Assessing intrarenal nonperfusion and vascular leakage in acute kidney injury with multinuclear (1) H/(19) F MRI and perfluorocarbon nanoparticles.
Assessing intrarenal nonperfusion and vascular leakage in acute kidney injury with multinuclear (1) H/(19) F MRI and perfluorocarbon nanoparticles.
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DOI:
10.1002/mrm.24851
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发表时间:
2014-06
影响因子:
3.3
通讯作者:
Wickline, Samuel A.
中科院分区:
文献类型:
--
作者:
Hu, Lingzhi;Chen, Junjie;Yang, Xiaoxia;Senpan, Angana;Allen, John S.;Yanaba, Noriko;Caruthers, Shelton D.;Lanza, Gregory M.;Hammerman, Marc R.;Wickline, Samuel A.
We sought to develop a unique sensor-reporter approach for functional kidney imaging that employs circulating perfluorocarbon nanoparticles (PFC NPs) and 19F MRI. Because the detected 19F signal intensity directly reflects local blood volume, and the 19F R1 is linearly proportional to local blood oxygen content (pO2), 19F spin density weighted and T1 weighted images were utilized to generate quantitative functional mapping in both healthy and ischemia-reperfusion (acute kidney injury, AKI) injured mouse kidneys. 1H Blood-Oxygenation-Level-Dependant (BOLD) MRI was also employed as a supplementary approach to facilitate the compressive analysis of renal circulation and its pathological changes in AKI. Heterogeneous blood volume distribution and intrarenal oxygenation gradient were confirmed in healthy kidneys by 19F MRI. In a mouse model of AKI, 19F MRI, in conjunction with BOLR MRI, sensitively delineated renal vascular damage and recovery. In the cortico-medullary (CM) junction region, we observed 25% lower 19F signal (p<0.05) and 70% longer 1H T2* (p<0.01) in injured kidneys compared to contralateral kidneys at 24 hours after initial ischemia-reperfusion injury. We also detected 71% higher 19F signal (p<0.01) and 40% lower 1H T2* (p<0.05) in the renal medulla region of injured kidneys compared to contralateral kidneys. With demonstrated superior diagnostic capability, functional kidney 19F MRI using PFC NPs could serve as a new diagnostic measures for comprehensive evaluation of renal function and pathology.
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影响因子:
4.3
作者:
Cohn, Claudia S.;Cushing, Melissa M.
通讯作者:
Cushing, Melissa M.
DOI:
10.1159/000313738
发表时间:
2010-01-01
期刊:
CARDIORENAL SYNDROMES IN CRITICAL CARE
影响因子:
--
作者:
Bonventre, Joseph V.
通讯作者:
Bonventre, Joseph V.
影响因子:
2.9
作者:
DETRE, JA;ZHANG, WG;LEIGH, JS
通讯作者:
LEIGH, JS
影响因子:
4.4
作者:
Alford, SK;Sadowski, EA;Grist, TM
通讯作者:
Grist, TM
影响因子:
13.8
作者:
Boyd, Alan S.;Zic, John A.;Abraham, Jerrold L.
通讯作者:
Abraham, Jerrold L.