4.5 Article

Physiological system analysis of the kidney by high-temporal-resolutionT2*monitoring of an oxygenation step response

Journal

MAGNETIC RESONANCE IN MEDICINE
Volume 85, Issue 1, Pages 348-359

Publisher

WILEY
DOI: 10.1002/mrm.28399

Keywords

BOLD MRI; hyperoxia; hypoxia; kidney; oxygenation; step response

Funding

  1. German Research Foundation [394046635]
  2. Hong Kong Research Grant Council [RGC C7048-16G]
  3. National Natural Science Foundation of China [61671228, 61728107, 81871349]
  4. Science and Technology Program of Guangdong [2017B090912006, 2018B030333001]

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This study investigates the feasibility of characterizing renal oxygenation regulation using high-temporal-resolution monitoring of the T2* response. The results suggest that the implemented system analysis approach may aid in understanding the regulation of renal oxygenation, potentially offering imaging means for diagnosis and therapy of renal diseases.
Purpose Examine the feasibility of characterizing the regulation of renal oxygenation using high-temporal-resolution monitoring of theT2*response to a step-like oxygenation stimulus. Methods ForT2*mapping, multi-echo gradient-echo imaging was used (temporal resolution = 9 seconds). A step-like renal oxygenation challenge was applied involving sequential exposure to hyperoxia (100% O-2), hypoxia (10% O-2+ 90% N-2), and hyperoxia (100% O-2). In vivo experiments were performed in healthy rats (N = 10) and in rats with bilateral ischemia-reperfusion injury (N = 4). To assess the step response of renal oxygenation, a second-order exponential model was used (model parameters: amplitude [A], time delay [Delta t], damping constant [D], and period of the oscillation [T]) for renal cortex, outer stripe of the outer medulla, inner stripe of the outer medulla, and inner medulla. Results The second-order exponential model permitted us to model the exponentialT2*recovery and the superimposedT2*oscillation following renal oxygenation stimulus. The in vivo experiments revealed a difference inD(outer medulla)between healthy controls (D< 1, indicating oscillatory recovery) and ischemia-reperfusion injury (D> 1, reflecting aperiodic recovery). The increase inD(outer medulla)by a factor of 3.7 (outer stripe of the outer medulla) and 10.0 (inner stripe of the outer medulla) suggests that this parameter might be rather sensitive to (patho)physiological oxygenation changes. Conclusion This study demonstrates the feasibility of monitoring the dynamic oxygenation response of renal tissues to a step-like oxygenation challenge using high-temporal-resolutionT2*mapping. Our results suggest that the implemented system analysis approach may help to unlock questions regarding regulation of renal oxygenation, with the ultimate goal of providing imaging means for diagnostics and therapy of renal diseases.

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