{"title":"振荡经颅电刺激和调幅频率决定了光幻视的数量特征。","authors":"Che-Yi Hsu, Tzu-Ling Liu, Chi-Hung Juan","doi":"10.1111/ejn.16658","DOIUrl":null,"url":null,"abstract":"<p>Previous research demonstrated that transcranial alternating current stimulation (tACS) can induce phosphene perception. However, tACS involves rhythmic changes in the electric field and alternating polarity (excitatory vs. inhibitory phases), leaving the precise mechanism behind phosphene perception unclear. To disentangle the effects of rhythmic changes from those of alternating polarity, this study employs oscillatory transcranial direct current stimulation (otDCS), in which the current oscillation remains confined to either a positive or negative polarity, thereby eliminating the influence of polarity switching. We applied scalp electrical stimulations using both polarity-switching (tACS) and non-polarity-switching (otDCS) methods, with anodal or cathodal polarities, targeting the occipital lobe. All stimulations were performed using sinusoidal or amplitude modulation (AM) waveforms at threshold or suprathreshold intensities. Our results show that tACS results in faster response times compared to cathodal otDCS, but not anodal otDCS, while anodal otDCS elicits greater brightness perception than both cathodal otDCS and tACS. Additionally, AM frequency induced a higher threshold than the sinusoidal frequency, and response times were slower in the AM condition across all positive, negative, and polarity-switching stimulations. However, stimulation intensity in the anodal AM condition could influence speed ratings, unlike in cathodal or tACS conditions. Our findings reveal that both tACS and otDCS induce phosphenes, with significant differences between polarities and current oscillation types, indicating that both mechanisms are critical in phosphene induction. This study provides evidence linking phosphene occurrence to oscillatory current activity and highlights the robustness and impact of AM coding in visual perception.</p>","PeriodicalId":11993,"journal":{"name":"European Journal of Neuroscience","volume":"61 1","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11708813/pdf/","citationCount":"0","resultStr":"{\"title\":\"Oscillatory Transcranial Electrical Stimulation and the Amplitude-Modulated Frequency Dictate the Quantitative Features of Phosphenes\",\"authors\":\"Che-Yi Hsu, Tzu-Ling Liu, Chi-Hung Juan\",\"doi\":\"10.1111/ejn.16658\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Previous research demonstrated that transcranial alternating current stimulation (tACS) can induce phosphene perception. However, tACS involves rhythmic changes in the electric field and alternating polarity (excitatory vs. inhibitory phases), leaving the precise mechanism behind phosphene perception unclear. To disentangle the effects of rhythmic changes from those of alternating polarity, this study employs oscillatory transcranial direct current stimulation (otDCS), in which the current oscillation remains confined to either a positive or negative polarity, thereby eliminating the influence of polarity switching. We applied scalp electrical stimulations using both polarity-switching (tACS) and non-polarity-switching (otDCS) methods, with anodal or cathodal polarities, targeting the occipital lobe. All stimulations were performed using sinusoidal or amplitude modulation (AM) waveforms at threshold or suprathreshold intensities. Our results show that tACS results in faster response times compared to cathodal otDCS, but not anodal otDCS, while anodal otDCS elicits greater brightness perception than both cathodal otDCS and tACS. Additionally, AM frequency induced a higher threshold than the sinusoidal frequency, and response times were slower in the AM condition across all positive, negative, and polarity-switching stimulations. However, stimulation intensity in the anodal AM condition could influence speed ratings, unlike in cathodal or tACS conditions. Our findings reveal that both tACS and otDCS induce phosphenes, with significant differences between polarities and current oscillation types, indicating that both mechanisms are critical in phosphene induction. This study provides evidence linking phosphene occurrence to oscillatory current activity and highlights the robustness and impact of AM coding in visual perception.</p>\",\"PeriodicalId\":11993,\"journal\":{\"name\":\"European Journal of Neuroscience\",\"volume\":\"61 1\",\"pages\":\"\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-01-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11708813/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European Journal of Neuroscience\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/ejn.16658\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/ejn.16658","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
Oscillatory Transcranial Electrical Stimulation and the Amplitude-Modulated Frequency Dictate the Quantitative Features of Phosphenes
Previous research demonstrated that transcranial alternating current stimulation (tACS) can induce phosphene perception. However, tACS involves rhythmic changes in the electric field and alternating polarity (excitatory vs. inhibitory phases), leaving the precise mechanism behind phosphene perception unclear. To disentangle the effects of rhythmic changes from those of alternating polarity, this study employs oscillatory transcranial direct current stimulation (otDCS), in which the current oscillation remains confined to either a positive or negative polarity, thereby eliminating the influence of polarity switching. We applied scalp electrical stimulations using both polarity-switching (tACS) and non-polarity-switching (otDCS) methods, with anodal or cathodal polarities, targeting the occipital lobe. All stimulations were performed using sinusoidal or amplitude modulation (AM) waveforms at threshold or suprathreshold intensities. Our results show that tACS results in faster response times compared to cathodal otDCS, but not anodal otDCS, while anodal otDCS elicits greater brightness perception than both cathodal otDCS and tACS. Additionally, AM frequency induced a higher threshold than the sinusoidal frequency, and response times were slower in the AM condition across all positive, negative, and polarity-switching stimulations. However, stimulation intensity in the anodal AM condition could influence speed ratings, unlike in cathodal or tACS conditions. Our findings reveal that both tACS and otDCS induce phosphenes, with significant differences between polarities and current oscillation types, indicating that both mechanisms are critical in phosphene induction. This study provides evidence linking phosphene occurrence to oscillatory current activity and highlights the robustness and impact of AM coding in visual perception.
期刊介绍:
EJN is the journal of FENS and supports the international neuroscientific community by publishing original high quality research articles and reviews in all fields of neuroscience. In addition, to engage with issues that are of interest to the science community, we also publish Editorials, Meetings Reports and Neuro-Opinions on topics that are of current interest in the fields of neuroscience research and training in science. We have recently established a series of ‘Profiles of Women in Neuroscience’. Our goal is to provide a vehicle for publications that further the understanding of the structure and function of the nervous system in both health and disease and to provide a vehicle to engage the neuroscience community. As the official journal of FENS, profits from the journal are re-invested in the neuroscientific community through the activities of FENS.