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ORIGINAL ARTICLE |
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Year : 2016 | Volume
: 12
| Issue : 47 | Page : 471-474 |
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Assessment of In vitro antibacterial activity and cytotoxicity effect of Nigella sativa oil
Ayse Ruveyda Ugur1, Hatice Turk Dagi2, Bahadir Ozturk3, Gulsum Tekin3, Duygu Findik2
1 Department of Medical Microbiology, Konya Education and Research Hospital, Konya, Turkey 2 Department of Medical Microbiology, Faculty of Medicine, Selcuk University, Konya, Turkey 3 Department of Biochemistry, Faculty of Medicine, Selcuk University, Konya, Turkey
Date of Submission | 12-Oct-2015 |
Date of Decision | 30-Nov-2015 |
Date of Web Publication | 30-Sep-2016 |
Correspondence Address: Ayse Ruveyda Ugur Department of Medical Microbiology, Konya Education and Research Hospital, Meram Yeniyol Caddesi No. 97, 42090 Meram, Konya Turkey
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0973-1296.191459
Abstract | | |
Background: Methicillin resistance is a serious health concern since it has spread among Staphylococcus aureus and coagulase-negative Staphylococci (CoNS) that are frequent community and nosocomial pathogens worldwide. Methicillin-resistant strains are often resistant to other classes of antibiotics, making their treatment difficult. Nigella sativa oil is known to be active against Gram-positive cocci, yet its in vitro cytotoxicity is rarely investigated, is a proper and powerful candidate for treatment of methicillin-resistant isolates. Objectives: The aim of this study is to evaluate the in vitro antibacterial activity and cytotoxicity effect of N. sativa oil. Materials and Methods: The minimal inhibitory concentrations (MICs) of N. sativa oil were determined by broth microdilution method against four different American Type Culture Collection strains, 45 clinical isolates of methicillin-resistant S. aureus (MRSA), and 77 methicillin-resistant CoNS (MRCoNS). The effects of different dilutions (0.25 μg/mL, 0.5 μg/mL, and 1 μg/mL) of N. sativa oil on the proliferation of gingival fibroblasts were evaluated. Results: The MIC values of N. sativa oil against clinical isolates of Staphylococci were between <0.25 μg/mL and 1.0 μg/mL. Compared to the control group, there was no cytotoxic effect on the proliferation of the gingival fibroblasts. Conclusion: In the present study, the oil of N. sativa was very active against MRSA and MRCoNS and had no in vitro cytotoxicity at relevant concentrations. These findings emphasize that there is a requirement for further clinical trials on N. sativa oil for "safe" medical management of infections caused by methicillin-resistant Staphylococci. Abbreviation used: ATCC: American Type Culture Collection; CLSI: Clinical and Laboratory Standards Institute; CoNS: Coagulase-negative Staphylococci; DMEM: Dulbecco's modified Eagle's medium; DMSO: Dimethyl sulfoxide; FBS: Fetal bovine serum; HGF: Human gingival fi broblast; MIC: Minimal inhibitory concentration; MRCoNS: Methicillin-resistant CoNS;MRSA: Methicillin-resistant S. aureus Keywords: Cytotoxic effect, methicillin-resistant Staphylococci, microdilution, Nigella sativa
How to cite this article: Ugur AR, Dagi HT, Ozturk B, Tekin G, Findik D. Assessment of In vitro antibacterial activity and cytotoxicity effect of Nigella sativa oil. Phcog Mag 2016;12, Suppl S4:471-4 |
How to cite this URL: Ugur AR, Dagi HT, Ozturk B, Tekin G, Findik D. Assessment of In vitro antibacterial activity and cytotoxicity effect of Nigella sativa oil. Phcog Mag [serial online] 2016 [cited 2022 May 23];12, Suppl S4:471-4. Available from: http://www.phcog.com/text.asp?2016/12/47/471/191459 |

Summary
- The minimal inhibitory concentration (MIC) values of Nigella sativa oil against Staphylococcus aureus American Type Culture Collection (ATCC) 29213, Enterococcus faecalis ATCC 29212, Escherichia coli ATCC 25922, and Pseudomonas aeruginosa ATCC 27853 standard strains were 0.5 μg/mL, 2 μg/mL, 64 μg/mL, and 64 μg/mL, respectively
- The N. sativa oil showed an excellent antibacterial activity against clinical isolates of methicillin-resistant S. aureus and methicillin-resistant coagulase-negative Staphylococci with very low MIC range of <0.25-1.0 μg/mL
- The N. sativa oil exhibited no cytotoxic effect on the proliferation of the gingival fibroblasts.
Introduction | |  |
Methicillin resistance is a serious health concern since it has spread among Staphylococcus aureus and coagulase-negative Staphylococci (CoNS) that are frequent community and nosocomial pathogens worldwide. [1],[2] Methicillin-resistant strains are often resistant to other classes of antibiotics making their treatment difficult. [2] In the recent years, the need for new antimicrobial agents because of the rise in antibiotic resistance has led to a search for alternative sources of antimicrobials. [3] Medicinal plants offer a wide range of biodiversity of great value for pharmacology. It has been known since antiquity that herbs and their essential oils have varying degrees of antimicrobial and therapeutic activity. [4] The World Health Organization has been recently supporting countries to integrate traditional medicine with their national health care systems. [5]
Nigella sativa that belongs to family Ranunculaceae is commonly known as black seed or black cumin. [6] It has been shown to possess antimicrobial, immunomodulatory, anti-inflammatory, and antioxidant properties. [7] The antimicrobial activity of the oil and its constituents has been frequently studied so far. [8],[9],[10] Although there have been varying ranges of susceptibility results in the literature, Gram-positive bacteria such as Bacillus cereus, S. aureus, and Staphylococcus epidermidis have been commonly designated as the most susceptible species to N. sativa oil. [8] Moreover, significant antimicrobial activity against multidrug-resistant clinical bacterial isolates has been also reported. [11],[12],[13]
In this study, we aimed to investigate in vitro antibacterial activity and in vitro cytotoxicity effect of N. sativa oil, which has been so far merely studied.
Materials and Methods | |  |
Antibacterial activity
The in vitro antibacterial activity of N. sativa oil was evaluated against following strains of S. aureus American Type Culture Collection (ATCC) 29213, Enterococcus faecalis ATCC 29212, Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853, 45 clinical isolates of methicillin-resistant S. aureus (MRSA), and 77 clinical isolates of methicillin-resistant CoNS (MRCoNS).
The minimal inhibitory concentrations (MICs) of N. sativa oil were determined by broth microdilution method according to the Clinical and Laboratory Standards Institute (CLSI) guidelines. [14] 10.24 mg of cold pressed N. sativa oil (purchased from ZADE Vital, Konya, Turkey) was dissolved in 10 mL of dimethyl sulfoxide (DMSO) to prepare a stock solution. The serial dilutions from the stock solution were made ranging from 256 μg/mL to 0.25 μg/mL using Mueller-Hinton broth (Becton Dickinson, Sparks, MD, USA) in 96-well microplates. The bacterial suspension containing approximately 5 × 10 5 colony-forming units/mL was prepared from a 24 h culture plate. From this suspension, 100 μL was inoculated into each well. A sterility control well and a growth control well were also studied for each strain. The plates were incubated at 35°C for 24 h. The MICs were read as the lowest concentrations of N. sativa that inhibit the appearance of visible growth. These experiments were carried out in duplicate.
Cell culture
The optimal seeding concentration (10.000 cells/well) for proliferation experiments of the human gingival fibroblasts (HGFs) was determined, and then, cells were allowed to adhere for 19 h in Dulbecco's modified Eagle's medium (DMEM) with 10% fetal bovine serum (FBS). The media were changed to DMEM with %5 FBS containing N. sativa. xCELLigence cell index (CI) impedance measurements were performed according to the instructions of the supplier.
Proliferation experiments
Cytotoxic effect of the selected dilutions of N. sativa oil (0.25 μg/mL, 0.5 μg/mL, and 1 μg/mL), equal to the MICs at which the Staphylococci were susceptible to, were evaluated on the proliferation of gingival fibroblast cells by a real-time cell analyzer (xCELLigence, Roche Diagnostics GmbH, Penzbeerg, Germany). The cells were suspended in DMEM with 10% FBS. Then, 200 μL of the suspensions was seeded into wells (10.000 cells/well) of the E-plate 16. The gingival fibroblast cells were observed every 15 min during 95 h. After seeding, cells were held to attach to the E-plate for 19 h; then, the cells were exposed to 100 μL of medium containing dilutions of the N. sativa oil.
Results | |  |
Antibacterial activity
The MIC values of N. sativa oil against S. aureus ATCC 29213, E. faecalis ATCC 29212, E. coli ATCC 25922, and P. aeruginosa ATCC 27853 standard strains were 0.5 μg/mL, 2 μg/mL, 64 μg/mL, and 64 μg/mL, respectively.
The MIC values of N. sativa oil against clinical isolates of Staphylococci were between <0.25 μg/mL and 1.0 μg/mL. Of 45 MRSA strains, MICs of 41 isolates were <0.25 μg/mL, two were 0.5 μg/mL, and two were 1 μg/mL. Of 77 MRCoNS strains, MICs of 53 isolates were <0.25 μg/mL, 19 were 0.25 μg/mL, two were 0.5 μg/mL, and three were 1 μg/mL.
Proliferation experiments
For the N. sativa oil applications, cytotoxic effect at concentrations up to 1 μg/mL was not observed on the gingival fibroblasts when compared to the control group. CI of all NS oil concentrations was not significantly different after the treatment [Figure 1]. | Figure 1: Dynamic monitoring of cell adhesion and proliferation using the xCELLigence system. The effects of different dilutions of Nigella sativa oil on the proliferation of human gingival fibroblasts at a density of 10,000 cells per well in E-Plates 96 were observed during 95 h
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Discussion | |  |
N. sativa seed oil consists of oleoresins and essential oil components, including thymoquinone, dithymoquinone, thymohydroquinone, p-cymene, carvacrol, 4-terpineol, α-thujene, t-anethol, longifolene, thymol, and pinene. [15] Thymoquinone (30-52.6%) and p-cymene (7-25.8%) were reported as its major components. [15],[16] Antimicrobial activity of N. sativa oil is attributed mainly to its phenolic constituents of the essential oil compartment. Thus, thymoquinone followed by its related compounds such as thymohydroquinone, dithymoquinone, and thymol along with carvacrol plays major role in antimicrobial activity. [8],[17],[18] Other constituents, oleoresins, linoleic acid, and oleic acid, may also have minor antimicrobial activity. [15] Indeed, whole essential oil was reported to have higher antibacterial activity than the combinations of its prominent constituents, suggesting that the minor components potentiate the antimicrobial activity. [19],[20],[21],[22]
Although our findings regarding the antibacterial activity of N. sativa oil against Gram-positive and Gram-negative bacteria were in agreement with other studies in terms of Gram-positive bacteria being more susceptible, our results were inconsistent with most of previously published works in terms of much lower MICs against Gram-positive ATCC strains and clinical isolates of Staphylococci. This discrepancy may be explained by several factors such as differences in the extraction methods, antibacterial assay methods used, percentage of active components in the oils, quality and composition of the active constituents, and type of microorganisms selected. [8],[19],[23],[24]
In fact, the oil composition and antimicrobial activities of a specific plant may differ depending on geographical locations where it is cultivated and on harvesting periods. [24],[25],[26],[27] It was reported that genetic differences between N. sativa seeds grown in the different countries exist and the genetic polymorphisms took place over time seem to cause distinct varieties. [28] Moreover, differences in the antimicrobial activities of the essential oils may be obtained depending on the species, subspecies, or varieties. [25] Indeed, comparison of data belonging to previously published works becomes more complicated because of the lack of a standardized method for investigating the antimicrobial activity of natural compounds such as oils obtained from various herbs. Yet, disk diffusion and broth microdilution methods are most applied technics to investigate the antimicrobial activity of plant and seed oils. [8],[15],[17],[29] The solvents utilized to dissolve these oils or their constituents are also quite diverse. [8],[16],[29],[30] CLSI recommends DMSO, ethyl alcohol, polyethylene glycol, and carboxymethyl cellulose as solvents for water-insoluble drugs without mentioning naturally existing antimicrobial compounds. [14] The units used for the MIC values that are reported as mg/mL, μg/mL, μL/mL, ppm, μL/well, and %(v/v) also differ between articles making comparison of results very difficult. [16],[19] Considering vast studies in the literature, it is obvious that there is a need to standardize every step of antimicrobial susceptibility tests for essential oils and their components. However, this subject is beyond our scope.
In the present study, we investigated the antibacterial activity of the whole N. sativa oil by broth microdilution method. Our findings presented at least three-fold lower MIC values against Staphylococci when compared to previously published works, most of which have studied active components instead of the entire oil of the N. sativa seed. [12],[17],[30],[31],[32] It was previously reported that the MIC value of 12.5 μg/mL of the N. sativa seed extract was the lowest concentration at which all the tested microorganisms (E. coli, B. subtilis, S. aureus, P. aeruginosa, Candida albicans, Aspergillus niger) were inhibited suggesting that further dilutions may possess antimicrobial activity against Staphylococci. [29] In point of fact, it has been severally shown that Staphylococci are more susceptible to N. sativa oil and its components than other bacteria. [8],[32],[33]
In the present study, an excellent activity of the N. sativa oil was observed with very low MICs against clinical isolates of MRSA and MRCoNS. Our findings were in agreement with literature reporting thymoquinone, the most active constituent, to have substantial antimicrobial activity against MRSA. [34],[35] Although Hannan et al. [12] reported higher MIC ranges (0.2-0.5 mg/mL) against MRSA, their results indicated that N. sativa has inhibitory effect on MRSA. In another study, the multidrug-resistant S. aureus isolates from diabetic wounds were susceptible to various concentrations of N. sativa oil. [11] Some experiments on animals show that N. sativa oil has significant in vivo antibacterial activity on S. aureus infections. [9],[36] It is also noteworthy to mention that MICs against methicillin susceptible and methicillin-resistant Staphylococci did not differ significantly in our study (P > 0.05) as in several other works. [17],[30] Moreover, a few studies demonstrated that N. sativa essential oil and thymoquinone can effectively inhibit S. aures biofilm formation, suggesting that N. sativa oil deserves further investigations on methicillin-resistant Staphylococci. [31],[37]
The seed extracts of N. sativa are characterized by a low level of toxicity. Although potential toxicity of the N. sativa seed oil was investigated in animal experiments to determine LD 50 values, its in vitro cytotoxicity effect has been rarely studied. It was reported that the extract of N. sativa seed was not toxic when administered to rats intraperitoneally at a daily dose of 50 mg/kg. [38] In addition, experimental animals were not affected when N. sativa oil at doses of 10 mL/kg was administered orally. [39],[40] In the present study, in vitro cytotoxicity assay of N. sativa oil on the fibroblast cells did not represent cytotoxic effect at the relevant dilutions when compared to the control group. Kadan et al. [41] reported that cytotoxic effect of 50% ethanol/water extract of N. sativa on the human hepatocellular carcinoma and the rat L6 muscle cell line exhibited at concentrations higher than 500 μg/mL. Although this concentration was much higher than concentrations we investigated, the results should not be compared with each other because the subject materials are different in composition and nature.
Conclusion | |  |
The oil of N. sativa was very active against MRSA and MRCoNS and had no in vitro cytotoxicity at concentrations up to 1 μg/mL in the present study. These findings emphasize that there is a requirement for further clinical trials on N. sativa oil for "safe" medical management of infections caused by methicillin-resistant Staphylococci.
Acknowledgment
HGFs used in this study have been provided by Dr. Sema Hakký (Selcuk University Faculty of Dentistry, Konya, Turkey).
The authors declare that they have no competing interests.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
References | |  |
1. | Dhawan B, Rao C, Udo EE, Gadepalli R, Vishnubhatla S, Kapil A. Dissemination of methicillin-resistant Staphylococcus aureus SCCmec type IV and SCCmec type V epidemic clones in a tertiary hospital: Challenge to infection control. Epidemiol Infect 2015;143:343-53.  [ PUBMED] |
2. | Murugesan S, Perumal N, Mahalingam SP, Dilliappan SK, Krishnan P. Analysis of antibiotic resistance genes and its associated SCCmec types among nasal carriage of methicillin resistant coagulase negative Staphylococci from community settings, Chennai, Southern India. J Clin Diagn Res 2015;9:DC01-5. |
3. | Carson CF, Riley TV. Non-antibiotic therapies for infectious diseases. Commun Dis Intell Q Rep 2003;27 (Suppl): S143-6.  [ PUBMED] |
4. | Singh G, Marimuthu P, Murali HS, Bawa AS. Antioxidative and antibacterial potentials of essential oils and extracts isolated from various spice materials. J Food Saf 2005;25:130-45. |
5. | |
6. | Paarakh PM. Nigella sativa Linn. A comprehensive review. Indian J Nat Prod Resour 2010;1:409-29. |
7. | Ali BH, Blunden G. Pharmacological and toxicological properties of Nigella sativa. Phytother Res 2003;17:299-305.  [ PUBMED] |
8. | Kokoska L, Havlik J, Valterova I, Sovova H, Sajfrtova M, Jankovska I. Comparison of chemical composition and antibacterial activity of Nigella sativa seed essential oils obtained by different extraction methods. J Food Prot 2008;71:2475-80.  [ PUBMED] |
9. | Hanafy MS, Hatem ME. Studies on the antimicrobial activity of Nigella sativa seed (black cumin). J Ethnopharmacol 1991;34:275-8.  [ PUBMED] |
10. | Toppozada HH, Mazloum HA, el-Dakhakhny M. The antibacterial properties of the Nigella sativa L. seeds. Active principle with some clinical applications. J Egypt Med Assoc 1965;48:187-202. |
11. | Emeka LB, Emeka PM, Khan TM. Antimicrobial activity of Nigella sativa L. seed oil against multi-drug resistant Staphylococcus aureus isolated from diabetic wounds. Pak J Pharm Sci 2015;28:1985-90.  [ PUBMED] |
12. | Hannan A, Saleem S, Chaudhary S, Barkaat M, Arshad MU. Anti bacterial activity of Nigella sativa against clinical isolates of methicillin resistant Staphylococcus aureus. J Ayub Med Coll Abbottabad 2008;20:72-4.  [ PUBMED] |
13. | Islam MH, Ahmad IZ, Salman MT. Antibacterial activity of Nigella sativa seed in various germination phases on clinical bacterial strains isolated from human patients. JBPR 2012;4:8-13. |
14. | Clinical and Laboratory Standard Institute. Performance Standards for Antimicrobial Susceptibility Testing; Twenty-First Informational Supplement, CLSI Document M100-S21. Wayne: Clinical and Laboratory Standard Institute; 2011. |
15. | Singh S, Das SS, Singh G, Schuff C, de Lampasona MP, Catalán CA. Composition, in vitro . antioxidant and antimicrobial activities of essential oil and oleoresins obtained from black cumin seeds (Nigella sativa L.). Biomed Res Int 2014;2014:918209. |
16. | Shaaban HA, Sadek Z, Edris AE, Saad-Hussein A. Analysis and antibacterial activity of Nigella sativa essential oil formulated in microemulsion system. J Oleo Sci 2015;64:223-32.  [ PUBMED] |
17. | Halawani E. Antibacterial activity of thymoquinone and thymohydroquinone of Nigella sativa L. and their interaction with some antibiotics. Adv Biol Res 2009;3:148-52. |
18. | Ghosheh OA, Houdi AA, Crooks PA. High performance liquid chromatographic analysis of the pharmacologically active quinones and related compounds in the oil of the black seed ( Nigella sativa L.). J Pharm Biomed Anal 1999;19:757-62.  [ PUBMED] |
19. | Burt S. Essential oils: Their antibacterial properties and potential applications in foods - A review. Int J Food Microbiol 2004;94:223-53.  [ PUBMED] |
20. | Bassolé IH, Juliani HR. Essential oils in combination and their antimicrobial properties. Molecules 2012;17:3989-4006. |
21. | Mourey A, Canillac N. Anti-listeria monocytogenes activity of essential oils components of conifers. Food Control 2002;13:289-92. |
22. | Anwar S, Ahmesd N, Habibatni S, Abusamra Y. Ajwain ( Trachyspermum Ammi L.) oils. In: Preed VR, editor. Essential Oils in Food Preservation, Flavor and Safety. London: Academic Press; 2015. p. 181-92. |
23. | Mith H, Duré R, Delcenserie V, Zhiri A, Daube G, Clinquart A. Antimicrobial activities of commercial essential oils and their components against food-borne pathogens and food spoilage bacteria. Food Sci Nutr 2014;2:403-16. |
24. | Karakaya S, El SN, Karagözlü N, Sahin S. Antioxidant and antimicrobial activities of essential oils obtained from oregano ( Origanum vulgare ssp. hirtum) by using different extraction methods. J Med Food 2011;14:645-52. |
25. | Sarac N, Ugur A. Antimicrobial activities of the essential oils of Origanum onites L. Origanum vulgare L. subspecies hirtum (Link) Ietswaart, Satureja thymbra L. and Thymus cilicicus Boiss. and Bal. growing wild in Turkey. J Med Food 2008;11:568-73. |
26. | McGimpsey JA, Douglas MH, Van Klink JL, Beauregard DA, Perry NB. Seasonal variation in essential oil yield and composition from naturalized Thymus vulgaris L. in New Zealand. Flavour Fragr J 1994;9:347-52. |
27. | D′Antuono LF, Moretti A, Lovato AF. Seed yield, yield components, oil content and essential oil content and composition of Nigella sativa L. and Nigella damascena L. Ind Crops Prod 2002;15:59-69. |
28. | Al-Huqail A, Al-Saad F. DNA fingerprinting and genotyping of four black seed ( Nigella sativa L.) Taxa. J King Abdul Univ Meteorol Environ Arid Land Agric Sci 2010;21:93-108. |
29. | Bakathir HA, Abbas NA. Detection of the antibacterial effect of Nigella sativa ground seeds with water. Afr J Tradit Complement Altern Med 2011;8:159-64. |
30. | Dadgar T, Asmar M, Saifi A, Mazandarani M, Bayat H, Moradi A, et al. Antibacterial activity of certain Iranian medicinal plants against methicillin-resistant and sensitive Staphylococcus aureus. Asian J Plant Sci 2006;5:861-6. |
31. | Chaieb K, Kouidhi B, Jrah H, Mahdouani K, Bakhrouf A. Antibacterial activity of Thymoquinone, an active principle of Nigella sativa and its potency to prevent bacterial biofilm formation. BMC Complement Altern Med 2011;11:29.  [ PUBMED] |
32. | Toama MA, El-Alfy TS, El-Fatatry HM Antimicrobial activity of the volatile oil of Nigella sativa Linneaus seeds. Antimicrob Agents Chemother 1974;6:225-6. |
33. | Kabbashi AS, Garbi MI, Osman EE, Dahab MM, Koko WS, Abuzeid N. In vitro antimicrobial activity of ethanolic seeds extracts of Nigella sativa (Linn) in the Sudan. Afr J Microbiol Res 2015;9:788-92. |
34. | Liu M, Koya S, Furuta H, Matsuzaki S. Growth-inhibiting activity of anthraquinones and benzoquinones against methicillin resistant Staphylococcus aureus (MRSA). Dokkyo J Med Sci 1996;23:85-93. |
35. | Salman MT, Khan RA, Shukla I. Antimicrobial activity of Nigella sativa Linn. seed oil against multi-drug resistant bacteria from clinical isolates. NPR 2008;7:10-4. |
36. | Hosseinzadeh H, Bazzaz BSF, Haghi MM. Antibacterial activity of total extracts and essential oil of Nigella Sativa L. seeds in mice. Pharmacologyonline 2007;2:429-35. |
37. | Manju S, Malaikozhundan B, Vijayakumar S, Shanthi S, Jaishabanu A, Ekambaram P, et al. Antibacterial, antibiofilm and cytotoxic effects of Nigella sativa essential oil coated gold nanoparticles. Microb Pathog 2016;91:129-35.  [ PUBMED] |
38. | el Daly ES. Protective effect of cysteine and Vitamin E, Crocus sativus and Nigella sativa extracts on cisplatin-induced toxicity in rats. J Pharm Belg 1998;53:87-93.  [ PUBMED] |
39. | Khanna T, Zaidi FA, Dandiya PC. CNS and analgesic studies on Nigella sativa. Fitoterapia 1993;5:407-10. |
40. | Zaoui A, Cherrah Y, Mahassini N, Alaoui K, Amarouch H, Hassar M. Acute and chronic toxicity of Nigella sativa fixed oil. Phytomedicine 2002;9:69-74.  [ PUBMED] |
41. | Kadan S, Saad B, Sasson Y, Zaid H. In vitro evaluations of cytotoxicity of eight antidiabetic medicinal plants and their effect on GLUT4 Translocation. Evid Based Complement Alternat Med 2013;2013:549345.  [ PUBMED] |
Authors | |  |
Dr. Ayse Ruveyda Ugur, is a medical microbiologist at Konya Education and Research Hospital. She completed her medical education (2009) and her specialist training in medical microbiology (2015) at Selcuk University Faculty of Medicine. She has experience and proficiency in medical laboratory management, including diagnostic methods, antimicrobial susceptibility testing, antimicrobial policies, and hospital policies for infection control.
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