American Cancer Advocates
                                              
 Investing in your health,...not your disease!

THERAPEUTIC SUBSTANCES
******



DREAMING THE IMPOSSIBLE!

****



How Can This Be?

Aloe vera, alpha/beta quinone injections, chlorella and blue green algae...

DMSO, sulphur in garlic, mangosteen, Coenzyme q-10, sea- weed...

wheatgrass/barley grass, chlorophyll, ozone / peroxide,
ESSIAC tea, polyphenols, bioflavenoids, pau d'arco...

 Tumeric, Cayenne,  Citrate, alkaline salts, 
and several fatty acids,
 are all
vastly different
 substances!
 
Yet, every single one of these are still being used to treat cancer, hepatitis, auotimmunes, fungal infections, and HIV in a sporadic
 non-uniform fashion.

Don't believe it?

Well, start typing these substances into your search engine along with the name of different diseases and see the mountains of new research that has been done on alternative substances.
 
Type in "DMSO and Cancer"  then type in
"DMSO and Viruses" ... and finally type,

"DMSO and Autoimmune."

What did you find?

Try the same search over and over again
 using a different substance now!

After you have glanced over five or six substances
and cross-reference each to virus, cancer, and
autoimmune disease it should have
become obvious that these
substances all share one
special connection.



Well, what is that connection?


How could it be possible that  one substance can help with cancer much less cross-treat more than one disease, because in
 pharmaceuticals very, very few meds are used to
cross treat other illnesses that appear
to be completely different 
illnesses?

How could it be that a dozen different substances  can
treat cancer and other diseases?

Could they all be doing the same thing in our bodies?


It would seem unlikely that all these substances with the exact same disease profiles are all fighting all these illnesses, each by
their own different mechansm, ...

and then also feature 
different mechanisms in
a second disease?

Why is this unlikely?

If ten different substances treated three separate illnesses with different mechanism for each illness, that would mean there would
be thirty completely different mechanisms
of action in a group of ten 
therapeutic substances.
 
It would, on the surface, appear that it is likely that these substances
 have similar mechanisms in each
disease being treated.

That would be the 
simplest and most logical explanation for a dozen
different substances treating
 so many same diseases.

This makes perfect sense if we use an anaerboic disease model.

The explanation would be this:

"All of these substances treat cellular hypoxia."

Do you not see?

If all of these substances could somehow improve anaerobic conditions within the cells and tissues, we could actually predict each one would then
 be used in cross-treating any
 condition which hates
 oxygen.

We could also predict that if we examined their chemical compositionsthen we will find oxygen as a significant sub unit or a
 common element

...in each and every one of
 these substances.

Well, both those predictions were found to be true. Thus validating the
 anaerobic disease model and hypoxia
 treatment hypothesis.



DRAWBACKS IN ALTERNATIVE MEDICINES


If this framented population of natural pathologists, homeopathologists, orthomolecular practitioners can't figure out the exact mechanisms
 of action to their own therapies,
 
then how can
we feel confident in the treatment?

....and
how can these therapies ever reach their
maximum potential?

(Mixed results from alternative medicine hurts alternative medicine.)

 
We all should really push aggressively to maximize the above therapies as only oxygen promoting
 therapies.

Ask yourself why every single one of these above substances in this list are  being used to cross-treat every kind of horrible disease
 known to man?

There is only one simple answer!

These diseases are anaerobic and the subsequent treatments
 are in fact aerobic!
Period!

Now, everything becomes so easy to understand.
 

***  

 

The Common Element in Alternative Meds

All of these different substances have been examined and found to contain an oxygen potentiator
or oxygen donor.

Just look,...it's true!

Of all the alternative treatments that have withstood time
 or have been universally adopted by practitioners
 most either contain chlorophyll 
 or another oxygen donor
 like peroxide/ozone!

One therapy actually attracts greater concentrations
of oxygen into the cell,
(alkaline.)


"Why is the AMA using
 ozone/chlorophyll for cancer!


They stimulate the chlorophyll with U.V. light!



 It's all about Oxygen?

****


OK! WHY OXYGEN?


 
Cancers and Virus are anaerobic, they don’t live or metabolize oxygen, and it’s
 basic biology now!

 Why would autoimmune disease respond to oxygen you ask?
  If they are Viruses then they are
 still anaerobic illnesses!

How much simpler can it get?


***




         
OXYGEN POTENTIATORS VS. OXYGEN DONORS



Our research revealed that most touted therapies  in the alternative markets contain varying levels of
oxygen donors,  resembling chains of
the quinone structures,
(phenols.)

Those that did not fit this structural theme actually attracted greater concentrations of the O2 molecule into  cells,
dissolved into and O2 salt, or
they manufactured O2.

but still there is an O2 relationship!

The quinone,( known as the "q" in Coq10,) is actually used
as an oxidizer industrially.
 
Why?

It donates oxygen!

h-quinone is used by a beetle to boil peroxide in his abdomen! Oxidation of quinone releases so much oxygen that
this bug shoots a blast of hot steam as a defense
 mechanism,as oxygen supports
this rapid combustion.

 Oxygen and quinone are nearly synonomous it would seem!
 
So, oxygen donors start as small as a quinone ring and then  become gradually more complex in chains adding
more and more of these
 quinone rings. 

These sometimes are s0-called anti oxidants and for
one moment consider this reaction.

(Carbon ring)-OH + OH- ==>(Carbon ring) =O + H2O


Please, someone tell me what happens now.... to this double
bonded oxygen on the right that is highlighted
in Yellow? 

This means metabolites of most anti oxidants become
pro oxidant!!!!



OTHER OXYGEN DONORS

The other small donors of oxygen are Sulphur, (So4,) mineral oxides, ozone, (O3,) and peroxide, (H2O2.)

Other classes of oxygen donors consist of chlorophyll,
 ( has two separate reactions,)
 and of course,
 DMSO.
**


What are...
OXYGEN POTENTIATORS?


A third way to increase intercellular O2 is through
 raised alkalinity! 

 To understand this is not difficult.

Otto Warburg won a Nobel Prize for showing how very strong metalic salts could increase oxygen, not in blood,
but inside of  cells.
 
As oxygen is exchanged from donors to recipients, oxygen very strong negative polarity.

At this moment alkaline cytoplasm means more O2 absorbed into and then accross cell membranes
and into the cell. 

Oxygen being a gas, always seeks to go from highest concentration to lowest concentration.

We measure this pressure as partial pressure. But if there is a chemical/magnetic force repelling oxygen,...these negative ions will resist the  contradictory force of partial pressure,
 thereby inhibitting oxygen from
crossing through the cell
membrane.

Remember that similar charges repell!

 
Oxygen is negatively charged, so by making the inside of cells more possitively charged, oxygen will be attracted like
a magnet into the cell. (Brewer/Warburg)

How simple is that?

This is exactly why electron donors like heparin, vitamin c, and other aromatic compounds actually increase permeability
 of cancer cell membranes to alkaline substances.
Also why the exact same substances are
used to potentiate chemotherapy.


WHERE DO I FIND THESE SUBSTANCES

      
         

Here is a basic rundown on the different herbs and compounds that all contain an oxygen delivery mechanism, the active ingredients that restore/elevate oxygen. 


* Please remember that most protocols also recommending large doses of Ascorbates.

 

Wheat grass and Barley grass- very high in chlorophyll and alkaline minerals, smaller in polysaccharides, large am’t of amino acids.

 

Blue-green algae and seaweed- Very high in chlorophyll and alkaline minerals, glycolproteins,  amino acid, ( which can be -COOH-donors.)


Aloe Vera-
only modest chlorophyll, high alkaline minerals, polyphenols, lipopolysacharides, complex carbohydrates, amino acids, (can be donors) b-quinone, (an highly reactive O2 donor!)


Essiac herbs- very high alkaline minerals,  complex carbohydrates, lipopolysacharrides, amino acids, and numberous oxygen donors, ie., b- quinone, oxalates, mineral oxides, polyphenols, and chlorophyll.


DMSO
- Takes oxygen to cytoplasm and the mitochondria. DMSO breaks down into DMSO and MSM. MSM strives to pick up spare oxygen and this reaction produces MSMO. (This is MSM with a oxygen attached.)

 These two salts then strip and donate oxygen back and forth, operating like and oxygen pump.  (Always trying to stay in equilibrium to one another.)   The oxygen is subject to partial pressure laws.
PhD. Biochemist explains,...
http://www.krysalis.net

Peroxide/Ozone -  Donate oxygen. {H2O2} and {O3}

Cesium Chloride- Alkaline metalic salt which attracts oxygen into the cell.
(do not consume at the same time with potassium)


Coenzyme Q
- same principle/ different mechanism, works inside mitochondria, compliments the increased density of O2 by increasing the actual amount of O2 your body can effectively burn at one time. It's really a fuel pump for oxygen combustion and should be apart of every single oxygen protocol. It is foolish not to use this compound for cancer protocols

Most complex oxygen donors are:

 
Bioflaveniods, Elligiac Acid, Tannins, fatty acids, polyphenols...

....and these can be found in fermented products, green tea, cinnaminic acid, grape seed, apple skins. Decreased absorbtion of these molecules is a trade off for their large structures.
 

*********

The Structures of
POLYPHENOLS


SIMPLEST MOLECULES

                        

                        Hydro quinones rapidly donate H+  to free radicals  becoming b-quinone

                                 





                                                          
SLIGHTLY LARGER MOLECULE





Anthracene rapidly absorbs energy, UV light,  attatches to any loose o2 molecules, stripping them away from oxides, and donors.  Then it becomes:



                           


686- Anthraquinone              and                 Xanthone


Then donating oxygen to cytoplam it becomes:




                   Xanthene-      an aromatic compound which releases it's final O2 molecule to become anthracene again. This cycle operates like a oxygen pump.





Other Xanthone like products:

Novartis is manufacturing ASA404,...code named for carboxylated
xanthone!  Shhhhh! I didn't tell you!

File:Vadimezan.png

"Vandimazin"







                                                                 

  
                  More  Complex Quinones,(Phenols)


        
         Quercetin (flavonoid)






                      
                                                       Highly Complex Polyphenols




Extremely complex chains!

Long/medium chain fatty acids, amino acids, glyco nutrients, cinnaminic acid, tannins, etc. many containing carboxyl group, (O=C-OH) This becomes carboxylate and is associated with dozens of anti cancer substances.
 You should ask why?

Fatty acid carbon chain/ note carboxyl group!
                  File:Fatty acid numbering.png



Dr.William Koch was a pioneer in his time using the smallest form of phenolic compounds to treat almost every pathology known to man, …he in essence developed a
uniform theory on disease in practice,
but not in theory.

Way ahead of his time, Koch agreed with Warburg and called Cancer and anaerobic pathology.  Used quinones.

 

 

KOCH'S QUINONE THEORY 

His quinone therapy is now being used and considered in
other countries, mainly socialized medicine. He even
exploited carboxylated quinones. This
molecule is associated to dozens
of anti cancer substances.

Carboxylic Acid
File:Carboxylic-acid.svg
Found in dozens of anti cancer
compounds!


Quinones themselves are a class of polyphenol and should be called monophenol. They are cheap!

They are very unique in their phenol structure as they are smallest ringed molecule that can carry,
….you guessed it,…oxygen!

Xanthones are three ringed quinones period.

... is it any guess why they are used alternatively to
treat several bad, bad diseases?
***
 
 DOWNSIDE OF POLYPHENOLS

These larger molecules are means they are carrying many more donor sites containing oxygen.


However, before their ability to liberate the larger portions of oxygen they must first donated of hydrogen to
other chemical reactions before oxygen
 becomes double bonded to
carbon, and naked.

Therefore the amount of available O2 will diminish as the blood concentrations increases until hydrogren donation
reaches a saturation level or an equilibrium. 

This then would be seen in treatment settings
as mixed efficacy if metabolic equilibrium inhibbits
oxygen donation due to ph balance.

Mixed efficacy isn't good enough for cancer in our book!

Meaning, the patient improves, lived several years longer, but disease still did not completely resolve. So....If a patient
outlives his prognosis by 6 years; this is
good
 and bad,
this is mixed efficacy.
 
So, the larger or more complicated these quinone units become the more donor sites it will have containing oxygen. 

Xanthones and quinones are even more permeable than polyphenols as they are smaller and enter
cytoplasm faster, cross the brain barrier,
infiltrate fatty and fibrous tissues
much easier than the
complex polyphenols!

They can come hydrogenated or not and therefore may have more consistent efficacy in treatment settings in
their non-hydrogenated forms.
 
Quinones are permeable to nerve sheaths, fibrous tissue, fatty tissue, and mitochondria membranes. They are
reported to cross the blood
barrier of the brain.

 This may be, in fact, the complete answer to anaerobic pathologies as Dr.William Koch illustrated for us by chronicling
 his fantastic successes.

 Many aromatic compounds are wonderful electron donors as well and this characteristic is anti
cancer as well.

Electron donors, by nature, increase cancer cell-wall permeability, as cell transport is driven by an electromagnetic
polarity pulling in positively charged
molecules towards a
negative center.

Understandably, the more electrons inside the cancer cell means fewer H+ ions, (less acidic.)

Xanthones also carry oxygen and release oxygen very easily. It has very high permeability it easily lets go of its oxygen 
due to its weaker bonds. Xanthones are
 found in Mangosteen.

....described as cytotoxic, fungicidal, bacterialcidal, and not described  as oxygen therapy by naturalists!

This is puzzling because a Dr. Koch, manufactured a quinone complex and touted it as a treatment for
all diseases as early as
 1930's and 40‘s.
 
He even made a firm oxygen connection to cancer and
 anaerobes and tied it to Warburg’s Nobel Prize
 winning  work where cancer was officially
 classified as both anaerobic
 and acidic.

The oxygen connection was no secret back the the 1940’s,
 at least with the disease of cancer.
 
The A.M.A. has finally vindicated Dr. Koch using molecular oxygen for cancer today. A cancer therapy using
ozone and chlorophyll.

Many practitioners have always used herbs containing these compounds since the beginning of homeopathy
and natural pathology. 

Why are they still being used and now by AMA?

The anti-cancer/ anti-viral herbs which contain quinones are:

1) Aloe vera

2) Essiac preparation

3) Amazon factor preparation

4) Pau de Arco extract

5) Quinine sulfate

6) Tumeric

7) Fermented wheat germ

8) Mangosteen, (three ringed quinone)

The next more complex molecules can contain as many as nine or ten rings.

Polyphenols and Bioflavenoids

1) Green and white tea

2) Apple skin extract

3) Grape skin extract

4) Aloe (moderate)

5) Essiac Herbs- (high)

6) Fermented products

7)Olive Leaf

                           


TANNINS AND FATTY ACIDS

1) Spices and spice extracts (cinnamon etc)

2) Matumba bark- Tannins procyanidins

3) Apple seeds/ grape seeds extract

4) Essiac herbs

5) Aloe skin latex-

6) Grape seed

7) Bitter fruits

8) Tea's

9)Clove oil/essential oils



 
OTHER OXYGEN DONORS
(note similarities)



Citrate




Sulfate


Chlorophyllin
(note carboxyl groups)

Chlorophyllin.png


Dmso
structural formula of the DMSO molecule, with bond lengths and angles



Ozone
Ozone-1,3-dipole.png



Peroxide

Structural formula of hydrogen peroxide

Carboxylate
File:Carboxylate-resonance-2D.png
COO-(H)



IMPROVING TODAY"S THERAPIES

So, the next time you consider alternative treatments you need to understand what will make that treatment better, more effective!!!

Sure some of these substances have other therapeutic substances like amino acids, polysacharides,....however, the familiar theme is concrete, never changing from substance to substance. 

But who needs a scientist or a doctor to tell us the obvious.


"If a disease hates oxygen, maybe we should try to give it more oxygen!"



Please call for comments or questions
 602 754 1584          602 754 1584

Email Us

 

 

 

 

                                                        RESEARCH ARTICLES

Below is an example of cross treating,...we predicted cancer therapies could treat other diseases that are anaerobic. This would be strong indicator that oxygen donation is the mechanism of action.

 

SSR Super Quinone

This liquid homeopathic type formulation developed over 50 years ago by Dr. Koch has had a long history of providing a profound impact on reversing all chronic health issues. Of most importance for HIV/Aids is its ability to help halt the replication of viruses and other pathogens in the body.

As a historical note, in Germany SSR is used to treat many different diseases. German authorities say that SSR Super Quinone treats: HIV, cancer, chronic infectious diseases like hepatitis, autoimmune diseases, is a replacement for vaccinations of diseases such as chicken pox and measles, and basically treats any and all disease.

From “Cancerfightingstrategies.com”

SSR Super Quinone and Koch TMT Homeopathic Remedies

Developed by Dr. William F. Koch, Super Quinone and Koch's full line of TMT homeopathic remedies have for over 60 years been used time and again to conquer cancer and other major illnesses. Composed of homeopathic sized methylglyoxal quinone molecules, one of their main functions is their ability to repair damaged respiratory enzymes in cells. This is fundamental to the development of cancer.

As a historical note, in Germany they have been used to treat many different diseases. German authorities on these remedies say that they treat: Cancer, HIV, chronic infectious diseases, autoimmune diseases, can be a replacement for vaccinations of diseases such as chicken pox and measles, and basically treat any and all disease. (Heart disease is intimately connected to free radical damage and bacterial infections.) Because the Super Quinone and TMT molecules are extremely small, it has no problem working on diseases of the brain.

From “Avemarresearch.com”

Curcumin

, the most important component of turmeric —a spice component of curry—commonly

adopted as an anti-inflammatory compound in eastern medicinalpractices, shows inhibition of

NF-kB activation in a concentration-dependent manner in endothelial cells w33x.

Resveratrol

, an edible polyphenolic stilbene found in the skin of red grapes, which has antioxidant

properties similar to vitamin E, has been reported as being capable of suppressing IL-1binduced

activation of NF-kB in acute myeloid leukemia cells w34x.

A fermented wheat germ extract with standardized benzoquinone content

(Avemar) has shown an improvement of clinical and laboratory parameters

on mice subject to SLE w35x. Authors postulate that results may be related to a rebalancing

of the lymphocytes subclasses Th1yTh2 (inhibition of IL4 and IL10 production). This product

contains large amounts of chinolonics and falconoid having an intense anti-oxidant activity. It is

therefore likely that the immunomodulatory therapeutic effect can be ascribed to them w35.

From: a1arthritisremedies.com

 

Mangosteen supplementation is also an area which should be explored in regards to pain relief. Mangosteen is said to have properties which reduce pain. many consider this an arthritis remedy in itself.

Mangosteen is also packed full of powerful xanthones which can boost the immune system. Many types of arthritis are thought to be an

autoimmune disorder

Aloe Approved for Use in Feline Leukemia

Although untested on human malignancies, acemannan has been approved for veterinary use in injectable form for fibrosarcomas and feline leukemia (FeLV), caused by a retrovirus as is AIDS. Over 70% of cats with FeLV die within 8 weeks of onset of clinical signs, yet acemannan has shown impressive results. After 6 injections of acemannan (2 mg/kg) over a six-week period, re-examination after 6 more weeks showed 71% of 44 cats were alive and in good health.(9) Researchers believe the mechanism to be related to increased secretion of tumor necrosis factor, interleukin, and interferon leading to increased initiation of immune attack.

 

 

Aloe Indicated as Adjunct to AZT

Preliminary studies indicate the potential usefulness of aloe as an adjunct to current AIDS therapy (i.e., AZT).

Three studies conducted by H.R. McDaniel, Ph.D., et al., demonstrated that 500-800 mg. of acemannan per day in HIV-1 infected patients 1) raised CD8 levels and maintained CD4 levels; 2) significantly increased circulating monocytes/macrophages and improved phagocytic activity; 3) significantly improved Modified Walter Reed Clinical (MWR) scoring, absolute T-4, absolute T-8, and p24 core antigen levels.(2,3,4)

Researchers believe that acemannan may potentiate the antiviral drug azidothymidine (AZT), reducing the amount of AZT required by as much as 90%.(5)

  

REFERENCES

1. Womble, D., and Helderman, J.H. Enhancement of all-responsiveness of human lymphocytes by acemannan. Int. J. Immunopharmacol 10(8):967-74, 1988.

2. McDaniel, H.R., Ph.D., et al. CD4 and CD8 lymphocyte levels in acemannan (ACM)-treated HIV-1 infected longer-term survivors. Int. Conf. AIDS 9(1):438, 1993.

3. McDaniel, H.R., et al. An increase in circulating monocyte/macrophages (MM) is induced by oral acemannan (ACE-M) in HIV-1 patients. Am. J. Clin. Pathol. 94:516-17, 1990.

4. McDaniel, H.R., et al. Extended survival and prognostic criteria for acemannan(ACE-M) treated HIV-1 patients. Antiviral Res. 13(Suppl. 1):117, 1990.

5. Werbach, Melvyn R., M.D. and Murray, Michael T., N.D. Botanical Influences on Illness: A sourcebook of clinical research. Tarzana, CA: Third Line Press, 1994.

6. Kahlon, J.B., et al. In vitro evaluation of the synergistic antiviral effects of acemannan in combination with azidothymidine and acyclovir. Mol. Biother. 3:214-23, 1991.

7. Ghannam, N. The antidiabetic activity of aloes: Preliminary clinical and experimental observations. Hormone Res. 24:288-94., 1986.

8. Shida, T., et al. Effect of aloe extract on peripheral phagocytosis in adult

 

Aloe Vera

 

This natural solution is vital for sufferers of all auto-immune disorders, IBD, Ulcerative Colitis (UC), Crohn's Disease, Irritable Bowel Syndrome (IBS), Diverticulitis, Diverticulosis, Chronic Fatigue Syndrome, Ulcers, Arthritis,  Allergies, Digestive Problems...

By Robert E. Willner, M.D., Ph.D.The Aloe plant has become the basic ingredient of a large number of commercial preparations in the form of creams, lotions, gels and shampoos. The juice of the Aloe is being used for cleansing of the colon and intestinal problems. Toxicity and side effects are relatively rare and not usually severe. Almost every conceivable benefit has been claimed for Aloe over the centuries - most of them justified.Because it is a plant, chemical analysis has revealed a host of substances, one of which has been shown in mice to have anti-leukemic activity. (S.N. Kupchan, 1976)The anti-cancer activity of Aloe indicate that its action is through stimulation of the scavenging white blood cells of the immune system. (L. Ralamboranto, Archives of the Pasteur Institute, 1982)The many studies carried out by Russian scientists have done more to establish a respectable place in modern medicine for Aloe than any other group of investigators. N.V. Gribel and V.G. Pashinskii, in Vopr Onkol., 1986, showed that Aloe juice reduced tumor mass and the frequency of metastases in rats.R. Berkow in the Merck Manual, wrote of Aloe’s ability to protect individuals with weakened immune systems against infection.S. Solar, publishing in the Archives of the Pasteur Institute in 1980, showed that Aloe could prevent infection in mice if used several days before exposure.J.Y. Brossat and his group, in the same journal the following year, demonstrated that Aloe was effective in preventing serious infections from bacteria, parasites and even fungus. These studies give great credence to those individuals who drink Aloe on a daily basis as a protective against disease.Y. Sato wrote of Aloe’s protective effect on the skin against X-rays and K. Saki demonstrated its protection of the liver, particularly against alcohol. All of this evidence makes Aloe a logical choice in health maintenance and, in particular, as a cancer preventative because of its obvious protection and benefits to the immune system.

 

Tumor Inhibitors 114 Aloe Emodin: AntileukemicPrinciple Isolated From Rhamnus Frangula L

Kupchan SM; Karim A

Lloydia 39(4):223-4 1976 Jul-Aug

A systematic fractionation of an ethanol-water (1:1) extract of the seeds of Rhamnus frangula L., guided by assays for tumor-inhibitory activity, led to the isolation of Aloe emodin. This compound was found to show significant antileukemic activity against the P-388 lymphocytic leukemia in mice. A noteworthy vehicle-dependence of the testing results is reported. In the light of this vehicle-dependence, the re-examination of other anthraquinone derivatives is recommended.

 

Cancer Research

Tizard I; Kemp M

Texas A&M

Research by the immunologist Ian Tizard, Ph.D. and virologist Maurice Kemp, Ph.D. from Texas A&M led to the discovery that Aloe mucopolysaccharide is taken into a special leukocyte, the macrophage, and this cell is stimulated to release messenger molecules called cytokines (interferons, interleukines, prostaglandins, tumor necrosis factor and stem-cell growth factors.) Tumors release a chemical that attracts blood circulation so that malignant cells have a supply to the tumor and it therefore dies. All of the immune modulating effects from Aloe contribute greatly to the prevention and healing of malignant cells.

 

Anticancer Effects Of Aloe On Sarcoma 180 In ICR Mouse & On Human Cancer Cell Lines

Jeong HY; Kim JH; Hwang SJ; Rhee DK
Coll. Pharm., Sung Kyun Kwan Univ.Yakhak Hoeji 38 (3). 1994. 311-321

Anticancer effects of Aloe on sarcoma 180 in ICR mouse or human cancer cells were determined. Sarcoma 180 cells were inoculated subcutaneously into male ICR mouse to determine effect of Aloe on tumor growth, or inoculated intraperitoneally into male ICR mouse to determine effect of Aloe on life span prolongation, followed by oral administration of Aloe vera (10 mg/kg/day, 50 mg/kg/day) or Aloe arborescens (10 mg/kg/day, 100 mg/kg/day) once a day for 14 days. The administration of Aloe vera or Aloe arborescens did not suppress tumor growth. However the life span of ICR mouse was prolonged to 19% (P lt 0.05), 22% (P lt 0.05), and 32% (P lt 0.05) by administration of Aloe vera 10 mg/kg/day, Aloe vera 50 mg/kd/day, and Aloe arborescens 100 mg/kg/day, respectively. To determine anticancer effect of Aloe in vitro, Aloe extract was added to the culture of human gastric cancer cells (SNU-1) and colorectal cancer cells (SNU-C2A), and concentration of Aloe to inhibit cancer cell growth was determined using MTT (3 - (4, 5-dimethylthiazol-2-yl) -2, 5-diphenyltetrazolium bromide) cytotoxicity assay. High ID-50 values of Aloe vera and Aloe arborescens against gastric cancer cell line (SNU-1) and colorectal cancer cell line (SNU-C2A) suggest that Aloe gel does not have anticancer effect on these specific human cancer cells although high concentration of Aloe inhibited growth of human cancer cells significantly.

 

 

Antimutagen Of Aloe Plants

Nakasugi, Tohru; Komai, Koichiro

Res. Lab. Med, Prod. Plant Origin

Kinki Daigaku Nogakubu Kiyo (1994), 27, 47-54

 

An antimutagen from Aloe Arborescens Mill was isolated and identified. Methanol exts. from dried leaves of A. arborescens inhibited frameshift mutation induced by 3-amino-1-methyl-5H-pyrido [4, 3b] indole in Salmonella typhimurium TA98. The antimutagen isolated from the methanol exts. was identified as the anthraquinone Aloe-emodin. Aloe-emodin inhibited frameshift mutation by 60.3% at 0.1 mM/plate and 86.3% at 1.0 mM/plate whereas barbaloin, monoglucoside of Aloe-emodin, did not. Fresh A. aborescens leaves contained 1.17 ug/g (wet wt.) of Aloe-emodin. Aloe-emodin was also detected in A. ferox, A. vera, A. eru, and A. compacta by HPLC. These Aloe species may have substances that are useful for prevention of some forms of cancer

 

 

Jacob Labs and Aloe 

Beta-glucomannans are a class of very long chain sugars derived from plants, which have been shown in laboratory and clinical studies to have a wide variety of immune stimulating and protective effects within the body. In studying the different sources of this polymer, it has been discovered that the aloe barbadensis plant contains the greatest concentration of acetylated polymannans, which is also the most active form of mannans. These long-chain complex polysaccharides are often called beta-glucomannans, mucopolysaccharides or Acemannan. These aloe polysaccharides have been shown to have many effects in the body, mostly impacting the gastrointestinal and immune systems, which are intricately related. Before elaborating on their beneficial effects, it is appropriate to discuss the type of pathology often present in individuals experiencing immune system depression.The most striking commonality found in individuals suffering with immune depressive conditions such as Epstein-Barr virus, chronic fatigue syndrome, systemic candidiasis, HIV infection and others, is the high incidence of digestive dysfunction and maldigestion. This has several effects that contribute to stress on the immune system and weakening it.

 http://www.hepatitiscfree.com/aloe_vera_book.htm

References:

1. Byeon SW, et al., "Aloe barbadensis extracts reduce the production of interleukin-10 after exposure to ultraviolet radiation" J Invest Dermatol, 1998 May;110(5):811-7

2. Chithra P, et al., "Influence of Aloe vera on the glycosaminoglycans in the matrix of healing dermal wounds in rats" J Ethnopharmacol, 1998 Jan;59(3):179-86

3. Chithra P, et al., "Influence of aloe vera on the healing of dermal wounds in diabetic rats" J Ethnopharmacol, 1998 Jan;59(3):195-201

4. Chithra P, et al.,"Influence of Aloe vera on collagen characteristics in healing dermal wounds in rats" Mol Cell Biochem, 1998 Apr;181(1-2):71-6

5. Chithra P, et al.,"Influence of Aloe vera on collagen turnover in healing of dermal wounds in rats" Indian J Exp Biol,1998 Sep;36(9):896-901

6. Davis RH, et al., "Anti-inflammatory and wound healing activity of a growth substance in Aloe vera" J Am Podiatr Med Assoc, 1994 Feb;84(2):77-81

7. Davis RH, et al., "Processed Aloe vera administered topically inhibits inflammation" J Am Podiatr Med Assoc, 1989 Aug;79(8):395-7

8. Davis RH, et al., "Wound healing: Oral and topical activity of Aloe vera" J Am Podiatr Med Assoc, 1989 Nov;79(11):559-62

9. Desai KN, et al., "The preventive and therapeutic potential of the squalene-containing compound, Roidex, on tumor promotion and regression" Cancer Lett, 1996 Mar 19;101(1):93-6

10. Odes HS, et al., "A double-blind trial of a celandin, aloe vera and psyllium laxative preparation in adult patients with constipation" Digestion, 1991; 49(2): 65-71

11. Schmidt JM, et al., "Aloe vera dermal wound gel is associated with a delay in wound healing" Obstet Gynecol, 1991 Jul;78(1):115-7

12. Shamaan NA, et al., "Vitamin C and aloe vera supplementation protects from chemical hepatocarcinogenesis in the rat" Nutrition, 1998 Nov-Dec;14(11-12):846-52

13. Strickland FM, et al., "Inhibition of UV-induced immune suppression and interleukin-10 production by plant oligosaccharides and polysaccharides" Photochem Photobiol, 1999 Feb;69(2):141-7

14. Strickland FM, et al., "Prevention of ultraviolet radiation-induced suppression of contact and delayed hypersensitivity by Aloe barbadensis gel extract" J Invest Dermatol, 1994 Feb;102(2):197-204

15. Stuart RW, et al., "Upregulation of phagocytosis and candidicidal activity of Macrophages exposed to the immunostimulant acemannan" Int J Immunopharmacol, 1997 Feb;19(2):75-82

16. Sydiskis RJ, et al., "Inactivation of enveloped viruses by anthraquinones extracted from plants" Antimicrob Agents Chemother, 1991 Dec;35(12):2463-6

17. Syed TA, et al., "Management of psoriasis with Aloe vera extract in a hydrophilic cream: a placebo-controlled, double-blind study" Trop Med Int Health, 1996 Aug;1(4):505-9

18. Visuthikosol V, et al., "Effect of aloe vera gel to healing of burn wound a clinical and histologic study" J Med Assoc Thai, 1995 Aug;78(8):403-

 

CHOROPHYLL AND ALGAE

Since chlorella has a true nucleus, it is a more evolved organism than the other common green micro-algae and therefore may offer superior-quality RNA/DNA. This particular aspect of its RNA/DNA, measured by the CGF, strengthens immunity by improving the activity of T- and B-cells, which defend against viruses and other invading microorganisms, and macrophages, which destroy cancer and cellular debris in general.
Healing With Whole Foods by Paul Pitchford, page 194

For cancer, AIDS <http://www.newstarget.com/AIDS.html>, Epstein-Barr syndrome, multiple sclerosis, rheumatoid arthritis, tumors, Candida overgrowth, excessive mucus, edema, and other conditions associated with dampness, wild blue-green is generally the most useful. Individuals who are not particularly excessive will benefit from a moderate dosage of 1.5-2 grams. The upper dosage ranges of cereal grass, chlorella (excellent for disorders with immune malfunction), spirulina <http://www.newstarget.com/spirulina.html>, and dunaliella are also beneficial additions (often spirulina and dunaliella are used together). One may choose the one or two most appropriate of these green foods <http://www.newstarget.com/green_foods.html> based on their properties.
Healing With Whole Foods by Paul Pitchford, page 204

Chlorella helps protect the body in its fight against both viruses and cancer. A series of studies during the 1980s showed that tumor growth in mice could be reduced or stopped by injecting a water solution of chlorella…
Herbal Medicine Healing Cancer by Donald R Yance Jr, page 231

This research, says Tim Sara, president of Nature's Balance, a major U.S. supplier of chlorella, "has confirmed that serum levels of albumin are extremely accurate indicators of overall health status and that low albumin levels exist at the onset and progression of virtually every nonhereditary, degenerative disease <http://www.newstarget.com/degenerative_disease.html> process, including cancers and cardiovascular heart disease." A series of studies with rats demonstrated that chlorella supplementation increases albumin levels by 16% to 21%.
Heart Disease by Burton Goldberg, page 131

Research in the 1940s indicating that chlorophyllin solutions slowed the growth of certain anaerobicbacteria in the test tube and accelerated the healing of experimental wounds in animals led to the use of topical chlorophyllin solutions and ointments in the treatment of persistent open wounds in humans

The Dark and light reaction of chlorophyll 

In the dark reactions of photosynthesis (also known as the Calvin Cycle), carbon dioxide (CO2) is converted into glucose through a series of complicated reactions involving ATP (adenosine triphosphate) and NADPH2 (nicotinamide adenine dinucleotide phosphate), two essential compounds synthesized during the light reactions of daylight. Ordinary C-3 plants form a 3-carbon compound called phosphoglyceric acid (PGA) during the initial steps of the dark reactions. The PGA is converted into another 3-carbon compound called phosphoglyceraldehyde (PGAL). Two PGAL molecules combine to form a 6-carbon glucose molecule. The following equation shows the overall reactants and products of photosynthesis:  

6 CO2 + 6 H2O (ATP & NADPH2 from Light Reactions) = C6H12O6 + 6 O2

Note: The oxygen liberated during the light reactions of photosynthesis comes from water.

 

Glycolysis overview Cancer

Cancer’s chief metabolic respiration is glycolysis. This fact is old, (Otto Warburg.)

 

 Chlorophyllin as an effective antioxidant against membrane damage in vitro and ex vivo.
Kamat JP, Boloor KK, Devasagayam TP.Cell Biology Division, Bhabha Atomic Research Centre, 400 085, Mumbai, India.

Chlorophyllin (CHL), the sodium-copper salt and the water-soluble analogue of the ubiquitous green pigment chlorophyll, has been attributed to have several beneficial properties. Its antioxidant ability, however, has not been examined in detail. Using rat liver mitochondria as model system and various sources for the generation of reactive oxygen species (ROS) we have examined the membrane-protective properties of CHL both under in vitro and ex vivo conditions. Oxidative damage to proteins was assessed as inactivation of the enzymes, cytochrome c oxidase and succinic dehydrogenase besides formation of protein carbonyls. Damage to membrane lipids was measured by formation of lipid hydroperoxides and thiobarbituric acid reactive substances. The effect of this compound on the antioxidant defense system was studied by estimating the level of glutathione and superoxide dismutase. ROS were generated by gamma-radiation, photosensitization, ascorbate-Fe(2+), NADPH-ADP-Fe(3+) and the peroxyl radical generating agent, azobis-amidopropane hydrochloride. Our results show that CHL is highly effective in protecting mitochondria, even at a low concentration of 10 microM. The antioxidant ability, at equimolar concentration, was more than that observed with ascorbic acid, glutathione, mannitol and tert-butanol. When CHL was fed to mice at a dose of 1% in drinking water, there was a significant reduction in the potential for oxidative damage in cell suspensions from liver, brain and testis. To examine the possible mechanisms responsible for the observed antioxidant ability we have studied the reaction of CHL with the potent ROS in the form of hydroxyl radical and singlet oxygen. The compound shows a fairly high rate constant with singlet oxygen, in the order of 1.3x10(8) M(-1) s(-1). In conclusion, our studies showed that CHL (Chlorophyllin) is a highly effective antioxidant, capable of protecting mitochondria against oxidative damage induced by various ROS.

Scientists have combined two molecules that occur naturally in blood to engineer a molecular complex that uses solar energy to split water into hydrogen and oxygen, says research published today in the Journal of the American Chemical Society.

 Glycolosis produces NADPH2, in mammals, and this is a needed chemical to facilitate the CO2 eating reactions of chlorophyll in mammals. To argue that chlorophyll can’t perform its function in mammals, only in plants is incorrect.New York Journal of Bichemestry






DMSO is generally used in alternative medicine with liquid ionic cesium chloride.

DMSO helps cesium chloride get inside of cancer cells, though cesium chloride is perfectly capable of doing this by itself. What DMSO is really used for is to get the cesium chloride through the skin, into the blood stream.

DMSO is especially effective with brain cancer patients because of how quickly it gets past the blood-brain barrier, but it can be used productively with any type of cancer. 

In a case study, one brain cancer patient had a tumor in his brain pressing against one of his optic nerves. When he mixed DMSO with the cesium chloride he could literally feel the cesium chloride and DMSO getting into his tumor within 15 minutes. He could feel it because his tumor was pressing against an optic nerve.  

http://www.cancertutor.com/Cancer/DMSO.html

  

DMSO and MSM
The Biochemical Oxygen Transport Pair

A new insight into their biochemistry that explains the claims for their wide-ranging health and energy benefits

David W. Gregg, Ph.D.

188 Calle La Montana
Moraga, CA 94556
Phone/Fax (925) 284-5434
 

A First-Line Treatment for A Multitude of Medical Diseases/Disorders

Once it is understood that DMSO (& MSM) acts as a profoundly effective oxygen transport system, this opens up the opportunity to use this information to treat a multitude of medical disorders, immediate and long term that are caused by a deficiency of oxygen transport. As one example, it has been reported that DMSO is greatly helpful in minimizing the damage from a traumatic brain injury due to a blow to the head or a stroke. Now the explanation as to why it helps is clear. Brain cells, more than any other cells in the body cannot tolerate a lack of oxygen for an extended period of time. The DMSO will enhance oxygen transport to the brain cells until there is sufficient healing to where blood flow and the conventional oxygen transport system is reestablished.

In the Health Note for Crohn's Disease I describe a mechanism where the DMSO stimulates a mechanism that enhances the transport of iron from the intestine to the rest of the cells in the body. This is a very specialized mechanism, which is not the primary health benefit mechanism that will be discussed here. The primary mechanism discussed here is how I believe DMSO, in combination with its spontaneously generated oxidized form, MSM, act as an antioxidant pair, in the same sense as I discuss other antioxidants in the previous Health Note, in other words the biochemistry of how DMSO and MSM act together to enhance metabolism. 

The most important attribute of DMSO in our fight against the herpes virus is it's unique ability to enter the cell itself. Lacking a genetic material to exist on it's own, viruses can only replicate (multiply) within a cell. Once inside the cell the herpes virus is protected by the protein coating of the cell making most antiviral drugs ineffective against the herpes virus. (Of course, big pharmaceutical companies don't want you to know that.) DMSO contains oxygen. Viruses cannot exist in an elevated oxygen (or alkaline) environment. Applied properly DMSO enters the cell and kills the herpes virus. This is an indisputable fact.

 

 

DMSO is very safe. Dr. Morton Walker in his book "

 

DMSO - Nature's Healer" states "Compared to aspirin DMSO is a much safer drug." And in "DMSO - The complete up-to-date guidebook",

 

 

Inhibition of Bovine Virus by Aromatic Cationic Molecules

M. Daniel Givens,1 

* Christine C. Dykstra,1 Kenny V. Brock,1 David A. Stringfellow,1 Arvind Kumar,2 Chad E. Stephens,2 Hakan Goker,2 and David W. Boykin2

 MATERIALS AND METHODS
Compounds. All of the compounds screened in this study were synthesizedin the laboratory of one of the authors (D.W.B.). Stock solutionsof 5 or 10 mM were made in sterile distilled water or dimethylsulfoxide (DMSO) and stored at -80°C until use. While screeningresults for 41 compounds are described, 52 additional compoundswere screened.
  

  RESULTS

 

Screening assays. During screening assays at both 25 and 5 µM concentrations,4 of 93 molecules were visibly toxic to MDBK cells in the expo)
. At a concentration of only
25 µM, eight additional molecules were visibly toxic tothe MDBK cells. Screening assays identified 5 of 93 aromaticcationic molecules that were selected for determination of CC50,CC10, IC90, and IC50 for BVDV in cell




Dimethyl sulfoxide blocks herpes simplex virus-1 productive infection in vitro acting at different stages with positive cooperativity. Application of micro-array analysis

1Dept. of Mol. Biol. & Biochem, U. Calif. Irvine, 19172 Jamboree Road, Irvine, CA 92697, USA
2Genomic Technology & Informatics Centre, University of Edinburgh, Summerhall EH9 1QH, UK
BMC Infectious Diseases 2002,
2:9     doi:10.1186/1471-2334-2-9
The electronic version of this article is the complete one and can be found online at:
http://www.biomedcentral.com/1471-2334/2/9
© 2002 Aguilar et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserve



DMSO Still Worthwhile Treatment For PBS/IC

Main Category: Urology / Nephrology News
Article Date: 04 Apr 2006 - 0:00 PST

Rossberger and colleagues from Goteborg, Sweden retrospectively studied 28 patients, 13 with ulcerative and 15 with nonulcerative IC who were treated with a 6 week course of intravesical solution of 50% DMSO. Some went on to monthly maintenance. Four to 28 could not complete the initial course of therapy because of symptom flare. Of the remaining 24 patients, 9 were classified as successful, having varying degrees of improvement and requiring no other treatments for their condition. Both ulcerative and nonulcerative patients showed responses. Almost half of patients had urethral irritation or pain after the first instillation, but these side effects were transitory. In clinical studies with DMSO, changes in the ocular refractive index or the development of lens opacity in humans have not been encountered. Despite this, eye examinations during extended treatment with DMSO are encouraged by some physicians because of experimental Recurrent herpes simplex in the mouse: inflammation in the skin and activation of virus in the ganglia following peripheral stimulation

DA Harbour, TJ Hill and WA Blyth

The originally infected ear of mice latently infected in the cervicalganglia with herpes simplex virus (HSV) was treated with one of fivestimuli: stripping with cellophane tape, irradiation with u.v. light, orthe application of xylene, dimethyl sulphoxide (DMSO) or retinoic acid.Each of these stimuli induced the appearance of infectious virus in theganglia 1 to 5 days later, most frequently after 1 to 3 days. Virus wasalso isolated from the treated ears, most frequently 3 to 5 days afterstimulation. In a proportion of mice treated with cellophane tapestripping, xylene, retinoic acid or DMSO, clinical recurrent disease wasobserved, although in the case of DMSO this proportion was low. Some of thephysiological changes induced in the skin by the five stimuli were studied.Treatment with DMSO, cellophane tape stripping or xylene induced almostimmediate inflammation in the skin as judged by extravasation of Evans bluedye. Studies with inhibitors suggested that this was mediated by aneurogenic factor together with histamine or 5- hydroxytryptamine, or bothof these. In addition, with the exception of mice treated with DMSO, thelevels of prostaglandins of the E and F classes in the skin of the ear wereelevated 1 to 3 days after treatment. These results are discussed withreference to the mechanisms by which recurrent herpetic disease develops.



Successful Treatment of Lupus Erythematosus Cystitis With DMSO

By Jose R. Sotolongo, Jr., MD; Frederick Swerdlow, MD; Howard I. Schiff, MD; Hans E. Schapira, MD
Departments of Urology and Medicine, Mount Sinai Medical Center
New York, Ny
 

Abstract 

Systemic lupus erythematosus patients sometimes present with pathologicallu confirmed lupus. Treatment with prednisone has not been observed to be successful. Two patients are presented who were successfully treated with intravesical dimethyl sulfoxide (DMSO).

Systemic Lupas erythematosus (SLE) is an autoimmune disease entity with multiorgan involvement. Although the involvement of the genirourinary tract has been traditionally represented by lomerulonephritis, the appearance of interstitial cystitis-like signs and symptoms has recently been postulated as a manifestation of the SLE constellation.

 

1,2 Attempts to treat this aspect of the disease with steroids have been largely unsuccessful,1,2 although at least 1 recent case treated successfully with prednisone has appeared in the literature. 3

We present 2 cases of interstitial cystitis, hereafter referred to as lupus cystitis, sucessfully treated with intravesical dimethyl sulfoxide (DMSO).  

1. Harvey AM, et al: Systemic lupus erythematosus; review of the literature and clinical analysis of 138 cases. Medicine 33: 291 1954.

2. DuBois EL, and Tuffanelli DL: Clinical manifestation of systemic lupus erythmatosus. JAMA 190: 104 1964.

3. Silk MR: Bladder antibodies in interstitial cystitis. J. Urol 103: 307 1970.

4. Gordon HL, Rosen RD, Hersh EM, and Yium JJ: Immunologic aspects of interstitial cystitis. J. Urol 109: 228 1973.

5. Huston DP, and Steinberg AD: Animal model of human ststemic lupus erythematosus. Yale Biol Med 52: 289 1979.

6. Walker SE, et al: Palmerston North mice, a new animal model of systemic lupus erythmatosus. J. Lab Clin Med 92: 923 1965.

7. Kligman AM: Topical pharmacology and toxicology of dimethyl sulfoxide. JAMA 193: 923 1965.

8. Persky L, Stewart BH: The use of dimethy sulfoxide in the treatment of genitourinary disorders. Ann NY Acad Sci 141: 551 1967.

9. Cohen AS, et al: Preliminary criteria of the classification of systemic lupus erythematosus, Bull Rheumat Dis 21: 643 1971.

A Partially Unified Theory Of Disease by  

Dr. Cordell E. Logan

 

Autoimmune problems are real, and more so in present-day times.

 

Dr. Royal Lee seems correct in his early findings of the mechanism and treatment for what we now call autoimmune diseases.

Sometimes, it seems people get their book or paper published by taking a far left or a far right stand. Controversy brings attention. Some are so hung up on one idea, such as the idea of keeping the body more alkaline and totally being against the “germ” theory, that they drive every thing else into that wall also. It is not a matter of compromising to make all sides happy; it is a matter of looking at a more total picture which then may seem to moderate the various positions.

There are researchers who claim that bacteria, or other micro-organisms, appear to be a major factor in many diseases. The public has been informed that stomach ulcers are caused by Helicobacter pylori. Inflammation is now believed to be a major contributor to heart disease. This, along with an associated infection, lead to what is called vulnerable plaque. Indeed, the plaque, which can be seen by standard tests, can be reversed by diet, proper nutrition supplements, exercise, and intravenous chelation.

Bacteria, fungi, viruses, and parasites are indeed secondary (long supported by naturopathic physicians, the oldest medical professional in the world). This does not exclude the possibility that these organisms can come from the outside. One case is the flu in 1918, the most devastating illness of the 20th century, far surpassing any war in modern history. The war effort of World War I simply took too much away from the people so their diets and immune systems were weakened (the introduction of processed foods began on a large scale then). It killed in nine months more than the war killed in four years. Whether originating from the inside (the microzymas) or from the outside, the end purpose is the same: to clean up the mess (the degenerated body tissues). Nature inexorable moves along. Toxic wastes are usually acid, which leads to a body too acid. Thus, alkaline foods (raw vegetables mostly) are in order. However, our stomachs need to be acid, which helps not only to digest foods (especially proteins), but also to kill pathogenic organisms that may have come in (we don

t live in a perfect world).

Reference:

1. Young, R.O., with S.R. Young. Sick and Tired? Reclaim your Terrain. Woodland Publishing, POBox 160, Pleasant Grove, UT 84062. 1999. ISBN 1-58054-030-9.

2. Logan, C.E. Medicine at the Crossroads: A Global View from Agriculture to Complementary Medicine. Cordell E. Logan, 1994 W. Carriage Ave. Riverton, UT 84065. 1993. ISBN 0-9636519-0-0.

3. Gordon, G.F. Heart Disease: America’s No. 1 Killer Surgery for the Treatment of Heart Disease is Coming to an End! Townsend Letter for Doctors & Patients. Nov. 1999. #1 96- pp70-74.

 

Cesium Therapy in Cancer patients

by H.E. Sartori

 

 Treatment was performed on 50 patients during the last three years at Life Sciences Universal Medical Clinics in Rockville MD and in Washington D.C. All patients were terminal subjects with generalized metastatic disease. Forty-seven of the 50 patients studies had received maximal modalities of treatment, i.e., surgery, radiation, and various chemotherapy, before metabolic Cs-treatment was initiated. Three patients were comatose and 14 of the patients were considered terminal due to previous treatments outcome and cancer complications. The type of cancer of the patients studied and their number is detailed in table 1.

The Cs-treatment was given in conjunction of other supportive compounds under diet control in addition to the utilization of specific compounds to produce adequate circulation and oxygenation. According to individual cases CsCl was given at daily dosages of 6 to 9 grams in 3 equally divided doses, with vitamin A-emulsion (100,000 to 300,000 U), vitamin C (4 to 30 grams), zinc (80 to 100 mg) selenium (600 to 1,200 mcg) and amygdalin (1,500 mg) in addition to other supplementations according to the specific needs of the patient. The diet consisted mainly of whole grains, vegetables, linolenic acid rich oils (linseed, walnut, soy, wheat germ) and other supplemental food. To increase efficiency of the treatment and improve the circulation and oxygenation, the patients received the chelating agent EDTA, dimethylsulfoxide (DMSO) and also a combination of vitamins, K and Mg salts.Results

Table 1 summarizes the results of the Cs-treatment of 50 cancer patients studied over 3 years. They had generalized metastatic disease, except for 3 patients. Initial death occurrences fir the initial 2 week treatment was in the same order and magnitude of these recorded for the 12 month period. The percent of survival of breast, colon, prostate, pancreas, and lung cancer accounted to approximately, 50% recovery which was higher than that noted for liver cancer and the lymphoma patients treated. An overall 50% recovery from cancer by the Cs-therapy was determined in the 50 patients treated. Data from the autopsy made indicated the absence of tumors in patient dying within 14 days of the Cs-treatment. One of the most striking effects of the treatment was the disappearance of pain in all patients within 1 to 3 days after initiation of the Cs-therapy.

Lack of oxygen and high levels of acidity go together. One reason for this: "In the electron transport scheme during oxidative metabolism, electrons are transferred along a set of electron acceptors, ending up, ultimately with the combination of hydrogen and oxygen to form water. However, when there is an oxygen deficiency, the loss of electrons can result in the accumulation of positive hydrogen ions, which lead to blood acidification." - Sandra Goodman, PhD, Germanium - The Health and Life Enhancer, Chapter 4. You can read her book on the Internet here:  

http://www.positivehealth.com/permit/Articles/Nutrition/Germanium/chapter4.htm

 




CSCL and Viruses

Cancer Tutor Focuses on the Rare Alternative Cancer Treatments
Which are Potent Enough To Provide Cancer Patients, Including Those
Given Up On By Orthodox Medicine, a Significant Chance of Survival

 The Theory Behind the Treatment

 Part of the treatment is actually a treatment for AIDS (i.e. something that will work for any virus), modified for other possible causes of type 1 diabetes.

This treatment kills viruses by using cesium chloride, rubidium, germanium (known by itself to kill viruses) and indium to kill the viruses with alkalinity. These are all highly alkaline minerals.

 

 

Ozone therapies-

Licensed only in a few states inside the U.S.A. and it’s approved in many other countries.

This therapy has been around longer than any of the oxygen related therapies. There is so much evidence of cross treating with ozone therapies for viruses, cancer, and autoimmune that I will not address ozone very much. The information is out there, it’s public record, but even the promoters of ozone/peroxide therapy miss the mark with respect to autoimmune disorders, failing to make the viral-link, but they do misquote a Nobel Prize Winning Chemist stating autoimmune disorders were anaerobic disorders.

The promoters of ozone were right about mode of action, but when missing the viral connection they failed accurately to link ozone’s effectiveness to autoimmune disorders. Anaerobic conditions don’t generally make white cells attack us! They left a gray area which again prevents patients from turning to ozone/peroxide therapies. They don’t understand the link between anaerobic conditions and collagen inflammation, and neither do the promoters. They missed the anaerobic virus-link. If ozone practitioners would just say they are treating anaerobic viruses with ozone,…more patients would flock to their services.

People with various degenerative diseases are sometimes found to have low venous oxygen saturation. With proper care, the venous oxygen saturation level rises and their health & vitality improve dramatically.

Arterial oxygen saturation should be very high. "High O2 tensions were lethal to cancer tissue, 95% being very toxic, whereas in general, normal tissue were not harmed by high oxygen tensions. Indeed, some tissues were found to require high O2 tensions...", J.B. Kizer, quoted in

McCabe, page 82. An "Oximeter" device to measure your blood oxygen level is available from www.rgarden.com for $199. 


OTHER THERAPIES ARE BEING USED TO CROSS TREAT CANCER AND ANAEROBIC DISEASES

Do not these also have oxygen link?


Benefits for Aids/HIV

UNIVERSITY of CALIFORNIA at BERKELEY REPORT


AIDS is caused by the human immunodeficiency virus (HIV), which attacks a specific type of white blood cells known as T-lymphocytes. About 20 million people throughout the world are infected with HIV. A massive research effort has produced better treatments, resulting in longer survival and improved quality of life for those with access to the treatments. But there is still no vaccine or cure. The only real defense against AIDS is prevention.

What makes HIV so difficult to control is that it targets and destroys immune cells called t-helper cells, the body's first line of defense against infection. Once these t-cells are decimated the body is vulnerable to a host of infections of diseases. When t-cells are are weakened by HIV, they lose their ability to produce and transport glutathione, a major cellular antioxidant. Once this happens, they succumb to oxidative stress causing further destruction. Not surprisingly, HIV-positive patients have considerably lower glutathione, as well as other antioxidant, levels.

AIDS/HIV and Alpha Lipoic Acid

In the test tube, ALA prevents replication of HIV in cultured human cells. There is also evidence that ALA bolsters the antioxidant defenses in HIV-positive people. In one study, lipoic acid (150mg, 3 times daily) was given orally to 12 HIV patients. At the end of 2 weeks, all of the patients had an increase in in blood glutathione levels, and 9 patients had an increase in the number of t-helper cells - a sign that their immune system was stronger.

In vitro, alpha-lipoic acid has been shown to have synergistic effects when combined with AZT, with the combination of the two showing stronger inhibition of HIV replication than either had when used alone. In vitro research done at Kumamoto University in Japan has shown that alpha-lipoic acid significantly depresses both HIV tat gene activity and HIV infectivity, and is active in both acute and chronically infected cells. Other in vitro research done in the Department of Molecular and Cell Biology at the University of California, Berkeley, has shown that alpha-lipoic acid inhibits NF-kappa B activity.

German in vitro research has also shown that alpha-lipoic acid inhibits the infectivity of virus particles and suppresses viral replication, and follow-up in vivo studies by the same researchers showed that it does have antiviral effects in HIV+'s, reducing viral titers just as had been predicted by the in vitro research. Since NF-kappa B is, in essence, an on-off switch for the activation of HIV, and tat inhibition is considered a promising antiviral approach, and anything non-toxic that effectively suppresses viral replication and reduces infectivity is immensely desirable, alpha lipoic acid may be a very important part of a comprehensive antiviral approach

 

 

ALPHA-LIPOIC ACID MAY HELP REDUCE INFLAMMATION

October 11, 2002.The incidence of inflammatory diseases such as arthritis increases with age. Free radicals promote inflammatory reactions, which antioxidants have been successful at diminishing. Scientists recently stimulated the inflammatory response of white blood cells, resulting in an increase of Intracellular Adhesion Molecule 1 (ICAM-1), which encourages white blood cells to stick to other cells, thereby inflaming tissues. Alpha-lipoic acid, a potent antioxidant, was then added to the mix. Researchers said the acid reduced the activity of ICAM-1 to levels in normal, un-stimulated cells in a dose-dependent manner. It also lowered the activity of NFkB (NFkB can increase the activity of genes responsible for inflammation). According to the study, these changes suggest that alpha-lipoic acid may help reduce the effects of inflammatory diseases such a rheumatoid arthritis and psoriasis.

Cancer and Alpha Lipoic Acid



Free radical damage can promote the activity of a particular cell protein called NF kappa B. (NF-kB) NF-kB works to promote inflammation and genetic changes that have been linked with the development of cancer. Studies at the University of California at Berkley have found that when cells are bathed in ALA, NF-kB is inhibited thus preventing cell mutations from replicating. Researchers believe that this has significant implications in inhibiting the formation of cancerous tumors.

MayoClinic

Coenzyme Q-

Associated with improvement of following conditions:

Abnormal heart rhythms,
amyotrophic lateral sclerosis (ALS),
asthma,
atherosclerosis,
Bell's palsy,
blood flow disorders,
breathing difficulties,
cancer,
cerebellar ataxia,
chronic fatigue syndrome,
chronic obstructive pulmonary disease (COPD),
deafness, gingivitis, hair loss (and hair loss from chemotherapy),
heart irregular beats,
hepatitis B,
high cholesterol,
immune system diseases, 
kidney failure, leg swelling (edema), life extension,
liver enlargement or diseaseung cancer
lung diseasemacular
egenerationMELAS syndromemetastatic disease,
MIDD (maternally inherited diabetes mellitus and deafness)
muscle wasting, nutrition, obesityPapillon-Lefevre Syndrome,
physical performance
prevention of muscle damage from "statin" cholesterol-lowering drugs,
psychiatric disorders,
QT-interval shortening;
reduction of phenothiazine drug side effects,
 reduction of tricyclic antidepressant (TCA) drug side effects,
 stomach ulcer, swelling.


HIV/AIDS

There is limited evidence that natural levels of CoQ10 in the body may be reduced in people with HIV/AIDS. There is no reliable scientific research showing that CoQ10 supplements have any effect on this disease. C Breast cancer

Several studies in women with breast cancer report reduced levels of CoQ10 in diseased breast tissue or blood. It has been suggested by some researchers that raising CoQ10 levels with supplements might be helpful. However, it is not clear if CoQ10 is beneficial in these patients, or if the low levels of CoQ10 may actually be a part of the body's natural response to cancer, helping to fight disease. Supplementation with CoQ10 has not been proven to reduce cancer, and has not been compared to other forms of treatment for breast cancer. C

MORE ON QUINONES AND POLYPHENOLS

Apple skins and seeds (Extract) related to quinones only these are larger molecules with a lot more available oxygen attached. Note the structure and the number of -OH molecules that are available to donate oxygen first the hydrogen, but then the oxygen .