<?xml version="1.1" encoding="utf-8"?>
<article xsi:noNamespaceSchemaLocation="http://jats.nlm.nih.gov/publishing/1.1/xsd/JATS-journalpublishing1-mathml3.xsd" dtd-version="1.1" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><front><journal-meta><journal-id journal-id-type="publisher-id">CBR</journal-id><journal-title-group><journal-title>Cell Biology Research</journal-title></journal-title-group><issn>TBA</issn><eissn>2529-7627</eissn><publisher><publisher-name>WHIOCE PUBLISHING PTE. LTD.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.18063/CBR.v6i4.1014</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title>Application of Integrated Animal and Cell Experiment Teaching Model in Demonstrating Ferroptosis in Cerebral Ischemia-Reperfusion Injury</title><url>https://artdesignp.com/journal/CBR/6/4/10.18063/CBR.v6i4.1014</url><author>SunGuangjie,HuangBingcang</author><pub-date pub-type="publication-year"><year>2025</year></pub-date><volume>6</volume><issue>4</issue><history><date date-type="pub"><published-time>2025-12-26</published-time></date></history><abstract>Traditional molecular medicine experimental teaching often suffers from a disconnection between theory and practice, as well as fragmented experimental content, making it difficult for students to integrate multi-level knowledge to address complex scientific problems. To address this, we redesigned our Molecular Medicine Experimental Techniques course around the pathophysiology of cerebral ischemia-reperfusion injury (CIRI), with a focus on the mechanism of ferroptosis. Our integrated pedagogical model links an in vivo transient middle cerebral artery occlusion (tMCAO) mouse model with an in vitro oxygen-glucose deprivation/reoxygenation (OGD/R) model in HT22 neuronal cells. Within this&amp;nbsp;framework, students first observe in vivo phenotypes in the tMCAO model, including increased brain iron content, downregulated GPX4 expression, and accumulation of the lipid peroxidation marker 4-HNE. They then use the OGD/R cell model to validate key ferroptosis features at the molecular and ultrastructural levels, such as enhanced lipid peroxidation, glutathione depletion, and mitochondrial damage. This &amp;ldquo;phenotype-to-mechanism&amp;rdquo; approach allows students to intuitively understand the role of ferroptosis in CIRI while systematically mastering the full research cycle,&amp;nbsp;from establishing disease models and applying multi-technique assays to integrating and interpreting data. By translating a cutting-edge scientific topic into a coherent experimental teaching module, this reform effectively bridges the gap between theoretical knowledge and hands-on research practice. It fosters students&amp;rsquo; integrative scientific thinking and enhances their ability to tackle complex biomedical questions, offering a transferable paradigm for advancing high-level experimental training in molecular medicine.</abstract><keywords>Cerebral ischemia-reperfusion injury, Ferroptosis, Molecular medicine experimental techniques, Teaching reform</keywords></article-meta></front><body/><back><ref-list><ref id="B1" content-type="article"><label>1</label><element-citation publication-type="journal"><p>[1] Feigin VL, Brainin M, Norrving B, et al., 2025, World Stroke Organization: Global Stroke Fact Sheet 2025.&amp;nbsp;Int J Stroke, 20(2): 132-144.
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