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Introduction: An objective and precise pain evaluation is of significant clinical value, and electroencephalography as a non-invasive physiological signal has been demonstrated to correlate with subjective pain perception. This study aimed to analyze the EEG changes in patients with lumbar disk herniation (LDH) under traditional Chinese medicine small needle knife and to further explore the feasibility of EEG as an indicator of pain assessment in patients with LDH.
Methods: This study conducted resting-state electroencephalography on 20 patients with LDH before and after treatment and on 20 healthy controls, respectively. Following the spectral analysis of the EEG signals with continuous wavelet transform, power ratios were extracted for four frequency bands (θ, α, β and γ). Significance tests were conducted within the LDH group and between the LDH and healthy controls, as well as correlation analyses of EEG characteristics with pain scales in four regions of interest.
Results: A significant reduction in subjective pain intensity was observed after small needle knife, with a 32.86 and 38.41% reduction in the Visual Analog Scale (VAS) and modified Japanese Orthopedic Association (mJOA) scores, respectively. Alpha accounted for a significantly higher of the four regions, while theta in the frontal, occipital and beta in the central were significantly lower. HC had fewer EEG oscillations in the theta band compared to LDH. The constructed alpha/beta features demonstrated a significant negative correlation with VAS in the frontal ( = -0.361, = 0.022) and parietal ( = -0.341, = 0.031), as well as with mJOA in the frontal ( = -0.416, = 0.007), central ( = -0.438, = 0.004), and parietal ( = -0.390, = 0.013) regions.
Conclusion: EEG power ratios showed significantly different results in LDH groups, and between patients and HC. The alpha/beta features of the frontal and parietal constructed in this study showed correlations with subjective pain scores and might serve as a biomarker of pain status in the short term in LDH.
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http://dx.doi.org/10.3389/fnins.2025.1507245 | DOI Listing |
Beilstein J Org Chem
August 2025
Department of Natural Sciences and Sustainable Resources, Institute of Organic Chemistry, BOKU University, 1190 Vienna, Austria.
Nonreducing disaccharides are prevalent in non-mammalian glycans and glycolipids, serving as pivotal structural components in mycobacterial glycans, microbial oligosaccharide and nucleoside antibiotics, as well as biologically active mimetics of bacterial pathogen-associated molecular patterns (PAMPs). As integral components of PAMPs, 1,1'-linked disaccharide-containing biomolecules play important roles in host-pathogen interactions, cellular signaling, and pathogenesis. Accessing complex biomolecules containing nonreducing disaccharides is often hindered by difficulties in isolating them from natural sources, which can result in impure or degraded products, particularly when sensitive functional groups are involved.
View Article and Find Full Text PDFPLoS Pathog
September 2025
Institut de Chimie des Substances Naturelles, CNRS, Université Paris-Saclay, Gif-sur-Yvette, France.
Respiratory syncytial virus (RSV), the most common cause of bronchiolitis and pneumonia in infants, elicits a remarkably weak innate immune response. This is partly due to type I interferon (IFN) antagonism by the non-structural RSV NS1 protein. It was recently suggested that NS1 could modulate host transcription via an interaction with the MED25 subunit of the Mediator complex.
View Article and Find Full Text PDFBiochem Biophys Res Commun
September 2025
Beamline Development and Application Section, Bhabha Atomic Research Centre, Mumbai, 400085, India. Electronic address:
The UPF0235 UniProt family proteins are conserved across archaea, bacteria, and eukaryotes; however, they remain functionally uncharacterized. Here, we report the high resolution (1.3 Å) crystal structure of UPF0235 protein (PF1765, UniProt: Q8U052) from Pyrococcus furiosus.
View Article and Find Full Text PDFInt J Biol Macromol
September 2025
Department of Biomedical Science, Acharya Narendra Dev College, University of Delhi, Govindpuri, Kalkaji, 110019, New Delhi, India. Electronic address:
Mycobacteriophage-encoded LysinB enzymes target mycolyl ester linkages in mycolyl-arabinogalactan-peptidoglycan of mycobacterium hosts and generally exhibit a globular architecture. Here, we present the structural and functional characterization of a novel Mycobacterium fortuitum prophage-encoded modular LysinB (LysinB_MF), which contains the α/β hydrolase domain and a distinct peptidoglycan-binding domain (PGBD). The enzyme's active site features the conserved Ser-Asp-His catalytic triad common to esterases and forms a funnel-like topology.
View Article and Find Full Text PDFCell Rep
September 2025
Shanghai Institute of Hematology, State Key Laboratory of Medical Genomics, National Research Center for Translational Medicine at Shanghai, Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China; Pôle de Recherches Sino-Français en Science du Vivant et Gé
RNA helicase DDX3X is generally implicated in inflammasome activation and anti-viral responses. We characterize the common features of scattered DDX3X mutations in lymphoid cancers using molecular dynamics simulation and crystallization, thereby demonstrating their crucial role in Epstein-Barr virus (EBV) lytic gene-driven oncogenic processes. The DDX3X mutation is significantly related to impaired stimulator of interferon genes (STING)/ interferon regulatory factor 7 (IRF-7)/interferon (IFN)-α/β-mediated innate immunity, overexpression of EBV lytic gene BNLF2b, and increased formation of R-loops.
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