Transcranial alternating current stimulation of the cerebellum (ctACS) is an emerging neuromodulation technique that can potentially be leveraged to treat neurological disorders and improve learning in healthy individuals. Yet, the effects of ctACS on the neuronal circuits of the cerebellum is elusive. We implanted carbon fiber bundle electrodes in the interpositus nucleus of the cerebellum and an array electrode on the posterior surface of the skull for stimulation in chronic rats. Multi-unit activities (MUA) were recorded from three unanesthetized and quietly resting animals during transcranial application of the current stimuli at various frequencies (10 Hz-300 Hz) and amplitudes as well as after harmaline induced tremors. A frequency-spectrum based method for assessing the modulation strength from the MUA was developed. The results show that the interpositus MUA can be modulated transcranially in a range of frequencies with a peak modulation around 50 Hz. This agrees with an earlier report in general [1] although the peak frequency is lower. This study demonstrates the feasibility of entraining the activity of the cerebellar nuclear cells in awake animals by transcranial application of AC stimulation, as well as the detection of harmaline induced tremor from the MUAs. Future research will be directed towards testing the ctACS effects on this animal model of essential tremor.
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http://dx.doi.org/10.1109/EMBC53108.2024.10782504 | DOI Listing |
Brain Struct Funct
March 2025
The School of Biomedical Sciences, Faculty of Medicine, The University of Queensland, Brisbane, QLD, 4072, Australia.
The Hippo signalling cascade is an evolutionarily conserved pathway critical for the development of numerous organ systems and is required for the development of many parts of the mammalian nervous system, including the cerebellum. The Hippo pathway converges, via the nuclear YAP/TAZ co-transcription factors, on transcription factors of the TEA Domain (TEAD) family (TEAD1-4) and promotes the expression of pro-proliferative genes. Despite the importance of TEAD function, our understanding of spatial and temporal expression of this family is limited, as is our understanding of which TEAD family members regulate Hippo-dependent organ development.
View Article and Find Full Text PDFEur J Neurol
March 2025
Department of Neurology and Institute of Neurology, Huashan Hospital, Fudan University, Shanghai, China.
Background And Purpose: Whether microglial activation plays an important role in the pathogenesis of autoimmune encephalitis (AE), such as anti-leucine-rich, glioma-inactivated-1 (LGI1) encephalitis, remains unknown. [F]-DPA714 PET targeting the translocator protein (TSPO) is a novel method to detect neuroinflammation via visualizing activated microglia. In this study, we aimed to investigate the application of [F]-DPA714 PET in anti-LGI1 encephalitis.
View Article and Find Full Text PDFMol Ther
March 2025
Department of Biochemistry and Molecular Biology, Universitat Autònoma de Barcelona, 08193 Bellaterra, Spain; Institute of Neurosciences, Universitat Autònoma de Barcelona, 08193 Bellaterra, Spain; UAB-VHIR Joint Unit, Vall d'Hebron Institut de Recerca, 08035 Barcelona, Spain; Biomedical Research Networking Center on Neurodegenerative Diseases (CIBERNED), Institute of Health Carlos III, 28031 Madrid, Spain. Electronic address:
Megalencephalic leukoencephalopathy with subcortical cysts (MLC) is an ultrarare, infantile-onset leukodystrophy characterized by white matter edema for which there is no treatment. More than 70% of diagnosed cases result from biallelic loss-of-function mutations in the astrocyte-specific gene MLC1, leading to early-onset macrocephaly, cerebellar ataxia, epilepsy, and mild cognitive decline. To develop a gene therapy for MLC, we administered an adeno-associated viral vector capable of crossing the murine blood-brain barrier, delivering the human MLC1 cDNA under the control of a human astrocyte-specific promoter, to 10-month-old Mlc1 mice.
View Article and Find Full Text PDFCroat Med J
February 2025
Abdul Aziz Mohamed Yusoff, Department of Neurosciences, School of Medical Sciences, Universiti Sains Malaysia, Health Campus, 16150 Kubang Kerian, Kelantan, Malaysia,
Chiari malformation type 1 (CM 1) is a rare and complex neurological condition. This congenital condition affects the lower posterior fossa, where the brain connects to the spinal cord. Although the exact cause of CM 1 remains unclear, genetic predisposition plays a considerable role in structural defects of the cerebellum.
View Article and Find Full Text PDFJ Headache Pain
March 2025
Harbin Medical University, Harbin, Heilongjiang, 150088, China.
Background: Vestibular migraine (VM) is a disorder characterized by recurrent episodes of dizziness or vertigo and is often accompanied by headache. The mechanisms underlying vestibular dysfunction and pain in VM remain unclear.
Methods: Chronic migraine (CM) and VM models were induced by NTG and kainic acid, respectively.
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