Rose Jim, Martin Claudio, MacDonald Tammy, Ellis Chris
Department of Physiology, University of Westsern Ontario, London, Canada.
Microcirculation. 2006 Jan;13(1):41-7. doi: 10.1080/10739680500383472.
NADH fluorescence microscopy has been used as an index of the metabolic state of tissue but is associated with various obstacles such as low spatial resolution and quenching effects of blood pigments that prevent reliable monitoring of tissue bioenergetics. The objective of this study was to develop a system to monitor tissue bioenergetics in vivo using NADH fluorescence microscopy in the rat ileal mucosa.
Using an inverted microscope with an epifluorescence unit and an intensified charge-coupled device camera, NADH fluorescence images were visualized. Fluorescence intensity was measured of beta-NADH solutions at varying concentration (n = 6) and pH (n = 3) and in ex vivo (n = 6) and in vivo (n = 6) preparations of ileal mucosa of Sprague-Dawley rats anesthetized with isoflurane.
Intravital fluorescence microscopy reveals a map of the microcirculation that permits visualization of NADH fluorescence and intercapillary areas. The system was adjusted so a linear relationship between physiological concentrations of beta-NADH and fluorescence was achieved (r(2) = 0.98, p < .0001). Decreasing the pH of the solution had no effect on fluorescence intensity and fluorescence intensity in an anoxic ex vivo ileal segment was similar to that of the in vivo ileum after ischemia. Ischemia also resulted in spatial heterogeneity that was abolished by the addition of a 550-nm LP filter.
With this system, intravital NADH fluorescence microscopy provides the high resolution necessary to reliably monitor tissue bioenergetics in the rat ileal mucosa.
烟酰胺腺嘌呤二核苷酸(NADH)荧光显微镜已被用作组织代谢状态的指标,但它存在各种障碍,如空间分辨率低和血液色素的淬灭效应,这妨碍了对组织生物能量学的可靠监测。本研究的目的是开发一种系统,利用NADH荧光显微镜在大鼠回肠黏膜中监测体内组织生物能量学。
使用带有落射荧光装置的倒置显微镜和增强型电荷耦合器件相机,观察NADH荧光图像。测量了不同浓度(n = 6)和pH值(n = 3)的β-NADH溶液以及用异氟烷麻醉的Sprague-Dawley大鼠回肠黏膜的离体(n = 6)和体内(n = 6)制剂中的荧光强度。
活体荧光显微镜揭示了微循环图谱,可观察到NADH荧光和毛细血管间区域。对该系统进行了调整,使β-NADH的生理浓度与荧光之间呈现线性关系(r² = 0.98,p <.0001)。溶液pH值降低对荧光强度无影响,缺氧离体回肠段的荧光强度与缺血后体内回肠的荧光强度相似。缺血还导致了空间异质性,添加550 nm长波通(LP)滤光片可消除这种异质性。
利用该系统,活体NADH荧光显微镜提供了可靠监测大鼠回肠黏膜组织生物能量学所需的高分辨率。