Nolan A M, Erhardt W
Institute of Experimental Surgery, Technical University, Munich, FRG.
J Vet Pharmacol Ther. 1990 Mar;13(1):29-35. doi: 10.1111/j.1365-2885.1990.tb00744.x.
The alpha 2 agonist xylazine produced a dose-dependent decrease in mean arterial blood pressure in conscious rabbits when injected intrathecally (i.t.) through a cannula previously implanted under general anaesthesia. Intrathecal administration of 200 and 400 micrograms of xylazine produced a significant reduction in arterial blood pressure from control values (maximum depressions of 25% and 33%, respectively). There was little effect on cardiac output and arterial carbon-dioxide tension and no effect on respiratory rate, arterial oxygen tension and pulse rate. Intrathecal injection of 100 microliters of 0.9% saline had no effect. Intravenous (i.v.) tolazoline (0.5 mg/kg) abolished xylazine-induced hypotension (200 micrograms) in four rabbits. Contrast radiography revealed that 100 microliters of solution injected i.t. in anaesthetized rabbits spread distally over eight vertebral spaces. There was little rostral spread. It was concluded that xylazine-induced hypotension following i.t. injection was due to local activation of alpha 2 adrenoceptors present in the thoracic spinal cord. It is postulated that spinal alpha 2 adrenoceptors may play an important role in the hypotension recorded in animals after parenteral injection of xylazine.
α2 激动剂赛拉嗪在通过先前在全身麻醉下植入的套管鞘内注射(i.t.)时,可使清醒家兔的平均动脉血压呈剂量依赖性下降。鞘内注射200微克和400微克赛拉嗪可使动脉血压较对照值显著降低(最大降幅分别为25%和33%)。对心输出量和动脉二氧化碳张力影响很小,对呼吸频率、动脉血氧张力和脉搏率无影响。鞘内注射100微升0.9%生理盐水无作用。静脉注射(i.v.)妥拉唑啉(0.5毫克/千克)可消除4只家兔中赛拉嗪(200微克)诱导的低血压。造影显示,在麻醉家兔中鞘内注射100微升溶液可向远侧扩散至8个椎间隙。向头侧扩散很少。得出的结论是,鞘内注射后赛拉嗪诱导的低血压是由于胸段脊髓中存在的α2肾上腺素能受体的局部激活。据推测,脊髓α2肾上腺素能受体可能在动物经胃肠外注射赛拉嗪后记录到的低血压中起重要作用。