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HOMEOPATHY AS CARRIER OF ENZYMATIC DATA THE POLYMORPHIC RESONANCE FACTORS OF HOMEOPATH WITH ENZYMATIC REVIEW
In The Promorpheus we discussed in detail the lock-and-key phenomenon: how it started historically in biology, and how it is used to explain much of biological phenomena. This lock-and-key phenomenon depends on the morphic shape of receptor site and intervening molecule. Thus the shape of both sides of this interaction is highly important. The shape and attraction effect is held in place by the Trivector and subspace field. This trivector field is an expression of the voltage, amperage and resistance factors induced by the Quantum Electrodynamics of the molecules. However, as we have pointed out in The Promorpheus, it goes beyond just the shape of these molecules; there also must be a quantic understanding of how these two molecules are drawn together. The drawing together of these molecules goes beyond the simple chemical understanding of their shape. We must understand the short- and long-range forces of these various chemicals. The theoretical side of this is covered in The Promorpheus, which we now recommend. In this treatise we endeavor to understand how a quantum quality control technique can be developed for understanding the polymorphic structure of homeopathy, and how it might be utilized. All life depends on enzymatic function. An enzyme acts as a catalyst to allow two compounds to blend into a third with much less energy than it would if the enzyme were not present. Thus enzymes are essential to life. Enzymes work through the magnetic action of these compounds as they draw in the entities magnetically. Then through the shape receptor parts of the enzyme they allow the transition of these
compounds to maneuver with much less energy than normal. The magnetic capacities of the the molecules is an expression of the inductance and voltage part of the Trivector state. The electrostatic capacities are a reflection of the amperage or capacitance vector. The resistance part of the vector is a reflection of the electron transport abilities of the item. Enzymes have powerful magnetic parts of thier trivector patterns. The Trivector fields of thousands of homeopathic substances have been measured by the staff of New Vistas. This is used in the Quantum Quality Control process of Homeopathic manufacture. The trivector field of a patient can be measured with the Quantum Med C.I. Then the reaction of a patient's trivector field to the trivector field of these thousands of substances can then give us the electrophysical reactivity pattern of the patient giving us insight to thier health. Biology also works on shape receptors at the cellular level. Every cell has internal and external shape receptors. These shape receptors receive commands from various compounds as they enter a lock-and-key phenomenon. As pointed out inThe Promorpheus, there is an elasticity factor in this lock-and-key phenomenon. The compounds need not be exact, but can have some plasticity. Thus a key in biology can have many forms that might approximate the perfect key. This was developed by biology, because if there were a preciseness, it would be difficult for biology to exist in response to a cold, cruel environment. Mutagenic compounds inside various organisms would not activate receptor sites if the locks would only accept a specific shape of key. So biology had to develop a plasticity or elastic component to be able to use keys that weren't quite appropriate. This phenomenon can also be reversed. We can see that there are certain types of locks that also have an elastic component, in that they can be triggered by more diverse types of keys. The shape receptor sites in biology are concentrated mostly in the nasal pharynx area of the body, although every cell within the body has shape receptor sites.
We can see that a compound such as belladonna will have a specific type of shape at the molecular level. Belladonna is associated with atropine. Thus the atropine within belladonna produces pharmacological effects on an organism. It makes them red as a beat, dry as a bone, mad as a hatter. This is the pharmacological activity of belladonna. This belladonna also has its polymorphic structure, or shape structure. A structure held in place by the trivector and subspace field. Water and alcohol seem to be able to capture different types of shapes. Water and alcohol have a liquid crystal type of organization. The liquid crystal structure of water is accountable because of the angle of the hydrogen elements inside the combination of hydrogen and oxygen making up the H2O molecule. With a touch of alcohol these compounds can be utilized to make many shapes. Water alone can only make five of the eight great polygon shapes known in topology. If we have the collection of all eight great polygonal structures known in topology, we can make any known structure or shape. The trivector electrical field can be retained into the paramagnetic substance of water and alcohol. This effect is measured in the Quantum Quality Control. The reaction effect is measured with the Quantum Med C.I. Thus the belladonna shape can be imprinted into the water and alcohol mixture via the process of succussion. It will take mechanical energy for this liquid crystal of water and alcohol (a collection of the valent forces of the little dipole magnetic of the molecule of water) to exist. The structure of belladonna can be imparted into the water and alcohol by the mechanical action of succussion, which then imparts the shape tendency into the liquid crystal of the water and alcohol trivector field. Now at very dilute amounts, such as 60x or 1000x, we can see that this structure is inside the water and alcohol from our freezing work with the cyroliquid microscope. The shape of belladonna can come into the nasal pharynx of the patient and trigger an unconscious process of the brain. It is fooled into thinking that belladonna is coming. The brain thinks that belladonna is coming because its shape
receptor has been triggered in the nasal pharynx. Thus the brain will turn on the antiredness, anti-dryness and anti-madness device. In other words, homeopathy has a reversal component, partially because of the shape receptor triggering that can be accomplished through the polymorphic structure of the water and alcohol. In the sections of this book dealing with the device, we can see how the cyroliquid microscope can freeze the water and alcohol, and then, with a polarized filter, be able to examine the shear lines that develop along the freezing patterns inside the compound. This will allow us to analyze and quality control the polymorphic structure of the compound. As we have found from our research, the polymorphic structure is more evident in the "x" formulas than it is in the "c" formulas. The "x" formulas, with one part per ten dilution, have a greater ability to impart the polymorphic structure into the water and alcohol than do the "c". The "c" formulas have a greater polymorphic structure than the "m" formulas or the "lm" formulas. Thus the polymorphic effect of homeopathy is greatest in the "x" formulas. This also points to why many manufacturers prefer to use "x" formulas rather than "c". Even though there is less work in developing "c" and "m" formulas, there seems to be more polymorphic structural energy in the "x" potencies. In providing high quality, the work pays off. Let us now examine some of the background information on enzymes, to see how they work in a polymorphic structural fashion. As we have pointed out before, all organisms are a dramatic collection of chemical reactions that are highly dependent on enzymatic interchange. In the Natural Repertory of Dr. Nelson we can see a review of the cellular enzymatic process, and how the krebs cycle has extreme complexity in maintaining cellular metabolism. These enzymes will control both the kind and the rate of reaction inside the cellular process. Enzymes are made up of amino acids found in other proteins. Enzymes have a distinct three-dimensional structure that allows for confirmation of the
least energy content. Enzymes involve the same kinds of bonds that appear to be represented during ordinary organic reactions. Enzymes also use structures supplied by amino acid residues and prosthetic groups. Enzymes are able to bring chemical groups together through a particular geometric conformation. Thus enzymes bring these groups through the utilization of bio-photonic virtual forces along the lines of QED. Using quantum electrodynamics principles enzymes can bring these things together through electromagnetic reactivity. Enzymes have high specific binding action in their compounds. The amino acid residues at the binding site closely fit only a few compounds. To use the technical nomenclature, an enzyme will have high specificity for its substrates. Some enzymes are more plastic than others. "Substrate" means a compound whose reaction is catalyzed by an enzyme. Thus an enzyme allows the substrate to become a type of product. The catalytic mechanism comes from the presence in proteins of groups known to be effective catalysts for ordinary organic reactions. An amino acid side chain is then capable of donating or accepting protons. This will allow the side chain to act as a general acid or base catalyst. Hydroxyl groups and amino groups can act as nucleophiles. Around enzymes there are designs to reinforce catalytic properties. Nucleophiles in effect donate electrons to bond other groups lacking filled electron orbitals. Enzymes have peculiar catalytic effects due to the combination of specific binding in the presence of catalytic groups. In regular chemical reactions compounds will contort into an unfavorable configuration before they change into something else. The formation of the less probable intermediate state allows us to calculate the activation energy barrier that must be overcome for the reaction to ensue. Thus in a typical chemical reaction there is a thermodynamic randomness to the organization of the molecules that limits the activity. Inside an enzymatic pathway the enzyme holds the items in a specific geometric pattern, which then allows this to proceed. As we
have shown in The Promorpheus, this is a quantic process, and not a random or thermodynamic process. There are three stages in the normal enzymatic reaction: one is the formation of a complex between the enzyme and substrate; two is the conversion of this complex to an enzyme intermediate complex; and three is the further conversion of the complex between the enzyme and the product that can dissociate. Thus, through geometric maneuvering, we can see how enzymes can minimize the amount of energy between the enzyme and the substrate, and the enzyme and product complexes. Thus the activation barrier is dramatically reduced with the presence of these quantum enzymes. The binding of substrate to enzyme serves not only to confine particular reactions to a few compounds, but also serves in the creation of a complex that spontaneously favors the formation of increasingly more reactive configurations. The enzyme provides catalytic groups in the single-molecule range. This will eliminate the need for collision between two or more molecules during the course entropy. It also will align the substrate at favorable geometric angles so that the catalytic group and its interaction is facilitated through a process known as orbital steering. The enzyme also provides binding groups at positions that stabilize the reactive intermediate or propinquity effect. The suffix "ase" was put onto enzymes for classification in the development of a nomenclature. The commission of the International Union of Biochemistry created a more systematic nomenclature. Six types of designation are used in this nomenclature.
1. Oxidoreductases. These are enzymes catalyzing all of the reactions in which one compound is oxidized and another compound is reduced: dehydrogenases reductases oxidases peroxidases hydroxylases oxygenases
2. Transferases. These are enzymes catalyzing reactions not involving oxidation and reduction in which a group containing C, N, P or S is transferred from one substrate to another: transferases trans--ases (such as transaminase, transketolase, transaldolase, transmethylase)
3. Hydrolases. These are enzymes catalyzing hydrolytic cleavages or their reversal. (They do not include enzymes catalyzing the addition or removal of water from one compound, such as fumarase or enolase.) This included all of the enzymes named as: esterases amidases peptidases phosphatases glycosidases
4. Lyases. These are enzymes catalyzing the cleavage of C -- C, C -- O, C -- N bonds, etc., without a hydrolysis or oxidation-reduction:
decarboxylases aldolases synthases (but not properly named synthetases) cleavage enzymes (such as citrate or 3-hydroxy-3-methylglutaryl CoA cleavage enzymes) hydrases or hydratases or dehydratases deaminases nucleotide cyclases
5. Isomerases. These are enzymes catalyzing intramolecular rearrangements not involving a net change in the concentration of compounds other than the substrate: isomerases racemases mutases
6. Ligases. These are enzymes catalyzing all of the reactions involving the formation of bonds between two substrate molecules that are coupled to the cleavage of a pyrophosphate bond in ATP or another energy donor. They include all of the enzymes now named as synthetases, except in cases where this name has been misapplied. The name synthetase was originally defined to include those enzymes now being defined as ligases, but it was later applied to enzymes catalyzing the formation of compounds by other mechanisms. Thus one sometimes sees glycogen synthetase or *-aminolevulinate synthetase even though the reactions catalyzed by these enzymes do not involve the cleavage of a high-energy phosphate bond. The term "synthase" was later coined to cover these enzymes, which are lyases in the IUB nomenclature.
Contained within each of these groups and types of enzymes are further subdivisions. These are given numbers.
1. Oxidoreductases 1. With NAD or NADP as acceptor 27. L-lactate:NAD oxidoreductase EC 1.1.1.27 (lactate dehydrogenase)
2. Transferases 4. Glycosyltransferases 1. Hexosyltransferases 18. "-1,4-Glucan:"-1,4-glucan 6-glycosyltransferase EC2.4.1.18 (1.4-"-glucan branching enzyme) 7. Transferring phosphorus-containing groups 1. Phosphotransferases with an alcohol group as acceptor 2. ATP:D-glucose 6-phosphotransferase EC 2.7.1.2. (glucokinase)
3. Hydrolases 4. Acting on peptide bonds 21. Serine proteases 4. No systematic name given EC 3.4.21.4 (trypsin)
5. Isomerases 1. Racemases and epimerases 3. Acting on carbohydrates and derivatives 1. D-Ribulose 5- phosphate 3-epimerase EC 5.1.3.1. (ribulosephosphate 3-epimerase)
6. Ligases 2. Forming C - S bonds 1. Acid-thiol ligases 3. Acid: CoA ligase (AMP-forming) EC 6.2.1.3. (acyl CoA synthetase)
One of the simple experiments we have performed in the polymorphic structure part of homeopathy involved enzymatic activity that could be documented in a test tube. Using homeopathic forms of the enzyme at 30x or greater, where none of the chemical enzyme exists, we can still see that the enzyme effect can be produced by the homeopathic inside a test tube, showing us that homeopathy can work in the polymorphic structure. One simple experiment is to take oatmeal prepared in one batch. The oatmeal has large protein molecules that make it bind together in the bowl. In the presence of various protease (enzymes) these bonds break, and the oatmeal becomes more
liquid. In the study we used eleven cups of oatmeal. Three controls of water and alcohol were put in, and also a 1x of various digestive enzymes. A 3x, 6x, 12x, 24x, 60x and 100x of the latter were also put into separate containers of oatmeal. As we can see from the table, there is some enzymatic activity occurring beyond the control in the 30x, 60x, and 100x, where there is no known enzyme within the bottle. Enzyme Effectiveness Percent Effect on Protein 6x 12x 24x 80% 80% 15% 30% 2% 30%
3x 95% 95%
30x 1% 25%
60x 0% 20%
100x 0% 15%
Thus the form of the enzyme gets into the water and alcohol, and then allows the water and alcohol to have enzymatic action in breaking up the oatmeal molecules. Many other enzyme studies have also been done validating this polymorphic hypothesis. There are special types of inclusion compounds called clath rate compounds. Here the host molecules form a crystal lattice that contain empty spaces into which certain guest molecules can fit. In cage clath rates the cavity is a space completely surrounded by a network of host molecules. Some gas hydrates are examples. Structures such as a hydrogen-bond network of water molecules can enclose these different gaseous molecules within them, such as methane, argon and nitrogen. Also this can account for some of the containment of these compounds within homeopathy. Thus a clath rate compound is a well-defined addition compound formed by the inclusion of molecules in a cavity existing in a crystal lattice. Part of the theory of our homeopathics is that the clath rate structure of water can organize itself into a crystal network that can impart these various polymorphic structures. Another possibility is that of the morphic resonance of shape structure. This is covered in The Promorpheus, Bio-Quantum Matrix, and Quantum Vibrational Medicine. The actual morphological structure of a thought, an idea, a compound, an enzyme, a protein, a carbohydrate, a lipid, etc. can have echoing effects throughout the universe. This morphic resonance can be explained through Dr. Einstein's theory of space, geometry, time and matter. Once an object takes shape it will more probably exist in the universe. This type of morphic resonance is becoming a more undeniable part of our science through the existence of fractal dynamics and the work of Feynman and Feigenbaum. In the Natural Repertory is an article titled "A New Perspective on Research", in which we find that looking for dramatic statistical research events is no longer necessary for us to
find some truth, and that there can be fractal chaotic dynamics that can be analyzed with a fuzzy type of arithmetic and nonlinear systems. Thus homeopathy, the polymorphic structure and the continuity of these shapes also must be analyzed with softer statistic criteria than has been developed before in the pharmaceutical industry. This morphic resonance is also very much akin to the work of Plato. He proposed a world of forms that existed outside reality. This world of ideal shapes dictated and had effects on reality. This type of morphic form resonance outlined by Plato also should be reviewed and perhaps rethought and entered into the form of medicine we know as homeopathy.