What does it do? Bromelain is one of a group of proteolytic enzymes (enzymes capable of digesting protein). It is widely
believed that most orally ingested enzymes are destroyed by the digestive juices prior to
being absorbed. However, there is evidence that significant amounts of bromelain can be
absorbed intact.1 Proteolytic enzymes other than bromelain are often used
with people who suffer from malabsorption. Although
bromelain in combination with other enzymes and ox bile has been reported to help digest
food,2 it is generally not used for this purpose. However, bromelain does
contribute to the digestion of protein, and may therefore be used as a digestive aid. Although
many doctors assume that other proteolytic enzymes, such as those found in pancreatin, are
more effective than bromelain in helping digestion and absorption, almost no research compares
the relative effects of these enzymes.
Bromelain is an anti-inflammatory agent and for this reason is helpful in healing minor injuries, particularly sprains and strains, muscle
injuries, and the pain, swelling, and tenderness that
accompany sports injuries.3 4 5 Topically applied bromelain
in the form of a cream may be beneficial for cleaning debris from burns 6 and frostbite,7 possibly enhancing
the rate of healing.8 This use of bromelain should be supervised by a doctor.
Also as a result of its anti-inflammatory effect, bromelain has been found to dramatically
reduce postoperative swelling in controlled human research.9 Double-blind research
has found bromelain effective in reducing swelling, bruising,10 and pain, for women
having minor surgery in conjunction with giving birth (episiotomy).11
The anti-inflammatory effect of bromelain is the probable reason this enzyme has been found
effective for people suffering from
sinusitis.12 Some of the evidence supporting bromelain in the treatment of
sinusitis comes from double-blind research.13
Bromelain, in combination with trypsin (another enzyme) may enhance the effect of
antibiotics in people with a urinary tract infection. In a
double-blind study, 100% of people who received bromelain/trypsin in combination with antibiotics had a resolution of their infection, compared to only 46% of those who received
antibiotics alone.14
Again, probably due to its anti-inflammatory action, bromelain was reported to help
patients with rheumatoid arthritis in
preliminary research.15 In that trial, in which bromelain was given for varying
(3-week to 13-month) periods, 73% had good to excellent results.
Bromelain is a natural blood thinner because it prevents excessive blood platelet
stickiness.16 This may explain, in part, the positive reports in a few clinical
trials of bromelain to decrease symptoms of angina and
thrombophlebitis.17 18 In addition, bromelain reduces the thickness of
mucus, which may benefit patients with asthma or chronic
bronchitis.19
Preliminary evidence in both animals and people suggests that bromelain may possess
antitumor activity, though the true importance of this effect is poorly
understood.20
Bromelain can induce beneficial changes in white blood cells with possible effects on immune function.21 22 However,
whether these effects would help people with immune system problems remains unclear.
Where is it found? Bromelain is found mostly in the stems of
pineapples and is available as a dietary
supplement.
Bromelain has been used in
connection with the following conditions (refer to the individual
health concern for complete information):
Who is likely to be deficient? Since bromelain is not
essential, deficiencies of this plant-based enzyme do not
exist.
How much is usually taken? Assessing the right amount of
bromelain to take is complicated. Most bromelain research was conducted years ago, when
amounts used were listed in units of activity that no longer exist. These old units do not
precisely convert to new ones. Today, bromelain is measured in MCUs (milk clotting units) or
GDUs (gelatin dissolving units). One GDU equals approximately 1.5 MCU. Strong products contain
at least 2,000 MCU (1,200–1,333 GDU) per gram (1,000 mg). A supplement containing 500 mg
labeled “2,000 MCU per gram” would have 1,000 MCU of activity. Some doctors
recommend as much as 3,000 MCU taken three times per day for several days, followed by 2,000
MCU three times per day.23 Much of the research uses smaller amounts, more like the
equivalent of approximately 500 MCU taken four times per day. However, most of the bromelain
used in the studies was enteric-coated in order to prevent it from being destroyed by gastric
juice. It is likely, therefore, that currently available bromelain preparations (which
typically are not enteric-coated) are of lower potency than the bromelain used in most
studies.
Are there any side effects or interactions? Bromelain is
generally safe and free of side effects when taken in moderate amounts. However, one
preliminary report indicates increased heart rate with the use of bromelain.24 In
addition, some people are allergic to bromelain. One woman reportedly developed a hives and
severe swelling after taking bromelain, even though she had tolerated bromelain on two other
occasions previously.25 Because bromelain acts as a blood thinner and little is
known about how bromelain interacts with blood-thinning drugs, people should avoid combining
such drugs with bromelain in order to reduce the theoretical risk of excessive bleeding.
Are there any drug interactions? Certain medications may
interact with bromelain. Refer to the drug interactions
safety check for a list of those medications.
References:
1. Izaka K, Yamada M, Kawano T, Suyama T. Gastrointestinal absorption and
anti-inflammatory effect of bromelain. Jpn J Pharmacol 1972;22:519–34.
2. Balakrishnan V, Hareendran A, Nair CS. Double-blind cross-over trial
of an enzyme preparation in pancreatic steatorrhea. J Assoc Physicians India
1981;29:207–9.
3. Seligman B. Bromelain: an anti-inflammatory agent. Angiology
1962;13:508–10.
4. Cirelli MG. Treatment of inflammation and edema with bromelain.
Delaware Med J 1962;34:159–67.
5. Masson M. Bromelain in the treatment of blunt injuries to the
musculoskeletal system. A case observation study by an orthopedic surgeon in private practice.
Fortschr Med 1995;113:303–6.
6. Levensen S. Supportive therapy in burn care. Debriding agents. J
Trauma 1979;19(11 Suppl):8–30.
7. Ahle NW, Hamlet MP. Enzymatic frostbite eschar debridement by
bromelain. Ann Emerg Med 1987;16:1063–5.
8. Hayashi M. Pharmacological studies of Shikon and Tooki. (3) Effect of
topical application of the ether extracts and Shiunko on inflammatory reactions. Nippon
Yakurigaku Zasshi 1977;73:205–14 [in Japanese].
9. Seltzer AP. Minimizing post-operative edema and ecchymoses by the use
of an oral enzyme preparation (bromelain). EENT Monthly 1962;41:813–7.
10. Howat RCL, Lewis GD. The effect of bromelain therapy on episiotomy
wounds—a double blind controlled clinical trial. J Obstet Gynaecol Br
Commonwealth 1972;79:951–3.
11. Zatuchni GI, Colombi DJ. Bromelains therapy for the prevention of
episiotomy pain. Obstet Gynecol 1967;29:275–8.
12. Taub SJ. The use of Ananase in sinusitis. A study of 60 patients.
EENT Monthly 1966;45:96–8.
13. Ryan RE. A double-blind clinical evaluation of bromelains in the
treatment of acute sinusitis. Headache 1967;7:13–7.
14. Mori S, Ojima Y, Hirose T, et al. The clinical effect of proteolytic
enzyme containing bromelain and trypsin on urinary tract infection evaluated by double blind
method. Acta Obstet Gynaecol Jpn 1972;19:147–53.
15. Cohen A, Goldman J. Bromelains therapy in rheumatoid arthritis.
Pennsylvania Med J 1964;67:27–30.
16. Heinicke R, van der Wal L, Yokoyama M. Effect of bromelain (Ananase)
on human platelet aggregation. Experientia 1972;28:844–5.
17. Nieper HA. Effect of bromelain on coronary heart disease and angina
pectoris. Acta Med Empirica 1978;5:274–8.
18. Seligman B. Oral bromelains as adjuncts in the treatment of acute
thrombophlebitis. Angiology 1969;20:22–6.
19. Schafer A, Adelman B. Plasma inhibition of platelet function and of
arachidonic acid metabolism. J Clin Invest 1985;75:456–61.
20. Kelly GS. Bromelain: a literature review and discussion of its
therapeutic applications. Altern Med Rev 1996;1:243–57 [review].
21. Desser L, Rehberger A, Paukovits W. Proteolytic enzymes and amylase
induce cytokine production in peripheral blood mononuclear cells in vitro. Cancer
Biother 1994;9:253–63.
22. Munzig E, Eckert K, Harrach T, et al. Bromelain protease F9 reduces
the CD44 mediated adhesions of human peripheral blood lymphocytes to human umbilical vein
endothelial cells. FEBS Lett 1995;351:215–8.
23. Gaby AR. The story of bromelain. Nutr Healing May 1995:3, 4,
11.
24. Gutfreund AE, Taussig SJ, Morris AK. Effect of oral bromelain on
blood pressure and heart rate of hypertensive patients. Hawaii Med J
1978;37:143–6.
25. Nettis E, Napoli G, Ferrannini A, Tursi A. IgE-mediated allergy to
bromelain. Allergy 2001;56:257–8.
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The information presented in Healthnotes is for informational
purposes only. It is based on scientific studies (human, animal, or in vitro),
clinical experience, or traditional usage as cited in each article. The results reported may
not necessarily occur in all individuals. For many of the conditions discussed, treatment with
prescription or over-the-counter medication is also available. Consult your doctor,
practitioner, and/or pharmacist for any health problem and before using any supplements or
before making any changes in prescribed medications. Information expires December 2003.
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