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Article

Effects of Nigella sativa Oil Fractions on Reactive Oxygen Species and Chemokine Expression in Airway Smooth Muscle Cells

by
Asma Mosbah
1,2,*,
Hanane Khither
2,
Camélia Mosbah
3,
Abdelkader Slimani
4,
Abdelkader Mahrouk
1,
Salah Akkal
4 and
Gema Nieto
5,*
1
Laboratory of Applied Biochemistry, Faculty of Natural and Life Sciences, University Constantine 1, Constantine 25000, Algeria
2
Laboratory of Applied Biochemistry, Faculty of Natural and Life Sciences, University of Ferhat Abbas Setif 1, Setif 19000, Algeria
3
Laboratory of Natural Substances, Bioactive Molecules and Biotechnological Applications, Larbi Ben M’hidi University, Oum El Bouagui 04000, Algeria
4
Unit of the Valorization of Natural Resources, Bioactive Molecules and Physicochemical and Biological Analysis, Faculty of Exact Sciences, University Constantine 1, Constantine 25000, Algeria
5
Department of Food Technology, Food Science and Nutrition, Faculty of Veterinary Sciences, Regional Campus of International Excellence “Campus Mare Nostrum”, University of Murcia, Espinardo, 30071 Murcia, Spain
*
Authors to whom correspondence should be addressed.
Plants 2023, 12(11), 2171; https://doi.org/10.3390/plants12112171
Submission received: 19 April 2023 / Revised: 14 May 2023 / Accepted: 24 May 2023 / Published: 30 May 2023
(This article belongs to the Special Issue Valorization of Food Industry By-Products for Applications as Food Additives)
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Abstract

:
Background: many previous studies have demonstrated the therapeutic potential of N. sativa total oil fractions, neutral lipids (NLs), glycolipids (GLs), phospholipids (PLs), and unsaponifiable (IS) in asthma patients. We therefore tested its effect on airway smooth muscle (ASM) cells by observing its ability to regulate the production of glucocorticoid (GC)-insensitive chemokines in cells treated with TNF-α/IFN-γ, and its antioxidative and reactive oxygen species (ROS) scavenging properties. Materials and methods: the cytotoxicity of N. sativa oil fractions was assessed using an MTT assay. ASM cells were treated with TNF-α/IFN-γ for 24 h in the presence of different concentrations of N. sativa oil fractions. An ELISA assay was used to determine the effect of N. sativa oil fractions on chemokine production (CCL5, CXCL-10, and CXCL-8). The scavenging effect of N. sativa oil fractions was evaluated on three reactive oxygen species (ROS), O2•−, OH•, and H2O2. Results: our results show that different N. sativa oil fractions used at 25 and 50 µg/mL did not affect cell viability. All fractions of N. sativa oil inhibited chemokines in a concentration-dependent manner. Interestingly, the total oil fraction showed the most significant effect of chemokine inhibition, and had the highest percentage of ROS scavenging effect. Conclusion: these results suggest that N. sativa oil modulates the proinflammatory actions of human ASM cells by inhibiting the production of GC-insensitive chemokines.

1. Introduction

Asthma is a chronic inflammatory condition of the respiratory system (airways) characterized by airway inflammation, intermittent airflow obstruction, and bronchial hyper-responsiveness. Approximately 5 to 10% of patients with severe asthma are poorly responsive to high doses of glucocorticoids (GCs) (oral or inhaled) [1]. Airway inflammation plays a pivotal role in asthma severity by promoting excessive contraction of the airway smooth muscle (ASM) and remodeling of the airways, both contributing to an acute asthma attack. ASM may also participate in progression/perpetuation of the airway inflammation via its ability to produce a large array of cytokines, growth factors, and chemokines, which are capable of attracting different immune cells, including T cells, eosinophils, and neutrophils [2]. ASM has been also implicated in the poor response of severe asthma patients to GCs by being refractory to their anti-inflammatory action [3]. It was suggested that development of GC insensitivity in ASM cells could result from the concerted action of different inflammatory cytokines. Indeed, treatment of ASM cells with both TNF-α and IFN-γ stimulated the expression of a number of proasthmatic proteins (cytokines, adhesion molecules, transcription factors, etc.) that were clearly insensitive to fluticasone [3]. The underling mechanisms of GC insensitivity involved the over-activation of the transcription factor IRF-1, expression of dominant negative GRβ, and the protein phosphatase PP5 [3]. Collectively, these observations suggest that targeting these proinflammatory and GC-insensitive pathways in ASM cells may offer new therapeutic avenues for asthma.
GC insensitivity may also derive from reactive oxygen species (ROS). Inflammatory cells, such as T cells, helper T cells, mast cells, macrophages, basophils, and eosinophils, which are involved in airway inflammation in asthma [4], produce different reactive oxygen species [5]. ROS have been involved in the pathogenesis of asthma as evidenced by the increased markers of oxidative stress in various lung specimens including sputum, lungs, exhaled breath, and blood, which often correlate with disease severity or poor control [6,7]. Oxidative stress may contribute to the progression and/or aggravation of asthma via multiple mechanisms including alteration of the epithelium or ASM cells, leading to proremodeling and proinflammatory actions [6]. Indeed, oxidative stress stimulates the production of various proinflammatory mediators, chemokines, adhesion molecules, and eosinophil granule proteins [7,8,9,10]. Evidence suggests that ROS may promote the development of GC insensitivity by interfering with GC receptor (GRα) signaling pathways, including inhibition of histone deacetylase 2 (HDAC2) activity and/or interference with GRα nuclear trafficking [11].
Nigella sativa (N. sativa) is an herbaceous plant, native to Southern Europe, North Africa and Southeast Asia [12,13,14]. This plant is traditionally used worldwide for culinary and medicinal purposes [15,16]. N. Sativa has been shown to have numerous properties, including immune-stimulatory, anti-inflammatory, hypoglycemic, antihypertensive, antimicrobial, antiparasitic, antioxidant, and anticancer actions [17,18,19,20]. N. sativa and its constituents have been traditionally used to relieve respiratory disorders such as asthma, bronchospasm, and chest congestion, although the precise mechanisms of action have not been elucidated [21]. Few studies have examined whether N. sativa has antiasthma properties. Indeed, it was reported that N. sativa supplementation improved asthma control, reduction in exacerbations, inflammatory markers such as IFN-γ, and blood eosinophils [22,23]. N. sativa also exerts immunomodulatory and therapeutic effects in patients with allergic diseases (allergic rhinitis, bronchial asthma, and atopic eczema), possibly via the inhibition of proinflammatory cytokines, downregulating PGD2 and COX-2 expressions, and decrease of airway inflammatory cell infiltration [24,25]. In vitro studies reported the beneficial role of carvacrol, one of the key components of N. sativa, in guinea pig tracheal preparations. Carvacrol was reported to exert broncho relaxant and functionally antagonistic effects on muscarinic receptors [26], histamine (H1) receptors [27], an inhibitory effect on calcium [28], and an opening effect on potassium channels [29]. A boiled extract of N. sativa indicated a bronchodilatory effect on asthmatic patients by increasing pulmonary function [30].
To manage patients with severe asthma, the chronic administration of high doses of GC is required, which is often associated with serious adverse effects. In corticosteroid-resistant asthma, the need exists for novel therapies. Clinical trials are oriented toward natural biomolecules extracted from medicinal plants for the treatment of various diseases. In this study, we provide the first evidence that N. sativa and its fractions, neutral lipids (NLs), glycolipids (GLs), phospholipids (PLs), and unsaponifiable (IS), could exert therapeutic effects in asthma by inhibiting the production of GC-insensitive chemokines in human ASM cells, a clinically relevant cell model.

2. Results

2.1. Extraction Yield

The total oil and its fraction yields are summarized in Table 1.

2.2. Analysis of N. sativa Total Oil Lipid Components Using Gas Chromatography–Mass Spectrophotometer (GC–MS)

The total oil of N. sativa was analyzed using GC–MS. The obtained chromatogram exhibited multiple peaks at various retention times and intensities (Figure 1).
Compounds corresponding to these peaks were identified based on their molecular weights. The chemical compositions of N. sativa TO identified by GC–MS are listed in Table 2. In total, 18 constituents were identified in the TO fraction obtained from Algerian N. sativa seeds using the GC–MS technique.
To determine the efficiency of N. sativa oil fractions, antiradical, anti-inflammatory, and cell viability assays were performed. The half-maximal inhibitory concentration (IC50) values of N. sativa oil fractions were determined.

2.3. Antiradical Assays

Antiradical properties of N. sativa oil fractions were compared using different reactive oxygen species (O2•−, OH•, and H2O2). All assays showed a similar trend in the scavenging of free radicals. Figure 2 indicates that TO has the highest scavenging effect, followed by PL, GL, and NL. However, this scavenging effect remained lower than that of positive control α-tocopherol.
For superoxide anion radical, total oil (TO) presents the best scavenging activity, with an IC50 of 0.0172 mg/mL, followed by phospholipids (PLs), glycolipids (GLs), and neutral lipids (NFs) fractions, with an IC50 of 0.0197, 0.0261, and 0.0680 mg/mL, respectively. The same pattern was also reported for hydroxyl radical and H2O2 scavenging capacity, when TO showed the highest antiradical activity with an IC50 of 0.105, at the concentration of 0.440 mg/mL, followed by PL 0.132, at the concentration of 0.465 mg/mL, GL 0.330, at the concentration of 0.626 mg/mL and, NF 0.460, at 0.930 mg/mL, respectively.

2.4. MTT Assay

To investigate the effect of N. sativa oil fractions on cell viability, ASM cells were treated with 25 and 50 µg/mL N. Sativa TO fractions for 24 h and 48 h, and subjected to the MTT colorimetric assay.
The percent cell viability of ASM cells against N. sativa oil fractions, as observed by the MTT assay, is presented in Figure 3. The results show that all fractions of N. sativa oil demonstrate no toxic activity on ASM cells at the used dosages and treatment periods.

2.5. Anti-Inflammatory Activity of N. sativa Oil Fractions

In the present study, we aimed to investigate the effect of N. sativa oil fractions on the expression of chemokines in ASM cells treated with TNF-α and IFN-γ.
As shown in Figure 4, both TNF-α and IFN-γ increased chemokine production in ASM cells from subjects with asthma compared to unstimulated ASM cells (the basal). Interestingly, the different N. sativa fractions induced a dose-dependent inhibition of chemokine production, with the highest inhibition achieved at 50 µg/mL for all fractions. In ASM-treated cells, TO Inhibited CCL5 secretion by 43.33%, CXCL-10 secretion by 40.03%, and CXCL-8 secretion by 47.62% (n = 6). The NF fraction inhibited CCL5 secretion by 41.66%, CXCL-10 secretion by 36.25 %, and CXCL-8 secretion by 39.53%. The PL fraction inhibited CCL5 secretion by 40.05%, CXCL-10 secretion by 31.25%, and CXCL-8 secretion by 29.48%. The GL fraction inhibited CCL5 secretion by 36.33%, CXCL-10 secretion by 37.50%, and CXCL-8 secretion by 42.26%. IS inhibited CCL5 secretion by 38.02%, CXCL-10 secretion by 35.62%, and CXCL-8 secretion by 28.11% (Figure 4).

3. Discussion

The present study aimed to explore the anti-inflammatory effect of different fractions of N. sativa oil in terms of chemokine secretion in human ASM cells. This study found that N. sativa TO and derived fractions suppressed the production of GC-insensitive chemokine action by human ASM cells, and possess ROS scavenging activity. This study shows the potential benefit of N. sativa by acting on ASM cells, a key player in the pathogenesis of asthma.
The chemical composition of N. sativa TO identified by GC–MS indicated the presence of linoleic acid (18:2n-6), oleic acid (18:1n-9), palmitic acid (16:0), and stearic acid based on comparative value for the standards present in the database. Comparing our results with those reported by Ramadan et al. (2003) [31], which used Egyptian N. sativa, indicated that linoleic acid, oleic acid, and palmitic acid measured for Egyptian TO were higher than that of Algerian TO. Another study showed that the concentrations of fatty acids (oleic, linoleic, palmitic, and stearic acids) in Algerian N. sativa oil were higher than those of Indian and Ethiopian plants [32] (Table 3). These differences with regard to the qualitative and quantitative aspects of N. sativa could be explained by the genetic properties of seeds, geographical origin, storage conditions, harvest duration, and extraction methods.
The present report also confirmed the radical scavenging property of the different N. sativa oil fractions by showing their ability to scavenge O2•−, OH•, and H2O2 in a dose-dependent manner. The total oil (TO) showed the highest scavenging capacity in all assays, followed by phospholipids (PLs), glycolipids (GLs), and neutral fraction (NFs). Our results of the antiradical activities are in agreement with previous studies showing that TO and PLs presented a potent source of antioxidant compounds, which may explain the therapeutic effect exerted by these fractions [33,34]. The characterization by GC–MS showed the existence of many antioxidant fatty acids, such as linoleic, oleic, palmitic, and stearic acids, and 14 other hydrocarbons. The antioxidant activity of TO and different polar and apolar fractions could be explained by the phytochemical analysis due to the presence of polyphenols, diene functional groups, and unsaturated fatty acids, which are known for their antioxidant activity [31]. Palmitic, oleic, and linoleic acids have been reported to exert a potent antioxidant effect in different assays [35,36,37]. Oxidative stress is involved in the pathophysiology of many human diseases, including asthma. The evidence showed that both increased ROS production by inflammatory cells infiltrated within the airways and/or impairment of the antioxidant responses could contribute to asthma severity and exacerbations [38,39,40]. The inflammatory answer is an important factor to the exacerbation of ROS production in organ injury. The study conducted by Fusco et al. (2020) showed increased plasma levels of proinflammatory cytokines, particularly TNF-α, IL6, and IL-1β, after intestinal ischemia/reperfusion injury [41].
A number of previous studies have shown the therapeutic benefit of N. sativa administered via different routes (i.p., orally) in experimental models of asthma (rat, mouse) sensitized and challenged with ovalbumin [42]. N. sativa was shown to reduce allergen-induced airway inflammatory markers (Th2 cytokines, white blood cells) and lung histological changes. Our present report shows that these beneficial effects could result from the radical scavenging activity of N. sativa.
ASM has been considered as an important player in the pathogenesis of asthma via its contribution to airway remodeling, abnormal lung function, and airway inflammation [43,44]. Indeed, ASM cells can secrete a variety of inflammatory mediators, including chemokines, which could regulate airway inflammation via the recruitment and activation of various key inflammatory cells, monocytes, eosinophils, and T cells [45]. In cultured ASM cells, a combination of both TNF-α and IFN-γ leads to the synergistic production of various proinflammatory chemokines (CXCL-8, CCL-11, CX3CL-1, CCL5, and CXCL-10, among others) [30,46]. In addition, chemokine production by TNF-α and IFN-γ has been shown to be insensitive to GCs via multiple mechanisms [3], thus representing a unique cellular model to dissect the mechanisms of GC insensitivity in asthma, or find new strategies to reverse it. We made the novel finding that N. sativa and its fractions inhibited the production of GC-insensitive chemokines (CCL5, CXCL-8, and CXCL-10) induced by TNF-α and IFN-γ in ASM cells from both healthy and asthmatic patients. Although we have not dissected the underlying mechanisms by which N. sativa suppressed the production of inflammatory chemokines, it is possible that N. sativa interfered with the function of key transcription factors such as NF-κB, IRF-1, and STATs. Additional studies are clearly needed to address these possibilities. These inhibitory actions were not due to any cytotoxic effect as assessed by the MTT assay. Together, our results suggest that the anti-inflammatory actions of N. sativa, seen in various animal models of allergic asthma [42], may derive from their capacity to suppress chemokine production from ASM cells.
Previous studies have confirmed the ability of N. sativa and its fractions to exert therapeutic action using isolated airway preparations from asthmatic patients [30]. Essential oil of N. sativa exhibited an inhibitory effect on the cyclooxygenase and 5-lipoxygenase pathways of arachidonic acid metabolism and membrane lipid peroxidation. Similarly, Boskabady et al. (2008) showed that different N. sativa fractions (n-hexane, dichloromethane, methanol, and aqueous) can relax isolated tracheal ring preparations, and the most potent relaxant effect was detected for methanol and dichloromethane fractions [47]. The therapeutic effect of N. sativa on airway preparations may result from a direct action on ASM cells via several mechanisms, including (1) interfering with calcium channel blocking activity [28], (2) modulation of potassium channels [29], (3) inhibition of muscarinic receptor function [26], (4) histaminic antagonistic activity receptor [27], and (5) activation of β2-adrenoceptors [48]. Together, these results strongly support a therapeutic action of N. sativa and its fractions in asthma via their action on ASM cells.
Herbal extracts showed complex mechanisms of action compared with conventional drugs, which may involve proinflammatory cytokine secretion through various molecular signaling pathways. Several mechanisms of action have been suggested for N. sativa extracts. In the present study, the inhibition of the production of GC-insensitive chemokines (CCL5, CXCL-8, and CXCL-10) induced by TNF-α and IFN-γ may involve the mechanism of Th1/Th2 cytokine modulation, which is attributed to the inhibition of the signal transducer and activator of transcription-6 (STAT6) signaling pathway [49,50].
It is important to mention some of the limitations of the present study. First, we have not provided any mechanisms to explain the anti-inflammatory actions of N. sativa or its fractions. Looking at the activity of different cytokine-associated transcriptions may address this issue. We have also limited our study at the preventive action of N. sativa (2 h preincubation prior cytokines), and it is not known whether the in vitro beneficial action of N. sativa would still be seen if used therapeutically (after cytokines). Finally, it would also be interesting to repeat these experiments in ASM cells obtained from nonsevere asthma patients, which exhibit an abnormal phenotype including a constitutive state of GC insensitivity [51].

4. Materials and Methods

4.1. Materials

All solvents, chemical compounds (fatty acids, MTT, xanthine), and biological compounds (TNF-α, IFN-γ, XOR) were purchased from Sigma-Aldrich (Darmstadt, Germany). Commercial organic solvents methanol, hexane, chloroform, acetone, and DMSO were of analytical grade (∼99.5%). ELISA kits were performed using R&D System Duoset kits (Minneapolis, MN, USA).

4.2. Collection of the N. sativa Plant

Seeds of N. sativa used in this study were collected from Algerian Sahara, Bechar in 2016. The plant was identified by Dr. Houssine Laouar from Setif 1 University, Algeria. The specimen was deposited at the Natural Biological Resources Development laboratory at Setif 1 University, Algeria. Seeds were cleaned with water, dried, and stored in darkness at 4 °C until use.

4.3. Human Airway Smooth Muscle (ASM) Cell Culture

Primary human ASM cells were obtained from consenting healthy subjects and asthmatic patients (Glenfield Hospital patients and staff 6). ASM cells were isolated from endobronchial biopsies as described previously [52,53,54,55]. Written informed consent was gained from all participants prior to their involvement.
This study was approved by the Leicestershire, Northamptonshire, and Rutland Research Ethics Committee (references: 4977, 04/Q2502/74, and 08/H0406/189).
All experiments involving human ASM cells were performed in Dr Amrani’s laboratory at the University of Leicester.

4.4. Preparation of Extracts

N. sativa seed powder (30 g) was extracted in methanol solvent (400 mL) using a Soxhlet extractor for two hours at room temperature (27 °C). Methanol was evaporated at reduced pressure at 40 °C using a rotary evaporator (BÜCHI 461). The resulting extract was mixed with 200 mL of hexane solvent in a bulb for settling, until the formation of two distinct phases: methanol (green color) and hexane (yellow color). The latter phase was recovered, and hexane solvent was evaporated at 40 °C to obtain total oil (TO), characterized by a greenish color.
The extracted oil fraction was then applied on a silica gel column to be separated into the neutral lipids fraction (NF), glycolipids (GLs), phospholipids (PLs), and unsaponifiable (IS). The eluting solvents for NF, GLs, and PLs were chloroform, acetone, and methanol, respectively. Solvents were evaporated with a rotary evaporator, and the percentage of each fraction was calculated as described previously [56,57,58,59,60,61,62,63,64].

4.5. Analysis of N. sativa Total Oil Lipid Components Using GC–MS

Gas chromatography–mass spectrometry (GC–MS) analysis was used for the quantitative analysis of 18 lipid compounds of N. sativa. The test was performed according to the method of Dalli et al. [65].
On dry lipid extract, 1 mL of BF3 was added (boron trifluoride–methanol solution 14%). The mixture was transmethylated at 100 °C to remove nonpolar lipids. Methyl esters were extracted two times with hexane in the presence of water. Fatty acid methyl esters were analyzed using the gas chromatography–mass spectrometry electron impact ionization method (HP/MSD Agilent 5890), operating in the scan mode (m/z = 25–2000). Samples were injected into an HP-5MS capillary column (length: 30 m, inner diameter: 0.25 mm, film thickness: 0.25 μm) and eluted by helium at 0.3 mL/min with a split ratio of 1/10. Injector and detector temperatures were 240 °C. Analysis was carried out with an ionization energy of 70 eV (filament temperature: 150 °C, current: 600 mA, potential PM: 600 V).
Fatty acid methyl esters were identified by their retention times in comparison to those of commercial standard data bank provided by the Chemstation software (NIST 2002 and Wiley version 7.0).

4.6. Superoxide Anion Radical (O2•−) Scavenging Assay

The ability of total oil and its fractions to scavenge superoxide anions produced with the xanthine/xanthine oxidoreductase (XOR) system was evaluated according to Robak and Gryglewski’s method (1988) [63].
Reaction medium was composed of xanthine (100 µM) and cytochrome c (25 µM) prepared in phosphate buffer saturated with oxygen (50 mM Na2HPO4/NaH2PO4, pH 7.4) and different concentrations of total oil and its fractions. The reaction was started with the addition of XOR enzyme. After one minute, the reduced cytochrome c was detected spectrophotometrically at 550 nm. The percentage of reduced cytochrome c was determined using the following relationship:
Inhibition % = (AC − AS/AC) × 100
AC:
Absorbance of control.
AS:
Absorbance of samples.

4.7. Hydroxyl Radical (OH•) Scavenging Assay

This experiment was carried out using the Smirnoff and Cumbes method (1989) [64]. The final volume of the reaction medium was 3.0 mL, and contained 1.0 mL FeSO4 (1.5 mM), 0.7 mL hydrogen peroxide (6 mM), 0.3 mL salicylate sodium (20 mM), and 1 mL of different concentrations of total oil and its fractions. After incubation at 37 °C for 1 h, salicylate hydroxyl complex absorption was measured at 562 nm. The percentage of OH• inhibition was calculated using the following formula:
Inhibition % = [1 − (A1 − A2)/A0] × 100
A0:
Absorbance of control (without extract).
A1:
Absorbance of extracts.

4.8. Hydrogen Peroxide (H2O2) Scavenging Assay

The ability of TO and its fractions to scavenge H2O2 was determined according to Ruch et al. [65].
H2O2 solution (40 mM) was prepared in phosphate buffer (pH 7.4). The reaction mixture consisted of 1.2 mL of H2O2 solution (40 mM in phosphate buffer, pH 7.4) and 2 mL of extracts or standard. Absorbance was measured after 10 min at 230 nm. The percentage of H2O2 scavenging was calculated using the following formula:
Inhibition % = (AC − AE)/AC × 100
AC:
Absorbance of control.
AE:
Absorbance of samples

4.9. Cell Viability Assay

Cell viability was evaluated using a 3-(4,5-dimethylthiazol-2-yl)- 2,5-diphenyl-2H- tetrazolium bromide (MTT) assay [66]. N. sativa TO and its fractions NF, GLs, PLs, and unsaponifiable (IS) were dissolved in DMSO (0.01%). For each fraction, two standard concentrations were made, i.e., 25 and 50 µg/mL from the initial stock solution prepared at a concentration of 100 mg of extract/1 mL of dimethyl sulfoxide (DMSO).
This test was conducted using 24-well microplates. ASM cells were incubated with the medium for one week to ensure their growth, washed with PBS, and serum-starved using DMEM supplemented with antibiotics, 4 mML-glutamine, 20 mM HEPES (pH 7.4), and 0.1% BSA. ASM cells were then incubated with different concentrations of TO and their respective fractions NF, GLs, PLs, and IS (25 and 50 µg/mL) for 24 and 48 h. The medium was aspirated and 200 μL of a medium consisting of 5% of fetal bovine serum (FBS) and 0.5 mg/mL of MTT solvent was added to each well for four hours. Following the incubation, cell supernatants were removed and replaced with 200 μL of dimethyl sulfoxide (DMSO). Basal was treated with vehicle only and DMSO. The absorbance was read at 570 nm by an ELISA reader, and the comparison was conducted against the basal.

4.10. Measurement of the Different CCL5, CXCL-10, and CXCL-8 in Human ASM Cell Supernatants

All ELISA assays for CCL5, CXCL-10, and CXCL-8 were performed using Duoset ELISAs (R&D Systems, Minneapolis, MN, USA), as previously reported [52].
Cultured ASM cells were treated in duplicate with NF, GLs, PLs, and IS at two concentrations of 25 and 50 µg/mL for two hours, followed by treatment with recombinant human TNF-α (10 ng/mL) and IFN-γ (25 ng/mL) (R&D Systems) for 24 h before supernatants were collected for chemokine assays using ELISA [52,67]. The light absorbance was recorded at a wavelength of 450 nm for the three chemokines.

4.11. Statistical Analysis

The comparison between multiple groups was made using one-way ANOVA followed by the Bonferroni post hoc test for comparisons between specific groups. The comparison between two groups was made using paired or unpaired t-tests, and p < 0.05 was taken as statistically significant.

5. Conclusions

The present study demonstrates that N. sativa TO, NF, GL, PL, and IS fractions differentially change the production of chemokines known to play a key role in the pathogenesis of asthma. We also show that N. sativa has radical scavenging activity. These results are still insufficient to claim that N. sativa has anti-inflammatory properties. In vivo data should be provided. Understanding how these different fractions exert an effect on GC-insensitive features in ASM cells may offer new therapeutic options for asthma.

Author Contributions

Experimental, writing—original draft preparation, resources, H.K., C.M. and A.M. (Asma Mosbah); writing—review and editing, G.N.; in vitro experiment, A.M. (Abdelkader Mahrouk) and H.K.; supervision, S.A.; validation and supervision, S.A. and A.M. (Asma Mosbah); writing, A.S., G.N. and A.M. (Asma Mosbah). All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the Algerian Ministry of Higher Education and Scientific Research (MERS).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

We are greatly indebted to Amrani Yassin for allowing us to perform some of the experiments in his lab.

Conflicts of Interest

The authors declare no conflict of interest.

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Plants 12 02171 g001 550
Figure 1. Gas chromatography–mass spectrometry (GC–MS)chromatogram of fatty acid compounds in N. sativa total oil (TO).
Figure 1. Gas chromatography–mass spectrometry (GC–MS)chromatogram of fatty acid compounds in N. sativa total oil (TO).
Plants 12 02171 g001
Plants 12 02171 g002 550
Figure 2. Scavenging effect of total oil (TO), phospholipids (PLs), glycolipids (GLs), and neutral fraction (NF) (A) superoxide anion radical (O2•−), (B) hydroxyl radical (OH•), and (C) hydrogen peroxide (H2O2). α-Tocopherol was used as positive control. Values were expressed as the mean ± SD of experiments performed in triplicate, * p < 0.05, ** p < 0.001.
Figure 2. Scavenging effect of total oil (TO), phospholipids (PLs), glycolipids (GLs), and neutral fraction (NF) (A) superoxide anion radical (O2•−), (B) hydroxyl radical (OH•), and (C) hydrogen peroxide (H2O2). α-Tocopherol was used as positive control. Values were expressed as the mean ± SD of experiments performed in triplicate, * p < 0.05, ** p < 0.001.
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Plants 12 02171 g003 550
Figure 3. Cell proliferation (MTT assay) results of airway smooth muscle (ASM) cells following treatment with N. sativa oil fractions at concentrations of (50 µg/mL) (A) and (25 µg/mL) (B) for 48 h of incubation. All values are expressed as mean ± SEM from two different replicates.
Figure 3. Cell proliferation (MTT assay) results of airway smooth muscle (ASM) cells following treatment with N. sativa oil fractions at concentrations of (50 µg/mL) (A) and (25 µg/mL) (B) for 48 h of incubation. All values are expressed as mean ± SEM from two different replicates.
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Plants 12 02171 g004a 550Plants 12 02171 g004b 550
Figure 4. Nigella sativa oil fractions differentially regulate chemokine secretion in airway smooth muscle (ASM) cells stimulated for 24 h with TNF-α (10 ng/mL) and IFN-γ (25 ng/mL) compared to unstimulated ASM cells (the basal). Levels of CCL5 (A,B), CXCL-10 (C,D), and CXCL-8 (E,F) were analyzed as described in the Materials and Methods section. Results shown as mean ± SEM of n = 6 different donors. TO: total oil, NF: neutral fraction, GL: glycolipids, PL: phospholipids, IS: unsaponifiable * p < 0.05, ** p < 0.001, ns = not significant.
Figure 4. Nigella sativa oil fractions differentially regulate chemokine secretion in airway smooth muscle (ASM) cells stimulated for 24 h with TNF-α (10 ng/mL) and IFN-γ (25 ng/mL) compared to unstimulated ASM cells (the basal). Levels of CCL5 (A,B), CXCL-10 (C,D), and CXCL-8 (E,F) were analyzed as described in the Materials and Methods section. Results shown as mean ± SEM of n = 6 different donors. TO: total oil, NF: neutral fraction, GL: glycolipids, PL: phospholipids, IS: unsaponifiable * p < 0.05, ** p < 0.001, ns = not significant.
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Table
Table 1. Yield of N. sativa oil fractions.
Table 1. Yield of N. sativa oil fractions.
FractionsYield (g/mL)Yield (%)
Total oil (TO)11.7913.61 of seeds weight
Neutral lipids (NLs)10.0893.97 of TO
Glycolipids (GLs)0.352.98 of TO
Phospholipids (FLs)0.131.11 of TO
Table
Table 2. Fatty acids composition of N. sativa total oil.
Table 2. Fatty acids composition of N. sativa total oil.
Retention Time (min)ComponentsContent (%)
14.44o-Cymen3.5
15.15Gamma-Terpinene1.04
15.82p-Cymene0.19
16.54m-Cymene0.19
19.32Alpha-Longipinene0.16
21.67(+)-Longifolene1.59
22.95Squalene0.53
16.25Cumene0.12
16.921-Ethyl-3,5-Dimethyl-Benzene0.51
18.59Prehnitol0.38
22.62(E)5-Octadecene0.75
23.64Heptadecane1.04
23.94Not identified26.21
30.74Sandaracopimaradiene3.28
29.89Palmitic acid8.81
32.51Stearic acid4.09
32.90Oleic acid22.58
33.72Linoleic acid25.03
Table
Table 3. Comparison of total oil fatty acid contents of Nigella ativa L. from Algeria, Egypt, India, and Ethiopia [32].
Table 3. Comparison of total oil fatty acid contents of Nigella ativa L. from Algeria, Egypt, India, and Ethiopia [32].
Fatty Acid CompositionTotal Oil Content (%)
AlgerianEgyptianIndianEthiopian
Oleic acid22.5824.719.0917.63
Linoleic acid25.0351.850.2461.25
Palmitic acid8.8118.410.8311.36
Stearic acid4.092.072.472.81
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Mosbah, A.; Khither, H.; Mosbah, C.; Slimani, A.; Mahrouk, A.; Akkal, S.; Nieto, G. Effects of Nigella sativa Oil Fractions on Reactive Oxygen Species and Chemokine Expression in Airway Smooth Muscle Cells. Plants 2023, 12, 2171. https://doi.org/10.3390/plants12112171

AMA Style

Mosbah A, Khither H, Mosbah C, Slimani A, Mahrouk A, Akkal S, Nieto G. Effects of Nigella sativa Oil Fractions on Reactive Oxygen Species and Chemokine Expression in Airway Smooth Muscle Cells. Plants. 2023; 12(11):2171. https://doi.org/10.3390/plants12112171

Chicago/Turabian Style

Mosbah, Asma, Hanane Khither, Camélia Mosbah, Abdelkader Slimani, Abdelkader Mahrouk, Salah Akkal, and Gema Nieto. 2023. "Effects of Nigella sativa Oil Fractions on Reactive Oxygen Species and Chemokine Expression in Airway Smooth Muscle Cells" Plants 12, no. 11: 2171. https://doi.org/10.3390/plants12112171

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