Affiliations:
Department of Psychology, Institute of Neuroscience, University of Oregon, Eugene, OR, USA
Correspondence:
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Correspondence to: Michael Wehr, Department of Psychology, Institute of Neuroscience, 1254 University of Oregon, Eugene, OR 97403, USA. E-mail: wehr@uoregon.edu.
Abstract: Background:Effective treatment of Alzheimer’s disease (AD) will hinge on early detection. This has led to the search for early biomarkers that use non-invasive testing. One possible early biomarker is auditory temporal processing deficits, which reflect central auditory pathway dysfunction and precede cognitive and memory declines in AD. Gap detection is a measure of auditory temporal processing, is impaired in human AD, and is also impaired in the 5XFAD mouse model of AD. Gap detection deficits appear as early as postnatal day 60 in 5XFAD mice, months before cognitive deficits or cell death, supporting gap detection as an early biomarker. However, it remains unclear how gap detection deficits relate to the progression of amyloid pathology in the auditory system. Objective:To determine the progression of amyloid pathology throughout the central auditory system and across age in 5XFAD mice. Methods:We quantified intracellular and extracellular antibody labelling of Aβ42 in 6 regions of the central auditory system from p14 to p150. Results:Pathology appeared first in primary auditory cortex (A1) as intracellular accumulation of Aβ42 in layer 5 pyramidal neurons by age p21. Extracellular plaques appeared later, by age p90, in A1, medial geniculate body, and inferior colliculus. Auditory brainstem structures showed minimal amyloid pathology. We also observed pathology in the caudal pontine reticular nucleus, a brainstem structure that is outside of the central auditory pathway but which is involved in the acoustic startle reflex. Conclusion:These results suggest that Aβ42 accumulation, but not plaques, may impair gap detection.
