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Basic and Clinical research about High Frequency Oscillations (600 Hz)

Basic and Clinical research about High Frequency Oscillations (600 Hz)
高频振荡(600 Hz)的基础和临床研究
批准号:
13671568
负责人:
YAMAMOTO Ken
金额:
$2.5万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2001
资助国家:
日本
项目状态:
已结题
起止时间:
2001 至 2002

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中文摘要
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英文摘要
High frequency oscillations (HFOs) are a burst of spike-like wavelets separated from somatosensory evoked potentials (SEPs) by digital bandpass filters. SEPs are generated by pyramidal cells in the cerebral cortex, while HFOs reflect activities of inhibitory interneurons. One hypothesis states that anesthetic drugs initiate anesthetic action by, enhancement of gamma-aminobutyric acid (GABA) action. Therefore, we investigated the effect of sevoflurane and midazolam on SEPs and HFOs. In Wistar male rats, SEPs and HFOs evoked by direct electric stimulation of the ischiatic nerve were recorded in the soma tosensory cortex1. First, we examined whether ketamine infusion was an appropriate anesthetic method for this investigation. The analgesic effect of ketamine was certified by a planter test with heat radiation, while s bowing no change in the latencies and dose dependently increasing of the amplitudes of SEPs and HFOs. We concluded that ketamine infusion was acceptable2. Sevoflurane inhal … More ation prolonged the latency of SEPs, and caused characteristic biphasic changes of amplitude ; a low concentration of sevoflurane increased the amplitude of SEPs ; a high concentration of sevoflurane decreased the amplitude dose dependently. This phenomenon can be explained as follows : a low concentration of sevoflurane acts on only the cortical level GABA receptors, as a result, excitation of the pyramidal cells could reach the surface of the cortex without decay, because GABA stops diverting flow to dendrites. On the other hand, a high concentration of sevoflurane acts on not only the cortical but also thalamic GABA receptors, and it decreases the amount of afferent excitation3. Midazolam prolonged the latencies of SEPs and HFOs, and the length of prolonged latencies was equal at each peak. The amplitudes of early SEPs did not show any change, whereas those of late S EPs decreased. On the contrary, the amplitudes of all HFOs' peaks were markedly decreased. The action site of midazolam is assumed to be in the thalamus or below it Less
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