{"title":"APOE4, activation of latent form HSV-1, A beta accumulation and AD progression","authors":"Weiqi Mo","doi":"10.54254/2753-8818/44/20240488","DOIUrl":null,"url":null,"abstract":"The role of APOE4 in Alzheimers disease progression is an area of ongoing research. The core objective of this paper is to investigate the intricate interplay between APOE4, HSV-1, A, and AD progression. Methodology involves assessing A Levels, Spatial Recognition Memory, and Exploratory Behavior in HSV-1-infected Fx5AD Mice with APOE4, alongside monitoring specific biomarkers to confirm HSV-1 activation status. Our expected experimental outcomes suggest that APOE4 accelerates latent HSV-1 activation, leading to heightened A aggregation. Thus, we hypothesize that APOE4 may expedite latent HSV-1 activation, thereby facilitating A accumulation and AD advancement. The investigation of relationship between APOE4, HSV-1, A, and AD progression could give valuable insights into further experiments and treatments of AD.","PeriodicalId":341023,"journal":{"name":"Theoretical and Natural Science","volume":"121 7","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Theoretical and Natural Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.54254/2753-8818/44/20240488","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The role of APOE4 in Alzheimers disease progression is an area of ongoing research. The core objective of this paper is to investigate the intricate interplay between APOE4, HSV-1, A, and AD progression. Methodology involves assessing A Levels, Spatial Recognition Memory, and Exploratory Behavior in HSV-1-infected Fx5AD Mice with APOE4, alongside monitoring specific biomarkers to confirm HSV-1 activation status. Our expected experimental outcomes suggest that APOE4 accelerates latent HSV-1 activation, leading to heightened A aggregation. Thus, we hypothesize that APOE4 may expedite latent HSV-1 activation, thereby facilitating A accumulation and AD advancement. The investigation of relationship between APOE4, HSV-1, A, and AD progression could give valuable insights into further experiments and treatments of AD.