OSCR

Impact of aging on neck vasculature and brain biochemistry in female mice.

Overview

Authors: Allison R Jones1, Amin Jarrahi1, Kylee Karpowich2, EllaGrey Moody3, Lily Renner1, Lindsay P Brown4, Caitlin M Tressler5,6, A Colleen Crouch1
  1. Department of Biomedical Engineering, University of Tennessee, Knoxville, Tennessee, USA
  2. Department of Psychology, University of Tennessee, Knoxville, Tennessee, USA
  3. Department of Biochemistry & Cellular and Molecular Biology, University of Tennessee, Knoxville, Tennessee, USA
  4. Department of Chemistry, University of Tennessee, Knoxville, Tennessee, USA
  5. The Johns Hopkins University Applied Imaging Mass Spectrometry Core and Service Center, Division of Cancer Imaging Research, The Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA
  6. The Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA
Institutions: University of Tennessee at Knoxville (United States); Johns Hopkins University (United States); Johns Hopkins Medicine (United States); Sidney Kimmel Comprehensive Cancer Center (United States)
Journal: Physiological reports, volume 14, issue 17, article e71059
Dates: received 13 April 2026; accepted 5 August 2026; published online 30 August 2026; in print September 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.14814/phy2.71059 · PMID 42670228 · PMCID PMC13527430 · OpenAlex W7204792934
Open access: gold, a free copy (OpenAlex)
Status: data only
Categories: genetics / omics (modality), other (modality), histology / microscopy (modality), mouse (organism)
Methods: Statistics, Smoothing, state filtering, decompositions, Connectivity
Keywords: aging in female mice, brain lipidomics, MALDI mass spectrometry imaging, neck vascular biomechanics, neurovascular aging, wall shear stress
MeSH: Aging*, Brain*, Brain Chemistry*, Neck*, Animals, Female, Hemodynamics, Mice, Mice, Inbred C57BL (* major topic)
Topic: Barrier Structure and Function Studies (Neurology, Neuroscience), according to OpenAlex
Funding: NIH HHS (S10 OD030500, NIH S10 OD030500)
Citations: not cited yet (Europe PMC); 78 references in the paper
Research resources: RRID:SCR_028273

Abstract

Age‐related changes in large‐vessel biomechanics may contribute to neurovascular dysfunction and region‐specific biochemical remodeling in the brain, with important implications for female health. This study investigated the impact of aging on neck vasculature and brain lipid biochemistry in female C57BL/6NHsd mice by comparing young (12 weeks; n = 10) and middle‐aged (52 weeks; n = 10) cohorts using ultrasound imaging, histology, and mass spectrometry. In vivo ultrasound quantified carotid and jugular hemodynamics, including wall shear stress (WSS), circumferential cyclic strain (CCS), pulsatility index, and volumetric flow. Ex vivo assessments included spatial lipid mapping in vessels and brain, and histology staining to quantify elastin‐to‐collagen ratios. Middle‐aged females exhibited reduced carotid systolic velocity, systolic WSS, and body weight–normalized carotid volumetric flow compared to young controls, while pulsatility index and CCS showed non‐significant decreases. Histology revealed a reduction in the carotid elastin‐to‐collagen ratio, consistent with vascular remodeling. Lipidomic profiling identified age‐dependent shifts in lipid headgroups, including decreases across multiple brain lipid classes, increased N‐acylethanolamides, alongside increases in carotid cardiolipin and lysophosphatidylethanolamine. Hippocampal spectra showed clearer age‐related separation than whole‐brain analyses. Correlation analyses identified moderate to strong associations between vascular biomechanics and lipid features across tissues, supporting coordinated neurovascular and biochemical aging in female mice.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

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Data

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Data availability statement

All data associated with this study are available in the Dryad Digital Repository. Additional information is available from the corresponding author upon reasonable request.

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 8 authors, 6 keywords, 9 MeSH terms, 1 funder, 74 references, 1 RRID.

Cite

This paper

Jones, A. R., Jarrahi, A., Karpowich, K., Moody, E., Renner, L., Brown, L. P., Tressler, C. M., & Crouch, A. C. (2026). Impact of aging on neck vasculature and brain biochemistry in female mice. Physiological reports, 14(17), e71059. https://doi.org/10.14814/phy2.71059

BibTeX

@article{jones2026impact,
author = {Jones, Allison R and Jarrahi, Amin and Karpowich, Kylee and Moody, EllaGrey and Renner, Lily and Brown, Lindsay P and Tressler, Caitlin M and Crouch, A Colleen},
title = {{Impact of aging on neck vasculature and brain biochemistry in female mice}},
journal = {Physiological reports},
year = {2026},
month = sep,
volume = {14},
number = {17},
pages = {e71059},
publisher = {Wiley},
issn = {2051-817X},
doi = {10.14814/phy2.71059},
url = {https://doi.org/10.14814/phy2.71059},
pmid = {42670228},
pmcid = {PMC13527430}
}

RIS

TY - JOUR
AU - Jones, Allison R
AU - Jarrahi, Amin
AU - Karpowich, Kylee
AU - Moody, EllaGrey
AU - Renner, Lily
AU - Brown, Lindsay P
AU - Tressler, Caitlin M
AU - Crouch, A Colleen
TI - Impact of aging on neck vasculature and brain biochemistry in female mice
T2 - Physiological reports
J2 - Physiol Rep
PY - 2026
DA - 2026/09/01
VL - 14
IS - 17
SP - e71059
SN - 2051-817X
PB - Wiley
DO - 10.14814/phy2.71059
UR - https://doi.org/10.14814/phy2.71059
LA - en
ER -

CSL-JSON

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