Saraví F D, Saldeña T A, Cincunegui L M
Cátedra de Física Biológica, Facultad de Ciencias Médicas, Universidad Nacional de Cuyo, Mendoza, República Argentina.
Acta Gastroenterol Latinoam. 1996;26(3):159-65.
Electrogenic epithelial transport depends on oxidative metabolism. Acute hypoxia and subsequent reoxygenation effects on short-circuit current (Isc), transepithelial potential difference (PD) and tissue resistivity (TR) of rat distal colon were assessed. The tissue was mounted in an Ussing chamber filled with Ringer-HCO3-solution at 37 degrees C and bubbled with 95% O2- 5% CO2 which was switched to 95% N2- 5% CO2 for inducing hypoxia; afterwards normal oxygenation was resumed. The effect of 5, 10, 15 and 20 min-hypoxic periods was assessed in isolated mucosa preparations. Recovery was complete after 10- and 15-min hypoxia, but not after 20-min hypoxia. After 5-min hypoxia, an overshoot of Isc and PD was seen on reoxygenation. This effect was further characterized comparatively in mucosa-submucosa and isolated mucosa preparations. In the former (n = 10), control values were Isc = 71.7 +/- 8.6 microA. cm-2, PD = 9.7 +/- 1.6 mV and TR = 134.9 +/- 13.6 omega cm2. A 5-min hypoxia reduced Isc by 47.2 +/- 7.3% and PD by 61.5 +/- 4.9%. Peak values on reoxygenation were 28.1 +/- 4.1% for Isc and 16.8 +/- 5.4% for PD, over controls values. In the isolated mucosa (n = 9), control values were Isc = 52.04 +/- 5.5 microA. cm-2, PD = 5.0 +/- 0.8 mV and TR = 101.04 +/- 10.5 omega. cm2. In hypoxia, Isc decreased by 64.5 +/- 7.6% and PD by 57.2 +/- 7.8%. On reoxygenation peak values of 78.0 +/- 19.0% and 87.5 +/- 17.1%, respectively, were seen. The response to a 5 min-hypoxia was comparable, but that to reoxygenation was weaker and slower, in mucosa-submucosa than in isolated mucosa preparations. This may be explained by a hindrance to oxygen diffusion caused by the submucosal tissue. TR did not change with any period of hypoxia tested, but decreased slightly (8.9 +/- 1.3%) upon reoxygenation in the mucosa-submucosa preparations. Ouabain (10(-3) M) markedly blunted the response to reoxygenation. We conclude that hypoxic periods of 20 min lead to irreversible functional deterioration. Hypoxia decreases electrogenic transepithelial pumping, which may allow sodium to accumulate intracellularly and, if the hypoxia is short enough to prevent damage to the epithelium, increase sodium pump activity when oxygenation is resumed.
电生性上皮运输依赖于氧化代谢。评估了急性缺氧及随后的复氧对大鼠远端结肠短路电流(Isc)、跨上皮电位差(PD)和组织电阻(TR)的影响。将组织置于充满37℃林格氏碳酸氢盐溶液的尤斯灌流室中,用95%O₂ - 5%CO₂鼓泡,然后切换为95%N₂ - 5%CO₂以诱导缺氧;之后恢复正常氧合。在分离的黏膜制剂中评估了5、10、15和20分钟缺氧期的影响。10分钟和15分钟缺氧后恢复完全,但20分钟缺氧后未完全恢复。5分钟缺氧后,复氧时Isc和PD出现过冲。在黏膜 - 黏膜下层和分离的黏膜制剂中对该效应进行了比较进一步表征。在前者(n = 10)中,对照值为Isc = 71.7±8.6μA·cm⁻²,PD = 9.7±1.6mV,TR = 134.9±13.6Ω·cm²。5分钟缺氧使Isc降低47.2±7.3%,PD降低61.5±4.9%。复氧时的峰值Isc比对照值高28.1±4.1%,PD高16.8±5.4%。在分离的黏膜(n = 9)中,对照值为Isc = 52.04±5.5μA·cm⁻²,PD = 5.0±0.8mV,TR = 101.04±10.5Ω·cm²。缺氧时,Isc降低64.5±7.6%,PD降低57.2±7.8%。复氧时分别出现78.0±19.0%和87.5±17.1%的峰值。黏膜 - 黏膜下层对5分钟缺氧的反应与分离的黏膜制剂相当,但复氧时的反应比分离的黏膜制剂弱且慢。这可能是由于黏膜下层组织对氧扩散的阻碍所致。在所测试的任何缺氧期TR均未改变,但在黏膜 - 黏膜下层制剂复氧时略有降低(8.9±1.3%)。哇巴因(10⁻³M)显著减弱了复氧反应。我们得出结论,20分钟的缺氧期会导致不可逆的功能恶化。缺氧会降低电生性跨上皮泵浦,这可能使钠在细胞内蓄积,并且如果缺氧时间足够短以防止上皮受损,那么复氧时钠泵活性会增加。