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首页> 外文期刊>Advances in Experimental Medicine and Biology >Chronic hypoxia induces changes in the central nervous system processing of arterial chemoreceptor input.
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Chronic hypoxia induces changes in the central nervous system processing of arterial chemoreceptor input.

机译:慢性缺氧会引起中枢神经系统处理动脉化学感受器输入的变化。

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摘要

Chronic hypoxia increases the hypoxic ventilatory response (HVR) in awake rats and the phrenic nerve response to carotid sinus nerve stimulation in anesthetized rats. An increased O2 sensitivity of the arterial chemoreceptors contributes to the increase in the HVR, but changes in the CNS processing of afferent information from arterial chemoreceptors are also involved. Adult male Sprague-Dawley rats were exposed to 0-7 days of hypobaric hypoxia (PIO2 = 80 Torr). Ventilation was measured in rats exposed to 0, 2 and 7 days of hypoxia using whole-body plethysmography. Ventilation increased after 2 days and remained elevated after 7 days of hypoxia. Following dopamine D2 receptor (D2-R) blockade in the CNS, frequency significantly decreased after 0 and 7 days of hypoxia, but did not change significantly after 2 days of hypoxia. In anesthetized rats, the phrenic nerve response to carotid sinus nerve stimulation was reduced following systemic D2-R blockade in control rats and those exposed to 7 days of hypoxia. After 2 days of hypoxia, there was no effect of blocking systemic D2-R. To determine whether changes in D2-R mRNA precede physiological changes, competitive RT-PCR was used to quantify D2-R mRNA in micropunches from the nucleus tractus solitarius (NTS) in normoxic and chronically hypoxic rats. In hypoxia, D2-R mRNA in the caudal NTS initially increased (6-12 hours) and then decreased below control levels (24 hours-7 days). These results show that chronic hypoxia causes time-dependent changes in D2-R that could result in changes in the ventilatory response to hypoxia.
机译:慢性缺氧会增加清醒大鼠的低氧通气反应(HVR),并在麻醉大鼠中增加对颈动脉窦神经刺激的神经反应。动脉化学感受器的O2敏感性增加导致HVR的增加,但是也涉及CNS处理来自动脉化学感受器的传入信息的变化。成年雄性Sprague-Dawley大鼠暴露于低压缺氧0-7天(PIO2 = 80托)。使用全身体积描记法对暴露于缺氧0、2和7天的大鼠进行通气测量。缺氧2天后通气增加,缺氧7天后通气保持升高。在中枢神经系统中多巴胺D2受体(D2-R)阻滞后,缺氧0和7天后频率显着降低,但缺氧2天后频率没有明显变化。在麻醉的大鼠中,对照组和暴露于缺氧7天的大鼠的全身D2-R阻断后,对颈动脉窦神经刺激的phr神经反应降低。缺氧2天后,没有阻断全身D2-R的作用。为了确定D2-R mRNA的变化是否先于生理学变化,使用竞争性RT-PCR定量测定了常氧和慢性低氧大鼠的孤束核(NTS)微穿孔中的D2-R mRNA。在缺氧状态下,尾部NTS中的D2-R mRNA最初升高(6-12小时),然后降至低于对照水平(24小时7天)。这些结果表明,慢性缺氧会引起D2-R的时间依赖性变化,这可能导致对缺氧的通气反应发生变化。

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