Chronic Inhibition of Nitric Oxide Synthases Impairs Spatiotemporal Learning and Memory to a Similar Extent in C57BL/6 and hAPP23+/− Mice

Author:

Hendrickx Jhana O.1ORCID,Calus Elke2,De Deyn Peter Paul23ORCID,Van Dam Debby23ORCID,De Meyer Guido R. Y.1ORCID

Affiliation:

1. Laboratory of Physiopharmacology, University of Antwerp, Wilrijk, 2610 Antwerp, Belgium

2. Laboratory of Neurochemistry and Behaviour, Experimental Neurobiology Unit, Wilrijk, 2610 Antwerp, Belgium

3. Department of Neurology and Alzheimer Center Groningen, University Medical Center Groningen, University of Groningen, 9713 AV Groningen, The Netherlands

Abstract

Due to global population growth, age-related disorders like cardiovascular disease and dementia are anticipated to increase. Recent data suggests a connection between cardiovascular disease and neurodegeneration, especially focusing on arterial stiffness (AS) and Alzheimer’s disease (AD). In light of this, we conducted a study to explore the impact of long-term nitric oxide synthase (NOS) isoform inhibition, which leads to AS, on neurobehavioral performance. We also compared these effects in an AD model and control mice. C57BL/6 and hAPP23+/− mice (an established AD model) were given 0.5 mg/mL N(G)-Nitro-L-Arginine Methyl Ester (L-NAME) in their drinking water for 16 weeks. Our findings indicate that chronic non-selective NOS inhibition increased AS and reduced spatiotemporal learning and memory in both C57BL/6 and hAPP23+/− mice. These effects were consistent across both groups, emphasizing the role of neuronal NOS (nNOS) in cognitive aging, regardless of genetic predisposition to AD.

Funder

University of Antwerp

Research Foundation-Flanders

Medical Research Foundation Antwerp, Neurosearch Antwerp

Hercules Foundation

Publisher

MDPI AG

Subject

Pharmacology

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