Puke M J, Luo L, Xu X J
Department of Anaesthesiology and Intensive Care, Karolinska Hospital, Stockholm, Sweden.
Eur J Pharmacol. 1994 Aug 1;260(2-3):227-32. doi: 10.1016/0014-2999(94)90341-7.
Two putative agonists of subtypes of alpha 2-adrenoceptors, guanfacine (alpha 2A) and ST-91 ([2,6-dicthylphenylamino]-2-imidazoline, alpha 2C), were applied intrathecally and their effects on autotomy behaviour and on the flexor reflex before and after sciatic nerve section were examined. Neither drug influenced autotomy during a 17-day observation period. Both drugs dose dependently depressed the flexor reflex in rats with intact sciatic nerves. After axotomy, the sensitivity of the flexor reflex to guanfacine and ST-91 was moderately increased compared to normals. ST-91 i.t. at high doses evoked motor discharges, an effect which was reversed by the alpha 1-adrenoceptor antagonist, WB4101 (2-[2,6-dimethyoxyphenoxyethyl]-aminomethyl-1,4-benzodioxane). Thus, the effect of i.t. clonidine on the flexor reflex and autotomy behaviour observed previously may not involve its action on alpha 2A- and alpha 2C-adrenoceptors. Furthermore, due to its motor effect which may involve activation of alpha 1-adrenoceptors, ST-91 may not be a suitable tool to study the physiological function of spinal alpha 2C-adrenoceptors.
鞘内注射两种假定的α2 -肾上腺素能受体亚型激动剂,胍法辛(α2A)和ST - 91([2,6 - 二乙基苯氨基]-2 -咪唑啉,α2C),并检测它们对坐骨神经切断前后自残行为和屈肌反射的影响。在17天的观察期内,两种药物均未影响自残行为。两种药物均剂量依赖性地抑制坐骨神经完整大鼠的屈肌反射。轴突切断后,与正常大鼠相比,屈肌反射对胍法辛和ST - 91的敏感性适度增加。高剂量鞘内注射ST - 91可诱发运动放电,该效应可被α1 -肾上腺素能受体拮抗剂WB4101(2 - [2,6 - 二甲氧基苯氧基乙基]-氨基甲基-1,4 -苯并二恶烷)逆转。因此,先前观察到的鞘内注射可乐定对屈肌反射和自残行为的影响可能不涉及其对α2A -和α2C -肾上腺素能受体的作用。此外,由于其可能涉及α1 -肾上腺素能受体激活的运动效应,ST - 91可能不是研究脊髓α2C -肾上腺素能受体生理功能的合适工具。