Animal models of Alzheimer's disease: Applications, evaluation, and perspectives
- PMID: 36317468
- PMCID: PMC9700500
- DOI: 10.24272/j.issn.2095-8137.2022.289
Animal models of Alzheimer's disease: Applications, evaluation, and perspectives
Abstract
Although great advances in elucidating the molecular basis and pathogenesis of Alzheimer's disease (AD) have been made and multifarious novel therapeutic approaches have been developed, AD remains an incurable disease. Evidence shows that AD neuropathology occurs decades before clinical presentation. AD is divided into three stages: preclinical stage, mild cognitive impairment (MCI), and AD dementia. In the natural world, some animals, such as non-human primates (NHPs) and canines, can develop spontaneous AD-like dementia. However, most animals do not develop AD. With the development of transgenic techniques, both invertebrate and vertebrate animals have been employed to uncover the mechanisms of AD and study treatment methods. Most AD research focuses on early-onset familial AD (FAD) because FAD is associated with specific genetic mutations. However, there are no well-established late-onset sporadic AD (SAD) animal models because SAD is not directly linked to any genetic mutation, and multiple environmental factors are involved. Moreover, the widely used animal models are not able to sufficiently recapitulate the pathological events that occur in the MCI or preclinical stages. This review summarizes the common models used to study AD, from yeast to NHP models, and discusses the different applications, evaluation methods, and challenges related to AD animal models, as well as prospects for the evolution of future studies.
近年来,虽然人们对阿尔茨海默病(Alzheimer’s disease,AD)的分子学基础和发病机制的研究均取得了较大进展,各种新的治疗方法层出不穷,但就目前而言,阿尔茨海默病仍是一种不治之症。有证据表明,AD神经病理学改变在出现临床表现的几十年之前就有可能发生。AD大致可以分为三个阶段:临床前阶段、轻度认知障碍(Mild cognitive impairment,MCI)阶段和AD痴呆阶段。自然界中有一些动物,如非人类的灵长类动物和犬科动物,可以自发的形成AD样痴呆,但大多数动物不会发展出AD样表现。随着转基因技术的发展,无脊椎动物和脊椎动物都被广泛用于揭示AD的发病机制和研究治疗方法。大多数AD研究集中在早发型AD(即家族型AD),因为家族性AD与特定的基因突变相关。与之相对应的晚发型AD(即散发型AD),由于其与基因突变没有直接联系,且涉及多种环境因素,目前还没有完善的散发型AD动物模型。此外,目前广泛使用的动物模型还不能充分再现MCI或临床前阶段发生的一系列病理改变。该文从酵母模型到非人灵长类动物模型系统综述了目前用于研究AD的常用模型,在此基础上讨论了AD动物模型的不同应用、评价方法、面临的挑战以及未来研究的发展前景。.
Keywords: Alzheimer’s disease; Amyloid-β; Animal models; Neuroinflammation; Tau protein.
Figures
Similar articles
-
Neurons derived from sporadic Alzheimer's disease iPSCs reveal elevated TAU hyperphosphorylation, increased amyloid levels, and GSK3B activation.Alzheimers Res Ther. 2017 Dec 1;9(1):90. doi: 10.1186/s13195-017-0317-z. Alzheimers Res Ther. 2017. PMID: 29191219 Free PMC article.
-
Spontaneous and familial models of Alzheimer's disease: Challenges and advances in preclinical research.Life Sci. 2023 Sep 1;328:121918. doi: 10.1016/j.lfs.2023.121918. Epub 2023 Jul 6. Life Sci. 2023. PMID: 37422070 Review.
-
Tau Cleavage Contributes to Cognitive Dysfunction in Strepto-Zotocin-Induced Sporadic Alzheimer's Disease (sAD) Mouse Model.Int J Mol Sci. 2021 Nov 10;22(22):12158. doi: 10.3390/ijms222212158. Int J Mol Sci. 2021. PMID: 34830036 Free PMC article.
-
The oDGal Mouse: A Novel, Physiologically Relevant Rodent Model of Sporadic Alzheimer's Disease.Int J Mol Sci. 2023 Apr 9;24(8):6953. doi: 10.3390/ijms24086953. Int J Mol Sci. 2023. PMID: 37108119 Free PMC article.
-
Advance of sporadic Alzheimer's disease animal models.Med Res Rev. 2020 Jan;40(1):431-458. doi: 10.1002/med.21624. Epub 2019 Jul 22. Med Res Rev. 2020. PMID: 31328804 Review.
Cited by
-
Effect of heatwaves on mortality of Alzheimer's disease and other dementias among elderly aged 60 years and above in China, 2013-2020: a population-based study.Lancet Reg Health West Pac. 2024 Oct 8;52:101217. doi: 10.1016/j.lanwpc.2024.101217. eCollection 2024 Nov. Lancet Reg Health West Pac. 2024. PMID: 39430125 Free PMC article.
-
Advancing Alzheimer's Research With Zebrafish Models: Current Insights, Addressing Challenges, and Charting Future Courses.Cureus. 2024 Aug 15;16(8):e66935. doi: 10.7759/cureus.66935. eCollection 2024 Aug. Cureus. 2024. PMID: 39280389 Free PMC article. Review.
-
Alzheimer's Disease: Models and Molecular Mechanisms Informing Disease and Treatments.Bioengineering (Basel). 2024 Jan 1;11(1):45. doi: 10.3390/bioengineering11010045. Bioengineering (Basel). 2024. PMID: 38247923 Free PMC article. Review.
-
Diverse Efficacy of Dimethyl Fumarate in Alleviating the Late Streptozotocin-Induced Cognitive Impairment and Neuropathological Features in Rat.Mol Neurobiol. 2024 Oct;61(10):7751-7766. doi: 10.1007/s12035-024-04024-8. Epub 2024 Mar 2. Mol Neurobiol. 2024. PMID: 38430351
-
Convergent transcriptomic and genomic evidence supporting a dysregulation of CXCL16 and CCL5 in Alzheimer's disease.Alzheimers Res Ther. 2023 Jan 21;15(1):17. doi: 10.1186/s13195-022-01159-5. Alzheimers Res Ther. 2023. PMID: 36670424 Free PMC article.
References
-
-
Adalbert R, Nogradi A, Babetto E, Janeckova L, Walker SA, Kerschensteiner M, et al. 2009. Severely dystrophic axons at amyloid plaques remain continuous and connected to viable cell bodies.
Brain ,132 (Pt 2): 402–416.
-
-
- Ahlijanian MK, Barrezueta NX, Williams RD, Jakowski A, Kowsz KP, McCarthy S, et al Hyperphosphorylated tau and neurofilament and cytoskeletal disruptions in mice overexpressing human p25, an activator of cdk5. Proceedings of the National Academy of Sciences of the United States of America. 2000;97(6):2910–2915. doi: 10.1073/pnas.040577797. - DOI - PMC - PubMed
-
- Albert MS, Dekosky ST, Dickson D, Dubois B, Feldman HH, Fox NC, et al The diagnosis of mild cognitive impairment due to Alzheimer's disease: recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease. Alzheimer's & Dementia:Translational Research & Clinical Interventions. 2011;7(3):270–279. - PMC - PubMed
-
- Alzheimer's Association 2013 Alzheimer's disease facts and figures. Alzheimer's & Dementia. 2013;9(2):208–245. - PubMed
-
-
Ankarcrona M, Mangialasche F, Winblad B. 2010. Rethinking Alzheimer's disease therapy: are mitochondria the key?.
Journal of Alzheimer's Disease ,20 Suppl 2 : S579–S590.
-
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases