Brain injury following cardiac arrest (CA) is thought to be caused by a sudden loss of blood flow resulting in disruption in oxygen delivery, neural function and metabolism. However, temporal trajectories of the brain's physiology in the first few hours following CA have not been fully characterized. Furthermore, the extent to which these early measures can predict future neurological outcomes has not been determined. The present study sought to perform dynamic measurements of cerebral blood flow (CBF), oxygen extraction fraction (OEF) and cerebral metabolic rate of oxygen (CMRO 2) with MRI in the first 3 hours following the return of spontaneous circulation (ROSC) in a rat CA model. It was found that CBF, OEF and CMRO 2 all revealed a time-dependent increase during the first 3 hours after the ROSC. Furthermore, the temporal trajectories of CBF and CMRO 2 , but not OEF, were different across rats and related to neurologic outcomes at a later time (24 hours after the ROSC) (P < .001). Rats who manifested better outcomes revealed faster increases in CBF and CMRO 2 during the acute stage. When investigating physiological parameters measured at a single time point, CBF (ρ = 0.82, P = .004) and CMRO 2 (ρ = 0.80, P = .006) measured at $ 3 hours post-ROSC were positively associated with neurologic outcome scores at 24 hours. These findings shed light on brain physiological changes following CA, and suggest that MRI measures of brain perfusion and metabolism may provide a potential biomarker to guide post-CA management. K E Y W O R D S cardiac arrest, cerebral blood flow, cerebral metabolic rate of oxygen, MRI, neurologic deficit score, oxygen consumption, phase contrast, TRUST 1 | INTRODUCTION Cardiac arrest (CA) carries a low survival rate ($10%) and unfavorable outcomes. 1,2 Poor functional outcomes and mortality in CA are primarily driven by brain injury that occurs from a sudden loss of blood supply to the brain. The lack of blood flow leads to rapid changes in intracellular and extracellular ion concentrations with the development of intracellular acidosis. Furthermore, the failure of maintaining ionic balance results in membrane disruption, irreversible neuronal injury and, eventually, cell death. 3 As a critical management strategy for CA, effective cardiopulmonary