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dc.contributor.authorErdogan, Mumin Alper
dc.contributor.authorBozkurt, Mehmet Fatih
dc.contributor.authorErbas, Oytun
dc.date.accessioned2024-02-04T13:29:36Z
dc.date.available2024-02-04T13:29:36Z
dc.date.issued2023
dc.identifier.issn0736-5748
dc.identifier.issn1873-474X
dc.identifier.urihttps://doi.org/10.1002/jdn.10248
dc.identifier.urihttp://hdl.handle.net/11446/4693
dc.description.abstractBackgroundA neurodevelopmental disease, autism spectrum disorder (ASD) occurs in males three times more commonly than girls. Higher prenatal testosterone exposure may result in autistic-like behaviour in boys, according to earlier research. It is unclear how fetal testosterone affects the development of autism. In this study, we tested the hypothesis that prenatal testosterone exposure in an animal model may result in autistic behaviours by modifying serotonin, dopamine, IGF-1 and oxytocin levels. Materials and MethodsGroup 1 (control, n = 6) and Group 2 (testosterone undecanoate, n = 6) of female rats were randomly assigned. For 2-3 days during the oestrus cycle, female rats were housed with a reproductive male (three females/one male). On the 10th day of gestation, rats in Group 1 received 1 ml/kg% 0.9 NaCl saline, whereas rats in Group 2 received 250 mg/kg testosterone undecanoate. Until weaning on postnatal day 21 (P21), the mothers were permitted to care for their pups. On P21, 40 littermates-10 male and female for control and 10 male and female from mothers that exposed to testosterone-were arbitrarily split up and housed. On P50, these mature rats were tested for their behaviour. The rats were then sacrificed. The brain tissue was subjected to histological examinations as well as biochemical tests for homovanillic acid (HVA), 5-Hydroxyindoleacetic acid (5-HIAA), oxytocin and insulin-like growth factor-1 (IGF-1). ResultsThe groups differed significantly in the behavioural examinations (three-chamber social test, passive avoidance learning analysis, open field test), with the testosterone-exposed groups exhibiting autistic symptoms to a higher extent. When compared with the control groups, testosterone exposure caused significant histological changes in the hippocampus CA1 and CA3 areas, including gliosis and cell death of neurons. In the testosterone-exposed groups, HVA, 5-HIAA and IGF-1 tissue expressions in the brain elevated, whereas oxytocin levels reduced. These findings point to a potential connection between neurodevelopmental disorders like ASD and exposure to testosterone during gestation. ConclusionOverall, we revealed that prenatal testosterone exposure led to autistic traits by elevating serotonin, dopamine and IGF-1 levels while lowering oxytocin levels.en_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.relation.ispartofInternational Journal Of Developmental Neuroscienceen_US
dc.identifier.doi10.1002/jdn.10248
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectautism spectrum disordersen_US
dc.subjectdopamineen_US
dc.subjectIGF-1en_US
dc.subjectoxytocinen_US
dc.subjectserotoninen_US
dc.subjecttestosteroneen_US
dc.titleEffects of prenatal testosterone exposure on the development of autism-like behaviours in offspring of Wistar ratsen_US
dc.typearticleen_US
dc.departmentDBÜen_US
dc.identifier.issue2en_US
dc.identifier.volume83en_US
dc.identifier.startpage201en_US
dc.identifier.endpage215en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-temp[Erdogan, Mumin Alper] Izmir Katip Celebi Univ, Fac Med, Dept Physiol, Izmir, Turkiye; [Bozkurt, Mehmet Fatih] Afyon Kocatepe Univ, Fac Vet Med, Dept Pathol, Afyon, Turkiye; [Erbas, Oytun] Demiroglu Bilim Univ, Fac Med, Dept Physiol, Istanbul, Turkiyeen_US
dc.authoridBozkurt, Mehmet Fatih/0000-0002-1669-0988
dc.authoridErdogan, Mumin/0000-0003-0048-444X
dc.authoridErbas, Oytun/0000-0001-5427-8428
dc.identifier.pmid36573444en_US
dc.identifier.scopus2-s2.0-85146451100en_US
dc.identifier.wosWOS:000917849200001en_US
dc.authorwosidBozkurt, Mehmet Fatih/R-5895-2016


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