USPEH- ЦЕНТР ОМОЛОЖЕНИЯ И ПРАКТИЧЕСКОЙ ПСИХОЛОГИИ
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Аватар пользователя Viorel  Bungau
Viorel Bungau

Dear Professor, I want to promote energy assessment by Energo-Electro-Photography (Virtual Scanning) in cancer and generally become a diagnostic method, and rebalance energy irradiation with light color (color therapy). Please join me in this research proposal, as leader, because I can not go alone.Please inform me your opinion about this hypothesis. The basic idea of this theory is that the oxidation of hydrogen and carbon atoms, arising from the degradation of carbohydrates, is by two distinct processes based on oxidation-reduction electron transfer and photochemical process of energy release on the basis of color complementary, predominance of one or another depending on intracellular acid-base balance. Final biological oxidation, the production of CO2 and H2O, should be reconsidered in the sense that a distinction must be made between the oxidation of carbon and hydrogen oxidation. In the case of carbon atoms, cytochrome oxidase must have an alkaline chemical structure, to be colored green and so can absorb additional red energy carbon atoms derived from carbohydrate. For the oxidation of H atom cytochrome oxidase must have a acidic chemical structure, to be colored red, and so can absorb additional green energy hydrogen atom derived from carbohydrate. We propose an experiment to prove that the final biological oxidation, in addition to its oxidation-reduction, with formation of H2O and CO2,there is a photochemical effect, by which energy is transferred from the H atom, or C, process is done selct, the colors, complementary colors on the basis of the structures involved are colored (red hemoglobin Fe, Mg chlorophyll green, blue ceruloplasmin Cu, Fe cytochrome oxidase red, green cytochrome oxidase with Cu etc.). The basic idea is that if life pigments (chlorophyll, hemoglobin, cytochromes), which provides energy metabolism of the cell, are colored, we can control their activities through chromotherapy, on the basis of complementary color and energy rebalance the body, with a figured COLOR ELECTROPHOTOGRAPHY (VIRTUAL SCANNING). In my opinion, at the basis of malign transformation is a disturbance of energetical metabolism, which reached a level that cell can not correct (after having succeeded before, many times), disturbance that affects the whole body in different degrees and requires corection from outside starting from the ideea that the final biological oxidizing takes place through photochemical process with releasing and receieving energy. I SUGGEST TO YOU AN EXPERIMENT: TWO PLANTS, A RED (CORAL) LIGHT ONLY, IN BASIC MEDIUM, WITH ADDED COPPER, WILL GROW, FLOWER AND FRUIT WILL SHORT TIME, AND THE OTHER ONLY BLUE-GREEN LIGHT(TOURQUOISE), IN AN ACID MEDIUM, WITH ADDED COPPER CHELATOR , WHICH GROWS THROUGHOUT WILL NOT GROW FLOWERS AND FRUIT WILL DO. CULTURE OF NEOPLASTIC TISSUE, IRRADIATED WITH MONOCHROMATIC BLUE-GREEN (TOURQUOISE) LIGHT, IN AN ALKALINE MEDIUM, WITH ADDED COPPER, WILL IN REGRESSION OF THE TISSUE CULTURE. CULTUREOF NEOPLASTIC TISSUE, IRRADIATED WITH RED (RED CORAL) LIGHT, IN AN ACID MEDIUM, WITH ADDED COPPER CHELATOR, WILL LEAD TO EXAGERATED AND ANARCHICAL MULTIPLICATION. If in photosynthesis is the direct effect of monochromatic irradiation, in the final biological oxidation effect is reversed. Exogenous irradiation with green, induces endogenous irradiation with red, and vice versa. "About Carcinogenesis." Final biological oxidation, the production of CO2 and H2O, should be reconsidered in the sense that a distinction must be made between the oxidation of carbon and hydrogen oxidation. In the case of carbon atoms, cytochrome oxidase must have an alkaline chemical structure, to be colored green and so can absorb additional red energy carbon atoms derived from carbohydrate. For the oxidation of H atom cytochrome oxidase must have a acidic chemical structure, to be colored red, and so can absorb additional green energy hydrogen atom derived fromcarbohydrate.In my opinion, at the basis of malign transformation is a disturbance of energeticalmetabolism, which reached a level that cell can not correct (after having succeeded before, many times), disturbance that affects the whole body in different degrees and requires corection from outside starting from the ideea that the final biological oxidizing takes place through photochemical process with releasing and receieving energy. "Duality of cytochrome oxidase. Proliferation (growth) and Differentiation (maturation) cell." Cytochrome oxidase is present in two forms, depending on the context of acid-base internal environment : 1.- Form acidic (acidosis), which contains two Iron atoms, will be red, will absorb the additional green energy of the hydrogen atom, derived from carbohydrates, with formation of H2O, metabolic context that will promote cell proliferation. 2.-Form alkaline(alkalosis), containing two Copper atoms, will be green, will absorb the additional red energy of the carbon atom, derived from carbohydrates, with formation of CO2, metabolic context that will promote cell differentiation. It is known that in conditions of acidosis (oxidative potential), the principle electronegativity metals, Copper is removed from combinations of the Iron. So cytochrome oxidase will contain two atoms of iron instead of copper atoms, which changes its oxidation-reduction potential, but (most important), and color, which radically change its absorption spectrum, based on the principle of complementary colors. According to the principle electronegativity metals, under certain conditions the acid-base imbalance (acidosis), iron will replace copper in combination,leading to changing oxidation-reduction potential, BUT THE COLOR FROM GREEN, TO REED, to block the final biological oxidation and the appearance of aerobic glycolysis. In the final biological oxidation, in addition to an oxidation-reduction process takes place and a photo-chemical process,based on complementary colors, the first in the electron transfer, the second in the energy transfer. A body with cancer disease will become chemically color "red"(Acid, as evidenced by laboratory), and in terms of energy, "green"(visible by color Electrophotography ;Virtual Scanning). A healthy body will become chemically color"green"(Alkaline,as evidenced by laboratory) and in terms of energy, "red" (visible by Electrophotography ; Virtual Scanning). "Green body" with alkaline chemical structure, with energy connection type C = O, and red energy , from the oxidation of the carbon energy C = O derived from carboxylic acids. "Red body" with acid chemical structure, with connections Carbon non-energy C-OH, (non-energy, phenolic acids, with strong oxidizing, prone to multiplication), and green energy , which comes from oxidation of hydrogen atoms derived from carbohydrates). Carbon Energy O ::C:: O; Non-Energy Carbon :O: C :O: I want to promote energy assessment by Energo-Electro-Photography (Virtual Scanning) in cancer and generally become a diagnostic method, and rebalance energy irradiation with light color (color therapy). Please support me in this research, as leader of the project. This process is carried out based on complementary colors, which are coenzymes oxidative dehydrogenation and oxidative decarboxylation is colored . It reveals the importance of acid-base balance, the predominance of the acidic or basic, as an acid structure (red), not only can gain energy from the carbon atom red (the principle of complementarity), but can not assimilate (under the same principle). It must therefore acid-base balance of internal environment, and alkalinization his intake of organic substances by the electron donor. By alkalinization (addition of electrons) will occur neutralize acid structures, the red, they become leucoderivat, colorless, and inactive, while the basic, which because of acidosis became neutral, colorless and inactive, will be alkaline in electron contribution, will be in green, and will absorb red energy from the carbon atom. So, on two kinds of vital energy, it is clear correlation between the chemical structure of the cell (body),and type of energy that can produce and use. Thus a cell with acidic chemical structure, can produce only energy by oxidative dehydrogenation (green energy), because the acid can only be active coenzymes with acid chemical structure, red, will absorb the complementarity only green energy of hydrogen. Basic structures which should absorb red energy from carbon , are inactive due to acid environment, which in turn chemically in leucoderivat, so colorless structures, inactive. Conversion of these structures to normal, operation by alkalinization could be a long lasting process, therefore, we use parallel chromotherapy, based on the fact that these COENZYMES INVOLVED IN BIOLOGICAL OXIDATION FINALS ARE COLORED AND PHOTOSENSITIVE. If we can determine the absorption spectrum at different levels, we can control energy metabolism by chromotherapy - EXOGENOUS MONOCHROMATIC IRRADIATION . Energy absorption in biological oxidation process itself, based on complementary colors, the structures involved (cytochromes), is the nature of porphyrins, in combination with a metal becomes colored, will absorb the complementary color, corresponding to a specific absorption spectrum, it will be in - ENDOGENOUS MONOCHROMATIC IRRADIATION. This entitles us to believe that: In photosynthesis,light absorption and its storage form of carbohydrates, are selected,the colors, as in cellular energy metabolism, absorption of energy bythe degradation of carbohydrates, is also done selectively, based on complementary colors. Thus, exogenous irradiation with monochromatic green will neutralize, by complementarity, coenzymes red, acidic. In will reactivate alkaline coenzymes, which have become due acidosis leucoderivat, so colorless and inactive. Without producing CO2, carbonic anhydrase can not form H2CO3, severable and thus transferred through mitochondrial membrane. Will accumulate in the respiratory Flavin, OH groups, leading to excessive hydroxylation, followed by consecutive inclusion of amino (NH2). It is thus an imbalance between the hydrogenation-carboxylation and hydroxylation-amination, in favor of the latter. This will predominate AMINATION and HYDROXYLATION at the expense CARBOXYLATION and HYDROGENATION, leading to CONVERSION OF STRUCTURAL PROTEINS IN NUCLEIC ACIDS. Meanwhile, after chemical criteria, not genetic, it synthesizes the remaining unoxidized carbon atoms, nucleic bases "de novo" by the same process of hydroxylation-amination,leading to THE SYNTHESIS OF NUCLEIC ACIDS "DE NOVO". Please get involved in this project as a scientific leader. Sincerely yours, Dr. Viorel Bungau

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