Gillis R A, Kellar K J, Quest J A, Namath I J, Martino-Barrows A, Hill K, Gatti P J, Dretchen K
Department of Pharmacology, Georgetown University, School of Medicine, Washington.
Drugs. 1988;35 Suppl 6:20-33. doi: 10.2165/00003495-198800356-00004.
The major purpose of our study was to determine whether urapidil acts in the central nervous system (CNS) to lower arterial blood pressure. Once demonstrating a CNS antihypertensive action of urapidil we further set out to determine: (1) the relative role of a CNS antihypertensive action to the total antihypertensive effect of urapidil; (2) the brain site of action for the antihypertensive effect of urapidil; and, (3) the receptor mechanism whereby urapidil acts in the CNS to lower arterial blood pressure. Studies were conducted in chloralose-anaesthetised cats, and arterial blood pressure and heart rate were monitored. Drugs were administered intravenously (IV), into the cerebral ventricles (ICV), topically by application to the ventral surface of the medulla and by microinjection into specific nuclei. Receptor binding studies were also conducted using rat cerebral cortex homogenates. We found that injection of urapidil into the fourth ventricle decreased arterial pressure. Local application of urapidil to the ventral medullary surface also decreased arterial blood pressure. Microinjection of urapidil into one of the nuclei associated with the ventral surface of the medulla, the rostral part of the nucleus reticularis lateralis (rLRN), produced a similar degree of antihypertensive effect. The effect of urapidil was not altered by alpha 1-receptor blockade. Instead, the urapidil effect resembled that produced by drugs that stimulate serotonin (5-hydroxytryptamine)-1A receptors (B695-40 and 8-OH-DPAT). Furthermore, urapidil was found to have the highest potency for binding to serotonin-1A receptor sites (as compared to alpha 1- and alpha 2-receptor sites). Urapidil administered IV was shown to lower arterial blood pressure in part by blocking peripheral alpha 1-adrenoceptors but also, in high doses, by acting in the CNS to decrease central sympathetic outflow. These data indicate that urapidil is a unique drug, possessing both peripheral and CNS actions which contribute to its antihypertensive effect. Urapidil may also be unique in that its central action may involve activation of serotonin-1A receptors.
我们研究的主要目的是确定乌拉地尔是否通过作用于中枢神经系统(CNS)来降低动脉血压。一旦证实乌拉地尔具有中枢性降压作用,我们进一步着手确定:(1)中枢性降压作用在乌拉地尔总降压效果中的相对作用;(2)乌拉地尔降压作用的脑内作用部位;以及(3)乌拉地尔在中枢神经系统中降低动脉血压的受体机制。研究在氯醛糖麻醉的猫身上进行,并监测动脉血压和心率。药物通过静脉注射(IV)、脑室内注射(ICV)、局部应用于延髓腹侧面以及微量注射到特定核团给药。还使用大鼠大脑皮层匀浆进行了受体结合研究。我们发现,向第四脑室注射乌拉地尔可降低动脉压。将乌拉地尔局部应用于延髓腹侧面也可降低动脉血压。将乌拉地尔微量注射到与延髓腹侧面相关的核团之一,即外侧网状核的头端部分(rLRN),产生了相似程度的降压效果。乌拉地尔的作用不受α1受体阻断的影响。相反,乌拉地尔的作用类似于刺激5-羟色胺(5-羟色胺)-1A受体的药物(B695-40和8-OH-DPAT)所产生的作用。此外,发现乌拉地尔与5-羟色胺-1A受体位点结合的效力最高(与α1和α2受体位点相比)。静脉注射乌拉地尔显示,其降低动脉血压部分是通过阻断外周α1肾上腺素能受体,但在高剂量时也通过作用于中枢神经系统来减少中枢交感神经输出。这些数据表明,乌拉地尔是一种独特的药物,具有外周和中枢作用,这两种作用均有助于其降压效果。乌拉地尔可能还具有独特之处,即其中枢作用可能涉及5-羟色胺-1A受体的激活。