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dc.contributor.authorMakav, Mustafa
dc.contributor.authorEroğlu, Hüseyin Avni
dc.date.accessioned2022-08-10T13:06:07Z
dc.date.available2022-08-10T13:06:07Z
dc.date.issued2021en_US
dc.identifier.citationMakav, M., & Eroğlu, H. A. (2021). Recuperative effect of estrogen on rotenone-induced experimental model of Parkinson’s disease in rats. Environmental Science and Pollution Research, 28(17), 21266–21275. https://doi.org/10.1007/s11356-020-11985-5en_US
dc.identifier.issn0944-1344 / 1614-7499
dc.identifier.urihttps://doi.org/10.1007/s11356-020-11985-5
dc.identifier.urihttps://hdl.handle.net/20.500.12428/3657
dc.description.abstractParkinson’s disease (PD) is described as the loss of dopaminergic neurons located in the substantia nigra (SN) region of the brain and a progressive motor failure. Increased frequency of PD in women, especially after menopause, suggests the effect of estrogen. This view has been supported with empirical studies. Therefore, the effect of estrogen in an experimental model of Parkinson’s disease induced by rotenone was investigated. A total of 32 female Wistar Albino rats were randomly assigned to four groups (control group, ovariectomy group, Parkinson’s group, Parkinson’s + estrogen group). The Parkinson’s group received rotenone subcutanously at the dose of 2.5 mg/kg bw, on the 1st, 2nd, 3rd 4th, 6th, 9th, 12th, 15th, 18th, and 21st days animals in the Parkinson’s + estrogen group received retonon as in the Parkinson’s group and was additionally subcutaneously given estrogen (implant containing 0.5 mg 17 β-estradiol lasting for 21 days). The rats were subjected to rotarod, pole, and swimming tests at the end of the experiment for comparison of their motor activities, and then, histopathological and biochemical analyses were performed on the tissues that were extracted. The rotarod results revealed that Parkinson’s group had the shortest time (32.33 ± 3.98 sn) than the groups of control (92.50 ± 12.60 s) ovariectomy (71.42 ± 10.58 s), and Parkinson’s + estrogen (71.37 ± 9.26 s). The results of pole disclosed that return and landing time prolonged for Parkinson’s group when compared with other groups (return time for control 2.98 ± 0.38 s, ovariectomy 3.02 ± 0.75 s, Parkinson 5.91 ± 0.33 s, Parkinson’s + estrogen 3.48 ± 0.42 s and landing time for control 5.30 ± 0.59 s, ovariectomy 5.45 ± 0.73 s, Parkinson 9.80 ± 0.90 s, Parkinson’s + estrogen 5.37 ± 1.02 s). Parkinson’s group had longest (90.71 ± 12.56 s) swimming time to reach the target when compared with control (33.16 ± 8.68 s), ovariectomy (47.37 ± 12.19 s), and Parkinson’s + estrogen (49.82 ± 5.78 s). Histopathological examination indicated a significant difference in tyrosine hydroxylase-stained cells (dopaminergic neurons and dopamine) between the Parkinson’s + estrogen group and the Parkinson’s group. The biochemical analyses of Caspas-3 activation in SN and striatum (STR) was significantly different between the Parkinson’s + estrogen group and the Parkinson’s group, but this difference was not observed in STR while evaluating Bcl-2. The results of this study suggested that estrogen may have a recuperative effect on PD.en_US
dc.language.isoengen_US
dc.publisherSpringeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectParkinson’s Diseaseen_US
dc.subjectEstrogenen_US
dc.subjectCaspase-3en_US
dc.subjectBcl-2en_US
dc.subjectRotenoneen_US
dc.titleRecuperative effect of estrogen on rotenone-induced experimental model of Parkinson’s disease in ratsen_US
dc.typearticleen_US
dc.authorid0000-0002-1040-3255en_US
dc.relation.ispartofEnvironmental Science and Pollution Research (ESPR)en_US
dc.departmentFakülteler, Tıp Fakültesi, Temel Tıp Bilimleri Bölümüen_US
dc.identifier.volume28en_US
dc.identifier.issue17en_US
dc.identifier.startpage21266en_US
dc.identifier.endpage21275en_US
dc.institutionauthorEroğlu, Hüseyin Avni
dc.identifier.doi10.1007/s11356-020-11985-5en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorwosidABF-4291-2021en_US
dc.authorscopusid56500220800en_US
dc.identifier.wosqualityQ2en_US
dc.identifier.wosWOS:000605574100003en_US
dc.identifier.scopus2-s2.0-85099235673en_US
dc.identifier.pmidPMID: 33410082en_US


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