BROWN D A
Br J Pharmacol Chemother. 1962 Aug;19(1):111-9. doi: 10.1111/j.1476-5381.1962.tb01431.x.
The intra-arterial injection of chloral hydrate potentiated the transmission of nerve impulses through the cat superior cervical ganglion, antagonized the ganglionblocking action of hexamethonium, and greatly enhanced the ganglion-stimulant action of acetylcholine. Effects on the ganglion-stimulant actions of carbachol, nicotine, tetramethylammonium and potassium chloride were slight or absent. Chloral hydrate itself usually had no direct stimulant action. The neuromuscular-blocking action of tubocurarine on the isolated rat diaphragm preparation was completely and rapidly reversed by chloral hydrate. This reversal was prevented by previoustreatment of the muscle with neostigmine. Chloral hydrate potentiated the actions of acetylcholine and nicotine on the isolated rabbit duodenum, and, in concentrations exceeding 1 mg/ml., produced a spasm which was abolished by hyoscine but not by mepyramine. It was concluded that these eserine-like effects were manifestations of an anticholinesterase action of chloral hydrate. Neither chloralose nor trichlorethanol showed evidence of this property.
水合氯醛动脉内注射增强了神经冲动通过猫颈上神经节的传递,拮抗了六甲铵的神经节阻断作用,并大大增强了乙酰胆碱的神经节兴奋作用。对氨甲酰胆碱、尼古丁、四甲铵和氯化钾的神经节兴奋作用影响轻微或无影响。水合氯醛本身通常无直接兴奋作用。氯醛水合物可完全且迅速逆转筒箭毒碱对离体大鼠膈肌标本的神经肌肉阻断作用。预先用新斯的明处理肌肉可防止这种逆转。水合氯醛增强了乙酰胆碱和尼古丁对离体兔十二指肠的作用,且浓度超过1mg/ml时会产生痉挛,该痉挛可被东莨菪碱消除,但不能被美吡拉敏消除。得出的结论是,这些类似毒扁豆碱的作用是水合氯醛抗胆碱酯酶作用的表现。氯醛糖和三氯乙醇均未显示出这种特性的证据。