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Colasanti, A.

Publications and source records attributed to Colasanti, A..

2 recordsLinked to original sources

A Double Challenge: Cerebral Blood Flow During Concurrent Breath-Hold and Motor Task

Background/Hypothesis: Challenging the brain with simultaneous global and local demands may reveal functional constraints not apparent with either challenge alone. Here, we combine breath-holding with a motor task to investigate how a global vascular challenge modifies the local neurovascular response. Methods: Fourteen healthy adults underwent arterial spin labelling magnetic resonance imaging during three conditions: finger tapping with normal breathing, 25-second inspiratory breath-holding, and finger tapping during breath-holding. Cerebral blood flow responses were assessed using whole brain voxelwise analyses and motor regions of interest. Results: In the primary motor cortex, the increase in cerebral blood flow relative to baseline was approximately halved during the combined breath-holding and motor task challenge compared with motor task alone (26.5% vs 51.3%; p<0.001). Supplementary motor area responses were also smaller (23.2% vs 41.2%), but the difference was not statistically significant (p=0.092). Regional perfusion reductions were less extensive during the combined challenge than during breath-holding alone. These regional effects occurred without significant global grey- or white-matter perfusion changes from baseline. Conclusion/Interpretation: Combining global and local challenges revealed constraints on task-evoked perfusion increases not apparent during motor activation alone. This approach could help assess whether impaired cerebrovascular reserve compromises the brains capacity to meet local functional demands.

physiology↗

The effects of acute Methylene Blue administration on cerebral blood flow and metabolism in humans and rats

Methylene Blue (MB) is a brain-penetrating drug with putative neuroprotective, antioxidant and metabolic enhancing effects. In vitro studies suggest that MB enhances mitochondrial complexes activity. However, no study has directly assessed the haemodynamic and metabolic effects of MB in the human brain. We used in vivo neuroimaging to measure the effect of MB on cerebral blood flow (CBF) and brain metabolism in humans and in rats. Two doses of MB (0.5 and 1 mg/kg in humans; 2 and 4 mg/kg in rats; iv) induced reductions in global cerebral blood flow (CBF) in humans (F(1.74, 12.17)5.82, p=0.02) and rats (F(1,5)26.04, p=0.0038). Human cerebral metabolic rate of oxygen (CMRO2) was also significantly reduced (F(1.26, 8.84)8.01, p=0.016), as was the rat cerebral metabolic rate of glucose (CMRglu) (t=2.6(16) p=0.018). This was contrary to our hypothesis that MB will increase CBF and energy metrics. Nevertheless, our results were reproducible across species and dose dependent. One possible explanation is that the concentrations used, although clinically relevant, reflect MBs hormetic effects, i.e., higher concentrations produce inhibitory rather than augmentation effects on metabolism. Additionally, here we used healthy volunteers and healthy rats with normal cerebral metabolism where MBs ability to enhance cerebral metabolism might be limited.

neuroscience↗