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The responses of cortical neurones to monoamines under differing anaesthetic conditions

机译:皮质神经元在不同麻醉条件下对单胺的反应

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摘要

1. Noradrenaline, isoprenaline, 5-hydroxytryptamine and acetylcholine have been applied into the environment of single neurones in the cat cerebral cortex by micro-iontophoresis. The influence of anaesthesia on the neuronal responses to these drugs was studied.2. In general, excitation of neurones by noradrenaline occurred commonly in both unanaesthetized encéphale isolé (48%) and N2O-halothane anaesthetized preparations (57%) while depressions were less frequent (24 and 20% respectively). The picture differed markedly in barbiturate anaesthetized animals where excitation was uncommon (12%) and the majority of cells (59%) was depressed by noradrenaline. Although fewer cells were studied, similar differences were obtained with isoprenaline and 5-hydroxytryptamine for the three types of preparation. In sharp contrast, the vast majority of cells was excited by acetylcholine in each of the preparations: encéphale isolé 84%; N2O-halothane 92%; barbiturate anaesthetized preparations 85%.3. The differing neuronal responses observed in these experimental situations were not the result of variations in the depth of anaesthesia.4. Although the depths at which neurones were encountered within the cortex did not differ in N2O-halothane and encéphale isolé preparations, significantly more cells were found in deeper layers of cortex in barbiturate preparations. The proportion of cells excited or depressed by noradrenaline was generally similar at each depth in the three preparations used.5. The distribution of rates of cell firing was strikingly similar in each preparation, and most of the cells studied had frequencies below 10/sec.6. The direction in which a cell responds to noradrenaline is mainly determined by the type of anaesthetic used, and not by the depth of anaesthesia, the rate of cell firing, or cell depth within the cortex. This suggests important differences in the central pharmacology of halothane and barbiturates.
机译:1.通过微离子电渗疗法将去甲肾上腺素,异戊二烯,5-羟色胺和乙酰胆碱用于猫大脑皮层的单个神经元环境。研究了麻醉对这些药物神经元反应的影响。2。通常,去甲肾上腺素对异戊二烯(48%)和N2O-氟烷麻醉(57%)的神经元兴奋通常发生在抑郁症(分别为24%和20%)的情况下。在巴比妥酸盐麻醉的动物中,图片明显不同,其中兴奋不常见(12%),而大多数细胞(59%)被去甲肾上腺素抑制。尽管研究的细胞较少,但对于三种类型的制剂,异丙肾上腺素和5-羟基色胺可获得相似的差异。与之形成鲜明对比的是,每种制剂中的绝大多数细胞都被乙酰胆碱激发:异戊烯脑84%; N2O-氟烷92%;巴比妥酸盐麻醉制剂85%3。在这些实验情况下观察到的不同神经元反应不是麻醉深度变化的结果。4。尽管在N2O-氟烷和脑啡肽中,皮层中遇到神经元的深度没有差异,但是在巴比妥酸盐制剂中,深层皮层中发现的细胞明显更多。在使用的三种制剂中,去甲肾上腺素兴奋或抑制的细胞比例在每个深度通常相似。5。在每种制剂中,细胞发射速率的分布惊人地相似,并且大多数研究细胞的频率低于10 / sec.6。细胞对去甲肾上腺素反应的方向主要取决于所用麻醉剂的类型,而不取决于麻醉深度,细胞发射速率或皮层内细胞深度。这表明氟烷和巴比妥类药物在中心药理学上存在重要差异。

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