THE NEW VITAMIN Mi
took some 25 plus years following Dr. Kohler’s death until the EAP salts would turn into a biologically active substance of the dimension not yet fathomable. Following the cell membrane model of the Swiss scientist Buchi, colamine phosphate is integrated into the cell membrane in a way that it is localized on the outside on the external cell membrane, mainly at the entrance Spots into the so-called free lipid pore. From communications by Dr. Pressman, New York, we know today that colamine phosphates are part of the so-called neurotransmitters, i.e. substances necessary for conducting an electric signal to biological structures. In addition, the substance is obviously necessary to retain said charges, especially of calcium, on the membrane surface. The resulting change is extremely significant because, in this way, the cell membranes can function like an electric condenser, except that the areas containing the charge do not consist of metal as they do in technology but of biologically retained (bound) calcium linings. Colamine phosphate salts, and calcium salt, in particular, are therefore indispensable in supporting the condenser function of the cell membrane. We will refer back to this lifedeciding factor later.
From approximately 1963 on, we started to apply calcium and magnesium-EAP clinically with the intention of protecting the cell membranes against unwanted intruders, e.g. antibodies, toxins and viruses. These unwanted intruders can only enter through the so-called free lipid pore of the cell membrane, at whose entrance – as mentioned before – the colamine phosphate is in position. We presumed, therefore, that the supply of calcium EAP would have a special sealing function because of the rejective effect of calcium. Our expectation proved to be correct. Already in 1971, Monninghoff, Munster, W. Germany, published electron microscopic research demonstrating in a spectacular manner how the sealing of cell membranes with calcium-EAP (and also with calcium aspartate) could prevent penetration of peroxidase granules. Peroxidase granules can be followed very well by electron microscopy in an experimental setting since they provide a highly suitable testing model.
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By Hans A. Nieper, M.D. of Hannover, Germany Translated from Aug/Sept 1988 raum & zeit(“space & time”) This material is reprinted by permission from the May-July 1996 issue of Australasian Health & Healing29 Terrace St. (P.O. Box 206) Kingscliff, NSW 2487 Australia Tel: (02) 6674-2407 Fax: (02) 6674-3633