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Berberine
Dave Johnson's Proletariat Protocol
Information on nutritional supplements people with ALS have been taking
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<languages/> [[Special:MyLanguage/Information on nutritional supplements people with ALS have been taking|Tietoa ALS-potilaiden käyttämistä lisäravinteista]] * [https://en.wikipedia.org/wiki/Berberine Wikipedia-sivu] * [http://examine.com/supplements/Berberine/ Examine.com] kertoo berberinestä: :* alkaloidi, jota uutetaan useista perinteisessä kiinalaisessa lääketieteessä käytetystä kasveista :* käytetään lisäravinteena '''tulehdusta vähentävien''' ja '''diabetesta vastustavien''' vaikutusten takia :* voi myös '''parantaa suoliston terveyttä''' ja '''alentaa kolesterolia''' :* kykenee '''alentamaan glukoosin tuotantoa maksassa'''. :* 1500 mg kolmena 500 mg annoksena otettuna on ihmis- ja eläinkokeiden perusteella yhtä tehokas kuin 1500 mg metformiinia tai 4 mg glibenclamidea (tyypin II diabetekseen käytettäviä lääkkeitä). Tehokkuutta mitattiin aineiden kyvyllä vähentää tyypin II diabeteksen biomarkkereita. :* Saattaa myös lisätä mielialalääkkeiden tehoa ja auttaa kehoa pääsemään eroon rasvasta. Näistä hyödyistä tarvitaan kuitenkin lisänäyttöä ennen kuin berberineä voidaan suositella ko. tarkoituksiin. :* Päämekanismi on osin diabetestä ja tulehdusta vastustavan vaikutuksen takana. :* Kykenee aktivoimaan AMPK-entsyymiä ja samalla w while inhibiting Protein-Tyrosine Phosphatase 1B (PTP1B). According to Wikipedia, the half-life ''in vivo'' seems to be 3-4 hours, thus suggesting administration three times a day if steady levels are to be achieved. == Effect of berberine on ALS == In rat cerebral cortex, berberine inhibits synaptosomal glutamate release.{{#pmid:23840629|Lin2013}} By downregulating several proinflammatory pathways{{#pmid:19208854|Jeong2009}} it presumably reduces the neuroinflammatory component of ALS. Berberine activates AMPK apparently by inhibiting mitochondria{{#pmid:19208854|Jeong2009}}, resulting into increased glycolysis. ''Note: progression seems to correlate with AMPK activation in SOD1 ALS but with AMPK inactivation in TDP-43 ALS{{#pmid:24595038|Perera2014}} .'' In a study{{#pmid:21086546|Campisi2011}} on rat astrocyte primary cultures, berberine and the alkaloid extract of B. aetnensis roots were able to restore the oxidative status modified by glutamate and the levels of TG2 to control values. Consequently berberine or the alkaloid extract of B. aetnensis roots are able to ameliorate the excessive production of glutamate, protein misfolding and aggregation, mitochondrial fragmentation, and neurodegeneration. Berberine is a PPAR gamma inhibitor{{#pmid:18520050|Zhou2008}}. ''Note: the significance of this for ALS needs further elaboration.'' It may be helpful against leaky gut, which is hypothetized to be a part of ALS pathology [source needed]. ==Cautions and risks== On the negative side, berberine has been found to '''impair muscle metabolism''' by two mechanisms. It impairs mitochondrial function stimulating the expression of [http://www.pnas.org/content/98/25/14440.full atrogin-1] without affecting phosphorylation of forkhead transcription factors. The increase in atrogin-1 not only stimulates protein degradation but also suppresses protein synthesis, causing muscle atrophy.{{#pmid:20522589|Wang2010}} It has also been found{{#pmid:20393601|Sarna2010}} to restore SOD1 activity inhibited by lipopolysaccharides. == Discussion threads on the ALSTDI forum == * [http://www.alstdi.org/forum/yaf_postst48627_berberine.aspx Berberine] * [http://www.alstdi.org/forum/default.aspx?g=posts&t=46945 Berberine Suppresses Pro-Inflammatory Responses]: :''In adipose tissue of obese db/db mice, BBR treatment significantly down-regulated the expression of pro-inflammatory genes such as TNFalpha, IL-1beta, IL-6, MCP-1, iNOS and COX2. Consistently, BBR inhibited LPS-induced expression of pro-inflammatory genes including IL-1beta, IL-6, iNOS, MCP-1, COX 2, and MMP9 in peritoneal macrophages and RAW 264.7 cells. Upon various pro-inflammatory signals including LPS, free fatty acids, and hydrogen peroxide, BBR suppressed the phosphorylation of MAPKs such as p38, ERK, and JNK, and the level of reactive oxygen species in macrophages.''{{#pmid:17971514|Yin2008}} * [http://www.alstdi.org/forum/yaf_postst54133_ampk-activation-status-in-different-types-of-als.aspx AMPK activation status in different types of ALS]: :''While AMPK activation in motor neurons correlates with progression in mutant SOD1-mediated disease, AMPK inactivation mediated by PP2A is associated with mutant TDP-43-linked ALS.'' * [http://www.alstdi.org/forum/yaf_postst50860_interesting--leaks-and-neuro-diseases.aspx Interesting - leaks in neuro diseases] :''According to a 2010 study, berberine ameliorated damage to the tight junctions of intestinal epithelial cells induced by pro-inflammatory cytokines (in vitro). Berberine may thus serve as a targeted therapeutic agent for restoring barrier function in intestinal disease states.[16]'' == Regulated pathways == == Where to get it == * [http://www.amazon.co.uk/Swanson-Berberine-400mg-60-Capsules/dp/B006MRK8LG Amazon.co.uk (400 mg capsules)] == References == [[Category:Supplement data pages]]
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