Hageman G R, James T N, Urthaler F
Am Heart J. 1983 Sep;106(3):547-53. doi: 10.1016/0002-8703(83)90700-7.
Serotonin activates a cardiogenic hypertensive chemoreflex characterized by sudden hypertension. This study in 16 awake and 12 anesthetized dogs was conducted to examine the influence of changes in breathing or heart rate as they may influence the reflex hypertension. In all 28 dogs, either anesthetized or awake, there is a variable but brief initial reflex bradycardia and in all dogs there is transient ventilatory stimulation, but the response in every dog was characterized by hypertension within at most 10 seconds after administering serotonin. Treatment with atropine regularly eliminated the reflex bradycardia and caused the hypertension to appear soon (average of 6 seconds to maximal level). Atropine did not alter the reflex stimulation of breathing. Since atropine eliminated any transient bradycardia (and associated hypertension) but did not prevent reflex changes in breathing, we do not believe that breathing alteration plays any significant hemodynamic role in this reflex.
血清素激活一种以突然高血压为特征的心源性高血压化学反射。本研究对16只清醒犬和12只麻醉犬进行,旨在研究呼吸或心率变化对反射性高血压的影响,因为这些变化可能会影响反射性高血压。在所有28只犬(无论是麻醉的还是清醒的)中,都有一个可变但短暂的初始反射性心动过缓,并且所有犬都有短暂的通气刺激,但每只犬的反应都以在给予血清素后最多10秒内出现高血压为特征。用阿托品治疗通常可消除反射性心动过缓,并使高血压很快出现(平均6秒达到最大水平)。阿托品并未改变呼吸的反射性刺激。由于阿托品消除了任何短暂的心动过缓(以及相关的高血压),但并未阻止呼吸的反射性变化,因此我们认为呼吸改变在该反射中不发挥任何重要的血液动力学作用。