Mechanisms of impaired cerebral hemodynamics and memory resilience differ by sex: A role for mineralocorticoid receptors in VCID

INTRODUCTION: Chronic hypertension is associated with cerebral hypoperfusion and is a primary risk factor for vascular contributions to cognitive impairment and dementia (VCID). Aldosterone, a key mediator of hypertension, causes cerebrovascular dysfunction via its mineralocorticoid receptor (MR). METHODS: The effects of MR signaling during hypertension on hemodynamics in two cognition-centric brain regions were determined in both sexes using an established model of VCID (spontaneously hypertensive rat, SHR) and MR antagonist eplerenone. Long-term and spatial working memory were tested, and absolute brain blood flow and brain oxygenation were measured in vivo in CA1 of dorsal hippocampus and medial prefrontal cortex (mPFC). RESULTS: Hypertension differentially impaired hemodynamics in a sex- and region-dependent manner. Female SHR had more pervasive hypoperfusion than males that did not affect flow-metabolism coupling. Eplerenone treatment in females restored perfusion in mPFC and hippocampus, improved working memory, but did not protect hippocampal-dependent memory. Eplerenone had no effect in male SHR, indicating the MR-dependent mechanism of VCID is sex-specific. DISCUSSION: This study advances our understanding of how chronic hypertension compromises brain blood flow, suggests that resilience of memory function differs by domain, and that efficacy of interventions depend upon sex.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-11-04
DOI
https://doi.org/10.64898/2026.10.31.763340
Primary Topic
Neurological Disease Mechanisms and Treatments
Type
preprint
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preprint

Mechanisms of impaired cerebral hemodynamics and memory resilience differ by sex: A role for mineralocorticoid receptors in VCID

Jared Luchetta, Abbie C. Chapman, Emily J. Baumoel, Emily D. Schellinger et al.
bioRxiv (Cold Spring Harbor Laboratory)
Neurological Disease Mechanisms and Treatments
preprint

Mechanisms of impaired cerebral hemodynamics and memory resilience differ by sex: A role for mineralocorticoid receptors in VCID

Jared Luchetta, Abbie C. Chapman, Emily J. Baumoel, Emily D. Schellinger, Gianna M. DeMarco, Dinlin Chen, Gabrielle A Bernstein, Maya E Westbrook, James Bloete
preprint en

Abstract

INTRODUCTION: Chronic hypertension is associated with cerebral hypoperfusion and is a primary risk factor for vascular contributions to cognitive impairment and dementia (VCID). Aldosterone, a key mediator of hypertension, causes cerebrovascular dysfunction via its mineralocorticoid receptor (MR). METHODS: The effects of MR signaling during hypertension on hemodynamics in two cognition-centric brain regions were determined in both sexes using an established model of VCID (spontaneously hypertensive rat, SHR) and MR antagonist eplerenone. Long-term and spatial working memory were tested, and absolute brain blood flow and brain oxygenation were measured in vivo in CA1 of dorsal hippocampus and medial prefrontal cortex (mPFC). RESULTS: Hypertension differentially impaired hemodynamics in a sex- and region-dependent manner. Female SHR had more pervasive hypoperfusion than males that did not affect flow-metabolism coupling. Eplerenone treatment in females restored perfusion in mPFC and hippocampus, improved working memory, but did not protect hippocampal-dependent memory. Eplerenone had no effect in male SHR, indicating the MR-dependent mechanism of VCID is sex-specific. DISCUSSION: This study advances our understanding of how chronic hypertension compromises brain blood flow, suggests that resilience of memory function differs by domain, and that efficacy of interventions depend upon sex.

bioRxiv (Cold Spring Harbor Laboratory)
Binghamton University (US)
Neurological Disease Mechanisms and Treatments
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Mechanisms of impaired cerebral hemodynamics and memory resilience differ by sex: A role for mineralocorticoid receptors in VCID — Jared Luchetta, Abbie C. Chapman, et al. · bioRxiv (Cold Spring Harbor Laboratory) (2026) | TGRS Research Map | TGRS