dickkopf-1* (Dkk-1) via alkaline phosphatase activity, releasing ascorbic acid into the cell; leading to neurogenesis.
*Seriously? What does the rest of that sentence even mean?
Posted 15 May 2013 - 01:17 AM
dickkopf-1* (Dkk-1) via alkaline phosphatase activity, releasing ascorbic acid into the cell; leading to neurogenesis.
Posted 15 May 2013 - 01:37 AM
dickkopf-1* (Dkk-1) via alkaline phosphatase activity, releasing ascorbic acid into the cell; leading to neurogenesis.
*Seriously? What does the rest of that sentence even mean?
Posted 15 May 2013 - 02:25 AM
It means that L-Threonate is turned into intracellular Ascorbic Acid by alkaline phosphatase activity where it neutralises the DKK-1 protein; allowing normal, young level neurogenesis.
My apologies for oversimplifying the sentence in an effort to make it more readable.
Edited by ta5, 15 May 2013 - 02:26 AM.
Posted 15 May 2013 - 11:52 AM
Maybe L-Threonate and maybe not Magnesium-L-Threonate. I don't think you can say they will share the same effects.
Edited by Logic, 15 May 2013 - 12:38 PM.
Posted 15 May 2013 - 12:14 PM
Maybe L-Threonate and maybe not Magnesium-L-Threonate. I don't think you can say they will share the same effects.
Read the studies!
I THINK that you cant get L-Threonate on its own: You have to chelate something like Magnesium or Calsium to get it?
Edited by ta5, 15 May 2013 - 12:15 PM.
Posted 15 May 2013 - 01:11 PM
Maybe L-Threonate and maybe not Magnesium-L-Threonate. I don't think you can say they will share the same effects.
Read the studies!
I THINK that you cant get L-Threonate on its own: You have to chelate something like Magnesium or Calsium to get it?
I had looked at the abstracts you posted in your other thread.
Maybe L-Threonate and maybe not Magnesium-L-Threonate. I don't think you can say they will share the same effects.
Edited by ScienceGuy, 15 May 2013 - 01:16 PM.
Posted 16 May 2013 - 01:51 AM
Posted 16 May 2013 - 02:15 AM
Posted 16 May 2013 - 04:03 AM
Folks, forget the trivial increase in magnesium. Does not matter and can be reached in very many different ways... After all, the increases in brain magnesium levels from mg threonate are too small to really matter much...
1. Problem: Vitamin C in the ascorbic acid form does not cross the BBB to brain. Traditionally, it was thought that it was the dehydroascorbic acid form how vitamin C got to the brain...
Edited by ScienceGuy, 16 May 2013 - 04:07 AM.
Posted 16 May 2013 - 04:12 AM
To clarify, ESTER-C comprises circa 10% as CALCIUM THREONATE-DEHYDROASCORBATE (i.e. THREONATE bonded to the DEHYDROASCORBIC ACID form of VITAMIN C), and hence it does in fact readily cross the BLOOD BRAIN BARRIER (BBB); N.B. this is outlined in its PATENT INFORMATON which you can find here: US PATENT NUMBER WO2008103926 A1
Hence one of my reasons for recommending it as a highly bioactive way of supplementing with THREONATE and IMO preferred to MAGNESIUM L-THREONATE which is very expensive to boot
Posted 16 May 2013 - 06:06 AM
Rock on. Sounds like we agree.
...next patent magnesium compounds coming from China will be "magnesium cocaine" for "chronic fatigue syndrome" and "magnesium sildenafil" for erectile dysfunction. Raising magnesium levels in your scrotum will do wonders for your sex life, they'll say
Posted 16 May 2013 - 12:11 PM
Posted 16 May 2013 - 12:18 PM
Gawd damn it Science Guy! Please, let me spend my money frivolously, especially if I feel a placebo effect from an expensive supplement I've been purchasing since January 1st. It grows hair for pete's sake! I need to enjoy the perception that I've stumbled upon something great before most others on the forums have discovered it's 'true' beneficial properties.
Next thing you're going to tell me is that you agree with the thread I posted entitled, "Fish Oils do Nothing". (sigh)
Posted 16 May 2013 - 12:36 PM
Posted 16 May 2013 - 01:03 PM
Of course, I did not suffer through Grad school to get a paper without knowing anything about research, various research methodologies and inherent biases easily detected in published studies.
I will say though, that if this Mag-T product I've been taking in the mornings doesn't actually improve cognition without any sedation, than it truly is a placebo effect. If this turns out to be the case, please send me your 'samples' - but, if you'd be so kind, give it a cool name or put it in a colorful capsule or something will ya?
Posted 25 June 2013 - 04:33 AM
http://www.nutraingr...pected-mid-2012
Human data on memory-boosting magnesium compound expected mid-2012
By Elaine Watson , 30-Nov-2011
Preliminary results of a human study into Magtein - a patent-pending magnesium compound called magnesium-L-threonate claimed to boost memory and cognitive function - will be available next year.
Given the intense interest in cognitive health ingredients, Magtein – which is self-affirmed GRAS, soluble in water, odorless, tasteless and colorless - has already attracted a lot of interest in the dietary supplements and food sector following the publication of a high-profile animal study conducted by scientists at MIT in the journal Neuron last year.
This showed that Magtein – developed by Magceutics and distributed by AIDP on an exclusive basis - could increase learning ability, working memory, and short- and long-term memory in young and aged rats.
It also showed that common magnesium compounds do not effectively improve brain magnesium levels (Enhancement of Learning and Memory by Elevating Brain Magnesium, Slutsky I, Abumaria N, Wu LJ, Huang C, Zhang L, Li B, Zhao X, Govindarajan A, Zhao MG, Zhuo M, Tonegawa S, Liu G. Neuron. 2010 Jan 28;65(2):165-77).
Food firms interested but waiting for results of human trial
A human study, which has just started at the University of Southern California, is now looking at whether these results can be replicated in people, said an AIDP spokesman.
“The human clinical study is a double-blind, placebo controlled study with 40 individuals. Preliminary results will be available by mid-2012.”
He did not disclose the age or cognitive abilities of the volunteers are being studied, what biomarkers will be monitored and what cognitive tests will be performed, adding: “As this study is in the initial phases, the design details are confidential at this point.
“But we will be happy to share more when the study is completed.”
Edited by blood, 25 June 2013 - 04:34 AM.
Posted 25 June 2013 - 12:25 PM
Posted 25 June 2013 - 09:30 PM
Posted 26 June 2013 - 02:14 AM
I've been using Magnesium Chloride Hexahydrate Oil. Great results. I've tried different topical magnesiums but this one seems to be great. Bought from Earthshiftproducts.
Will be testing out Magesium L-Threonate soon and will compare results now that I've actually found a magnesium that I can feel the effects. I'm guessing that the oil will be more effective. One oil I tried left a milky white residue and dried my skin out really bad. Mag oil by Life flo was the name.
Posted 26 June 2013 - 05:47 AM
I'd be very interested to see the results as well. Sometimes these things take longer than expected.
Posted 26 June 2013 - 05:58 AM
I'd be very interested to see the results as well. Sometimes these things take longer than expected.
Another possibility is that the results were disappointing, and it was decided not to release them.
Posted 26 June 2013 - 01:24 PM
I'd be very interested to see the results as well. Sometimes these things take longer than expected.
Another possibility is that the results were disappointing, and it was decided not to release them.
The test they should do is to feed one group of folks Magnesium Threonate, another an equal amount of something like Ester-C that has plain Vit C, dehydroascorbic acid and threonic acid in it ... as well as have a third placebo group. Then see which groups improves most in terms of memory and cognitive function. I would bet my money on it being the Ester-C group, but I would also not bet my money on the folks with a patent for Magnesium Threonate not ever doing such a study
Posted 26 June 2013 - 03:54 PM
*snip* it is indeed L-THREONIC ACID / THREONATE that should be the focus here, as it is indeed clearly what is responsible for the alleged NEUROGENESIS effect and not the MAGNESIUM component
To clarify, ESTER-C comprises circa 10% as CALCIUM THREONATE-DEHYDROASCORBATE (i.e. THREONATE bonded to the DEHYDROASCORBIC ACID form of VITAMIN C), and hence it does in fact readily cross the BLOOD BRAIN BARRIER (BBB); N.B. this is outlined in its PATENT INFORMATON which you can find here: US PATENT NUMBER WO2008103926 A1
Hence one of my reasons for recommending it as a highly bioactive way of supplementing with THREONATE and IMO preferred to MAGNESIUM L-THREONATE which is very expensive to boot
Edited by Luddist, 26 June 2013 - 04:49 PM.
Posted 26 June 2013 - 04:47 PM
Posted 26 June 2013 - 06:05 PM
Edited by Luddist, 26 June 2013 - 06:11 PM.
Posted 26 June 2013 - 07:37 PM
Hi,
Human clinical trial will be finished in the middle of September. The time it take to finish a human clinical trial is always longer that what people anticipate. Fortunately, we are close to finish.
If you are interested in science, we just published anther people showing that MgT can prevent Alzheimer disease in animal model.
Best,
Guosong
Abstract
Profound synapse loss is one of the major pathological hallmarks associated with Alzheimer's disease (AD) and might underlie memory impairment. Our previous work demonstrated that the magnesium ion is a critical factor in controlling synapse density/plasticity. Here, we investigated whether elevation of brain magnesium by the use of a recently developed compound, magnesium-l-threonate (MgT), can ameliorate the AD-like pathologies and cognitive deficits in the APPswe/PS1dE9 mice, a transgenic (Tg) mouse model of AD. MgT treatment reduced Aβ plaque and prevented synapse loss and memory decline in the Tg mice. Strikingly, MgT treatment was effective even when given to the mice at the end stage of their AD-like pathological progression. To explore how elevation of brain magnesium ameliorates the AD-like pathologies in the brains of Tg mice, we studied molecules critical for APP metabolism and signaling pathways implicated in synaptic plasticity/density. In the Tg mice, the NMDAR/CREB/BDNF signaling was downregulated, whereas calpain/calcineurin/Cdk5 neurodegenerative signaling and β-secretase (BACE1) expression were upregulated. MgT treatment prevented the impairment of these signaling pathways, stabilized BACE1 expression, and reduced soluble APPβ and β-C-terminal fragments in the Tg mice. At the molecular level, elevation of extracellular magnesium prevented the high-Aβ-induced reductions in synaptic NMDARs by preventing calcineurin overactivation in hippocampal slices. Correlation studies suggested that the protection of NMDAR signaling might underlie the stabilization of BACE1 expression. Our results suggest that elevation of brain magnesium exerts substantial synaptoprotective effects in a mouse model of AD and may have therapeutic potential for treating AD in humans.
Edited by Luddist, 26 June 2013 - 07:38 PM.
Posted 27 June 2013 - 02:28 AM
Posted 27 June 2013 - 06:10 AM
Posted 27 June 2013 - 04:31 PM
Respect for Dr. Liu. But he's the guy with the patent. Kind of like listening to stock brokers or realtors as to whether prices will rise. Guess the answer?
Edited by Luddist, 27 June 2013 - 04:32 PM.
Posted 11 July 2013 - 09:40 PM
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