR= multi drug resistant.
Thus adding an inhibitor helps prevent the pathogen from "spitting out" the beneficial chemical out.
Berberine chloride works by interferring with DNA winding and unwinding.
Berberine chloride inhibits ...well...
Berberine also inhibits DNA topoisomerase I and II in biochemical system (14,15), and in fact, several classes of compounds that inhibit eukaryotic topoisomerase I or II have antitumor activity (16).
Many of our antibiotics inhibit one topisomerase or the other! - the PATHOGEN'S DNA.
Berberine inhibits both!!!
Several cancer drugs (including those currently being made) also focus on the topoisomerases. - OUR DNA (which is damaged).
I wish all the websites that discuss berberine would be specific...chloride or sulfate?!
Frontline blocks chloride channels in the tick and thus destroys Bb in the tick.
Tamoxifen blocks chloride channels in breast cancer cells (but adding EPA - omega 3 helps a LOT somehow effecting cancer cells' normal resistance to cell death).
Logically...if Bb is triggering the opening of the chloride channels (and sodium channels), why not make use of that fact and send in berberine chloride?
Would the sulfate form be less likely to go into the effected cells?
Any biochemists reading? Does berberine chloride and berberine sulfate have different effects on cells? All cells or just certain ones?
P.S. I think the KIND of Mg given IV after "photon therapy" was Mg CHLORIDE.
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Marnie
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posted
1. PGC-1alpha interacts with PPARy. = PPAR gamma.
2. These studies suggest that BBR (berberine) works on multiple molecular targets as an
***inhibitor of PPARgamma and alpha, ***
and is a potential weight reducing, hypolipidemic, and hypoglycemic drug.
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