Written by: Sylvia P. Onusic, PhD, CNS, LDN
This article is copyrighted by Walkabout Health Products LLC, 2019

Hundreds of recent studies show that vitamin K2 (MK-4), the “Activator-X” of Dr. Weston A. Price, (Onusic, 2017) is required in many life-sustaining and life-givingprocesses. The vitamin K2- menaquinone (MK) family has many members, MK-3 to MK-13 but only one appears as a food source, MK-4. However, it appears that all menaquinones are not interchangeableand MK-4 is the only form that is not the product of bacterial synthesis. The body prefers and uses vitamin K2 in the form of menaquinone-4 (MK-4) in its many processes and this also includes pregnancy. MK-4 is found in the brain, pancreas, salivary glands, heart, kidneys, cartilage, sternum and in breast milk. The body prefers MK-4 as far as the fetus is concerned, over other available forms of vitamin K2. (Onusic, 2017) https://walkabouthealthproducts.com/emu-oil-dr-weston-price-activator-x/

Studies dating back to the late 1980’s – 1990’s show that Mother Nature chooses MK-4 for the unborn child every time, even when MK-7 from natto is readily available in the diet, and even present in the placenta. Japanese scientists divided a group of Japanese women into two groups: Group A, composed of women consuming a normal diet; and Group B, whose subjects ate a diet high in natto, a fermented soybean food which is high in menaquinone-7 (MK-7).

In one of the few studies ever conducted on the presence of vitamin K2 in the placenta and umbilical cord of newborn babies, Dr. Hidekazu Hiraike and his colleagues found that the placenta blocked MK-7 from passing into the fetus, acting as a natural evolutionary control mechanism. The researchers measured MK-4, MK-6, MK-7, as well as vitamin K1 in the placenta. However, they found that only the MK-4 and vitamin K1 passed into the child. (Hirakie et al., 1998).

MK-7 was found in the maternal blood plasma and the placental tissues of both groups. The maternal plasma of MK-7 in Group A (normal diet) was .70 nanograms per milliliter (ng/ml) and the maternal plasma of group B (eating high amounts of natto regularly) was 3.55 ng/ml.  Levels of MK-7 in the placentas of Group A were 1.08 ng/g and significantly higher levels of MK-7 were found in the placenta of Group B at 10.82 ng/g. (Hirakie et al, 1998) (See Graph 1 below.)

Only Vitamin K2 MK-4 is utilized directly by the fetus.

Graph 1: Levels of MK-7

Scientists who promote MK-7 say that it has a longer half-life and circulates longer in the plasma, therefore it is more bioavailable. Here is a true account of what actually happens in the body. Although high levels of MK-7 were circulating in the blood, none found its way into the fetus. It is also not found in any organ. Intestinal bacteria make it for their own use. Humans  absorb fat soluble vitamins in the small intestine where bile is required; they cannot absorb MK-7 made by bacteria in the colon.

Despite the high levels of MK-7 in the natto Group B, no MK-7 was found in the umbilical cord blood, meconium and amniotic fluid of any of the babies. However, MK-4 and vitamin K1 (both from food sources not injection) were found in the cord blood, meconium and amniotic fluid. It appeared that the placental tissues effectively blocked the passage of MK-7 while allowing MK-4 into the fetus. 

Vitamin K2 MK-4 placental carrier protein

Dr. Hideaki Iioka and his team also found in 1992 that MK-4 is transported into the placenta by a carrier protein as the result of an existing transport carrier system in the brush border membrane of the human placenta. This carrier could be the reason that MK-4 reaches the fetus and MK-7 does not. It could also be the reason that MK-4 is often not detected in the blood because it is attached to a carrier protein. Even though all other fat-soluble vitamins (A, D, E) are carried in the blood by a carrier protein (Kono et al, 2015), very few researchers acknowledge or have explored the presence of a vitamin K2 MK-4 carrier protein in other tissues.

In Dr. Hirake’s study, the MK-7 found in the pregnant women’s plasma and placenta was from their diet and not from an injection or supplement. Many supplements on the market contain vitamin K2 in the form of MK-7. MK-7 is also found in prenatal vitamins. Pregnant women taking a MK-7 supplement are unknowingly participating in a human experiment. The outcome of taking MK-7 by pregnant women is untested– no study has examined the effect of MK-7 from supplements on pregnant women and their unborn babies.

Food sources of MK-4

Food sources of vitamin K2, containing MK-4, have been safely used by moms and babies for thousands of years. MK-4 is found in breast milk and levels are affected by diet. Excellent sources of pre-formed vitamin K2 MK-4 are butter, ghee, egg yolk, goose liver, goose meat, chicken liver, organ meats and Australian emu oil (Walkabout Brand). Fair sources are hard cheeses, organ meats, and other poultry. Sauerkraut contains a very small amount of MK-4, with the longer chains such as MK-9 predominating. (Elder et al, 2006; Schurgers et al, 2002) Traditional weaning foods for babies were chicken liver and egg yolk, both excellent sources of
MK-4.

Natural food forms vs. bacterially fermented forms

MK-4 and MK-7 do not substitute for one another. They are structurally different and are derived from different sources. No matter how much vitamin K-2 a pregnant woman takes in the form of a MK-7 supplement or natto, at least in this study, none of the MK-7 passed into the baby’s blood.

Can excess MK-7 harm the fetus?

Vitamin K2 in the form of the MK-4 is naturally found in foods and recognized by the body. MK-7, a patented form of vitamin K2, is now found in prenatal vitamins which some pregnant women take during their entire pregnancy.

Researchers promoting MK-7 have not investigated the concerns raised here regarding the safety of MK-7. In fact, in 2007, the FDA raised concerns about fetal death in experimental groups of rats, with the company NattoPharma who distributes MenaQ-7, when they were trying to attain GRAS (generally regarded as safe) status in the U.S. (GRAS petition, 2007)

What exactly happened to the MK-7 in the placenta if it did not pass through to the baby? It remained in the placenta. But can excess MK-7 in the placenta cause harm to the fetus? No studies have examined this possibility.

Calcified placenta, osteocalcin, MK-7 and the fetal skull

The placenta is a circular organ attached to the uterine wall of pregnant women that protects, nourishes, and maintains the fetus through the umbilical cord. In a few studies, researchers concluded that MK-7 acts as a cofactor in forming osteocalcin that deposits calcium in bones. (Inaba, Sato, Yamashita, 2015) Excess calcification in the placenta could cause a decrease in blood supply, thus less oxygen, a condition called” small for gestational age” and other defects. If MK-7 is involved in creating vitamin K dependent proteins in the placenta, this process could result in an increase in osteocalcin, which does pass into the infant. The bones of the fetal skull are not fused yet so that the baby can pass easily through the birth canal. Could increased mineralization as a result of the osteocalcin, reach the bones and other tissues of the unborn? (Israels et al. 1995).

If the infant cannot use the MK-7 as shown in this study, why take the chance?

Safety of natto and MK-7

In the study described here the natto consumed by the women in Group B was a natural product. Bacillus subtilis is the bacteria that produces MK-7 in the soybeans. However, the amount of MK-7 which can be produced by the traditional natto fermentation process is limited –and the entire product is consumed, not just the bacterial product itself. The Bacillus group of bacteria is extremely large. Dr. H. Almquist, one of the discoverers of vitamin K2 that turned out to be MK-7, actually isolated it from decayed fishmeal.

Commercial production of MK-7

To produce more MK-7 and deliver it in a supplement form, scientists have developed and patented alternative ways of growing large amounts of MK-7 from mutated forms of bacteria on a variety of substrates such as soy, chickpeas, mung bean, corn waste, and then extracting the bacteria from the substrate with toxins such as hexane. Almost all MK-7 supplements on sale are made by these methods. (Sato et al, 2001) One form of MK-7 is totally the product of genetic engineering, Kappa Bioscience, K2Vital (Moller et al. European Patent EP 2 819 928 B1).

Fermentation of soy, histamines, glutamates and biogenic amines

Fermentation produces histamines, glutamate, and biogenic amines (Spano, 2010) that can cause allergic reactions after ingested. Soybeans, soy protein, and soy derivatives contain glutamate, as would natto. The food additive MSG, monosodium glutamate, is created by fermenting starch, corn sugar or molasses from sugarcane or sugar beets. This kind of glutamate production does not require disclosure by the USFDA. Too much of the excitotoxin, glutamate excites the neurons in the brain, causes anxiety, sleeplessness, headache, rash, etc., and even neuron death. (Science Direct) Excitotoxins: The Taste That Kills, by neurologist, Dr. Russell Blaylock, gives detailed information on the effects of glutamates on the brain.

J-Oil Mills, Ajinomoto, NattoPharma, MenaQ7

But another piece of the MK-7 puzzle: the company that is one of the largest producers of MSG, selling it under the name “Ajinomoto Umami Super Seasoning,” https://bit.ly/2v4vawr, is Ajinomoto, now transformed into J-Oil Mills, the company that makes the “natural” form of MK-7 from natto-derived substances and distributed by NattoPharma as MenaQ7 (cision.com, 2007). In fact, the bioengineer Toshiro Sato, appears to be the main researcher employed by J-Oil Mills who developed the patented process to produce the “natural” MK-7, MenaQ7, (Sato et al, 2001) and author who collaborated with Dutch researchers on several occasions on research papers about MK-7 that are widely circulated and quoted. (Sato, Schurgers, 2012)

Does this sound like a “natural” product?

Quote: “Menaquinone-7 (MK-7) is a highly bioactive homologue of vitamin K. We obtained a diphenylamine-resistant mutant strain D200-41 from Bacillus subtilis strain MH-1 which was isolated from fermented soybeans, natto. The mutant strain exhibited decreased production of MK-6. Using strain D200-41, efficient production of MK-7 was achieved. We found that, compared with an agitated and aerated culture, production of MK-7 was increased by static culture. The sporulation of the cells progressed more slowly in a static culture than in an agitated culture. The maximum concentration of MK reached about 60 mg/l in a medium containing 10% soybean extract, 5% glycerol, 0.5% yeast extract and 0.05% K2HPO4 (pH 7.3) when D200-41 cells as well as MH-1 cells were statically cultured at 45°C for 5 d after being cultured with shaking at 37°C for 1 d.” (Sato et al, 2001)

Toxicity

Many sources state that vitamin K2 cannot become toxic, even when taken in high amounts. However, it is a fat-soluble vitamin and, like other fat-soluble vitamins, is stored in the body. Hypervitaminosis (high levels of a vitamin) has been documented with all the other fat-soluble vitamins, not from food sources, but from artificial supplements. Toxicity can be caused by intake of fortified foods (cereals, grain products, crackers, etc.) AS WELL but natural foods rarely deliver dangerous levels of fat-soluble vitamins (Sizer, 2008). Food products that contain higher levels of natural pre-formed vitamin K2 MK-4, like Australian emu oil (Walkabout Brand), butter, ghee, and egg yolk, are naturally found in a food matrix, unlike MK-7, a single isolate supplement produced by a fermentation process.

 



Dr. Onusic is a board certified clinical nutritionist licensed to practice dietetics and nutrition. She completed dietetic studies, a Master of Science and PhD at Penn State University. She is a frequent contributor to the journal, Wise Traditions in Food, Farming and the Healing Arts. Her website, Nutrition Power, can be found at drsylviaonusic.com. Sylvia is the mother of two sons and lives in western Pennsylvania

 


References

View References