Kira Shaw

@kirasha.bsky.social

Wellcome CDA fellow at University of Manchester | Postdoc at Sheffield University 🏢, interested in neurovascular coupling in health, ageing and neurodegeneration 🧠🔬

Delighted to share our latest review in Nature Reviews Neuroscience! We examine the growing evidence that vascular dysfunction plays a key role in cognitive decline in ageing and dementia, and argue that preserving/restoring CBF should be central to future therapies. www.nature.com/articles/s41...

The vascular contribution to cognitive decline in ageing and dementia - Nature Reviews Neuroscience

Growing evidence suggests that reduced cerebral blood flow contributes to cognitive decline in ageing and dementia. Attwell and colleagues discuss the underlying mechanisms and functional consequences...

nature.com

Come and join us in Manchester... We are looking for candidates interested in vascular health and neurodegeneration. This project is specifically exploring how menopause may increase Alzheimer's risk. We also have a postdoc position available: www.jobs.manchester.ac.uk/Job/JobDetai...

Research Associate in Neuroscience :Oxford Road

jobs.manchester.ac.uk

Dementia Researcher@dementiaresearcher.bsky.social · last yr.

Research Technician vacancy at University of Manchester. Join Dr Kira Shaw @kirasha.bsky.social & Dr Ingo Schiessl on a Wellcome project exploring how menopause may increase Alzheimer’s risk. Closing date: 12th August www.dementiaresearcher.nihr.ac.uk/job/universi...

I'm pleased to share our new paper about the impact of locomotion on haemodynamic responses across the brain's vascular compartments in SPIE: Neurophotonics. www.spiedigitallibrary.org/journals/neu... Please read the comments below for a 'Bluetorial' on our findings... 👇

Voluntary locomotion induces an early and remote hemodynamic decrease in the large cerebral veins

SignificanceBehavior regulates dural and cerebral vessels, with spontaneous locomotion inducing dural vessel constriction and increasing stimulus-evoked cerebral hemodynamic responses. It is vital to investigate the function of different vascular network components, surrounding and within the brain, to better understand the role of the neurovascular unit in health and neurodegeneration.AimWe characterized locomotion-induced hemodynamic responses across vascular compartments of the whisker barrel cortex: artery, vein, parenchyma, draining, and meningeal vein.ApproachUsing 2D-OIS, hemodynamic responses during locomotion were recorded in 9- to 12-month-old awake mice: wild-type, Alzheimer’s disease (AD), atherosclerosis, or mixed (atherosclerosis/AD) models. Within the somatosensory cortex, responses were taken from pial vessels inside the whisker barrel region [(WBR): “whisker artery” and “whisker vein”], a large vein from the sagittal sinus adjacent to the WBR (draining vein), and meningeal vessels from the dura mater (which do not penetrate cortical tissue).ResultsWe demonstrate that locomotion evokes an initial decrease in total hemoglobin (HbT) within the draining vein before the increase in HbT within WBR vessels. The locomotion event size influences the magnitude of the HbT increase in the pial vessels of the WBR but not of the early HbT decrease within the draining veins. Following locomotion onset, an early HbT decrease was also observed in the overlying meningeal vessels, which unlike within the cortex did not go on to exceed baseline HbT levels during the remainder of the locomotion response. We show that locomotion-induced hemodynamic responses are altered in disease in the draining vein and whisker artery, suggesting this could be an important neurodegeneration biomarker.ConclusionsThis initial reduction in HbT within the draining and meningeal veins potentially serves as a “space-saving” mechanism, allowing for large increases in cortical HbT associated with locomotion. Given this mechanism is impacted by disease, it may provide an important target for vascular-based therapeutic interventions.

spiedigitallibrary.org

I am excited to have been awarded a Wellcome Trust CDA fellowship to study whether menopause enhances AD risk by exacerbating vascular dysfunction. I will be starting my lab in Manchester in January 2026, and would love to connect with other researchers interested in sex differences and AD 🧠🩸 🔬.