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HP-43: Stimulation of insulin secretion, protective and restorative effect of thymoquinone on β-cell line

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dc.contributor.author TACHOUR, Rechda Amel
dc.contributor.author REZGUI, Abdelmalek
dc.contributor.author Djaouida, CHARIF
dc.contributor.author TACHERFIOUT, Mustapha
dc.contributor.author HAB, Fatma Zahra
dc.contributor.author DERGUINE, Rania
dc.contributor.author GACI, Kamel
dc.contributor.author AGRED, Rym
dc.contributor.author BENMANSEUR, Anfel
dc.contributor.author KHETTAL, Bachra
dc.contributor.author SOBHI, Widad
dc.date.accessioned 2026-01-18T08:20:41Z
dc.date.available 2026-01-18T08:20:41Z
dc.date.issued 2023-10-05
dc.identifier.uri http://depot.umc.edu.dz/handle/123456789/14795
dc.description.abstract Our study elucidates the protective and restorative effect of thymoquinone on β-cell line, and its potential impact on the stimulation of insulin secretion, and its effect on oxidative stress. Objectives: Study the effect of Thymoquinone on viability and stimulation of insulin secretion of β-cell line and its protective and restorative effect on these cells, in order to find a solution to type 1 diabetes. Methods: A cytotoxic study was conducted on EMT6 and NIT-1 cell lines using the XTT kit. To reveal the insulin stimulation potential, NIT-1 cells were incubated for 24h, then Thymoquinone was added at different concentrations, the insulin level was measured using the Mouse Ins1/Insulin-1 ELISA. Then to determine the protective effect of Thymoquinone, NIT-1 culture was performed, and Thymoquinone was added for 24 h. After that, the STZ was added for 24h. To measure the cell viability the XTT reagent was added. The oxidative stress markers (MDA, SOD, and GSH) assay was performed in a supernatant of beta cells treated with Thymoquinone. Finally, the STZ was added before Thymoquinone for the restorative effect, and cell viability was determined. Results and discussion: The results show low cytotoxicity of Thymoquinone, on both EMT6 and NIT-1 cell lines, a highly significant difference (around 100%) of insulin secretion between the cells of control and the cells treated with Thymoquinone was mentioned. The results indicate that STZ caused cell death of approximately 45% of untreated β NIT-1line cells. However, the cells treated with TQ then exposed to STZ were protected against its cytotoxicity because we only noted the death of about 15% of cells. The results of the restorative effect demonstrate that there is an 12-14% improvement in viability of cells treated with thymoquinone compared with cells treated only with STZ. Conclusion: Thymoquinone has demonstrated a strong stimulation of insulin secretion by β-cell line with low cytotoxicity. Thymoquinone can be suggested as a solution for type 1 diabetes fr_FR
dc.language.iso en fr_FR
dc.publisher université frères mentouri constantine1 fr_FR
dc.subject Thymoquinone fr_FR
dc.subject Type 1 Diabetes fr_FR
dc.subject β cell line fr_FR
dc.subject Streptozotocin fr_FR
dc.subject protective effect fr_FR
dc.subject insulin secretion fr_FR
dc.title HP-43: Stimulation of insulin secretion, protective and restorative effect of thymoquinone on β-cell line fr_FR
dc.type Article fr_FR


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