Lundy P M
Can J Physiol Pharmacol. 1978 Oct;56(5):857-62. doi: 10.1139/y78-134.
Following intravenous administration of the cholinesterase reactivator HS-6 (30 mg/kg), blood pressure fell (up to 50 mmHg) and maximal blood levels of HS-6 reached 242 microgram/ml. HS-6 attenuated the pressor response resulting from carotid occlusion and the depressor effect of vagal stimulation. Doses of HS-6 below those used to protect against soman in different animal species (10--30 mumol/kg) progressively blocked the ganglion-stimulating effects of nicotine and dimethylphenylpiperazinium but not the pressor effect following adrenaline, a pattern similar to that produced by hexamethonium but only 1/84 as potent. HS-6, like hexamethonium and mecamylamine, progressively blocked the contraction of the nictitating membrane of the cat resulting from preganglionic stimulation. The results indicate that HS-6 possesses ganglion-blocking properties at doses likely to be used in the protection against soman poisoning. The ganglion-blocking properties of the drug may be a factor in the beneficial effects of HS-6.
静脉注射胆碱酯酶复活剂HS-6(30毫克/千克)后,血压下降(最高达50毫米汞柱),HS-6的最大血药浓度达到242微克/毫升。HS-6减弱了颈动脉闭塞引起的升压反应以及迷走神经刺激的降压作用。在不同动物物种中,低于用于防护梭曼的剂量(10 - 30微摩尔/千克)的HS-6逐渐阻断了尼古丁和二甲基苯基哌嗪鎓的神经节刺激作用,但不阻断肾上腺素后的升压作用,这种模式与六甲铵产生的模式相似,但效力仅为其1/84。与六甲铵和美加明一样,HS-6逐渐阻断了节前刺激引起的猫瞬膜收缩。结果表明,HS-6在可能用于防护梭曼中毒的剂量下具有神经节阻断特性。该药物的神经节阻断特性可能是HS-6产生有益作用的一个因素。