Bromelain is an extract obtained from the pineapple plant and is used as a traditional folk remedy for several ailments. In this review, a comprehensive electronic database search was carried out to compile available literature on therapeutic implications of bromelain.
Pharmaceutical value of bromelain has been demonstrated in different surgical sub-specialties. Diverse biological processes like anti-inflammatory, anti-oedematous, analgesic, anti-thrombotic, exfoliation etc. are involved in bromelain's therapeutic actions, mediated through the kallikrein-kinin and arachidonic acid pathways as well as through effects on cell mediated immunity.
Bromelain equals non-steroidal anti-inflammatory drugs as an anti-inflammatory agent, but has been shown to have fewer side effects. In Europe it is approved for oral and topical use, mainly for surgical wounds, inflammation due to trauma and surgery, and debridement of deep burns. Literature suggests a promising role of bromelain in surgical care. More clinical trials to establish its utility as an anti-inflammatory agent in surgical care are recommended.
Keywords: Bromelain, Pineapple, Wound healing, Inflammation, Anti-inflammatory, debridement.
Bromelain is a crude extract derived from pineapple plant (Ananas comosus) and contains mixture of proteolytic enzymes and non-enzymatic substances. It is used as a folk remedy by many native cultures like Philippines, Hawaii etc. Several research studies have shown beneficial effects of bromelain in diverse health-related conditions. Bromelain's relevance is evident from reports of its beneficial effects in resolving swelling, inflammation, bruising and pain associated with trauma and surgery. Bromelain is not only effective but also has fewer adverse effects as compared to non-steroidal anti-inflammatory drugs (NSAIDs).1-6
In this review, we present the current available scientific literature covering mechanism of action and therapeutic role of bromelain in surgical care and related conditions. Bibliographic search with emphasis on key words 'bromelain, surgery, inflammation, wound' and phrases 'bromelain in surgical care and surgical wound, anti-inflammatory effect of bromelain etc. was carried out from available data using PubMed database filter (year 1957-2016), Google Scholar, Ovid and specific journals were also searched individually. Total 2,880 articles were searched in which 1,550 were with anti-inflammatory effect of bromelain in surgical care. Out of these articles, only most pertinent research articles with oral administered bromelain (separately or in proteolytic enzyme complex) or topical application of bromelain in different surgical care practices were selected. Those articles with intravenous route of bromelain administration as well as those involving bromelain effects on cancer and combination therapies were excluded. Our aim was to review and explore current evidence based primary data with respect to application of bromelain therapy in surgical practice.
Bromelain has two main sources: Fruit bromelain (EC 22.214.171.124) extracted from pineapple fruit and Stem bromelain (EC 126.96.36.199) extracted from inedible pineapple stem.7 Stem bromelain is economical to produce; hence it is the more commonly available commercial product. It is composed of endopeptidases (ananain, comosain), phosphatases, glucosidases, peroxidases, escharase, cellulases, glycoproteins, proteinase inhibitors (cystatin), calcium and carbohydrate.8-11 The proteolytic activity of bromelain is sensitive to storage conditions and biochemical processing thus, it is not practical to take therapeutic amount of bromelain by oral consumption of raw pineapple fruit as a substitute for bromelain supplements.12
Mechanism of action
Several in vivo and in vitro studies have been conducted on the anti-inflammatory activity of bromelain but the actual mechanism of anti-inflammatory effect is not fully established.
(a) Kallikrein-kinin pathway
Studies show that bromelain's anti-inflammatory and analgesic activity is due to lowering plasmakinin (bradykinin) at inflammatory site and lowering prostaglandin E2 levels. In vitro experiments showed that bromelain activates plasma prekallikrein by activation of factor XII.13 In rat experiments, it is shown that bromelain-derived plasminogen activator leads to production of plasmin. The plasmin cleaves Hageman factor in a way that results in a strong release of kallikrein but a weak release of thrombin. Intravenous bromelain administration in rats markedly reduced plasma prekallikrein and high molecular weight kininogen 15 minutes after the injection, and the effect lasted for 72 hours.14
Bromelain has been demonstrated to inhibit thrombus formation when administered orally and intravenously.15,16 The effect may be related to reduction in levels of high molecular weight kininogen and weak release of thrombin.
(b) Arachidonic acid pathway
It is also demonstrated that bromelain increases platelet cyclic adenosine monophosphate (cAMP) levels thus increasing prostaglandin (PG) I2 and PGE1 levels. A possible mechanism is suggested that the dominant endogenous prostaglandins being produced must be from the group that increases platelet cAMP levels (prostacyclin, PGE1, etc.). In in-vivo experimentally-induced inflammatory reaction in rats, bromelain was tested for its action on eicosanoids production. It was identified that arachidonic acid cascade was affected by bromelain.17 Bromelain, when administered orally in doses of 10 and 20 mg/kg, significantly decreased PGE2 and substance P concentrations in the exudate in rats with subcutaneous carrageenan-induced inflammation. In in-vitro experiment, PGE 2 levels were not affected by bromelain although substance P level was increased.18
(c) Cell Mediated Immunity
In in-vitro and in-vivo studies, it was observed that bromelain has anti-inflammatory effect by modulating leukocyte cell surface molecules like CD 14, CD 44, CD 16, CD 21, CD 128 a and b which are involved in leukocyte homing, cellular adhesion, induction of pro-inflammatory mediators and immunomodulatory effect on T cells by inhibition of T cell signal transduction, producing effect on Th1, Th2 and immunosuppressive cytokines, etc. Bromelai also reduce P-selectin mediated neutrophil recruitment.19-21
Therapeutic uses of bromelain in trauma and surgical care
Several clinical studies have demonstrated beneficial effects of bromelain (Table)
in a variety of conditions related to surgical practice, as described below:
1. Orthopaedics: In a clinical trial, patients with long bone fractures were treated with oral bromelain as a proteolytic enzyme combination containing 90 mg bromelain per tablet after surgery. Significant reduction in pain and swelling with accelerated healing was observed as compared to group of patients who were treated with standard anti-inflammatory analgesics.22
2. Obstetrics: Bromelain, administered orally, has been shown to be effective in reducing pain, ecchymosis and edema due to episiotomy in a placebo-controlled, double blind study.23 Another study showed a trend of similar reduction but the difference did not achieve statistical significance.24
3. Otolaryngology: In a randomized, placebo-controlled study, it has been reported that oral bromelain minimizes ecchymosis and edema after rhinoplasty.25
4. Dentistry: In patients who had undergone surgery for impacted third molar, a randomized controlled study showed that treatment with oral bromelain reduces post-operative erythema, pain and inflammation.26 Other randomized, double-blind, placebo-controlled clinical trial showed significant reduction in pain by bromelain compared to placebo and diclofenac, while yet another trial showed non-significant reduction in inflammation.27,28
5. Ophthalmology: In a double-blind, placebo-controlled clinical trial on patients undergoing cataract surgery, it was demonstrated that oral bromelain administered two days prior to surgery and five days post-operatively resulted in significant reduction in inflammation and pain as compared to the placebo group.29
In a series of patients suffering from blunt trauma injuries to the musculoskeletal system, treatment with bromelain resulted in subjective improvement in swelling, pain, and tenderness at the site of injury with good tolerability, although there was no control group.30
In a placebo controlled clinical trial, when subjects with artificially induced haematoma were treated with bromelain, there was a more rapid resorption of the haematoma and a significantly lower volume of haematoma as compared to placebo group. 31 The mechanism of resolution was not reported but in separate animal studies, inhibition of bradykinin generation at injury site and increase in serum fibrinolytic activity were observed, suggesting the probable mechanism of haematoma resolution.32,33
Literature shows mixed results for bromelain use in treatment of sprains and strains. According to some research studies it appears to reduce swelling, bruising, redness and tenderness, and promotes rapid recovery and healing. A double-blind placebo-controlled study was conducted on patients having sports related ankle injuries. Patients treated with oral bromelain had faster recovery as compared to placebo group.34 In three small double-blind studies, oral bromelain significantly healed bruises and improved mild athletic injuries as compared to placebo group.35-37
Contrary to this, in one big double-blind, placebo-controlled randomized trials, patients with acute unilateral sprain of the lateral ankle joint were treated either separately or in combination with oral bromelain, trypsin or a bioflavonoid rutin. Results showed significant difference in pain, swelling and range of motion as compared to placebo treated group.38
Topical application of bromelain to skin wounds and burns has been shown to be a safe and effective method for debridement of necrotic tissue and is an alternate to surgical debridement.39,40 Local application of bromelain has been shown to be rapid, effective, non-invasive, safe, easily performed at the bedside with minimal or no blood loss and negligibly interfere with natural wound healing processes.41
Debridement of necrotic tissue is due to a non-proteolytic component Escharase having molecular weight of 45,000 Daltons and is present in bromelain extract which also helps in healing. Houck described method of isolating escharase from stem of pineapple plant. Escharase helps in digestion, dissection and separation of non-viable, devitalized tissue, especially eschar tissue between the viable native and the non-viable denatured burn tissue.42
A multi-center, open-label, randomized, controlled clinical trial was conducted on patients 4 to 55 years of age with deep partial and full thickness burns. Patients were treated with a bromelain-rich topical agent NexoBrid which was applied for 4 hours or by standard of care. There was reduced time from to complete debridement, need for surgery and need for autografting in bromelain treatment group.43
It has been reported that oral administration of bromelain significantly lowers adenosine phosphate induced platelet aggregation. Antiplatelet activity was determined ex vivo.44 In one study, effect of bromelain was assessed on human plasma fibrin (ogen) and blood coagulation. Bromelain showed dual action on blood coagulation: at low concentration showed procoagulant effect and at high concentration anticoagulant effect.45 These findings are of concern for surgeons and care needs to be exercised in patients with bleeding disorders while prescribing bromelain.
Contrary to above mentioned findings, some authors identified that bromelain does not significantly affect blood clotting mechanism in healthy volunteers. In one clinical trial, healthy volunteers and breast cancer patients were treated with oral bromelain. The activated partial thromboplastin time increased from 38 to 46 seconds, leaving prothrombin time and plasminogen unchanged.46 In another clinical trial, patients with oedema and inflammation were treated with 40 mg oral bromelain 4 times daily for 1 week. There was no significant effect on bleeding, coagulation and prothrombin time suggesting that therapeutic amount of bromelain does not affect blood clotting.47
On the basis of available positive research evidence, the German Commission E approved bromelain as an effective remedy to treat inflammation after ear, nose, throat and trauma surgeries.48 In the United States, bromelain is "generally recognized as safe" (21CFR184.1024) by the U.S. Food and Drug Administration (FDA), though no approved therapeutic indications are available due to lack of required body of research evidence.
Although bromelain is generally safe, there are rare reports of nausea, vomiting, diarrhea, allergic reaction and unusual menstrual bleeding.49,50 As safety data is scarce, it is advisable that pregnant women, patients with bleeding disorders, hypertension, liver disease and kidney disease should avoid bromelain. 51,52
Bromelain's role against platelet aggregation may increase the risk of bleeding during and after surgery. It should be administered in patients under doctor's supervision with special precautions. It is recommended that bromelain should not be combined with anticoagulant drugs such as warfarin, clopidogrel etc. and should not be administered in bleeding disorders.
Therapeutic management with bromelain is based on medical condition for which it is being taken.
u The German Commission E recommended dosing in ENT surgeries and trauma to be 80 - 320 mg orally 2 - 3 times per day for 8 days. For certain conditions higher doses are also prescribed.
u For debridement of deep thermal skin burns, bromelain is applied topically once for 4 hours in the form of debrase gel dressing. Treatment is provided in specialized burn centers under strict observation. Bromelain gel should not be applied to more than 15% of the patients total body surface area and to the broken skin.
Bromelain is not recommended in children as there is no reliable safety data available. A Paediatric Investigation Plan (EMEA-000142-PIP02-09-M03) has been agreed by European Medicines Agency (Decision number P/0072/2014) and its proposed date of completion is March 2019.48
Literature search of 59 years suggest a promising role of bromelain in surgical care on account of its anti-inflammatory effect. Pineapple extracted Bromelain may be used as a therapeutic agent in surgical care.
In surgical practice, further exploration of bromelain's role as a therapeutic anti-inflammatory agent remains to be established through more number of randomized controlled clinical trials.
1.Lapeyre-Mestre M, Grolleau S, Montastruc JL, Association Française des Centres Régionaux de Pharmacovigilance (CRPV). Adverse drug reactions associated with the use of NSAIDs: a case/noncase analysis of spontaneous reports from the French pharmacovigilance database 2002-2006. Fundam Clin Pharmacol. 2013; 27:223-30.
2.de la Barrera-Núñez MC, Yáñez-Vico RM, Batista-Cruzado A, Heurtebise-Saavedra JM, Castillo-de Oyagüe R, Torres-Lagares D. Prospective double-blind clinical trial evaluating the effectiveness of Bromelain in the third molar extraction postoperative period. Med Oral Patol Oral Cir Bucal. 2014; 19:e157-62.
3.Ho D, Jagdeo J, Waldorf HA. Is There a Role for Arnica and Bromelain in Prevention of Post-Procedure Ecchymosis or Edema? A Systematic Review of the Literature. Dermatol Surg. 2016; 42: 445-63.
4.Sahbaz A, Aynioglu O, Isik H, Ozmen U, Cengil O, Gun BD, et al. Bromelain: a natural proteolytic for intra-abdominal adhesion prevention. Int J Surg. 2015; 14: 7-11.
5.Shetty V, Mohan A. A prospective, randomized, double-blind, placebo-controlled clinical trial comparing the efficacy of systemic enzyme therapy for edema control in orthognathic surgery using ultrasound scan to measure facial swelling. J Oral Maxillofac Surg. 2013; 71:1261-7.
6.Klein G, Kullich W. Short-Term Treatment of Painful Osteoarthritis of the Knee with Oral Enzymes. Clinical Drug Investigation. 2000; 19:15-23.
7.Hale LP, Greer PK, Trinh CT, James CL. Proteinase activity and stability of natural bromelain preparations. Int Immunopharmacol. 2005; 5:783-93.
8.Nadzirah KZ, Zainal S, Noriham A, Normah I. Efficacy of selected purification techniques for bromelain. IFRJ. 2013; 20:43-6.
9.Napper AD, Bennett SP, Borowski M, Holdridge MB, Leonard MJ, Rogers EE, et al. Purification and characterization of multiple forms of the pineapple-stem-derived cysteine proteinases ananain and comosain. Biochem J. 1994; 301:727-35.
10.Irene D, Chen BJ, Lo SH, Liu TH, Tzen JT, Chyan CL. Resonance assignments and secondary structure of a phytocystatin from Ananas comosus. Biomol NMR Assign. 2012; 6:99-101.
11.de Lencastre Novaes LC, Jozala AF, Lopes AM, de Carvalho Santos-Ebinuma V, Mazzola PG, Pessoa Junior A. Stability, purification, and applications of bromelain: A review. Biotechnol Prog. 2016; 32:5-13.
12.Bhattacharya R, Bhattacharyya D. Preservation of natural stability of fruit "bromelain" from Ananas comosus (pineapple). J Food Biochem. 2009; 33:1-19.
13.Oh-ishi S, Uchida Y, Ueno A, Katori M. Bromelian, a thiolprotease from pineapple stem, depletes high molecular weight kininogen by activation of Hageman factor (Factor XIII). Thromb Res. 1979; 14:665-72.
14.Uchida Y, Katori M. Independent consumption of high and low molecular weight kininogens in vivo. Adv Exp Med Biol. 1986; 198:113-8.
15.Felton GE. Fibrinolytic and antithrombotic action of bromelain may eliminate thrombosis in heart patients. Med Hypotheses. 1980; 6: 1123-33.
16.Maurer HR. Bromelain: biochemistry, pharmacology and medical use. Cell Mol Life Sci. 2001; 58:1234-45.
17.Vellini M, Desideri D, Milanese A, Omini C, Daffonchio L, Hernandez A, et al. Possible involvement of eicosanoids in the pharmacological action of bromelain. Arzneimittelforschung. 1986; 36:110-2.
18.Gaspani L, Limiroli E, Ferrario P, Bianchi M. In vivo and in vitro effects of bromelain on PGE(2) and SP concentrations in the inflammatory exudate in rats. Pharmacology. 2002; 65:83-6.
19.Banks JM, Herman CT, Bailey RC. Bromelain Decreases Neutrophil Interactions with P-Selectin, but Not E-Selectin, In Vitro by Proteolytic Cleavage of P-Selectin Glycoprotein Ligand-1. PloS One. 2013; 8:e78988.
20.Hale LP, Greer PK, Sempowski GD. Bromelain treatment alters leukocyte expression of cell surface molecules involved in cellular adhesion and activation. Clin Immunol. 2002; 104:183-90.
21.Muller S, Marz R, Schmolz M, Drewelow B, Eschmann K, Meiser P. Placebo-controlled randomized clinical trial on the immune modulating activities of low- and high-dose bromelain after oral administration - new evidence on the antiinflammatory mode of action of bromelain. Phytother Res. 2013; 27:199-204.
22.Kamenicek V, Holan P, Franek P. [Systemic enzyme therapy in the treatment and prevention of post-traumatic and postoperative swelling]. Acta Chir Orthop Traumatol Cech. 2001; 68:45-9.
23.Golezar S. Ananas comosus Effect on Perineal Pain and Wound Healing After Episiotomy: A Randomized Double-Blind Placebo-Controlled Clinical Trial. Iran Red Crescent Med. 2016; 18: e21019.
24.Howat RCL, Lewis GD. The effect of bromelain therapy on episiotomy wounds-a double blind controlled clinical trial. BJOG. 1972; 79:951-3.
25.Seltzer AP. Minimizing post-operative edema and ecchymoses by the use of an oral enzyme preparation (bromelain). A controlled study of 53 rhinoplasty cases. Eye Ear Nose Throat Mon. 1962; 41:813-7.
26.Ordesi P, Pisoni L, Nannei P, Macchi M, Borloni R, Siervo S. Therapeutic efficacy of bromelain in impacted third molar surgery: a randomized controlled clinical study. Quintessence Int. 2014; 45:679-84.
27.Majid OW, Al-Mashhadani BA. Perioperative bromelain reduces pain and swelling and improves quality of life measures after mandibular third molar surgery: a randomized, double-blind, placebo-controlled clinical trial. J Oral Maxillofac Surg. 2014; 72:1043-8.
28.María C, Barrera-Núñez dl, Yáñez-Vico RM, Batista-Cruzado A, Heurtebise-Saavedra JM, Castillo-de Oyagüe R, et al. Prospective double-blind clinical trial evaluating the effectiveness of Bromelain in the third molar extraction postoperative period. Med Oral Patol Oral Cir Bucal. 2014; 19:e157-62.
29.Spaeth GL. The effect of bromelains on the inflammatory response caused by cataract extraction: a double-blind study. Eye Ear Nose Throat Mon. 1968; 47: 634-9.
30.Masson M. Bromelain in blunt injuries of the locomotor system. A study of observed applications in general practice. Fortschr Med. 1995; 113:303-6.
31.Woolf RM, Snow JW, Walker JH, Broadbent TR. Resolution of an Artifically Induced Hematoma and the Influence of a Proteolytic Enzyme. J Trauma. 1965; 5:491-4.
32.Pirotta F, De Giuli-Morghen C. Bromelain: a deeper pharmacological study. Note I. Antiinflammatory and serum fibrinolytic activity after oral administration in the rat. Drugs Exp Clin Res. 1978; 4: 1-20.
33.Kumakura S, Yamashita M, Tsurufuji S. Effect of bromelain on kaolin-induced inflammation in rats. Eur J Pharmacol. 1988; 150:295-301.
34.Baumuller M. The application of hydrolytic enzymes in blunt wounds to the soft tissue and distortion of the ankle joint: a double blind clinic al trial (Translated from German). Allgemeinmedizin. 1990; 19:178-82.
35.Zuschlag JM. Double-blind clinical study using certain proteolytic enzyme mixtures in karate fighters: Working paper. Mucos Pharma GmbH (Germany). 1988; 1-5.
36.Deitrick RE. Oral proteolytic enzymes in the treatment of athletic injuries: a double-blind study. Pa Med. 1965; 68: 35-7.
37.Rathgeber WF. The use of proteolytic enzymes (chymoral) in sporting injuries. S Afr Med J. 1971; 45: 181-3.
38.Kerkhoffs GM, Struijs PA, de Wit C, Rahlfs VW, Zwipp H, van Dijk CN. A double blind, randomised, parallel group study on the efficacy and safety of treating acute lateral ankle sprain with oral hydrolytic enzymes. Br J Sports Med. 2004; 38:431-5.
39.Cordts T, Horter J, Vogelpohl J, Kremer T, Kneser U, Hernekamp JF. Enzymatic debridement for the treatment of severely burned upper extremities - early single center experiences. BMC Dermatol. 2016; 16:8.
40.Krieger Y, Bogdanov-Berezovsky A, Gurfinkel R, Silberstein E, Sagi A, Rosenberg L. Efficacy of enzymatic debridement of deeply burned hands. Burns. 2012; 38: 108-12.
41.Koller J, Bukovcan P, Orsag M, Kvalteni R, Graffinger I. Enzymatic necrolysis of acute deep burns--report of preliminary results with 22 patients. Acta Chir Plast. 2008; 50: 109-14
42.Houck JC, Chang CM, Klein G. Isolation of an effective debriding agent from the stems of pineapple plants. Int J Tissue React. 1983; 5:125-34.
43.Rosenberg L, Krieger Y, Bogdanov-Berezovski A, Silberstein E, Shoham Y, Singer AJ. A novel rapid and selective enzymatic debridement agent for burn wound management: a multi-center RCT. Burns. 2014; 40:466-74.
44.Heinicke RM, van der Wal L, Yokoyama M. Effect of bromelain (Ananase) on human platelet aggregation. Experientia. 1972; 28: 844-5.
45.Errasti ME, Prospitti A, Viana CA, Gonzalez MM, Ramos MV, Rotelli AE, et al. Effects on fibrinogen, fibrin, and blood coagulation of proteolytic extracts from fruits of Pseudananas macrodontes, Bromelia balansae, and B. hieronymi (Bromeliaceae) in comparison with bromelain. Blood Coagul Fibrinolysis. 2016; 27: 441-9.
46.Eckert K, Grabowska E, Stange R, Schneider U, Eschmann K, Maurer HR. Effects of oral bromelain administration on the impaired immunocytotoxicity of mononuclear cells from mammary tumor patients. Oncol Rep. 1999; 6: 1191-9.
47.Cirelli MG, Smyth RD. Effects of bromelain anti-edema therapy on coagulation, bleeding, and prothrombin times. J New Drugs. 1963; 3:37-9.
48.European Medicines Agency-EMA/113587/2014. [Online] 2014 [cited 2015 December 14]. Available from: URL: http://www.ema.europa.eu/docs/en_GB/document_library/PIP_decision/WC500166523.pdf
49.Worm M, Reese I, Ballmer-Weber B, Beyer K, Bischoff SC, Classen M, et al. Guidelines on the management of IgE-mediated food allergies: S2k-Guidelines of the German Society for Allergology and Clinical Immunology (DGAKI) in collaboration with the German Medical Association of Allergologists (AeDA), the German Professional Association of Pediatricians (BVKJ), the German Allergy and Asthma Association (DAAB), German Dermatological Society (DDG), the German Society for Nutrition (DGE), the German Society for Gastroenterology, Digestive and Metabolic Diseases (DGVS), the German Society for Oto-Rhino-Laryngology, Head and Neck Surgery, the German Society for Pediatric and Adolescent Medicine (DGKJ), the German Society for Pediatric Allergology and Environmental Medicine (GPA), the German Society for Pneumology (DGP), the German Society for Pediatric Gastroenterology and Nutrition (GPGE), German Contact Allergy Group (DKG), the Austrian Society for Allergology and Immunology (AE-GAI), German Professional Association of Nutritional Sciences (VDOE) and the Association of the Scientific Medical Societies Germany (AWMF). Allergo J Int. 2015; 24:256-93.
50.Brien S, Lewith G, Walker AF, Middleton R, Prescott P, Bundy R. Bromelain as an adjunctive treatment for moderate-to-severe osteoarthritis of the knee: a randomized placebo-controlled pilot study. QJM. 2006; 99:841-50.
51.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.
52.Bromelain. Monograph. Altern Med Rev. 2010; 15:361-8.
This journal is a member of and subscribes to the principles of the Committee on Publication Ethics.