Effects of Frankincense Compounds

Boswellia trees, found throughout the Middle East and parts of Africa and Asia, are the source of frankincense oil. Since antiquity, frankincense has been traded as a precious commodity, but it has also been used for the treatment of chronic disease, inflammation, oral health, and microbial infection.

  • inflammation
  • oral health
  • frankincense
  • infection
  • microbiology

1. Introduction

The increasing rate of antibiotics drug resistance, the cost of drugs, and the lack of access to healthcare systems for many people [1][2], especially in less developed countries, support the need for studying traditional medicines for sustainable, cost-effective therapeutic purposes. Frankincense is one of the common sources for traditional medicine [3]. The word “frankincense” is derived from an old French term “franc encens” and means “pure incense” or “pure and noble high-quality incense”. [4] Traditionally, frankincense gum has been burned for the pleasant fragrance it produces. It can be produced as a hardened resin or gum-like material discharged by the Boswellia sacra Flück. tree through cuts made in the trunk. Figure 1 shows the B. sacra tree, a member of the Boswellia genus. Frankincense has been traded and used as one of the most valuable materials since the beginning of written history [5].
Figure 1. Boswellia sacra in Wadi Dawkah, a natural park of frankincense-producing trees in Oman. Boswellia sacra photo from Wikimedia.org.
The Boswellia genus includes around thirty species and is usually found in the arid regions of tropical Africa, the Arabian Peninsula, and South Asia [6], where moisture is supplied by morning mist. For example, Boswellia serrata Roxb. is found in India, Boswellia sacra in the Arabian Peninsula, Boswellia papyrifera (Caill. ex Delile) Hochst. and Boswellia rivae Engl. in Ethiopia, Boswellia neglecta S.Moore in Eritrea, and Boswellia carterii and Boswellia frereana Birdw. in North Africa and Somalia [7]. However, frankincense is obtained mostly from B. frereanaB. sacraB. papyrifera, and B. serrata, which grow in Somalia, Yemen, Oman, India, and Pakistan [8]. Although many Boswellia species are known to produce frankincense, B. serrata (India), B. sacra (Oman), and B. carterii (Somalia) are the major sources of commercial frankincense [9]
The oleoresin from the Boswellia trees has been considered as a treasure for more than a millennium due to its aromatic and medicinal applications [4]. Frankincense resin is secreted as a milky-white, sticky liquid when the plant is injured, and it is also known as olibanum [10]. Olibanum is produced mainly by four different species of Boswellia, which are B. serrata, B. carteriiiB. frereana, and B. sacra [10][11]. The oleo gum resin produced by members of the genus Boswellia helps the plant defend against various infections and pests [12] and has been used in religious ceremonies, perfume production, and as a phytomedicine since antiquity [13]. Recently, the essential oils derived from frankincense are gaining high economic importance internationally for aromatherapy and perfumery [14].

2. Description of Frankincense Resins, Oils, and Boswellic Acids

The resin is available in yellowish, bluish, and greenish shades, and is composed of 3–8% volatile oils containing various terpenes and sesquiterpenes, 60–70% resin, and 27–35% gum [15]. In the mid-twentieth century, it was found that the gum contains two types of polysaccharides [16]. More recently, the composition showed that the monosaccharides present were predominantly galactose, arabinose, and glucuronic acid, along with small amounts of rhamnose and glucose [17]. However, recent scientific advancements allow us to identify the molecular content of diverse frankincense products such as incense mixtures, components of conventional medicines, and archaeological specimens.
The concentrated volatile, aromatic liquid obtained from different parts of the plant such as roots, seeds, leaves, flowers, and resins is called an essential oil. Mostly, a distillation process is used to extract the essential oil from Boswellia plants [18]. The main chemical constituents of frankincense oil are pentacyclic triterpenoids [19], tetracyclic triterpenoids [20], and a variety of other oils [21]. The most common characteristic and intensely studied component in frankincense are the pentacyclic triterpenoids [7][22].
The major active components of frankincense are the boswellic acids (BA), which are extracted from the woody parts of different Boswellia trees. The representative phytochemicals are β-boswellic acid, acetyl-β-boswellic acid (ABA), 11-keto-β-boswellic acid (KBA), 3-acetyl-11-keto-β-boswellic acid (AKBA), α-boswellic acid, and acetyl-α-boswellic acid. Figure 2 shows the chemical structure of the main BA.
Figure 2. Chemical structure of common boswellic acids found in frankincense. Two-dimensional chemical structures were obtained from Pub Chem. Pub Chem CIDs are as follows: α-boswellic acid, 637234; acetyl-α-boswellic acid, 15181201; β-boswellic acid, 168928; acetyl-β-boswellic acid (ABA), 11386458; 11-keto-β-boswellic acid (KBA), 9847548; 3-acetyl-11-keto-β-boswellic acid (AKBA), 11168203.
The chemical composition and yield vary according to different factors such as the geographical region of the tree, the wood surface area, the collection season, the collection method, the age of the tree, and the storage conditions [23]. For instance, the gum resin from B. serrata has relatively similar quantities of 11-keto-β-boswellic acid (3–4.7%) and acetyl-11-keto-β-boswellic acid (2.2–2.9%) [7]. However, the resin from B. carterii contains 0.5% 11-keto-β-boswellic acid and 3.3% acetyl-11-keto-β-boswellic acid [7].
The gum resin of B. carterii reported from Somalia has α-thujene (19.2%), sabinene (9.4%), limonene (7.8%), and α-pinene (7.2%) as the main constituents [24]. This is a native plant of the Red Sea region of North-East Africa, where it is abundant in Somalia and Ethiopia. Other studies on the composition of the oleo resin reported different components in different concentrations. For instance, Wahab reported that the oil contains 62.1% esters, 15.4% alcohols, 9.9% monoterpene hydrocarbons, and 7.1% diterpenes [25], and Wang et al. reported octyl acetate (60.0%), octanol (12.7%), and p-cymene (8.7%) [26]. The gas chromatography–mass spectrometry (GC/MS) analysis of the hydro-distillate of B. carterii resin showed the presence of 40 different constituents. The major constituents were verticiol (14.48%), isobutylcyclopentane (12.25%), n-octyl acetate (9.20%), and 9-oxabicyclo-[6.1.0]-non-3-yne (9.12%) [27]. However, the composition of the resin differs due to different factors such as climate, geography, season of the year, and the extraction conditions. This notion is corroborated by a report from Chen et al. (2013) which observed low concentrations of the above components [28], while other studies reported higher concentrations of n-octyl acetate [28][29].
Boswellia dalzielii, which grows in West Africa, is an understudied species. However, a study conducted using essential oil from 21 oleoresin samples from northern Nigeria and two samples from Ghana revealed that α-pinene was the dominant component (21.7–76.6%), followed by α-thujene (2.0–17.6%), myrcene (up to 35.2%), p-cymene (0.3–15.6%), and limonene (1.1–32.9%) [30]. It was reported that out of the 29 compounds obtained from the essential oil from leaves, α-pinene was the dominant component (45.7%) [31]. On the other hand, it was also reported that out of 50 compounds isolated, δ-3-carene (27.7%) was the dominant one [32].

3. Modern Medicinal Uses of Frankincense

Many plant components from Boswellia are used to treat chronic diseases with comparatively few side effects [33][34]. Indian traditional medicine practice narrates that Boswellia decoctions were used to treat various gastrointestinal tract conditions such as diarrhea, flatulence, alimentary stoppage, and vomiting [35][36][37][38]. It was believed that the decoctions contain active ingredients from Boswellia, which are useful in treating the above-mentioned diseases. Furthermore, the extract was used to treat bronchitis, asthma, hoarseness, dyspnea, cough, and cold [39][40].
The gum extracts or resins from Boswellia sp. and their triterpenes, especially BA, have attracted the attention of pharmacologists, medicinal chemists, and biochemists as therapeutic agents due to their efficacy in treating rheumatoid arthritis and chronic inflammation without side effects and toxicity. The gum exudate obtained from the bark of the tree B. serrata, also called Indian olibanum, has been extensively used in the treatment of arthritis, asthma, ulcers, and skin diseases by practitioners of Indian traditional medicine [15][25]. It has also been widely used in various formulations for the treatment of inflammation related disorders in the past decade [15][41]. One study analyzed the effects of gum resins of B. serrata (900 mg daily divided in three doses for 6 weeks) on human patients suffering from chronic colitis [33][42]. The authors found that out of 20 patients treated with Boswellia gum resin, 18 patients showed an improvement in one or more parameters, including stool properties, histopathology and scanning electron microscopy characterization, hemoglobin, serum ion, calcium, phosphorus, proteins, total leukocytes, and eosinophils [33][42]. The control group (10 patients) was given sulfasalazine at a dose of 1 g three times a day for 6 weeks. The authors reported that 6 out of 10 patients in the control group showed similar improvements with the same parameters tested in the B. serrata group. This study demonstrates that a gum resin preparation from B. serrata might be effective in the treatment of chronic colitis, with minimal side effects [33][42]. The same research group evaluated the effects of B. serrata gum resin on the treatment of patients with bronchial asthma [40]. Their data demonstrated that 70% of patients treated with 300 mg thrice daily for 6 weeks showed improvement of disease, evident by the disappearance of physical symptoms and signs such as dyspnea, rhonchi, number of attacks, as well as a decrease in eosinophilic counts. The control group (treated with placebo) only showed 27% of improvements in symptoms [40]. These data imply that gum resin from B. serrata could serve as a pharmacological agent in the treatment of bronchial asthma.
Gum resin from B. serrata was reported to be a potential remedy for inflammation, and it has been used as a folk medicine for topical and systemic inflammatory diseases for centuries [15]. The oleo gum resin of B. carterii has been used in folk medicine to treat cough and asthma and as an embalming fluid for human corpses. In addition, it has been used as an incense, respiratory antiseptic, and diuretic stimulant [25].
The oleo gum resin of B. serrata and B. carterii were also used in traditional medicine in different countries to treat rheumatic and other inflammatory diseases, including Crohn’s disease and ulcerative colitis [42][43][44]. However, B. serrata was reported to be the least effective in recurrent infections [45]. In addition, frankincense extracts and oils were used as antiseptic agents in mouthwash and also used to treat cough and asthma [43]. Furthermore, recent studies on animals and humans have demonstrated the efficacy of resin gum of B. serrata to treat inflammatory bowel disease, asthma, osteoarthritis, and rheumatoid arthritis [42][46][47].
Though frankincense has been known for its medicinal properties since antiquity, it is still widely used in modern medical treatment. In 2010, Moussaieff and Mechoulam reviewed Boswellia resin constituents in vitro, in vivo, and in clinical trials studies [48]. Indeed, in Ayurvedic medicine, different parts of the Boswellia tree and derived extracts are used for the treatment of respiratory, gastrointestinal, immune system, and skin conditions. Most of the published work focuses on the pharmacological activities of boswellic acids, specifically on their anti-inflammatory, analgesic, and anti-arthritic properties. As an example, there is growing evidence to support the clinical efficacy of Boswellia in osteoarthritis patients. However, there is inadequate evidence to demonstrate the clinical efficacy in rheumatoid arthritis patients [49]. The application of frankincense to treat different diseases of recent times is discussed below and summarized in Figure 3. Frankincense has been used to treat both infections and chronic diseases.
Figure 3. Modern medicinal uses of Boswellia.

4. Antimicrobial Activity of Frankincense

In general, the bioactive natural compounds produced by different plants are considered better alternatives to synthetic antimicrobial and antioxidant agents. Different compounds obtained from Boswellia resins, particularly BA and their derivatives, exhibited diverse biological activities. As considered in this section, the antimicrobial effects can vary depending on the study and the amount of bioactive compounds present in the frankincense extracts.

The oleo gum resin essential oils from B. carterii (Somalia), B. papyrifera (Ethiopia), B. serrata (India), and B. rivae (Ethiopia) were individually tested against different fungi and Gram-positive and Gram-negative bacteria. The essential oils exhibited significant antifungal activity against both C. albicans and C. tropicalis, with the essential oils from B. carterii and B. papyrifera showing the best activity [50]. The MIC values for C. albicans and C. tropicalis were 12.86 and 12.86 μg/mL (B. serrata), 6.16 and 6.16 μg/mL (B. carterii), 6.09 and 6.09 μg/mL (B. papyrifera), and 2.65 and 27.38 μg/mL (B. rivae), respectively, compared with the MIC of 0.15 μg/mL for amphoterecin B. The essential oil of B. rivae resin exhibited the best activity against C. albicans [50]. Limonene present in the essential oils is thought to be responsible for the antifungal activity [51], since oleo gum resin essential oils without limonene lack antifungal activity. The oleo gum resins also showed significant antibacterial effects against Gram-positive S. aureus and S. epidermidis, with MIC values ranging from 3.52 to 107.20 μg/mL. These values can be compared with the MIC of 1 μg/mL for vancomycin and 2 μg/mL for amikacin used as controls in the experiments [50]. The frankincense compounds against Gram-negative E. coli and P. aeruginosa showed MIC ranging from 6.60 to 107.18 μg/mL, compared to the vancomycin MIC of 10 and 5 μg/mL for E. coli and P. aeruginosa, respectively. It is noteworthy that some of the frankincense compounds had antimicrobial effects at concentrations that were comparable or very close to concentrations of the standard antibiotics used in the in vitro experiments. Future studies might confirm and expand the results to in vivo and clinical models.

Dental caries and periodontitis remain two of the major oral diseases that affect more than half of the global population [52]. Periodontitis is often referred as a common inflammatory disease in humans. The etiology of these diseases has been linked to certain bacterial species, plaque and biofilm formation, and the resultant inflammatory states. Current therapies for treating periodontal disease place an emphasis on biofilm removal. This is exercised via a combination of mechanical (such as scaling and root planing) and antibiotic treatments. However, these treatment modalities are still unable to fully remove biofilms. This has led to an interest in incorporating herbal extracts into current treatment regimens.

Many studies have been performed using the resin of B. serrata. As noted above, this resin contains boswellic acid, which are the active components in its anti-inflammatory effects. In addition, both the boswellic acid and the essential oils of B. serrata exhibit antimicrobial properties. Of the four major boswellic acids, acetyl-11-keto-β-boswellic acid (AKBA), has consistently demonstrated the greatest antibacterial effects. In fact, several studies have determined that AKBA is the most active component in the resin of B. serrata and other Boswellia species [53].

In terms of antibacterial effectiveness, AKBA isolated from B. serrata demonstrated activity against Streptococcus mutans, Enterococcus faecalis, Enterococcus faecium, Actinomyces viscosus, Streptococcus sanguinis, Fusobacterium nucleatum, Prevotella intermedia, and Porphyromonas gingivalis. Furthermore, the post-antibiotic effects of AKBA were determined to be greater than those of ciprofloxacin, and AKBA was also shown to inhibit biofilms of the cariogenic bacteria S. mutans [53].

In a double-blinded, randomized clinical trial, the effectiveness of traditional scaling and root planing methods were compared to the use of B. serrata extract or powder [54]. The results indicated that the addition of B. serrata extract or powder to traditional scaling and root planing treatments leads to better gingival health as measured by gingival, plaque, and bleeding indices, as well as probed pocket depths [54]. The authors concluded that the anti-inflammatory properties of B. serrata extract had results comparable or even superior to traditional scaling and root planing treatments. Given its antibacterial, antifungal, and antioxidant properties, it is not surprising that frankincense also has promising beneficial effects on oral health.

5. Anti-Inflammatory Effects of Frankincense

Many patients consuming non-steroidal anti-inflammatory drugs (NSAID) suffer from adverse effects of the drugs on the gastrointestinal or cardiovascular systems. Many efforts have been made to develop drugs that avoid these complications, but the goal is still far from being achieved. Hence, it is necessary to search for novel, alternative drugs. In this context, B. serrata and other Boswellia species have gained prominence as potential alternatives as anti-inflammatory herbal remedies. The anti-inflammatory properties of boswellic acids have been well-established by several studies with cells in vitro, and preclinical, and clinical trials [4][7].
Studies on animals and humans have shown the anti-inflammatory potential of B. serrata gum resin to treat different inflammatory disorders such as inflammatory bowel disease, rheumatoid arthritis, osteoarthritis, and asthma [46]. Corticosteroids are essential to control cerebral edema but they also cause severe negative impacts. In contrast, the gum resin of B. serrata was found to control the peritumoral brain edema associated with glioma [55].
The anti-inflammatory activity of B. serrata is due to the presence of α- and β-boswellic acid and other pentacyclic triterpenic acids. These compounds inhibit pro-inflammatory processes by acting on 5-lipooxygenase and cyclo-oxygenase and on the complement system [39][56][57]. Inhibition of prostaglandin synthesis plays only a minimal role in the anti-inflammatory effect of BAs. However, inhibition of 5-lipoxygenase by BA decreases production of leukotrienes, whereas chronic inflammatory diseases are associated with increased leukotriene activity [56].
BA is involved in the inhibition of inflammation induced by factors such as histamine, prostaglandins, leukotriene, 5-lipooxygenase, human leukocyte elastase, cytokines, tumor necrosis factor, and free oxygen radicals. Figure 4 summarizes the inhibitory effects induced by BAs. To demonstrate the anti-inflammatory activity of the gum resin of Boswellia species, experiments were conducted in animal models. Carrageenan-induced mouse paw edema and rat pleurisy models were employed to test the effectiveness of defined BAs in vivo. This study also demonstrated the suppression of PGE2 formation by BAs via interference with mPGES1, which may represent a biochemical basis for the anti-inflammatory effectiveness of BAs [58].
Figure 4. Schematic diagram showing anti-inflammatory effects of boswellic acids and Boswellia extracts.
Some limitations of this study must be considered. First, more studies are required to elucidate the antimicrobial and anti-inflammatory mechanisms exerted by frankincense extracts and compounds. Secondly, more studies, including pre-clinical and randomized clinical trials, are needed to better understand the beneficial effects of frankincense extracts and compounds on human health. 

This entry is adapted from 10.3390/molecules27134174

References

  1. Yu, D.; Ryu, K.; Zhi, S.; Otto, S.J.G.; Neumann, N.F. Naturalized Escherichia coli in Wastewater and the Co-evolution of Bacterial Resistance to Water Treatment and Antibiotics. Front. Microbiol. 2022, 13, 810312.
  2. Ventola, C.L. The antibiotic resistance crisis: Part 1: Causes and threats. Pharm. Ther. 2015, 40, 277–283.
  3. Al-Yasiry, A.R.; Kiczorowska, B. Frankincense—Therapeutic properties. Postepy Hig. Med. Dosw. (Online) 2016, 70, 380–391.
  4. Efferth, T.; Oesch, F. Anti-inflammatory and anti-cancer activities of frankincense: Targets, treatments and toxicities. Semin. Cancer Biol. 2022.
  5. Van Wyk, B.E. A review of commercially important African medicinal plants. J. Ethnopharmacol. 2015, 176, 118–134.
  6. Eslamieh, J. Cultivation of Boswellia, 2nd ed.; A Book’s Mind: Fort Collins, CO, USA, 2017.
  7. Abdel-Tawab, M.; Werz, O.; Schubert-Zsilavecz, M. Boswellia serrata: An overall assessment of in vitro, preclinical, pharmacokinetic and clinical data. Clin. Pharmacokinet. 2011, 50, 349–369.
  8. Britannica, The Editors of Encyclopaedia. Frankincense. Available online: https://www.britannica.com/topic/frankincense (accessed on 21 February 2022).
  9. Bokelmann, J.M. Medicinal Herbs in Primary Care: An Evidence-Guided Reference for Healthcare Providers. In Frankincense/Boswellia (Boswellia serrata/sacra/carterii): Bark Resin; Bokelmann, J.M., Ed.; Medicinal Herbs in Primary Case; Elsevier: Amsterdam, The Netherlands, 2021; pp. 351–360.
  10. Shah, S.A.; Rathod, I.S.; Suhagia, B.N.; Pandya, S.S.; Parmar, V.K. A simple high-performance liquid chromatographic method for the estimation of boswellic acids from the market formulations containing Boswellia serrata extract. J. Chromatogr. Sci. 2008, 46, 735–738.
  11. Chevrier, M.R.; Ryan, A.E.; Lee, D.Y.; Zhongze, M.; Wu-Yan, Z.; Via, C.S. Boswellia carterii extract inhibits TH1 cytokines and promotes TH2 cytokines in vitro. Clin. Diagn. Lab. Immunol. 2005, 12, 575–580.
  12. Barnett, J.R.; Langenheim, J.H. Plant resins: Chemistry, evolution, ecology and ethnobotany. Ann. Bot. 2004, 93, 2.
  13. Hughes, L. The Funerals of the Russian Emperors and Empresses. In Monarchy and Religion: The Transformation of Royal Culture in Eighteenth-Century Europe; Schaich, M., Ed.; Oxford University Press: Oxford, UK, 2007; pp. 395–419.
  14. Berhanu, Y.; Vedeld, P.; Angassa, A.; Aune, J.B. The contribution of frankincense to the agro-pastoral household economy and its potential for commercialization—A case from Borana, southern Ethiopia. J. Arid Environ. 2020, 186, 104423.
  15. Yuan, G.; Wahlqvist, M.L.; He, G.; Yang, M.; Li, D. Natural products and anti-inflammatory activity. Asia Pac. J. Clin. Nutr. 2006, 15, 143–152.
  16. Jones, J.K.N.; Nunn, J.R. The Structure of Frankincense Gum. J. Am. Chem. Soc. 1955, 77, 5745–5746.
  17. Hosain, N.A.; Ghosh, R.; Bryant, D.L.; Arivett, B.A.; Farone, A.L.; Kline, P.C. Isolation, structure elucidation, and immunostimulatory activity of polysaccharide fractions from Boswellia carterii frankincense resin. Int. J. Biol. Macromol. 2019, 133, 76–85.
  18. Amri, A.S.L.; Jesil, A.; Salim, A.; Saravanam, A.M. Extraction of Essential Oil from Frankincense Using Steam Distillation. Int. J. Trend Res. Dev. 2019, 6, 3.
  19. Siddiqui, M.Z. Boswellia serrata, a potential antiinflammatory agent: An overview. Indian J. Pharm. Sci. 2011, 73, 255–261.
  20. Wang, F.; Li, Z.L.; Cui, H.H.; Hua, H.M.; Jing, Y.K.; Liang, S.W. Two new triterpenoids from the resin of Boswellia carterii. J. Asian Nat. Prod. Res. 2011, 13, 193–197.
  21. Ren, P.; Ren, X.; Cheng, L.; Xu, L. Frankincense, pine needle and geranium essential oils suppress tumor progression through the regulation of the AMPK/mTOR pathway in breast cancer. Oncol. Rep. 2018, 39, 129–137.
  22. Shen, T.; Lou, H.X. Bioactive constituents of myrrh and frankincense, two simultaneously prescribed gum resins in chinese traditional medicine. Chem. Biodivers. 2008, 5, 540–553.
  23. Vuddanda, P.R.; Singh, S.; Velaga, S. Boswellic acid—Medicinal use of an ancient herbal remedy. J. Herb. Med. 2016, 6, 8.
  24. Chiavari, G.; Galletti, G.C.; Piccaglia, R.; Mohamud, M.A. Differentiation between Resins Boswellia carterii and Boswellia frereana (Frankincense) of Somali Origin. J. Essent. Oil Res. 1990, 3, 2.
  25. Wahab, S.M.; Aboutabl, E.A.; El-Zalabani, S.M.; Fouad, H.A.; De Pooter, H.L.; El-Fallaha, B. The essential oil of olibanum. Planta Med. 1987, 53, 382–384.
  26. Wang, W.; Zhu, Y.; Liu, L.; Ling, D.; Qin, X.; Tian, J. Analysis of the Chemical Constituents of Essential Oil of Boswellia carterii Birdwood from Somali. Chin. J. Pharm. Anal. 1993, 13, 3.
  27. Mohamed, A.A.; Ali, S.I.; Kabiel, H.F.; Hegazy, A.K.; Kord, M.A.; EL-Baz, F.K. Assessment of Antioxidant and Antimicrobial Activities of Essential Oil and Extracts of Boswellia carterii Resin. Int. J. Pharmacogn. Phytochem. Res. 2015, 7, 8.
  28. Chen, Y.; Zhou, C.; Ge, Z.; Liu, Y.; Liu, Y.; Feng, W.; Li, S.; Chen, G.; Wei, T. Composition and potential anticancer activities of essential oils obtained from myrrh and frankincense. Oncol. Lett. 2013, 6, 1140–1146.
  29. Mikhaeil, B.R.; Maatooq, G.T.; Badria, F.A.; Amer, M.M. Chemistry and immunomodulatory activity of frankincense oil. Z. Nat. C 2003, 58, 230–238.
  30. DeCarlo, A.; Johnson, S.; Okeke-Agulu, K.I.; Dosoky, N.S.; Wax, S.J.; Owolabi, M.S.; Setzer, W.N. Compositional analysis of the essential oil of Boswellia dalzielii frankincense from West Africa reveals two major chemotypes. Phytochemistry 2019, 164, 24–32.
  31. Dimas Kubmarawa, I.A.O.; Okorie, D.A.; Olawore, N.O.; Kasali, A.A. Constituents of the Essential Oils of Boswellia dalzielii Hutch. from Nigeria. J. Essent. Oil Res. 2011, 18, 2.
  32. Kohoude, M.J.; Gbaguidi, F.; Agbani, P.; Ayedoun, M.A.; Cazaux, S.; Bouajila, J. Chemical composition and biological activities of extracts and essential oil of Boswellia dalzielii leaves. Pharm. Biol. 2017, 55, 33–42.
  33. Gupta, I.; Parihar, A.; Malhotra, P.; Gupta, S.; Ludtke, R.; Safayhi, H.; Ammon, H.P. Effects of gum resin of Boswellia serrata in patients with chronic colitis. Planta Med. 2001, 67, 391–395.
  34. Roy, N.K.; Parama, D.; Banik, K.; Bordoloi, D.; Devi, A.K.; Thakur, K.K.; Padmavathi, G.; Shakibaei, M.; Fan, L.; Sethi, G.; et al. An Update on Pharmacological Potential of Boswellic Acids against Chronic Diseases. Int. J. Mol. Sci. 2019, 20, 4101.
  35. Iram, F.; Khan, S.A.; Husain, A. Phytochemistry and potential therapeutic actions of Boswellic acids: A mini-review. Asian Pac. J. Trop. Biomed. 2017, 7, 513–523.
  36. Padhi, M.; Mahapatra, S. Boswellia serrata: A review of its traditional uses, phytochemistry and pharmacology. Int. Rev. Biophys. Chem. (IREBIC) 2013, 4, 74–83.
  37. Catanzaro, D.; Rancan, S.; Orso, G.; Dall’Acqua, S.; Brun, P.; Giron, M.C.; Carrara, M.; Castagliuolo, I.; Ragazzi, E.; Caparrotta, L.; et al. Boswellia serrata Preserves Intestinal Epithelial Barrier from Oxidative and Inflammatory Damage. PLoS ONE 2015, 10, e0125375.
  38. Borrelli, F.; Capasso, F.; Capasso, R.; Ascione, V.; Aviello, G.; Longo, R.; Izzo, A.A. Effect of Boswellia serrata on intestinal motility in rodents: Inhibition of diarrhoea without constipation. Br. J. Pharmacol. 2006, 148, 553–560.
  39. Ammon, H.P. Boswellic acids in chronic inflammatory diseases. Planta Med. 2006, 72, 1100–1116.
  40. Gupta, I.; Gupta, V.; Parihar, A.; Gupta, S.; Ludtke, R.; Safayhi, H.; Ammon, H.P. Effects of Boswellia serrata gum resin in patients with bronchial asthma: Results of a double-blind, placebo-controlled, 6-week clinical study. Eur. J. Med. Res. 1998, 3, 511–514.
  41. Shah, B.A.; Qazi, G.N.; Taneja, S.C. Boswellic acids: A group of medicinally important compounds. Nat. Prod. Rep. 2009, 26, 72–89.
  42. Gupta, I.; Parihar, A.; Malhotra, P.; Singh, G.B.; Ludtke, R.; Safayhi, H.; Ammon, H.P. Effects of Boswellia serrata gum resin in patients with ulcerative colitis. Eur. J. Med. Res. 1997, 2, 37–43.
  43. Banno, N.; Akihisa, T.; Yasukawa, K.; Tokuda, H.; Tabata, K.; Nakamura, Y.; Nishimura, R.; Kimura, Y.; Suzuki, T. Anti-inflammatory activities of the triterpene acids from the resin of Boswellia carteri. J. Ethnopharmacol. 2006, 107, 249–253.
  44. Langmead, L.; Rampton, D.S. Review article: Complementary and alternative therapies for inflammatory bowel disease. Aliment. Pharmacol. Ther. 2006, 23, 341–349.
  45. Holtmeier, W.; Zeuzem, S.; Preiss, J.; Kruis, W.; Bohm, S.; Maaser, C.; Raedler, A.; Schmidt, C.; Schnitker, J.; Schwarz, J.; et al. Randomized, placebo-controlled, double-blind trial of Boswellia serrata in maintaining remission of Crohn’s disease: Good safety profile but lack of efficacy. Inflamm. Bowel Dis. 2011, 17, 573–582.
  46. Poeckel, D.; Werz, O. Boswellic acids: Biological actions and molecular targets. Curr. Med. Chem. 2006, 13, 3359–3369.
  47. Krieglstein, C.F.; Anthoni, C.; Rijcken, E.J.; Laukotter, M.; Spiegel, H.U.; Boden, S.E.; Schweizer, S.; Safayhi, H.; Senninger, N.; Schurmann, G. Acetyl-11-keto-beta-boswellic acid, a constituent of a herbal medicine from Boswellia serrata resin, attenuates experimental ileitis. Int. J. Colorectal. Dis. 2001, 16, 88–95.
  48. Moussaieff, A.; Mechoulam, R. Boswellia resin: From religious ceremonies to medical uses; a review of in-vitro, in-vivo and clinical trials. J. Pharm. Pharmacol. 2010, 61, 1281–1293.
  49. Yu, G.; Xiang, W.; Zhang, T.; Zeng, L.; Yang, K.; Li, J. Effectiveness of Boswellia and Boswellia extract for osteoarthritis patients: A systematic review and meta-analysis. BMC Complement. Med. Ther. 2020, 20, 225.
  50. Camarda, L.; Dayton, T.; Di Stefano, V.; Pitonzo, R.; Schillaci, D. Chemical composition and antimicrobial activity of some oleogum resin essential oils from Boswellia spp. (Burseraceae). Ann. Chim. 2007, 97, 837–844.
  51. Shao, Y.; Ho, C.T.; Chin, C.K.; Badmaev, V.; Ma, W.; Huang, M.T. Inhibitory activity of boswellic acids from Boswellia serrata against human leukemia HL-60 cells in culture. Planta Med. 1998, 64, 328–331.
  52. Eke, P.I.; Borgnakke, W.S.; Genco, R.J. Recent epidemiologic trends in periodontitis in the USA. Periodontology 2000 2020, 82, 257–267.
  53. Raja, A.F.; Ali, F.; Khan, I.A.; Shawl, A.S.; Arora, D.S. Acetyl-11-keto-beta-boswellic acid (AKBA); targeting oral cavity pathogens. BMC Res. Notes 2011, 4, 406.
  54. Khosravi Samani, M.; Mahmoodian, H.; Moghadamnia, A.; Poorsattar Bejeh Mir, A.; Chitsazan, M. The effect of Frankincense in the treatment of moderate plaque-induced gingivitis: A double blinded randomized clinical trial. Daru 2011, 19, 288–294.
  55. Winking, M.; Sarikaya, S.; Rahmanian, A.; Jodicke, A.; Boker, D.K. Boswellic acids inhibit glioma growth: A new treatment option? J. Neurooncol. 2000, 46, 97–103.
  56. Ammon, H.P. Modulation of the immune system by Boswellia serrata extracts and boswellic acids. Phytomedicine 2010, 17, 862–867.
  57. Knaus, U.; Wagner, H. Effects of boswellic acid of Boswellia serrata and other triterpenic acids on the complement system. Phytomedicine 1996, 3, 77–80.
  58. Siemoneit, U.; Koeberle, A.; Rossi, A.; Dehm, F.; Verhoff, M.; Reckel, S.; Maier, T.J.; Jauch, J.; Northoff, H.; Bernhard, F.; et al. Inhibition of microsomal prostaglandin E2 synthase-1 as a molecular basis for the anti-inflammatory actions of boswellic acids from frankincense. Br. J. Pharmacol. 2011, 162, 147–162.
More
This entry is offline, you can click here to edit this entry!
Top