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Acitretin reverses early functional network degradation in a mouse model of familial Alzheimer’s disease

Bibliographic

Year of Publication:
2021
Contact PI Name:
Albrecht Stroh
Contact PI Affiliation:
Institute for Pathophysiology Johannes Gutenberg University, Mainz, Germany
Co-Authors:
Eduardo Rosales Jubal, Miriam Schwalm, Malena dos Santos Guilherme, Florian Schuck, Sven Reinhardt, Amanda Tose, Zeke Barger, Mona K. Roesler, Nicolas Ruffini, Anna Wierczeiko, Michael J. Schmeisser, Ulrich Schmitt, Kristina Endres
Primary Reference (PubMED ID):
Funding Source:
Alfred Dollwet Foundation
Focus Program Translational Neurosciences (FTN)
Johannes Gutenberg University Mainz
Study Goal and Principal Findings:

Aberrant activity of local functional networks underlies memory and cognition deficits in Alzheimer's disease (AD). Hyperactivity was observed in microcircuits of mice AD-models showing plaques, and also recently in early stage AD mutants prior to amyloid deposition. However, early functional effects of AD on cortical microcircuits remain unresolved. Using two-photon calcium imaging, we found altered temporal distributions (burstiness) in the spontaneous activity of layer II/III visual cortex neurons, in a mouse model of familial Alzheimer's disease (5xFAD), before plaque formation. Graph theory (GT) measures revealed a distinct network topology of 5xFAD microcircuits, as compared to healthy controls, suggesting degradation of parameters related to network robustness. After treatment with acitretin, we observed a re-balancing of those network measures in 5xFAD mice; particularly in the mean degree distribution, related to network development and resilience, and post-treatment values resembled those of age-matched controls. Further, behavioral deficits, and the increase of excitatory synapse numbers in layer II/III were reversed after treatment. GT is widely applied for whole-brain network analysis in human neuroimaging, we here demonstrate the translational value of GT as a multi-level tool, to probe networks at different levels in order to assess treatments, explore mechanisms, and contribute to early diagnosis.

Bibliographic Notes:
Eduardo Rosales Jubal (Competence Center for Methodology and Statistics, Luxembourg Institute of Health, Luxembourg) and Albrecht Stroh (Institute for Pathophysiology Johannes Gutenberg University, Mainz, Germany) are corresponding authors on this paper.

Therapeutic Agent

Therapeutic Information:
Therapy Type:
Small Molecule
Therapeutic Agent:
Acitretin
Therapeutic Target:
Retinoic Acid Receptors

Animal Model

Model Information:
Species:
Mouse
Model Type:
APPxPS1
Strain/Genetic Background:
C57BL/6J

Experimental Design

Is the following information reported in the study?:
Power/Sample Size Calculation
Randomized into Groups
Blinded for Treatment
Blinded for Outcome Measures
Pharmacokinetic Measures
Pharmacodynamic Measures
Toxicology Measures
ADME Measures
Biomarkers
Dose
Formulation
Route of Delivery
Duration of Treatment
Frequency of Administration
Age of Animal at the Beginning of Treatment
Age of Animal at the End of Treatment
Sex as a Biological Variable
Study Balanced for Sex as a Biological Variable
Number of Premature Deaths
Number of Excluded Animals
Statistical Plan
Genetic Background
Inclusion/Exclusion Criteria Included
Conflict of Interest

Outcomes

Outcome Measured
Outcome Parameters
Behavioral
Morris Water Maze
Histopathology
beta Amyloid Deposits
Biochemical
Brain-Buffer Soluble beta Amyloid Peptide 42
Brain-Formic Acid Soluble beta Amyloid Peptide 42
Brain-Derived Neurotrophic Factor (BDNF)
Glial Fibrillary Acidic Protein (GFAP)
Glutamate Ionotropic Receptor AMPA Type Subunit 1 (GluR1)
Ionized Calcium Binding Adaptor Molecule 1 (Iba1)
Neuronal Nitric Oxide Synthase (nNOS/NOS1)
Nitric Oxide (NO)
Nuclear Factor kappa B-RelA (NFkB-p65)
Immunochemistry
Brain-beta Amyloid Deposits
Gephyrin
Homer 1
Vesicular GABA Transporter (VGAT)
Vesicular Glutamate Transporter 1 (VGLUT1)
Microscopy
Synaptic Density
Imaging
In Vivo Two-Photon Calcium Imaging