bromelain enzyme benefits

Bromelain

(Ananas comosus)

Contents

Bromelain Description                                                           

Bromelain is a protein-eating enzyme found in the Pineapple plant, a member of the Bromeliad family of plants, hence its name. Pineapple is thought to have originated in South America where it was prized for its sweet taste and medicinal value. Trading amongst the native tribes helped spread it throughout Central America and the Caribbean and eventually around the world.

Historically, pineapple has been used in a variety of ways; as a digestive aid, as an anti-inflammatory, and as a blood thinner, to name a few. However, since being introduced as a therapeutic compound in 1957, studies have shown it to hold great promise for an even wider range of healing effects.

 Key Uses of Bromelain
  • Anti-Inflammatory
  • Cardiovascular and Circulatory Improvement: helps reduce blood clotting in the arteries
  • Helps digestion
  • Stimulates immune system and healing response
  • Bromelain Clinical Applications 

    Bromelain is indicated for the treatment of swelling and inflammation due to its inhibition of inflammatory agents. It has also been shown to inhibit platelet aggregation.

    How Bromelain Works

    Bromelain appears to inhibit a number of aspects involved in the Coagulation Cascade, a biochemical process that triggers blood clotting and inflammation at wound sites and/or in the body in general. It has been shown to interfere with the development of fibrin among the different blood components resulting in a subsequent decrease of platelet aggregation or blood clots, and contributing to improved circulation.

    Further, Bromelain inhibits inflammation and associated pain by inhibiting pro-inflammatory mediators. By keeping these inflammatory biochemicals which trigger swelling, redness, heat and pain from moving into and constricting tissues, inflammation is reduced, circulation improves and tissues start to heal. It also appears to have the advantage of selectively controlling some of the biochemical causes of pain and inflammation rather than the often-uncontrolled effect of NSAIDS. Bromelain has also shown in animal studies, to have a stimulating effect on the development of plasmin which contributes to tissue healing and which also inhibits some of the precursors to the coagulation process.

    Bromelain research has shown great potential in other areas of treatment. It appears to significantly stimulate the immune system by promoting the production of cytokines in cells. It also appears to potentiate antibiotics and supplements such as glucosamine and preliminary testing indicates it may have a significant anti-tumor effect.

    Bromelain Safety

    Bromelain is considered safe even at high dosages. No toxicity was report in a 6 month study where dogs 750/mg/Kg daily. The typical dose for humans is between 450 and 2,000 mg per day. Some reported allergies have been report with Bromelain. These can occur in individuals with allergies to Pineapple or other members of the Bromeliaceae family. A small percentage of people who are sensitive to honeybee venom, latex, birch pollen, carrot, celery, fennel, cypress pollen, grass pollen, papain have also experience allergies to bromelain.

    Bromelain Side Effects

    Because of Bromelain's anti-coagulant properties, patients using anti-coagulant medications should consult with their physicians before using.

    Other reported side effects are stomach upset and diarrhea, increased heart rate, nausea, vomiting, irritation of mucus membranes, and menstrual problems. Not recommended for pregnant women due to lack of research.

    Bromelain Recommended Amounts

    Because herbs also contain active chemical substances which can and will interact with others, no herb or drug should be taken without first consulting with one's physician.

    A variety of doses have been used and studied. Research in the 1960s and 1970s indicated 120 to 240 milligrams of bromelain concentrate tablets daily in three to four divided doses for up to one week to treat inflammation. The German expert panel, the Commission E, has recommended 80 to 320 milligrams (200 to 800 FIP units) taken two to three times per day. Effects of bromelain may occur at lower doses, and treatment may be started at a low dose and increased as needed.

    Bromelain Research

    1) Seligman B. Bromelain-an anti-inflammatory agent thrombophlebitis. No toxicity. Angiology 1962;13:508-510.

    2) Felton G. Does Kinin released by pineapple stem bromelain stimulate production of prostaglandin E1-like compound. Haw Med J 1976;2:39-47.

    3) Mynott TL, Luke RK, Chandler DS. Oral administration of protease inhibits enterotoxigenic Escherichia coli receptor activity in piglet small intestine. Gut 1996;38:28-32.

    4) Taussig SJ, Nieper HA. Bromelain: its use in prevention and treatment of cardiovascular disease, present status. J IAPM 1979;6:139-151.

    5) Giacca S. Clinical experiments with bromelain in peripheral venous diseases and chronic bronchitic states. Minerva Med 1965;56:Suppl.104.

    6) Nieper HA. Effect of bromelain on coronary heart disease and angina pectoris. Acta Med Empirica 1978;5:274-278.

    7) Nieper HA. Decrease of the incidence of coronary heart infarct by Mg- and K-orotate and bromelain. Acta Med Empirica 1977;12:614-618.

    8) Masson M. Bromelain in blunt injuries of the locomotor system. Fortschr Med 1995;113:303-306.

    9) Tassman GC, Zafran JN, Zayon GM. Evaluation of a plant proteolytic enzyme for the control of inflammation and pain. J Dent Med 1964;19:73-77.

    10) Blonstein JL. Control of swelling in boxing injuries. Practitioner 1960;185:78.

    11) Mojcik C, Shevach E. Adhesion molecules: a rheumatologic perspective. Arthritis Rheum 1997;40:991-1004.

    12) Bodi T. The effects of oral bromelains on tissue permeability to antibiotics and pain response to bradykinin: double blind studies on human subjects. Clin Med 1966;73:61-65.

    13) Uhlig G, Seifert J. Die Wirkung proteolytischer Enzyme auf das posttraumatische Syndrom. Fortschritte der Medizin 1981;15:554-556.

    14) Cohen A, Goldman J. Bromelain therapy in rheumatoid arthritis. Penn Med J 1964;67:27-30.

    15) Leipner J, Iten F, Saller R. Therapy with proteolytic enzymes in rheumatic disorders. Biodrugs 2001;15:779

    16) Klein G, Kullich W. Short-term treatment of painful osteoarthritis of the knee with oral enzymes: a randomised, double-blind study versus Diclofenac. Clin Drug Invest 2000;19:15-23.

    17) Singer F, Singer C, Oberleitner H. Phlyoenzym versus diclofenac in the treatment of activated osteoarthritis of the knee. Int J Immunother 2001;17:135-141.

    18) Tilwe GH, Beria S, Turakhia NH, Daftary GV, Schiess W. Efficacy and tolerability of oral enzyme therapy as compared to diclofenac in active osteoarthritis of the knee joint: an open randomised controlled clinical trial. Journal of the Association of Physicians of India. JAPI 2001;49:621.

    19) Walker AF, Bundy R, Hicks SM, Middleton RW. Bromelain reduces mild acute knee pain and improves well being in a dose dependant fashion in an open study of otherwise healthy adults. Phytomedicine 2002;9:681-686.

    20) Bellamy N, Buchanan W, Goldsmith C, Campbell J, Stitt L. Validation study of WOMAC: a health status instrument for measuring clinically important patient relevant outcomes to anti-rheumatic drug therapy in patients with osteoarthritis of the hip or knee. Rheumatology 1988;15:1833-1840.

    21) Felton G. Does Kinin released by pineapple stem bromelain stimulate production of prostaglandin E1-like compound. Haw Med J 1976;2:39-47.

     


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