Balaszczuk A M, Arranz C T, Martinez Seeber A
Departamento de Ciencias Biológicas, Facultad de Farmacia y Bioquímica, U.B.A., Argentina.
Arch Int Physiol Biochim. 1987 Jun;95(2):167-71. doi: 10.3109/13813458709104530.
Baroreflex control of cardiovascular parameters was studied in control, atropine- and guanethidine-treated rats. Baroreceptor activity was tested by the relationship between the increase in blood pressure produced by a phenylephrine administration (bolus ov infusion) and the induced bradycardia. No differences were observed in basal arterial blood pressure and heart rate between treated- and control rats. Baroreceptor sensitivity was lower in atropine- or guanethidine-treated rats than in control animals. Baroreceptor activity has two components: a first, rapid, predominantly parasympathetic and a second, slower, that is mediated by both parasympathetic and sympathetic efferent pathways.
在对照大鼠、阿托品处理大鼠和胍乙啶处理大鼠中研究了压力反射对心血管参数的控制。通过去氧肾上腺素给药(推注或输注)引起的血压升高与诱发的心动过缓之间的关系来测试压力感受器活性。处理组大鼠和对照组大鼠的基础动脉血压和心率未观察到差异。阿托品或胍乙啶处理的大鼠的压力感受器敏感性低于对照动物。压力感受器活性有两个组成部分:第一个是快速的,主要是副交感神经介导的;第二个是较慢的,由副交感神经和交感神经传出途径共同介导。