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Current Traditional Medicine

Editor-in-Chief

ISSN (Print): 2215-0838
ISSN (Online): 2215-0846

Review Article

Asafetida (Ferula asafoetida) and its Potential Risks on Respiratory Disorders

Author(s): Maryam Salavatifar, Mohaddese Mahboubi* and Sepideh Sotoudeh Nia

Volume 9, Issue 6, 2023

Published on: 27 January, 2023

Article ID: e281222212243 Pages: 9

DOI: 10.2174/2215083809666221228124031

Price: $65

Abstract

Ferula asafoetida is an endemic species in Iran and is rich in oleo-gum resin with high economic value in the world. One important application of F. assafoetida is its traditional use for the management of respiratory ailments. The aim of this review was to collect papers dealing with F. asafoetida oleo-gum resin in respiratory tract’s diseases in modern medicine. For preparing the manuscript the scientific databases (Google scholar, PubMed, Springer, Science Direct, Magiran), books, thesis, etc. were searched using the keywords of “Ferula asafoetida”, “Ferula scorodesma”, “Scorodesma foetida”, “Northex asafoetida” plus “respiratory tract”, "respiratory disorder" “infection”, “cough”, “trachea”, “traditional medicine” up to Feb 2022 and the collected data were summarized, analyzed, and discussed. The results of the investigation confirmed the traditional belief on the efficacy of Ferula asafoetida in the treatment of respiratory viral infection (Coronavirus, influenza), cigarette smoking, asthma, cough and cancer, but most studies were limited to in vitro. There was only one registered randomized, blinded, placebo controlled clinical trial for 300 mg F. asafoetida aqueous extract capsules (three times a day for 14 days) on 40 patients with COVID-19 without any published results. Although, the studies implied the efficacy of F. asafoetida in the treatment of respiratory treatments, but design large clinical studies for evaluating its efficacy and safety is essential in future investigations.

Graphical Abstract

[1]
Barzegar A, Salim MA, Badr P, et al. Persian asafoetida vs. sagapenum: Challenges and opportunities. Res J Pharmacogn 2020; 7(2): 71-80.
[2]
Mozaffararian V. A dictionary of Iranian plant names. Tehran, Iran: Farhang Moaser 2013; pp. 228-9.
[3]
Takeoka G. Instrumental analysis of food Flavors-4 volatile constituents of asafoetida. In: ACS Symposium Series. Washington, DC: American Chemical Society 2001; 794: pp. 33-44.
[4]
Zargari A. Medicinal Plants. Tehran: Tehran University Publication 1996; pp. 592-601.
[5]
Boghrati Z, Iranshahi M. Ferula species: A rich source of antimicrobial compounds. J Herb Med 2019; 16: 100244.
[http://dx.doi.org/10.1016/j.hermed.2018.10.009]
[6]
Salehi M, Naghavi MR, Bahmankar M. A review of Ferula species: Biochemical characteristics, pharmaceutical and industrial applications, and suggestions for biotechnologists. Ind Crops Prod 2019; 139: 111511.
[http://dx.doi.org/10.1016/j.indcrop.2019.111511]
[7]
Sultana A, Asma K, Rahman K, Rahman S. Oleo-gum-resin of Ferula asafoetida: A traditional culinary spice with versatile pharmacological activities. J Res J Rec Sci 2015; 2277: 2502.
[8]
Mahboubi M. The beneficial effects of Ferula asafoetida oleo-gum resin in gastrointestinal disorders. Bull Fac Pharm Cairo Univ 2022; 59(1): 50-63.
[http://dx.doi.org/10.54634/2090-9101.1025]
[9]
Aggarwal H, Kotwal N. Foods used as ethno-medicine in Jammu. Stud Ethno-Med 2009; 3(1): 65-8.
[http://dx.doi.org/10.1080/09735070.2009.11886340]
[10]
Rollinger JM, Steindl TM, Schuster D, et al. Structure-based virtual screening for the discovery of natural inhibitors for human rhinovirus coat protein. J Med Chem 2008; 51(4): 842-51.
[http://dx.doi.org/10.1021/jm701494b] [PMID: 18247552]
[11]
Evans WC. Trease and Evans Pharmacognosy. London: Saunders 2002; pp. 299-300.
[12]
Srinivasan K. Spices as influencers of body metabolism: An overview of three decades of research. Food Res Int 2005; 38(1): 77-86.
[http://dx.doi.org/10.1016/j.foodres.2004.09.001]
[13]
Appendino G, Maxia L, Bascope M, et al. A meroterpenoid NF-kappaB inhibitor and drimane sesquiterpenoids from Asafetida. J Nat Prod 2006; 69(7): 1101-4.
[http://dx.doi.org/10.1021/np0600954] [PMID: 16872156]
[14]
Kapoor L. CRC handbook of Ayurvedic medicinal plants. (1st ed.), Boca Raton: CRC press 2018.
[http://dx.doi.org/10.1201/9781351070997]
[15]
Mahran G, El Alfy T. Phytochemical study of volatile oil of Afghanian asafetida. Bull Facult Pharm 1973; 12(2): 101-7.
[16]
Singh YN. Traditional medicine in Fiji: Some herbal folk cures used by Fiji Indians. J Ethnopharmacol 1986; 15(1): 57-88.
[http://dx.doi.org/10.1016/0378-8741(86)90104-2] [PMID: 3713228]
[17]
Seabrook W. Adventures in arabia among the bedouins, druses, whirling dervishes, & Yezidee Devil Worshipers. In: Blue Ribbon Books. International kindle paper white 1927; 347.
[18]
Lilly E. Lilly's Hand Book of Pharmacy and Therapeutics: Hansebooks. 2016; p. 342.
[19]
Ahmad M, Zafar M, Shahzadi N, Yaseen G, Murphey TM, Sultana S. Ethnobotanical importance of medicinal plants traded in Herbal markets of Rawalpindi-Pakistan. J Herb Med 2018; 11: 78-89.
[http://dx.doi.org/10.1016/j.hermed.2017.10.001]
[20]
Arruda E, Cintra OA, Hayden FG. Respiratory tract viral infections. Trop Infect Dis. 2006; pp. 637-59.
[21]
Lee CL, Chiang LC, Cheng LH, et al. Influenza A (H1N1) antiviral and cytotoxic agents from Ferula assa-foetida. J Nat Prod 2009; 72(9): 1568-72.
[http://dx.doi.org/10.1021/np900158f] [PMID: 19691312]
[22]
Ghannadi A, Amree S. Volatile oil constituents of Ferula gummosa Boiss. from Kashan, Iran. J Essent Oil Res 2002; 14(6): 420-1.
[http://dx.doi.org/10.1080/10412905.2002.9699908]
[23]
Hassan MZ, Osman H, Ali MA, Ahsan MJ. Therapeutic potential of coumarins as antiviral agents. Eur J Med Chem 2016; 123: 236-55.
[http://dx.doi.org/10.1016/j.ejmech.2016.07.056] [PMID: 27484512]
[24]
Ghannadi A, Fattahian K, Shokoohinia Y, Behbahani M, Shahnoush A. Anti-viral evaluation of sesquiterpene coumarins from Ferula assa-foetida against HSV-1. Iran J Pharm Res 2014; 13(2): 523-30.
[PMID: 25237347]
[25]
Dissanayake K, Perera W. Medicinal importance of Ferula asafetida oligogum resins against infective diseases. J Med Plants Stud 2020; 8: 135-9.
[26]
Moradi M-T, Karimi A, Lorigooini Z, Pourgheysari B, Alidadi S. in vitro anti influenza virus activity, antioxidant potential and total phenolic content of twelve Iranian medicinal plants. Marmara Pharm J 2017; 21(4): 843-51.
[http://dx.doi.org/10.12991/mpj.2017.10]
[27]
Amini H, Naghavi M, Iranshahi M, Yazdanfar N, Nasiri J. Chemical composition of different parts of Ferula assa-foetida L. using GC-MS. Majallah-i Ulum-i Giyahan-i Zirai-i Iran 2019; 50(3): 89-96.
[28]
Kavoosi G, Rowshan V. Chemical composition, antioxidant and antimicrobial activities of essential oil obtained from Ferula assa-foetida oleo-gum-resin: Effect of collection time. Food Chem 2013; 138(4): 2180-7.
[http://dx.doi.org/10.1016/j.foodchem.2012.11.131] [PMID: 23497874]
[29]
Lan J, Ge J, Yu J, et al. Structure of the SARS-CoV-2 spike receptor-binding domain bound to the ACE2 receptor. Nature 2020; 581(7807): 215-20.
[http://dx.doi.org/10.1038/s41586-020-2180-5] [PMID: 32225176]
[30]
Carlos AJ, Ha DP, Yeh DW, et al. The chaperone GRP78 is a host auxiliary factor for SARS-CoV-2 and GRP78 depleting antibody blocks viral entry and infection. J Biol Chem 2021; 296: 100759.
[http://dx.doi.org/10.1016/j.jbc.2021.100759] [PMID: 33965375]
[31]
Subbarao K, Mahanty S. Respiratory virus infections: Understanding COVID-19. Immunity 2020; 52(6): 905-9.
[http://dx.doi.org/10.1016/j.immuni.2020.05.004] [PMID: 32497522]
[32]
Maurya AK, Mishra N. In silico validation of coumarin derivatives as potential inhibitors against main protease, NSP10/NSP16-methyltransferase, phosphatase and endoribonuclease of SARS CoV-2. J Biomol Struct Dyn 2021; 39(18): 7306-21.
[http://dx.doi.org/10.1080/07391102.2020.1808075] [PMID: 32835632]
[33]
Natesh J, Mondal P, Penta D, Abdul Salam AA, Meeran SM. Culinary spice bioactives as potential therapeutics against SARS-CoV-2: Computational investigation. Comput Biol Med 2021; 128: 104102.
[http://dx.doi.org/10.1016/j.compbiomed.2020.104102] [PMID: 33190011]
[34]
Rajapaksa R, Perera BT, Nisansala M, Perera W, Dissanayake K. Potential of inhibiting the receptor binding mechanism of sarscov- 2 using phytochemical extracts of medicinal herb; moleculer docking study. Nature reports 2020; 10: 17699.
[35]
DeMuri GP, Gern JE, Eickhoff JC, Lynch SV, Wald ER. Dynamics of bacterial colonization with Streptococcus pneumoniae, Haemophilus influenzae, and Moraxella catarrhalis during symptomatic and asymptomatic viral upper respiratory tract infection. Clin Infect Dis 2018; 66(7): 1045-53.
[http://dx.doi.org/10.1093/cid/cix941] [PMID: 29121208]
[36]
Durham AL, Adcock IM. The relationship between COPD and lung cancer. Lung Cancer 2015; 90(2): 121-7.
[http://dx.doi.org/10.1016/j.lungcan.2015.08.017] [PMID: 26363803]
[37]
Lennon FE, Salgia R. Mitochondrial dynamics: Biology and therapy in lung cancer. Expert Opin Investig Drugs 2014; 23(5): 675-92.
[http://dx.doi.org/10.1517/13543784.2014.899350] [PMID: 24654596]
[38]
Ito K, Caramori G, Adcock IM. Therapeutic potential of phosphatidylinositol 3-kinase inhibitors in inflammatory respiratory disease. J Pharmacol Exp Ther 2007; 321(1): 1-8.
[http://dx.doi.org/10.1124/jpet.106.111674] [PMID: 17021257]
[39]
Seltzer AP. Anti-smoking lozenge. J Natl Med Assoc 1975; 67(4): 311-3.
[PMID: 1159862]
[40]
Bagheri SM, Hedesh ST, Mirjalili A, Dashti-R MH. Evaluation of anti-inflammatory and some possible mechanisms of antinociceptive effect of Ferula assa-foetida oleo gum resin. J Evid Based Complementary Altern Med 2016; 21(4): 271-6.
[http://dx.doi.org/10.1177/2156587215605903] [PMID: 26427790]
[41]
Iranshahi M, Askari M, Sahebkar A, Litina HD. Evaluation of antioxidant, anti-inflammatory and lipoxygenase inhibitory activities of the prenylated coumarin umbelliprenin. Daru 2009; 17(2): 99-103.
[42]
Zamani Taghizadeh Rabe S, Iranshahi M, Mahmoudi M. In vitro anti-inflammatory and immunomodulatory properties of umbelliprenin and methyl galbanate. J Immunotoxicol 2016; 13(2): 209-16.
[http://dx.doi.org/10.3109/1547691X.2015.1043606] [PMID: 26004404]
[43]
Iranshahy M, Iranshahi M. Traditional uses, phytochemistry and pharmacology of asafoetida (Ferula assa-foetida oleo-gum-resin)-a review. J Ethnopharmacol 2011; 134(1): 1-10.
[http://dx.doi.org/10.1016/j.jep.2010.11.067] [PMID: 21130854]
[44]
Niimi A. Cough and asthma. Curr Respir Med Rev 2011; 7(1): 47-54.
[http://dx.doi.org/10.2174/157339811794109327] [PMID: 22081767]
[45]
Barnes PJ. Theophylline. Pharmaceuticals (Basel) 2010; 3(3): 725-47.
[http://dx.doi.org/10.3390/ph3030725] [PMID: 27713276]
[46]
Bayrami G, Boskabady MH, Iranshahi M, Gholamnezhad Z. Relaxant effects of asafoetida extract and its constituent umbelliprenin on guinea-pig tracheal smooth muscle. Chin J Integr Med 2013; 12: 1-6.
[http://dx.doi.org/10.1007/s11655-013-1550-3] [PMID: 24338082]
[47]
Rath B, Maharana CS, Rath S, Mahakul DJ. Evaluation of bronchoprotective effect of Ferula asafetida in Guinea pigs. IOSR J Dent Med Sci 2017; 16(3): 19-22.
[http://dx.doi.org/10.9790/0853-1603131922]
[48]
Khazdair MR, Boskabady MH, Kiyanmehr M, Hashemzehi M, Iranshahi M. The inhibitory effects of Ferula assafoetida on muscarinic receptors of guinea-pig tracheal smooth muscle. Jundishapur J Nat Pharm Prod 2015; 10(3): e20008.
[http://dx.doi.org/10.17795/jjnpp-20008]
[49]
Kiyanmehr M, Boskabady MH, Khazdair MR, Hashemzehi M. Possible mechanisms for functional antagonistic effect of Ferula assafoetida on muscarinic receptors in tracheal smooth muscle. Malays J Med Sci 2016; 23(1): 35-43.
[PMID: 27540324]
[50]
Gholamnejad Z, Byrami G, Boskabady MH, Iranshahi M. Possible mechanism(s) of the relaxant effect of asafoetida (Ferula assa-foetida) oleo-gum-resin extract on guinea-pig tracheal smooth muscle. Avicenna J Phytomed 2012; 2(1): 10-6.
[51]
Fatehi M, Farifteh F, Fatehi-Hassanabad Z. Antispasmodic and hypotensive effects of Ferula asafoetida gum extract. J Ethnopharmacol 2004; 91(2-3): 321-4.
[http://dx.doi.org/10.1016/j.jep.2004.01.002] [PMID: 15120456]
[52]
Esmaeili H, Sharifi M, Esmailidehaj M, Rezvani ME, Hafizibarjin Z. Vasodilatory effect of asafoetida essential oil on rat aorta rings: The role of nitric oxide, prostacyclin, and calcium channels. Phytomedicine 2017; 36: 88-94.
[http://dx.doi.org/10.1016/j.phymed.2017.10.002] [PMID: 29157833]
[53]
Lee JH, Choi S, Lee Y, et al. Herbal compound farnesiferol C exerts antiangiogenic and antitumor activity and targets multiple aspects of VEGFR1 (Flt1) or VEGFR2 (Flk1) signaling cascades. Mol Cancer Ther 2010; 9(2): 389-99.
[http://dx.doi.org/10.1158/1535-7163.MCT-09-0775] [PMID: 20103598]
[54]
Fong Y, Tang CC, Hu HT, et al. Inhibitory effect of trans-ferulic acid on proliferation and migration of human lung cancer cells accompanied with increased endogenous reactive oxygen species and β-catenin instability. Chin Med 2016; 11(1): 45.
[http://dx.doi.org/10.1186/s13020-016-0116-7] [PMID: 27733866]
[55]
Valiahdi SM, Iranshahi M, Sahebkar A. Cytotoxic activities of phytochemicals from Ferula species. Daru 2013; 21(1): 39.
[http://dx.doi.org/10.1186/2008-2231-21-39] [PMID: 23701832]
[56]
Khaghanzadeh N, Mojtahedi Z, Ramezani M, Erfani N, Ghaderi A. Umbelliprenin is cytotoxic against QU-DB large cell lung cancer cell line but anti-proliferative against A549 adenocarcinoma cells. Daru 2012; 20(1): 69.
[http://dx.doi.org/10.1186/2008-2231-20-69] [PMID: 23351548]
[57]
Kim KH, Lee HJ, Jeong SJ, et al. Galbanic acid isolated from Ferula assafoetida exerts in vivo anti-tumor activity in association with anti-angiogenesis and anti-proliferation. Pharm Res 2011; 28(3): 597-609.
[http://dx.doi.org/10.1007/s11095-010-0311-7] [PMID: 21063754]
[58]
Oh BS, Shin EA, Jung JH, et al. Apoptotic effect of galbanic acid via activation of caspases and inhibition of Mcl-1 in H460 non-small lung carcinoma cells. Phytother Res 2015; 29(6): 844-9.
[http://dx.doi.org/10.1002/ptr.5320] [PMID: 25753585]
[59]
Appendino G, Tagliapietra S, Mario Nano G, Jakupovic J. Sesquiterpene coumarin ethers from asafetida. Phytochemistry 1993; 35(1): 183-6.
[http://dx.doi.org/10.1016/S0031-9422(00)90530-2]
[60]
Nabiev AA, Khasanov TK, Malikov VM. A new terpenoid coumarin from Ferula kopetdaghensis. Chem Nat Compd 1982; 18(1): 44-6.
[http://dx.doi.org/10.1007/BF00581594]
[61]
Yang JR, An Z, Li ZH, Jing S, Qina HL. Sesquiterpene coumarins from the roots of Ferula sinkiangensis and Ferula teterrima. Chem Pharm Bull 2006; 54(11): 1595-8.
[http://dx.doi.org/10.1248/cpb.54.1595] [PMID: 17077560]
[62]
Abd El-Razek MH, Wu YC, Chang FR. Sesquiterpene coumarins from Ferula foetida. J Chin Chem Soc 2007; 54(1): 235-8.
[http://dx.doi.org/10.1002/jccs.200700035]
[63]
Caglioti L, Naef H, Arigoni D, Jeger O. Zur Kenntnis der sesquiterpene und azulene. Uer die inhaltsstoffe der asafoetida II. Farnesiferol B und C. Helv Chim Acta 1959; 42(7): 2557-70.
[http://dx.doi.org/10.1002/hlca.19590420727]

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