Abstract

BackgroundChronic noise exposure has been associated with tau hyperphosphorylation and Alzheimer’s disease (AD)-like pathological changes, but the underlying mechanism is unknown. In this study, we explored the effects of long-term noise exposure on the corticotropin-releasing factor (CRF) system in the hippocampus and its role in noise-induced tau phosphorylation.MethodsSixty-four rats were randomly divided into the noise-exposed group and the control group, and rats in the exposure group were exposed to 95 dB SPL white noise for 30 consecutive days. The levels of CRF, CRFR1, CRFR2, and total tau and phosphorylated tau (p-tau) at Ser396 (S396) and Thr205 (T205) in the hippocampus were measured at different time points after the final noise exposure. The co-localized distribution of CRF and p-tau (T205) in the hippocampus was evaluated using double-labeling immunofluorescence.ResultsLong-term exposure to noise for 30 consecutive days significantly increased the expression of CRF and CRFR1 and their mRNAs levels in the hippocampus, which persisted for 7 days after final exposure. In contrast, CRFR2 was raised for 3–7 days following the last exposure. These alterations were also concomitant with the phosphorylation of tau at S396 and T205. Furthermore, there was co-localization of p-tau and CRF in hippocampal neurons.ConclusionChronic noise leads to long-lasting increases in the hippocampal CRF system and the hyperphosphorylation of tau in the hippocampus. Our results also provide evidence for the involvement of the CRF system in noise-induced AD-like neurodegeneration.

Highlights

  • Chronic noise exposure has been associated with tau hyperphosphorylation and Alzheimer’s disease (AD)-like pathological changes, but the underlying mechanism is unknown

  • Chronic noise exposure causes abnormalities of the corticotropin-releasing factor (CRF) system in the hippocampus To assess the influence of chronic noise exposure on the CRF system, we examined the expression levels of CRF, CRF receptor 1 (CRFR1), and CRFR2 by using RT-PCR and Western blotting, respectively

  • Results showed that the expression levels of CRF and CRFR1 mRNA and protein in hippocampus were significantly increased after exposure to noise for 30 days, with an increasing trend that persisted for up to 7 days after the final noise exposure (Fig. 2a–f)

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Summary

Introduction

Chronic noise exposure has been associated with tau hyperphosphorylation and Alzheimer’s disease (AD)-like pathological changes, but the underlying mechanism is unknown. We explored the effects of long-term noise exposure on the corticotropin-releasing factor (CRF) system in the hippocampus and its role in noise-induced tau phosphorylation. Supporting a role for CRF in AD neuropathology, work from many laboratories has demonstrated that both CRF overexpression and acute or repeated exposure to stressors induce phosphorylation of tau and accumulation of Aβ within the hippocampus, a process that is dependent on CRFR1 [11, 12]. We have investigated the effects of longterm noise exposure on the CRF signaling system and explored the relationship between CRF and noiseinduced AD-like changes in the rat hippocampus. Our data could implicate CRF-dependent mechanisms in the neuropathophysiology induced by environmental noise

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