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催眠药物依托咪酯在模型神经系统(颊神经节,东风螺)中的作用。

Effects of the hypnotic drug etomidate in a model nervous system (Buccal ganglia, Helix pomatia).

作者信息

Altrup U, Lehmenkühler A, Speckmann E J

机构信息

Institut für Experimentelle Epilepsieforschung, Münster, F.R.G.

出版信息

Comp Biochem Physiol C Comp Pharmacol Toxicol. 1991;99(3):579-87. doi: 10.1016/0742-8413(91)90290-a.

Abstract
  1. Effects of the hypnotic drug etomidate were studied with intracellular recordings of the identified neurons B1 to B4 of the buccal ganglia of Helix pomatia. 2. At threshold doses of 10 mumol/l, etomidate mainly affected interneuronal networks. 3. In concentrations above 200 mumol/l, the drug induced typical epileptic activities (paroxysmal depolarization shifts, PDS). Neurons B1 to B4 generated epileptic activities in differential concentration ranges. PDS were synchronized via electrical contacts. PDS could be blocked by the "calcium antagonist" verapamil but not by a block of chemical synaptic transmission. 4. In comparison with the epileptogenic drug pentylenetrazol, effective doses of etomidate to induce PDS were about 100 times lower.
摘要
  1. 利用细胞内记录法,对苹果螺颊神经节中已鉴定的神经元B1至B4进行研究,以探究催眠药依托咪酯的作用。2. 在阈剂量10微摩尔/升时,依托咪酯主要影响中间神经元网络。3. 浓度高于200微摩尔/升时,该药物诱发典型的癫痫活动(阵发性去极化漂移,PDS)。神经元B1至B4在不同浓度范围内产生癫痫活动。PDS通过电接触同步。PDS可被“钙拮抗剂”维拉帕米阻断,但化学性突触传递阻断剂无效。4. 与致癫痫药物戊四氮相比,诱导PDS的依托咪酯有效剂量约低100倍。

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