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Effect of Apomorphine on the Wakefulness—Sleep Cycle of the Common Frog Rana temporaria

机译:阿扑吗啡对普通蛙蛙温度觉觉-睡眠周期的影响

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摘要

This work considers effects of introduction into spinal lymphatic sac of dopamine agonist— apomorphine (APO)—at doses of 0.1, 1.0, 2.0, and 4.0 mg/kg body weight on the common frog wakefulness—sleep cycle (WSC). Usually the frog WSC is represented by wakefulness and three types of passive-protective behavior: the immobility states of the type of catalepsy, catatonia, and cataplexy that are characterized by high thresholds of arousal and by different (corresponding to the name) skeletal muscle tones. These immobility forms are considered as homologues of mammalian stress-reaction, hibernation, and sleep. Low apomorphine doses produced in WSC a marked decrease of portion of wakefulness and an increase of the immobility state of the catalepsy type; high doses, on the contrary, initially promoted in CNS an increase of wakefulness and the state of catalepsy by demonstrating thereby its stressogenic action; after this, in WSC there increased the portion of the sleep-like immobility state of the catalepsy type that is considered a functional homologue of sleep of homoiothermal animals. In spectra of electrograms of the frog telencephalon the representation of waves of the delta diapason rose. Taking into account that the states of catalepsy and cataplexy in frogs are under control of anterior hypothalamus, it can be suggested that manifestations of cataplexy (sleep) in frog are due to the low level of dopaminergic activity, whereas manifestations of catalepsy (the homologue of stress reaction) are due to the high dopamine content in the anterior hypothalamic structures. Comparative analysis of changes in WSC of amphibians and mammals in response to administration of dopamine and its agonists allows thinking that the role of the dopaminergic neurotransmitter system in regulation of the vertebrate WSC certainly consists in that the low level of activity of this system facilitates development of sleep (catalepsy), whereas the high level provides reaction of arousal and is actively included in the system providing stress-reaction.
机译:这项工作考虑了以0.1、1.0、2.0和4.0 mg / kg体重的剂量将多巴胺激动剂阿扑吗啡(APO)引入脊髓淋巴囊对普通青蛙的觉醒-睡眠周期(WSC)的影响。通常,青蛙WSC表现为清醒和三种被动保护行为:僵直,僵直和瘫痪类型的固定状态,其特征是唤醒阈值高,并且骨骼肌音调不同(对应于名称) 。这些固定形式被认为是哺乳动物应激反应,冬眠和睡眠的同系物。 WSC中产生的低阿扑吗啡剂量明显降低了僵住症类型的清醒部分并增加了不动状态;相反,高剂量最初通过证明其引起压力的作用而在中枢神经系统中促进了清醒和僵直状态的增加;此后,在WSC中,僵尸症类型的睡眠样不动状态的比例增加了,这被认为是同温动物睡眠的功能同源物。在青蛙末脑的电描记图谱中,三角洲扩散的波的表示上升了。考虑到青蛙的僵直和瘫痪状态处于下丘脑前部的控制之下,因此可以认为青蛙的僵直(睡眠)表现是由于多巴胺能活动水平低下,而僵直的表现是应力反应)是由于下丘脑前部结构中的多巴胺含量高。比较分析两栖动物和哺乳动物的WSC响应多巴胺及其激动剂的给药变化,可以认为多巴胺能神经递质系统在调节脊椎动物WSC中的作用肯定在于该系统的低水平活性促进了WSC的发育。睡眠(僵直),而高水平会引起唤醒反应,并积极地包含在系统中,从而产生压力反应。

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