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乙酰胆碱诱导的丘脑底核神经元兴奋的药理学特性。

Pharmacological properties of acetylcholine-induced excitation of subthalamic nucleus neurones.

作者信息

Feger J, Hammond C, Rouzaire-Dubois B

出版信息

Br J Pharmacol. 1979 Mar;65(3):511-5. doi: 10.1111/j.1476-5381.1979.tb07859.x.

Abstract
  1. In 15 rats anaesthetized with ketamine, microiontophoretically applied acetylcholine (ACh) excited all 58 cells studied in the subthalamic nucleus (STN). 2. The ACh-evoked excitation was slow in onset and outlasted the ACh application. There was no sign of desensitization when the ACh application was prolonged or repeated. The excitation was prolonged by a concomitant application of physostigmine. 3. Acetyl-beta-methyl choline and oxotremorine were effective cholinomimetics. Nicotine had no effect. 4. The ACh excitation was antagonized by stropine and scopolamine but not by mecamylamine. 5. It was condluded that STN ACh receptors are muscarinic in character. 6. Since large microiontophoretic applications of Mg2+ did not suppress ACh-evoked excitation, it is suggested that ACh acts postsynaptically. 7. The excitatory response of STN cells to striatal or pallidal stimulation was unaffected by atropine administered either microiontophoretically to single cells or intravenously (3 mg/kg) to the whole animal.
摘要
  1. 在15只用氯胺酮麻醉的大鼠中,微量离子透入法施加的乙酰胆碱(ACh)使丘脑底核(STN)中所研究的全部58个细胞兴奋。2. ACh诱发的兴奋起效缓慢且持续时间长于ACh施加时间。当ACh施加时间延长或重复时,没有脱敏迹象。同时应用毒扁豆碱可延长兴奋时间。3. 乙酰-β-甲基胆碱和氧化震颤素是有效的拟胆碱药。尼古丁无作用。4. ACh兴奋被东莨菪碱和阿托品拮抗,但不被美加明拮抗。5. 得出结论:STN的ACh受体具有毒蕈碱特性。6. 由于大量微量离子透入法施加Mg2+并未抑制ACh诱发的兴奋,提示ACh作用于突触后。7. 对单细胞微量离子透入法给予阿托品或对整个动物静脉注射(3mg/kg)阿托品,均不影响STN细胞对纹状体或苍白球刺激的兴奋反应。

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