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Protease Enzymes

Rich Distributing Enzymes Plus Intestinal Flora

Protease enzymes hydrolyze large protein molecules into smaller polypeptides and amino acids. Human and animal studies have provided irrefutable evidence that proteolytic enzymes, preferably taken on an empty stomach, can and are absorbed intact from the gastrointestinal tract into the undesirable and often detrimental protein factions in the extra-cellular fluids. In particular, this increased proteolytic activity has been found to help reduce the effects of acute inflammation. When there is cellular injury, insoluble fibrin clots develop at the periphery of the inflamed area, enclosing the damaged tissue preventing the migration of disease-causing agents of toxins to other areas of the body. During the reparative process, serum proteolytic enzymes, known as plasmins, begin breaking down the fibrin clots into smaller, soluble peptides and amino acids. Although the immediate fibrin deposits is one of the most important defense mechanisms in the body, an imbalance between the number of fibrin clots formed and the amount of piasmin present to dissolve the clot has been found to cause exaggerated inflammatory symptoms such as more extensive edema; more pain; complete stoppage of circulation to the area; a delay of the phagocytic stage of inflammation; and delayed healing with excess scar formation. Proteolytic enzymes given to human subjects suffering from inflammation; and delayed healing with excess scar formation. Proteolytic enzymes given to human subjects suffering from inflammation have experienced a dramatic resorption of the edemic fluid and relief of the heat, redness, swelling from inflammation have experienced a dramatic resorption of the edemic fluid and relief of the heat, redness, swelling and pain. Protease supplementation has been shown to be beneficial for acute inflammation involving soft tissue (sports injuries), bones, respiratory tract or the ears, nose, throat, and/or gums.

A Boost To The Immune System

Adequate proteolytic activity in the bloodstream is vital to a healthy immune system. Human lymphocytes have proteolytic enzymes bound on the surface of their cell membranes which are capable of digesting the protein components of various pathogens. In addition, lymphocytic proteases have an increased affinity for infected cells due to the presence of foreign proteins in the cell membrane. Immunological studies have shown that oral administration of proteolytic enzymes increases antibody and lymphocyte production and so aid the immunological response. Exogenous proteases exhibit a unique selectivity for foreign non-living proteins. Normal, living cells are protected against lysis by an inhibitor mechanism. Viruses are cell parasites consisting of nucleic acids covered by a protein film which do not show any of the characteristics of life until after a successful cellular invasion. In vitro studies have found that, during their extra-cellular phase, the viral envelope can be hydrolyzed or at least inactivated by proteolytic activity leading to a loss of infectivity of several types of viruses in man including six different influenza Type A viruses and cold viruses. Although bacteria and parasites cannot be inactivated directly be exogenous proteolytic enzymes (due to the protective mechanism in their cell membranes), these enzymes can breakdown undigested protein, cellular dedris and toxins in the blood. For example, proteases can hydrolyze undigested dietary protein that enters the blood through openings made in the intestinal wall by the toxins and mycelia of Candida yeast. Supplementation of high-potency proteases allows the immune system to focus its full attention upon the bacterial or parasitic invasion.

The Problem With Undigested Proteins

The inability to properly digest protein can negatively affect many metabolic processes of the body. Protease supplementation helps the body utilize protein to produce hormones and to carry calcium to structural tissue and the nervous system. In a healthy nervous system, calcium and protein are integrally involved in the release of neurotransmitters which propagate transmission of nerve impulses. Magnesium concentrations in the extra-cellular fluids determine how much calcium may enter a nerve cell. When extra-cellular levels of protein, calcium and magnesium are low, irregular nervous reactions or anxiety can result. Magnesium also plays a vital role in maintaining mental and emotional balance by regulating the formation of the brain neurotransmitter dopamine and by promoting the formation of beneficial Prostaglandins. Proper protein, calcium and magnesium assimilation is imperative to the improvement of the irritability, anxiety and other psychological imbalances associated with PMS and menopause. In addition, studies have shown that people suffering from fungal infestations such as Candidiasis tend to be deficient in magnesium.

Protein Digestion Leads To Better Calcium Utilization

Calcium ions initiate and control muscle fiber contractions. A decrease in ionized serum calcium results in severe intermittent spastic contractions of the muscle known as tetany. As protein utilization is improved, more calcium ions are bound by circulating proteins thus educing the extra-cellular calcium ion concentration. To avoid the possibility of a tetanic response, it is necessary to supplement calcium when taking high-potency protease enzymes. We should note that drinking ionized alkaline water produced by our alkaline water ionizers may eliminate the need to supplement on calcium. Readily-soluble Calcium and Magnesium are included in Rich Distributing's Enzymes Plus Intestinal Flora to prevent the complications that could result from a deficiency of dietary calcium and/or magnesium.

In addition to Protease, cellulose, lipase and amylase are provided in Rich Distributing's Enzymes Plus Intestinal Flora formula to help utilize other important food nutrients.

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