Differentiating sensitivity of post-stimulus undershoot under diffusion weighting: implication of vascular and neuronal hierarchy

• Published in: PloS one 2008-08, Vol.3 (8), p.e2914-e2914
• Main Authors: Harshbarger, Todd B, Song, Allen W
• Format: Article
• Language: English
• Subjects: Blood; Blood Flow Velocity - physiology; Blood vessels; Blood Vessels - drug effects; Blood Vessels - physiology; Blood volume; Brain; Brain - physiology; Brain Mapping; Cerebrovascular Circulation - physiology; Diffusion; Functional magnetic resonance imaging; Humans; Magnetic Resonance Imaging; Medical imaging; Metabolic rate; Metabolism; Mobility; Neurobiology; Neurons; Neurons - drug effects; Neurons - physiology; Neurophysiology; NMR; Nuclear magnetic resonance; Oxygen; Oxygen - blood; Oxygen metabolism; Oxygenation; Photic Stimulation; Physiology; Radiology and Medical Imaging/Magnetic Resonance Imaging; Signal Transduction - physiology; Studies; Trends; Visual perception; Visual signals; Visual stimuli; Weighting
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0002914

The widely used blood oxygenation level dependent (BOLD) signal during brain activation, as measured in typical fMRI methods, is composed of several distinct phases, the last of which, and perhaps the least understood, is the post-stimulus undershoot. Although this undershoot has been consistently observed, its hemodynamic and metabolic sources are still under debate, as evidences for sustained blood volume increases and metabolic activities have been presented. In order to help differentiate the origins of the undershoot from vascular and neuronal perspectives, we applied progressing diffusion weighting gradients to investigate the BOLD signals during visual stimulation. Three distinct regions were established and found to have fundamentally different properties in post-stimulus signal undershoot. The first region, with a small but focal spatial extent, shows a clear undershoot with decreasing magnitude under increasing diffusion weighting, which is inferred to represent intravascular signal from larger vessels with large apparent diffusion coefficients (ADC), or high mobility. The second region, with a large continuous spatial extent in which some surrounds the first region while some spreads beyond, also shows a clear undershoot but no change in undershoot amplitude with progressing diffusion weighting. This would indicate a source based on extravascular and small vessel signal with smaller ADC, or lower mobility. The third region shows no significant undershoot, and is largely confined to higher order visual areas. Given their intermediate ADC, it would likely include both large and small vessels. Thus the consistent observation of this third region would argue against a vascular origin but support a metabolic basis for the post-stimulus undershoot, and would appear to indicate a lack of sustained metabolic rate likely due to a lower oxygen metabolism in these higher visual areas. Our results are the first, to our knowledge, to suggest that the post-stimulus undershoots have a spatial dependence on the vascular and neuronal hierarchy, and that progressing flow-sensitized diffusion weighting can help delineate these dependences.