Publication | Open Access
Focal physiological uncoupling of cerebral blood flow and oxidative metabolism during somatosensory stimulation in human subjects.
2.1K
Citations
28
References
1986
Year
Brain CirculationCerebral Metabolic RateSocial SciencesCerebral Vascular RegulationHuman SubjectsMultiple Sequential AdministrationsNeurologyFocal Physiological UncouplingNeuroimagingBrain StimulationNervous SystemCerebral Blood FlowNeurostimulationReperfusion InjuryBrain ImagingNeurophysiologyPhysiologyElectrophysiologyNeuroscienceCentral Nervous SystemBrain ElectrophysiologyMedicine
The study hypothesizes that cerebral blood flow is dynamically regulated by neuronal firing independent of oxygen metabolism. The authors used sequential 15O radiotracer PET scans to measure CBF and CMRO₂ in human subjects. In healthy adults, CBF and CMRO₂ are tightly coupled at rest (r≈0.87), but somatosensory stimulation induces focal uncoupling, with CBF increasing ~29% while CMRO₂ rises only ~5%, and stimulus duration does not alter this effect.
Coupling between cerebral blood flow (CBF) and cerebral metabolic rate of oxygen (CMRO2) was studied using multiple sequential administrations of 15O-labeled radiotracers (half-life, 123 sec) and positron emission tomography. In the resting state an excellent correlation (mean r, 0.87) between CBF and CMRO2 was found when paired measurements of CBF and CMRO2 from multiple (30-48) brain regions were tested in each of 33 normal subjects. Regional uncoupling of CBF and CMRO2 was found, however, during neuronal activation induced by somatosensory stimulation. Stimulus-induced focal augmentation of cerebral blood flow (29% mean) far exceeded the concomitant local increase in tissue metabolic rate (mean, 5%), when resting-state and stimulated-state measurements were obtained in each of 9 subjects. Stimulus duration had no significant effect on response magnitude or on the degree of CBF-CMRO2 uncoupling observed. Dynamic, physiological regulation of CBF by a mechanism (neuronal or biochemical) dependent on neuronal firing per se, but independent of the cerebral metabolic rate of oxygen, is hypothesized.
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