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1.
Physiol Meas ; 44(12)2023 Dec 18.
Article in English | MEDLINE | ID: mdl-38029444

ABSTRACT

Objective. Due to individual differences, it is greatly challenging to realize the multiple types of emotion identification across subjects.Approach. In this research, a hierarchical feature optimization method is proposed in order to represent emotional states effectively based on peripheral physiological signals. Firstly, sparse learning combined with binary search is employed to achieve feature selection of single signals. Then an improved fast correlation-based filter is proposed to implement fusion optimization of multi-channel signal features. Aiming at overcoming the limitations of the support vector machine (SVM), which uses a single kernel function to make decisions, the multi-kernel function collaboration strategy is proposed to improve the classification performance of SVM.Main results. The effectiveness of the proposed method is verified on the DEAP dataset. Experimental results show that the proposed method presents a competitive performance for four cross-subject  types of emotion identification with an accuracy of 84% (group 1) and 85.07% (group 2). Significance. The proposed model with hierarchical feature optimization and SVM with multi-kernel function collaboration demonstrates superior emotion recognition accuracy compared to state-of-the-art techniques. In addition, the analysis based on DEAP dataset composition characteristics presents a novel perspective to explore the emotion recognition issue more objectively and comprehensively.


Subject(s)
Emotions , Support Vector Machine , Humans , Emotions/physiology , Algorithms
2.
Glia ; 69(7): 1709-1722, 2021 07.
Article in English | MEDLINE | ID: mdl-33660902

ABSTRACT

Oligodendroglial lineage cells go through a series of morphological changes before myelination. Prior to myelination, cell processes and membrane structures enlarge by approximately 7,000 times, which is required to support axonal wrapping and myelin segment formation. Failure of these processes leads to maldevelopment and impaired myelination. Quetiapine, an atypical antipsychotic drug, was proved to promote oligodendroglial differentiation and (re)myelination, pending detailed effects and regulatory mechanism. In this study, we showed that quetiapine promotes morphological maturation of oligodendroglial lineage cells and myelin segment formation, and a short-term quetiapine treatment is sufficient to induce these changes. To uncover the underlying mechanism, we examined the effect of quetiapine on the Oligodendrocyte transcription factor 1 (Olig1). We found that quetiapine upregulates Olig1 expression level and promotes nuclear Olig1 translocation to the cytosol, where it functions not as a transcription modulator, but in a way that highly correlates with oligodendrocyte morphological transformation. In addition, quetiapine treatment reverses the negative regulatory effect of the Olig1-regulated G protein-coupled receptor 17 (GPR17) on oligodendroglial morphological maturation. Our results demonstrate that quetiapine enhances oligodendroglial differentiation and myelination by promoting cell morphological transformation. This would shed light on the orchestration of oligodendroglia developmental mechanisms, and provides new targets for further therapeutic research.


Subject(s)
Basic Helix-Loop-Helix Transcription Factors , Oligodendroglia , Axons/metabolism , Basic Helix-Loop-Helix Transcription Factors/metabolism , Cell Differentiation/physiology , Myelin Sheath/metabolism , Oligodendroglia/metabolism , Quetiapine Fumarate/metabolism , Quetiapine Fumarate/pharmacology
3.
Plant Sci ; 252: 290-299, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27717465

ABSTRACT

Drought stress is a major factor limiting wheat growth and productivity. Late embryogenesis abundant (LEA) proteins are tolerant to water-related stress. To reveal the regulatory mechanisms of LEA proteins under drought stress, we cloned a novel group 3 LEA gene, namely, TaDlea3, from wheat (Triticum aestivum L.) Shaanhe 6. Subcellular localization assay showed that TaDlea3 protein accumulated in the cytoplasm. Quantitative real-time polymerase chain reaction results revealed that TaDlea3 expression was induced by drought stress. Western blot results indicated that TaDlea3 protein expression gradually increased with drought stress during four different developmental stages. Under normal conditions, no obvious phenotype difference was observed between the transgenic and wild-type seedlings. Meanwhile, the overexpression of TaDlea3 in Arabidopsis resulted in enhanced tolerance to drought stress, as determined by the assessment of antioxidant enzyme activities. Our results provide a basis for highly detailed functional analyses of LEA proteins and offer a promising approach for improving the tolerances of wheat cultivars to drought stress through genetic engineering.


Subject(s)
Plant Proteins/physiology , Stress, Physiological/genetics , Triticum/physiology , Antioxidants/metabolism , Arabidopsis/genetics , Cloning, Molecular , Droughts , Gene Expression Regulation, Plant , Phylogeny , Plant Proteins/genetics , Plant Proteins/metabolism , Plants, Genetically Modified/physiology , Protoplasts/metabolism , RNA, Messenger/metabolism , Real-Time Polymerase Chain Reaction , Seedlings/genetics , Seedlings/growth & development , Seedlings/metabolism , Sequence Analysis, Protein , Nicotiana/genetics , Nicotiana/metabolism , Triticum/genetics , Triticum/growth & development
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