长期高海拔缺氧对胎羊和成年羊冠状动脉张力和细胞内钙反应的影响。

Satoshi Kono, Virginia M Stiffel, Raymond D Gilbert
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引用次数: 2

摘要

目的:我们之前的研究表明,暴露于长期缺氧后,胎儿冠状动脉血流维持在控制水平,尽管心输出量减少了25%。我们还证明,从长期缺氧胎儿中分离出来的冠状动脉血管环,在充氧良好的沐浴系统中研究,在KCl的作用下,去极化诱导的收缩强度显着降低。为了研究长期缺氧后胎儿冠状血管对kcl诱导的收缩反应降低的机制,我们同时测量了张力和细胞内钙,以及l型Ca2+通道密度和敏感性。方法:将怀孕母羊饲养在海拔3820 m,饲养约110 d。在妊娠138 ~ 141天,处死长期缺氧动物和对照动物,分离胎儿和成年左冠状动脉前降支(LAD),在充氧浴系统中进行研究。同时测量张力和细胞内钙([Ca2+]i)对KCl浓度增加的响应,此外,在KCl最大浓度的一半下测量对钙通道阻滞剂硝苯地平的敏感性。我们还用(+)-[3H]PN200-110测量了l型Ca2+通道密度。结果:l型Ca2+通道密度在长期缺氧的胎儿中下降了约31%,但在成人LAD中没有。在所有浓度的KCl下,长期缺氧的胎儿和成人LAD的张力均显著降低。[Ca2+]i在长期缺氧动物的胎儿和成年LAD中静止时较低,在所有KCl浓度下均升高至较低水平。在所有浓度的KCl下,张力与[Ca2+]i的比值也较低。硝苯地平的敏感性不变。结论:l型Ca2+通道密度的降低和对KCl的[Ca2+]i反应的降低,以及对[Ca2+]i的张力反应的降低,可能与长期缺氧胎儿LAD去极化诱导的收缩减少有关。在缺氧的成年人中,[Ca2+]i的减少和对[Ca2+]i的张力反应的降低可能与kcl诱导的收缩的低张力反应有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of long-term, high-altitude hypoxia on tension and intracellular calcium responses in coronary arteries of fetal and adult sheep.

Objectives: We have previously shown that after exposure to long-term hypoxia, fetal coronary flow is maintained at control levels despite a 25% reduction in cardiac output. We also demonstrated that coronary vascular rings isolated from the long-term hypoxic fetuses and studied in well-oxygenated bath system displayed significantly reduced depolarization-induced contraction strength in response to KCl. To study the mechanism of reduced fetal coronary vascular responses to KCl-induced contractions following exposure to long-term hypoxia, we measured tension and intracellular calcium simultaneously, as well as L-type Ca2+ channel density and sensitivity.

Methods: Pregnant ewes were housed at altitude (3820 m) for approximately 110 days. At 138 to 141 days of gestation, long-term hypoxic and control animals were killed and fetal and adult left anterior descending coronary artery (LAD) was isolated and studied in a well-oxygenated bath system. Tension and intracellular calcium ([Ca2+]i) were measured simultaneously in response to increasing concentrations of KCl and, in addition, the sensitivity to the calcium channel blocker nifedipine was measured at a half maximal concentration of KCl. We also measured L-type Ca2+ channel density with (+)-[3H]PN200-110.

Results: L-type Ca2+ channel density was decreased by approximately 31% in the long-term hypoxic fetal, but not adult, LAD. Tension in the long-term hypoxic fetal and adult LAD was significantly lower at all concentrations of KCl. [Ca2+]i was lower at rest in both fetal and adult LAD from long-term hypoxic animals and increased to lower levels at all concentrations of KCl. The ratio of tension to [Ca2+]i was also lower at all concentrations of KCl. Sensitivity to nifedipine was unchanged.

Conclusions: The reduced L-type Ca2+ channel density and the reduced [Ca2+]i response to KCl, as well as the reduced tension response to [Ca2+]i, could potentially be involved in the reduction in depolarization-induced contractions in LAD from long-term hypoxic fetuses. In hypoxic adults, reduced [Ca2+]i and reduced tension response to [Ca2+]i may be involved in the lower tension response to KCl-induced contractions.

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