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Cardiovascular responses to peripheral chemoreflex activation and comparison of different methods to evaluate baroreflex gain in conscious mice using telemetry

机译:心血管对周围化学反射激活的反应以及使用遥测技术评估清醒小鼠压力反射增益的不同方法的比较

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摘要

Peripheral chemoreceptors located in the carotid bodies are the primary sensors of systemic hypoxia. Although the pattern of responses elicited by peripheral chemoreceptor activation is well established in rats, lambs, and rabbits, the cardiovascular responses to peripheral chemoreflex activation in conscious mice have not been delineated. Here we report that stimulation of peripheral chemoreceptors by potassium cyanide (KCN) in conscious mice elicits a unique biphasic response in blood pressure that is characterized by an initial and robust rise followed by a decrease in blood pressure, which is accompanied by a marked reduction in heart rate. The depressor and bradycardic responses to KCN were abolished by muscarinic receptor blockade with atropine, and the pressor response was abolished by α-adrenergic receptor blockade with prazosin, suggesting that vagal and sympathetic drive to the heart and sympathetic drive to the vasculature mediate these cardiovascular responses. These studies characterized the chemoreflex in conscious mice and established the reliability of using them for studying hypoxia-related diseases such as obstructive sleep apnea. In another series of experiments, two methods for analyzing baroreflex sensitivity were compared: the classical pharmacological approach using phenylephrine and sodium nitroprusside (i.e., the Oxford technique) or the sequence method for analyzing spontaneous baroreflex activity. Our findings indicate that both methods are reliable, and the sequence method certainly has its benefits as a predictive tool in the context of long-term noninvasive studies using telemetry. However, for absolute determination of baroreflex function, analysis of spontaneous baroreflex activity should be complemented by the classical pharmacological method.
机译:位于颈动脉体的周围化学感受器是系统性缺氧的主要传感器。尽管在大鼠,羔羊和兔子中已经很好地确定了由周围化学感受器激活引起的反应模式,但尚未明确意识小鼠对周围化学感受器激活的心血管反应。在这里,我们报告说,在有意识的小鼠中,氰化钾(KCN)对周围化学感受器的刺激会引起血压的独特双相反应,其特征是初始且稳定的升高,然后降低血压,同时伴随着显着的血压降低。心率。阿司匹林对毒蕈碱受体的阻滞作用可消除对KCN的抑郁和缓动反应,而对哌唑嗪的α-肾上腺素能受体的阻滞作用可消除对KCN的降压和缓动反应,这表明迷走神经和交感神经对心脏的驱动力以及交感神经对脉管系统的驱动作用介导了这些心血管反应。这些研究对清醒小鼠的化学反射进行了表征,并确立了将其用于研究与低氧相关疾病(如阻塞性睡眠呼吸暂停)的可靠性。在另一系列实验中,比较了两种分析压力感受器反射敏感性的方法:使用去氧肾上腺素和硝普钠的经典药理方法(即牛津技术)或分析自发压力感受器反射活性的序列方法。我们的发现表明,这两种方法都是可靠的,并且在使用遥测技术进行的长期非侵入性研究的背景下,测序方法无疑具有其作为预测工具的优势。但是,对于绝对压力反射功能的绝对测定,应通过经典药理学方法对自发压力反射活性进行分析。

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