Arena Alessandro, Lamanna Jacopo, Gemma Marco, Ripamonti Maddalena, Ravasio Giuliano, Zimarino Vincenzo, De Vitis Assunta, Beretta Luigi, Malgaroli Antonio
Università Vita-Salute San Raffaele, Milan, Italy.
Neurobiology of Learning Unit, Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy.
J Physiol. 2017 Jan 1;595(1):321-339. doi: 10.1113/JP272215. Epub 2016 Aug 13.
The mechanisms of action of anaesthetics on the living brain are still poorly understood. In this respect, the analysis of the differential effects of anaesthetics on spontaneous and sensory-evoked cortical activity might provide important and novel cues. Here we show that the anaesthetic sevoflurane strongly silences the brain but potentiates in a dose- and frequency-dependent manner the cortical visual response. Such enhancement arises from a linear scaling by sevoflurane of the power-law relation between light intensity and the cortical response. The fingerprint of sevoflurane action suggests that circuit silencing can boost linearly synaptic responsiveness presumably by scaling the number of responding units and/or their correlation following a sensory stimulation.
General anaesthetics, which are expected to silence brain activity, often spare sensory responses. To evaluate differential effects of anaesthetics on spontaneous and sensory-evoked cortical activity, we characterized their modulation by sevoflurane and propofol. Power spectra and the bust-suppression ratio from EEG data were used to evaluate anaesthesia depth. ON and OFF cortical responses were elicited by light pulses of variable intensity, duration and frequency, during light and deep states of anaesthesia. Both anaesthetics reduced spontaneous cortical activity but sevoflurane greatly enhanced while propofol diminished the ON visual response. Interestingly, the large potentiation of the ON visual response by sevoflurane was found to represent a linear scaling of the encoding mechanism for light intensity. To the contrary, the OFF cortical visual response was depressed by both anaesthetics. The selective depression of the OFF component by sevoflurane could be converted into a robust potentiation by the pharmacological blockade of the ON pathway, suggesting that the temporal order of ON and OFF responses leads to a depression of the latter. This hypothesis agrees with the finding that the enhancement of the ON response was converted into a depression by increasing the frequency of light-pulse stimulation from 0.1 to 1 Hz. Overall, our results support the view that inactivity-dependent modulation of cortical circuits produces an increase in their responsiveness. Among the implications of our findings, the silencing of cortical circuits can boost linearly the cortical responsiveness but with negative impact on their frequency transfer and with a loss of the information content of the sensory signal.
麻醉剂对活体大脑的作用机制仍未得到充分理解。在这方面,分析麻醉剂对自发和感觉诱发皮质活动的不同影响可能会提供重要且新颖的线索。我们在此表明,麻醉剂七氟醚能强烈抑制大脑活动,但会以剂量和频率依赖的方式增强皮质视觉反应。这种增强源于七氟醚对光强度与皮质反应之间幂律关系的线性缩放。七氟醚作用的特征表明,回路抑制可能通过缩放响应单元的数量和/或感觉刺激后它们的相关性来线性增强突触反应性。
全身麻醉剂预期会抑制大脑活动,但通常会保留感觉反应。为了评估麻醉剂对自发和感觉诱发皮质活动的不同影响,我们对七氟醚和丙泊酚对其的调节作用进行了表征。利用脑电图数据的功率谱和爆发抑制率来评估麻醉深度。在浅麻醉和深麻醉状态下,通过可变强度、持续时间和频率的光脉冲诱发皮质的开反应和关反应。两种麻醉剂都降低了自发皮质活动,但七氟醚极大地增强了开视觉反应,而丙泊酚则使其减弱。有趣的是,七氟醚对开视觉反应的大幅增强被发现代表了光强度编码机制的线性缩放。相反,两种麻醉剂都抑制了皮质关视觉反应。七氟醚对关成分的选择性抑制可通过对开通路的药理学阻断转化为强烈的增强,这表明开反应和关反应的时间顺序导致了后者的抑制。这一假设与以下发现一致:通过将光脉冲刺激频率从0.1赫兹增加到1赫兹,开反应的增强会转化为抑制。总体而言,我们的结果支持这样一种观点,即皮质回路的非活动依赖性调节会导致其反应性增加。我们研究结果的影响之一是,皮质回路的抑制可以线性增强皮质反应性,但对其频率传递有负面影响,并导致感觉信号信息内容的丢失。