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Real-time assessment of in vivo renal ischemia using laser autofluorescence imaging

机译:使用激光自发荧光成像实时评估体内肾脏缺血

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摘要

Potentially transplantable kidneys experience warm ischemia, and this injury is difficult to quantify. We investigate optical spectroscopic methods for evaluating, in real time, warm ischemic kidney injury and reperfusion. Vascular pedicles of rat kidneys are clamped unilaterally for 18 or 85 min, followed by 18 or 35 min of reperfusion, respectively. Contralateral, uninjured kidneys serve as controls. Autofluorescence and cross-polarized light scattering images are acquired every 15 s using 335-nm laser excitation (autofluorescence) and 650±20-nm linearly polarized illumination (light scattering). We analyze changes of injured-to-normal kidney autofluorescence intensity ratios during ischemia and reperfusion phases. The effect of excitation with 260 nm is also explored. Average injured-to-normal intensity ratios under 335-nm excitation decrease from 1.0 to 0.78 at 18 min of ischemia, with a return to baseline during 18 min of reperfusion. However, during 85 min of warm ischemia, average intensity ratios level off at 0.65 after 50 min, with no significant change during 35 min of reperfusion. 260-nm excitation results in no autofluorescence changes with ischemia. Cross-polarized light scattering images at 650 nm suggest that changes in hemoglobin absorption are not related to observed temporal behavior of the autofluorescence signal. Real-time detection of kidney tissue changes associated with warm ischemia and reperfusion using laser spectroscopy is feasible. Normalizing autofluorescence changes under 335 nm using the autofluorescence measured under 260-nm excitation may eliminate the need for a control kidney.
机译:潜在的可移植肾脏会经历温暖的局部缺血,这种损伤很难量化。我们研究光学光谱法,以实时评估温暖的缺血性肾损伤和再灌注。大鼠肾脏的血管蒂被单侧钳夹18或85分钟,然后分别进行18或35分钟的再灌注。对侧未损伤的肾脏作为对照。使用335 nm激光激发(自发荧光)和650±20 nm线性偏振照明(光散射)每15 s获取一次自发荧光和交叉偏振光散射图像。我们分析了缺血和再灌注阶段中损伤至正常肾脏自身荧光强度比率的变化。还探讨了260 nm激发的影响。在335 nm激发下的平均损伤强度与正常强度之比在缺血18分钟时从1.0降低至0.78,在再灌注18分钟后恢复至基线。然而,在热缺血的85分钟内,平均强度比在50分钟后稳定在0.65,而在35分钟的再灌注过程中没有明显变化。 260 nm激发导致缺血后自发荧光无变化。 650 nm处的交叉偏振光散射图像表明,血红蛋白吸收的变化与所观察到的自发荧光信号的时间行为无关。使用激光光谱法实时检测与热缺血和再灌注有关的肾脏组织变化是可行的。使用在260 nm激发下测量的自发荧光将335 nm下的自发荧光变化归一化可以消除对对照肾脏的需求。

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