Evidence map›Paper›PMID 42551659›Full record

ArticleNeurobiology of disease2026

Chronic hypertension and social isolation disrupt the blood-brain barrier and memory in a sex-dependent manner.

Anduela Thaqi, Gianna M DeMarco, Emily D Schellinger, Dinlin Chen, Jared Luchetta, Abbie C Chapman

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Article in Neurobiology of disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Anduela ThaqiDepartment of Psychology, Binghamton University - SUNY, Binghamton, NY 13902, United States of America.
Gianna M DeMarcoDepartment of Psychology, Binghamton University - SUNY, Binghamton, NY 13902, United States of America.
Emily D SchellingerDepartment of Psychology, Binghamton University - SUNY, Binghamton, NY 13902, United States of America.
Dinlin ChenDepartment of Psychology, Binghamton University - SUNY, Binghamton, NY 13902, United States of America.
Jared LuchettaDepartment of Psychology, Binghamton University - SUNY, Binghamton, NY 13902, United States of America.
Abbie C ChapmanDepartment of Psychology, Binghamton University - SUNY, Binghamton, NY 13902, United States of America; The Center for Development and Behavioral Neuroscience, Binghamton University - SUNY, Binghamton, NY 13902, United States of America. Electronic address: achapman@binghamton.edu.

Funding

The Role of the Hippocampal Vasculature in Vascular Cognitive Impairment and DementiaR01NS127284 · NINDS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI Abbie C Chapman · 2022 to 2026
$2.5M
NINDS NIH HHS R01 NS127284
6 · The paper itself

Abstract

Chronic hypertension in mid-life is a leading cause of vascular cognitive impairment (VCI), the second leading cause of age-related cognitive decline. Further, social isolation is another risk factor for dementia, and disproportionately impacts middle-aged adults. However, mechanisms by which social isolation may compound chronic hypertension to damage the cerebrovasculature and contribute to VCI remain unclear. The current study used male and female adult Wistar rats and spontaneously hypertensive rats (SHR) to investigate how social isolation during chronic hypertension disrupted blood-brain barrier (BBB) and memory function. Half of the SHR were housed individually for three months, with remaining SHR and Wistar rats housed in groups and routinely handled (n = 8/group). At six months old, long-term and spatial working memory were assessed using object recognition and continuous y maze tasks, respectively. BBB permeability was measured in-vivo in dorsal hippocampus and prefrontal cortex and serum markers of inflammation assessed. Long-term memory function was impaired only in isolated male SHR, as recognition index was lower compared to socialized male Wistar and SHR (0.59 ± 0.07 vs. 0.70 ± 0.02 and 0.77 ± 0.03; p < 0.05 by 2way ANOVA), which was associated with increased BBB permeability in the hippocampus. In contrast, spatial working memory was only impaired in isolated female SHR that had a decreased alternation index compared to socialized female Wistar rats (0.59 ± 0.04 vs. 0.74 ± 0.02; p < 0.05 by 2way ANOVA). This sex-specific deficit was associated with greater BBB disruption in prefrontal cortex that correlated with elevated levels of circulating oxidative stress marker 8-isoprostane. These findings suggest that social isolation during chronic hypertension differentially impairs memory function in a sex-dependent manner. Overall, this study advances our understanding of cerebrovascular consequences of social isolation in adulthood and indicate brain region/memory domain dysfunction differ by sex during chronic hypertension.

Indexed as

Blood-Brain BarrierHypertensionMemorySex CharacteristicsSocial IsolationAnimalsChronic DiseaseFemaleMaleMaze LearningMemory, Short-TermRatsRats, Inbred SHRRats, WistarBlood-brain barrierChronic hypertensionSex differencesSocial isolationVascular cognitive impairment

Identifiers

PMID42551659
PMCPMC13559686

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.