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外侧膝状核中胆碱能感受细胞的研究。

A study of cholinoceptive cells in the lateral geniculate nucleus.

作者信息

Phillis J W, Tebĕcis A K, York D H

出版信息

J Physiol. 1967 Oct;192(3):695-713. doi: 10.1113/jphysiol.1967.sp008326.

Abstract
  1. The dorsal lateral geniculate nucleus (LGN) of the cat stains densely for acetylcholinesterase, which is present in intra-axonal and extracellular locations.2. Acetylcholine (ACh), cholinomimetic drugs, anticholinesterases and ACh antagonists were administered iontophoretically to neurones in the LGN.3. ACh excited eighty-six of 184 (46.7%) geniculate neurones and depressed seven (3.8%).4. The excitatory response to ACh was frequently larger than that to L-glutamate and had a comparable time course.5. There was a considerable variation in the proportion of ACh sensitive cells in different animals. ACh firing was facilitated by optic nerve or visual stimulation.6. Carbamylcholine was the most active of the choline esters tested, frequently exceeding ACh in potency. The other choline esters and nicotine were consistently less active than ACh.7. Anticholinesterases, eserine, neostigmine and edrophonium potentiated the action of ACh, and often caused excitation. Eserine caused an initial small enhancement in the amplitude of the focal potential evoked by optic nerve stimulation followed by a reduction in amplitude and prolongation of duration of the potential.8. Atropine and benzoquinonium effectively prevented the ACh excitation of many cells. Dihydro-beta-erythroidine failed to cause a significant reduction in the magnitude of the ACh response. All three ACh antagonists failed to reduce the excitant effects of optic nerve or visual stimulation.9. Stimulation of the mesencephalic reticular formation caused either an enhancement or a reduction in the excitability of ACh sensitive neurones in the LGN. Benzoquinonium abolished the excitatory effects of reticular formation stimulation.10. The findings presented in this paper suggest that ACh is the transmitter released by terminals of nerves of the reticular formation projection to the LGN.
摘要
  1. 猫的背外侧膝状核(LGN)对乙酰胆碱酯酶染色浓密,该酶存在于轴突内和细胞外位置。

  2. 将乙酰胆碱(ACh)、拟胆碱药物、抗胆碱酯酶药物和ACh拮抗剂通过离子导入法施用于LGN中的神经元。

  3. ACh使184个膝状神经元中的86个(46.7%)兴奋,使7个(3.8%)抑制。

  4. 对ACh的兴奋性反应通常比对L-谷氨酸的反应更大,且时间进程相似。

  5. 不同动物中对ACh敏感的细胞比例有相当大的差异。视神经或视觉刺激可促进ACh的发放。

  6. 氨甲酰胆碱是所测试的胆碱酯类中活性最高的,其效力常常超过ACh。其他胆碱酯类和尼古丁的活性始终低于ACh。

  7. 抗胆碱酯酶药物毒扁豆碱、新斯的明和依酚氯铵增强了ACh的作用,并常常引起兴奋。毒扁豆碱使视神经刺激诱发的局部电位幅度最初有小的增强,随后电位幅度减小,持续时间延长。

  8. 阿托品和苯喹铵有效地阻止了许多细胞对ACh的兴奋作用。二氢β-刺桐啶未能使ACh反应的幅度显著降低。所有这三种ACh拮抗剂都未能降低视神经或视觉刺激的兴奋作用。

  9. 刺激中脑网状结构可使LGN中对ACh敏感的神经元的兴奋性增强或减弱。苯喹铵消除了网状结构刺激的兴奋作用。

  10. 本文所呈现的研究结果表明,ACh是网状结构投射到LGN的神经末梢释放的神经递质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dad/1365537/fa061242b20b/jphysiol01117-0121-a.jpg

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