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大鼠海马切片中同步γ振荡的破坏:麻醉药物作用的共同机制。

Disruption of synchronous gamma oscillations in the rat hippocampal slice: a common mechanism of anaesthetic drug action.

作者信息

Faulkner H J, Traub R D, Whittington M A

机构信息

Biomedical Sciences Division, Imperial College School of Medicine, London.

出版信息

Br J Pharmacol. 1998 Oct;125(3):483-92. doi: 10.1038/sj.bjp.0702113.

Abstract
  1. At the molecular level much progress has been made towards elucidating the mechanisms of action of general and dissociative anaesthetics. However, little is known about how these molecular actions may lead to disruption of cognitive function. 2. A promising physiological correlate of cognitive function is the ability of spatially separate areas of the brain to synchronize firing patterns via mutual inhibitory, gamma-frequency (20-80 Hz) electrical oscillations. Here we examine the effects of five different anaesthetic/hypnotic agents with different primary mechanisms of action on these oscillations in the hippocampus. 3. Gamma oscillations were elicited simultaneously at two sites at either end of area CAI by tetanic stimulation. Such oscillations are synchronous between these areas even when separated by up to c. 4 mm in control conditions. 4. Agents which act directly on GABA(A) receptor-mediated inhibition had different effects on synchronous gamma oscillations. Thiopental (10-200 microm) markedly disrupted the oscillation and resulting synchrony whereas the benzodiazepines diazepam and temazepam (0.05-1.0 microM) had little effect. 5. The opiate morphine (10-200 microM) and dissociative agent ketamine (10-100 microM) had a different profile of effects on gamma oscillations. However, as with thiopental, both agents markedly disrupted between site synchrony. These three agents demonstrated this effect at aqueous concentrations relevant to anaesthetic ED50. 6. Using the hippocampus as a model neuronal network we propose that, despite differing primary mechanisms of action, anaesthetics may disrupt cognitive function by interfering with the mechanism of generation of synchronous firing patterns between spatially separate areas of the brain.
摘要
  1. 在分子水平上,人们在阐明全身麻醉药和解离麻醉药的作用机制方面已经取得了很大进展。然而,对于这些分子作用如何导致认知功能障碍却知之甚少。2. 认知功能一个有前景的生理相关因素是大脑中空间上分离的区域通过相互抑制的γ频率(20 - 80赫兹)电振荡来同步放电模式的能力。在此,我们研究了五种具有不同主要作用机制的麻醉/催眠药物对海马体中这些振荡的影响。3. 通过强直刺激在CA1区两端的两个位点同时诱发γ振荡。即使在对照条件下相隔多达约4毫米,这些区域之间的这种振荡也是同步的。4. 直接作用于GABA(A)受体介导的抑制作用的药物对同步γ振荡有不同影响。硫喷妥钠(10 - 200微摩尔)显著破坏振荡及由此产生的同步性,而苯二氮䓬类药物地西泮和替马西泮(0.05 - 1.0微摩尔)影响很小。5. 阿片类药物吗啡(10 - 200微摩尔)和解离性药物氯胺酮(10 - 100微摩尔)对γ振荡有不同的作用模式。然而,与硫喷妥钠一样,这两种药物都显著破坏位点间的同步性。这三种药物在与麻醉ED50相关的水溶液浓度下都表现出这种作用。6. 以海马体作为模型神经元网络,我们提出,尽管作用的主要机制不同,但麻醉药可能通过干扰大脑中空间上分离区域之间同步放电模式的产生机制来破坏认知功能。

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