This venerable water will prove its worth yet.
http://www.ncbi.nlm....pubmed/17159237
Posted 07 February 2008 - 02:17 PM
Posted 07 February 2008 - 03:07 PM
This venerable water will prove its worth yet.
http://www.ncbi.nlm....pubmed/17159237
Posted 07 February 2008 - 05:02 PM
Edited by caston, 07 February 2008 - 05:17 PM.
Posted 07 February 2008 - 05:52 PM
Posted 07 February 2008 - 06:24 PM
Posted 07 February 2008 - 07:02 PM
Those were in vitro studies. How do we go about defeating our physiological pH controls?
Posted 07 February 2008 - 07:08 PM
Posted 07 February 2008 - 07:46 PM
If I've gradually geared my body into slightly 'alkaline mode' over the last few years I'm happy, - well, I feel 10/10 better than ever, although I should try a trip of pots of coffee and McCrap for a few weeks, to note the difference. ;-)
What do you think about Daniel Reid's view?
The PH diet is funny. Replace ACIDIC with UNHEALTHY and ALKALINE with HEALTHY and it is actually not far off
Posted 07 February 2008 - 10:29 PM
I've been drinking the stuff for a couple of years now. The best time to take it is between meals, as the quantity of acid in your stomach during digestion will overwhelm the buffering capacity of the water.Six-month ERW [Electrolyzed-reduced water] treatment increased hematocrit and attenuated proinflammatory cytokines profile in the HD patients. In conclusion, ERW treatment administration is effective in palliating HD-evoked oxidative stress, as indicated by lipid peroxidation, hemolysis, and overexpression of proinflammatory cytokines in HD [hemodialysis]patients.
Posted 07 February 2008 - 10:45 PM
Posted 08 February 2008 - 03:43 AM
Hypochlourous acid reacts slowly with DNA and RNA as well as all nucleotides in vitro.[7][27] GMP is the most reactive because HOCl reacts with both the heterocyclic NH group and the amino group. Similarly TMP with only a heterocyclic NH group that is reactive with HOCl is the second most reactive. AMP and CMP which only have a slowly reactive amino group are less reactive with HOCl.[27] UMP has been reported to be reactive only at a very slow rate.[6][7] The heterocyclic NH groups are more reactive than amino groups and their secondary chloramines are able to donate the chlorine.[9] These reactions likely interfere with DNA base pairing and consistent with this, Prütz[27] has reported a decrease in viscosity of DNA exposed to HOCl similar to that seen with heat denaturation. The sugar moieties are unreactive and the DNA backbone is not broken.[27] NADH can react with chlorinated TMP and UMP as well as HOCl. This reaction can regenerate UMP and TMP and results in the 5-hydroxy derivative of NADH. The reaction with TMP or UMP is slowly reversible to regenerate HOCl. A second slower reaction that results in cleavage of the pyridine ring occurs when excess HOCl is present. NAD+ is inert to HOCl.[27][9]
Edited by s123, 08 February 2008 - 03:46 AM.
Posted 08 February 2008 - 03:55 AM
Posted 08 February 2008 - 04:12 AM
What the hell is in electrolyzed-reduced and alkalized water, anyway? Are they even related?
Posted 08 February 2008 - 04:15 AM
If I may answer my own question...What the hell is in electrolyzed-reduced and alkalized water, anyway? Are they even related?
Biochem Biophys Res Commun. 1997 May 8;234(1):269-74.
Electrolyzed-reduced water scavenges active oxygen species and protects DNA from oxidative damage.Shirahata S, Kabayama S, Nakano M, Miura T, Kusumoto K, Gotoh M, Hayashi H, Otsubo K, Morisawa S, Katakura Y.
Institute of Cellular Regulation Technology, Graduate School of Genetic Resources Technology, Kyushu University, Fukuoka, Japan. sirahata@grt.kyushu-u.ac.jp
Active oxygen species or free radicals are considered to cause extensive oxidative damage to biological macromolecules, which brings about a variety of diseases as well as aging. The ideal scavenger for active oxygen should be 'active hydrogen'. 'Active hydrogen' can be produced in reduced water near the cathode during electrolysis of water. Reduced water exhibits high pH, low dissolved oxygen (DO), extremely high dissolved molecular hydrogen (DH), and extremely negative redox potential (RP) values. Strongly electrolyzed-reduced water, as well as ascorbic acid, (+)-catechin and tannic acid, completely scavenged O.-2 produced by the hypoxanthine-xanthine oxidase (HX-XOD) system in sodium phosphate buffer (pH 7.0). The superoxide dismutase (SOD)-like activity of reduced water is stable at 4 degrees C for over a month and was not lost even after neutralization, repeated freezing and melting, deflation with sonication, vigorous mixing, boiling, repeated filtration, or closed autoclaving, but was lost by opened autoclaving or by closed autoclaving in the presence of tungsten trioxide which efficiently adsorbs active atomic hydrogen. Water bubbled with hydrogen gas exhibited low DO, extremely high DH and extremely low RP values, as does reduced water, but it has no SOD-like activity. These results suggest that the SOD-like activity of reduced water is not due to the dissolved molecular hydrogen but due to the dissolved atomic hydrogen (active hydrogen). Although SOD accumulated H2O2 when added to the HX-XOD system, reduced water decreased the amount of H2O2 produced by XOD. Reduced water, as well as catalase and ascorbic acid, could directly scavenge H2O2. Reduce water suppresses single-strand breakage of DNA b active oxygen species produced by the Cu(II)-catalyzed oxidation of ascorbic acid in a dose-dependent manner, suggesting that reduced water can scavenge not only O2.- and H2O2, but also 1O2 and .OH.
PMID: 9169001
Posted 08 February 2008 - 04:23 AM
Atomic hydrogen. A hydrogen radical... Would this form a hydronium radical? H3O.+ ?? Curious. Where would the high pH come from? Unexpected species breaking the assumptions behind pH electrodes?
Posted 08 February 2008 - 05:01 AM
You're probably right. I was just wildly speculating about the nature of the solvation of atomic hydrogen. I've never looked at the electrolysis of water, aside from doing it with a battery when I was a kid. I'd guess the vast majority of the H. would recombine to form H2, but some is bound to get lost. There would be so much water around that the most likely collision would be with H2O, and you might get some recombination to H3O., not H3O.+ (oops!) Maybe there is some ultimate reaction that generates hydroxyl ions. It's easy enough to see how that could happen in such a soup.Atomic hydrogen. A hydrogen radical... Would this form a hydronium radical? H3O.+ ?? Curious. Where would the high pH come from? Unexpected species breaking the assumptions behind pH electrodes?
I don't think that H3O.+ exists. The H3O+ complex is formed by a Lewis acid-base reaction. I don't see how a radical could do something similar.
Posted 08 February 2008 - 05:29 AM
What the hell is in electrolyzed-reduced and alkalized water, anyway? Are they even related?
Posted 08 February 2008 - 06:06 AM
But if there's no chloride, then you wouldn't get any bleach. The current carrier could be a little sulfuric acid, for example. Or sodium sulfate. I agree that most of the electrolysis would be conventional, forming H2 and O2, and most of whatever atomic H that was formed would probably recombine, but what becomes of the rest? I would expect that atomic hydrogen has some level of solubility in water; it can't be zero. There may well be radical species formed that have some level of enhanced stability relative to the free atom. Shirahata et al. find that it scavenges superoxide; no telling who reviewed the paper but Biochem Biophys Res Comm isn't a flaky journal. And that's a pretty easy experiment to run so if it was complete crap, you'd think someone would have said so by now. Someone somewhere must have done the experiments needed to characterize the radical species present after electrolysis of water, but I don't think that medline covers J Chem Phys, so you probably wouldn't find it there. I must say, this stuff attracts quacks like flies to poop, but while that's a red flag, it doesn't mean that it's wrong.What the hell is in electrolyzed-reduced and alkalized water, anyway? Are they even related?
There's a good diagram here.
At one electrode you get 2 H2O + 2 e- -> H2 + 2 OH-
At the other electrode you get 2 Cl- -> 2 e- + Cl2
If both electrodes are in the same jar, you get bleach, as noted by S123. If the electrodes are in separate jars connected by a salt bridge, you get molecular hydrogen and sodium hydroxide in one and chlorine gas in the other.
If you have calcium carbonate instead of salt, I think you'd get calcium hydroxide instead of sodium hydroxide, which would then turn into calcium carbonate as CO2 is absorbed from the atmosphere. You'd have to drink it before the carbonate forms in order for it to be alkaline. In the other jar you'd get CO2 and O2 instead of chlorine gas.
I cringed when I read "dissolved atomic hydrogen" in that abstract. Hydrogen atoms are highly reactive. They can exist in a flame or inside metals like palladium, but not in a room temperature solution. They'd either recombine to form inert molecular hydrogen or react with any organic material present.
Posted 08 February 2008 - 06:37 AM
Reduced water exhibits high pH, low dissolved oxygen (DO), high dissolved hydrogen (DH) and significant negative redox potential (RP) values.
Posted 08 July 2008 - 01:36 PM
Here's a previous study in diabetic mice by some of the same authors.Oxidative stress is produced under diabetic conditions and is likely involved in progression of pancreatic beta-cell dysfunction found in diabetes. Both an increase in reactive oxygen free radical species (ROS) and a decrease in the antioxidant defense mechanism lead to the increase in oxidative stress in diabetes. Electrolyzed reduced water (ERW) with ROS scavenging ability may have a potential effect on diabetic animals, a model for high oxidative stress. Therefore, the present study examined the possible anti-diabetic effect of ERW in two different diabetic animal models. The genetically diabetic mouse strain C57BL/6J-db/db (db/db) and streptozotocin (STZ)-induced diabetic mouse were used as insulin deficient type 1 and insulin resistant type 2 animal model, respectively. ERW, provided as a drinking water, significantly reduced the blood glucose concentration and improved glucose tolerance in both animal models. However, ERW fail to affect blood insulin levels in STZ-diabetic mice whereas blood insulin level was markedly increased in genetically diabetic db/db mice. This improved blood glucose control could result from enhanced insulin sensitivity, as well as increased insulin release. The present data suggest that ERW may function as an orally effective anti-diabetic agent and merit further studies on its precise mechanism.
Here's an in vitro study that's a bit over my head. I think the main point is that it reduced ROS produced by the cancer cells. Inhibitory effect of electrolyzed reduced water on tumor angiogenesis. (PMID 18175936)Oxidative stress is produced under diabetic conditions and involved in progression of pancreatic beta-cell dysfunction. Both an increase in reactive oxygen free radical species (ROS) and a decrease in the antioxidant defense mechanism lead to the increase in oxidative stress in diabetes. Electrolyzed reduced water (ERW) with ROS scavenging ability may have a potential effect on diabetic animals, a model for high oxidative stress. Therefore, the present study examined the possible anti-diabetic effect of ERW in genetically diabetic mouse strain C57BL/6J-db/db (db/db). ERW with ROS scavenging ability reduced the blood glucose concentration, increased blood insulin level, improved glucose tolerance and preserved beta-cell mass in db/db mice. The present data suggest that ERW may protects beta-cell damage and would be useful for antidiabetic agent.
StephenElectrolyzed reduced water (ERW) produced near the cathode during the electrolysis of water scavenged intracellular H(2)O(2) and decreased the release of H(2)O(2) from a human lung adenocarcinoma cell line, A549, and down-regulated both VEGF transcription and protein secretion in a time-dependent manner.
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