| Literature DB >> 35222678 |
Mansour Miran1, Keyvan Amirshahrokhi2, Yousef Ajanii3, Reza Zadali4, Maxwell W Rutter5, Ayesheh Enayati6, Farahnaz Movahedzadeh7,8.
Abstract
Aromatic oleo-gum-resin secreted from B. sacra, reputed as frankincense, is widely used in traditional medicine to treat Alzheimer's disease, gastric disorders, hepatic disorders, etc. Frankincense is also used in the cosmetic, perfume, and beverage and food industries. Frankincense is a rich resource for bioactive compounds, especially boswellic acids and derivatives. Although several reports have described frankincense's constituents and pharmacological activities, there is no comprehensive study that covers the valuable information on this species. Therefore, the current review will focus on the phytochemistry, traditional uses, and pharmacological activities of B. sacra.Entities:
Year: 2022 PMID: 35222678 PMCID: PMC8881160 DOI: 10.1155/2022/8779676
Source DB: PubMed Journal: Evid Based Complement Alternat Med ISSN: 1741-427X Impact factor: 2.629
Figure 1A photograph of frankincense gum resin taken from https://nagaadgums.com.
Figure 2Photographs of (a) tree growing in control habitat; (b) tree growing in wild habitats given by Khan et al. [5].
Figure 3The chemical composition of the volatile oil of B. sacra resin.
Figure 4Sesquiterpenoids isolated from B. sacra.
Figure 5Structure of isolated diterpenoids from B. sacra.
Figure 6Structure of isolated triterpenoids from B. sacra.
Figure 7Basic structure of triterpenoids in BAs.
Figure 8Structure of isolated boswellic acids and derivatives from B. sacra.
Figure 9Frankincense B. sacra essential oil (https://www.amazon.com).
The pharmacological profiles of B. sacra gum resin and its phytochemicals.
| Activity | Extract/compounds | Dose and treatment period | Model | Results | Mechanism | Reference |
|---|---|---|---|---|---|---|
| Anticancer | Essential oil, 11-keto-b-boswellic acid | 100 | T47D, MCF7, MDA-MB-231, MCF10-2A | Reduced cell viability, elevated cell death, suppressed cellular network formation, disrupted spheroid development of breast cancer cells, caused the breakdown of multicellular tumor spheroids (T47D), no cytotoxity on MCF10-2A, inhibited caspases in the MDA-MB-231, anti-invasive | (+) cleaved caspase-3(−) caspase-8 p43/p41, caspase-9 p37/p35, pro-caspase-3, Akt, PARP, ERK1/2(Thr202/Tyr204), cdk4, cyclin D1 | [ |
| Essential oil, 11-keto-b-boswellic acid | 100 | MIA PaCa-2, Panc-28, BxPC-3, DANG | [ | |||
| Essential oil | 30 | Heterotopic xenograft mouse | Suppressed viability, reduced cell growth, antiproliferative, antiapoptotic, induced cytotoxicity, reduced tumor volume, anti-tumor | (+) Caspase-3 activation, apoptosis(−) cyclin D1, cdk4, caspase-8 p43/p41, caspase-9p37/p35, procaspase-3, PARP, Akt ser (473), ERK1/2(Thr202/Tyr204), proliferating | [ | |
| 3 mL daily, oral, 25 months | A 52-year-old male with urothelial cell carcinoma | (+) No(−) AST, ALT, bilirubin, creatinine, BUN | ||||
| Methanolic extract, Boswellic acids | 6.25–100 | Human pancreatic (PANC1), colon (HCT116), lung adenocarcinoma (MOR), breast cancer MCF7 and MDA-MB-231, the human prostate cancer LNCaP, and SerBob cell lines | Inhibited tumor growth, anticancer, improved kidney and liver function, decreased tumor volume | (+)-(−)- | [ | |
| Anti-tumor cytotoxicity, inhibited cell viability | ||||||
| Anti-inflammatory | Essential oil | 0.3%, inhalation, 8 weeks | Ovalbumin-induced BALB/c mice allergic asthma | Reduced eosinophils, decreased goblet cell hyperplasia, inhibited hyperresponsiveness, anti-inflammatory, immunity | (+) Th1, IFN- | [ |
| Analgesic | Methanolic extract, essential oils, subfractions | 300 mg/kg, orally | Acetic acid-induced writhes and formalin-induced pain in mice | Analgesic, inhibited writhes, inhibited licking, and biting response | (+) No(−) No | [ |
| Antimicrobial | Essential oil | 0.1 ml, treat, 24 h |
| Antifungal, antimicrobial | (+) No(−) No | [ |
| Resin essential oil | 2.5, 5, 7.5, 10 g/100 ml1, 2, 3, 4 ml/100 ml, incubated, 15 days |
| Inhibited microbial and aflatoxins, enhanced fungal growth, inhibited aflatoxin biosynthesis and secretion pathway | (+) Mycelial dry weights(−) Inhibited fungal growth and aflatoxins production | [ | |
| Anti-Alzheimer | Essential oil, (+) pinene | 0.5 mg/ml, incubated, 15 min | AChE, Jack bean urease | Anti-Alzheimer's disease, protected stomach ulcers | (+) No(−) AChE, urease enzyme | [ |
| Diterpenoids of ethanolic extract | 10 | Glutamate-induced toxicity rat cortical neurons, human neuroblastoma SK-N-SH cellsAChE model | Neuroprotection | (+) No(−) No | [ | |
| Boswellic acids, ethyl acetate fraction | 0.75 mM, 0.23, 0.46,0.93 mg/ml, incubated, 20 min | Anti-Alzheimer's disease | (+) No(−) AChE | [ | ||
| Hepatoprotective | Diterpenoids of ethanolic extract | 10 | Paracetamol-induced HepG2 cells | Hepatoprotective, inhibited damage | (+) No(−) No | [ |
| Methanolic extract | 250, 500 and 1000 mg/kg, oraly, 28-day | Safety and toxicological studies on rat | Reduced mean cellular hemoglobin (MCH), induced hypochromic normocytic anemia, may not be safe to use | (+)-(−)- | [ | |
| Wound healing | Methanolic extracts | 10–20 | H2O2- induced injury on adult human dermal fibroblasts | Improved proliferation, migration, and wound healing process | (+) pERK/ERK(−) ROS | [ |
Note. (+): increased or activated; (−): decreased or inhibited.