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Therapeutic Use of Nigella Sativa A Review

Nigella sativa also called prophetic medicine. Prophet Muhammad (Peace Be Upon on Him) recommended and used it to maintain health. Although the seeds of cumin (Cuminum cyminum L.) are widely used as a spice for their distinctive aroma, they are also commonly used in traditional medicine to treat a variety of diseases. The literature presents ample evidence for the biomedical activities of cumin, which have generally been ascribed to its bioactive constituents such as terpenes, phenols, and flavo
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0% found this document useful (0 votes)
67 views7 pages

Therapeutic Use of Nigella Sativa A Review

Nigella sativa also called prophetic medicine. Prophet Muhammad (Peace Be Upon on Him) recommended and used it to maintain health. Although the seeds of cumin (Cuminum cyminum L.) are widely used as a spice for their distinctive aroma, they are also commonly used in traditional medicine to treat a variety of diseases. The literature presents ample evidence for the biomedical activities of cumin, which have generally been ascribed to its bioactive constituents such as terpenes, phenols, and flavo
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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International Journal of Horticulture and Food Science 2021; 3(1): 06-12

E-ISSN: 2663-1067
P-ISSN: 2663-1075
IJHFS 2021; 3(1): 06-12 Therapeutic use of Nigella sativa: A review
Received: 04-10-2020
Accepted: 09-12-2020
Dr. Md. Shahab Uddin and Dr. ZN Nuri
Dr. Md. Shahab Uddin
Department of Unani
Medicine, Hamdard University Abstract
Bangladesh, Gazaria, Nigella sativa also called prophetic medicine. Prophet Muhammad (Peace Be Upon on Him)
Munshiganj, Bangladesh recommended and used it to maintain health. Although the seeds of cumin (Cuminum cyminum L.) are
widely used as a spice for their distinctive aroma, they are also commonly used in traditional medicine
Dr. ZN Nuri to treat a variety of diseases. The literature presents ample evidence for the biomedical activities of
Former Medical officer, cumin, which have generally been ascribed to its bioactive constituents such as terpenes, phenols, and
Hamdard Lab. (WQF) flavonoids. Those health effects of cumin seeds that are experimentally validated are discussed in this
Bangladesh review. Numerous pre-clinical and clinical trials have investigated its efficacy using the seed oil,
essential oil, and its main constituent thymoquinone (TQ). These investigations support its use either
independently or as an adjunct along with conventional drugs in respiratory problems, allergic rhinitis,
dyspepsia, metabolic syndrome, diabetes mellitus, inflammatory diseases, and different types of human
cancer. Multiple studies made in the last decades validate its health beneficial effects particularly in
diabetes, dyslipidemia, hypertension, respiratory disorders, inflammatory diseases, and cancer. Nigella
sativa seeds also possess immune stimulatory, gastroprotective, hepatoprotective, nephroprotective,
and neuroprotective activities. TQ is the most abundant constituent of volatile oil of N. sativa seeds,
and most of the medicinal properties of N. sativa are attributed mainly to TQ. All the available
evidence suggests that TQ should be developed as a novel drug in clinical trials.

Keywords: medicine, traditional, thymoquinone, diabetes, evidence

1. Introduction
Nigella sativa is an amazing herb with a rich historical and religious background. The seeds
of N. sativa are the source of the active ingredient of this plant. The actual importance of N.
sativa to the Muslims came from the holy saying of the Prophet Mohammed “Prayers and
peace be upon him” in the black seed is the medicine for every disease except death
(Ghaznavi, 1991) [47]. It is the same black seed referred by Prophet Mohammed as a panacea
(universal healer), that is a remedy for all ailments but cannot prevent ageing or death
(Ghaznavi, 1991) [47]. Historical use of black seeds has been mentioned in various religious
and ethnic books. Black seeds are identified as the curative black cumin in the holy bible; it
is also described as the melanthion of Hippocrates. In the Greco Arab/ Unani-Tibb system of
medicine which originate from Hippocrates, his contemporary Galen and Ibn- sina has
regarded black seed as a valuable remedy in hepatic and digestive disorder. The famous book
of medicine by Ibn-sina “The cannon of medicine (980- 1037) revealed historical importance
of this Black seeds as the seeds “That stimulates the body’s energy and help recovery from
fatigue (Ghaznavi, 1991; Chevallier, 1996) [87, 21]. Through thousand of years, until the time
being, millions of people in the mediterranean region and Far East countries use the oil of N.
sativa seeds daily as a natural protective and curative remedy. Historically, it has been
recorded that N. sativa seeds were prescribed by ancient Egyptian and Greek physicians to
treat headache, nasal congestion, toothache and intestinal worm, as well as a diuretic to
promote menstruation and milk production (Hajhashemi et al., 2004) [50].

2. Synonym of black seeds in various languages


English: Black cumins, Love-in-a-mist.
Arabic: Habatut Barakah; Sonez ; Habatut – sauda; Kamune-asvad.
Corresponding Author: Hindi: Kalonji.
Dr. Md. Shahab Uddin
Department of Unani
Sankrit: Krishana – Jiraka.
Medicine, Hamdard University Persian: Siyadanah (Ahmad et al., 2004; Chevallier, 1996) [5, 21].
Bangladesh, Gazaria,
Munshiganj, Bangladesh

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3. Morphology of the plant


N. sativa is a braky, self-branching plant of about 50 to 60
cm in height. Leaves are divided into linear segment 2 to 3
cm long; they are apposite in pairs on either side of the
stem. Its lower leaves are small, and petiolate and upper
leaves are long. The plant has finely divided foliage and
pale bluish or white flowers. The flowers grow terminally
on its branches. N. sativa reproduces with itself and forms a
fruit capsule which consist of many white trigonal seeds,
once the fruit capsule has matured, it opens up and the seeds
contained within are exposed to the air becoming black in
colour (black seeds), seeds are triangular in shape, black in
colour and possess a severe pungent smell, contains
considerable amount of oil (Chevallier, 1996) [21]. Fig 1b: (Thymol)

4. Scientific classification of the plant 6. Pharmacological activity


Kingdom: Plantae. There are many studies have been conducted particularly
Subkingdom: Tracheobionata that is, vascular plant. during the last two decades on the effect of N. sativa seeds
Supervision: Spermatophyte. extracts or its active compounds on the various body
Order: Ranunculus’s. systems in vivo or in vitro. The following is the selection of
Family: Ranunculaceae-Butter cup family. some of these studies.
Genera: Nigella.
Species: sativa 6.1. Antioxidant activity
Antioxidant action of N. sativa may explain its claimed
5. Chemical constituents usefulness in folk medicine. The essential oil of N. sativa
N. sativa seeds contain 36 to 28% fixed oil, proteins, was tested for a possible antioxidant activity. The essential
alkaloid, saponin and 0.4 to 2.5% essential oil. The fixed oil oil, thymoquinone and other components like carvacrol,
is mainly composed of unsaturated fatty acid that includes anethole and 4-terpineol demonstrated respectable radical
arachidonic, eicosadienoic, linoleic and linolenic acid. The scavenging property. The free radical scavenging effect of
saturated fatty acid present in the oil are palmitic, stearic thymol, thymoquinone and dithymoquinone were studied on
and myristic acid (Hajhashemi et al., 2004) [50]. The the reactions generating reactive oxygen species such as
essential oil present in the seeds was analyzed by gas superoxide anion radical, hydroxyl radical and singlet
chromatography-mass spectrometry (GC–MS). Many oxygen using the chemiluminescence and
components were characterized but the pharmacologically spectrophotometer methods (Kruk et al., 2000) [63].
active constituent of volatile oil are thymoquinone (Figure Thymoquinone and fixed oil of N. sativa were also reported
1a), dithymoquinone, thymol (Figure 1b) and to inhibit non-enzymatic peroxidation in ox brain
thymohydroquinone. Dithymoquinone is the dimerised form phospholipid liposomes (Houghton et al., 1995) [55]. The
of Thymoquinone (Ghosheh et al., 1999; Hajhashemi et al., antioxidant effect of thymoquinone (TQ) and a synthetic
2004) [48, 50]. The crystalline active principle, nigellone is the structurally related ter-butyl thymoquinone (TBHQ) were
only constituent of the carbonyl fraction of the oil. The other examined in vitro. Interestingly, both TQ and TBHQ
constituents of the volatile oil of the seed are p-cymene efficiently inhibited iron dependant microsomal lipid
carvacrol, t-anethole, 4-terpineol and longifoline. Four peroxidation in a concentration dependent manner (Badary
alkaloids have been reported as constituent of N. Sativa et al., 2003) [18, 19].
seeds. Nigellicine and nigellidine have an indazole nucleus
whereas nigellimine and N-oxide of nigellimine are 6.2. Hepatoprotective activity
isoquinolines (Atta-ur-Rehman, 1985a, b, 1995) [14, 15]. The protective action of thymoquinone against the
Recently, a triterpene saponin Alfa herein was isolated from hepatotoxin: terbutyl hyderoperoxide has been demonstrated
the seeds of N. sativa. α-heredin is known to have antitumor using isolated rat hepatocytes (Daba et al., 1998) [23]. In this
activity (Kumara and Haut, 2001) [64, 65]. study, the hepatoprotective activity of thymoquinone (TQ)
was compared with that of silybin a known hepatoprotective
agent. The mechanism of hepatoprotection of TQ is not
certain but may be related to the preservation of intracellular
gluathione (GSH), the depletion of which by oxidative stress
is known to increase the susceptibility of cells to irreversible
injury.

6.3. Anti-nephrotoxic activity


Administration of seed extract with cysteine, Vitamin E and
Crocus sativa before administrating the nephrotoxic drug
cisplatin was effective in ameliorating the biochemical and
physiological indices of nephrotoxicity (El-Dally et al.,
1996) [31]. This was also confirming with our previous
results and reported results of Nephroprotective activity of
Fig 1a: (Thymoquinone) N. sativa seed oil in nephrotoxicity induced by Cisplatin and

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Gentamycin (Tembhurne et al., 2008; Ali, 2004) [84, 10]. The writhing) conclude that the fixed oil of the seeds is
reason for the protective action is not certain but may be endowed with strong antinociceptive actions and these
related to the antioxidant action of the drug and the fact that actions were due to an opioid principle in the oil as they
the neprotoxic drug may induce its effects via generation of were antagonized by naloxone. In a study have used four
free radicals (El-Dally et al., 1996) [31]. Administration of different models of analgesia (hot plate test, tail pinched
thymoquinone with the drinking water before and during test, acetic acid induced writing and formalin induced pain)
ifosfamide treatment ameliorated the severity of ifosfamide for studying the analgesic activity of the drug. The
induced renal damage and improved most of the alteration mechanism of anti-inflammatory and analgesic effect seems
of biochemical parameters (Badary et al., 1996) [18, 19]. to be related to the inhibition of eicosanoid synthesis as
suggested by the study of Houghton et al. (1995) [55].
6.4. Antidiabetic activity
Al-Awadi and Gumma (1987) [7] have reported the use of a 6.8. Antinociceptive effects
plant mixture containing N. sativa, myrrh, gum, asafetida Study showed that the oral administration of N. sativa oil
and aloe by diabetics in Kuwait. They studied the effect of extracted from Egyptian N. sativa seeds produces a
these drugs for their glucose lowering effect in rats and suppressive effect on nociceptive responses caused by
found it to be effective. Further studies on the plant mixture thermal, mechanical and chemical nociceptive stimuli in
containing N. sativa revealed that the blood glucose mice, and that the antinociceptive effect of N. sativa oil is
lowering effect was due to the inhibition of hepatic partly attributable to its component, thymoquinone. It also
gluconeogenesis and the plant extract mixture may prove to revealed that at least the supraspinal opioid systems are
be useful therapeutic agent in the treatment of non-insulin involved in the antinociceptive effect of thymoquinone.
dependent diabetes mellitus (Al-Awadi et al., 1991)[6].
6.9. Anti-ulcer activity
6.5. Antimicrobial activity The aqueous extract of N. sativa seeds was effective in
The extract and the oil have been reported to have a broad reducing the ulcer index induced by Aspirin by about 36%
spectrum of activity against a number of microbes. In vitro (Rajkapoor et al., 1996) [77]. In other study oil of seed of N.
antibacterial effects of the essential oil showed pronounced sativa found to show protective effects on the formation of
activity even in 1:1000 dilutions against several organisms stress gastritis in hypothyroidal rats (Khaled et al., 2009)
[60]
that include Staphylococcus albus, E. coli, Salmonella typhi, . Recent clinical study is also supported with eradication
Vibrio cholera. The oil was more effective against gram of Helicobacter pylori in patient with non-ulcer dyspepsia
positive than gram negative organism. El-Kamali et al. (Salem et al., 2010) [79].
(1998) [34] using the plate diffusion method confirmed the
report and showed that essential oil was effective against 6.10. Anti-histaminic action
gram positive (Bacillus substilis and Staphylococcus The antihistaminic effect was first investigated by
aureus) and gram negative bacteria (E. coli and ElDakhakhany et al. (1982) [32] who reported the protective
Pseudomonas aeruginosa) the antibacterial effect was action of thymoquinone and carbonyl fraction of N. sativa
maximal when Bacillus substilis was used. The oil was against histamine-induced bronchospasm in guinea pigs.
found to have excellent antifungal activity particularly Furthermore, an in vitro study demonstrated that nigellone,
against Aspergillus species. In a study isolated from N. sativa, effectively inhibited the release of
using murine cytomegalovirus as a model intreaperitonneal histamine from mast cells, possibly through decrease in
administration of oil substantially decreased the viral load in intracellular calcium and inhibition of protein kinase C
liver and spleen (Salem et al., 2000) [79]. (Chakarvarti et al., 1993) [20]. These effects together with
analgesic and anti-inflammatory actions, perhaps can be
6.6. Antimalarial correlated with the use of N. sativa in eczema and asthma,
Various extracts of N. sativa found to show antiplasmodial for scorpion and spider stings and for the bites of cat, dog
activity against both in vivo and in vitro plasmodia and snake, recommended in the folk medicine (Al-Jishi et
infections. It shows 100% inhibition of the parasite growth al., 2003) [11].
(Plasmodium falciparum) at concentration 50 ug/ml. N.
sativa shows dose dependant activity against parasite (El- 6.11. Effect on cardiovascular system
Hadi et al., 2010) [32]. N. sativa alone or in combination with honey or garlic are
promoted for the treatment of hypertension which drew the
6.7. Analgesic and Anti-inflammatory activity attention of El-Tahir et al. (1993) [37, 38] to investigate the
Houghton et al. (1995) [55] reported that crude fixed oil of N. action of the volatile oil of N. sativa and its active
sativa and an active principle thymoquinone (TQ) inhibits constituent thymoquinone on the arterial blood pressure and
cycloxygenase and 5-lipooxygenase pathway of arachi heart of anaesthetized rats. Both agents produce a dose
donate metabolism in rat peritoneal leukocytes. The effect dependent decrease in the arterial blood processor and heart
was demonstrated via the dose dependant inhibition of the rates. These effects were significantly antagonized by
formation of thromboxane B2 and leukotrienes B4. This atropine, cyproheptadiene and hexamethonium. This
effect was later confirmed in experimental animal studies suggests that these effects were centrally antagonized
conducted using aqueous suspension of N. sativa crushed mainly via the involvement of 5-hydroxy tryptaminergic and
seed by Al-Ghamdi (2001) [8]. In this study, formation of muscarinic mechanism. Oral dose of 0.6 ml/kg/day of N.
edema in rat hind paw was inhibited and these effects were sativa extract produced a significant hypotensive effect in
comparable with Aspirin used as a standard antiflammatory spontaneously hypertensive rats. These findings were
drug using three antinociceptive tests in rats and mice significantly comparable with the standard anti-hypertensive
(hotplates test, tail pinched test, acetic acid induced drug nifedipine (Zaoui et al., 2002) [88, 89]. The effect of the

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drug was concluded to be partially due to its diuretic effect weeks) of N. sativa seeds in mice and rats were investigated
which was comparable to 0.5 mg/kg/day furosemide. In one through the determination, of LD50 values and examination
of study, two-month dietary supplementation with N. sativa of possible biochemical, hematological and
extract to normal rats has shown a homogenous cardiac histopathological changes. The low toxicity of N. sativa
hypertrophy and enhanced cardiac contractility at baseline fixed oil was evidenced by high LD50 values (11.915
conditions. The hearts of Nigella-treated rats developed a ml/kg), key hepatic enzyme stability and organ integrity
moderate but significant hypertrophy that was evident by an values. This suggests a wide margin of safety for therapeutic
increase in the heart weight to body weight ratio. The doses of fixed oil and N. sativa seeds. The LD50 value of
observed Nigella-induced cardiac hypertrophy was thymoquinone was found to be 2.4 g/kg. Inclusion of
associated with an increase in the baseline cardiac inotropic thymoquinone in the drinking water of mice at
properties (Yar et al.,2008) [87]. concentration of 0.03% for 90 days resulted in no signs of
toxicity except for significant decrease in fasting plasma
6.12. Effect on gastro-intestinal tract glucose concentration (Zaoui et al., 2002) [88, 89]. In a recent
In Unani medicine N. sativa is used for stomachache and as study of diazinon induced organ toxicity, with N. sativa
a digestive, carminative, laxative and anti-jaundice (Chopra seeds extract given orally for three and six weeks, the study
et al., 1956) [22]. Oral N. sativa powder was reported to observed attenuated extensive changes of hematological and
relieve flatulence. While Nigellone, an active principle of N. biochemical parameters in diazinontreated rats. Based upon
sativa was found to antagonize histamine induced these results, they suggested N. sativa seeds can be
contractions of guinea pig intestine. In addition, to this a considered as a promising therapeutic agent against
choleretic effect of N. sativa oil and its active principles hematotoxicity, immunotoxicity, hepatoxicity, nephrotxicity
(thymoquinone, thymohydroquinone and dithymoquinone) and cardiotoxicity induced by diazinon and may be against
reported, respectively (Mahfouz and ElDakhakhany, 1960) other chemical pollutants, environmental contaminants and
[67]
. El-Dakhakhani et al. (1965, 2000) [27, 28] investigated the pathogenic factors (Atef and Wafa, 2010) [13]. Some other
effect of N. sativa oil on gastric secretion and ethanol- studies also demonstrate that treatment with N. sativa
induced ulcer in rats. Reported to significant increase in resulted in significant decrease of haematological disorders
mucin content, glutathione level as well as a significant induced by aflatoxin and cadmium (Demir et al., 2006) [25].
decrease in mucosal histamine content and ulcer formation, No remarkable pathological changes were recorded in bone
with a protection ratio of 53.56%, was found in the N. sativa marrow of animals treated with suspension of N. sativa in
oil pretreated group. More recently, the crude extract of N. carbon tetrachloride induced bone marrow toxicity (Abou et
sativa was shown to cause a dose dependent (0.1 to 3.0 al., 2007 ) [3].
mg/ml) relaxation of spontaneous contractions of rabbit
jejunum as well as inhibition of K + - induced contractions 7. Conclusion
in a similar dose range, suggestive of calcium channel Most studies confirm its value in folk medicine as analgesic,
blockade (Gilani et al., 2001) [49]. Recently, Abdel-Sater anti-inflammatory, anti-oxidant, and anti-cancer, anti-
(2009) [1] investigated the protective effects of N. sativa on microbial, anti-parasitic, antihypertensive and as an immune
hypothyroidism induced development of acute cold restraint stimulant. However, controversial results have been
stress gastritis in rats. reported for its effect on the respiratory system, blood
coagulation and uterine motility. More work is needed to
6.13. Effect on immune system determine the pharmacokinetics, biochemical,
As a natural remedy, people take N. sativa seeds or oil is a pharmacodynamic and therapeutics of active components
promoter of good health and for the prophylaxis of common and their interactions with modern drugs and importance to
cold and Asthama. In view of that, El-Kadi et al. (1986) [33] human health with sufficient detail.
investigated the effect of N. sativa on immune system and
found that the drug has immuno potentiating properties in 8. References
human T-cells in vitro. This was confirmed by Haq et al. 1. Abdel-Sater KA. Gastroprotective effects of Nigella
(1995) [51] who showed that N. sativa seeds activate T- sativa oil on the formation of stress gastritis in
lymphocyte to secrete the interleukin, IL-3 and IL-1B hypothyroidal rats. Int. J. Physiol. Pathophysiol.
production. In further experiment, they purified the proteins Pharmacol 2009;1:143-149.
in the whole N. sativa seeds and it should be noted that 2. Abdulelah HAA, Zainal-Abidin BAH. In vivo anti-
some proteins have suppressive and others have stimulatory malarial tests of Nigella sativa (Black Seed) different
properties in lymphocyte culture (Haq et al., 1999) [52, 53]. extracts. Am. J. Pharmacol. Toxicol 2007;2:46-50.
3. Abou Gabal AA, Essawy AE, Abdel-Moneim AM,
6.14. Effect on reproductive system Hamed SS, Elzergy AA. The protective effect of black
Sixty days study of N. sativa seeds shows to increase in the seed (Nigella sativa) against carbon tetrachloride-
weight of reproductive organs, sperm motility and count in induced chromosomal aberrations and ultrastructural
cauda epidydimides and testicular ducts. Spermatogenesis changes of bone marrow cells. Arab J. Biotech
was found to increase at primary and secondary 2007;10(2):275-288.
spermatocyte. While in fertility, there was increase in 4. Abu El-Ezz NM. Effect of Nigella sativa and Allium
number of female pregnant rats (Mukhallad et al., 2009; Al- cepa oils on Trichinella spiralis in experimentally
Sa'aidi et al., 2009) [72, 12]. infected rats. J. Egypt. Soc. Parasit 2005;35:511-523.
5. Ahmad Z, Gafoor A, Aslam M. Nigella sativa – A
6.15. Toxicological report potential commodity in crop diversification
The seed extract and its constituent appear to have a low traditionally used in health care. Project on Introduction
level of toxicity. The toxicity of fixed oil (10 ml/kg for 12 of Medicinal herb and species as crop. Ministry of food,

~9~
International Journal of Horticulture and Food Science http://www.hortijournal.com

agriculture and livestock, Pakistan 2004. Obese Male. Acta. Med. Indones 2010;42(3):130-34.
6. Al-Awadi FM, Fatania H, Shamte U. The effect of a 25. Demir H Kanter, Coskun O, Uz YH, Koe A, Yildiz A.
plant mixture extract on liver gluconeogenesis in Effect of black cumin (Nigella sativa) on heart rate,
streptozotocin-induced diabetic rats. Diab. Res some hematological value, and pancreatic beta-cell
1991;18(4):163-168. damage in cadmium-treated rats. Biol. Trace. Elem. Res
7. Al-Awadi FM, Gumma KA. Studies on the activity of 2006;110:151-162.
individual plants of an anti-diabetic plant mixture. Acta. 26. Drozed AG, Komissarenko FN, Litvinenko EA.
Diabetol. Lat 1987;24(1):37-41. Coumarins of some species of Ranunaulaceae family.
8. Al-Ghamdi MS. Anti-inflammatory, analgesic and anti- Farm ZH 1973;25(4):57-60.
pyretic activity of Nigella sativa. J. Ethnopharmacol 27. El-Dakhakhani M, El-Halim MA, Aly SM. Effect of
2001;76:45-48. Nigella sativa oil on gastric secretion and ethanol-
9. Al-Hader A, Aqel M, Hasan Z. Hypoglycemic effect of induced ulcer in rats. J. Ethnopharmacol 2000;72(1-
volatile oil of Nigella sativa seeds. Int. J. Pharmacog 2):299-304.
1993;31(2):96-100. 28. El-DakhaKhani M, Mady NL, Halim MA. Nigella
10. Ali BH. The effect of Nigella sativa in gentamicin sativa L. oil protects against induced hepatotoxicity and
nephrotoxicity in rats. Am. J. Chin. Med improves serum lipid profile in rats.
2004;32(1):49-55. Arzneimittelforschung 2000;50(9):832-836.
11. Al-Jishi SA, Hoziafa BA. Effect of Nigella sativa on 29. El-Dakhakhany M. Studies on the chemical constitution
Blood hemostatic functions in rats. J. Ethnopharmacol of Egyptian N. sativa L. seeds. Planta Med.
2003;85:7-14. 1963;11(4):465-470.
12. Al-Sa'aidi JAA, Al-Khuzai ALD, Al-Zobaydi NFH. 30. EL-Dakhakhany M. Some pharmacological properties
Effect of alcoholic extract of Nigella sativa on fertility of some constituents of Nigella sativa L seeds: The
in male rats. Iraqi. J. Vet. Sci 2009;23:123-128. carbonyl fraction of essential oil. Proceeding of the 2nd
13. Atef M Al-Attar, Wafa'a A Al-Taisan. Preventive International conference on Islamic Medicine, Kuwait
Effects of Black Seed (Nigella sativa) extract on 1982, pp. 426-431.
Sprague Dawley Rats Exposed to Diazinon. Austr. J. 31. El-Dally ES. Protective effect of cysteine, Vitamin E,
Basic Appl. Sci 2010;4(5):957-968. C. Sativus and N. sativa extract on cisplatin induced
14. Atta-ur-Rehman S, Malik S, Cun-Hung H, Clardy J. toxicity in rats. J. Isl. Acad. Sci 1996;9(4):47-55.
Isolation and structure determination of nigellicine, a 32. El-Hadi MA, Bakri YM, Yousif G. Mohammed and
novel alkaloid from seeds of Nigella sativa. Hassan S. Khalid. Antiplasmodial Activity of Some
Tetrahedron Lett 1985a;26:2759-2762. Medicinal Plants Used in Sudanese Folk-medicine.
15. Atta-ur-Rehman S, Malik S, Sadiq H, Choudhary MI, Environ. Health Insights 2010;4:1-6.
Clardy J. Nigellidine, a new indazole alkaloid from 33. El-Kadi, Kandil O. Effect of Nigella sativa (the black
seeds of Nigella sativa. Tetrahedron Lett 1995;36:1993- seed) on immunity. Proceeding of the 4th International
1996. Conference on Islamic Medicine, Kuwait. Bull. Islamic
16. Ayaz E, Yilmaz H, Ozbek H, Tas Z, Orunc O. The Med 1986;4:344-348.
effect of Nigella sativa oil against Aspiculuris 34. El-Kamali HH, Ahmad AH, Mohammad AS, Yahia
tetraptera and Hymenolepis nana in naturally infected AAM. Antibacterial properties of essentials oils from
mice. Saudi Med. J 2007;28:1654-1657. Nigella sativa. Fitoterapia 1998;69:77-78.
17. Babayan VK, Koottungal D, Halaby GA. Proximate 35. El-Naggar ARM, El-Deib AEM. A study of some
analysis, fatty acid and amino acid composition of biological activities of Nigella sativa (black seeds)
Nigella sativa L seeds. J. Food Sci 1978;43(4):1314- “Habbat El-Barka”. J. Egypt Soc. Pharmacol. Exp. Ther
1315. 1992;11(2):781-800.
18. Badary A, Taha RA, Ayman M, El-Din G, Abdel- 36. El-Shenawy NS, Soliman MF, Reyad SI. The effect of
Wahab MH. Thymoquinone is a potent suprroxide antioxidant properties of aqueous garlic extract and
anion scavenger. Drug Chem. Toxicol 2003;26(2):87- Nigella sativa as anti schistosomiasis agents in mice.
98. Rev. Inst. Med. Trop 2008;50:29-36.
19. Badary OA. Thymoquinone attenuates afosfamide- 37. El-Tahir KE, Ashour M, Al-Harbi MM. The respiratory
induced Fanconi syndrome in rats and enhances its effects of the volatile oil of black seed (Nigella sativa)
antitumor activity in mice. J. Ethnopharmacol in guinea pigs: elucidation of the mechanism(s) of
1996;67:135-142. action. Gen. Pharmacol 1993;24(5):1115-1122.
20. Chakarvarti N. Inhibition of histamine release from 38. El-Tahir KE, Ashour MM, Al-Harbi MM. The
mast cells by nigellone. Ann. Allergy 1993;70(3):237- cardiovascular effects of the volatile oil of black seed
242. (Nigella sativa) in rats: elucidation of the mechanism(s)
21. Chevallier A. Encyclopedia of medicinal plants. New of action. Gen. Pharmacol 1993;24(5):1123-1131.
York, NY: DK Publishing 1996, p. 237. 39. El-Zawahry BH. Isolation of new hypotensive fraction
22. Chopra RN, Nayyer SL, Chopra IC. Glossary of Indian from Nigella sativa seed. Kongr. Pharm. Wiss
medicinal plants. India: CSIR 1956, pp. 176-188. 1964;23:193-203.
23. Daba MH, Abdel-Rehman MS. Hepatoprotective 40. Enomoto S, Asano R, Iwahori Y, Narui T, Okada Y,
activity of thymoquinone in isolated rat hepatocytes. Singab AN, et al. Hematological studies on black
Toxicol. Lett 1998;95:23-29. cumin oil from the seeds of Nigella sativa L. Biol.
24. Datau EA, Eko E, Surachmanto, Pandelaki K, Langi Pharm. Bull 2001;24(3):307-310.
FA. Efficacy of Nigella sativa on Serum Free 41. Fahrettin Y, Sacit C, Alpaslan T, Mustafa A, Nurten A,
Testosterone and Metabolic Disturbances in Central Hale C, et al. Nigella sativa relieves the deleterious

~ 10 ~
International Journal of Horticulture and Food Science http://www.hortijournal.com

effects of ischemia reperfusion injury on liver. World J. lower respiratory tract illness in children. Afr. J. Pharm.
Gastroenterol 2008;14(33):5204-5209. Pharmacol 2009;3(5):248-251.
42. Farah IO, Begum RA. Effect of Nigella sativa and 58. Keshri G, Singh MM, Lakshami V, Kamboj VP. Post-
oxidative stress on the survival pattern of MCF-7 breast coital contraceptive effect of the seeds of Nigella sativa
cancer cells. Biomed. Sci. Instrum 2003;39:359-364. in rats. Indian J. Physiol. Pharmacol 1995;39(1):59-62.
43. Farah KM, Atoji Y, Shimizu Y, Takewaki T. 59. Khadiga A, Abdel Ati AE, Mustafa HE. The effect of
Insulinotropic properties of Nigella sativa oil in dietary Nigella sativa seeds on the blood cholesterol
streptozotocin plus nicotinamide diabetic hamsters. and lipoprotein levels of rabbits. J. Animal Plant Sci
Res. Vet. Sci 2002;73:279-282. 2009;3(3):227-230.
44. Gad AM, El-Dakhakhany M, Hassan MM. Studies on 60. Khaled A, Abdel-Sater. Gastroprotective effects of
the chemical constitution of Egyptian Nigella sativa L Nigella sativa oil on the formation of stress gastritis in
oil. Planta Med 1963;11(2):134-138. hypothyroid rats. Int. J. Physiol. Pathophysiol.
45. Gali-Muhtasib H, Roessner A, Schneider-Stock R. Pharmacol 2009;1:143-149.
Thymoquinone: a promising anti-cancer drug from 61. Khanna T, Zaidi FA, Dandiya PC. CNS and analgesic
natural sources. Int. J. Biochem. Cell Biol studies of Nigella sativa . Fitoterapia 1993;5:407-410.
2006;38(8):1249-1253. 62. Khanna T, Zaidi FA, Dandiya PC. CNS and analgesic
46. Ghanya Al-Naqeep, Adel S, Al-Zubairi, Maznah I, studies of Nigella sativa. Fitoterapia 1993;5:407-410.
Zulkhairi HA, Norhaizan ME. Antiatherogenic 63. Kruk I, Michalska T, Klanda A. The effect of thymol
Potential of Nigella sativa Seeds and Oil in Diet- and its derivatives on reaction generating reactive
Induced Hypercholesterolemia in Rabbits. Evid. Based oxygen species. Chemosphere 2000;41:1059-1064.
Complement Alternat. Med 2011, 8. 64. Kumara SS, Huat BT. Extraction, isolation and
47. Ghaznavi KM. Tibbe-e-Nabvi aur Jadid Science, Al- characterization of anti-tumour principle, alpha-hedrin,
Faisal Nasheeran wa Tajeera-e- Kutab. Urdu Bazar from the seeds of Nigella sativa. Planta Med
Lahore, Pakistan 1991;1:228-236. 2001;67:29-22.
48. Ghosheh OA, Houdi AA, Crooks PA. High 65. Kumara SS, Huat BT. Extraction, isolation and
performance liquid chromatographic analysis of the characterization of anti-tumour principle, alpha-hedrin,
pharmacologically active quinines and related from the seeds of Nigella sativa. Planta Med
compounds in the oil of the black seed (Nigella sativa 2001;67:29-22.
L.). J. Pharm. Biomed. Anal 1999;19(5):757-762. 66. Le PM, Benhaddou-Andaloussi A, Settaf A, Cherrah Y,
49. Gilani AH, Aziz N, Khurram IM, Chaudhary KS, Iqbal Haddad PS. The petroleum ether extract of Nigella
A. Bronchodilator, spasmolytic and calcium sativa exerts lipid lowering action in the rats. J.
antagonistic activities of Nigella sativa seed (Kalonji): Ethnopharmacol 2004;94(2-3):251-259.
a traditional herbal product with multiple medicinal 67. Mahfouz M, El-Dakhakhany M. Some chemical and
uses. J. Pakistan Med. Assoc 2001;51(3):115-120. pharmacological properties of the new antiasthmatic
50. Hajhashemi V, Ghannadi A, Jafarabadi H. Black cumin drug “Nigellone”. Egypt Pharmacol. Bull 1960;42:411-
seed essential oil as a potential analgesic and anti- 424.
inflammatory. Phytother. Res 2004;18(3):195-199. 68. Mahmoud MR, El-Abhar HS, Salh S. The effect of
51. Haq A, Abdullatif M, Lobo PI, Khabar KS, Sheth KV, Nigella sativa oil against the liver damage induced by
Al-Sedairy ST. Nigella sativa: Effect on human Schistosoma mansoni infection in mice. J.
lympocytes and polymorphonuclear leucocyte Ethnopharmacol 2002;79(1):1-11.
phagocytic activity. Immunopharmacology 69. Matira K, Zesmin FD. Effects of the crude and the n-
1995;30(2):147-150. hexane extract of Nigella sativa Linn. (kalajira) upon
52. Haq A, Lobo I, Al-Tufail M, Rama NR, Sedairy ST. diabetic rats. Bangladesh J. Pharmacol 2008;4:17-20.
Immunomodulatory effect of Nigella sativa proteins 70. Merfort I, Wary V, Barakat H, Hussain A, Nawwar
fractionated by ion exchange chromatography. Int. J. AM. Flavonol triglyco sides from seeds of Nigella
Immunopharmacol 1999;21:283- 285. sativa. Phytochem 1997;46(2):359-363.
53. Haq A, Lobo PI, Al-Tufail M, Rama NR, Sedairy ST. 71. Muhammad AB, Muhammad T. Effect of Nigella
Immunomodulatory effect of Nigella sativa proteins sativa on Lipid Profile in Albino rats. Gomal J. Med.
fractionated by ion exchange chromatography. Int. J. Sci 2007;5(1):28-31.
Immunopharmacol 1999;21:283-285. 72. Mukhallad AM, Mohamad MJ, Mohamad P, Hatham
54. Hosseinzadeh H, Parvardeh S (2004). “Anticonvulsant D. Effects of Black Seeds (Nigella sativa) on
effects of thymoquinone, the major constituent of Spermatogenesis and Fertility of Male Albino Rats.
Nigella sativa seeds, in mice.” Phytomed Res. J. Med. Med. Sci 2009;4(2):386-390.
1999;11(1):56-64. 73. Nadia MH, Taha RA. Effects of Nigella sativa Oil and
55. Houghton PJ, Zarka R, Heras B, Hoult JR. Fixed oil of Thymoquinone on Oxidative Stress and Neuropathy in
Nigella sativa and derived thymoquinone inhibit Streptozotocin-Induced Diabetic Rats. Pharmacology
eicosanoid generation in leukocytes and membrane 2009;84:127-134.
lipid peroxidation. Planta Med 1995;61:33-36. 74. Nagi MN, Alam K, Badary OA, Al-Shabanah OA, Al-
56. Inayat UB, Fazal UR, Muhannad AK, Sarfaraz Khan. Sawaf HA, ALBekairy AM. Thymoquinone protects
Effect of Prophetic medicinal Kalonji (Nigella sativa against carbon tetracholide hepatotoxicity in mice via
L.) on Lipid Profile of Human Being: An In vivo an antioxidant mechanism. Biochem. Mol. Biol. Int
Approach. World Appl. Sci. J 2009;6(8):1053-1057. 1999;47:153-159.
57. Jameel A, Rahat AK, Ashraf MM. Study of Nigella 75. Najmi A, Nasiruddin M, Khan RA, Haque SF. Effect of
sativa oil in the management of wheeze associated Nigella sativa oil on various clinical and biochemical

~ 11 ~
International Journal of Horticulture and Food Science http://www.hortijournal.com

parameters of insulin resistance syndrome. Int. J. Diab.


Dev. Ctries 2008;28:11-14.
76. Perveen T, Haider S, Kanwal S, Haleem DJ. Repeated
administration of Nigella sativa decreases 5-HT
turnover and produces anxiolytic effects in rats, Pak. J.
Pharm. Sci 2009;22(2):139-144.
77. Rajkapoor B, Anandan R, Jayakar B. Anti-ulcer effect
of Nigella sativa and Pongamia pannata in rats.
Fitoterapia 1996;67:195-199.
78. Salama RB. Sterols in the seed oil of Nigella sativa.
Planta Med 1973;24(4):375-377.
79. Salem ML, Hossain MS. Protective effect of black seed
oil from Nigella sativa against murine cytomegalovirus
infection. Int. J. Immunopharmacol 2000;22:729-740.
80. Salomi MJ, Nair SC, Panikkar KR. Inhibitory effect of
Nigella sativa and Saffron (Crocus sativus) on chemical
carcinogenesis in mice. Nutr. Cancer 1991;16(1):67-72.
81. Salomi NJ, Nair SC, Jayawardhanan KK, Varghese CD,
Panikkar KR. Antitumour principles from Nigella
sativa seeds. Cancer Lett 1992;63(1):41-46.
82. Staphylakis PK, Gegiou D. The sterols of Nigella sativa
seed oil. Phytochem 1986;25:761-763.
83. Tarek El-Naggar, Mar´ıa Pilar G´omez-Serranillos,
OlgaMar´ıa P, Carmen A, Mar´ıa EC. Nigella sativa L.
Seed Extract Modulates the Neurotransmitter Amino
Acids Release in Cultured Neurons in Vitro. J. Biomed.
Biotechnol 2010, 398312.
84. Tembhurne SV, Firoj S, Jagtap AG. Nephroprotective
activity of Nigella sativa seeds against cisplatin induced
Nephrotoxicity in Mice. Indian J. Nat. Prod
2008;24(1):13-16.
85. Topozada HH, Masloum H, El-Dakhakhany M. The
anti-bacterial properties of Nigella sativa seeds: Active
principle with some clinical application. J. Egypt Med.
Assoc 1965;48:187-202.
86. Worthen DR, Ghosheh OA, Crooks PA. The in vitro
anti-tumour activity of some crude and purified
components of black-seed, Nigella sativa L. Anticancer
Res 1998;18(3A):1527-1532.
87. Yar T, El-Hariri M, EL-Bahai MN, Bamosa AO.
Effects of Nigella sativa supplementation for one
month on cardiac reserve in rats. Indian J. Physiol.
Pharmacol 2008;52(2):141-148.
88. Zaoui A, Cherrah Y, Aloui K, Mahassine N, Amarouch
H, Hassar M. Effect of Nigella sativa fixed oil on blood
homeostasis in rat. J. Ethnopharmacol 2002;79(1):23-
26.
89. Zaoui A, Cherrah Y, Mahassine N, Alaoui K, Hassar
M. Acute and chronic toxicity of Nigella sativa fixed
oil. Phytomed 2002;9:69-74.
90. Zhou Y, Shen K, Hou S, Qiu M, Luo Z. Experimental
study on apoptosis induced by elemene in glioma cells.
Ai Zheng. Chin. J. Cancer 2003;22(9):959-963.

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