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Prophetic Medicine-Nigella Sativa (Black cumin seeds) – Potential herb for COVID-19?

Naina Mohamed Pakkir Maideen1,*

1Dubai Health Authority, Dubai, United Arab Emirates

Correspondence to: *Corresponding Author Naina Mohamed Pakkir Maideen. Pharmacologist, Dubai Health Authority 4545, Dubai,, United Arab Emirates., Tel: +971-4216-4952, +971-5057-69833 Fax: +971-4224-4302 E-mail: nmmaideen@dha.gov.ae

Received: May 30, 2020; Revised: June 2, 2020; Accepted: June 8, 2020

This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

J Pharmacopuncture 2020; 23(2): 62-70

Published June 30, 2020 https://doi.org/10.3831/KPI.2020.23.010

Copyright © The Korean Pharmacopuncture Institute.

Abstract

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Coronavirus disease-19 (COVID-19) is caused by the severe acute respiratory syndrome coronavirus 2 (SARS CoV-2). Currently, the management of patients with COVID-19 depends mainly on repurposed drugs which include chloroquine, hydroxychloroquine, lopinavir/ritonavir, ribavirin, remdesivir, favipiravir, umifenovir, interferon-α, interferon-β and others. In this review, the potential of Nigella sativa (black cumin seeds) to treat the patients with COVID-19 analyzed, as it has shown to possess antiviral, antioxidant, anti-inflammatory, anticoagulant, immunomodulatory, bronchodilatory, antihistaminic, antitussive, antipyretic and analgesic activities. PubMed, Google Scholar, Science Direct, Directory of open access journals (DOAJ) and reference lists were searched to identify articles associated with antiviral and other properties of N.sativa related to the signs and symptoms of COVID-19. Various randomized controlled trials, pilot studies, case reports and in vitro and in vivo studies confirmed that N.sativa has antiviral, antioxidant, anti-inflammatory, immunomodulatory, bronchodilatory, antihistaminic, antitussive activities related to causative oraganism and signs and symptoms of COVID-19. N. sativa could be used as an adjuvant therapy along with repurposed conventional drugs to manage the patients with COVID-19.

Keywords

Nigella sativa, Black seeds, Antiviral, Antioxidant, Anti-inflammatory, Anticoagulant

1. Introduction

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Coronavirus disease-19 (COVID-19) is caused by the severe acute respiratory syndrome coronavirus 2 (SARS CoV-2) and this virus was first originated from Wuhan city of Hubei province of China spreading around the globe [1]. Around 5 million of COVID-19 cases have been reported across the world and 0.3 million deaths occurred among them, till 21st May 2020 [2].

The prominent symptoms of COVID-19 include fever, cough and dyspnea [3] and other symptoms noted in patients affected by COVID-19 may include chills, repeated shaking with chills, muscle pain, headache, sore throat and new loss of taste or smell [4]. In addition, the emergency warning signs of COVID-19 include difficulty breathing or shortness of breath, persistent pain or pressure in the chest, new confusion or inability to arouse and bluish lips or face and the patients experiencing any of these signs should get immediate medical attention [5].

The development of specific antiviral drugs and vaccines to treat COVID-19 patients will take months or years to complete. Hence, the treatments of COVID-19 depend mainly on repurposed drugs which include chloroquine, hydroxychloroquine, lopinavir/ritonavir, ribavirin, remdesivir, favipiravir, umifenovir, interferon-α, interferon-β and others. As of this time, there is no specific, effective and proven conventional medicine to manage patients affected by COVID-19 and as of April 2, 2020, there are 291 active clinical trials found specific to COVID-19. Among them 109 trials included pharmacological therapy for the treatment of COVID-19 in adult patients [6].

Similarly, the herbal medicine can contribute as an alternative measure to manage the patients with COVID-19 as there are many traditional herbs shown antiviral and other medicinal properties.

In this review, the potential of Nigella sativa (black cumin seeds) to treat the patients with COVID-19 analyzed, as Prophet Muhammad (PBUH) stated that “In the black cumin, there is a cure for every disease except death”. In addition, the black cumin is also mentioned in Holy Bible as “Curative black seed” and is described as ‘Melanthion of Hippocrates and Dioscorides’ and as ‘Glitch of Pliny’ [7].

N. sativa belongs to the Ranunculacea family and it is also known as black cumin seed, black seed, Habbatul Barakah, Habbatus sawda, kalonji, etc [8]. In traditional medicine, N. sativa has been used for centuries to treat various illnesses including asthma, common cold, headache, nasal congestion, rheumatic diseases, warts and many others [9]. More recently, N. sativa has been used to treat conditions like infections, cancer, diabetes, hypertension, obesity, cardiovascular diseases, and gastrointestinal problems [10]. The medicinal properties of N. sativa have been demonstrated in Unani, Chinese medicine, ayurveda and other medicinal systems [11].

Phytochemical screening of N.Sativa revealed that it contains various compounds including terpenes, flavanoids, phytosterols, tannins, coumarins, phenolic compounds, alkaloids, cardiac glycosides, saponins fatty acids, and volatile oils. The bioactive constituents of N. sativa include terpenes such as thymoquinone (TQ), dithymoquinone (DTQ), carvone, limonine, trans-anethol, and p-cymene, indazole alkaloids like nigellidine and nigellicine, and isoquinoline alkaloids including nigellicimine, nigellicimine-N-oxide and α-hederin [12].

As N.sativa possesses antiviral, antioxidant, anti-inflammatory, anticoagulant, immunomodulatory, bronchodilatory, antihistaminic, antitussive, antipyretic and analgesic activities (Fig. 1), it would be a potential herbal candidate to treat the patients with COVID-19 (Table 1). In addition, N.sativa has also shown anti-hypertensive, anti-obesity, anti-diabetic, anti-hyperlipidemic, anti-ulcer, and antineoplastic activities which would help the COVID-19 patients with comorbid conditions [13]. Moreover, the active constituents of N.sativa including nigellidine and α-hederin have been identified as potential inhibitors of SARS CoV-2 [14].

2. Methods

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PubMed, Google Scholar, Science Direct, Directory of open access journals (DOAJ) and reference lists were searched to identify articles associated with antiviral and other properties of N.sativa related to the signs and symptoms of COVID-19 using keywords such as Nigella sativa, black cumin, black seeds, antiviral, antioxidant, anti-inflammatory, immunomodulatory, bronchodilatory, antihistaminic, antitussive and COVID-19. All the studies assessing the antiviral effects and other medicinal properties related to the signs and symptoms of COVID-19 of N.sativa were included in this review.

3.Results

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3.1. Antiviral activity

Many clinical studies have proven that N. sativa is very much effective in treating patients infected with viruses such as Human Immunodeficiency Virus (HIV) as well as Hepatitis C Virus (HCV).

A study recruited 51 HIV-positive patients and they were administered with α-Zam (herbal concoction containing N. sativa and honey) for 16 months. All the patients were relieved of all the signs and symptoms of HIV infection within 4 weeks of commencement of α-Zam therapy. At the end of the herbal therapy, undetectable viral load has been noted in 41 patients and less than 1000 copies/ml of viral load in 10 patients. In addition to decreased viral load, the CD4 count of all participants has been increased [15]. Another study included six HIV-positive patients who took α-Zam (herbal concoction containing N. sativa and honey for 4 months and their signs and symptoms of HIV infection disappeared in 20 days of α-Zam treatment. Moreover, at the end of 4 months, the viral load (HIV-RNA) of the patients decreased consistently to an undetectable level along with increased body weight and CD4 count [16].

Moreover, a complete seroreversion was evidently reported in a 46-year-old HIV positive patient who took 10ml of N.sativa concoction (60% of N.sativa seeds and 40% of honey) two times daily for 6 months. Repeated HIV tests of the patient have shown sustained seroreversion (undetectable viral (HIV-RNA) load) and normal CD4 count since 24 months without N.sativa therapy [17]. Similarly, a sustained seroreversion was noted in a 27-year-old HIV infected pregnant woman who was not eligible for antiretroviral therapy, received 10ml of N.sativa and honey mixture (60% of N.sativa seeds and 40% of honey) three times daily for a year. Repeated serology assessments for 10 years have shown undetectable viral load and CD4 count not less than 750 cells/μL [18].

The administration of soft gelatin capsules of N. sativa seed oil (450 mg) three times daily for 3 months to patients with Hepatitis C Virus (HCV) who were not eligible for Interferon-α therapy, resulted in significant decrease in viral load, increased Total Antioxidant Capacity (TCA) and improved laboratory biomarkers such as total protein, red blood cell, and platelet count, decreased fasting blood glucose, and postprandial glucose in both diabetic and non-diabetic HCV patients and reduced lower-limb edema [19] while, the administration of ethanolic extract of N. sativa in HCV patients found to decrease viral load significantly, to augment α-fetoprotein and other liver function parameters and to overall clinical condition [20] and the administration of combination of natural products (N.sativa, honey, Blue green® tablet, vitamin D3, and linolenic acid) along with chloroquine in 195 HCV patients who were not eligible for Interferon-α therapy, lead to negative HCV-RNA in 6 months among 42.1% of study participants and in 12 months among 54.9% of participants and 64.3% of participants achieved end of treatment response in 18 months [21].

The in vitro and in vivo studies of N.sativa has also shown antiviral efficacy against some other viruses like Murine cytomegalovirus (MCMV) [22], Papaya Ring Spot Virus [23], Hepatitis C Virus (HCV) [24], Avian influenza (H9N2) [25], Newcastle disease virus (NDV) [26] and Peste des Petits Ruminants (PPR) Virus [27]. It has been proposed that antiviral efficacy of N.sativa might be due to raised serum levels of interferon-gamma, increased CD4 count, augmented suppressor function and enhanced numbers of macrophages [22].

3.2. Antioxidant activity

The pathogenesis of SARS-CoV infection is associated with overproduction of reactive oxygen species (ROS) and a deprived antioxidant system [28]. COVID-19 infection can induce the overproduction of numerous reactive oxygen species (ROS) like H2O2, (•O2 −), (•OH), etc. through the stimulation of immunocytes such as macrophages and neutrophils. Multiple organ failure can occur due to excessive ROS which would oxidize cellular proteins and membrane lipids and destroy normal cells in lung and other organs including heart. Hence, potential antioxidants such as Vitamin C (ascorbic acid) and Vitamin E could be recommended to prevent organ damages [29].

N. sativa has shown some potential antioxidant properties in previous studies and its antioxidant activity may help to alleviate oxidative damages to the organs. A randomized controlled clinical trial of 50 obese volunteer women found that N. sativa oil significantly increased the levels of superoxide dismutase (SOD) which is important antioxidant enzyme acting against oxidative stress in the body [30].

In addition, a placebo controlled participant blinded clinical trial of 114 type 2 diabetic patients consisting equal number of participants in control group and N. sativa group, determined that the patients who received 2gm of N. sativa daily for 1 year have shown enhanced antioxidant defense system through significant elevation in total antioxidant capacity (TAC), superoxide dismutase (SOD), and glutathione levels [31]. Significant reduction of plasma levels of malondialdehyde (MDA) and increased activity of erythrocyte glutathione peroxidase (GSH-Px) and superoxide dismutase were reported in thirty postmenopausal women who took N. sativa seed and Allium sativum concomitantly for 2 months [32].

N. sativa has been reported for its effective antioxidant activities of in vivo and in vitro studies too. N. sativa oil has been shown to produce marked antioxidant activity in human pre-adipocytes [33], and the pre-treatment of human retinal pigment epithelial cells with thymoquinone of N. sativa protected them from hydrogen peroxide-induced oxidative stress through the activation of the nuclear factor erythroid 2-related factor 2 (Nrf2)/ Heme oxygenase-1 (HO-1) pathway [34]. And the bioactive constituents of N. sativa like thymoquinone, carvacrol, t-anethole and 4-terpineol demonstrated variable antioxidant activity [35].

3.3. Anti-inflammatory activity

Inflammation plays a crucial role in tissue damage occurring due to many chronic diseases like asthma, rheumatoid arthritis, cancer, diabetes, cardiovascular disorders, Alzheimer’s disease, epilepsy and various infections [36]. The patients with severe COVID-19 observed with high levels of circulating inflammatory cytokines such as IL-6, IL-7 and tumor necrosis factor (TNF) and also of inflammatory chemokines including CC-chemokine ligand 2 (CCL2), CCL3 and CXC-chemokine ligand 10 (CXCL10). Disease severity and death are associated with excessive inflammatory response to SARS-CoV-2 infection [37]. The Janus kinase (JAK) inhibitor like Baricitinib is preferred as an anti-inflammatory agent to treat COVID-19 patients, as it has low plasma protein binding and has minimal interaction potential with CYP enzymes and drug transporters [38].

Previous studies have confirmed the anti-inflammatory activity of N. sativa which may reduce the effects of cytokine storm. A placebo controlled study of 40 female patients with rheumatoid arthritis (RA) who received N. sativa oil capsules (500 mg) twice daily, has shown improvement in number of inflamed joints, incidence of morning stiffness, and disease activity score [39] and a randomized, double blind, placebo-controlled clinical trial of 42 patients with rheumatoid arthritis (RA) where the participants of intervention group received 2 capsules of N. sativa oil (500mg), each day for 8 weeks and the levels of nitric oxide (NO) and malondialdehyde (MDA) decreased significantly in participants treated with N. sativa. The anti-inflammatory effect of N. sativa probably due to the inhibition of nuclear factor kappa B (NF-κB) [40].

Another randomized double blind, placebo-controlled clinical trial of 90 volunteer obese women who were divided equally in to intervention group (treated with the supplementation of 3g of N. sativa oil daily) and a placebo group. The participants of both the groups were on low-calorie diet along with their supplementation for 8 weeks. The systemic inflammatory biomarkers including Tumor necrosis factor-α (TNF-α) and C-reactive protein (CRP) were reduced in N. sativa treated group compared to placebo group [41]. The anti-inflammatory activity of N. sativa further revealed in another randomized double blind, placebo-controlled clinical trial of 43 patients with type 2 diabetes mellitus. Among them 23 patients were assigned to intervention group who were supplemented with 500mg of N. sativa capsules two times daily and 20 patients kept in placebo group, for 8 weeks. The serum levels of malondialdehyde (MDA) and nitric oxide (NO) decreased significantly in patients supplemented with N. sativa [42]. The anti-inflammatory activity of N. sativa further revealed in another randomized double blind, placebo-controlled clinical trial of 96 patients with Behcet's disease (BD) divided randomly as intervention group (received 1000mg/day of N. sativa oil capsules) and placebo group. The patients who received N. sativa showed significant reduction in the serum levels of malondialdehyde (MDA) and no significant changes were found in other parameters studied such as tumor necrosis factor-α (TNF-α), Interleukin -10 (IL-10) and high sensitivity C-reactive protein (hs- CRP) probably due to lower dose of N. sativa [43].Thymoquinone of N. sativa inhibited the formation of leukotrienes (LTC4 and LTB4) in human blood cells, probably due to the inhibition of 5-lipoxygenase and LTC4 synthase enzymes [44].

3.4. Immunomodulatory effect

Over activation of immune system could be found in hospitalized COVID-19 patients and it is described as a cytokine storm, which can lead to multiple organ failure. And it has been suggested that the need for ventilators and extracorporeal membrane oxygenation (ECMO) might be avoided by early and aggressive immunomodulatory treatment [45].

Certain active ingredients of N. sativa and its oil have shown beneficial immunomodulatory effects through the augmentation of immune responses related to T lymphocytes and natural killer cells [46]. A clinical study recruited 24 patients with allergic rhinitis sensitive to house dust mites and 7 healthy volunteers, administered with conventional doses of allergen-specific immunotherapy for 30 days. After a month of immunotherapy, 12 patients among 24 received the 2 g/day oral supplementation of N. sativa seed for 30 days that resulted in significant raise of CD8 counts and polymorphonuclear leukocyte (PMN) along with improved clinical symptoms [47] and a randomized, double-blinded placebo-controlled clinical trial of 43 female patients with mild to moderate rheumatoid arthritis (RA) revealed that administration of capsules of 500mg N. sativa oil 2 times daily for 2 months resulted in modulation of T lymphocytes such as decreased CD8+ (suppressive lymphocyte), and increased percentage of CD4+CD25+ and the ratio of CD4+/CD8+ [48].

3.5. Anticoagulant activity

Significant coagulopathy is attributed to severe COVID-19 infection [49] and to prevent venous thromboembolism, it is recommended to administer prophylactic dose of low molecular weight heparin (LMWH) in COVID-19 patients and the treatment dose of LMWH in patients with significantly higher d-dimer concentrations [50].

A clinical study of 94 patients (43 men and 51 women) with type 2 diabetes mellitus who were randomly divided into three groups receiving capsules containing 500 mg of grounded N. sativa seeds in different doses of 1, 2, and 3 g of N. sativa daily for 12 weeks. The patients treated with 2 g/day of N. sativa seeds showed a significant increase in Partial thromboplastin time (PTT) along with a significant reduction in the systolic blood pressure, diastolic blood pressure, mean arterial pressure, and heart rate at the end of the study. Administration of NS seeds increased the PTT but not Prothrombin Time (PT) which indicates the inhibition of the intrinsic pathway of the clotting mechanism [51].

In vitro coagulation assays of thromboelastography (TEG) and activated partial thromboplastin time (aPTT) using pancreatic cancer cell lines, tested the anticoagulant effect of Thymoquinone of N. sativa and it has been determined that Thymoquinone reversed the cancer-associated thrombosis (CAT) by returning tissue factor (TF) and inflammation to basal levels. Moreover, Thymoquinone inhibited the activity of factor Xa significantly, at higher concentrations (0.8-1.6 mg/mL) [52].

Another set of in vitro coagulation assays of thrombin time (TT), prothrombin time (PT), and activated partial thromboplastin time (aPTT) testing the anticoagulant effect of N. sativa seed extract revealed that it has prolonged the coagulation time transiently. The prolongation of TT, PT and aPTT indicates that N. sativa inhibit the coagulation activity of extrinsic, common and intrinsic pathways probably due to the presence of coumarin like substance [53].

3.6. Bronchodilatory effect

A randomized double blind clinical trial of 15 patients with asthma who received 50 and 100 mg/kg of boiled extract of N. sativa seeds, showed a relatively potent bronchodilatory effect through a short significant increase in peak expiratory flow (PEF), forced expiratory volume in one second (FEV1), maximal expiratory flow (MEF), maximal mid expiratory flow (MMEF), and specific airway conductance [54].

Another randomized single-blind placebo-controlled clinical trial of 73 patients with asthma divided randomly in to 3 groups receiving placebo, 1 capsule of 500 mg ground seeds of N. sativa 2 times daily and 2 capsules of 500 mg ground seeds of N. sativa 2 times daily respectively, for 12 weeks along with maintenance inhaled therapy. The patients treated with N. sativa have shown significant improvements in forced expiratory volume in one second (FEV1), peak expiratory flow (PEF), serum interferon-γ, and asthma control test (ACT) score and a significant reduction of fractional exhaled nitric oxide (FeNO) and serum total immunoglobulin E (IgE). Adjuvant therapy with N. sativa could decrease the exacerbations and improve overall control of asthma [55].

3.7. Antihistaminic activity

A randomized single-blind clinical trial of 20 patients with seasonal allergic rhinitis who were administered with 250 mg of N. sativa seeds orally for days, has shown a significant reduction of seasonal allergic rhinitis symptoms score [56] and a randomized single-blind uncontrolled comparative clinical trial conducted on 47 patients with seasonal allergic rhinitis who were orally administered with either N. sativa (250 mg/day) or montelukast (10 mg/day) for 2 weeks, randomly. The administration of N. sativa led to a significant reduction of daytime and ophthalmic symptoms and total eosinophil count comparable to montelukast [57].

Another randomized double blind clinical trial of 66 patients with allergic rhinitis has shown that the administration of N. sativa oil capsules (0.5 ml/day) for 4 weeks resulted in reduction of clinical symptoms such as nasal itching, rhinorrhea, sneezing attacks, nasal congestion, turbinate hypertrophy and mucosal pallor [58]. A total of 68 allergic rhinitis patients with different severities (mild, moderate and severe) were topically administered with 1 drop of N. sativa seed oil in each nostril 3 times daily for 6 weeks and at the end of the study the patients with mild, moderate and severe allergic rhinitis symptoms were relieved of 100%, 68.7% and 58.3% respectively [59]. It has been proposed that N. sativa may exert its antihistaminic activity through the inhibition of release of histamine and leukotrines and blocking histamine receptors [56].

3.8. Antitussive property

The antitussive property of N. sativa was demonstrated in guinea pigs using the aerosols of 2 different concentrations of aqueous and macerated extracts, one concentration of boiled extract, and was compared with the aerosols of codeine, and saline. After 10 minutes of exposure of aerosols of different solutions, the animals were induced with coughs by the aerosol of citric acid, and it has been noted that the number of coughs produced in animals exposed to N. sativa and codeine were significantly less compared to saline treated animals [60].

The antitussive property of thymoquinone of N. sativa was also evaluated in guinea pigs induced with coughs by the aerosol of 20% citric acid and it was compared with codeine. The intraperitoneal injections of thymoquinone and codeine reduced the number of coughs significantly. Pretreatment of animals with naloxone (2 mg/kg) abolished the antitussive effect of thymoquinone and codeine indicating that thymoquinone exerts antitussive activity by its anti-inflammatory, bronchodilatory effects mediated probably through opioid receptors [61].

4. Conclusion

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Various randomized controlled trials, pilot studies, case reports and in vitro and in vivo studies confirmed that N. sativa has antiviral, antioxidant, anti-inflammatory, immunomodulatory, bronchodilatory, antihistaminic, antitussive activities related to causative oraganism and signs and symptoms of COVID-19. In addition, N. sativahas also shown anti-hypertensive, anti-obesity, anti-diabetic, anti-hyperlipidemic, anti-ulcer, and antineoplastic activities which would help the COVID-19 patients with comorbid conditions. Moreover, the active constituents of N. sativa such as nigellidine and α-hederin have been identified as potential inhibitor of SARS CoV-2. N. sativa could be used as an adjuvant therapy along with repurposed conventional drugs to manage the patients with COVID-19. Adjuvant therapy of N. sativa may reduce the adverse effects of conventional medicines by helping to decrease their doses. However, more randomized controlled trials are required to confirm the potential beneficial effects of N. sativa to treat the patients with COVID-19, as an alternative herbal medicine.

CONFLICTS OF INTEREST

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Conflict of Interest

The authors declare that there are no conflicts of interest.

Figures

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Fig. 1.

Potential Pharmacological activities of N. sativa to manage COVID-19


Tables

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Drugs used for arthritis. Conventional Disease Modifying Anti-Rheumatic Drugs (DMARDs)

S.NoPharmacological ActivityType of StudyNo. of ParticipantsFindings
1Antiviral (Anti-HIV)Pilot study [15]51Undetectable viral load noted in 41 patients and less than 1000 copies/ml of viral load in 10 patients.
CD4 count of all participants has been increased.
2Antiviral (Anti-HIV)Pilot study [16]6Undetectable viral load (HIV-RNA) in all patients.
Increased body weight
Increased CD4 count.
3Antiviral (Anti-HIV)Case report [17]1Complete seroreversion.
Normal CD4 count.
4Antiviral (Anti-HIV)Case report [18]1Sustained seroreversion.
CD4 count not less than 750 cells/μL.
5Antiviral (Anti-HCV)Pilot study [19]30Significant decrease in viral load.
Increased Total Antioxidant Capacity (TCA).
Improved laboratory biomarkers such as total protein, red blood cell, and platelet count.
Decreased fasting blood glucose and postprandial glucose in both diabetic and non-diabetic HCV patients.
Reduced lower-limb edema
6Antiviral (Anti-HCV)Pilot study [20]60Significant decrease in viral load.
Augmentation of α-femiddlerotein and other liver function parameters.
7Antiviral (Anti-HCV)Pilot study [21]195Negative HCV-RNA
8AntioxidantRandomized controlled clinical trial [30]50Significant raise of levels of superoxide dismutase (SOD).
9AntioxidantPlacebo controlled participant blinded clinical trial [31]114Significant elevation of total antioxidant capacity (TAC), superoxide dismutase (SOD), and glutathione levels.
10Antioxidant Pilot study [32]30Significant reduction of plasma levels of malondialdehyde (MDA).
Increased activity of erythrocyte glutathione peroxidase (GSH-Px) and superoxide dismutase.
11Anti-inflammatoryPlacebo controlled study [39]40Improvement in number of inflamed joints, incidence of morning stiffness, and disease activity score.
12Anti-inflammatoryRandomized, double blind, placebo-controlled clinical trial [40]42Significant decrease in the levels of malondialdehyde (MDA) and nitric oxide (NO).
13Anti-inflammatoryRandomized double blind, placebo-controlled clinical trial [41]90Significant reduction of systemic inflammatory biomarkers including Tumor necrosis factor-α (TNF-α) and C-reactive protein (CRP).
14Anti-inflammatoryRandomized double blind, placebo-controlled clinical trial [42]43Significant reduction of serum levels of malondialdehyde (MDA) and nitric oxide (NO).
15Anti-inflammatoryRandomized double blind, placebo-controlled clinical trial [43]96Significant reduction of serum levels of malondialdehyde (MDA).
16ImmunomodulatoryPilot study [47]24Significant raise of CD8 counts and polymorphonuclear leukocyte (PMN).
Improved clinical symptoms.
17ImmunomodulatoryRandomized double blind, placebo-controlled clinical trial [48]43Decreased CD8+ and increased percentage of CD4+CD25+ and the ratio of CD4+/CD8+.
18AnticoagulantRandomized double blind, placebo-controlled clinical trial [51]94Significant increase in Partial thromboplastin time (PTT).
Significant reduction of systolic blood pressure, diastolic blood pressure, means arterial pressure, and heart rate.
19BronchodilatoryRandomized double blind clinical trial [54]15Short significant increase in peak expiratory flow (PEF), forced expiratory volume in one second (FEV1), maximal expiratory flow (MEF), maximal mid expiratory flow (MMEF), and specific airway conductance.
20BronchodilatoryRandomized single-blind placebo-controlled clinical trial [55]73Significant improvements in forced expiratory volume in one second (FEV1), peak expiratory flow (PEF), serum interferon-γ, and asthma control test (ACT) score.
Significant reduction of fractional exhaled nitric oxide (FeNO) and serum total immunoglobulin E (IgE).
21AntihistaminicRandomized single-blind clinical trial [56]20Significant reduction of seasonal allergic rhinitis symptoms score.
22AntihistaminicRandomized single-blind uncontrolled comparative clinical trial [57]47Significant reduction of daytime and ophthalmic symptoms and total eosinophil count comparable to montelukast.
23AntihistaminicRandomized double blind clinical trial [58]66Reduction of clinical symptoms such as nasal itching, rhinorrhea, sneezing attacks, nasal congestion, turbinate hypertrophy and mucosal pallor.
24AntihistaminicPilot study [59]68Relief of symptoms of allergic rhinitis.

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Article

Review Article

J Pharmacopuncture 2020; 23(2): 62-70

Published online June 30, 2020 https://doi.org/10.3831/KPI.2020.23.010

Copyright © The Korean Pharmacopuncture Institute.

Prophetic Medicine-Nigella Sativa (Black cumin seeds) – Potential herb for COVID-19?

Naina Mohamed Pakkir Maideen1,*

1Dubai Health Authority, Dubai, United Arab Emirates

Correspondence to:*Corresponding Author Naina Mohamed Pakkir Maideen. Pharmacologist, Dubai Health Authority 4545, Dubai,, United Arab Emirates., Tel: +971-4216-4952, +971-5057-69833 Fax: +971-4224-4302 E-mail: nmmaideen@dha.gov.ae

Received: May 30, 2020; Revised: June 2, 2020; Accepted: June 8, 2020

This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Coronavirus disease-19 (COVID-19) is caused by the severe acute respiratory syndrome coronavirus 2 (SARS CoV-2). Currently, the management of patients with COVID-19 depends mainly on repurposed drugs which include chloroquine, hydroxychloroquine, lopinavir/ritonavir, ribavirin, remdesivir, favipiravir, umifenovir, interferon-α, interferon-β and others. In this review, the potential of Nigella sativa (black cumin seeds) to treat the patients with COVID-19 analyzed, as it has shown to possess antiviral, antioxidant, anti-inflammatory, anticoagulant, immunomodulatory, bronchodilatory, antihistaminic, antitussive, antipyretic and analgesic activities. PubMed, Google Scholar, Science Direct, Directory of open access journals (DOAJ) and reference lists were searched to identify articles associated with antiviral and other properties of N.sativa related to the signs and symptoms of COVID-19. Various randomized controlled trials, pilot studies, case reports and in vitro and in vivo studies confirmed that N.sativa has antiviral, antioxidant, anti-inflammatory, immunomodulatory, bronchodilatory, antihistaminic, antitussive activities related to causative oraganism and signs and symptoms of COVID-19. N. sativa could be used as an adjuvant therapy along with repurposed conventional drugs to manage the patients with COVID-19.

Keywords: Nigella sativa, Black seeds, Antiviral, Antioxidant, Anti-inflammatory, Anticoagulant

1. Introduction

Coronavirus disease-19 (COVID-19) is caused by the severe acute respiratory syndrome coronavirus 2 (SARS CoV-2) and this virus was first originated from Wuhan city of Hubei province of China spreading around the globe [1]. Around 5 million of COVID-19 cases have been reported across the world and 0.3 million deaths occurred among them, till 21st May 2020 [2].

The prominent symptoms of COVID-19 include fever, cough and dyspnea [3] and other symptoms noted in patients affected by COVID-19 may include chills, repeated shaking with chills, muscle pain, headache, sore throat and new loss of taste or smell [4]. In addition, the emergency warning signs of COVID-19 include difficulty breathing or shortness of breath, persistent pain or pressure in the chest, new confusion or inability to arouse and bluish lips or face and the patients experiencing any of these signs should get immediate medical attention [5].

The development of specific antiviral drugs and vaccines to treat COVID-19 patients will take months or years to complete. Hence, the treatments of COVID-19 depend mainly on repurposed drugs which include chloroquine, hydroxychloroquine, lopinavir/ritonavir, ribavirin, remdesivir, favipiravir, umifenovir, interferon-α, interferon-β and others. As of this time, there is no specific, effective and proven conventional medicine to manage patients affected by COVID-19 and as of April 2, 2020, there are 291 active clinical trials found specific to COVID-19. Among them 109 trials included pharmacological therapy for the treatment of COVID-19 in adult patients [6].

Similarly, the herbal medicine can contribute as an alternative measure to manage the patients with COVID-19 as there are many traditional herbs shown antiviral and other medicinal properties.

In this review, the potential of Nigella sativa (black cumin seeds) to treat the patients with COVID-19 analyzed, as Prophet Muhammad (PBUH) stated that “In the black cumin, there is a cure for every disease except death”. In addition, the black cumin is also mentioned in Holy Bible as “Curative black seed” and is described as ‘Melanthion of Hippocrates and Dioscorides’ and as ‘Glitch of Pliny’ [7].

N. sativa belongs to the Ranunculacea family and it is also known as black cumin seed, black seed, Habbatul Barakah, Habbatus sawda, kalonji, etc [8]. In traditional medicine, N. sativa has been used for centuries to treat various illnesses including asthma, common cold, headache, nasal congestion, rheumatic diseases, warts and many others [9]. More recently, N. sativa has been used to treat conditions like infections, cancer, diabetes, hypertension, obesity, cardiovascular diseases, and gastrointestinal problems [10]. The medicinal properties of N. sativa have been demonstrated in Unani, Chinese medicine, ayurveda and other medicinal systems [11].

Phytochemical screening of N.Sativa revealed that it contains various compounds including terpenes, flavanoids, phytosterols, tannins, coumarins, phenolic compounds, alkaloids, cardiac glycosides, saponins fatty acids, and volatile oils. The bioactive constituents of N. sativa include terpenes such as thymoquinone (TQ), dithymoquinone (DTQ), carvone, limonine, trans-anethol, and p-cymene, indazole alkaloids like nigellidine and nigellicine, and isoquinoline alkaloids including nigellicimine, nigellicimine-N-oxide and α-hederin [12].

As N.sativa possesses antiviral, antioxidant, anti-inflammatory, anticoagulant, immunomodulatory, bronchodilatory, antihistaminic, antitussive, antipyretic and analgesic activities (Fig. 1), it would be a potential herbal candidate to treat the patients with COVID-19 (Table 1). In addition, N.sativa has also shown anti-hypertensive, anti-obesity, anti-diabetic, anti-hyperlipidemic, anti-ulcer, and antineoplastic activities which would help the COVID-19 patients with comorbid conditions [13]. Moreover, the active constituents of N.sativa including nigellidine and α-hederin have been identified as potential inhibitors of SARS CoV-2 [14].

2. Methods

PubMed, Google Scholar, Science Direct, Directory of open access journals (DOAJ) and reference lists were searched to identify articles associated with antiviral and other properties of N.sativa related to the signs and symptoms of COVID-19 using keywords such as Nigella sativa, black cumin, black seeds, antiviral, antioxidant, anti-inflammatory, immunomodulatory, bronchodilatory, antihistaminic, antitussive and COVID-19. All the studies assessing the antiviral effects and other medicinal properties related to the signs and symptoms of COVID-19 of N.sativa were included in this review.

3.Results

3.1. Antiviral activity

Many clinical studies have proven that N. sativa is very much effective in treating patients infected with viruses such as Human Immunodeficiency Virus (HIV) as well as Hepatitis C Virus (HCV).

A study recruited 51 HIV-positive patients and they were administered with α-Zam (herbal concoction containing N. sativa and honey) for 16 months. All the patients were relieved of all the signs and symptoms of HIV infection within 4 weeks of commencement of α-Zam therapy. At the end of the herbal therapy, undetectable viral load has been noted in 41 patients and less than 1000 copies/ml of viral load in 10 patients. In addition to decreased viral load, the CD4 count of all participants has been increased [15]. Another study included six HIV-positive patients who took α-Zam (herbal concoction containing N. sativa and honey for 4 months and their signs and symptoms of HIV infection disappeared in 20 days of α-Zam treatment. Moreover, at the end of 4 months, the viral load (HIV-RNA) of the patients decreased consistently to an undetectable level along with increased body weight and CD4 count [16].

Moreover, a complete seroreversion was evidently reported in a 46-year-old HIV positive patient who took 10ml of N.sativa concoction (60% of N.sativa seeds and 40% of honey) two times daily for 6 months. Repeated HIV tests of the patient have shown sustained seroreversion (undetectable viral (HIV-RNA) load) and normal CD4 count since 24 months without N.sativa therapy [17]. Similarly, a sustained seroreversion was noted in a 27-year-old HIV infected pregnant woman who was not eligible for antiretroviral therapy, received 10ml of N.sativa and honey mixture (60% of N.sativa seeds and 40% of honey) three times daily for a year. Repeated serology assessments for 10 years have shown undetectable viral load and CD4 count not less than 750 cells/μL [18].

The administration of soft gelatin capsules of N. sativa seed oil (450 mg) three times daily for 3 months to patients with Hepatitis C Virus (HCV) who were not eligible for Interferon-α therapy, resulted in significant decrease in viral load, increased Total Antioxidant Capacity (TCA) and improved laboratory biomarkers such as total protein, red blood cell, and platelet count, decreased fasting blood glucose, and postprandial glucose in both diabetic and non-diabetic HCV patients and reduced lower-limb edema [19] while, the administration of ethanolic extract of N. sativa in HCV patients found to decrease viral load significantly, to augment α-fetoprotein and other liver function parameters and to overall clinical condition [20] and the administration of combination of natural products (N.sativa, honey, Blue green® tablet, vitamin D3, and linolenic acid) along with chloroquine in 195 HCV patients who were not eligible for Interferon-α therapy, lead to negative HCV-RNA in 6 months among 42.1% of study participants and in 12 months among 54.9% of participants and 64.3% of participants achieved end of treatment response in 18 months [21].

The in vitro and in vivo studies of N.sativa has also shown antiviral efficacy against some other viruses like Murine cytomegalovirus (MCMV) [22], Papaya Ring Spot Virus [23], Hepatitis C Virus (HCV) [24], Avian influenza (H9N2) [25], Newcastle disease virus (NDV) [26] and Peste des Petits Ruminants (PPR) Virus [27]. It has been proposed that antiviral efficacy of N.sativa might be due to raised serum levels of interferon-gamma, increased CD4 count, augmented suppressor function and enhanced numbers of macrophages [22].

3.2. Antioxidant activity

The pathogenesis of SARS-CoV infection is associated with overproduction of reactive oxygen species (ROS) and a deprived antioxidant system [28]. COVID-19 infection can induce the overproduction of numerous reactive oxygen species (ROS) like H2O2, (•O2 −), (•OH), etc. through the stimulation of immunocytes such as macrophages and neutrophils. Multiple organ failure can occur due to excessive ROS which would oxidize cellular proteins and membrane lipids and destroy normal cells in lung and other organs including heart. Hence, potential antioxidants such as Vitamin C (ascorbic acid) and Vitamin E could be recommended to prevent organ damages [29].

N. sativa has shown some potential antioxidant properties in previous studies and its antioxidant activity may help to alleviate oxidative damages to the organs. A randomized controlled clinical trial of 50 obese volunteer women found that N. sativa oil significantly increased the levels of superoxide dismutase (SOD) which is important antioxidant enzyme acting against oxidative stress in the body [30].

In addition, a placebo controlled participant blinded clinical trial of 114 type 2 diabetic patients consisting equal number of participants in control group and N. sativa group, determined that the patients who received 2gm of N. sativa daily for 1 year have shown enhanced antioxidant defense system through significant elevation in total antioxidant capacity (TAC), superoxide dismutase (SOD), and glutathione levels [31]. Significant reduction of plasma levels of malondialdehyde (MDA) and increased activity of erythrocyte glutathione peroxidase (GSH-Px) and superoxide dismutase were reported in thirty postmenopausal women who took N. sativa seed and Allium sativum concomitantly for 2 months [32].

N. sativa has been reported for its effective antioxidant activities of in vivo and in vitro studies too. N. sativa oil has been shown to produce marked antioxidant activity in human pre-adipocytes [33], and the pre-treatment of human retinal pigment epithelial cells with thymoquinone of N. sativa protected them from hydrogen peroxide-induced oxidative stress through the activation of the nuclear factor erythroid 2-related factor 2 (Nrf2)/ Heme oxygenase-1 (HO-1) pathway [34]. And the bioactive constituents of N. sativa like thymoquinone, carvacrol, t-anethole and 4-terpineol demonstrated variable antioxidant activity [35].

3.3. Anti-inflammatory activity

Inflammation plays a crucial role in tissue damage occurring due to many chronic diseases like asthma, rheumatoid arthritis, cancer, diabetes, cardiovascular disorders, Alzheimer’s disease, epilepsy and various infections [36]. The patients with severe COVID-19 observed with high levels of circulating inflammatory cytokines such as IL-6, IL-7 and tumor necrosis factor (TNF) and also of inflammatory chemokines including CC-chemokine ligand 2 (CCL2), CCL3 and CXC-chemokine ligand 10 (CXCL10). Disease severity and death are associated with excessive inflammatory response to SARS-CoV-2 infection [37]. The Janus kinase (JAK) inhibitor like Baricitinib is preferred as an anti-inflammatory agent to treat COVID-19 patients, as it has low plasma protein binding and has minimal interaction potential with CYP enzymes and drug transporters [38].

Previous studies have confirmed the anti-inflammatory activity of N. sativa which may reduce the effects of cytokine storm. A placebo controlled study of 40 female patients with rheumatoid arthritis (RA) who received N. sativa oil capsules (500 mg) twice daily, has shown improvement in number of inflamed joints, incidence of morning stiffness, and disease activity score [39] and a randomized, double blind, placebo-controlled clinical trial of 42 patients with rheumatoid arthritis (RA) where the participants of intervention group received 2 capsules of N. sativa oil (500mg), each day for 8 weeks and the levels of nitric oxide (NO) and malondialdehyde (MDA) decreased significantly in participants treated with N. sativa. The anti-inflammatory effect of N. sativa probably due to the inhibition of nuclear factor kappa B (NF-κB) [40].

Another randomized double blind, placebo-controlled clinical trial of 90 volunteer obese women who were divided equally in to intervention group (treated with the supplementation of 3g of N. sativa oil daily) and a placebo group. The participants of both the groups were on low-calorie diet along with their supplementation for 8 weeks. The systemic inflammatory biomarkers including Tumor necrosis factor-α (TNF-α) and C-reactive protein (CRP) were reduced in N. sativa treated group compared to placebo group [41]. The anti-inflammatory activity of N. sativa further revealed in another randomized double blind, placebo-controlled clinical trial of 43 patients with type 2 diabetes mellitus. Among them 23 patients were assigned to intervention group who were supplemented with 500mg of N. sativa capsules two times daily and 20 patients kept in placebo group, for 8 weeks. The serum levels of malondialdehyde (MDA) and nitric oxide (NO) decreased significantly in patients supplemented with N. sativa [42]. The anti-inflammatory activity of N. sativa further revealed in another randomized double blind, placebo-controlled clinical trial of 96 patients with Behcet's disease (BD) divided randomly as intervention group (received 1000mg/day of N. sativa oil capsules) and placebo group. The patients who received N. sativa showed significant reduction in the serum levels of malondialdehyde (MDA) and no significant changes were found in other parameters studied such as tumor necrosis factor-α (TNF-α), Interleukin -10 (IL-10) and high sensitivity C-reactive protein (hs- CRP) probably due to lower dose of N. sativa [43].Thymoquinone of N. sativa inhibited the formation of leukotrienes (LTC4 and LTB4) in human blood cells, probably due to the inhibition of 5-lipoxygenase and LTC4 synthase enzymes [44].

3.4. Immunomodulatory effect

Over activation of immune system could be found in hospitalized COVID-19 patients and it is described as a cytokine storm, which can lead to multiple organ failure. And it has been suggested that the need for ventilators and extracorporeal membrane oxygenation (ECMO) might be avoided by early and aggressive immunomodulatory treatment [45].

Certain active ingredients of N. sativa and its oil have shown beneficial immunomodulatory effects through the augmentation of immune responses related to T lymphocytes and natural killer cells [46]. A clinical study recruited 24 patients with allergic rhinitis sensitive to house dust mites and 7 healthy volunteers, administered with conventional doses of allergen-specific immunotherapy for 30 days. After a month of immunotherapy, 12 patients among 24 received the 2 g/day oral supplementation of N. sativa seed for 30 days that resulted in significant raise of CD8 counts and polymorphonuclear leukocyte (PMN) along with improved clinical symptoms [47] and a randomized, double-blinded placebo-controlled clinical trial of 43 female patients with mild to moderate rheumatoid arthritis (RA) revealed that administration of capsules of 500mg N. sativa oil 2 times daily for 2 months resulted in modulation of T lymphocytes such as decreased CD8+ (suppressive lymphocyte), and increased percentage of CD4+CD25+ and the ratio of CD4+/CD8+ [48].

3.5. Anticoagulant activity

Significant coagulopathy is attributed to severe COVID-19 infection [49] and to prevent venous thromboembolism, it is recommended to administer prophylactic dose of low molecular weight heparin (LMWH) in COVID-19 patients and the treatment dose of LMWH in patients with significantly higher d-dimer concentrations [50].

A clinical study of 94 patients (43 men and 51 women) with type 2 diabetes mellitus who were randomly divided into three groups receiving capsules containing 500 mg of grounded N. sativa seeds in different doses of 1, 2, and 3 g of N. sativa daily for 12 weeks. The patients treated with 2 g/day of N. sativa seeds showed a significant increase in Partial thromboplastin time (PTT) along with a significant reduction in the systolic blood pressure, diastolic blood pressure, mean arterial pressure, and heart rate at the end of the study. Administration of NS seeds increased the PTT but not Prothrombin Time (PT) which indicates the inhibition of the intrinsic pathway of the clotting mechanism [51].

In vitro coagulation assays of thromboelastography (TEG) and activated partial thromboplastin time (aPTT) using pancreatic cancer cell lines, tested the anticoagulant effect of Thymoquinone of N. sativa and it has been determined that Thymoquinone reversed the cancer-associated thrombosis (CAT) by returning tissue factor (TF) and inflammation to basal levels. Moreover, Thymoquinone inhibited the activity of factor Xa significantly, at higher concentrations (0.8-1.6 mg/mL) [52].

Another set of in vitro coagulation assays of thrombin time (TT), prothrombin time (PT), and activated partial thromboplastin time (aPTT) testing the anticoagulant effect of N. sativa seed extract revealed that it has prolonged the coagulation time transiently. The prolongation of TT, PT and aPTT indicates that N. sativa inhibit the coagulation activity of extrinsic, common and intrinsic pathways probably due to the presence of coumarin like substance [53].

3.6. Bronchodilatory effect

A randomized double blind clinical trial of 15 patients with asthma who received 50 and 100 mg/kg of boiled extract of N. sativa seeds, showed a relatively potent bronchodilatory effect through a short significant increase in peak expiratory flow (PEF), forced expiratory volume in one second (FEV1), maximal expiratory flow (MEF), maximal mid expiratory flow (MMEF), and specific airway conductance [54].

Another randomized single-blind placebo-controlled clinical trial of 73 patients with asthma divided randomly in to 3 groups receiving placebo, 1 capsule of 500 mg ground seeds of N. sativa 2 times daily and 2 capsules of 500 mg ground seeds of N. sativa 2 times daily respectively, for 12 weeks along with maintenance inhaled therapy. The patients treated with N. sativa have shown significant improvements in forced expiratory volume in one second (FEV1), peak expiratory flow (PEF), serum interferon-γ, and asthma control test (ACT) score and a significant reduction of fractional exhaled nitric oxide (FeNO) and serum total immunoglobulin E (IgE). Adjuvant therapy with N. sativa could decrease the exacerbations and improve overall control of asthma [55].

3.7. Antihistaminic activity

A randomized single-blind clinical trial of 20 patients with seasonal allergic rhinitis who were administered with 250 mg of N. sativa seeds orally for days, has shown a significant reduction of seasonal allergic rhinitis symptoms score [56] and a randomized single-blind uncontrolled comparative clinical trial conducted on 47 patients with seasonal allergic rhinitis who were orally administered with either N. sativa (250 mg/day) or montelukast (10 mg/day) for 2 weeks, randomly. The administration of N. sativa led to a significant reduction of daytime and ophthalmic symptoms and total eosinophil count comparable to montelukast [57].

Another randomized double blind clinical trial of 66 patients with allergic rhinitis has shown that the administration of N. sativa oil capsules (0.5 ml/day) for 4 weeks resulted in reduction of clinical symptoms such as nasal itching, rhinorrhea, sneezing attacks, nasal congestion, turbinate hypertrophy and mucosal pallor [58]. A total of 68 allergic rhinitis patients with different severities (mild, moderate and severe) were topically administered with 1 drop of N. sativa seed oil in each nostril 3 times daily for 6 weeks and at the end of the study the patients with mild, moderate and severe allergic rhinitis symptoms were relieved of 100%, 68.7% and 58.3% respectively [59]. It has been proposed that N. sativa may exert its antihistaminic activity through the inhibition of release of histamine and leukotrines and blocking histamine receptors [56].

3.8. Antitussive property

The antitussive property of N. sativa was demonstrated in guinea pigs using the aerosols of 2 different concentrations of aqueous and macerated extracts, one concentration of boiled extract, and was compared with the aerosols of codeine, and saline. After 10 minutes of exposure of aerosols of different solutions, the animals were induced with coughs by the aerosol of citric acid, and it has been noted that the number of coughs produced in animals exposed to N. sativa and codeine were significantly less compared to saline treated animals [60].

The antitussive property of thymoquinone of N. sativa was also evaluated in guinea pigs induced with coughs by the aerosol of 20% citric acid and it was compared with codeine. The intraperitoneal injections of thymoquinone and codeine reduced the number of coughs significantly. Pretreatment of animals with naloxone (2 mg/kg) abolished the antitussive effect of thymoquinone and codeine indicating that thymoquinone exerts antitussive activity by its anti-inflammatory, bronchodilatory effects mediated probably through opioid receptors [61].

4. Conclusion

Various randomized controlled trials, pilot studies, case reports and in vitro and in vivo studies confirmed that N. sativa has antiviral, antioxidant, anti-inflammatory, immunomodulatory, bronchodilatory, antihistaminic, antitussive activities related to causative oraganism and signs and symptoms of COVID-19. In addition, N. sativahas also shown anti-hypertensive, anti-obesity, anti-diabetic, anti-hyperlipidemic, anti-ulcer, and antineoplastic activities which would help the COVID-19 patients with comorbid conditions. Moreover, the active constituents of N. sativa such as nigellidine and α-hederin have been identified as potential inhibitor of SARS CoV-2. N. sativa could be used as an adjuvant therapy along with repurposed conventional drugs to manage the patients with COVID-19. Adjuvant therapy of N. sativa may reduce the adverse effects of conventional medicines by helping to decrease their doses. However, more randomized controlled trials are required to confirm the potential beneficial effects of N. sativa to treat the patients with COVID-19, as an alternative herbal medicine.

CONFLICTS OF INTEREST

Conflict of Interest

The authors declare that there are no conflicts of interest.

Fig 1.

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Figure 1.

Potential Pharmacological activities of N. sativa to manage COVID-19

Journal of Pharmacopuncture 2020; 23: 62-70https://doi.org/10.3831/KPI.2020.23.010

Table 1 . Drugs used for arthritis. Conventional Disease Modifying Anti-Rheumatic Drugs (DMARDs).

S.NoPharmacological ActivityType of StudyNo. of ParticipantsFindings
1Antiviral (Anti-HIV)Pilot study [15]51Undetectable viral load noted in 41 patients and less than 1000 copies/ml of viral load in 10 patients.CD4 count of all participants has been increased.
2Antiviral (Anti-HIV)Pilot study [16]6Undetectable viral load (HIV-RNA) in all patients.Increased body weightIncreased CD4 count.
3Antiviral (Anti-HIV)Case report [17]1Complete seroreversion.Normal CD4 count.
4Antiviral (Anti-HIV)Case report [18]1Sustained seroreversion.CD4 count not less than 750 cells/μL.
5Antiviral (Anti-HCV)Pilot study [19]30Significant decrease in viral load.Increased Total Antioxidant Capacity (TCA).Improved laboratory biomarkers such as total protein, red blood cell, and platelet count.Decreased fasting blood glucose and postprandial glucose in both diabetic and non-diabetic HCV patients.Reduced lower-limb edema
6Antiviral (Anti-HCV)Pilot study [20]60Significant decrease in viral load.Augmentation of α-femiddlerotein and other liver function parameters.
7Antiviral (Anti-HCV)Pilot study [21]195Negative HCV-RNA
8AntioxidantRandomized controlled clinical trial [30]50Significant raise of levels of superoxide dismutase (SOD).
9AntioxidantPlacebo controlled participant blinded clinical trial [31]114Significant elevation of total antioxidant capacity (TAC), superoxide dismutase (SOD), and glutathione levels.
10Antioxidant Pilot study [32]30Significant reduction of plasma levels of malondialdehyde (MDA).Increased activity of erythrocyte glutathione peroxidase (GSH-Px) and superoxide dismutase.
11Anti-inflammatoryPlacebo controlled study [39]40Improvement in number of inflamed joints, incidence of morning stiffness, and disease activity score.
12Anti-inflammatoryRandomized, double blind, placebo-controlled clinical trial [40]42Significant decrease in the levels of malondialdehyde (MDA) and nitric oxide (NO).
13Anti-inflammatoryRandomized double blind, placebo-controlled clinical trial [41]90Significant reduction of systemic inflammatory biomarkers including Tumor necrosis factor-α (TNF-α) and C-reactive protein (CRP).
14Anti-inflammatoryRandomized double blind, placebo-controlled clinical trial [42]43Significant reduction of serum levels of malondialdehyde (MDA) and nitric oxide (NO).
15Anti-inflammatoryRandomized double blind, placebo-controlled clinical trial [43]96Significant reduction of serum levels of malondialdehyde (MDA).
16ImmunomodulatoryPilot study [47]24Significant raise of CD8 counts and polymorphonuclear leukocyte (PMN).Improved clinical symptoms.
17ImmunomodulatoryRandomized double blind, placebo-controlled clinical trial [48]43Decreased CD8+ and increased percentage of CD4+CD25+ and the ratio of CD4+/CD8+.
18AnticoagulantRandomized double blind, placebo-controlled clinical trial [51]94Significant increase in Partial thromboplastin time (PTT).Significant reduction of systolic blood pressure, diastolic blood pressure, means arterial pressure, and heart rate.
19BronchodilatoryRandomized double blind clinical trial [54]15Short significant increase in peak expiratory flow (PEF), forced expiratory volume in one second (FEV1), maximal expiratory flow (MEF), maximal mid expiratory flow (MMEF), and specific airway conductance.
20BronchodilatoryRandomized single-blind placebo-controlled clinical trial [55]73Significant improvements in forced expiratory volume in one second (FEV1), peak expiratory flow (PEF), serum interferon-γ, and asthma control test (ACT) score.Significant reduction of fractional exhaled nitric oxide (FeNO) and serum total immunoglobulin E (IgE).
21AntihistaminicRandomized single-blind clinical trial [56]20Significant reduction of seasonal allergic rhinitis symptoms score.
22AntihistaminicRandomized single-blind uncontrolled comparative clinical trial [57]47Significant reduction of daytime and ophthalmic symptoms and total eosinophil count comparable to montelukast.
23AntihistaminicRandomized double blind clinical trial [58]66Reduction of clinical symptoms such as nasal itching, rhinorrhea, sneezing attacks, nasal congestion, turbinate hypertrophy and mucosal pallor.
24AntihistaminicPilot study [59]68Relief of symptoms of allergic rhinitis.

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