Pertovaara A, Kemppainen P, Kauppila T
Department of Physiology, University of Helsinki, Finland.
Pharmacol Biochem Behav. 1991 Feb;38(2):287-92. doi: 10.1016/0091-3057(91)90280-f.
In the pentobarbitone-anesthetized cat, the threshold of the tooth pulp-elicited jaw-opening reflex was elevated in a dose-dependent way (30-100 micrograms/kg, IP) following the administration of medetomidine, an alpha-2-adrenoceptor agonist. This elevation was significantly reduced by atipamezole (1 mg/kg, IP), an alpha-2-adrenoceptor antagonist. The inhibitory interaction between two successive dental stimuli applied to the same tooth (in-field inhibition) was suppressed by a lower dose of medetomidine (30 micrograms/kg) than the threshold elevation to single electrical pulses (55 micrograms/kg). Only the highest dose of medetomidine used (100 micrograms/kg) significantly influenced the temporally facilitated (in-field facilitation) response. In comparison, cocaine, a nonspecific monoaminergic agent, did not produce a significant threshold elevation of the tooth pulp-elicited jaw-opening reflex (1-25 mg/kg, IP). It is concluded that medetomidine, through an action on alpha-2-adrenoceptors, can suppress a predominantly nociceptive trigeminal reflex in anesthetized cats. The threshold evoked by single electric pulses, in-field inhibition, and in-field facilitation display differential sensitivities to medetomidine effects.
在戊巴比妥麻醉的猫中,给予α2肾上腺素能受体激动剂美托咪定(30 - 100微克/千克,腹腔注射)后,牙髓诱发的下颌张开反射阈值呈剂量依赖性升高。α2肾上腺素能受体拮抗剂阿替美唑(1毫克/千克,腹腔注射)可显著降低这种升高。与单次电脉冲阈值升高(55微克/千克)相比,较低剂量的美托咪定(30微克/千克)即可抑制施加于同一颗牙齿的两个连续牙科刺激之间的抑制性相互作用(场内抑制)。仅所用的最高剂量美托咪定(100微克/千克)对时间性易化(场内易化)反应有显著影响。相比之下,非特异性单胺能药物可卡因(1 - 25毫克/千克,腹腔注射)并未使牙髓诱发的下颌张开反射阈值显著升高。得出的结论是,美托咪定通过作用于α2肾上腺素能受体,可抑制麻醉猫中主要为伤害性的三叉神经反射。单次电脉冲诱发的阈值、场内抑制和场内易化对美托咪定效应表现出不同的敏感性。