尼麦角林对正常血压或自发性高血压大鼠心率的影响。中枢α -1受体的可能参与]。

Journal de pharmacologie Pub Date : 1986-01-01
A M Huchet, H Schmitt
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引用次数: 0

摘要

研究了nicergoline(一种优先阻断α - 1-肾上腺素能受体的药物)在麻醉的正常血压或自发性高血压(SH)大鼠中的心血管作用。尼麦角碱(300微克/公斤,静脉注射)可显著降低对照组、双迷走神经切除或β -阻断的正常血压或高血压大鼠的血压和心率。在双侧迷走神经切断和β -阻断的大鼠中,尼麦角碱降低了平均血压,但不再改变心率。因此,我们推测尼麦角林可能通过抑制中枢α 1-肾上腺素受体而降低交感神经张力并增加迷走神经活动。与血压正常的SHR组相比,双迷走神经切除SHR组尼科麦角碱诱导的心动过缓更严重。脑室内注射尼麦角林(30微克/千克)没有改变血压正常对照组、双迷走神经切除或β -阻断大鼠的心率。相反,大池注射尼科麦角碱(30微克/千克)可引起三组正常血压大鼠明显的心动过缓。在所有接受尼麦角林集中治疗的组中,血压都以同样的方式降低。综上所述,尼麦角碱可能通过外周α -肾上腺素受体阻断降低血压,并通过抑制主要分布于脑干的α - 1-肾上腺素受体调节自主神经活动。
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[The effects of nicergoline on the heart rate in the normotensive or spontaneously hypertensive rat. Possible participation of central alpha-1 receptors].

The cardiovascular effects of nicergoline, a preferential alpha 1-adrenoceptor blocking drug, were studied in anaesthetized normotensive or spontaneously hypertensive (SH) rats. Nicergoline (300 micrograms/kg, i.v.) significantly reduced blood pressure and heart rate in control, bivagotomized or beta-blocked normotensive or SH rats. In bilaterally vagotomized and beta-blocked rats, nicergoline reduced mean blood pressure but did no longer modify heart rate. Thus, it is postulated that nicergoline could reduce the sympathetic tone and increase the vagal nerve activity, possibly by inhibiting central alpha 1-adrenoceptors. The nicergoline--induced bradycardia was greater in bivagotomized SHR than in normotensive ones. Intracerebroventricular injections of nicergoline (30 micrograms/kg) did not modify heart rate in normotensive control, bivagotomized or beta-blocked rats. On the contrary, nicergoline (30 micrograms/kg) injected into the cisterna magna induced a significant bradycardia in the three groups of normotensive rats. Blood pressure was reduced in the same way in all groups centrally treated by nicergoline. In conclusion, it seems that nicergoline reduces blood pressure by peripheral alpha-adrenoceptor blockade and modulates the autonomic nervous activity by inhibiting alpha 1-adrenoceptors mainly localized in the brainstem.

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