Izumi H, Nakamura I
Departments of Autonomic Neuroscience and Hospital Pharmacy, Tohoku University School of Dentistry, Sendai 980-8575, Japan.
Am J Physiol Regul Integr Comp Physiol. 2000 Jul;279(1):R332-9. doi: 10.1152/ajpregu.2000.279.1.R332.
In anesthetized cats, we 1) compared the effects of antihypertensive agents (nifedipine, clonidine, phentolamine, propranolol, and nitroprusside) on the parasympathetic vasodilations elicited by lingual nerve (LN) stimulation in the lower lip and tongue and 2) investigated the mechanisms underlying the inhibitory effect of nifedipine on parasympathetic lower lip vasodilation. At the doses used, each antihypertensive agent reduced systemic arterial blood pressure by approximately 20 mmHg; however, the parasympathetic vasodilation elicited by LN stimulation was significantly reduced only by nifedipine. This inhibitory effect of nifedipine was not seen when LN was stimulated during ongoing repetitive stimulation of the superior cervical sympathetic trunk at 1-Hz frequency. This suggests that the ability of lip and tongue blood vessels to relax to parasympathetic stimulation is not directly impaired by this calcium channel blocker and that the inhibitory effects of nifedipine seen here probably resulted from an action on postsynaptic sites in vascular smooth muscle that caused a reduction in preexisting sympathetic vasoconstrictor tone (by inhibiting calcium influx into the vascular smooth muscle cell).
在麻醉猫中,我们:1)比较了抗高血压药物(硝苯地平、可乐定、酚妥拉明、普萘洛尔和硝普钠)对舌神经(LN)刺激下唇和舌头所引发的副交感神经血管舒张的影响;2)研究了硝苯地平对副交感神经下唇血管舒张抑制作用的潜在机制。在所使用的剂量下,每种抗高血压药物均使体循环动脉血压降低约20 mmHg;然而,仅硝苯地平显著降低了LN刺激所引发的副交感神经血管舒张。当在以1 Hz频率持续重复刺激颈上交感神经干期间刺激LN时,未观察到硝苯地平的这种抑制作用。这表明该钙通道阻滞剂并未直接损害唇和舌血管对副交感神经刺激的舒张能力,此处观察到的硝苯地平的抑制作用可能是由于其作用于血管平滑肌的突触后位点,导致预先存在的交感神经血管收缩张力降低(通过抑制钙流入血管平滑肌细胞)。