La Trobe

Post-stroke cognitive impairment and brain hemorrhage are augmented in hypertensive mice

Version 2 2025-01-21, 00:29
Version 1 2025-01-08, 03:32
journal contribution
posted on 2025-01-21, 00:29 authored by David Wong ZhangDavid Wong Zhang, Tayla Gibson HughesTayla Gibson Hughes, Hericka Bruna Figueiredo GalvaoHericka Bruna Figueiredo Galvao, Cecilia Lo, Quynh Nhu DinhQuynh Nhu Dinh, Shenpeng ZhangShenpeng Zhang, Hyun Ah KimHyun Ah Kim, Sharmalee Selvaraji, Andrew N Clarkson, Thiruma ArumugamThiruma Arumugam, Grant DrummondGrant Drummond, Christopher SobeyChristopher Sobey, Michael De SilvaMichael De Silva
Hypertension is a major risk factor for both stroke and cognitive impairment, but it is unclear whether it may specifically affect post-stroke cognitive impairment. We assessed the effect of hypertension and/or stroke on brain injury, cognitive outcome, and the brain transcriptomic profile. C57BL/6J mice (n = 117; 3–5 mo.) received s.c. infusion of either saline or angiotensin II followed by sham surgery or photothrombotic stroke targeting the prefrontal cortex seven days later. Cognitive function was assessed with the Barnes maze and RNA sequencing was used to quantify transcriptomic changes in the brain. Angiotensin II treatment produced spontaneous hemorrhaging after stroke. In the Barnes maze, hypertensive mice that received stroke surgery had an increased escape latency compared to other groups (day 3: hypertensive + stroke = 166.6 ± 6.0 s vs. hypertensive + sham = 122.8 ± 13.8 s vs. normotensive + stroke = 139.9 ± 10.1 s vs. normotensive + sham = 101.9 ± 16.7 s), consistent with impaired cognition. RNA sequencing revealed >1500 differentially expressed genes related to neuroinflammation in hypertensive + stroke vs. normotensive + stroke, which included genes associated with apoptosis, microRNAs, autophagy, anti-cognitive biomarkers and Wnt signaling. Overall, we show that the combination of hypertension and stroke resulted in greater learning impairment and brain injury.

Funding

The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work was supported by Project Grants to CGS from the National Health and Medical Research Council of Australia (NHMRC; GNT1064686 and GNT1085323) and a Senior Research Fellowship to CGS (GNT1079467). David Wong Zhang was supported by an Australian Government Research Training Program Scholarship and a La Trobe University Postgraduate Research Scholarship.

History

Publication Date

2024-06-17

Journal

Cerebrovascular and Brain Metabolism Reviews

Volume

44

Issue

12

Pagination

18p. (p.1517-1534)

Publisher

Raven Press

ISSN

1040-8827

Rights Statement

© The Author(s) 2024. This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).

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