Guest guest Posted September 11, 2008 Report Share Posted September 11, 2008 I know that curcumin's limitations for viable treatment is bioavailability. In humans they havent achieved more than 0.1uM free curcumin in plasma even with piperine at like 12 grams per day, but here they report 5uM, like 50x greater. Could this be true? See http://www.ncbi.nlm.nih.gov/pubmed/18417733 " Oral gavage of an optimized lipidated curcumin formulation (Verdure Sciences, Noblesville, Indiana) resulted in 11-fold higher levels of curcumin in plasma and 4-fold higher levels in brain compared to equal doses of curcumin powder or curcumin-piperine extracts. A 5 mg curcumin dose delivered by acute gavage in this lipid rich formulation (n=5) resulted in 2.15 ± 0.744 µM mouse brain curcumin levels after 3 hrs. After 2 weeks lipidated formulation at 500 ppm curcumin in chow (n=5) we observed 5.79 ± 1.22 µM mouse brain curcumin, well above the 1-2 µM range of EC50's for the inhibition of iNOS, IL-1ß, PGE2 and isoprostanes. This suggests oral delivery can achieve our target tissue levels. " http://www.ncbi.nlm.nih.gov/pubmed/18417733 Am I reading this right? Curtis " Anyone who has never made a mistake has never tried anything new. " - Einstein Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 13, 2008 Report Share Posted September 13, 2008 Curtis, I am not a scientist so had a hard time reading the link, etc. Is this on the market? Also, how would eating the actual turmeric root work? Thanks GB , " curtsummerlin " <curtsummerlin wrote: > > I know that curcumin's limitations for viable treatment is > bioavailability. In humans they havent achieved more than 0.1uM free > curcumin in plasma even with piperine at like 12 grams per day, but > here they report 5uM, like 50x greater. Could this be true? See > http://www.ncbi.nlm.nih.gov/pubmed/18417733 > > " Oral gavage of an optimized lipidated curcumin formulation (Verdure > Sciences, Noblesville, Indiana) resulted in 11-fold higher levels of > curcumin in plasma and 4-fold higher levels in brain compared to > equal doses of curcumin powder or curcumin-piperine extracts. A 5 mg > curcumin dose delivered by acute gavage in this lipid rich > formulation (n=5) resulted in 2.15 ± 0.744 µM mouse brain curcumin > levels after 3 hrs. After 2 weeks lipidated formulation at 500 ppm > curcumin in chow (n=5) we observed 5.79 ± 1.22 µM mouse brain > curcumin, well above the 1-2 µM range of EC50's for the inhibition of > iNOS, IL-1ß, PGE2 and isoprostanes. This suggests oral delivery can > achieve our target tissue levels. " > > http://www.ncbi.nlm.nih.gov/pubmed/18417733 > > Am I reading this right? > > Curtis > > " Anyone who has never made a mistake has never tried anything new. " - > Einstein > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 17, 2008 Report Share Posted September 17, 2008 Okay, I am completely clueless as to what you are talking about but am extremely interested. Are you saying that tumeric root can help or cure alzheimers? Can you put this in layman's terms for me. Thanks; Beva Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 18, 2008 Report Share Posted September 18, 2008 Beva Turmeric is good for a lot of things. Evidently scientists at UCLA have come up with a process that makes turmeric much more effective for Alzheimer's than the usual form of turmeric. I presume that they used a form similiar to what most people buy commercially. That is why I wrote Mr. Ebersole. It is in scientific terms and I think that the only ones who really know about it are the scientists because of the language. GB , Beva <beva1960 wrote: > > Okay, I am completely clueless as to what you are talking about but am extremely interested. Are you saying that tumeric root can help or cure alzheimers? Can you put this in layman's terms for me. > > Thanks; > Beva > Quote Link to comment Share on other sites More sharing options...
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