首页> 美国卫生研究院文献>The Journal of Physiology >Developmental changes in isolated rat type I carotid body cell K+ currents and their modulation by hypoxia.
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Developmental changes in isolated rat type I carotid body cell K+ currents and their modulation by hypoxia.

机译:分离的大鼠I型颈动脉体细胞K +电流的发育变化及其受缺氧的调节。

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摘要

1. Whole-cell patch-clamp recordings were used to investigate possible age-related changes in K+ currents of type 1 carotid body cells isolated from the rat. K+ current density increased with age, as measured in cells isolated from 4-day-old, 10-day-old and adult rats (> or = 5 weeks old). 2. The proportion of current reversibly inhibited by high [Mg2+] (6 mM), low [Ca2+] (0.1 mM) solutions, indicative of the proportion of current attributable to activation of Ca(2+) -sensitive K+ (KCa) channels, was significantly smaller in cells of 4-day-old rats compared with 10-day-old rats, despite inward Ca2+ current densities being similar in these two age groups. Inhibition of K+ currents by high [Mg2+], low [Ca2+] solutions was similar in 10-day-old and adult type 1 cells. 3. Hypoxia (PO2, 16-23 mmHg) caused reversible reductions in type I cells from rats of all age groups. However, reductions seen in cells of 4-day-old rats were significantly smaller than those seen in cells of 10-day-olds and adults. The degree of hypoxic inhibition in these latter two groups was not significantly different. 4. In the presence of high [Mg2+], low [Ca2+] solutions, hypoxia (PO2, 16-23 mmHg) was without significant effect on residual K+ currents in cells from all age groups. 5. These observations indicate that K+ current density increases with postnatal age in the rat. Between days 4 and 10, there appears to be a predominant enhancement of KCa channels, and over the same age range hypoxic sensitivity of K+ currents increases. Our findings demonstrate that this latter observation arises because hypoxia selectively inhibits KCa channels in cells at all ages studied. These results suggest an important role for KCa channels in postnatal maturation of hypoxic chemoreception in the rat carotid body.
机译:1.使用全细胞膜片钳记录来研究从大鼠分离的1型颈动脉体细胞的K +电流可能与年龄有关的变化。从4日龄,10日龄和成年大鼠(>或= 5周龄)分离的细胞中测得,K +电流密度随年龄增加而增加。 2.高[Mg2 +](6 mM),低[Ca2 +](0.1 mM)溶液可逆抑制的电流比例,表明归因于Ca(2+)敏感K +(KCa)通道激活的电流比例尽管这两个年龄组的内向Ca2 +电流密度相似,但与10天龄大鼠相比,4天龄大鼠的细胞中的β1明显更小。在10天龄和成年1型细胞中,高[Mg2 +]和低[Ca2 +]溶液对K +电流的抑制作用相似。 3.低氧(PO2,16-23 mmHg)导致所有年龄组大鼠的I型细胞可逆减少。但是,在4日龄大鼠的细胞中观察到的减少明显小于在10日龄及成年细胞中观察到的减少。后两组的低氧抑制程度无明显差异。 4.在存在高[Mg2 +]和低[Ca2 +]溶液的情况下,缺氧(PO2,16-23 mmHg)对所有年龄组细胞的残留K +电流均无显着影响。 5.这些观察结果表明,大鼠的K +电流密度随出生年龄的增加而增加。在第4天到第10天之间,KCa通道似乎主要增强,并且在相同年龄范围内,K +电流的低氧敏感性增加。我们的发现表明,后一种观察是由于缺氧选择性抑制了所有研究年龄细胞中的KCa通道。这些结果表明,KCa通道在大鼠颈动脉体内缺氧化学感受的产后成熟中具有重要作用。

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