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DOI: 10.3791/68435-v
Ecma Güvenilir1, Zeynep Yilmaz Şükranli2,3, Mai R. S. Abusalim1,2, Aslı Okan Oflamaz4, Züleyha Doğanyiğit4, Kemal Erdem Başaran2,5, Mehmet Dolanbay6, Minoo Rassoulzadegan2,7,8, Serpil Taheri2,3
1Gevher Nesibe Genome and Stem Cell Institute,Erciyes University, 2Betül Ziya Eren Genome and Stem Cell (GENKÖK) Center,Erciyes University, 3Department of Medical Biology,Erciyes University, 4Department of Histology and Embryology,Yozgat Bozok University, 5Department of Physiology,Erciyes University, 6Department of Obstetrics and Gynecology, Faculty of Medicine,Erciyes University, 7University of Nice Sophia Antipolis, 8Department of Medical Genetics,Erciyes University
Here, we present a protocol to induce hypoxia in neonatal mice by delivering them in controlled environments with varying oxygen concentrations. Mouse models subjected to oxygen variations at birth have durably varied the expression of miRNAs involved in the induction of behavioral phenotypic changes such as autism.
We studied how different levels of neonatal hypoxia affect brain development, behavior, and ASD related molecular changes in mice, emphasizing the severity dependent effects and need for early intervention. Research studies link neonatal hypoxia to autism-related brain changes. Focus is shifting to repurpose drugs targeting neuroinflammation and neuro-immune dysfunction to prevent neuronal damage and long-term cognitive decline.
We used hypoxia chambers, qPCR, behavioral tracking, and microscope to track molecular and structural changes in neonatal brains. A key challenge is translating molecular changes like microRNA dysregulation into behavior due to ASD's complexity. Limitations include species differences, lack of sex-specific analysis, and difficult controlling hypoxia therapy.
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