Some of the scientific literature suggests that Nigella sativa, and more specifically its primary active compound, thymoquinone, may exert a protective effect against certain adverse effects induced by anticancer treatments, particularly those related to oxidative stress.
These studies remain primarily experimental, but they offer valuable insights into the potential mechanisms involved. Several animal studies have shown that administration of oil or extracts of Nigella sativa can limit chemotherapy‐induced renal toxicity, particularly cisplatin, but also methotrexate, doxorubicin, or 5‐fluorouracil. These anticancer agents are known to generate a substantial production of reactive oxygen species, leading to oxidative damage in kidney cells.
In these experimental models, Nigella sativa (black seed) and thymoquinone reduce lipid peroxidation, enhance the activity of endogenous antioxidant enzymes such as superoxide dismutase and catalase, and improve biomarkers of renal function. From a histological perspective, a reduction in renal tissue lesions is also observed when black seed oil is administered both before and after exposure to chemotherapeutic agents.
Beyond the kidney, some studies suggest a broader hepatoprotective and antioxidant effect of the nigella. Seed extracts of Nigella sativa have notably shown an ability to mitigate the oxidative stress and liver damage induced by doxorubicin or exposure to gamma radiation. These findings suggest that thymoquinone’s antioxidant properties may, in certain experimental settings, help protect healthy tissues from treatment-related collateral damage without directly interfering with the treatments’ cytotoxic action on tumor cells.
For example, a study conducted on rats showed that a single dose of cisplatin (6 mg/kg) induced acute kidney injury via a massive production of free radicals. Oral administration of black seed oil (2 mL/kg), both before and after chemotherapy, made it possible to limit the rise in biomarkers of renal insufficiency, namely serum creatinine and blood urea. At the cellular level, black seed oil preserved the activity of enzymes responsible for proper tubular function in the kidneys, as well as those involved in carbohydrate metabolism. These biochemical results are supported by histological analysis, which reveals severe renal lesions in animals treated solely with cisplatin, compared to markedly attenuated damage in the group co-treated with black seed oil.
Effect of Nigella sativa, with and without cisplatin treatment, on urinary parameters in rats.
Source: KHAN F. & al. Protective effect of Nigella sativa oil on cisplatin induced nephrotoxicity and oxidative damage in rat kidney. Biomedicine & Pharmacotherapy (2017).
The overall data suggest a protective role of Nigella in attenuating chemotherapy-induced oxidative stress and renal tissue damage in a preclinical setting.
Another experimental study examined the ability of a Nigella sativa seed extract to attenuate the combined toxicity of doxorubicin and radiotherapy. In this protocol, rats received either doxorubicin, gamma irradiation, or both over several weeks, inducing marked oxidative stress and impaired liver function. These treatments led to a significant decrease in endogenous antioxidant defenses, accompanied by increases in lipid peroxidation markers and disruptions in hepatic enzyme activity. Daily oral administration of a Nigella sativa seed extract (2 g/kg), initiated before and continued during the anticancer treatments, was able to partially restore antioxidant parameters and improve markers of hepatic function compared to the groups exposed to doxorubicin and/or irradiation alone.
The antioxidant properties of nigella could help protect certain healthy tissues from treatment-induced oxidative damage, once again demonstrated exclusively in animal studies.