Tag Archives: Cell Biology

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The Healing Process: Role of the Immune System, Part 1 page 2

DISEASE AN INSIDE JOB, AS IS HEALING

Tony's picture 2 from PeggyWe saw how Dr. Royal Lee discovered protomorphogens in our last post.  In this post we will look at some of the other important players at the turn of the 20th Century who pioneered health-based healthcare as opposed to traditional medicine’s disease-based healthcare. 

At the same time Dr. Royal Lee was developing his theory of protomorphogens, Antoine Bechamp (1816-1908), a French Biologist, was working on a similar theory using a different name for these nuclear mineral proteins. In Dr. Sharon Rabb‘s words: 

Antoine  Bechamp was the most notable of scientists working along the same lines as Dr. Lee. Bechamp was a contemporary (and adversary) of Louis Pasteur. Bechamp’s theory, later confirmed by other scientists, was that “disease” is not produced primarily by invading bacteria but is actually perpetuated in an unhealthy, unbalanced body by the body’s own cells. The cells themselves produce pathogens like bacteria, fungi, and viruses instead of normal healthy cells. The theory also stated that all chronic and infectious illnesses have a microbial component not currently recognized by orthodox medicine. “Non-self” pathogens may provide a template for illness, but healthy individuals do not succumb. The existing toxic internal environment allows the disease to manifest. One does not really “catch” a cold — a cold is produced due to an imbalanced, toxic and malnourished environment. (underscores mine)

 Bechamp saw what he termed “mycrozymas” in the protoplasm of living cells and considered them to be the fundamental unit of living tissue (Lee’s PMGs). Bechamp disputed the “germ theory” and stated that the cause of disease was internal dysfunction not an external invasion. Invading pathogens could only cause illness in an unhealthy body by acting as a template to dividing cells. Pasteur, near the end of his life, confirmed Bechamp’s theories; however, traditional medicine was already firmly entrenched in the “germ theory” model.  (underscore mine)

This is unbelievable but very typical behavior on the part of medicine and the drug industry who can’t wait for the final results of extremely costly research to get a pill out on the market to enhance their bottom line.  Yet they do it notoriously and repeatedly with half-baked research and premature conclusions, which too many times results in deadly side effects and recall of the medicine.

As a side note, but very pertinent to how we got pointed in the wrong direction, here’s a telling piece of history from the introduction of R.B. Pearson’s book THE DREAM AND LIE OF LOUIS PASTEUR:

 Bechamp was one of France’s most prominent and active researchers and biologists. He taught in universities and medical schools, and published widely on cell biology, disease, botany and related subjects. His would probably be a household name today if it wasn’t for the activities of one Louis Pasteur, whom history has treated very kindly indeed, considering his fake science, his tendency to steal ideas (mainly from Bechamp), falsify experimental data, and in general make claims which had no basis in fact.

I’m not running off at the mouth by saying the above. It’s all quite well documented – Bechamp and Pasteur were both members of the French Academy of Sciences, and the papers they submitted, and their correspondance, both to each other and to other people, were all recorded. Even their verbal exchanges survive in the minutes of the meetings.

To cut a long story short, and it is a long story, Pasteur basically dug up the germ theory of disease and put his name on it. It wasn’t a new idea, although he claimed to have “discovered” germs all the same. The concept had actually been outlined by other people many years before, but of course, the whole idea is wrong anyway, so it hardly matters who thought of it first. In a few years, the germ theory of disease will be out there with the flat earth theory where it belongs. . . .  Another good book is Pasteur Exposed, written by Ethel Hume and first published in 1923, which goes into all the details of exactly how Bechamp’s ideas were twisted beyond recognition by Pasteur. None of this would matter a toss, of course, except for the minor point that western chemistry-based medicine is built on a foundation of unquestioning “Pasteurism”. (underscore mine)

At the same time, Dr. Royal Rife (1888 – 1971), pathologist and bacteriologist, was developing the first 100% sure cure for cancer in the 1920’s.  Here’s a piece of his story as told by Dr. Sharon Rabb:

Royal Rife, a friend of Dr. Lee, believed as did Bechamp in the theory of pleomorphism — the ability of a microorganism to change form in a living system. In other words, bacteria could change into a fungus or virus or vice versa. He also believed that the human body could produce these microorganisms instead of normal healthy cells. Rife invented a very powerful light microscope where he could see them “pleomorph”. He also invented a machine called the Rife machine which produced sound frequencies that “burst” specific microorganisms. He was able to see these pathogens, find the “resonant frequency” of the specific organism and produce the sound frequency–thus causing the organism (and it only) to self destruct. Rife used this machine to “terminate” cancer cells in infected individuals in the middle 1900’s. Several books have been written by Barry Lyons about Rife’s story, including The Cancer Cure that Worked. Rife was discredited and was finally run out of the country, a destitute man.

His lab and all of his equipment was burned to the ground by the medical society in Southern California.  His work was not to resurface again until the late 1990’s, thanks to the viral capacity of the internet to spread the word before anybody could stop it.  Rife machines are available and being used today in private homes and in alternative healthcare centers everywhere. For a full ten minute account of Dr. Rife’s story, click on this YouTube link: http://www.youtube.com/watch?v=AysfKyl8O9k&feature=related or copy and paste it in your web browser.  To view a picture of Royal Rife and his amazing electron Universal Microscope, along with another rendition of his story, click this link: http://www.rense.com/general31/rife.htm.

Another maverick scientist who agreed with the concept of pleomorphism was Gaston Naessens (1924). He developed the somatoscope in the late 1940s with a resolution of 150 angstroms. With the use of this scope, he identified the PMG (or somatid, or mycrozyma) and actually observed various microbes change forms to other pathogens. He clearly demonstrated the 16 stages of the “somatid cycle,” thus affirming that disease is not an issue of external invasion but an issue of weakened immune capacity. (The 16 stages show how single cells can “pleomorph” or change into other different microorganisms.)

To recap what went before and close this chapter. . . 

“. . . Dr. Lee refined the theories of Bechamp, Rife, Naessens and others and put them to practical use in formulating protomorphogens for virtually every tissue type. These PMGs have the potential to rebuild every organ and gland in the body. . . .   By providing the genetic material through the PMG, the body is able to “jump-start” the healing process and use the blueprints to reprogram healthy cell division.”  (Dr. Sharon Rabb)

For help with your particular health issue and to order supplements with protomorphogens, call me for a personal consultation at my office  (337) 497-1850, or my cell phone (337) 802-5510.  Consultations range from $45 (20 min) to $65 (40 min) and are payable by credit card. 

Join me next week as we tell the stories of  the major actors in the immune system and the role of the redox signaling molecule in immune response.  Thank you for following my blog.  I trust you find the articles interesting, informative and entertaining.  Your comments are most welcome as I love hearing from my readers.  Until my next post, 

Here’s to your health and healing,

Dr. Anthony Palombo

Email: tpal70@gmail.com    Website:HealingandAttunement.com

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The Healing Process: Role of the Immune System – Part I

  PROTOMORPHOGENS

    Here’s where our consideration of the Healing Process takes a turn away from the orthodox medical model and indoctrination and toward a more accurate understanding of the disease process : what causes it, where does it begin and how can it best be reversed by supporting the healing and re-building processes of the body. 

     Let us start with a recap of what we think we know about disease. Following Louis Pasteur’s “outside-in” thinking, medical science took off and developed on the basis of the theory that disease was brought into the body from the outside.  The “germ theory” gained popularity and soon we were developing antibiotics (literally, anti-life) to kill germs and pathogens of all kinds. We were given soaps, sprays and gels to sanitize ourselves and prevent the invasion of and contamination by these invaders.  And if we did get invaded, then we used antibiotics to “fight infection,” the body’s own natural way of dealing with harmful bacteria and viruses.  We even started “pasteurizing” our milk in an endeavor to kill the germs, only to kill the natural enzymes needed to digest the milk in the process.  Our blessed parents brought us up on whole milk we got from our cows and we gave our immune systems a good education on how to deal with sore throats (strep), boils (staph) and other symptoms of bacteria-fighting in our bodies, and we’re better off for it today.  The end result of all this waring against germs has been the adaptation of viruses and other pathogens to our powerful antibiotics and the appearance of super viruses and bacteria that are immune to our antibiotics, which has medical scientists deeply concerned.

Shortly after the time when Louis Pasteur (1822-1895) was selling his theory to medicine and the general public, another theory was put forward by Dr. Royal Lee and a scientist by the name of Antoine Bechamp.  Other important players in this arena were the renowned Dr. Royal Rife and Gaston Naessen, whose stories we will visit in my post next week.

Born the same year Louis Pasteur passed away, Dr. Royal Lee (1895-1967), a dentist who believed and proved conclusively that the health of the teeth was directly proportionate to and reflected the health of the body, developed and worked with a nutritional approach to the reversal of disease and the restoration of health.  His “Protomorphogen” discovery helped us turn the corner in our search for the real cause of disease and a natural solution to the cure of disease and to healing.  Today he is honored as the “Father of Natural Vitamins.”  His line of wholefood nutritional supplements and his legacy are kept alive and well-preserved by Standard Process Laboratories in Palmyra, Wisconsin.  

In his own words: 

“One of the biggest tragedies of human civilization is the precedence of chemical therapy over nutrition. It’s the substitution of artificial therapy over natural, of poisons over food, in which we are feeding people poisons trying to correct the reactions of starvation. You all know how ridiculous that it. But you all know how widely it’s being done.” Dr. Royal Lee, 1935

In a nutshell, here is the theory:  There are mineral protein essences secreted by the cells that carry the blueprint for cellular regulation and growth.  These “protomorphogens,” as Dr. Lee called them, help grow new and healthy cells and even help repair and rebuild cells that are damaged.  By enhancing the integrity of the body cells, invading pathogens (bacteria and viruses) are kept at bay.  They only attack sick and weak cells.  In Dr. Lee’s own words:

 A protomorphogen is a cell secretion given off by all living cells at all times in minute amounts that promotes the synthesis of protein for cell repair and cell maintenance on the outside of the cell wall, after which it is absorbed by the cell. Protomorphogens are chromosome end products, made in the cell nucleus, probably the agents by which the basic functions of the chromosome are exercised. All living proteins carry a protomorphogen component by which the protein is made specific in nature, specific in causing organic reactions, specific in function, specific in its ability to act as an antigen in provoking immune reactions. All antigens may be antigenic by reason of accompanying protomorphogens, in some cases instead of being attached to a protein molecule, the protomorphogen may be attached to a lipoid or polysaccharide aggregate. When a protein has been separated from a protomorphogen, it is said to be denatured and is no longer fully capable of antigenic action; that is, cannot create an antibody specific to it in the circumstance of its injection into an animal blood stream.

Since no cell can grow or maintain itself unless protomorphogens, as secreted by itself, are available in the pericellular [outside and around the cell] fluids, it is obvious that here we have the possible biological growth regulator. Suppose that the immune-body producing mechanism, heretofore looked upon only as a defense against invading organisms (cells) from the outside, were to be found to exert the same controlling action on every organ and cell of the body, we would have the answer to the long-sought questions of why animal organs and living creatures in general were able to regulate their cell growth exactly according to a well-ordered plan.

 We find, on investigation, that there is just such a reaction of the immune body producing mechanism (the reticuloendothelial system) and it has been described under the general designation of “Natural Tissue Antibody” (NTA).

IN CONCLUSION 

Protomorphogens are in reality mineral chains whose sequencing determine the amino acid (protein) structure of individual cell types. In living tissues these minerals are organically bound and accompanied by enzymes. . . .

. . . Dr. Lee refined the theories of Bechamp, Rife, Naessens and others and put them to practical use in formulating protomorphogens for virtually every tissue type. These PMGs have the potential to rebuild every organ and gland in the body. The concentration gradient both inside and outside the cell regulate this growth. The “health” of the cell regulates both the concentration gradient and “health” of the protomorphogen. The concentration and health of the protomorphogen also regulates the immune system in forming natural tissue antibodies (NTA). If an excess of PMGs accumulate outside the cell, normal cell division stops and an excess of autoimmune factor (NTA) can cause damage to the cell. The PMGs in living systems are “wrapped” in lipoid layers because of their potential toxicity to a living system. This is called “hypersensitivity” in immunological terms. The lipoid “wrapping” can be either incomplete or damaged in disease or malnutrition states.

Because of hypersensitivity, Lee chose not to use human genetic material in formulating his supplements – but rather to use animal tissue which would be taken orally. The PMGs are processed to be absorbed through the GI tract intact. The animal kingdom is removed from the human so that hypersensitivity is not a large issue. By providing the genetic material through the PMG, the body is able to “jump-start” the healing process and use the blueprints to reprogram healthy cell division  (underscore mine). Dr. Lee believed that every disease produced an autoimmune component which through the process of inflammation prevented normal cell division and caused most of the damage. This fact is being recognized by the medical profession more frequently in various illnesses.

Protomorphogens (PMGs) have two major functions: Control healthy cell growth and  Regulate immunity

Our own PMGs inhibit cell division. However, when taken orally in pill form (from other mammals), PMGs stimulate normal cell division and reduce the autoimmune component by reducing excessive amounts of the natural tissue antibodies. They stimulate the organ to regenerate new healthy tissue by supplying the blueprints or by “jump starting” the organ to manufacture more of its own PMG.

PMGs are taken from specific organs of other mammals. In supplying extracts of the specific organ to the organ that is diseased, we can influence the local nutrient environment of those particular cells. This increases the activity of the tissue which then increases the secretion of PMGs so that the net effect is the concentration of PMG is balanced. The tissue of the organ begins to grow and regenerate normal healthy cells and thus helps to reestablish normal growth patterns with control. . . .

. . . The theory of protomorphogens is fundamentally what stem cell research is about. 

For product information and to start benefiting from protomorphogen supplementation, simply contact me by email at tpal70@gmail.com. 

See you next week for another installation on the role of the Immune System in the Healing Process.  We will talk about other important players at the turn of the 20th Century who pioneered health-based healthcare as opposed to disease-based medicine.  

To your health,

Dr. Anthony Palombo 

Email:  tpal70@gmail.com 

Website: HealingandAttunement.com 


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The Healing Process: Role of the Redox Signaling Molecule

Redox Regulation of the Healing Process – New Science

We have come to the crux of our considerations around the Healing Process.  In this post we will see exactly how the healing process works and what players are involved.  Again, Dr. Gary Samuelson will tell the story in his own easy-to-read words.  We will start with two video clips: one of the process called “Covalent Bonding” and the other on how free radicals and antioxidants work in order to help us better understand how “free radicals” (oxidants) do their damage and how the antioxidants neutralize and disarm them by a simple exchange of electrons between “oxidants” (electron donors ) and “reductants” (electron acceptors).  At the end of the day, restoration of balance is the goal of the healing process, as we shall see, and the “villains” of the free radicals turn out to be essential players in the process of maintaining homeostasis.  This, I promise, will be a fascinating read.  Enjoy!  (Newcomers to my blog would enjoy reading the previous posts in this series on The Healing Process for background information.)

Video clips: Covalent Bonding (4:32), Free Radicals vs Antioxidants  (4:30)

Redox Regulation of the Healing Processes-New Science

Emerging science from the past five years has solidly established that the chemical balance of small reactive redox messengers is essential to the healing process and the regulation of the immune system. These small reactive “redox” molecules participate in the same homeostatic balancing act that is used to balance the proper amount of the various proteins inside the cell (as we already have discussed). These “redox” messengers are constantly being produced, mostly by the mitochondria in the cells, and then constantly being eliminated at the same rate by a variety of protective enzymes (generally called “antioxidants“) that are strategically stationed inside and outside of the cells.

Let us more closely examine these reactive “redox” messengers for a minute. They are made from simple rearrangements of the atoms in H20, NaGI and N2 and are put together by special molecular complexes in the cell. Some examples of redox signaling molecules are H202, H02, HOCI and NO. About half of the redox messengers can be categorized as “oxidants” and the other half, in fairness, can be categorized as “reductants.”  “Reductants” is a contrived nickname, the official name being energetic “electron acceptors.” Oxidants, incidentally, can also be referred to as energetic “electron donors” in the same sense.

Not much is said about “Reductants” in the literature. In fact this nickname was just fashioned to be able to talk about this group of electron acceptors in this booklet. The basic concept, however, is very familiar to chemists and physicists. The laws of conservation of charge, mass and energy dictate that every time an oxidant is made from a neutral solution, a reductant or combination of reductants must concurrently be made to counterbalance it. The electron acceptors must balance out the electron donors. The ability of the resulting molecules to oxidize or reduce the molecules in their environment is referred to as the “redox” potential, a key player and motivator for all of the chemical reactions that take place in nature.

The name “redox” itself comes from the ability of these messengers to “REDuce” and/or “OXidize” molecules in their environment. Reduction and oxidation are chemical terms that relate to the potential that the molecules have to “give away” (oxidize) or “accept” (reduce) electrons to and from other molecules in their environment. As mentioned, all chemical reactions taking place in the cell depend on this redox potential in order to happen. Redox messengers have the ability to change the redox potential of their environment, thereby altering the chemical reactions that take place. Strong reductants and oxidants can both be harmful and destructive to the cell if they are allowed to wander around at will.

The oxidants, in particular, have made a really bad name for themselves; several of them are free radicals that have high energy, unpaired electrons that will blow apart whatever they come into contact with (like tiny molecular cannons). Oxidants will damage DNA, blow holes in cellular membranes, destroy important proteins, etc. The reductants are also hazardous, they will grab electrons away from molecules (with the ferocity of small molecular sharks), thereby causing destruction. To be perfectly clear, reductants are not antioxidants. Reductants are simply the chemical counterparts of oxidants (much like acids and bases). Antioxidants, on the other hand, are a class of much larger organic molecules produced by genetic coding that act as catalysts capable of facilitating the reverse chemical processes needed to ultimately “untie” and neutralize both the oxidants and the reductants. Antioxidant cycles require both oxidants and reductants in order to work correctly.

Let us focus on the antioxidants for a minute. The antioxidants were historically considered as the heroes of the cell because they broke down the harmful oxidants by pulling them in and neutralizing them together with reductants, leaving just common harmless sea-water molecules in their wake. Over an antioxidant cycle (some of which are complex multi-step processes) the oxidants and reductants are neutralized [view clip], however the antioxidant itself remains unchanged, ready to do it all over again to the next set of oxidants and reductants. The antioxidant in this sense is a catalyst that speeds up the neutralization of oxidants with reductants and yet of itself remains unchanged. You can think of an antioxidant as a black box: reactive and potentially dangerous oxidants and reductants go into the box and harmless neutral sea-water molecules come out.

Ironically, the oxidants (that historically have been thought to be the villains) are now seen as central players to the healthy function of the cells. We have recently learned that we would not be able to live without either the reactive oxidants or the reductants. The truth be told, these tiny reactive molecules play an absolutely essential messenger role in our cells and tissues [my underscore]. The most critical aspect of healthy redox-messenger balance is in that the oxidants and reductants must be produced and eliminated in perfectly-balanced and equal portions. As long as there are equal portions of oxidants and reductants in the interior or exterior of the cell, the antioxidants can readily neutralize them both as fast as they are created. As discussed, the antioxidants need equal portions of oxidants and reductants in order to function, in the case of Glutathione (an abundant antioxidant made in our cells). The large mouth of the relatively huge antioxidant molecule lures in a reductant (that is electron hungry) and then lures in an oxidant (that has an energetic electron to donate) and then pulls them both together into the “active site” in the middle. At the active site, the reductant and oxidant are combined together, neutralizing them both. The resulting harmless molecules float away.  The antioxidant is then free to do it all again. If there is an ample supply of reductants and oxidants in the neighborhood, one antioxidant molecule can typically neutralize tens of millions of oxidant molecules every second, as measured in the lab.  [Emphasis and underscores mine]

This was a eye-opener for me when I first read it, and I believe it is crucial to a better understanding of homeostasis.  There are no “good” and “bad” players in this microcosm of the biological universe that comprises our bodies.  There’s only “appropriate” and “inappropriate” based on place and timing, balance and imbalance.  To quote a poet friend and colleague, “Nothing is wrong.  Everything matters.”  

The antioxidants are purposefully manufactured, sent to and positioned around the areas of the cell, such as the nucleus, that are vulnerable to oxidative damage. As equal portions of oxidants and reductants approach these protected areas, the antioxidants standing guard around these areas pull them in and neutralize them both. The antioxidants are thus able to keep these potentially harmful reactive molecules away from protected areas and corral and use them for their own best purposes. Consequently, the immune system uses large amounts of such oxidants, along with strong demolition enzymes, as its weapon of choice against harmful invading bacteria and viruses. The foreign invaders do not even stand a chance against these potent weapons. After the invaders have been torn apart and destroyed by the enzymes and oxidants, the surrounding antioxidants standing guard and other enzymes clean up the mess, toxins and hazards.

THE HEALING PROCESS DESCRIBED

The key to understanding how this redox balancing process helps the body heal itself comes when considering what happens when the cells become damaged or defective for some reason or another. There are thousands of different processes with thousands of different proteins taking place everywhere inside the cell. When something is not working right, how does the cell detect the damage? The answer lies in the fact that as the normal homeostatic balance that exists in healthy cells is disturbed, somewhere in the cell there is either a build-up or deficiency of the normal quantity of proteins. There is a high probability that this
growing imbalance will at some point make the metabolism of sugars less efficient. When this happens, the redox-messenger production in the mitochondria becomes unbalanced, producing many more oxidants than reductants or vice versa. In other words, the damage will ultimately manifest itself as a build–up of oxidants or reductants. This condition is called “oxidative stress” and is a real phenomenon seen (under the microscope) to occur in almost all defective or stressed cells (in both animals and plants).

An imbalance in the redox messengers, usually manifesting itself as oxidative stress, sends a clear signal that damage has occurred somewhere and that the cell is defective. The excess oxidants are not balanced by reductants and cannot be effectively neutralized by antioxidants. These oxidants end up causing even more damage to other parts of the cell. This clear signal for help causes the DNA to code for the “fix–it crew” and cytokine messengers that are sent out to alert the immune system. If this imbalance (oxidative stress condition) is not corrected by the attempts of the fix–it crew, the oxidants continue to build up. Then after about two hours, the fatally damaged cell starts a “programmed cell suicide” cascade (apoptosis) that will end up with the cell killing and dismantling itself. This is not a bad thing. Normal healthy neighboring cells will then be able to divide in order to fill in the vacancy. On the microscopic scale, this is essentially the healing process. [my underscore]

The oxidative stress condition in a stressed or damaged cell also causes the DNA to code for messengers to be sent to neighboring cells, advising them of its condition. Redox messengers can also be used as these intercellular messengers. If the damaged cell, such as those found in tumors, is not able to kill itself, then its neighboring healthy cells will send back “death domain” messengers as well as distress messengers to the immune system that will either cause the damaged cell to die or to be attacked by the immune system. This system is regularly used to detect and destroy practically all of the damaged and dysfunctional cells in the body. Remember, it only takes one undetected dysfunctional cell, out of the trillions that are successfully detected and killed, to start seeding an abnormal growth.”

This brings our series to a turning point.  The posts that will follow will look at the role of the immune system in healing and how this system is activated by the Redox Signaling Molecules.   View this video clip to prepare for the next consideration.

Clip:  The Healing Revolution – the Science Behind ASEA.

To your health and healing,

Dr. Tony Palombo

For information on ordering ASEA, click here.


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The Healing Process: Signaling Messengers and Diabetes

Redox Signaling Messengers

Like any community, the body cells depend on communication for their coordinated and harmonious function together. Communication depends on messengers, both inside the cell between the various actors and “micro machines”  and outside the cell between the one-hundred-billion cells that compose our bodies.  These next few posts will be about these messengers, most recently discovered among them being the Redox Signaling Messengers that turn out to be a most important players in the healing process.  We will have a look at a very significant scientific breakthrough in the field of health and healing.  Again, we will call upon Dr. Gary L. Samuelson to help us envision and understand the Healing Process as he presents it in his recently released booklet, The Science of Healing Revealed – New Insights into Redox Signaling.

How the Actors Work Together – The Signaling Messengers

So far in our abbreviated organization chart, a small sample of the cast of actors has been put together in order to provide a tiny taste of what they look like and what they do. There are thousands more (not listed, thankfully) that fill major roles inside and outside the cell; and the list is growing every day as new actors and roles are being discovered. The real story, however, lies not so much in what they look like or what their job description is, but in how they interact with each other and how they determine when and where to do their job.

For the most part, the cellular micro machinery is controlled by the various signaling messengers, as has already been mentioned, that go about carrying messages inside the individual cells (intracellular communication) as well as carrying messages between the cells (intercellular communication). As has also been mentioned, the very identity and behavior of the cell depends on the quantities and types of messengers being passed around in its surrounding environment.

The inner-cell (intracellular) messengers float around inside the seawater solution (cytosol) inside the cells. There are generally two types of intracellular messengers: (1) protein messengers that are coded by the DNA and built, delivered, passed around and modified by enzymes and cellular machinery and (2) a recently discovered network of messengers called “redox signaling and regulation” messengers made out of small, highly reactive molecules (ROS and RS) that are formed by the REDuction” and “OXidation'” (redox) of the very sea-water bath that surrounds all of this cellular machinery. These messengers modify the behavior of the machinery by changing the chemical potential in the salt-water environment where all of this machinery exists. Since these “redox” messengers are integrally involved in the healing process, they will be the topic of further investigation in this booklet.

The between-cell (intercellular) messengers are passed back and forth between cells. In order for them to work they must be able to leave one cell and “latch onto” or pass into surrounding cells. There are specific places built into the outer membranes of the cells, called “receptors” and “co-receptors,” where these messengers are allowed to “latch onto” the outside of the cell. Each different type of messenger molecule (called agonist) has its own custom-built latch (receptor) that allows it to pass a signal into the cell.

In many cases, the receptor itself, when latched, will cause intracellular messengers to be released to continue carrying the message into the cell. Most cells are stuck together with a scaffolding of adhesive molecules that allow messages to more easily be passed around among neighboring cells.

Redox messengers are able to alter the chemistry of the receptor latches that can either enhance or inhibit their ability to latch onto their messengers and pass messages into the cell. Sometimes the presence of these redox messengers themselves will spontaneously trigger a receptor to send messages into the cell.

In my next post we will explore further some amazing technology that has made it possible for us to enhance intra-and-inter-cellular communication.  Before leaving my blog, take a few minutes to view this video clip on the Redox Signaling Molecule (5 min).

Besides giving a visual demonstration of how these signaling messengers work, this clip presents recent groundbreaking technology that is being used to stabilize these highly reactive molecules outside the body and then use them as bio-active, non-toxic agents inside the body to assist in the healing process.

The end result of this research is a formulated “water” called “ASEA” that is now available to the public through network marketing.  I have become an associate distributor of this product because of the great promise it holds for my patients and clients at a foundational level in their healing and health maintenance, offering new solutions to longevity and quality of healthful living.  It also gives people a tool they can use safely and obtain directly from the company without the requirement of becoming a network marketer themselves, although that is available as well as a home-based business with minimal investment.  So, enjoy the clip! Until next week then, my best wishes . . .

To your health and healing,

Dr. Tony Palombo

For more information about ASEA and ordering instructions, simply click here.


Here’s a bonus for my readers concerned with their blood sugar levels and diabetes: The 39-day cure for Type II Diabetes.

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The Healing Process: The Cell, Part 3 Communication

The Signaling Messengers

We’ve been entertained and edified by the inner life of the cell — how it’s “micro machinery” makes protein molecules from amino acids in the ribosomes and produces its own energy (ATP) in the mitochondria.  We will now move on to learn how these inner parts of the cells communicate with one another, as well as how the cells communicate among themselves and with the various systems of the body.  Again, I will call upon Dr. Gary Samuelson to help tell the story from his booklet The Science of Healing Revealed – New Insights into Redox Signaling.

Looking at the simple molecular keys that control the kinase fuel gates that energize the machinery in the living cell gives us a first glimpse at a very important class of molecules and proteins that act as messengers that are sent off to make sure specific things happen or do not happen. As can be imagined, these signaling messengers serve a very important role in the working of the cells. They send signals between the machinery in the cell that determines how the cell’s machinery operates and responds to the normal changes in its environment as well as drastic alarms like threats, damage, lack of oxygen, changes in temperature, the arrival of a nerve signal, etc. They can also be sent as long distance messengers to send signals between cells and tissues, as well as general messengers released into the blood and lymph that affect the working of whole systems throughout the entire body, like adrenaline for example. A few of these are listed below. The rest of this booklet, however, is focused on the emerging science that explains, in part, how signaling messengers do what they do and the processes that keeps them controlled and balanced when the body is healthy.

Redox messengers – Reactive Oxygen Species (ROS) and Reduced SpeCies (RS) — The smallest and most fundamental universal signaling molecules in the body are the simple but extremely important reactive molecules that are formed from combinations of the atoms (Na, CI, H, 0, N) readily found in the salt water bath that fills the inside of the cells (cytosol). All of life’s players mentioned so far float around in this bath and can be surrounded by a balanced mixture of these reactive molecules…. “

Dr. Samuelson lists a few of these reactive molecules, such as Superoxide,  Hydrogen Peroxide, Hypochiorous Acid, Nitric Oxide, only four of some 20 of them.  Then there are these players:

Charged metal ions – Their movement alone makes the electric current that carries signals along our nerves and muscles. They also play signaling roles in hundreds of different life processes. Three examples or these are the Calcium ion (Ca2+), the Potassium ion (K+) and Sodium ion (Na+).

Cytokines  – The messengers that activate and regulate the immune system, controlling inflammation, white blood cell movement and natural cell death; Interleukins (regulate immune cells); Interferons (identify invaders,viruses).

Then there are the Endocrine messengers that control and regulate digestion, metabolism and organ function: Adrenaline, Insulin, Gastrin.  And the Hormone messengers that determine tissue growth and reproductive function: Testosterone, Estrogen and Progesterone.

Another group of fascinating players in the life of the cell are what are called the “Transcription Factors.“ These messengers cause the DNA inside the nucleus to call for increased production or reduction of certain specific proteins: NF-kappaB calls for inflammation; NRF2 calls for antioxidants; and TNF calls for tumor death.

Enzymes – the “break-it-down clean-it-up and recycle-it crew.”

There are enzymes in the cell that are assigned to the clean-up and recycling crew. They speed up the elimination of the cell’s “garbage,” breaking down the unneeded or excess molecules into smaller useful components.  Without these enzymes we would quickly die from the accumulation of excessive and possibly harmful unneeded molecules inside the cells.  They also protect the cells by breaking down toxins that come in from the outside environment.

In a very real sense, these enzymes are more than just the garbage disposal crew, they form an indispensable part of the system that maintains the chemical balance needed to sustain all of the life-critical processes that take place inside the cells. In the cell, molecules (large and small) are constantly in the process of being built up from smaller pieces and then torn back down into smaller pieces again.

Antioxiants – “The clean-up crew that is placed strategically in the cell, like guardians, to break down and eliminate the oxidants that would otherwise accumulate and cause damage.” They are: Glutathione Peroxldase (GPx) that breaks down various oxidants (free radicals), Superoxide Dismutase (SOD) that breaks down superoxides, and Catalase that breaks down hydrogen peroxide.

Proteases– The large protein break-it-down crew, used as digestive enzymes to break down food and used by cells to break down unneeded or defective proteins.  They are Trypsin, Chyotrypsin and Pepsinogen.

Other “Staff Members” are: Collagen, Cholesterol, Glucose, Triglycerides, Prostaglandin, Quinine, Oleic Acid, Cocaine, Caffeine, Levidopa, and Histamine.

As we can see, there are many and varied types of “actors” playing various and sundry roles to make life possible in our bodies so that we can live and serve in this earthly plane of existence.  It’s helpful to have them placed in a context the way Dr. Samuelson does in his booklet.

In my next post we will learn how all these actors work together via the signaling messengers, whose crucial role it is to keep all the actors in touch with one another and all the systems of the body well-informed on what’s going on with each part and within the whole body. Then we will be prepared to study and learn the important role chemical balance plays in the healing process, and how the body keeps everything balanced.  Until then,  if you haven’t viewed it already, take the time now to enjoy David Bolinsky’s “Fantastic Voyage Inside the Cell” (10 min).

My best to your health and healing,

Dr. Tony Palombo











 

 

 

 

 

 

 

 









 





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The Healing Process:The Cell, Part 1 Protein Synthesis

BASIC CONCEPTS

We’ve been considering the role of the cell in facilitating the healing process, sharing some of Dr. Gary Samuelson’s booklet The Science of Healing Revealed – New Insights into Redox Signaling. In this post we will look at the basic concept of the cell’s function in manufacturing protein molecules, the fundamental building blocks of our anatomy.

(Note: This post contains several video clips for your visual aid and entertainment. They are best viewed in full screen mode and with headphones. After viewing a clip, click the full screen option again to exit full screen mode, then click on the BACK arrow at the top left hand corner of the screen to return to the blog.)

We’ll start with this beautiful video clip of The Inner Life of the Cell (8 min).  Brief ABC Report (3 min).  If you have the time, enjoy  David Bolinsky’s  entertaining Fantastic Voyage inside the cell (10 min.)

An Overview of How Healthy Cells Work

All life processes take place inside of our cells. In the simplest definition, a cell is a tiny bag filled with salt water and organic chemicals. The bag itself is made out of a bi-lipid [phospholipid] membrane (3 thin sheet that has waterproof layers on both sides and a thin layer of fat [cholesterol] in between).

Note the need for cholesterol in the cell structure, not at all the “bad” thing medicine and pharma would have us believe.  Balance and ratio, as in all things, is the primary factor.

View clip Anatomy of a cell (3:38)

All of the materials that the cell needs to maintain life must be passed through this membrane into the inside of the cell and also all of the unneeded garbage that is generated inside tile cell needs to be passed back out through this membrane to the outside of the cell. The cell manufactures certain portals or gateways, called receptors and co-receptors, that are embedded in the cell membrane to let the materials in and out and to pass chemical messages from the outside to the inside of the cell and vice versa. Everything that affects the cell must be able either to pass through these portals or to diffuse through the membrane. (4:40)

(Click on picture for a larger view, then click on BACK arrow to return to blog)

In the middle of each cell there is another smaller double bag (made from two bi-lipid membranes) that contains the nucleus and DNA. The DNA [Deoxyibonucleic Acid] has encoded instructions on how and when to build the proteins that the cell uses. A DNA strand is made out of two molecular spines twisted into a double helix. Between the spines there can be found only four distinct types of molecules called nucleotides (labeled A,T,C,G)  which are arranged in sequenced groups like rungs on a ladder. Groups of three of these rungs are called “codons” (A-T-G1 for example).

The exact sequence of these codons in the DNA strand determines the specific order in which amino acids are chained together (called polypeptide chains) in order to form proteins, thousands and thousands of different varieties. Most of the cell’s machinery and inner structure is formed out of the proteins manufactured from these genetic instructions. One exception to this rule is the formation of an organelle called the Mitochondrion. The Mitochondria (plural) contain their own DNA (called mtDNA) formed in circular strands and they divide and reproduce inside the cell much like bacteria divide, but are controlled and regulated by protein messengers from the nucleus. The Mitochondria’s primary job is to efficiently produce the fuel (ATP) that energizes the micro machines inside the cell that carry out the life processes. There are anywhere from 10 to 5000 Mitochondria in a typical cell, taking up to 50% of the cell’s volume.

YouTube video clips:   DNA and RNA (1:45)   Protein Synthesis (3:30)  Transcription: From DNA to Flesh and Blood (4 min)

In theory, the DNA sequences of instructions (genes) inside any given cell in your body are entirely identical to the DNA sequences (genes) that are in every other cell (with the exception of the reproductive cells). Lately researchers have cloned whole animals by placing the DNA from a single skin cell inside an empty egg cell. The egg cell starts to divide and form a complete organism. The DNA package Inside every ceil in the animal has all of the instructions necessary to form a whole new animal. This begs the question: If the DNA in every cell is identical, then how does there come to be so many different varieties of cells and tissues, brain cells, bone cells, skin cells, liver cells, etc.? The answer to this question is found in the understanding that the individual cells do not act alone they are grouped and bound together into tissues.

The genes activated in the individual cells depend largely on messengers sent back and forth from their neighbors and are specific to where the cells are located in the body. After a while, the chemical (protein) messages sent from the surrounding cells activate the genes that determine the behavior of all the cells that collectively form similar tissue. So in a real sense, the cellular function is determined by the environment in which it lives.  Cells, in this sense, “become what they eat.”   [Underscore mine]

Cellular differentiation and “stem cells.”

The ability of a cell to change its form and function depending on the protein messengers surrounding it is called “cellular differentiation.” A cell gains its identity (brain, muscle, liver, etc.) from the messengers it finds around it and/or builds inside it. A recent triumph in science came when “stem cells” were discovered. These cells can take the form of any cell they come into contact with (they are undifferentiated cells). If you want to grow new brain cells, for example, then all that is required is to place stem cells in the brain. They will soon transform into new brain cells that fit flawlessly into their new environment as they are programmed to become new brain cells by their neighboring cells. This also happens if they are placed in the liver, heart, etc., the stem cells ultimately become similar to the cells that surround them. It is an interesting fact that the cells in your body can also genetically shift due to the intake of nutrients that you eat. What you eat can literally change the form and genetic function of your cells. There have been experiments with identical twins in mice, both having exactly the same DNA, that were fed different diets. One mouse grew shiny brown fur and was skinny. The other grew light gold fur and was fat and sickly. The only difference between the two mice was in what they ate.”

This point is one to give pause for deep consideration, so I will end this post with it.  It is this kernel of truth that emerged out of the fascinating work of world renown Cellular Biologist, Dr. Bruce Lipton.  Click on his name below when you have 35 minutes to relax and listen to this brilliant man as he tells his story of how he violated the central dogma that is the pillar of modern biomedicine.  This dogma is the concept, formulated by Francis Crick, co-founder along with Jim Watson of the DNA double helix molecule, that the flow of information in biology goes from DNA to RNA to protein, and since you body is made of protein, and protein is coded by the DNA in the cell, which carries your genetic heritage and fingerprint, your behavior is controlled by your genes, and you are a victim of your heredity past.  This is not the truth of the matter, but I’ll let Dr. Lipton tell his own story and leave you to your listening and learning pleasure . . . and with this prophetic pearl from Albert Einstein, who wrote: “The field is the sole governing agency of the particle.”

To your health and healing,

Dr. Tony Palombo

Video of  Dr. Bruce Lipton (35 min.)