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内侧膝状核中胆碱能感受神经元的特性

Properties of cholinoceptive neurones in the medial geniculate nucleus.

作者信息

Tebecis A K

出版信息

Br J Pharmacol. 1970 Jan;38(1):117-37. doi: 10.1111/j.1476-5381.1970.tb10341.x.

Abstract
  1. Acetylcholine (ACh), other cholinomimetics, cholinesterase inhibitors and cholinergic antagonists were administered iontophoretically to medial geniculate (MG) neurones and their effects on chemically or neurally evoked responses recorded extracellularly.2. Acetylcholine had excitant actions on 45% of the neurones tested. Most of these were of a slow time course. Desensitization to the excitant effects was frequently observed.3. Acetylcholine excited 91% of neurones activated antidromically by stimulation of the auditory cortex, 71% of neurones activated synaptically from the auditory cortex, 74% of neurones activated from the inferior colliculus and 100% of geniculo-cortical relay neurones.4. Acetylcholine had depressant effects, which were generally of a rapid time course, on 29% of MG neurones. No desensitization to the depressant effects was observed.5. On 4% of neurones, ACh had both excitant and depressant effects. Such "dual" effects were manifested either as an initial excitation followed by a depression, or as a depression followed by an excitation.6. Eserine, neostigmine and edrophonium potentiated both excitant and depressant actions of ACh on many cells. Neostigmine and edrophonium occasionally antagonized the effects of ACh.7. Atropine, hyoscine, dihydro-beta-erythroidine, hexamethonium and (+)-tubocurarine antagonized both excitant and depressant effects of ACh. The muscarinic blocking agents were usually more effective than the nicotinic agents.8. Carbamylcholine, acetyl-beta-methylcholine, nicotine, butyrylcholine, arecoline and pilocarpine had excitant, depressant or no effects on MG neurones. Generally, carbamylcholine was more potent than acetyl-beta-methylcholine and ACh, which were more potent than nicotine. Butyrylcholine, arecoline and pilocarpine were even less potent, often having no effect.9. The cholinomimetics generally had similar effects to those of ACh on the same neurones, but sometimes were quite different. Carbamylcholine, acetyl-beta-methylcholine and nicotine antagonized the effects of ACh on some neurones.10. The results suggest that cholinoceptive receptors on MG neurones are not homogeneous. Although there are possibly some purely muscarinic and purely nicotinic receptors, the majority appear to be of intermediate muscarinic-nicotinic type. These mediate either excitation or inhibition.
摘要
  1. 将乙酰胆碱(ACh)、其他拟胆碱药、胆碱酯酶抑制剂及胆碱能拮抗剂通过离子导入法作用于内侧膝状体(MG)神经元,并观察它们对细胞外记录的化学或神经诱发反应的影响。

  2. 乙酰胆碱对45%的受试神经元有兴奋作用。其中大多数作用的时间进程缓慢。对兴奋作用的脱敏现象经常可见。

  3. 乙酰胆碱兴奋了91%经听觉皮层刺激逆向激活的神经元、71%从听觉皮层突触激活的神经元、74%从下丘激活的神经元以及100%的膝状体 - 皮层中继神经元。

  4. 乙酰胆碱对29%的MG神经元有抑制作用,其作用时间进程通常较快。未观察到对抑制作用的脱敏现象。

  5. 在4%的神经元上,乙酰胆碱既有兴奋作用又有抑制作用。这种“双重”作用表现为先是兴奋后是抑制,或者先是抑制后是兴奋。

  6. 毒扁豆碱、新斯的明和依酚氯铵增强了乙酰胆碱对许多细胞的兴奋和抑制作用。新斯的明和依酚氯铵偶尔会拮抗乙酰胆碱的作用。

  7. 阿托品、东莨菪碱、二氢 - β - 刺桐啶、六甲铵和(+) - 筒箭毒碱拮抗乙酰胆碱的兴奋和抑制作用。毒蕈碱阻断剂通常比烟碱阻断剂更有效。

  8. 氨甲酰胆碱、乙酰 - β - 甲基胆碱、烟碱、丁酰胆碱、槟榔碱和毛果芸香碱对MG神经元有兴奋、抑制或无作用。一般来说,氨甲酰胆碱比乙酰 - β - 甲基胆碱和乙酰胆碱更有效,而乙酰胆碱又比烟碱更有效。丁酰胆碱、槟榔碱和毛果芸香碱效力更低,常常无作用。

  9. 拟胆碱药通常对同一神经元产生与乙酰胆碱相似的作用,但有时也有很大差异。氨甲酰胆碱、乙酰 - β - 甲基胆碱和烟碱在某些神经元上拮抗乙酰胆碱的作用。

  10. 结果表明,MG神经元上的胆碱能受体并非同质。虽然可能存在一些纯毒蕈碱型和纯烟碱型受体,但大多数似乎是中间型毒蕈碱 - 烟碱型。这些受体介导兴奋或抑制。

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Studies on cholinergic transmission in the medial geniculate nucleus.内侧膝状核胆碱能传递的研究。
Br J Pharmacol. 1970 Jan;38(1):138-47. doi: 10.1111/j.1476-5381.1970.tb10342.x.

本文引用的文献

3
The location of cholinesterase in the central nervous system.胆碱酯酶在中枢神经系统中的位置。
Q J Exp Physiol Cogn Med Sci. 1952;37(2):61-74. doi: 10.1113/expphysiol.1952.sp000983.
6
ACTIONS OF DRUGS ON SINGLE NEURONES IN THE BRAIN-STEM.药物对脑干中单神经元的作用。
Br Med Bull. 1965 Jan;21:15-8. doi: 10.1093/oxfordjournals.bmb.a070349.
8
THE EXCITATION OF THALAMIC NEURONES BY ACETYLCHOLINE.乙酰胆碱对丘脑神经元的兴奋作用。
Acta Physiol Scand. 1964 May-Jun;61:85-99. doi: 10.1111/j.1748-1716.1964.tb02945.x.

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