“Overshoot” of O2 Is Required to Maintain Baseline Tissue Oxygenation at Locations Distal to Blood Vessels

In vivo imaging of cerebral tissue oxygenation is important in defining healthy physiology and pathological departures associated with cerebral disease. We used a recently developed two-photon microscopy method, based on a novel phosphorescent nanoprobe, to image tissue oxygenation in the rat primary sensory cortex in response to sensory stimulation. Our measurements showed that a stimulus-evoked increase in tissue pO2 depended on the baseline pO2 level. In particular, during sustained stimulation, the steady-state pO2 at low-baseline locations remained at the baseline, despite large pO2 increases elsewhere. In contrast to the steady state, where pO2 never decreased below the baseline, transient decreases occurred during the “initial dip” and “poststimulus undershoot.” These results suggest that the increase in blood oxygenation during the hemodynamic response, which has been perceived as a paradox, may serve to prevent a sustained oxygenation drop at tissue locations that are remote from the vascular feeding sources.

[1]  Maiken Nedergaard,et al.  Two-photon NADH imaging exposes boundaries of oxygen diffusion in cortical vascular supply regions , 2010, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[2]  Sergei A. Vinogradov,et al.  Phosphorescent Pd Porphyrin−Dendrimers: Tuning Core Accessibility by Varying the Hydrophobicity of the Dendritic Matrix , 2002 .

[3]  Feng Gao,et al.  Oxygen microscopy by two-photon-excited phosphorescence. , 2008, Chemphyschem : a European journal of chemical physics and physical chemistry.

[4]  K. Oka,et al.  Dual responses of tissue partial pressure of oxygen after functional stimulation in rat somatosensory cortex , 2003, Brain Research.

[5]  D. Kleinfeld,et al.  Suppressed Neuronal Activity and Concurrent Arteriolar Vasoconstriction May Explain Negative Blood Oxygenation Level-Dependent Signal , 2007, The Journal of Neuroscience.

[6]  Egill Rostrup,et al.  Cerebral Blood Flow Response to Functional Activation , 2010, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[7]  David A. Boas,et al.  Quantitative cerebral blood flow with Optical Coherence Tomography , 2010, Optics express.

[8]  Kazuto Masamoto,et al.  Changes in Cerebral Arterial, Tissue and Venous Oxygenation with Evoked Neural Stimulation: Implications for Hemoglobin-Based Functional Neuroimaging , 2010, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[9]  Aleksander S Popel,et al.  Experimental and Theoretical Studies of Oxygen Gradients in Rat Pial Microvessels , 2008, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[10]  Emiri T. Mandeville,et al.  Two-photon high-resolution measurement of partial pressure of oxygen in cerebral vasculature and tissue , 2010, Nature Methods.

[11]  R. Buxton Neuroenergetics Review Article , 2022 .

[12]  David A Boas,et al.  Optical monitoring of oxygen tension in cortical microvessels with confocal microscopy. , 2009, Optics express.

[13]  A. Grinvald,et al.  Interactions Between Electrical Activity and Cortical Microcirculation Revealed by Imaging Spectroscopy: Implications for Functional Brain Mapping , 1996, Science.

[14]  A. Dale,et al.  Cortical depth-specific microvascular dilation underlies laminar differences in blood oxygenation level-dependent functional MRI signal , 2010, Proceedings of the National Academy of Sciences.

[15]  I A Silver,et al.  Tissue oxygen tension and brain sensitivity to hypoxia. , 2001, Respiration physiology.

[16]  E. P. Vovenko,et al.  Distribution of oxygen tension on the surface of arterioles, capillaries and venules of brain cortex and in tissue in normoxia: an experimental study on rats , 1999, Pflügers Archiv.

[17]  B. Chance,et al.  Intracellular Oxidation-Reduction States in Vivo , 1962, Science.

[18]  Afonso C. Silva,et al.  Spatiotemporal Evolution of the Functional Magnetic Resonance Imaging Response to Ultrashort Stimuli , 2011, The Journal of Neuroscience.

[19]  Winfried Denk,et al.  On the fundamental imaging-depth limit in two-photon microscopy , 2006 .

[20]  R. Freeman,et al.  Neurometabolic coupling in cerebral cortex reflects synaptic more than spiking activity , 2007, Nature Neuroscience.

[21]  M. Mintun,et al.  Brain work and brain imaging. , 2006, Annual review of neuroscience.

[22]  Winfried Denk,et al.  On the fundamental imaging-depth limit in two-photon microscopy , 2004, SPIE Photonics Europe.

[23]  R. Buxton,et al.  Modeling the hemodynamic response to brain activation , 2004, NeuroImage.

[24]  R. Freeman,et al.  Single-Neuron Activity and Tissue Oxygenation in the Cerebral Cortex , 2003, Science.

[25]  J. Detre,et al.  Dynamic Changes in Cerebral Blood Flow, O2 Tension, and Calculated Cerebral Metabolic Rate of O2 during Functional Activation Using Oxygen Phosphorescence Quenching , 2001, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[26]  Sergei A Vinogradov,et al.  Design of Metalloporphyrin-Based Dendritic Nanoprobes for Two-Photon Microscopy of Oxygen. , 2008, Journal of porphyrins and phthalocyanines.

[27]  Nikolas Offenhauser,et al.  Activity‐induced tissue oxygenation changes in rat cerebellar cortex: interplay of postsynaptic activation and blood flow , 2005, The Journal of physiology.

[28]  M. Raichle,et al.  Focal physiological uncoupling of cerebral blood flow and oxidative metabolism during somatosensory stimulation in human subjects. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[29]  B. Schoener,et al.  Intracellular Oxidation-Reduction States in Vivo , 1962, Science.

[30]  A. Grinvald,et al.  Increased cortical oxidative metabolism due to sensory stimulation: implications for functional brain imaging. , 1999, Science.

[31]  V. Jiménez‐Yuste,et al.  Hematopoietic cell transplantation using plasma and DMSO without HES, with non-programmed freezing by immersion in a methanol bath: results in 213 cases , 1998, Bone Marrow Transplantation.

[32]  Lihong V. Wang,et al.  Functional transcranial brain imaging by optical-resolution photoacoustic microscopy. , 2009, Journal of biomedical optics.

[33]  Erich Gnaiger,et al.  Polarographic Oxygen Sensors , 1983, Springer Berlin Heidelberg.

[34]  M. Ducros,et al.  Simultaneous two-photon imaging of oxygen and blood flow in deep cerebral vessels , 2011, Nature Medicine.

[35]  D. Kleinfeld,et al.  Stimulus-Induced Changes in Blood Flow and 2-Deoxyglucose Uptake Dissociate in Ipsilateral Somatosensory Cortex , 2008, The Journal of Neuroscience.