نمایش مختصر رکورد

dc.contributor.authorMohammadi, Elahehen_US
dc.contributor.authorMehri, Soghraen_US
dc.contributor.authorBadie Bostan, Hasanen_US
dc.contributor.authorHosseinzadeh, Hosseinen_US
dc.date.accessioned1399-07-09T12:38:14Zfa_IR
dc.date.accessioned2020-09-30T12:38:14Z
dc.date.available1399-07-09T12:38:14Zfa_IR
dc.date.available2020-09-30T12:38:14Z
dc.date.issued2017-12-01en_US
dc.date.issued1396-09-10fa_IR
dc.date.submitted2017-01-07en_US
dc.date.submitted1395-10-18fa_IR
dc.identifier.citationMohammadi, Elaheh, Mehri, Soghra, Badie Bostan, Hasan, Hosseinzadeh, Hossein. (2017). Protective effect of crocin against d-galactose-induced aging in mice. Avicenna Journal of Phytomedicine, 8(1), 14-23. doi: 10.22038/ajp.2017.21198.1801en_US
dc.identifier.issn2228-7930
dc.identifier.issn2228-7949
dc.identifier.urihttps://dx.doi.org/10.22038/ajp.2017.21198.1801
dc.identifier.urihttp://ajp.mums.ac.ir/article_9453.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/425444
dc.description.abstractObjective: Aging is a multifactorial phenomenon, which attribute to different diseases and abnormalities in living systems. Oxidative stress, which is an important factor in aging, exacerbates this process via different mechanisms. Crocin (CR), one of the active components of saffron showed strong antioxidant effects. In the present study, anti-aging property of crocin was investigated in mice.<br /> Materials and Methods: The model of aging was induced using administration of d-galactose (500 mg/kg, s. c.) for 42 days. Animals were treated with crocin (10, 20, 40 mg/kg, i.p.) during treatment with d-galactose.  At the end of treatment, levels of malondialdehyde (MDA) as a lipid peroxidation marker and glutathione content (GSH) in the liver and brain were measured. Also, biochemical factors including liver enzymes (ALT and AST), male sex hormones including testosterone and dehydroepiandrosterone-sulfate (DHEA-SO<sub>4</sub>) and pro-inflammatory markers such as tumor necrosis factor -α (TNF-α) and interlukine-6 (IL-6) in serum, were evaluated.<br /> Results: Administration of d-galactose led to induction of lipid peroxidation in liver and brain tissues, as well as elevation of AST, ALT, and pro-inflammatory cytokines and reduction of male sex hormones levels in serum. Interestingly, treatment of animals with crocin (10, 20 and 40 mg/kg) diminished lipid peroxidation in the liver and brain tissues while elevated GSH content. Also, a decline in serum levels of TNF-α and IL-6 and an elevation of male sex hormones were observed following treatment with crocin.<br /> Conclusion: Administration of crocin reduced d-galactose-induced aging in mice through inhibition of oxidative stress, reduction of inflammation and elevation of sex hormones.en_US
dc.format.extent606
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherMashhad University of Medical Sciencesen_US
dc.relation.ispartofAvicenna Journal of Phytomedicineen_US
dc.relation.isversionofhttps://dx.doi.org/10.22038/ajp.2017.21198.1801
dc.subjectD-galactoseen_US
dc.subjectCrocinen_US
dc.subjectCrocus sativusen_US
dc.subjectAgingen_US
dc.subjectOxidative stressen_US
dc.subjectPharmacologyen_US
dc.titleProtective effect of crocin against d-galactose-induced aging in miceen_US
dc.typeTexten_US
dc.typeOriginal Research Articleen_US
dc.contributor.departmentDepartment of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentPharmaceutical Research Center, Department of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentDepartment of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentPharmaceutical Research Center, Department of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.citation.volume8
dc.citation.issue1
dc.citation.spage14
dc.citation.epage23


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