MaitakeGold 404™ MD Fraction
The Medicinal Mushroom for Cellular
Immune Protection
written by Dr. Michael T. Murray
The The maitake mushroom (Grifola frondosa) is the source of immune enhancing compounds that are
being shown to offer significant health benefits.1,2 The commercial evolution of maitake has led to the
development of Maitake Gold 404™, a proprietary maitake extract developed by Dr. Hiroaki Nanba -
the world’s leading authority on maitake.
In the early 1980s, Dr. Nanba was researching the immune enhancing properties of mushrooms
when he came to the conclusion that maitake extracts demonstrated more pronounced antitumor
activity in animal tests than other mushroom extracts.3* One of the key benefits to maitake was the
ability to be quite effective when given orally. In contrast, the other mushrooms Dr. Nanba was studying
such as shiitake were only effective when injected into the bloodstream.
In 1984, Dr. Nanba identified a fraction of maitake that possessed a significant ability to stimulate
white blood cells known as macrophages (literal translation "big eaters").These specialized white blood
cells phagocytize or engulf foreign particles including cancer cells, bacteria, and cellular debris. Dr.
Nanba termed his discover maitake D-fraction.This fraction consisted of polysaccharide compounds
(beta-1,6 glucan and beta-1,3 glucan) and protein. In 1984 a patent was issued in Japan to Nanba and
others.
While other medicinal mushrooms have shown to have similar beta-glucan constituents, Dr. Nanba
found that the beta-glucans found in the maitake D-fraction have a unique and complex structure.The
biggest difference was a greater number of branching side chains. It is thought that the greater the
degree of branching, the higher the likelihood the beta-glucan fraction will reach and activate a greater
number of immune cells.4-6
Throughout the late 1980s and into the 1990s, Dr. Nanba and other Japanese researchers continued
to study maitake, trying to improve upon the antitumor and immunopotentiating activity of the Dfraction.
Further purification of the D-fraction yielded the MD-fraction (U.S. Patent #5,854,404), which
is even more bioactive than the D-fraction.7 It is important to point out that any research references
to the D-fraction also apply to the purer and more potent MD-fraction (i.e., Maitake Gold 404™).
The MD-fraction is produced in a similar manner to the D-fraction; however, Dr. Nanba added a
key step that removes some impurities found in the D-Fraction.7 The result is that the MD-fraction
provides superior results over the D-fraction. For example, in an antitumor test described in the
patent each solution was administered to mice with carcinomas.The researchers found the group
given the MD-fraction experienced a significantly stronger inhibitory effect on tumor growth than that
of the group given the D-fraction.The researchers also compared each fraction’s effects on white
blood cells (macrophage and killer T-cell activity) five days after each test substance was given.The
MD-fraction also exhibited stronger immune system potentiation compared to the D-fraction. Both
the D- and MD-fractions are considered to have low toxicity and high safety.
What are the other effects of maitake beta-glucan fractions
on the immune system and how does it fight cancer?
Maitake beta-glucan fractions exert profound effects on immune function.6,8-12* In a nutshell, it
appears that the beta-glucans in the maitake MD-fraction actually bind to receptors on the outer
membranes of macrophages and other white blood cells including natural killer (NK) cells and cytotoxic T-cells
(Tc). These immune cells are very important in protecting against and fighting cancer because they can attack
tumor cells directly.*
Just like a key in a lock, the binding of the beta-glucan literally flips white blood cells on and triggers a chain
reaction leading to increased immune activity. In addition to increasing the ability of the macrophages to engulf
and destroy cancer cells, microbes, and other foreign cells, the beta-glucan binding stimulates the production of
important signaling proteins of the immune system such as interleukin-1 interleukin-2, and lymphokines. These
immune activators ramp up defenses by activating immune cells.
Beta-glucans from Maitake Gold 404™ also stimulate the production of white blood cells within the bone
marrow - the major area for white blood cell production. Reduced bone marrow production means lowered
white cell counts and an increased risk of infection and cancer. This beneficial effect of the beta-glucan is put to
good use in cancer patients undergoing radiation therapy or chemotherapy.
Do other sources of
beta-glucans provide
the same benefit as
MaitakeGold 404™?
Beta-glucans are found in many other forms.
However, the unique branching pattern of maitake
MD-fraction makes it the ideal source of these
molecules. Beta-glucans from oats and barley, for
example, tend to form viscous gel. When consumed
with a meal, oat and barley beta-glucans act
as a good source of soluble fiber in lowering cholesterol
and blood sugar levels, but they really don’t
have much of an impact on the immune system.
Purified beta-glucans from the common baker’s
yeast (Saccharomyces cerevisiae) possess similar
benefit to maitake beta-glucan fractions, but may
not be as well absorbed.
How does maitake
beta-glucan fractions
inhibit tumor growth?
Maitake researchers have identified four primary
mechanisms by which maitake fights cancer:13-21
- By protecting healthy cells from becoming cancerous.*
- By enhancing the immune system’s ability to seek out and destroy cancer cells.*
- By helping the cell regain control of cell division and programmed cell death (apoptosis).*
- By helping to prevent the spreading (metastasis) of cancer.*
Another way in which maitake beta-glucan
fractions may inhibit cancer formation is via
enhancement of apoptosis, a distinct form of cell
death controlled by an internally encoded suicide
program.22* In cancerous cells, there is a tendency
of suppression of this natural process of cell death.
Instead of dying, the cancer cell multiplies. By promoting
apoptosis, cancer cells can literally be
turned off.
Does maitake have
any benefit against
the human immunodeficiency
virus (HIV)?
Yes. In the late 1980s, Japanese researchers
determined maitake D-fraction enhanced helper Tcells,
the target cells of HIV.26* This was one of
the earliest clinical indications that maitake may be
a potential treatment for HIV. Since then, test tube
studies have shown some promising results in
inhibiting HIV. Recently, the effect of the MDfraction
was studied in 35 HIV-positive subjects
for 360 days.27 The researchers monitored helper
T-cell (CD4+) counts, viral load, symptoms of
HIV infection, status of secondary disease, and
subjects' sense of well-being. Effects on the helper
T-cell count and viral load were variable: helper Tcells
increased in 20 patients, decreased in eight
patients, and remained static in four patients. Viral
load decreased in ten patients, increased in nine
patients, and was static in two patients. The big
change was that 85% of the patients reported an
increased sense of well-being with regard to various
symptoms and secondary diseases caused by HIV.
The researchers concluded that the MD-fraction
appears to work on several levels: by direct inhibition
of HIV, stimulation of the body's own natural
defense system against HIV, and making the body
less vulnerable to opportunistic disease.33
Can maitake betaglucan
fractions be
used during
chemotherapy?
According to preliminary data, maitake betaglucan
fractions appear to help reduce the side
effects of conventional chemotherapy (and radiation)
while at the same time enhancing its effectiveness.
23* In 1994, a group from China published
findings from a pilot study on 63 cancer
patient reporting a total effective rate against solid
tumors at higher than 95% and the effective rate
against leukemia higher than 90%. In a preliminary
study conducted by Dr. Nanba, 165 patients
with advanced cancer were given maitake extract.24
In the patients who were also on chemotherapy,
90% of the patients experienced a reduction in the
side effects common to chemotherapy including
hair loss, decreased white blood cell counts, nausea,
vomiting, and loss of appetite. Maitake was shown
to effectively reduce pain levels in 83% of the
patients. The results were best in breast, lung, and
liver cancers. Dr. Nanba reported significant
improvement in symptoms or regression of tumors
in 73.3% of patients with breast cancer, 66.6% in
lung cancer, and 46.6% in liver cancer. In contrast
to the incredible response rates claimed in the
Chinese study, in Dr. Nanba’s study less than 50%
of the leukemias and cancers of the prostate, brain,
stomach, and bone seemed to respond.
These preliminary studies need to be followedup
by larger, better controlled studies. It appears
that such studies are on the horizon as in February
1998 the U.S. Food and Drug Administration
approved an Investigational New Drug Application
(IND 54,589) for researchers to conduct a more
detailed pilot study on maitake D-fraction's potential
effects on advanced breast and prostate cancers.
What type of tumors
are inhibited by
maitake beta-glucan
fractions?
Preliminary studies in animal models have
shown maitake fractions inhibit the growth of
tumors in the colon, lungs, stomach, liver, prostate,
cervix, bladder, and brain, as well as leukemia.*
The significance of this inhibition in animal models
to the human condition is not clear at this time,
but it does give us an idea of the potential of
maitake beta-glucan fractions.
What is the proper
dosage for Maitake
Gold 404™?
The dosage of maitake extracts is based upon
the level of the D- or MD-fraction. The therapeutic
dosage range is based upon body weight, 0.5mg
to 1.0 mg for every 2.2 pounds (1 kg) of body
weight per day. That translates to a dosage of
approximately 35-70 mg of the D- or MD-fraction.
The dosage recommendation for prevention is
typically 5 to 15 mg of the D- or MD-fraction. For
best results take 20 minutes before meals or on an
empty stomach.
References
- Mayell M. Maitake extracts and their therapeutic potential. Altern Med Rev 2001;6:48-60
- Jones K. Maitake: a potent medicinal food. Alt Comp Ther 1998;4:420-429.
- Nanba H, Hamaguchi A, Kuroda H.The chemical structure of an antitumor polysaccharide in fruit bodies of Grifola frondosa (maitake). Chem Pharm Bull 1987;35:1162-1168.
- Adachi Y, Ohno N, Ohsawa M, et al. Change of biological activities of (1-3)-beta-D-glucan from Grifola frondosa upon molecular weight reduction by heat treatment. Chem Pharm Bull 1990;38:477-481.
- Okazaki M, Adachi Y, Ohno N,Yadomae T. Structure-activity relationship of (1Ñ>3)-beta-D-glucans in the induction of cytokine production from macrophages, in vitro. Biol Pharm Bull 1995;18:1320-1327.
- Borchers AT, Stern JS, Hackman RM, et al. Mushrooms, tumors, and immunity. Proc Soc Exp Biol Med 1999;221:281-293.
- Nanba H, Kubo K. Antitumor substance extracted from Grifola. U.S.Patent 5,854,404, issued December 29, 1998.
- Adachi Y, Okazaki M, Ohno N,Yadomae T. Enhancement of cytokine production by macrophages stimulated with (1Ñ>3)-beta-D-glucan, grifolan (GRN), isolated from Grifola frondosa. Biol Pharm Bull 1994;17:1554-1560.
- Adachi Y, Ohno N,Yadomae T. Activation of murine kupffer cells by administration with gel-forming (1Ñ>3)-beta-D-glucan from Grifola frondosa. Biol Pharm Bull 1998;21:278-283.
- Ohno N, Egawa Y, Hashimoto T, et al. Effect of beta-glucans on the nitric oxide synthesis by peritoneal macrophage in mice. Biol Pharm Bull 1996;19:608-612.
- Suzuki I, Itani T, Ohno N, et al. Effect of a polysaccharide fraction from Grifola frondosa on immune response in mice. J Pharmacobiodyn 1985;8:217-226.
- Suzuki I, Hashimoto K, Oikawa S, et al. Antitumor and immunomodulating activities of a beta-glucan obtained from liquid-cultured Grifola frondosa. Chem Pharm Bull 1989;37:410-413.
- Yamada Y, Nanba H, Kuroda H. Antitumor effect of orally administered extracts from fruit body of Grifola frondosa (maitake). Chemotherapy 1990;38:790-796.
- Adachi Y, Ohno N, Ohsawa M, et al. Physiochemical properties and antitumor activities of chemically modified derivatives of antitumor glucan "grifolan LE" from Grifola frondosa. Chem Pharm Bull1989;37:1838-1843.
- Mizuno T, Ohsawa K, Hagiwara N, Kuboyama R. Fractionation and characterization of antitumor polysaccharides from maitake, Grifola frondosa. Agric Biol Chem 1986;50:1679-1688.
- Ohno N, Asada N, Adachi Y,Yadomae T. Enhancement of LPS triggered TNF-alpha (tumor necrosis factor-alpha) production by (1Ñ>3)-beta-D-glucans in mice. Biol Pharm Bull 1995;18:126-133.
- Suzuki I, Itani T, Ohno N, et al. Antitumor activity of a polysaccharide fraction extracted from cultured fruiting bodies of Grifola frondosa. J Pharmacobiodyn 1984;7:492-500.
- Takeyama T, Suzuki I, Ohno N, et al. Host-mediated antitumor effect of grifolan NMF-5N, a polysaccharide obtained from Grifola frondosa. J Pharmacobiodyn 1987;10:644-651.
- Ohno N, Adachi Y, Suzuki I, et al. Antitumor activity of a beta-1,3-glucan obtained from liquid cultured mycelium of Grifola frondosa. J Pharmacobiodyn 1986;9:861-864.
- Yang DA. Inhibitory effect of Chinese herb medicine zhuling on urinary bladder cancer. An experimental and clinical study. Chung Hua Wai Ko Tsa Chih 1991;29:393-395,399.
- Suzuki I,Takeyama T, Ohno N, et al. Antitumor effect of polysaccharide grifolan NMF-5N on syngeneic tumor in mice. J Pharmacobiodyn 1987;10:72-77.
- Fullerton SA, Samadi AA,Tortorelis DG, et al. Induction of apoptosis in human prostatic cancer cells with beta-glucan (Maitake mushroom polysaccharide). Mol Urol 2000;4:7-13.
- Nanba H. Maitake D-fraction: healing and preventive potential for cancer. J Orthomol Med 1997;12:43-49.
- Nanba H. Results of non-controlled clinical study for various cancer patients using maitake D-fraction. Explore 1995;6:19-21.
- Nanba H, Kodama N, Schar D,Turner D. Effects of maitake (Grifola frondosa) glucan in HIV-infected patients. Mycoscience 2000;41:293-295.
- Hishida I, Nanba H, Kuroda H. Antitumor activity exhibited by oral administered extract from fruit body of Grifola frondosa (maitake). Chem Pharm Bull 1988;36:1819-1827.
- Nanba H, Kodama N, Shar D,Turner D. Effect of Maitake (Gifolia frondosa) glucan in HIV-infected patients. Mycoscience 2000;41:293-5.
*These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease. | |