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首页> 外文期刊>American Journal of Physiology >Cardiovascular phenotype and temperature control in mice lacking thyroid hormone receptor-beta or both alpha1 and beta.
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Cardiovascular phenotype and temperature control in mice lacking thyroid hormone receptor-beta or both alpha1 and beta.

机译:缺乏甲状腺激素受体-β或α1和β的小鼠的心血管表型和温度控制。

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We have used a telemetry system to record heart rate, body temperature, electrocardiogram (ECG), and locomotor activity in awake, freely moving mice lacking thyroid hormone receptor (TR)-beta or TR-alpha1 and -beta (TR-alpha1/beta). The TR-alpha1/beta-deficient mice had a reduced heart rate compared with wild-type controls. The TR-beta-deficient mice showed an elevated heart rate, which, however, was unresponsive to thyroid hormone treatment regardless of hormonal serum levels. ECG revealed that the TR-beta-deficient mice had a shortened Q-Tend time in contrast to the TR-alpha1/beta-deficient mice, which exhibited prolonged P-Q and Q-Tend times. Mental or pharmacological stimulation of the sympathetic nervous system resulted in a parallel increase in heart rate in all animals. A single injection of a nonselective beta-adrenergic-receptor blocker resulted in a parallel decrease in all mice. The TR-alpha1/beta-deficient mice also had a 0.4 degrees C lower body temperature than controls, whereas no difference was observed in locomotor activity between the different strains of mice. Our present and previous results support the hypothesis that TR-alpha1 has a major role in determining heart rate under baseline conditions and body temperature and that TR-beta mediates a hormone-induced increase in heart rate.
机译:我们已经使用遥测系统记录清醒,缺乏甲状腺激素受体(TR)-β或TR-alpha1和-beta(TR-alpha1 / beta的自由移动小鼠)的心率,体温,心电图(ECG)和运动活动)。与野生型对照组相比,TR-alpha1 / beta缺陷型小鼠的心律降低。 TR-beta缺陷型小鼠显示出较高的心率,但是,无论激素血清水平如何,对甲状腺激素治疗均无反应。心电图显示TR-beta缺陷小鼠的Q-Tend时间缩短,而TR-alpha1 / beta缺陷小鼠的P-Q和Q-Tend时间延长。交感神经系统的精神或药理刺激导致所有动物的心率平行增加。单次注射非选择性β-肾上腺素受体阻滞剂会导致所有小鼠的平行减少。 TR-alpha1 / beta缺陷型小鼠的体温也比对照组低0.4摄氏度,而不同品系的小鼠的运动能力没有差异。我们目前和以前的结果支持以下假设:TR-alpha1在确定基线条件和体温下的心率中起主要作用,而TR-β介导激素诱导的心率增加。

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