Wahl M, Unterberg A, Baethmann A
Int J Microcirc Clin Exp. 1985;4(1):3-18.
Vascular diameters and blood-brain-barrier (BBB) function were investigated in the parietal cortex of cats using an open skull window technique and intravital fluorescence microscopy. The cortical surface was superfused with artificial cerebrospinal fluid containing: bradykinin (BK), Na+-arachidonate (AA), or xanthine-oxidase (XO). Na+-fluorescein (MW: 376), fluorescein-isothiocyanate-labelled (FITC) albumin (MW: 67 000), or FITC-dextran (MW: 19 400-62 000) were given intravenously as blood-brain-barrier indicators of different molecular size. In control experiments, the effect of continuous exposure of the preparation to the light source used for fluorescence excitation was studied. Dependent on the molecular size of the tracer and light intensity, continuous light exposure led to extravasation and disturbances of the microcirculation in small veins. When Na+-fluorescein was employed as barrier indicator at a magnification of X 40, at least 55 min of continuous illumination were required to induce extravasation. Brief, i.e. 0.5-15 s and discontinuous illumination for taking microphotographs amounting to less than 20 min in total did not induce extravasation in control experiments of 3.5 h. Opening of the blood-brain-barrier was studied during superfusion with a hypertonic solution (2000 mOsmol 1(-1)). The results obtained with bradykinin, Na+-arachidonate, or xanthine-oxidase indicate that opening of the barrier can occur independently from a corresponding vasodilating reaction. BK, or AA led to initial venular leakage as a result of an increase of selective, or global barrier permeability. On the other hand, XO did not induce extravasation, although cerebral vessels were markedly dilated. Taken together, the experimental model presented is suitable to simultaneously analyze dynamic changes of the permeability of cerebral vessels in-vivo with excellent spatial resolution and of the cerebral vasomotor behaviour under physiological and pathological conditions.
利用开颅窗口技术和活体荧光显微镜,在猫的顶叶皮质中研究血管直径和血脑屏障(BBB)功能。用含缓激肽(BK)、Na + -花生四烯酸盐(AA)或黄嘌呤氧化酶(XO)的人工脑脊液对皮质表面进行灌流。静脉注射Na + -荧光素(分子量:376)、异硫氰酸荧光素标记的(FITC)白蛋白(分子量:67000)或FITC -葡聚糖(分子量:19400 - 62000)作为不同分子大小的血脑屏障指示剂。在对照实验中,研究了制剂持续暴露于用于荧光激发的光源的影响。根据示踪剂的分子大小和光强度,持续光照会导致小静脉血管外渗和微循环紊乱。当以40倍放大倍数使用Na + -荧光素作为屏障指示剂时,至少需要55分钟的持续光照才能诱导血管外渗。在对照实验中,持续3.5小时的短暂(即0.5 - 15秒)和间断光照(用于拍摄显微照片,总计少于20分钟)不会诱导血管外渗。在用高渗溶液(2000 mOsmol 1(-1))灌流期间研究血脑屏障的开放情况。用缓激肽、Na + -花生四烯酸盐或黄嘌呤氧化酶获得的结果表明,屏障的开放可以独立于相应的血管舒张反应而发生。BK或AA由于选择性或整体屏障通透性增加而导致最初的小静脉渗漏。另一方面,尽管脑血管明显扩张,但XO并未诱导血管外渗。综上所述,所呈现的实验模型适用于在体内同时分析脑血管通透性的动态变化,具有出色的空间分辨率,以及在生理和病理条件下的脑血管舒缩行为。