dc.contributor.author | Erdogan, Mumin Alper | |
dc.contributor.author | Turk, Miray | |
dc.contributor.author | Doganay, Gizem Dinler | |
dc.contributor.author | Sever, Ibrahim Halil | |
dc.contributor.author | Ozkul, Bahattin | |
dc.contributor.author | Sogut, Ibrahim | |
dc.contributor.author | Eroglu, Ebru | |
dc.date.accessioned | 2024-02-04T13:29:37Z | |
dc.date.available | 2024-02-04T13:29:37Z | |
dc.date.issued | 2023 | |
dc.identifier.issn | 1557-1890 | |
dc.identifier.issn | 1557-1904 | |
dc.identifier.uri | https://doi.org/10.1007/s11481-023-10089-4 | |
dc.identifier.uri | http://hdl.handle.net/11446/4701 | |
dc.description.abstract | Recent research on placental, embryo, and brain organoids suggests that the COVID-19 virus may potentially affect embryonic organs, including the brain. Given the established link between SARS-CoV-2 spike protein and neuroinflammation, we sought to investigate the effects of exposure to this protein during pregnancy. We divided pregnant rats into three groups: Group 1 received a 1 ml/kg saline solution, Group 2 received 150 mu g/kg adjuvant aluminum hydroxide (AAH), and Group 3 received 40 mu g/kg spike protein + 150 mu g/kg AAH at 10 and 14 days of gestation. On postnatal day 21 (P21), we randomly separated 60 littermates (10 male-female) into control, AAH-exposed, and spike protein-exposed groups. At P50, we conducted behavioral analyses on these mature animals and performed MR spectroscopy. Subsequently, all animals were sacrificed, and their brains were subject to biochemical and histological analysis. Our findings indicate that male rats exposed to the spike protein displayed a higher rate of impaired performance on behavioral studies, including the three-chamber social test, passive avoidance learning analysis, open field test, rotarod test, and novelty-induced cultivation behavior, indicative of autistic symptoms. Exposure to the spike protein (male) induced gliosis and neuronal cell death in the CA1-CA3 regions of the hippocampus and cerebellum. The spike protein-exposed male rats exhibited significantly greater levels of malondialdehyde (MDA), tumor necrosis factor alpha (TNF-alpha), interleukin-17 (IL-17), nuclear factor kappa B (NF-kappa B), and lactate and lower levels of brain-derived neurotrophic factor (BDNF) than the control group. Our study suggests a potential association between prenatal exposure to COVID-19 spike protein and neurodevelopmental problems, such as ASD. These findings highlight the importance of further research into the potential effects of the COVID-19 virus on embryonic and fetal development and the potential long-term consequences for neurodevelopment. | en_US |
dc.description.sponsorship | Scientific and Technological Research Council of Turkey (TUBITAK) [120Z305]; Istanbul Technical University Scientific Research Projects [TGA-2022-43373, TGA-2022- 43955]; Health Institutes of Turkey (TUSEB) [7162/8972]; TUBITAK 2211C Program | en_US |
dc.description.sponsorship | This research was supported by grants from the Scientific and Technological Research Council of Turkey (TUBITAK) under the project number 120Z305; Istanbul Technical University Scientific Research Projects with codes TGA-2022-43373 and TGA-2022- 43955; Health Institutes of Turkey (TUSEB) with the grant number 7162/8972; and the TUBITAK 2211C Program. There was no specific grant received from commercial or non-for-profit sectors. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Springer | en_US |
dc.relation.ispartof | Journal Of Neuroimmune Pharmacology | en_US |
dc.identifier.doi | 10.1007/s11481-023-10089-4 | |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | COVID-19 | en_US |
dc.subject | SARS-CoV-2 | en_US |
dc.subject | Spike protein | en_US |
dc.subject | Neurodegeneration | en_US |
dc.subject | Neuroinflammation | en_US |
dc.subject | Autism spectrum disorder | en_US |
dc.title | Prenatal SARS-CoV-2 Spike Protein Exposure Induces Autism-Like Neurobehavioral Changes in Male Neonatal Rats | en_US |
dc.type | article | en_US |
dc.department | DBÜ | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.volume | 18 | en_US |
dc.identifier.startpage | 573 | en_US |
dc.identifier.endpage | 591 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.department-temp | [Erdogan, Mumin Alper] Izmir Katip Celebi Univ, Fac Med, Dept Physiol, Izmir, Turkiye; [Turk, Miray; Doganay, Gizem Dinler] Istanbul Tech Univ, Grad Sch, Dept Mol Biol Genet & Biotechnol, TR-34469 Istanbul, Turkiye; [Doganay, Gizem Dinler] Istanbul Tech Univ, Fac Sci & Letters, Dept Mol Biol & Genet, TR-34469 Istanbul, Turkiye; [Sever, Ibrahim Halil] Demiroglu Bilim Univ, Fac Med, Dept Radiol, Istanbul, Turkiye; [Ozkul, Bahattin] Istanbul Atlas Univ, Sch Med, Dept Radiol, Istanbul, Turkiye; [Sogut, Ibrahim] Demiroglu Bilim Univ, Fac Med, Dept Biochem, Istanbul, Turkiye; [Eroglu, Ebru; Uyanikgil, Yigit] Ege Univ, Fac Med, Dept Histol & Embryol, Izmir, Turkiye; [Erbas, Oytun] Demiroglu Bilim Univ, Fac Med, Dept Physiol, Istanbul, Turkiye | en_US |
dc.authorid | Uyanikgil, Yigit/0000-0002-4016-0522 | |
dc.authorid | Uyanikgil, Yigit/0000-0002-4016-0522 | |
dc.authorid | Özkul, Bahattin/0000-0003-3339-8329 | |
dc.authorid | Eroglu, Ebru/0000-0002-8087-4159 | |
dc.authorid | Erdogan, Mumin/0000-0003-0048-444X | |
dc.authorid | Turk, Miray/0000-0003-0917-3605 | |
dc.identifier.pmid | 37889404 | en_US |
dc.identifier.scopus | 2-s2.0-85174926241 | en_US |
dc.identifier.wos | WOS:001088138600001 | en_US |
dc.authorwosid | Uyanikgil, Yigit/K-3544-2017 | |
dc.authorwosid | Uyanikgil, Yigit/M-2746-2019 | |
dc.authorwosid | Özkul, Bahattin/JVN-8696-2024 | |