Tsay B L, Lin M T
Neuroendocrinology. 1982;35(3):173-7. doi: 10.1159/000123377.
The effects of administration of thyrotrophic-releasing hormone (TRH) into the lateral cerebral ventricle on cardiovascular functions were assessed in both urethane-anesthetized and unanesthetized rats. Intracerebroventricular administration of TRH (10-60 micrograms in 5.0 microliters volume) caused a dose-dependent increase in both the heart rate and the mean arterial pressure. For example, both the heart rate and the arterial pressure rose almost immediately and reached their maximal levels about 4 min after an injection of 40 micrograms TRH. The cardiovascular responses recovered about 10 min after the TRH injection. In addition, reflex bradycardia was produced by intravenous infusion of epinephrine (1.0-5.0 micrograms/kg) in rats. Over the dose range of epinephrine used, a dose-dependent bradycardia was obtained. It was found that intracerebroventricular pretreatment of animals with TRH, although causing no change in the epinephrine-induced pressor effect, did reduce the epinephrine-induced reflex bradycardia in rats. However, intravenous pretreatment of animals with the same dose of TRH had no effect on the epinephrine-induced bradycardia. Thus, the data indicate that TRH acts through a central mechanism to inhibit reflex bradycardia mediated through baroreceptor reflexes in response to acute increase in blood pressure.
在氨基甲酸乙酯麻醉和未麻醉的大鼠中,评估了向侧脑室注射促甲状腺激素释放激素(TRH)对心血管功能的影响。脑室内注射TRH(5.0微升体积中含10 - 60微克)导致心率和平均动脉压呈剂量依赖性增加。例如,注射40微克TRH后,心率和动脉压几乎立即上升,并在约4分钟后达到最高水平。TRH注射后约10分钟,心血管反应恢复。此外,静脉注射肾上腺素(1.0 - 5.0微克/千克)可在大鼠中引发反射性心动过缓。在所使用的肾上腺素剂量范围内,可获得剂量依赖性心动过缓。研究发现,用TRH对动物进行脑室内预处理,虽然不会改变肾上腺素引起的升压效应,但确实会降低大鼠中肾上腺素引起的反射性心动过缓。然而,用相同剂量的TRH对动物进行静脉预处理,对肾上腺素引起的心动过缓没有影响。因此,数据表明TRH通过中枢机制起作用,以抑制在血压急性升高时通过压力感受器反射介导的反射性心动过缓。