Abstract

Age represents the highest risk factor for death due to cardiovascular disease. Heart failure (HF) is the most common cardiovascular disease in elder population and it is associated with cognitive impairment (CI), diminishing learning and memory process affecting life quality and mortality in these patients. In HF, CI has been associated with inadequate O2 supply to the brain; however, an important subset of HF patients displays CI with almost no alteration in cerebral blood flow. Importantly, nothing is known about the pathophysiological mechanisms underpinning CI in HF with no change in brain tissue perfusion. Here, we aimed to study memory performance and learning function in a rodent model of HF that shows no change in blood flow going to the brain. We found that HF rats presented learning impairments and memory loss. In addition, HF rats displayed a decreased level of Wnt/β-catenin signaling downstream elements in the hippocampus, one pathway implicated largely in aging diseases. Taken together, our results suggest that in HF rats CI is associated with dysfunction of the Wnt/β-catenin signaling pathway. The mechanisms involved in the alterations of Wnt/β-catenin signaling in HF and its contribution to the development/maintenance of CI deserves future investigations.

Highlights

  • Chronic heart failure (HF) is a recognized health care problem affecting at least 26 million people worldwide [1]

  • Mean arterial blood pressure (MABP) was decreased in HF rats compared to Sham rats (MABP: 101.1 ± 1.5 vs. 89.9 ± 8.3 mmHg; Sham vs. HF; p

  • HF is the most common cardiovascular disease in the elder population and it is associated with neurocognitive impairment

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Summary

Introduction

Chronic heart failure (HF) is a recognized health care problem affecting at least 26 million people worldwide [1]. HF is one of the most prevalent cardiovascular diseases in elderly and is a major cause of death, with a prevalence rising to ≥20% among people over 65 years of age [2]. It has been documented a strong association between HF and cognitive impairments (CI) [3,4]. An increasing body of evidence suggest that the presence and severity of sleep breathing disorders and cardiovascular autonomic imbalance contribute to age-related CI, in memory and learning process [16,17,18]. Identifying the pathophysiological mechanisms that contribute to CI in HFpEF will help to develop future treatments intended to improve quality of life in these patients

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