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New insights in animal models of neurotoxicity-induced neurodegeneration.

作者信息

Sanfeliu Coral, Bartra Clara, Suñol Cristina, Rodríguez-Farré Eduard

机构信息

Institut d'Investigacions Biomèdiques de Barcelona (IIBB), Consejo Superior de Investigaciones Científicas (CSIC), and Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.

PhD Program in Biotechnology, Facultat de Farmàcia i Ciències de l'Alimentació, Universitat de Barcelona, Barcelona, Spain.

出版信息

Front Neurosci. 2024 Jan 8;17:1248727. doi: 10.3389/fnins.2023.1248727. eCollection 2023.


DOI:10.3389/fnins.2023.1248727
PMID:38260026
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10800989/
Abstract

The high prevalence of neurodegenerative diseases is an unintended consequence of the high longevity of the population, together with the lack of effective preventive and therapeutic options. There is great pressure on preclinical research, and both old and new models of neurodegenerative diseases are required to increase the pipeline of new drugs for clinical testing. We review here the main models of neurotoxicity-based animal models leading to central neurodegeneration. Our main focus was on studying how changes in neurotransmission and neuroinflammation, mainly in rodent models, contribute to harmful processes linked to neurodegeneration. The majority of the models currently in use mimic Parkinson's disease (PD) and Alzheimer's disease (AD), which are the most common neurodegenerative conditions in older adults. AD is the most common age-related dementia, whereas PD is the most common movement disorder with also cases of dementia. Several natural toxins and xenobiotic agents induce dopaminergic neurodegeneration and can reproduce neuropathological traits of PD. The literature analysis of MPTP, 6-OH-dopamine, and rotenone models suggested the latter as a useful model when specific doses of rotenone were administrated systemically to C57BL/6 mice. Cholinergic neurodegeneration is mainly modelled with the toxin scopolamine, which is a useful rodent model for the screening of protective drugs against cognitive decline and AD. Several agents have been used to model neuroinflammation-based neurodegeneration and dementia in AD, including lipopolysaccharide (LPS), streptozotocin, and monomeric C-reactive protein. The bacterial agent LPS makes a useful rodent model for testing anti-inflammatory therapies to halt the development and severity of AD. However, neurotoxin models might be more useful than genetic models for drug discovery in PD but that is not the case in AD where they cannot beat the new developments in transgenic mouse models. Overall, we should work using all available models, either , , or , considering the seriousness of the moment and urgency of developing effective drugs.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e508/10800989/ff4d536eff6d/fnins-17-1248727-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e508/10800989/a4d22832db9d/fnins-17-1248727-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e508/10800989/ff4d536eff6d/fnins-17-1248727-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e508/10800989/a4d22832db9d/fnins-17-1248727-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e508/10800989/ff4d536eff6d/fnins-17-1248727-g002.jpg

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引用本文的文献

[1]
Neuroprotective Potential of Phytocompounds in the Treatment of Dementia: The State of Knowledge from the Scopolamine-Induced Animal Model of Alzheimer's Disease.

Curr Issues Mol Biol. 2025-8-8

[2]
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Int J Mol Sci. 2025-7-17

[3]
Neural organoids as advanced tools for neurotoxicity modeling.

Curr Res Toxicol. 2025-7-11

[4]
Gallic acid enhances memory, learning and reduces neuroinflammation in a rat model of scopolamine-induced cholinergic dysfunction.

Inflammopharmacology. 2025-4

[5]
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[6]
Systemic Neuroprotection by Chlorogenic Acid: Antioxidant and Anti-inflammatory Evaluation in Early Neurodegeneration Induced by 3-Nitropropionic Acid in Mice.

Neurochem Res. 2025-3-4

[7]
Licochalcone A prevents cognitive decline in a lipopolysaccharide-induced neuroinflammation mice model.

Mol Med. 2025-2-11

[8]
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Pharmacol Rep. 2025-4

[9]
Eugenol attenuates aluminium-induced neurotoxicity in rats by inhibiting the activation of STAT3 and NF-кB.

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[10]
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本文引用的文献

[1]
Are New Alzheimer Drugs Better Than Older Drugs?

JAMA Intern Med. 2023-7-31

[2]
The role of the microbiota-gut-brain axis and intestinal microbiome dysregulation in Parkinson's disease.

Front Neurol. 2023-5-25

[3]
Nigrostriatal 6-hydroxydopamine lesions increase alpha-synuclein levels and permeability in rat colon.

Neurobiol Aging. 2023-9

[4]
Investigation of the protective effect of long-term exercise on molecular pathways and behaviours in scopolamine induced alzheimer's disease-like condition.

Brain Res. 2023-9-1

[5]
Parkinson's Disease: Exploring Different Animal Model Systems.

Int J Mol Sci. 2023-5-22

[6]
An Insight into Cellular and Molecular Mechanisms Underlying the Pathogenesis of Neurodegeneration in Alzheimer's Disease.

Biomedicines. 2023-5-8

[7]
Amyloid-beta aggregation implicates multiple pathways in Alzheimer's disease: Understanding the mechanisms.

Front Neurosci. 2023-4-11

[8]
Sex and Gender Differences in Neurodegenerative Diseases: Challenges for Therapeutic Opportunities.

Int J Mol Sci. 2023-3-28

[9]
Dietary Protection against Cognitive Impairment, Neuroinflammation and Oxidative Stress in Alzheimer's Disease Animal Models of Lipopolysaccharide-Induced Inflammation.

Int J Mol Sci. 2023-3-21

[10]
Biomarkers and molecular mechanisms of Amyotrophic Lateral Sclerosis.

AIMS Neurosci. 2022-11-10

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