Please use this identifier to cite or link to this item: https://doi.org/10.1530/JME-17-0214
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dc.titleCurcumin exerts a protective effect against premature ovarian failure in mice
dc.contributor.authorYan, Z
dc.contributor.authorDai, Y
dc.contributor.authorFu, H
dc.contributor.authorZheng, Y
dc.contributor.authorBao, D
dc.contributor.authorYin, Y
dc.contributor.authorChen, Q
dc.contributor.authorNie, X
dc.contributor.authorHao, Q
dc.contributor.authorHou, D
dc.contributor.authorCui, Y
dc.date.accessioned2020-10-22T07:26:50Z
dc.date.available2020-10-22T07:26:50Z
dc.date.issued2018
dc.identifier.citationYan, Z, Dai, Y, Fu, H, Zheng, Y, Bao, D, Yin, Y, Chen, Q, Nie, X, Hao, Q, Hou, D, Cui, Y (2018). Curcumin exerts a protective effect against premature ovarian failure in mice. Journal of Molecular Endocrinology 60 (3) : 261-271. ScholarBank@NUS Repository. https://doi.org/10.1530/JME-17-0214
dc.identifier.issn09525041
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/179044
dc.description.abstractThis study was designed to investigate the protective effect of curcumin against d-galactose (d-gal)-induced premature ovarian failure (POF) in mice. A mouse POF model was induced by subcutaneous injection of d-gal (200 mg/kg/day) daily for 42 days. Mice in the curcumin group received both d-gal treatment and intraperitoneal injection of curcumin (100 mg/kg/day) for 42 days. Ovarian function, oxidative stress and apoptosis were evaluated. The P, E2 and SOD levels were higher, and the FSH, LH and MDA levels were significantly lower in the curcumin group than those in the d-gal group. The proportion of primordial follicles was also significantly higher in the curcumin group than that in the d-gal group. In addition, curcumin treatment after d-gal administration resulted in significantly lower Sod2, Cat, 8-OhdG, 4-HNE, NTY and senescence-associated protein P16 expression levels, higher Amh expression levels and less apoptosis in granulosa cells than was observed in the d-gal group. Moreover, the p-Akt, Nrf2 and HO-1 protein expression levels were significantly higher and the apoptosis-related cleaved caspase-3 and -9 protein expression levels were markedly lower in the curcumin group than in the d-gal group. In conclusion, curcumin effectively inhibited d-gal-induced oxidative stress, apoptosis and ovarian injury via a mechanism involving the Nrf2/HO-1 and PI3K/Akt signaling pathways, suggesting that curcumin is a potential protective agent against POF. © 2018 Society for Endocrinology Published by Bioscientifica Ltd.
dc.publisherBioScientifica Ltd.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectcaspase 3
dc.subjectcaspase 9
dc.subjectcurcumin
dc.subjectgalactose
dc.subjectmalonaldehyde
dc.subjectmessenger RNA
dc.subjectprotein kinase B
dc.subjectprotein p16
dc.subjectsuperoxide dismutase
dc.subject3-nitrotyrosine
dc.subject4-hydroxy-2-nonenal
dc.subject8-oxo-7-hydrodeoxyguanosine
dc.subjectaldehyde
dc.subjectcurcumin
dc.subjectcyclin dependent kinase inhibitor 2A
dc.subjectdeoxyguanosine
dc.subjectmessenger RNA
dc.subjectMuellerian inhibiting factor
dc.subjectprotective agent
dc.subjecttyrosine
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectantral follicle
dc.subjectapoptosis
dc.subjectArticle
dc.subjectcontrolled study
dc.subjectdevelopmental stage
dc.subjectenzyme immunoassay
dc.subjectfemale
dc.subjectgranulosa cell
dc.subjectimmunohistochemistry
dc.subjectmouse
dc.subjectmRNA expression level
dc.subjectnonhuman
dc.subjectovary function
dc.subjectovary tissue
dc.subjectoxidative stress
dc.subjectpremature ovarian failure
dc.subjectprimordial follicle
dc.subjectpriority journal
dc.subjectprotein expression level
dc.subjectTUNEL assay
dc.subjectWestern blotting
dc.subjectanimal
dc.subjectC57BL mouse
dc.subjectdisease model
dc.subjectdrug effect
dc.subjectgenetics
dc.subjectgonad
dc.subjecthypothalamus hypophysis system
dc.subjectmetabolism
dc.subjectovary
dc.subjectpathology
dc.subjectpremature ovarian failure
dc.subjectAldehydes
dc.subjectAnimals
dc.subjectAnti-Mullerian Hormone
dc.subjectApoptosis
dc.subjectCurcumin
dc.subjectCyclin-Dependent Kinase Inhibitor p16
dc.subjectDeoxyguanosine
dc.subjectDisease Models, Animal
dc.subjectFemale
dc.subjectGalactose
dc.subjectGonads
dc.subjectHypothalamo-Hypophyseal System
dc.subjectMice, Inbred C57BL
dc.subjectOvary
dc.subjectOxidative Stress
dc.subjectPrimary Ovarian Insufficiency
dc.subjectProtective Agents
dc.subjectRNA, Messenger
dc.subjectTyrosine
dc.typeArticle
dc.contributor.departmentPHARMACOLOGY
dc.description.doi10.1530/JME-17-0214
dc.description.sourcetitleJournal of Molecular Endocrinology
dc.description.volume60
dc.description.issue3
dc.description.page261-271
dc.published.statePublished
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