Hudlicka O, Milkiewicz M, Cotter M A, Brown M D
Department of Physiology, University of Birmingham, Birmingham B15 2TT, UK.
Exp Physiol. 2002 May;87(3):373-81. doi: 10.1113/eph8702285.
To investigate the role of hypoxia as a stimulus to the early upregulation of vascular endothelial growth factor (VEGF) in fast skeletal muscles during chronic low frequency stimulation, blood flow, oxygen consumption, VEGF expression and capillary : fibre ratio were measured in chronically stimulated tibialis anterior and extensor digitorum longus (EDL) muscles in rabbits and rats. No differences were found in blood flow, oxygen consumption and extraction between rabbit muscles stimulated for 2 or 4 days (8 h on-16 h off) and controls. Muscle P(O(2)) polarographically measured immediately at the end of stimulation on day 2 was also no different from control under resting conditions (10.7 +/- 1.6 vs. 9.5 +/- 1.2 Torr, n.s.). Unlike control muscles, however, P(O(2)) in 2 day stimulated muscles did not increase immediately after a further acute bout of contractions. This difference was not apparent after similar acute contractions in 4 day stimulated muscles. The involvement of VEGF in early angiogenesis in stimulated muscles was studied in serial cryosections of rat EDL. The proportion of capillaries positively immunostained for VEGF increased from 25 +/- 1 % to 40 +/- 1 % (P < 0.05) in muscles removed on day 2 immediately at the end of chronic stimulation; it decreased slightly after 16 h rest, and increased again after 4 days of stimulation. Capillary : fibre ratio was unchanged throughout the experiment. Capillary cell proliferation increased only after the rest period on day 2 (20-fold increase) and day 4 (12-fold increase), indicating angiogenesis in progress. Thus the timing of transient hypoxia and increase in capillary-linked VEGF in stimulated muscles, albeit in different species, was similar, and increased VEGF staining and capillary cell proliferation occurred even after the hypoxia had resolved. This suggests (1) a connection between hypoxia and VEGF during the early stages of stimulation, although ensuing capillary proliferation may thereafter rapidly correct for local hypoxia, and (2) that the subsequent angiogenesis and VEGF expression are dependent on factors other than hypoxia.
为研究缺氧在慢性低频刺激期间作为快速骨骼肌中血管内皮生长因子(VEGF)早期上调刺激因素的作用,对兔和大鼠经慢性刺激的胫骨前肌和趾长伸肌(EDL)测量了血流量、耗氧量、VEGF表达及毛细血管与肌纤维比例。在刺激2天或4天(8小时开启-16小时关闭)的兔肌肉与对照之间,血流量、耗氧量及氧摄取未发现差异。在第2天刺激结束时立即用极谱法测量的肌肉P(O₂)在静息条件下也与对照无差异(10.7±1.6对9.5±1.2托,无显著性差异)。然而,与对照肌肉不同,在2天刺激的肌肉中,进一步急性收缩后P(O₂)并未立即增加。在4天刺激的肌肉中进行类似急性收缩后,这种差异并不明显。在大鼠EDL的连续冰冻切片中研究了VEGF在刺激肌肉早期血管生成中的作用。在慢性刺激结束时立即于第2天取出的肌肉中,VEGF免疫染色阳性的毛细血管比例从25±1%增加到40±1%(P<0.05);休息16小时后略有下降,刺激4天后再次增加。在整个实验过程中毛细血管与肌纤维比例未变。毛细血管细胞增殖仅在第2天(增加20倍)和第4天(增加12倍)的休息期后增加,表明血管生成正在进行。因此,尽管在不同物种中,刺激肌肉中短暂缺氧和与毛细血管相关的VEGF增加的时间相似,并且即使在缺氧消除后VEGF染色增加和毛细血管细胞增殖仍会发生。这表明(1)在刺激早期缺氧与VEGF之间存在联系,尽管随后的毛细血管增殖可能迅速纠正局部缺氧,(2)随后的血管生成和VEGF表达依赖于缺氧以外的因素。