Hickey M J, Hurley J V, Morrison W A
Bernard O'Brien Institute of Microsurgery, St. Vincent's Hospital, Fitzroy, Victoria.
Am J Physiol. 1996 Oct;271(4 Pt 2):H1277-86. doi: 10.1152/ajpheart.1996.271.4.H1277.
The aim of these experiments was to describe clearly the spatial relationship between the no-reflow phenomenon and tissue injury in postischemic skeletal muscle. Using the rectus femoris muscle of anesthetized rabbits, we examined microvascular perfusion in untreated muscles and in muscles after 3.5 h of ischemia and 10 min, 1 h, and 24 h of reperfusion. Microvascular perfusion was assessed by infusion of biological ink and quantitation of 1) the area of capillary filling in histological sections, and 2) the ratio of perfused capillaries to muscle fibers in perfused areas (C/F). After 10 min of reperfusion, perfused cross-sectional area had decreased from 67.0 +/- 20.0 to 10.6 +/- 5.6 (SD)%, and C/F was also significantly reduced. These changes persisted for at least 24 h. After 10 min of reperfusion, flow was randomly distributed throughout the muscle. However, after 24 h, perfusion was confined to the peripheral tissue in areas that were also viable as demonstrated by nitro blue tetrazolium staining. These results show that in this model, in the early stages of reperfusion, flow is established in some areas, which are destined to become necrotic.
这些实验的目的是清晰描述缺血后骨骼肌中无复流现象与组织损伤之间的空间关系。我们使用麻醉兔的股直肌,检测未处理肌肉以及缺血3.5小时后再灌注10分钟、1小时和24小时的肌肉中的微血管灌注情况。通过注入生物墨汁并对以下两项指标进行定量来评估微血管灌注:1)组织学切片中毛细血管充盈面积;2)灌注区域内灌注毛细血管与肌纤维的比例(C/F)。再灌注10分钟后,灌注横截面积从67.0±20.0%降至10.6±5.6(标准差)%,C/F也显著降低。这些变化至少持续24小时。再灌注10分钟后,血流随机分布于整个肌肉。然而,24小时后,灌注局限于经硝基蓝四氮唑染色显示仍存活的外周组织区域。这些结果表明,在该模型中,再灌注早期,一些注定会发生坏死的区域会建立血流。