Key result
Thymoquinone improved testicular tissue, decreased apoptotic index and caspase 3 expressions, and increased testosterone levels compared to doxorubicin alone in rats.
Why the study?
Doxorubicin is widely used for cancer treatment, and thymoquinone is an antioxidant used to reduce drug side effects, motivating evaluation of its potential therapeutic effects on doxorubicin-induced testicular toxicity.
Does thymoquinone reduce doxorubicin-induced testicular toxicity in rats?
Does thymoquinone reduce doxorubicin-induced testicular toxicity in rats?
Thymoquinone attenuates doxorubicin-induced testicular toxicity, apoptosis, and oxidative stress in a rat model.
Answers are grounded in this paper and cite their sources.
May reduce doxorubicin testicular toxicity in rats; leaves open human translation for fertility preservation.
BACKGROUND: Doxorubicin (DOX) is used for treatment of many cancer types. Thymoquinone (THQ) is a powerful antioxidant agent used for reducing side effects of several drugs. The aim of this study is to determine possible therapeutic effects of THQ on doxorubicin-induced testicular toxicity in rats. METHODS: = 8): control, THQ, olive oil, DOX (a single dose of 15 mg/kg intraperitoneally (i.p.) on seventh day of the experiment), and DOX + THQ (10 mg/kg THQ per day and 15 mg/kg DOX i.p. on seventh day). Animals were euthanized, and testis tissues were evaluated histopathologically. Caspase 3 and HSP90 immunostaining were performed to determine the expression levels of these proteins among groups. Terminal deoxynucleotidyl transferase 2'-deoxyuridine, 5'-triphosphate nick-end labeling method was used for evaluation of apoptotic index. Moreover, serum testosterone levels and total antioxidant status (TAS) and total oxidant status (TOS) in testicular tissue were measured by ELISA assay. RESULTS: The DOX group had histopathological deterioration compared to the control group. There was an increase in apoptotic index, caspase 3 and HSP90 expressions in the DOX group. While TAS level of the DOX group decreased, TOS level increased when compared with the other groups. Serum testosterone levels in the DOX group decreased compared to the control group. However, there was improvement in testicular tissue in DOX + THQ group compared to the DOX group. There was a decrease in apoptotic index, caspase 3, and HSP90 expressions in DOX + THQ group compared to the DOX group. Testosterone level of DOX + THQ significantly increased compared to the DOX group. CONCLUSION: We suggest that THQ can be used as a protective agent to reduce the toxic effects of DOX.
No takes yet. Share an insight, caveat, or question.
Öztürk et al. (2020) studied Doxorubicin-induced testicular toxicity (n=40). Thymoquinone (THQ) vs. Doxorubicin (DOX) alone was evaluated on Testicular tissue histopathology, apoptotic index, and testosterone levels. Thymoquinone improved testicular tissue, decreased apoptotic index and caspase 3 expressions, and increased testosterone levels compared to doxorubicin alone in rats.
Synapse has enriched 10 related papers. Consider them for comparative context: