Pharmacological properties of feline red nucleus

R. Davis , P.C. Vaughan
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引用次数: 30

Abstract

Biogenic amines and related compounds, and certain amino acids were applied by microelectrophoresis onto single red nucleus neurons. The cats were either lightly anesthetized or specially prepared in the unanesthetized state.l-Glutamic anddl-homoeysteic acids were potent excitants while gamma-aminobutyric acid was a strong depressant of neuronal activity. Acetylcholine and carbamylcholine, 5-hydroxytryptamine and lysergic acid diethylamide, noradrenaline and dopamine and other phenylethylamines stopped brachio-rubral synaptic transmission, reduced “spontaneous” firing and amino-acid evoked firing of RN neurons. Parenterally administered drugs which disturb motor coordination, such as lysergic acid diethylamide, bufotenine and mephenesin depress directly or indirectly rubral neuronal activity. 4-Methoxyphenylethylamine when applied locally did depress rubral neurons. However, when applied intravenously 4-methoxyphenylethylamine caused a hypokinetic rigid syndrome to develop; parallel to the increases in muscle tension and electromyogram activity were increases in rubral neuronal firing. The evidence presented and from a Preliminary Note (H. McLennan) indicates that the transmitter released from the brachium fibers to excite rubral neurons is not acetylcholine. The rubro-cerebellar fibers may be cholinergic.

猫红核的药理性质
生物胺及其相关化合物和某些氨基酸通过微电泳应用于单个红核神经元。猫被轻微麻醉或在未麻醉状态下特别准备。l-谷氨酸和dl-同半胱氨酸是有效的兴奋剂,而γ -氨基丁酸是神经元活性的强抑制剂。乙酰胆碱和氨甲酰胆碱、5-羟色胺和麦角酸二乙胺、去甲肾上腺素和多巴胺等苯乙胺阻止臂-脑突触传递,减少RN神经元的“自发”放电和氨基酸诱发放电。肠外注射干扰运动协调的药物,如麦角酸二乙胺、丁氟替宁和甲苯二酚,可直接或间接抑制脑神经元活动。局部应用4-甲氧基苯乙胺可抑制脑区神经元。然而,当静脉注射4-甲氧基苯乙胺时,会导致低运动僵硬综合征的发生;与肌肉张力和肌电图活动的增加相平行的是脑皮层神经元放电的增加。初步记录(H. McLennan)提供的证据表明,从臂纤维释放的刺激小脑神经元的递质不是乙酰胆碱。红丘-小脑纤维可能是胆碱能纤维。
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