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5-羟色胺对皮层神经元的兴奋与抑制作用

Excitation and depression of cortical neurones by 5-hydroxytryptamine.

作者信息

Roberts M H, Straughan D W

出版信息

J Physiol. 1967 Nov;193(2):269-94. doi: 10.1113/jphysiol.1967.sp008357.

Abstract
  1. 5-Hydroxytryptamine (5-HT) and various 5-HT antagonists have been applied micro-electrophoretically from multibarrelled micropipettes into the environment of single neurones in the post-sigmoid and suprasylvian gyri of the cat cerebral cortex.2. In unanaesthetized animals (encéphale isolé) a high proportion of neurones (30%) were excited by 5-HT. This excitation usually had a rapid onset and was seen both in spontaneously active neurones and in otherwise quiescent neurones in which firing was induced by L-glutamate. Some neurones were so sensitive that the uncontrolled diffusion from micropipettes was sufficient to excite them. More cells were excited by 5-HT applied as a cation from solutions of the bimaleate salt than when solutions of the creatinine sulphate salt were used.3. In a high proportion of cells (33%) spontaneous firing or amino acid excitation was depressed by 5-HT.4. A mixed effect was seen in a small proportion (6%) of the cells tested; usually 5-HT caused an excitation initially which was followed by a depression. In other cells, desensitization occurred, and the excitatory effect of 5-HT was diminished or lost.5. When glutamate was used to excite otherwise quiescent cells, there was a significant increase in the number of cells excited by 5-HT and a significant decrease in the number of cells unaffected compared with spontaneously active cells.6. The micro-electrophoretic application of D-lysergic diethylamide (LSD 25), 2-brom LSD (BOL 148), methysergide (UML 491), or 2'- (3-dimethylaminopropylthio)cinnamanilide (SQ 10643) temporarily prevented excitation by 5-HT in half the cells tested. LSD and SQ 10643 were particularly potent in this respect. This antagonism of 5-HT excitation could still be seen when excitation of the cell by L-glutamate or acetylcholine (ACh) was unaffected.7. The depression induced by 5-HT was not prevented by the application of known 5-HT antagonists in the majority of the cells tested (93%). In two cells, however, the depression was reversibly prevented by these antagonists.8. Some cells tested with 5-HT were also tested with ACh or (-)-noradrenaline. The response of a cell to ACh was not significantly related to its response to 5-HT. The degree of correlation between the responses to noradrenaline and 5-HT was large, but not statistically significant with the small number of cells studied.9. The effects of 5-HT on cells in animals anaesthetized with alpha-chloralose did not differ significantly from its effects in unanaesthetized preparations. It is suggested that the use of this anaesthetic may prove a useful alternative to unanaesthetized preparations.10. The systemic injection of small quantities of thiopentone sodium selectively and reversibly reduced the sensitivity of some units to excitation by 5-HT at a time when the response to glutamate was unaffected. On other occasions, the 5-HT excitation was unaffected, though the response to glutamate was reduced.11. These results are discussed in relation to the possible nature of the 5-HT receptors in the cerebral cortex, and the interfering effects of anaesthesia on the response of brain cells to potential transmitter substances.
摘要
  1. 已用多管微量移液器将5-羟色胺(5-HT)及多种5-HT拮抗剂微量电泳施加于猫大脑皮质乙状结肠后回和颞上回单个神经元的周围环境中。

  2. 在未麻醉的动物(孤立脑)中,高比例的神经元(30%)被5-HT兴奋。这种兴奋通常起效迅速,在自发活动的神经元以及原本静止但由L-谷氨酸诱导放电的神经元中均可见到。一些神经元非常敏感,以至于微量移液器的非受控扩散就足以使其兴奋。与使用硫酸肌氨酸盐溶液相比,以顺丁烯二酸氢盐溶液形式作为阳离子施加的5-HT能使更多细胞兴奋。

  3. 在高比例的细胞(33%)中,5-HT抑制自发放电或氨基酸诱导的兴奋。

  4. 在一小部分(6%)受试细胞中观察到混合效应;通常5-HT最初引起兴奋,随后是抑制。在其他细胞中,出现脱敏现象,5-HT的兴奋作用减弱或消失。

  5. 当用谷氨酸兴奋原本静止的细胞时,与自发活动的细胞相比,被5-HT兴奋的细胞数量显著增加,未受影响的细胞数量显著减少。

  6. 微量电泳施加D-麦角酸二乙胺(LSD 25)、2-溴-LSD(BOL 148)、甲基麦角新碱(UML 491)或2'-(3-二甲氨基丙基硫代)肉桂苯胺(SQ 10643)可使受试细胞中的半数暂时免受5-HT的兴奋作用。LSD和SQ 10643在这方面尤为有效。当细胞对L-谷氨酸或乙酰胆碱(ACh)的兴奋作用未受影响时,仍可见到对5-HT兴奋作用的这种拮抗。

  7. 在大多数受试细胞(93%)中,已知的5-HT拮抗剂不能阻止5-HT诱导的抑制。然而,在两个细胞中,这些拮抗剂可可逆地阻止抑制。

  8. 一些用5-HT测试的细胞也用ACh或(-)-去甲肾上腺素进行了测试。细胞对ACh的反应与其对5-HT的反应无显著相关性。对去甲肾上腺素和5-HT反应之间的相关程度较大,但在研究的少量细胞中无统计学意义。

  9. 5-HT对用α-氯醛糖麻醉的动物细胞的作用与其在未麻醉制剂中的作用无显著差异。提示使用这种麻醉剂可能是未麻醉制剂的一种有用替代方法。

  10. 全身注射少量硫喷妥钠在对谷氨酸的反应未受影响时,能选择性且可逆地降低一些单位对5-HT兴奋的敏感性。在其他情况下,5-HT兴奋未受影响,而对谷氨酸的反应降低。

  11. 结合大脑皮质中5-HT受体的可能性质以及麻醉对脑细胞对潜在递质物质反应的干扰作用对这些结果进行了讨论。

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