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"Sung-Hye Park"

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"Sung-Hye Park"

Original Article

Brain disorders

Low-Frequency Repetitive Transcranial Magnetic Stimulation in the Early Subacute Phase of Stroke Enhances Angiogenic Mechanisms in Rats
Yookyung Lee, Byung-Mo Oh, Sung-Hye Park, Tai Ryoon Han
Ann Rehabil Med 2022;46(5):228-236.   Published online October 31, 2022
DOI: https://doi.org/10.5535/arm.22040
Objective
To characterize the repetitive transcranial magnetic stimulation (rTMS) induced changes in angiogenic mechanisms across different brain regions.
Methods
Seventy-nine adult male Sprague-Dawley rats were subjected to a middle cerebral artery occlusion (day 0) and then treated with 1-Hz, 20-Hz, or sham stimulation of their lesioned hemispheres for 2 weeks. The stimulation intensity was set to 100% of the motor threshold. The neurological function was assessed on days 3, 10, and 17. The infarct volume and angiogenesis were measured by histology, immunohistochemistry, Western blot, and real-time polymerase chain reaction (PCR) assays. Brain tissue was harvested from the ischemic core (IC), ischemic border zone (BZ), and contralateral homologous cortex (CH).
Results
Optical density of angiopoietin1 and synaptophysin in the IC was significantly greater in the low-frequency group than in the sham group (p=0.03 and p=0.03, respectively). The 1-Hz rTMS significantly increased the level of Akt phosphorylation in the BZ (p<0.05 vs. 20 Hz). Endothelial nitric oxide synthase phosphorylation was increased in the IC (p<0.05 vs. 20 Hz), BZ (p<0.05 vs. 20 Hz), and CH (p<0.05 vs. 20 Hz and p<0.05 vs. sham). Real-time PCR demonstrated that low-frequency stimulation significantly increased the transcriptional activity of the TIE2 gene in the IC (p<0.05).
Conclusion
Low-frequency rTMS of the ipsilesional hemisphere in the early subacute phase of stroke promotes the expression of angiogenic factors and related genes in the brain, particularly in the injured area.

Citations

Citations to this article as recorded by  
  • Intermittent theta-burst stimulation promotes neurovascular unit remodeling after ischemic stroke in a mouse model
    Jingjun Zhang, Ming Ding, Lu Luo, Dan Huang, Siyue Li, Shuying Chen, Yunhui Fan, Li Liu, Hongyu Xie, Gang Liu, Kewei Yu, Junfa Wu, Xiao Xiao, Yi Wu
    Neural Regeneration Research.2026; 21(8): 3598.     CrossRef
  • Neurovascular therapeutic potential of neuromodulation in Alzheimer’s disease
    Maria Luisa De Paolis, Claudio Zaccone, Marcello D’Amelio
    Neural Regeneration Research.2026; 21(10): 4876.     CrossRef
  • Evaluation of magnetic stimulation as a non-invasive technique in treating different causes of erectile dysfunction: a prospective cohort study
    Hasan El-Fakahany, Haythem Bassyouni, Sameh Fayek GamalEl Din, Mahmoud H. A. Montaser
    Basic and Clinical Andrology.2025;[Epub]     CrossRef
  • Novel emerging therapy for erectile dysfunction: efficacy and safety of flat magnetic stimulation
    Daniel Galimberti, Agustina Vila Echague, Ery A. Ko, Laura Pieri, Alessandra Comito, Irene Fusco, Tiziano Zingoni
    Archivio Italiano di Urologia e Andrologia.2024;[Epub]     CrossRef
  • Determining the Optimal Stimulation Sessions for TMS-Induced Recovery of Upper Extremity Motor Function Post Stroke: A Randomized Controlled Trial
    Yichen Lv, Jack Jiaqi Zhang, Kui Wang, Leilei Ju, Hongying Zhang, Yuehan Zhao, Yao Pan, Jianwei Gong, Xin Wang, Kenneth N. K. Fong
    Brain Sciences.2023; 13(12): 1662.     CrossRef
  • 9,462 View
  • 100 Download
  • 7 Web of Science
  • 5 Crossref
Case Report
Novel Mutation of the GNE Gene Presenting Atypical Mild Clinical Feature: A Korean Case Report
Young-Ah Choi, Sung-Hye Park, Youbin Yi, Keewon Kim
Ann Rehabil Med 2015;39(3):494-497.   Published online June 30, 2015
DOI: https://doi.org/10.5535/arm.2015.39.3.494

Glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase (GNE) myopathy is caused by mutations in GNE, a key enzyme in sialic acid biosynthesis. Here, we reported a case of GNE that presented with atypical mild clinical feature and slow progression. A 48-year-old female had a complaint of left foot drop since the age of 46 years. Electromyography (EMG) and muscle biopsy from left tibialis anterior muscle were compatible with myopathy. Genetic analysis led to the identification of c.1714G>C/c.527A>T compound heterozygous mutation, which is the second most frequent mutation in Japan as far as we know. Previous research has revealed that c.1714G>C/c.527A>T compound heterozygous mutation is a mild mutation as the onset of the disease is much later than the usual age of onset of GNE myopathy and the clinical course is slowly progressive. This was the first case report in Korea of the clinicopathological characteristics of GNE myopathy with GNE (c.1714G>C/c.527A>T compound heterozygous) mutation.

Citations

Citations to this article as recorded by  
  • Comparison of whole-body muscle imaging findings between GNE myopathy and other young adult-onset hereditary myopathies
    Pattira Boonsri, Suppakorn Yamutai, Pramot Tanutit, Jirakit Sattayapornpipat, Chariyawan Charalsawadi, Prut Koonalintip, Pornchai Sathirapanya, Suwanna Setthawatcharawanich, Rattana Leelawattana, Pat Korathanakhun, Vinay Kumar
    PLOS One.2026; 21(1): e0341031.     CrossRef
  • GNE myopathy with premature ovarian failure: Case report and review of the literature
    Shangyi Yang, Jine Yang
    Molecular Genetics and Metabolism Reports.2025; 44: 101240.     CrossRef
  • Recessive GNE Mutations in Korean Nonaka Distal Myopathy Patients with or without Peripheral Neuropathy
    Nasrin Tamanna, Byung Kwon Pi, Ah Jin Lee, Sumaira Kanwal, Byung-Ok Choi, Ki Wha Chung
    Genes.2024; 15(4): 485.     CrossRef
  • GNE myopathy (Nonaka myopathy)
    G.E. Rudenskaya, A.L. Chukhrova, O.P. Ryzhkova
    Annals of Clinical and Experimental Neurology.2019;[Epub]     CrossRef
  • GNE myopathy: from clinics and genetics to pathology and research strategies
    Oksana Pogoryelova, José Andrés González Coraspe, Nikoletta Nikolenko, Hanns Lochmüller, Andreas Roos
    Orphanet Journal of Rare Diseases.2018;[Epub]     CrossRef
  • Identification of a GNE homozygous mutation in a Han‐Chinese family with GNE myopathy
    Yuan Wu, Lamei Yuan, Yi Guo, Anjie Lu, Wen Zheng, Hongbo Xu, Yan Yang, Pengzhi Hu, Shaojuan Gu, Bingqi Wang, Hao Deng
    Journal of Cellular and Molecular Medicine.2018; 22(11): 5533.     CrossRef
  • GNE Myopathy in Turkish Sisters with a Novel Homozygous Mutation
    Gulden Diniz, Yaprak Secil, Serdar Ceylaner, Figen Tokucoglu, Sabiha Türe, Mehmet Celebisoy, Tülay Kurt İncesu, Galip Akhan
    Case Reports in Neurological Medicine.2016; 2016: 1.     CrossRef
  • 6,933 View
  • 35 Download
  • 6 Web of Science
  • 7 Crossref
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