Evidence Level
Moderate
7 Clinical Trials
10 Documented Benefits
3/5 Evidence Score

Black seed oil is pressed from the seeds of Nigella sativa, also called black cumin or kalonji, a spice with a long history in Middle Eastern, Persian and South Asian traditional medicine. Its main studied compound is thymoquinone, and the amount varies widely between commercial oils. Human trials, most of them small and short, have looked at blood pressure, cholesterol, blood sugar, body weight, oxidative stress markers, nasal and airway comfort, and indigestion. Trials have used about 0.5 to 1 g of oil a day in capsules, 2 g a day of Nigella sativa, or 5 mL of oil a day in honey. The oil tastes bitter and peppery, which some people find hard to take.

Studied Dose 5 mL of oil a day in a honey formulation for 8 weeks, as studied in functional dyspepsia (added to acid-reducing therapy); other trials used 0.5 to 1 g/day oil capsules or 2 g/day Nigella sativa. Thymoquinone content varies widely between oils.
Active Compound Thymoquinone; content varies widely between commercial oils. Branded forms include ThymoQuin® (TriNutra), standardized to 3% thymoquinone, and Thymocid® (Verdure Sciences), a cold-pressed black cumin seed oil. Isolated thymoquinone has its own page.

Benefits

Blood pressure reduction

A meta-analysis of 11 randomized trials (860 people) found black seed lowered systolic blood pressure by about 3.3 mmHg and diastolic by about 2.8 mmHg versus control over roughly 8 weeks, more with seed powder than with oil. A 28-day trial of a seed extract in 76 older adults with high blood pressure found no significant difference from placebo.

Blood sugar and HbA1c improvement

A pooled analysis of 7 trials in adults with type 2 diabetes found black seed lowered fasting blood sugar by about 18 mg/dL and HbA1c by about 0.7 percentage points versus control. The analysis included only a few studies and the effects were modest, so it is best seen as a complement to diet, exercise and any prescribed care.

Cholesterol and lipid improvements

Pooled trials show black seed lowers total cholesterol by about 16 mg/dL, LDL by about 14 mg/dL, and triglycerides by about 21 mg/dL. HDL did not change overall and rose only with seed powder. These are modest reductions, best viewed as support alongside diet and any prescribed care.

Nasal and airway comfort

In a 15-day trial of 65 adults with seasonal nasal allergy symptoms, a branded oil extract standardized to 5% thymoquinone (250 mg with piperine, twice daily) lowered nasal and eye symptom scores more than placebo; the maker ran the study. In a 4-week trial in people with asthma, 1 g a day of oil added to usual care improved asthma control scores, but lung function did not change significantly.

Inflammation markers

Pooled analyses of controlled trials found lower blood CRP with Nigella sativa seed or oil, and two of three analyses also found lower TNF-alpha; one found no change in IL-6. These are blood markers, not felt benefits, and the trials used varied products, doses and populations.

Body weight and BMI

A pooled analysis of randomized trials found black seed reduced body weight by about 1.8 kg (10 trials) and BMI by about 0.85 versus placebo, with large differences between trials; waist size did not change significantly. The effect is small, so it fits only as one part of a broader eating and activity plan.

Thymoquinone content varies between products

An analysis of 11 commercial black seed oils and capsules found thymoquinone ranging from about 3 to 809 mg per 100 g, a more than 250-fold spread. The authors called for thymoquinone content to be regulated so buyers know what they are getting; a label that states the thymoquinone amount is one way to know the dose.

Traditional use vs modern evidence

Black seed has a long history in Middle Eastern, Persian and South Asian traditional medicine, including a honey-based preparation for upper-stomach complaints. Modern human trials cover a narrower set of uses, mostly with small, short studies, so its traditional reputation reaches well beyond what has been tested.

Oxidative stress markers: lower MDA, higher antioxidant capacity

Three pooled analyses of controlled trials (10, 12 and 20 trials) in adults taking Nigella sativa seed or seed oil found lower blood malondialdehyde, a lipid peroxidation marker, and higher total antioxidant capacity; in the 12-trial analysis the effects were SMD -0.56 and 0.48, with moderate heterogeneity. A smaller 5-trial analysis found only higher SOD. These are lab markers, not felt benefits, and products and doses varied.

Indigestion and upper-stomach comfort

In a placebo-controlled trial of 70 people with functional dyspepsia (ongoing upper-stomach discomfort), 5 mL a day of the oil in honey for 8 weeks, added to acid-reducing medicine, lowered indigestion severity scores more than placebo. A second trial, of 2 g a day of Nigella sativa added to H. pylori treatment in 51 people, found no difference in indigestion.

Mechanism of action

1

NF-κB signaling and leukotriene formation

A review of mostly cell and animal studies describes thymoquinone acting on the NF-κB pathway, which controls inflammatory responses. In human blood cells in the test tube, thymoquinone blocked 5-lipoxygenase and the formation of leukotrienes, signaling molecules involved in airway and inflammatory responses. How much of this happens at supplement doses in people is not established.

2

Nrf2 activation and antioxidant enzymes

In cell and animal studies summarized in the same review, black seed and thymoquinone raised antioxidant enzyme activity, scavenged free radicals and acted on the Nrf2 pathway that controls responses to oxidative stress. Pooled human trials found higher blood antioxidant capacity, SOD and glutathione peroxidase, which fits this mechanism but does not prove it.

3

Cell energy sensing through AMPK

The same review describes thymoquinone acting on AMPK, an enzyme that senses a cell's energy status and adjusts its metabolism, in laboratory work. Whether this has anything to do with the blood sugar changes seen in human trials is unknown.

Clinical trials

1
Nigella sativa in Type 2 Diabetes: Meta-Analysis
PubMed

Meta-analysis of 7 trials of Nigella sativa on fasting blood sugar, HbA1c and blood lipids in type 2 diabetes (Daryabeygi-Khotbehsara et al. 2017, Complement Ther Med)

Adults with type 2 diabetes across 7 pooled clinical trials.

N. sativa lowered fasting blood sugar (about -17.8 mg/dL), HbA1c (about -0.7%), total cholesterol and LDL versus control. Triglycerides and HDL did not change significantly overall, though triglycerides fell in the oil subgroup. The authors note the analysis included only a few studies.

2
Nigella sativa Oil Add-On in Asthma: Randomized Trial
PubMed

Randomized, double-blind, placebo-controlled trial of N. sativa oil 500 mg twice daily for 4 weeks as add-on therapy; 80 enrolled, 60 completed. Outcomes: Asthma Control Test, pulmonary function, blood eosinophils. (Koshak et al. 2017, Phytother Res)

People with asthma (80 enrolled).

N. sativa oil as add-on therapy improved the Asthma Control Test score (21.1 vs 19.6, p=0.044) and lowered blood eosinophils versus placebo. The change in FEV1 did not reach statistical significance (p=0.17). This is a single small 4-week trial, and the oil was taken on top of usual asthma treatment.

3
Nigella sativa and Lipid Profile: Meta-Analysis
PubMed

Meta-analysis of 17 randomized controlled trials examining black seed effects on total cholesterol, LDL, HDL and triglycerides (Sahebkar et al. 2016, Pharmacol Res)

17 pooled randomized controlled trials.

N. sativa reduced total cholesterol (about -15.7 mg/dL), LDL cholesterol (about -14.1 mg/dL), and triglycerides (about -20.6 mg/dL) across 17 randomized trials. HDL did not change significantly. These reductions are modest. Effects varied by preparation, with oil favored for cholesterol and LDL.

4
Black Seed Oil in Honey and Indigestion Symptoms: RCT
PubMed

Double-blind, randomized, placebo-controlled trial of a traditional honey-based formulation giving 5 mL of N. sativa oil a day for 8 weeks, added to standard anti-secretory (acid-reducing) therapy (Mohtashami et al. 2015, J Ethnopharmacol)

70 people with functional dyspepsia by Rome III criteria, confirmed by upper endoscopy.

Hong Kong dyspepsia severity scores were significantly lower with the oil formulation than with placebo after 8 weeks (P<0.001), and fewer participants tested positive for H. pylori on a urease test. No serious adverse events were reported. Honey was part of the formulation and everyone also took acid-reducing medicine. A Cochrane review rated this single trial's result as high-certainty evidence.

5
Nigella sativa Added to H. pylori Treatment: Pilot RCT
PubMed

Double-blind, placebo-controlled pilot trial of 2 g/day N. sativa or placebo for 8 weeks, each added to quadruple H. pylori therapy (Alizadeh-Naini et al. 2020, Phytother Res)

51 people with H. pylori infection and functional dyspepsia.

Dyspepsia scores did not differ significantly between the groups. H. pylori eradication was higher with N. sativa (p = .01), and quality of life, food intake, body weight and BMI rose more than with placebo. IL-8, hs-CRP and malondialdehyde did not differ between groups.

6
Standardized Black Seed Oil and Seasonal Nasal Symptoms: RCT
PubMed

Randomized, double-blind, placebo-controlled trial of 250 mg Nigellin Amber (a supercritical-extracted N. sativa oil standardized to 5% thymoquinone) with 2.5 mg piperine, twice daily after food for 15 days. Most authors are employees of Sami-Sabinsa, which markets Nigellin Amber and supplied the product. (Majeed et al. 2024, Medicine (Baltimore))

65 adults aged 18 to 60 with two or more seasonal nasal allergy symptoms.

Total nasal and ocular symptom scores fell significantly more than with placebo, as did daily symptom episodes, and global impression of change was better. Serum IgE fell but not significantly versus placebo. No clinically significant changes in safety labs were seen. This was a single short, maker-run trial, and the capsule also contained piperine.

7
Nigella sativa Seed Extract and Blood Pressure in Older Adults: RCT
PubMed

Double-blind, randomized, placebo-controlled trial of 300 mg Nigella sativa seed extract twice daily for 28 days at three outpatient clinics in Jakarta, analyzed by intention to treat. Reported adverse events were indigestion in 6 participants, nausea in 3 and constipation in 2; no electrolyte, liver or kidney problems were seen. (Rizka et al. 2017, Acta Med Indones)

76 older adults with high blood pressure in Indonesia (38 per group).

Systolic blood pressure fell from about 160 to 146 mmHg with the extract and from about 161 to 148 mmHg with placebo, a difference that was not significant (p=0.36); diastolic pressure did not differ either (p=0.35). The authors concluded the extract was not shown to lower blood pressure in this group.

Side effects and drug interactions

Common Potential side effects

No serious adverse events were reported with 5 mL a day for 8 weeks in an indigestion trial
Digestive complaints can occur: in a 28-day trial of 600 mg a day of seed extract in older adults, reported side effects included indigestion (6 people), nausea (3) and constipation (2)
Avoid supplemental doses during pregnancy: safety in people has not been established, and in rats a high oral dose of thymoquinone (80 mg/kg) early in pregnancy caused complete pregnancy loss

Important Drug interactions

Diabetes medicines (insulin, metformin and others): may add to blood sugar lowering; monitor blood sugar
Warfarin: in lab tests, thymoquinone blocked warfarin breakdown by the liver enzyme CYP2C9, and modeling suggested that more than 1 g a day of black seed or its oil might affect warfarin; monitor INR and tell your doctor
Blood pressure medicines: may add to blood pressure lowering; monitor blood pressure
Cyclosporine: in rabbits, Nigella sativa lowered cyclosporine blood levels (AUC down about 56%); avoid combining without your transplant team
Phenytoin: in lab tests, thymoquinone blocked phenytoin breakdown by CYP2C9, and modeling suggested a possible clinically significant interaction with more than 1 g a day of black seed or its oil; do not combine without your doctor

Frequently asked questions about Black Seed Oil

How much black seed oil should I take?

Trials have used 0.5 to 1 g a day of oil in capsules, 2 g a day of Nigella sativa, or 5 mL (about 1 teaspoon) of oil a day in honey in an indigestion trial. Thymoquinone content varies widely between products, so the same amount of oil can deliver very different doses.

What is black seed oil used for?

Black seed oil (Nigella sativa, also called black cumin) has been studied in people for blood pressure, cholesterol, blood sugar, body weight, nasal and airway comfort, and indigestion. Most trials are small and short. Its main active compound is thymoquinone.

When and how should I take black seed oil?

Capsules in the seasonal allergy trial were taken after food. The oil has a strong, bitter, peppery taste, and one indigestion trial gave it in a honey formulation. The individual trials described here ran from 15 days to 8 weeks.

Is black seed oil safe during pregnancy?

Safety in pregnancy has not been established in people. In rats, a high oral dose of thymoquinone (80 mg/kg), the oil's main studied compound, given in the second week of pregnancy caused complete pregnancy loss, so supplemental doses are best avoided during pregnancy unless your doctor advises otherwise.

What is Black Seed Oil?

Black seed oil is pressed from the seeds of Nigella sativa, also called black cumin or kalonji, a spice with a long history in Middle Eastern, Persian and South Asian traditional medicine. Its main studied compound is thymoquinone, and the amount varies widely between commercial oils.

Is Black Seed Oil safe, and does it have side effects?

Side effects and cautions reported for Black Seed Oil include: No serious adverse events were reported with 5 mL a day for 8 weeks in an indigestion trial Digestive complaints can occur: in a 28-day trial of 600 mg a day of seed extract in older adults, reported side effects included indigestion (6 people), nausea (3) and constipation (2) It may also interact with some medications. Black Seed Oil is not right for everyone, so check with a healthcare provider first if you are pregnant or breastfeeding, have a medical condition, or take prescription medication.

Does Black Seed Oil interact with any medications?

Possible interactions include: Diabetes medicines (insulin, metformin and others): may add to blood sugar lowering; monitor blood sugar Warfarin: in lab tests, thymoquinone blocked warfarin breakdown by the liver enzyme CYP2C9, and modeling suggested that more than 1 g a day of black seed or its oil might affe… If you take prescription medication, check with a pharmacist or doctor before using it.

How strong is the scientific evidence for Black Seed Oil?

NutraSmarts rates the evidence for Black Seed Oil as Moderate (3 out of 5). It is backed by 7 study summaries and 21 cited references summarized on this page. A higher rating reflects more, larger, and better-designed human studies.

References(21 citations)

Evidence ratings on NutraSmarts are based on the totality of human clinical research, with emphasis on randomized controlled trials, meta-analyses, and systematic reviews. The references below directly support claims made throughout this page.

  1. Sahebkar A, Soranna D, Liu X, Thomopoulos C, Simental-Mendia LE, Derosa G, Maffioli P, Parati G. A systematic review and meta-analysis of randomized controlled trials investigating the effects of supplementation with Nigella sativa (black seed) on blood pressure. J Hypertens. 2016;34(11):2127-35. doi: 10.1097/HJH.0000000000001049.PubMedUsed to support: Meta-analysis of RCTs: short-term Nigella sativa modestly lowered systolic (about -3.3 mm Hg) and diastolic (about -2.8 mm Hg) blood pressure versus control. Supports a modest BP-lowering effect; trials were short.
  2. Sahebkar A, Beccuti G, Simental-Mendía LE, Nobili V, Bo S. Nigella sativa (black seed) effects on plasma lipid concentrations in humans: A systematic review and meta-analysis of randomized placebo-controlled trials. Pharmacol Res. 2016;106:37-50. doi: 10.1016/j.phrs.2016.02.008.PubMedUsed to support: Meta-analysis of 17 RCTs: Nigella sativa modestly reduced total cholesterol, LDL and triglycerides. Supports a modest lipid-lowering effect; effect sizes vary by preparation (oil vs powder).
  3. Daryabeygi-Khotbehsara R, Golzarand M, Ghaffari MP, Djafarian K. Nigella sativa improves glucose homeostasis and serum lipids in type 2 diabetes: A systematic review and meta-analysis. Complement Ther Med. 2017;35:6-13. doi: 10.1016/j.ctim.2017.08.016.PubMedUsed to support: Meta-analysis: Nigella sativa significantly reduced fasting blood glucose (about -17.8 mg/dL) and HbA1c (about -0.7%) in type 2 diabetes. Supports a modest glycemic benefit; based on only 7 trials.
  4. Koshak A, Wei L, Koshak E, Wali S, Alamoudi O, Demerdash A, Qutub M, Pushparaj PN, Heinrich M. Nigella sativa Supplementation Improves Asthma Control and Biomarkers: A Randomized, Double-Blind, Placebo-Controlled Trial. Phytother Res. 2017;31(3):403-409. doi: 10.1002/ptr.5761.PubMedUsed to support: RCT (80 asthmatics, 4 weeks): Nigella sativa oil as add-on therapy modestly improved asthma control scores and reduced blood eosinophils versus placebo. Supports a modest respiratory benefit; small, short trial.
  5. Mohit M, Farrokhzad A, Faraji SN, Heidarzadeh-Esfahani N, Kafeshani M. Effect of Nigella sativa L. supplementation on inflammatory and oxidative stress indicators: A systematic review and meta-analysis of controlled clinical trials. Complement Ther Med. 2020;54:102535. doi: 10.1016/j.ctim.2020.102535.PubMedUsed to support: Meta-analysis of 12 controlled trials. Nigella sativa lowered MDA (SMD -0.56, 95% CI -0.98 to -0.15, I2 64.7%) and raised total antioxidant capacity (SMD 0.48, 95% CI 0.09 to 0.87, I2 65.6%). It also lowered CRP, and the effect on TNF-alpha was not significant.
  6. Montazeri RS, Fatahi S, Sohouli MH, Abu-Zaid A, Santos HO, Găman MA, Shidfar F. The effect of nigella sativa on biomarkers of inflammation and oxidative stress: A systematic review and meta-analysis of randomized controlled trials. J Food Biochem. 2021;45(4):e13625. doi: 10.1111/jfbc.13625.PubMedUsed to support: Meta-analysis of 10 RCTs of Nigella sativa seed and seed oil. It found lower MDA and hs-CRP and higher TAC and SOD, with high heterogeneity (I2 77 to 99%), and subgroup results by dose, duration and oil. The authors say the small number of trials calls for caution.
  7. Kavyani Z, Musazadeh V, Golpour-Hamedani S, Moridpour AH, Vajdi M, Askari G. The effect of Nigella sativa (black seed) on biomarkers of inflammation and oxidative stress: an updated systematic review and meta-analysis of randomized controlled trials. Inflammopharmacology. 2023;31(3):1149-1165. doi: 10.1007/s10787-023-01213-0.PubMedUsed to support: Updated meta-analysis of 20 RCTs in 1,086 adults. Nigella sativa lowered MDA (SMD -2.15) and raised TAC (SMD 2.28), GPx (SMD 1.23) and SOD (SMD 2.05). It lowered CRP and TNF-alpha but not IL-6. The effect sizes are unusually large.
  8. Ardiana M, Pikir BS, Santoso A, Hermawan HO, Al-Farabi MJ. Effect of Nigella sativa Supplementation on Oxidative Stress and Antioxidant Parameters: A Meta-Analysis of Randomized Controlled Trials. ScientificWorldJournal. 2020;2020:2390706. doi: 10.1155/2020/2390706.PubMedUsed to support: Smaller meta-analysis of 5 placebo-controlled RCTs in 293 subjects. Nigella sativa raised SOD but had no significant effect on MDA or total antioxidant capacity. This is the discordant result disclosed on the page.
  9. Mohtashami R, Huseini HF, Heydari M, Amini M, Sadeqhi Z, Ghaznavi H, Mehrzadi S. Efficacy and safety of honey based formulation of Nigella sativa seed oil in functional dyspepsia: A double blind randomized controlled clinical trial. J Ethnopharmacol. 2015;175:147-52. doi: 10.1016/j.jep.2015.09.022.PubMedUsed to support: Double-blind RCT, 70 endoscopy-confirmed functional dyspepsia patients on standard anti-secretory therapy: 5 mL/day N. sativa oil in honey for 8 weeks lowered Hong Kong dyspepsia severity scores and H. pylori positivity versus placebo (P<0.001); no serious adverse events.
  10. Alizadeh-Naini M, Yousefnejad H, Hejazi N. The beneficial health effects of Nigella sativa on Helicobacter pylori eradication, dyspepsia symptoms, and quality of life in infected patients: A pilot study. Phytother Res. 2020;34(6):1367-1376. doi: 10.1002/ptr.6610.PubMedUsed to support: Double-blind pilot RCT, 51 H. pylori-infected people with functional dyspepsia: 2 g/day N. sativa plus quadruple therapy for 8 weeks raised eradication and quality of life, but dyspepsia scores did not differ from placebo.
  11. Báez G, Vargas C, Arancibia M, Papuzinski C, Franco JV. Non-Chinese herbal medicines for functional dyspepsia. Cochrane Database Syst Rev. 2023;6(6):CD013323. doi: 10.1002/14651858.CD013323.pub2.PubMedUsed to support: Cochrane review: versus placebo, Nigella sativa improved dyspepsia symptoms (SMD -1.59, 95% CI -2.13 to -1.05; 1 study, 70 participants; high certainty). Compared with other treatments it may provide little to no benefit.
  12. Majeed A, Majeed S, Parameswarappa AK, Murali A, Gudimallam S, Siddegowda C, Chandrashekar H, Mundkur L. A randomized, double-blind, placebo-controlled study to evaluate the benefits of a standardized Nigella sativa oil containing 5% thymoquinone in reducing the symptoms of seasonal allergy. Medicine (Baltimore). 2024;103(32):e39243. doi: 10.1097/MD.0000000000039243.PubMedUsed to support: RCT, 65 adults with seasonal nasal allergy symptoms: 250 mg Nigellin Amber oil (standardized to 5% thymoquinone, per the full text) with piperine twice daily for 15 days reduced nasal and ocular symptom scores versus placebo; IgE change not significant. Most authors employed by the maker (Sami-Sabinsa).
  13. Mousavi SM, Sheikhi A, Varkaneh HK, Zarezadeh M, Rahmani J, Milajerdi A. Effect of Nigella sativa supplementation on obesity indices: A systematic review and meta-analysis of randomized controlled trials. Complement Ther Med. 2018;38:48-57. doi: 10.1016/j.ctim.2018.04.003.PubMedUsed to support: Meta-analysis of 13 RCTs (875 subjects): N. sativa reduced body weight (-1.76 kg, 10 trials, I2 87%) and BMI (-0.85 kg/m2) versus placebo; waist circumference did not change significantly.
  14. Khaikin E, Chrubasik-Hausmann S, Kaya S, Zimmermann BF. Screening of Thymoquinone Content in Commercial Nigella sativa Products to Identify a Promising and Safe Study Medication. Nutrients. 2022;14(17):3501. doi: 10.3390/nu14173501.PubMedUsed to support: HPLC analysis of 6 black seed oils and 5 capsules: thymoquinone ranged from 3.08 to 809.4 mg/100 g. Supports the product-variability benefit.
  15. Al-Jenoobi FI, Al-Suwayeh SA, Muzaffar I, Alam MA, Al-Kharfy KM, Korashy HM, Al-Mohizea AM, Ahad A, Raish M. Effects of Nigella sativa and Lepidium sativum on cyclosporine pharmacokinetics. Biomed Res Int. 2013;2013:953520. doi: 10.1155/2013/953520.PubMedUsed to support: Rabbit study: 8 days of oral N. sativa lowered cyclosporine Cmax by 35.5% and AUC by 55.9%. Supports the cyclosporine interaction (animal data).
  16. Wang Z, Wang Z, Wang X, Lv X, Yin H, Jiang L, Xia Y, Li W, Li W, Liu Y. Potential food-drug interaction risk of thymoquinone with warfarin. Chem Biol Interact. 2022;365:110070. doi: 10.1016/j.cbi.2022.110070.PubMedUsed to support: In vitro study: thymoquinone competitively inhibited warfarin 7-hydroxylation (CYP2C9); modelling suggested N. sativa oil above 1 g/day might affect warfarin. Lab data only.
  17. Rizka A, Setiati S, Lydia A, Dewiasty E. Effect of Nigella sativa Seed Extract for Hypertension in Elderly: a Double-blind, Randomized Controlled Trial. Acta Med Indones. 2017;49(4):307-313..PubMedUsed to support: Double-blind RCT in 76 older adults with high blood pressure in Jakarta: 300 mg Nigella sativa seed extract twice daily for 28 days did not lower systolic (p=0.36) or diastolic (p=0.35) blood pressure significantly more than placebo. Reported adverse events included dyspepsia in 6 participants (15.7%), nausea in 3 (7.8%) and constipation in 2 (5.2%); no electrolyte, liver or kidney problems or orthostatic hypotension were seen.
  18. Mansour M, Tornhamre S. Inhibition of 5-lipoxygenase and leukotriene C4 synthase in human blood cells by thymoquinone. J Enzyme Inhib Med Chem. 2004;19(5):431-6. doi: 10.1080/14756360400002072.PubMedUsed to support: Test-tube study in human blood cells: thymoquinone inhibited formation of the leukotrienes LTC4 and LTB4 in a dose-dependent way, mainly by inhibiting 5-lipoxygenase (IC50 about 3 microM) and LTC4 synthase. Lab data, not a human trial.
  19. Sadeghi E, Imenshahidi M, Hosseinzadeh H. Molecular mechanisms and signaling pathways of black cumin (Nigella sativa) and its active constituent, thymoquinone: a review. Mol Biol Rep. 2023;50(6):5439-5454. doi: 10.1007/s11033-023-08363-y.PubMedUsed to support: Narrative review of mostly cell and animal studies: black seed and thymoquinone raised antioxidant enzyme activity, scavenged free radicals, and acted on Nrf2 and NF-κB signaling (oxidative stress and inflammation) and on AMPK (cell energy metabolism). Mechanistic background, not human outcomes.
  20. Wang Z, Wang X, Wang Z, Lv X, Yin H, Li W, Li W, Jiang L, Liu Y. Potential herb-drug interaction risk of thymoquinone and phenytoin. Chem Biol Interact. 2022;353:109801. doi: 10.1016/j.cbi.2022.109801.PubMedUsed to support: Lab study: thymoquinone competitively inhibited CYP2C9 hydroxylation of phenytoin (Ki about 4.45 microM); modeling predicted a possible clinically significant interaction with more than 18 mg/day of thymoquinone or more than 1 g/day of Nigella sativa or its oil. Lab and modeling data only.
  21. Abdollahzade Fard A, Saboory E, Tahmazi Y, Rasmi Y, Dindarian S, Parsamanesh N. Effect of orally-administrated thymoquinone during pregnancy on litter size, pentylenetetrazol-induced seizure, and body weight in rat offspring. Iran J Basic Med Sci. 2021;24(1):30-37. doi: 10.22038/ijbms.2020.47479.10930.PubMedUsed to support: Rat study: oral thymoquinone at 80 mg/kg in the second gestational week caused complete pregnancy loss, and in the third week halved litter size; 40 and 80 mg/kg lowered birth weight. The authors concluded that a high dose can be severely toxic for pregnancy. Animal data.