Positive and Negative Selective Allosteric Modulators of α5 GABAA Receptors: Effects on Emotionality, Motivation, and Motor Function in the 5xFAD Model of Alzheimer’s Disease

2021 ◽  
pp. 1-12
Author(s):  
Jovana Arandelović ◽  
Anja Santrač ◽  
Bojan Batinić ◽  
Lidija Todorović ◽  
Md Zubair Ahmed Khan ◽  
...  

Background: Positive and negative allosteric modulators of α5 GABAA receptors (PAM and NAM, respectively) are worthy of investigation as putative treatments of Alzheimer’s disease (AD). However, their potential to modify a dynamic range of behaviors in AD models needs to be systematically examined. Objective: The study aimed to assess effects of MP-III-022 as PAM and PWZ-029 as NAM on emotional reactivity, motivation, and motor function, as well as on gene expression of GABRA2, GABRA3 and GABRA5 subunit of GABAA receptors in prefrontal cortex (PFC) and hippocampus (HC) in 5xFAD mice, as an early-onset transgenic AD model. Methods: The 6-month-old 5xFAD transgenic and non-transgenic mice of both genders underwent a battery of reflexes and behavioral tests (sensorimotor tests, elevated plus maze, and open field) after 10-day intraperitoneal treatment with MP-III-022, PWZ-029, or solvent. The behavioral battery was followed by qPCR analysis of gene expression. Results: MP-III-022 induced a decline in motor function, while PWZ-029 further decreased emotionality of transgenic males, as compared to the transgenic control. No interfering effects on non-cognitive behavior were observed in female mice. In HC, both treatments reversed reciprocal GABRA2 and GABRA3 changes in transgenic females. In PFC, MP-III-022 decreased GABRA5 in both genders, while PWZ-029 increased GABRA2 in male transgenic animals. Conclusion: Gender-dependent protracted effects of PAMs and NAMs in AD model, with detrimental impact on motor capabilities of PAM, and attenuation of emotionality elicited by NAM in transgenic males, were revealed. This favors future research of α5 GABAA receptor modulation in females as more promising.

Author(s):  
Jannek M. Wagner ◽  
Marius E. Sichler ◽  
Eva M. Schleicher ◽  
Timon N. Franke ◽  
Caroline Irwin ◽  
...  

2018 ◽  
Vol 69 ◽  
pp. 74-90 ◽  
Author(s):  
Kathryn E. Hopperton ◽  
Marc-Olivier Trépanier ◽  
Nicholas C.E. James ◽  
Raphaël Chouinard-Watkins ◽  
Richard P. Bazinet

2015 ◽  
Vol 11 (7S_Part_7) ◽  
pp. P328-P328
Author(s):  
Paul M. McKeever ◽  
Andrew Hesketh ◽  
Giorgio Favrin ◽  
Stephen Oliver ◽  
Peter St. George-Hyslop ◽  
...  

2008 ◽  
Vol 4 ◽  
pp. T221-T221
Author(s):  
Clark A. Briggs ◽  
David J. Anderson ◽  
Won Choi ◽  
Paul E. Kroeger ◽  
Jinhe Li ◽  
...  

2001 ◽  
Vol 49 (11) ◽  
pp. 1469-1470 ◽  
Author(s):  
P. Pompei ◽  
R. Severini ◽  
D. Pediconi ◽  
M. Angeletti ◽  
A. Eleuteri ◽  
...  

2021 ◽  
Vol 6 (4) ◽  
pp. 8-21
Author(s):  
Y. V. Gorina ◽  
E. D. Khilazheva ◽  
Yu. K. Komleva ◽  
O. L. Lopatina ◽  
A. B. Salmina

Aim. To study the insulin (INS) gene expression, insulin and lactate levels, expression of Fe65 adapter protein, and level of oxidative DNA damage marker γH2AX in different brain areas in the experimental model of Alzheimer's disease.Materials and Methods. Male, 4-month-old C57BL/6 mice received either intrahippocampal injection of β-amyloid (C57BL/6 + Aβ 1-42) or phosphate-buffered saline (C57BL/6 + PBS). Insulin (INS) gene expression in the hippocampus and amygdala was assessed by means of reverse transcription-polymerase chain reaction. Levels of lactate and insulin in different brain areas were measured by enzyme-linked immunosorbent assay. Expression of Fe65 adapter protein and γH2AX in the hippocampus was studied by immunofluorescence staining followed by confocal microscopy.Results. We found an overexpression of the INS gene in the hippocampus and amygdala, an increase in lactate level in the hippocampus, and slightly increased insulin level in the amygdala of mice with Alzheimer's disease as compared with the control group. Neurodegeneration was accompanied by an elevated endothelial expression of Fe65 adapter protein (p= 0.04) and γH2AX in hippocampal neurons (p = 0.04).Conclusion. Alzheimer's disease neurodegeneration is accompanied by a disrupted insulin signaling and impaired glucose metabolism in the hippocampus and amygdala. This further leads to a neuronal accumulation of γH2AX and impaired amyloid precursor protein proteolysis because of insulin inability to inhibit its interaction with the Fe65 adapter protein and to prevent formation and deposition of β-amyloid.


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