{"title":"Investigation of in vitro neuronal activity processing using a CMOS-integrated ZrO2(Y)-based memristive crossbar","authors":"M.N. Koryazhkina, A.V. Lebedeva, D.D. Pakhomova, I.N. Antonov, V.V. Razin, E.D. Budylina, A.I. Belov, A.N. Mikhaylov, A.A. Konakov","doi":"10.1016/j.chaos.2024.115959","DOIUrl":null,"url":null,"abstract":"The influence of the epileptiform neuronal activity on the response of a CMOS-integrated ZrO<ce:inf loc=\"post\">2</ce:inf>(Y)-based memristive crossbar and its conductivity was studied. Epileptiform neuronal activity was obtained <ce:italic>in vitro</ce:italic> in the hippocampal slices of laboratory mice using 4-aminopyridine experimental model. Synaptic plasticity of the memristive crossbar induced by epileptiform neuronal activity pulses was detected. Qualitatively, the results obtained in the case of normal (without pathologies) and epileptiform neuronal activity with and without noise coincide. For quantitative analysis, the value of the relative change in synaptic weight has been calculated for such important biological mechanisms of synapses as paired-pulse facilitation/depression, post-tetanic potentiation/depression, and long-term potentiation/depression. It has been shown that average value of the relative change in synaptic weight and its scatter are smaller mainly in the case of epileptiform neuronal activity pulses. An effect of the influence of noise included in the neuronal activity was found, which consists in the fact that the current response of the memristive crossbar is smaller in the presence of noise. The results of this study can be used in the development of new generation hardware-implemented computing devices with high performance and energy efficiency for the tasks of restorative medicine and robotics. In particular, using these results, neurohybrid devices can be developed for processing epileptiform activity in real time and for its suppression.","PeriodicalId":9764,"journal":{"name":"Chaos Solitons & Fractals","volume":"54 1","pages":""},"PeriodicalIF":5.3000,"publicationDate":"2024-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chaos Solitons & Fractals","FirstCategoryId":"100","ListUrlMain":"https://doi.org/10.1016/j.chaos.2024.115959","RegionNum":1,"RegionCategory":"数学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATHEMATICS, INTERDISCIPLINARY APPLICATIONS","Score":null,"Total":0}
引用次数: 0
Abstract
The influence of the epileptiform neuronal activity on the response of a CMOS-integrated ZrO2(Y)-based memristive crossbar and its conductivity was studied. Epileptiform neuronal activity was obtained in vitro in the hippocampal slices of laboratory mice using 4-aminopyridine experimental model. Synaptic plasticity of the memristive crossbar induced by epileptiform neuronal activity pulses was detected. Qualitatively, the results obtained in the case of normal (without pathologies) and epileptiform neuronal activity with and without noise coincide. For quantitative analysis, the value of the relative change in synaptic weight has been calculated for such important biological mechanisms of synapses as paired-pulse facilitation/depression, post-tetanic potentiation/depression, and long-term potentiation/depression. It has been shown that average value of the relative change in synaptic weight and its scatter are smaller mainly in the case of epileptiform neuronal activity pulses. An effect of the influence of noise included in the neuronal activity was found, which consists in the fact that the current response of the memristive crossbar is smaller in the presence of noise. The results of this study can be used in the development of new generation hardware-implemented computing devices with high performance and energy efficiency for the tasks of restorative medicine and robotics. In particular, using these results, neurohybrid devices can be developed for processing epileptiform activity in real time and for its suppression.
期刊介绍:
Chaos, Solitons & Fractals strives to establish itself as a premier journal in the interdisciplinary realm of Nonlinear Science, Non-equilibrium, and Complex Phenomena. It welcomes submissions covering a broad spectrum of topics within this field, including dynamics, non-equilibrium processes in physics, chemistry, and geophysics, complex matter and networks, mathematical models, computational biology, applications to quantum and mesoscopic phenomena, fluctuations and random processes, self-organization, and social phenomena.