Research on Brain Networks of Human Balance Based on Phase Estimation Synchronization.

Phase synchronization serves as an effective method for analyzing the synchronization of electroencephalogram (EEG) signals among brain regions and the dynamic changes of the brain. The purpose of this paper is to study the construction of the functional brain network (FBN) based on phase synchronization, with a special focus on neural processes related to human balance regulation. This paper designed four balance paradigms of different difficulty by blocking vision or proprioception and collected 19-channel EEG signals. Firstly, the EEG sequences are segmented by sliding windows. The phase-locking value (PLV) of core node pairs serves as the phase-screening index to extract the valid data segments, which are recombined into new EEG sequences. Subsequently, the multichannel weighted phase lag index (wPLI) is calculated based on the new EEG sequences to construct the FBN. The experimental results show that due to the randomness of the time points of body balance adjustment, the degree of phase synchronization of the datasets screened by PLV is more obvious, improving the effective information expression of the subsequent EEG data segments. The FBN topological structures of the wPLI show that the connectivity of various brain regions changes structurally as the difficulty of human balance tasks increases. The frontal lobe area is the core brain region for information integration. When vision or proprioception is obstructed, the EEG synchronization level of the corresponding occipital lobe area or central area decreases. The synchronization level of the frontal lobe area increases, which strengthens the synergistic effect among the brain regions and compensates for the imbalanced response caused by the lack of sensory information. These results show the brain regional characteristics of the process of human balance regulation under different balance paradigms, providing new insights into endogenous neural mechanisms of standing balance and methods of constructing brain networks.

Compound 225# inhibits the proliferation of human colorectal cancer cells by promoting cell cycle arrest and apoptosis induction.

Colorectal cancer (CRC) ranks as the second leading cause of cancer­related death worldwide due to its aggressive nature. After surgical resection, >50% of patients with CRC require adjuvant therapy. As a result, eradicating cancer cells with medications is a promising method to treat patients with CRC. In the present study, a novel compound was synthesized, which was termed compound 225#. The inhibitory activity of compound 225# against CRC was determined by MTT assay, EdU fluorescence labeling and colony formation assay; the effects of compound 225# on the cell cycle progression and apoptosis of CRC cells were detected by flow cytometry and western blotting; and the changes in autophagic flux after the administration of compound 225# were detected using the double fluorescence fusion protein mCherry­GFP­LC3B and western blotting. The results demonstrated that compound 225# exhibited antiproliferative properties, inhibiting the proliferation and expansion of CRC cell lines in a time­ and dose­dependent manner. Furthermore, compound 225# triggered G2/M cell cycle arrest by influencing the expression of cell cycle regulators, such as CDK1, cyclin A1 and cyclin B1, which is also closely related to the activation of DNA damage pathways. The cleavage of PARP and increased protein expression levels of PUMA suggested that apoptosis was triggered after treatment with compound 225#. Moreover, the increase in LC3­II expression and stimulation of autophagic flux indicated the activation of an autophagy pathway. Notably, compound 225# induced autophagy, which was associated with endoplasmic reticulum (ER) stress. In accordance with the in vitro findings, the in vivo results demonstrated that compound 225# effectively inhibited the growth of HCT116 tumors in mice without causing any changes in their body weight. Collectively, the present results demonstrated that compound 225# not only inhibited proliferation and promoted G2/M­phase cell cycle arrest and apoptosis, but also initiated cytoprotective autophagy in CRC cells by activating ER stress pathways. Taken together, these findings provide an experimental basis for the evaluation of compound 225# as a novel potential medication for CRC treatment.

Impacts of multiple environmental factors on soil bacterial community assembly in heavy metal polluted paddy fields.

Soil microorganisms play pivotal roles in driving essential biogeochemical processes in terrestrial ecosystems, and they are sensitive to heavy metal pollution. However, our understanding of multiple environmental factors interaction in heavy metal polluted paddy fields to shape microbial community assembly remain limited. In the current study, we used 16S rRNA amplicon sequencing to characterize the microbial community composition in paddy soils collected from a typical industry town in Taihu region, eastern China. The results revealed that Cd and Pb were the major pollutant, and Proteobacteria, Acidobacteria and Chloroflexi were the dominate indigenous bacterial phyla. Linear regression and random forest analysis demonstrated that soil pH was the most important predictor of bacterial diversity. Mantel analysis showed that bacterial community structure was mainly driven by pH, CEC, silt, sand, AK, total Cd and DTPA-Cd. The constructed bacterial co-occurrence network, utilizing a random matrix theory-based approach, exhibited non-random with scale-free and modularity features. The major modules within the networks also showed significant correlations with soil pH. Overall, our study indicated that soil physiochemical properties made predominant contribution to bacterial community diversity, structure and their association in Cd/Pb polluted paddy fields. These findings expand our knowledge of the key environmental drivers and co-occurrence patterns of bacterial community in polluted paddy fields.